EMBRYOPSIDA Pirani & Prado

Gametophyte dominant, independent, multicellular, initially ±globular, not motile, branched; showing gravitropism; acquisition of phenylalanine lysase* [PAL], flavonoid synthesis*, microbial terpene synthase-like genes +, triterpenoids produced by CYP716 enzymes, CYP73 and phenylpropanoid metabolism [development of phenolic network], xyloglucans in primary cell wall, side chains charged; plant poikilohydrous [protoplasm dessication tolerant], ectohydrous [free water outside plant physiologically important]; thalloid, leafy, with single-celled apical meristem, tissues little differentiated, rhizoids +, unicellular; chloroplasts several per cell, pyrenoids 0; glycolate metabolism in leaf peroxisomes [glyoxysomes]; centrioles/centrosomes in vegetative cells 0, microtubules with γ-tubulin along their lengths [?here], interphase microtubules form hoop-like system; metaphase spindle anastral, predictive preprophase band + [with microtubules and F-actin; where new cell wall will form], phragmoplast + [cell wall deposition centrifugal, from around the anaphase spindle], plasmodesmata +; antheridia and archegonia +, jacketed*, surficial; mblepharoplast +, centrioles develop de novo, bicentriole pair coaxial, separate at midpoint, centrioles rotate, associated with basal bodies of cilia, multilayered structure + [4 layers: L1, L4, tubules; L2, L3, short vertical lamellae] (0), spline + [tubules from L1 encircling spermatid], basal body 200-250 nm long, associated with amorphous electron-dense material, microtubules in basal end lacking symmetry, stellate array of filaments in transition zone extended, axonemal cap 0 [microtubules disorganized at apex of cilium]; male gametes [spermatozoids] with a left-handed coil, cilia 2, lateral; oogamy; sporophyte +*, multicellular, growth 3-dimensional*, cuticle +*, plane of first cell division transverse [with respect to long axis of archegonium/embryo sac], sporangium and upper part of seta developing from epibasal cell [towards the archegonial neck, exoscopic], with at least transient apical cell [?level], initially surrounded by and dependent on gametophyte, placental transfer cells +, in both sporophyte and gametophyte, wall ingrowths develop early; suspensor/foot +, cells at foot tip somewhat haustorial; sporangium +, single, terminal, dehiscence longitudinal; meiosis sporic, monoplastidic, MTOC [MTOC = microtubule organizing centre] associated with plastid, sporocytes 4-lobed, cytokinesis simultaneous, preceding nuclear division, quadripolar microtubule system +; wall development both centripetal and centrifugal, 1000 spores/sporangium, sporopollenin in the spore wall* laid down in association with trilamellar layers [white-line centred lamellae; tripartite lamellae]; plastid transmission maternal; nuclear genome [1C] <1.4 pg, main telomere sequence motif TTTAGGG, KNOX1 and KNOX2 [duplication] and LEAFY genes present, ethylene involved in cell elongation; chloroplast genome with close association between trnLUAA and trnFGAA genes [precursors for starch synthesis], tufA, minD, minE genes moved to nucleus; mitochondrial trnS(gcu) and trnN(guu) genes +.

Many of the bolded characters in the characterization above are apomorphies of more or less inclusive clades of streptophytes along the lineage leading to the embryophytes, not apomorphies of crown-group embryophytes per se.

All groups below are crown groups, nearly all are extant. Characters mentioned are those of the immediate common ancestor of the group, [] contains explanatory material, () features common in clade, exact status unclear.


Sporophyte well developed, branched, branching dichotomous, potentially indeterminate; hydroids +; stomata on stem; sporangia several, terminal; spore walls not multilamellate [?here].


Sporophyte long lived, cells polyplastidic, photosynthetic red light response, stomata open in response to blue light; plant homoiohydrous [water content of protoplasm relatively stable]; control of leaf hydration passive; plant endohydrous [physiologically important free water inside plant]; PIN[auxin efflux facilitators]-mediated polar auxin transport; (condensed or nonhydrolyzable tannins/proanthocyanidins +); xyloglucans with side chains uncharged [?level], in secondary walls of vascular and mechanical tissue; lignins +; roots +, often ≤1 mm across, root hairs and root cap +; stem apex multicellular [several apical initials, no tunica], with cytohistochemical zonation, plasmodesmata formation based on cell lineage; vascular development acropetal, tracheids +, in both protoxylem and metaxylem, G- and S-types; sieve cells + [nucleus degenerating]; endodermis +; stomata numerous, involved in gas exchange; leaves +, vascularized, spirally arranged, blades with mean venation density ca 1.8 mm/mm2 [to 5 mm/mm2], all epidermal cells with chloroplasts; sporangia adaxial, columella 0; tapetum glandular; ?position of transfer cells; MTOCs not associated with plastids, basal body 350-550 nm long, stellate array in transition region initially joining microtubule triplets; archegonia embedded/sunken [only neck protruding]; suspensor +, shoot apex developing away from micropyle/archegonial neck [from hypobasal cell, endoscopic], root lateral with respect to the longitudinal axis of the embryo [plant homorhizic].


Sporophyte growth ± monopodial, branching spiral; roots endomycorrhizal [with Glomeromycota], lateral roots +, endogenous; G-type tracheids +, with scalariform-bordered pits; leaves with apical/marginal growth, venation development basipetal, growth determinate; sporangium dehiscence by a single longitudinal slit; cells polyplastidic, MTOCs diffuse, perinuclear, migratory; blepharoplasts +, paired, with electron-dense material, centrioles on periphery, male gametes multiciliate; nuclear genome size [1C] = 7.6-10 pg [mode]; chloroplast long single copy ca 30kb inversion [from psbM to ycf2]; mitochondrion with loss of 4 genes, absence of numerous group II introns; LITTLE ZIPPER proteins.


Sporophyte woody; stem branching lateral, meristems axillary; lateral root origin from the pericycle; cork cambium + [producing cork abaxially], vascular cambium bifacial [producing phloem abaxially and xylem adaxially].


Growth of plant bipolar [roots with positive geotropic response]; plants heterosporous; megasporangium surrounded by cupule [i.e. = unitegmic ovule, cupule = integument]; pollen lands on ovule; megaspore germination endosporic [female gametophyte initially retained on the plant].


Plant evergreen; nicotinic acid metabolised to trigonelline, (cyanogenesis via tyrosine pathway); microbial terpene synthase-like genes 0; primary cell walls rich in xyloglucans and/or glucomannans, 25-30% pectin [Type I walls]; lignin chains started by monolignol dimerization [resinols common], particularly with guaiacyl and p-hydroxyphenyl [G + H] units [sinapyl units uncommon, no Maüle reaction]; roots often ≥1 mm across, stele diarch to pentarch, xylem and phloem originating on alternating radii, cork cambium deep seated; stem apical meristem complex [with quiescent centre, etc.], plasmodesma density in SAM 1.6-6.2[mean]/μm2 [interface-specific plasmodesmatal network]; eustele +, protoxylem endarch, endodermis 0; wood homoxylous, tracheids and rays alone, tracheid/tracheid pits circular, bordered; mature sieve tube/cell lacking functioning nucleus, sieve tube plastids with starch grains; phloem fibres +; cork cambium superficial; leaf nodes 1:1, a single trace leaving the vascular sympodium; leaf vascular bundles amphicribral; guard cells the only epidermal cells with chloroplasts, stomatal pore with active opening in response to leaf hydration, control by abscisic acid, metabolic regulation of water use efficiency, etc.; axillary buds +, exogenous; prophylls two, lateral; leaves with petiole and lamina, development basipetal, lamina simple; sporangia borne on sporophylls; spores not dormant; microsporophylls aggregated in indeterminate cones/strobili; grains monosulcate, aperture in ana- position [distal], primexine + [involved in exine pattern formation with deposition of sporopollenin from tapetum there], exine and intine homogeneous, exine alveolar/honeycomb; ovules with parietal tissue [= crassinucellate], megaspore tetrad linear, functional megaspore single, chalazal, sporopollenin 0; gametophyte ± wholly dependent on sporophyte, development initially endosporic [apical cell 0, rhizoids 0, etc.]; male gametophyte with tube developing from distal end of grain, male gametes two, developing after pollination, with cell walls; female gametophyte initially syncytial, walls then surrounding individual nuclei; embryo cellular ab initio, suspensor short-minute, embryonic axis straight [shoot and root at opposite ends], primary root/radicle produces taproot [= allorhizic], cotyledons 2; embryo ± dormant; chloroplast ycf2 gene in inverted repeat, trans splicing of five mitochondrial group II introns, rpl6 gene absent; ??whole nuclear genome duplication [ζ - zeta - duplication], 2C genome size (0.71-)1.99(-5.49) pg, two copies of LEAFY gene, PHY gene duplications [three - [BP [A/N + C/O]] - copies], 5.8S and 5S rDNA in separate clusters.


Lignans, O-methyl flavonols, dihydroflavonols, triterpenoid oleanane, apigenin and/or luteolin scattered, [cyanogenesis in ANA grade?], lignin also with syringyl units common [G + S lignin, positive Maüle reaction - syringyl:guaiacyl ratio more than 2-2.5:1], hemicelluloses as xyloglucans; root cap meristem closed (open); pith relatively inconspicuous, lateral roots initiated immediately to the side of [when diarch] or opposite xylem poles; epidermis probably originating from inner layer of root cap, trichoblasts [differentiated root hair-forming cells] 0, hypodermis suberised and with Casparian strip [= exodermis]; shoot apex with tunica-corpus construction, tunica 2-layered; starch grains simple; primary cell wall mostly with pectic polysaccharides, poor in mannans; tracheid:tracheid [end wall] plates with scalariform pitting, wood parenchyma +; sieve tubes enucleate, sieve plate with pores (0.1-)0.5-10< µm across, cytoplasm with P-proteins, not occluding pores of plate, companion cell and sieve tube from same mother cell; ?phloem loading/sugar transport; nodes 1:?; dark reversal Pfr → Pr; protoplasm dessication tolerant [plant poikilohydric]; stomata randomly oriented, brachyparacytic [ends of subsidiary cells level with ends of pore], outer stomatal ledges producing vestibule, reduction in stomatal conductance with increasing CO2 concentration; lamina formed from the primordial leaf apex, margins toothed, development of venation acropetal, overall growth ± diffuse, secondary veins pinnate, fine venation hierarchical-reticulate, (1.7-)4.1(-5.7) mm/mm2, vein endings free; flowers perfect, pedicellate, ± haplomorphic, protogynous; parts free, numbers variable, development centripetal; P = T, petal-like, each with a single trace, outer members not sharply differentiated from the others, not enclosing the floral bud; A many, filament not sharply distinguished from anther, stout, broad, with a single trace, anther introrse, tetrasporangiate, sporangia in two groups of two [dithecal], each theca dehiscing longitudinally by a common slit, ± embedded in the filament, walls with at least outer secondary parietal cells dividing, endothecium +, cells elongated at right angles to long axis of anther; tapetal cells binucleate; microspore mother cells in a block, microsporogenesis successive, walls developing by centripetal furrowing; pollen subspherical, tectum continuous or microperforate, ektexine columellate, endexine lamellate only in the apertural regions, thin, compact, intine in apertural areas thick, orbicules +, pollenkitt +; nectary 0; carpels present, superior, free, several, spiral, ascidiate [postgenital occlusion by secretion], stylulus at most short [shorter than ovary], hollow, cavity not lined by distinct epidermal layer, stigma ± decurrent, carinal, dry; suprastylar extragynoecial compitum +; ovules few [?1]/carpel, marginal, anatropous, bitegmic, micropyle endostomal, outer integument 2-3 cells across, often largely subdermal in origin, inner integument 2-3 cells across, often dermal in origin, parietal tissue 1-3 cells across, nucellar cap?; megasporocyte single, hypodermal, functional megaspore lacking cuticle; female gametophyte lacking chlorophyll, four-celled [one module, nucleus of egg cell sister to one of the polar nuclei]; ovule not increasing in size between pollination and fertilization; pollen grains bicellular at dispersal, germinating in less than 3 hours, siphonogamy, pollen tube unbranched, growing towards the ovule, between cells, growth rate (20-)80-20,000 µm/hour, apex of pectins, wall with callose, lumen with callose plugs, penetration of ovules via micropyle [porogamous], whole process takes ca 18 hours, distance to first ovule 1.1-2.1 mm; male gametophytes tricellular, gametes 2, lacking cell walls, ciliae 0, double fertilization +, ovules aborting unless fertilized; fruit indehiscent, P deciduous; mature seed much larger than fertilized ovule, small [<5 mm long], dry [no sarcotesta], exotestal; endosperm +, ?diploid [one polar nucleus + male gamete], cellular, development heteropolar [first division oblique, micropylar end initially with a single large cell, divisions uniseriate, chalazal cell smaller, divisions in several planes], copious, oily and/or proteinaceous, embryo short [<¼ length of seed]; plastid and mitochondrial transmission maternal; Arabidopsis-type telomeres [(TTTAGGG)n]; nuclear genome [2C] (0.57-)1.45(-3.71) [1 pg = 109 base pairs], ??whole nuclear genome duplication [ε/epsilon event]; ndhB gene 21 codons enlarged at the 5' end, single copy of LEAFY and RPB2 gene, knox genes extensively duplicated [A1-A4], AP1/FUL gene, palaeo AP3 and PI genes [paralogous B-class genes] +, with "DEAER" motif, SEP3/LOFSEP and three copies of the PHY gene, [PHYB [PHYA + PHYC]]; chloroplast chlB, -L, -N, trnP-GGG genes 0.

[NYMPHAEALES [AUSTROBAILEYALES [[CHLORANTHALES + MAGNOLIIDS] [MONOCOTS [CERATOPHYLLALES + EUDICOTS]]]]]: wood fibres +; axial parenchyma diffuse or diffuse-in-aggregates; pollen monosulcate [anasulcate], tectum reticulate-perforate [here?]; ?genome duplication; "DEAER" motif in AP3 and PI genes lost, gaps in these genes.

[AUSTROBAILEYALES [[CHLORANTHALES + MAGNOLIIDS] [MONOCOTS [CERATOPHYLLALES + EUDICOTS]]]]: phloem loading passive, via symplast, plasmodesmata numerous; vessel elements with scalariform perforation plates in primary xylem; essential oils in specialized cells [lamina and P ± pellucid-punctate]; tension wood + [reaction wood: with gelatinous fibres, G-fibres, on adaxial side of branch/stem junction]; anther wall with outer secondary parietal cell layer dividing; tectum reticulate; nucellar cap + [character lost where in eudicots?]; 12BP [4 amino acids] deletion in P1 gene.

[[CHLORANTHALES + MAGNOLIIDS] [MONOCOTS [CERATOPHYLLALES + EUDICOTS]]] / MESANGIOSPERMAE: benzylisoquinoline alkaloids +; sesquiterpene synthase subfamily a [TPS-a] [?level], polyacetate derived anthraquinones + [?level]; outer epidermal walls of root elongation zone with cellulose fibrils oriented transverse to root axis; P more or less whorled, 3-merous [?here]; pollen tube growth intra-gynoecial; extragynoecial compitum 0; carpels plicate [?here]; embryo sac monosporic [spore chalazal], 8-celled, bipolar [Polygonum type], antipodal cells persisting; endosperm triploid.

[MONOCOTS [CERATOPHYLLALES + EUDICOTS]]: (veins in lamina often 7-17 mm/mm2 or more [mean for eudicots 8.0]); (stamens opposite [two whorls of] P); (pollen tube growth fast).

[CERATOPHYLLALES + EUDICOTS]: ethereal oils 0 [or next node up]; fruit dry [very labile].

EUDICOTS: (Myricetin +), asarone 0 [unknown in some groups, + in some asterids]; root epidermis derived from root cap [?Buxaceae, etc.]; (vessel elements with simple perforation plates in primary xylem); nodes 3:3; stomata anomocytic; flowers (dimerous), cyclic; protandry common; K/outer P members with three traces, ("C" +, with a single trace); A ?, filaments fairly slender, anthers basifixed; microsporogenesis simultaneous, pollen tricolpate, apertures in pairs at six points of the young tetrad [Fischer's rule], cleavage centripetal, wall with endexine; G with complete postgenital fusion, stylulus/style solid [?here]; seed coat?

[PROTEALES [TROCHODENDRALES [BUXALES + CORE EUDICOTS]]]: (axial/receptacular nectary +).

[TROCHODENDRALES [BUXALES + CORE EUDICOTS]]: benzylisoquinoline alkaloids 0; euAP3 + TM6 genes [duplication of paleoAP3 gene: B class], mitochondrial rps2 gene lost.

[BUXALES + CORE EUDICOTS]: mitochondrial rps11 gene lost.

CORE EUDICOTS / GUNNERIDAE: (ellagic and gallic acids +); leaf margins serrate; compitum + [one position]; micropyle?; γ whole nuclear genome duplication [palaeohexaploidy, gamma triplication], x = 21, 2C genome size (0.79-)1.05(-1.41) pg, PI-dB motif +; small deletion in the 18S ribosomal DNA common.

[ROSIDS ET AL. + ASTERIDS ET AL.] / PENTAPETALAE: root apical meristem closed; (cyanogenesis also via [iso]leucine, valine and phenylalanine pathways); flowers rather stereotyped: 5-merous, parts whorled; P = K + C, K enclosing the flower in bud, with three or more traces, C with single trace; A = 2x K/C, in two whorls, internal/adaxial to C, alternating, (numerous, but then usually fasciculate and/or centrifugal); pollen tricolporate; G [5], (G [3, 4]), whorled, placentation axile, style +, stigma not decurrent; compitum +; endosperm nuclear; fruit dry, dehiscent, loculicidal [when a capsule]; RNase-based gametophytic incompatibility system present; floral nectaries with CRABSCLAW expression; (monosymmetric flowers with adaxial/dorsal CYC expression).



[CARYOPHYLLALES + ASTERIDAE]: seed exotestal; embryo long.

ASTERIDAE / ASTERANAE Takhtajan  - Back to Main Tree

Nicotinic acid metabolised to its arabinosides; (iridoids +); tension wood decidedly uncommon; C enclosing A and G in bud, (connate [sometimes evident only early in development, petals then appearing to be free]); anthers dorsifixed?; if nectary +, gynoecial; G [2], style single, long; ovules unitegmic, integument thick [5-8 cells across], endothelium +, nucellar epidermis does not persist; exotestal [!: even when a single integument] cells lignified, esp. on anticlinal and/or inner periclinal walls; endosperm cellular.

Note: In all node characterizations, boldface denotes a possible apomorphy, (....) denotes a feature the exact status of which in the clade is uncertain, [....] includes explanatory material; other text lists features found pretty much throughout the clade. Note that the particular node to which many characters, particularly the more cryptic ones, should be assigned is unclear. This is partly because homoplasy is very common, in addition, basic information for all too many characters is very incomplete, frequently coming from taxa well embedded in the clade of interest and so making the position of any putative apomorphy uncertain. Then there are the not-so-trivial issues of how character states are delimited and ancestral states are reconstructed (see above).

Age. The age of crown-group asterids has been estimated at ca 128 m.y., mid Early Cretaceous (K. Bremer et al. 2004a), (128-)126(-122) m.y. by Wikström et al. (2015) or (140.8-)125.4(-109.4) m.y. by Tank and Olmstead (pers. comm.); Wikström et al. (2003: c.f. topology) suggest an age of (122-)117, 107(-102) m.y. (117-107.8 m.y. in Schenk & Hufford 2010), Janssens et al. (2009) an age of ca 128 m.y., while Anderson et al. (2005: only Cornales and Ericales sampled) give an age of ca 109 m. years. Soltis et al. (2008) suggest ages of 130-115(-86) m.y.a., Magallón and Castillo (2009) ca 106.35 m.y., Sun et al. (2013) 104-99 m.y., and Magallón et al. (2015) ca 114.6 m.y.; other estimates range from around (122-)114, 106(-100) m.y. (Bell et al. 2010), 113-104 m.y. (Zeng et al. 2017), 135.9-132.4 m.y. (Nylinder et al. 2012: suppl.), 167-103 m.y. (Schneider et al. 2004), (103-)93(-81) m.y. (N. Zhang et al. 2012), as old as ca 141 m.y. (Z. Wu et al. 2014) or 160-117 m.y.a. (Barba-Montoya et al. 2018) or as young as (89-)84(-80) m.y.a. (Moore et al. 2010: 95% HPD).

Martínez-Millán (2010) evaluated the asterid fossil record, which for the most part is not very rich (the Cornaceae-Alangiaceae area is an exception), and provided a series of fossil-based ages for asterid clades, with asterids going back to the Late Cretaceous ca 89.3 m.y. (Turonian), with Cornales, Ericales, and lamiids and campanulids/asterids I and II all being found in the fossil record by ca 83.5 m.y. (Late Santonian-Early Campanian). There are reports of earlier fossils, including Eoëpigynium burmensis, from 110-97 m.y. (Poinar et al. 2007; Poinar 2011 - flowers 4-merous, perhaps Cornales, but also perhaps Saxifragales, Myrtales, Asterales..., K quite well developed) and fossils of some 124 m.y. age that are perhaps Sarraceniaceae (Ericales) (Li 2005). Finally the Late Cretaceous Scandianthus (Friis & Skarby 1982) shows phenetic similarity with Vahliaceae, Hydrangeaceae, Phyllonomaceae, Escalloniaceae, and even some Saxifragaceae s. str. (Friis et al. 2011). These earlier fossils are difficult to integrate into the phylogeny.

Evolution: Divergence & Distribution. For a review of the fossils attributed to asterids, see Martínez-Millán (2010), where the focus is on how the papers reporting these fossils presented their data, also Manchester et al. (2015).

Wikström et al. (2015) provide dates throughout the asterids, and they tend to be younger - e.g. 3-16(-22: Dipsacales) m.y. younger (see Table 3, but not Gentianales) - than those in K. Bremer et al. (2004a); Wikström et al. (2015) suggest that this is largely because of the taxa included, how they calibrated the root node and how they treated divergence rates. Thus although Bremer et al. (2004a) thought that Cornales and Ericales diverged soon after the origin of the stem group asterids ca 128 m.y.a., mid Early Cretaceous, and the other asterid orders all diverged over 100 m.y.a., i.e. in the Early Cretaceous, Wikström et al. (2015) found that much of the divergence within the campanulids, but not the other major groups, occurred in the Late Cretaceous, and in general family divergences were in the Late Cretaceous.

K. Bremer et al. (2001) and Stull et al. (2018) suggest some morphological synapomorphies for asterids and some groupings within them. In general, where many characters are to be placed on the tree depends on resolution of relationships within Ericales and Cornales, and even then the pattern of gain-loss of some of these features is liable to be complex (Stull et al. 2018). Some characters common in asterids, including those of wood anatomy - for a survey of wood anatomy of Sympetalae in the old sense, see Carlquist (1992b) - probably have functional and logical linkages that also must be taken into account. Thus the presence of a tenuinucellate nucellus is linked with that of unitegmic ovules (see also Erbar & Leins 2011), the development of an endothelium (Kapil & Tiwari 1978), and a simple exotestal (see above) seed type (Netolitzky 1926); that of sympetalous monosymmetric flowers with epipetalous stamens, etc.

Ericales and Cornales in particular show much variation in the degree of sympetaly, stamen number and development, adnation of stamens to corolla, and in ovule morphology and anatomy; some of this variation is like that found in rosids, Dilleniales, etc., and is unlike that in the lamiid + campanulid/asterid I + II clade. They may also have ellagic acid, which has a rather similar distribution; interestingly, Ericales and Cornales contain the only families in which both iridoids and ellagic acid occur (Cornaceae, Symplocaceae, Ericaceae and Fouqueriaceae - Bate-Smith 1984). For further discussion of this variation, see the euasterids. Geraniol synthase is involved in an early step in iridod synthesis, diverting resources that might otherwise be used in monoterpene synthesis into iridoids, "non-canonical monoterpenes" (Boachon et al./Mint Evolutionary Genomics Consortium 2018). For possible additional synapomorphies in this area, see the section on chemistry, morphology, etc., below.

Ecology & Physiology. Leaf size increases and plant height shows a notable decrease at this node (Cornwell et al. 2014), although the former character subsequently decreases both in Ericaceae and in the euasterids.

See Batashev et al. (2013 and literature) for the anatomy of minor-vein phloem (the typology is complex) and its physiological implications.

Plant-Animal Interactions. Iridoids, common in asterids, have been implicated in herbivore preferences, deterring some and attracting others (e.g. see discussion under Plantaginaceae, Scrophulariaceae, etc.: Bowers 1980, 1988; Dobler et al. 2011); iridoids have a bitter taste and are emetics for vertebrates, at least. However, they are sometimes sequestered by the insect eating the plant and used in its defence against predators (Dyer & Bowers 1996; Nishida 2002 for a summary) - confusing the issue, iridoids may also be synthesized de novo by the insect (Burse et al. 2009 - Chrysomelina). Indeed, overall herbivory here is relatively low (Turcotte et al. 2014: see caveats). Insect preferences can be striking: Uraniidae (moths) are found on Dipsacales, Lamiales, Gentianales - and also Daphniphyllaceae, an iridoid-containing member of Saxifragales (Lees & Smith 1991), while larvae of Nymphalidae-Melitaeini butterflies are also almost restricted to asterids, although they are also quite common on Asteraceae and Acanthaceae, which, although asterids, lack iridoids; Melitaeini distinguish between plants with route I secoiridoids, which they eat, and route II decarboxylated iridoids, which they rarely eat (Wahlberg 2001). Pentzold et al. (2014) discuss how insects can get around iridoid defences. Iridoids may also be involved in plant-plant relationships. Parasite Orobanchaceae may produce toxic iridoid aglucones in their hosts and so increase their effect on the latter (Rank et al. 2004), while iridoids from roots of Verbascum (Scrophulariaceae) may depress germination of competitors (Pardo et al. 2004). Volatile iridoids, such as those found in Lamiaceae-NNepetoideae, may have yet other functions (Boachon et al. 2018).

Chemistry, Morphology, etc. Albach et al. (2001a) discussed iridoid distribution, etc., in the asterids, as do Soltis et al. (2005b). Mølgaard and Ravn (1988) and Rønsted et al. (2002) outlined the systematic utility of caffeic acid derivatives; chlorogenic acid, an ester of caffeic and quinic acid, is especially common in asterids, but also occurs elsewhere (see also also Lamiales and Boraginaceae in particular for other derivatives).

Characteristic of the whole clade - although with numerous exceptions (derived), is the Baileyan wood anatomical syndrome of predominantly solitary vessels, scalariform perforation plates, mainly opposite vessel pitting, very long vessel elements and fibres at least 800 and 2190 µm long respectively, non-septate fibres with distinctly bordered pits, and diffuse to diffuse-in-aggregates and scanty paratracheal axial parenchyma (Lens et al. 2008). Compound leaves are relatively uncommon in asterids, and when they occur the leaflets are often not articulated and/or distinct (but c.f. Araliaceae!), however, elements of development are largely identical in very different-looking compound leaves (Bharathan et al. 2002; Blein et al. 2008). Taxa with stipules are also fairly uncommon.

Taxa with apetalous flowers are uncommon in asterids, as are taxa with a tube-forming hypanthium (c.f. in rosids). Monosymmetry may have arisen some fifteen times here, with several reversals in Lamiales and Dipsacales (Jabbour et al. 2008: see also Donoghue et al. 1998; Ree & Donoghue 1999); monosymmetric flowers may have one, or rarely two, spurs (Jabbour et al. 2008).

For a discussion on corolla tube development, see below.

The direction of contortion in flowers with contorted petals tends to be consistent - again, c.f. rosids, where it may be labile even within an individual (Endress 1999, 2001b, 2010c)), although exactly where the switch might occur on the tree is unclear. Lee et al. (2004) suggest that the CRABS CLAW gene is expressed in the rather different nectaries in the rosids (receptacular nectary) and asterids (gynoecial nectary) that they sampled; Bernadello (2007) surveyed nectary variation in asterids.

Endress (2010c) noted that ovules in this clade are frequently unvascularized, although the exact distribution of this feature is unclear; taxa with vascularized ovules are also quite common (e.g. Guignard 1893). The integument, when single, is often dermal in origin, as is the inner integument of other angiosperms, while the outer integument is largely subdermal (but c.f. monocots: see Bouman 1984; de Toni & Mariath 2009 - I have not looked at this character in detail). A suggestion might then be that the single integument of asterids corresponds to the inner integument of many bitegmic angiosperms, but since a number of Cornales and Ericales in particular have bitegmic ovules, the story is unlikely to be simple. Indeed, the nature of the single integument so common here has occasioned much speculation, and it may well be a composite structure (Bouman & Calis 1977; Kelley et al. 2009; McAbee et al. 2005; Endress 2011b; Lora et al. 2015). Many asterids also have anatropous ovules, and curvature of the ovules in other angiosperms is commonly associated with the presence of a second integument (Endress 2011b). In the characterizations below, the asterid seed coat is described as being testal, although the term "testa" technically refers to that part of the seed coat that is derived from the outer integument. Commonly only the outer epidermal layer of cells is thickened and lignified, and this mostly on the anticlinal and the inner periclinal walls. This type of seed coat was called the Ericaceous-type seed by Huber (1991), and he emphasized its wide distribution; note that Caryophyllales have an strictly exotestal seed. Arillate seeds are decidedly uncommon in asterids, in part because the seeds are frequently very small.

Phylogeny. See the Dilleniales page for a discussion on the relationships of the asterids; Caryophyllales or Santalales (or the two as a combined clade) may be their sister group.

The monophyly of the asterids is well established (e.g. Olmstead et al. 1992, 1993, 2000; P. Soltis 1999); Albach et al. (1998) suggest the four main groupings recognised here. Relationships in phylogenies proposed by K. Bremer et al. (2001: analysis of 2 genes + morphology) and Albach et al. (2001b: analysis of four genes) are largely congruent. Differences were almost entirely in taxa not assigned to orders by A.P.G. (1998), although many of these have since been placed in orders, relationships in the provisional Bayesian analyses of Lundberg (2001b, d) pointing the way to relationships currently accepted. B. Bremer et al. (2002) provide an early comprehensive phylogeny of the clade, although with minimal sampling within families, using three coding and three non-coding chloroplast markers. Both B. Bremer et al. (2003) and Olmstead (2000) suggest that there is strong support for Cornales being the sister to all other asterids; see also Albach et al. (2001), Soltis et al. (2003) and J. Li and Zhang (2010). Although Hilu et al. (2003) reverse the positions of Cornales and Ericales, they sequenced the matK gene alone; Caiophora (Loasaceae) appears in Asterales, far separate from the other members of the family - a case of mistaken identity? Morton (2011: nuclear Xdh gene) found some support for an {Ericales + Cornales] clade, but sampling in the latter was poor (see also N. Zhang et al. 2012: weak support, nuclear genes; Zeng et al. 2017: not the focus of the study). Qiu et al. (2010: four mitochondrial genes, support for relationships mercifully poor) found Ericaceae to be sister to a clade [paraphyletic Cornales + rest of asterids] while Lee et al. (2011) even found Vaccinium to be sister to Caryophyllales in some analyses, with Cyclamen sister to Panax.... Tank and Donoghue (2010) provide a largely resolved tree of relationships between asterid orders, and the topology of the tree here is the same as theirs (Fiz-Palacios et al. 2011 have additional suggestions). For trees produced by analyses of 18S/26S nuclear ribosomal data, see Maia et al. (2014); very few deeper relationships have much support.

Previous Relationships. The distinction between all other angiosperms and the asterids partly corresponds to the distinction between the crassinucellate and tenuinucellate groups of Young and Watson (1970: phenetic analyses). However, there are also substantial differences, for example, Young and Watson included Apiaceae-Araliaceae in their crassinucellate group. Philipson (1974) further emphasized the distinction between the crassinucellate and tenuinucellate groups of Young and Watson, linking the two via Celastraceae, Grossulariaceae and Brexiaceae (here Celastrales, Saxifragales, and Crossosomatales, all rosids and not immediately related to asterids); Theales, Primulales and Ebenales together made up a separate lineage (here part of Ericales). Later Philipson (1977) resurrected van Tieghem's (1901) names Unitegminae and Bitegminae for these two groups; integument number and nucellus condition are correlated. General morphology indeed suggests such relationships, as Hufford (1992a) found even with phylogenetic analyses - Theaceae, Paracryphiaceae, Apiaceae and Araliaceae were members of Rosidae (but Pittosporaceae were sister to Polemoniaceae).

Synonymy: Aquifolianae Doweld, Aralianae Takhtajan, Asteranae Takhtajan, Balsaminanae Doweld, Boraginanae Doweld, Brunianae Doweld, Campanulanae Reveal, Cornanae Reveal, Diapensianae Doweld, Dipsacanae Takhtajan, Ericanae Takhtajan, Escallonianae Doweld, Eucommianae Reveal, Gentiananae Reveal, Lamianae Takhtajan, Lecythidanae Reveal, Loasanae Reveal, Oleanae Takhtajan, Phellinanae Doweld, Primulanae Reveal, Solananae Reveal Sarracenianae Reveal, Theanae Reveal, Vahlianae Doweld - Asteridae Takhtajan, Cornidae Reveal, Ericidae C. Y. Wu, Lamiidae Reveal, Theidae Doweld - Asclepiadopsida Brongniart, Asteropsida Brongniart, Bignoniopsida Nees, Campanulopsida Bartling, Caprifoliopsida Endlicher, Coffeopsida Brongniart, Convolvulopsida Brongniart, Diospyropsida Brongniart, Ericopsida Bartling, Ligustropsida Meisner, Loniceropsida Brongniart, Myrsinopsida Bartling, Plantaginopsida Meisner, Primulopsida Brongniart, Rubiopsida Bartling, Selaginopsida Brongniart, Solanopsida Brongniart, Styracopsida Bartling, Verbenopsida Brongniart

CORNALES Dumortier  - Main Tree.

Iridoids diverse, ellagic acid +, flavones 0; vessel elements with scalariform perforation plates; nodes 3:3; inflorescence cymose; (flowers 4-merous), K "small", C often valvate, apparently free [tube formation early]; A basifixed; G inferior, with disc-like nectary, ventral carpellary bundles in the carpel wall [= transseptal bundles, i.e. vascular bundles to ovules go over the top of the septum and then down; no bundles run up the central axis of the gynoecium]; ovule 1/carpel, apical; fruit drupaceous, with apical germination valve(s) in the stone, K persistent. - 6 families, 51 genera, 590 species.

Note: In all node characterizations, boldface denotes a possible apomorphy, (....) denotes a feature the exact status of which in the clade is uncertain, [....] includes explanatory material; other text lists features found pretty much throughout the clade. Note that the particular node to which many characters, particularly the more cryptic ones, should be assigned is unclear. This is partly because homoplasy is very common, in addition, basic information for all too many characters is very incomplete, frequently coming from taxa well embedded in the clade of interest and so making the position of any putative apomorphy uncertain. Then there are the not-so-trivial issues of how character states are delimited and ancestral states are reconstructed (see above).

Age. Wikström et al. (2001) suggest figures of (106-)101, 94(-89) m.y. for the age of crown group Cornales and Anderson et al. (2005) similar ages of 101-97 m.y.; Janssens et al. (2009) date the group to (117.1-)104(-90.9) m.y. and K. Bremer et al. (2004a) to some 112 m.y.a., 115.3-105.1 m.y. in Schenk and Hufford (2010: note topology) basically includes both. Magallón and Castillo (2009) estimate 101.55 m.y. as its age, Lemaire et al. (2011b) (123-)106(-92) m.y., while around 104.1 m.y. is the age in Magallón et al. (2015: note topology) and (117-)102(-90) m.y. in Wikström et al. (2015). Some time in the Turonian, i.e. older than 89.8 m.y., perhaps to 93.9 m.y., is the estimate in Atkinson et al. (2018: Fig. 3), while at (95.6-)90.7(-86.9) m.y., the estimate in Tank and Olmstead (pers. comm.) is similar.

Fruits readily assignable to Cornales because of their distinctive anatomy are very well represented in the fossil record (Manchester et al. 2007, 2015). They can be dated to the Cretaceous-Maastrichtian, ca 70 m.y.a. (Nyssa), Lower Campanian ca 82 m.y.a. (Atkinson 2015), ca 80 m.y.a. (Atkinson 2016: inc. Suciacarpa - septal bundles), some 84 m.y.a. (Stockey et al. 2016a - Eydeia - septal vascular bundles), Coniacian, ca 87 m.y.a. (Takahashi et al. 2002: Hironoia - bundles in central axis), and ca 89 m.y.a. from North America, material from three genera, with characters like germination flaps, rows of vascular bundles in the septae but no central bundles, and endocarp with sclereids or fibres on the inside (Atkinson et al. 2017b). Atkinson et al. (2017a) also described fossil fruits from the Upper Campanian on Vancouver Island ca 74 m.y. old; see also Martínez-Millán (2010), Atkinson et al. (2016), also Nyssaceae below.

The Late Cretaceous Silvianthemum suecicum, from rocks in southern Sweden ca 83.5 m.y.o., has tricolp(or)ate pollen, eight stamens (but a 5-merous perianth), the anthers appear to be dorsifixed, and there are three short, adaxially grooved styles (Friis 1990; see also Martínez-Millán 2010; Friis et al. 2011, 2013b). Bertilanthus scanicus, from the same rocks, has glandular hairs and stamens opposite the petals (Friis & Pedersen 2012). Although initially thought to be close to Quintinia (Paracryphiales), a position within Cornales was suggested by Beaulieu et al. (2013), which is more in accord with the morphology (and geography) of these fossils; Friis et al. (2013b) opt for a close linkage between Quintinia and the fossils, but they think that the phylogenetic position of Quintinia/Paracryphiales may be incorrect. Scandianthus, also Late Cretaceous and previously associated with Vahlia, may also belong in this area, indeed, there is quite a diversity of such 'saxifragalean' flowers in the fossil record (Friis et al. 2011: p. 489). Neither of the fossils mentioned was included in the study of Cornalean fossils by Atkinson (2018).

Evolution: Divergence & Distribution. In general, family identification of fossils is unclear, and they tend to have a mixture of characters of Cornaceae s.l. and Nyssaceae s.l.. In the comprehensive morphological analysis of Atkinson (2018) a number of fossils were associated with stem or crown Nyssaceae, while some were stem [Cornaceae + Nyssaceae], but in neither case was there much support. Interestingly, the morphospace occupied by these fossils overlapped only partly with that occupied by extant members of the order (Atkinson 2018).

Endress (2011a) thought that the inferior ovary of Cornales might be a "key innovation" - but whether for all or just a part of the clade would depend on its topology, and anyhow the clade is not very speciose, if morphologically quite diverse.

Chemistry, Morphology, etc. The strands of apotracheal parenchyma are relatively long (at least 9 cells long) in Cornaceae s.l. (inc. Curtisiaceae) when compared with some of their putative relatives (Noshiro & Baas 1998). Spirally-thickened vessels holding the two halves of transversely-torn leaves together are quite common... Leaf teeth of Nyssaceae and Hydrangeaceae have a clear apex with a foramen, higher order laterals are involved (Hickey & Wolfe 1975).

The petals are often free, but corolla tube formation, when known, is early (e.g. Reidt & Leins 1994). Atkinson et al. (2016) described Cretaceous endocarps assignable to Cornales, they might have longituinally or tranversely elongated fibres, or no fibres at all, or both (Atkinson 2016), and the outer surface of the fruit might be ridged or smooth. There is considerable variation in seed size in this clade (Moles et al. 2005a), but seed size is not incorporated into the family characterisations.

For more details, see Faure (1924: general), Grayer et al. (1999: saponins) and Gousiadou et al. (2016: iridoids), Jahnke (1986: inflorescence), Ferguson (1977: pollen), Sato (1976: embryology), and Takahashi et al. (2002: fruits), mostly as Cornaceae s.l..

Phylogeny. Molecular studies (e.g. Xiang et al. 1993) early suggested a break-up of the old, broadly circumscribed Cornaceae; the core remains here. Relationships between genera in this core have been unclear for some time, but at least some aggregation of the families they represent was clearly in order (e.g. Albach et al. 2001b; Xiang et al. 2002). Indeed, relationships in Cornales as a whole were unclear. Although Cornus is sister to Mastixiaceae in some morphological trees (Murrell 1993), it is not nearly so close in rbcL trees (Xiang et al. 1993, 1997). For the relationships of Grubbiaceae and Hydrostachyaceae (placement of the latter is particularly difficult, see below), see especially Hempel et al. (1995), Xiang (1999), Soltis et al. (1997, 2000, 2007a), Savolainen et al. (2000b), Fan and Xiang (2003) and Xiang et al. (2002). There has been support for a sister group relationship between Grubbiaceae and Curtisiaceae for quite some time (e.g. Fan & Xiang 2001).

The phylogenetic position of Hydrostachyaceae, a much-modified aquatic herb, has long presented problems. The embryology of the family shows certain similarities with that of Crassulaceae, but relationships neither there nor with Podostemaceae (see below) can be maintained given what we now know about relationships of these clades. Members of sympetalous groups, especially Lamiales, show similarities to Hydrostachyaceae in ovary structure (apical septae) and in ovule and endosperm development. However, although the coenocytic micropylar haustorium is well developed, the chalazal endosperm cell, which remains undivided, is barely haustorial, and the two carpels are collateral, rather than superposed as in most Lamiales (Jäger-Zürn 1965; see also Rauh & Jäger-Zürn 1966, 1967 [strongly supporting a relationship with Lamiales]; Leins & Erbar 1988, 1990). However, in some Orobanchaceae (e.g.) the chalazal haustorium is also very poorly developed (Tiagi 1963), as in Lamiales basal to Calceolariaceae. A position within Hydrangeaceae has also seemed to be quite likely (Xiang 1999; see also Hempel et al. 1995; Olmstead et al. 2000; Albach et al. 2001; Wikström et al. 2001; Fan & Xiang 2001; Xiang et al. 2002; Bell et al. 2010 - even in Xiang et al. 2011 this position cannot be excluded), but note that Hydrostachyaceae has a very long branch; what about the mitochondrial coxII.i3 intron (Joly et al. 2001)? As Albach et al. (2001) note, few morphological characters support this position, but one could argue that this is perhaps to be expected of any highly-derived aquatic plant... Schenk and Hufford (2010: support weak) and Magallón et al. (2015) placed Hydrostachyaceae as sister to all other Cornales.

In a five-gene analysis Burleigh et al. (2009) found that there was strong support (97% ML bootstrap) for a position of Hydrostachys within Lamiales, largely because of the matK sequence added. Where in the Lamiales Hydrostachys might be placed was unclear, although it would probably be in a clade that excluded Oleaceae, at least. More comprehensive analyses are needed; Calceolaria and other clades below it in Lamiales other than Oleaceae were not sampled. Indeed, although morphologically Hydrostachyaceae are more or less at home in Lamiales (and I initially thought that they might end up there), more comprehensive analyses (Schäferhoff et al. 2010) exclude them from that order; a sequence used by Burleigh et al. (2009) was similar to that of Avicennia (Acanthaceae)... However, the focus of the work by Schäferhoff et al. (2010) was on relationships within Lamiales, so they did not place Hydrostachyaceae with confidence.

Xiang et al. (2011) found a set of relationships [[Cornaceae [Curtisiaceae + Grubbiaceae]], Nyssaceae s.l., [Hydrostachyaceae [Hydrangeaceae + Loasaceae]]]]. Here taxon sampling is good and many of the relationships are well supported, however, nuclear 26S rDNA data alone suggested somewhat different relationships than did the six chloroplast genes, with Hydrostachys being embedded in Cornaceae s.l.. Using chloroplast genes alone a position of Nyssaceae as sister to [Hydrostachyaceae [Hydrangeaceae + Loasaceae]] had good support, and relationships suggested by this chloroplast phylogeny are followed here (see also most relationships in Schenk & Hufford 2010, but some nodes with weak support). However, there is little in the way of morphology to pin to the basal nodes, and as Xiang et al. (2011) noted, this new topology makes character evolution interesting. Morphological analyses (fruit characters) of extant and especially fossil members of Cornales found quite strong support (93% bootstrap) for a [Cornaceae, Nyssaceae, Curtisiaceae, Grubbiaceae] clade (Atkinson 2018), but not for much else. Stronger support for relationships in the order would be reassuring.

Previous Relationships. 11/15 of the genera of Cornaceae s.l. have been placed in monotypic families, or the family has been circumscribed very broadly, as by Mabberley (1997). Previous inhabitants of the old Cornaceae may be found in this site in Garryaceae (Garryales), Montiniaceae (Solanales), Argophyllaceae (Asterales) and Griseliniaceae (Apiales).

Includes Cornaceae, Curtisiaceae, Grubbiaceae, Hydrangeaceae, Hydrostachyaceae, Loasaceae, Nyssaceae.

Synonymy: Alangiales Martius, Grubbiales Doweld, Hortensiales J. Presl, Hydrangeales Martius, Hydrostachyales Reveal, Loasales Berchtold & J. Presl, Nyssales Martius, Philadelphales Link - This is the asterid IV group of some early phylogenetic studies.

[Cornaceae [Grubbiaceae + Curtisiaceae]]: sieve tube plastids also with polygonal protein crystalloids; leaves opposite, bases joined by a line/ridge; flowers small; drupe longitudinally grooved, walls with nests of sclereidal cells, endocarp sclereidal, germinaton valve elongate.

Age. This node may be around 97-95.5 m.y.o. (Tank et al. 2015: Table S1, S2) or 102.4-82.9 m.y. (Schenk & Hufford 2010).

CORNACEAE Berchtold & J. Presl, nom. cons.  - Back to Cornales


Trees and shrubs (stoloniferous subshrubs); (plants Al accumulators), route I secoiridoids, also route II decarboxylated iridoids, isoquinoline alkaloids, triterpenoid saponins, flavonols, +, (fructan sugars accumulated as isokestose oligosaccharides [inulins] - some Cornus), tanniniferous; (mucilage +); (laticifers +); (vessel elements with simple perforation plates); sclereids +; petiole bundle(s) arcuate (with adaxial inverted plate [and with wing bundles]), or D-shaped or annular (with inverted medullary bundle); hairs T-shaped, unicellular, (stellate), walls often with crystals; (leaves spiral or two-ranked), lamina vernation conduplicate(-flat) or curved (both -plicate) or involute, margins entire (lobed), secondary veins pinnate or actinodromous; (inflorescence capitate); flowers 4(-10)-merous; K notably small, connate or not, (decussate), C (decussate); stamens = and opposite sepals (-4x, anthers long - Alangium); pollen with complex endaperture [a pore joining two lateral thinnings parallel to the colpus], often starchy, exine with granules or spinules [?Alangium]; G 1-2(-3)-locular, style short (long, with long arms), stigma truncate to capitate, dry; ovules apotropous, parietal tissue ca 3 cells across (0 - red-fruited Cornus), hypostase 0; (megaspore mother cells several), (embryo sac tetrasporic, 8-nucleate, antipodals polyploid [Fritillaria type]); drupe 1-2-seeded, wall sclereidal, (with cavities - subgenus Cornus), septum with (elongated and) isodiametric sclereids, germination valve elongate; testa of elongated cells, much compressed, (ca 6 cells thick, vascularized - Alangium); endosperm (also nuclear), hemicellulosic, embryo chlorophyllous; n = 8-11; (plastid transmission biparental).

2[list]/85: Cornus (65). Scattered, not S. South America (map: see van Steenis & van Balgooy 1966; Aubréville 1974; Fl. Austral. 8. 1984; Meusel et al. 1978; Hultén & Fries 1986; Xiang & Thomas 2008; Trop. Afr. Fl. Pl. Ecol. Distr. 6. 2011). [Photos - Habit, [Photo: Cornus Inflorescence, Flower, Fruit.]

Age. An age of (82-)67(-47) m.y. is suggested for crown-group Cornaceae (Bell et al. 2010); Wikström et al. (2001) suggest an age of (79-)73, 64(-58) m.y..

Divergence & Distribution. Xiang and Thomas (2008) thought that stem-group Cornus was Late Cretaceous in age, ca 80 m.y. old, substantial diversification having occurred by ca 66 m.y. ago. Fruits of Cornus subg. Cornus have distinctive alveolate endocarps and are known from the Palaeocene of North Dakota in rocks about 58 m.y. old; they have six locules (Manchester et al. 2010b). Manchester et al. (2015) also discuss the fossil record, and they note that pollen of Alangium can be confused with that of Pelliciera (Ericales).

For a careful study reconstructing ancestral areas and characters in Cornus, see Xiang and Thomas (2008); the results depended much on the methods used, etc..

Pollination Biology. The floral organ B (some, but not all, i.e. not PI, but AP3) and C genes are expressed in the large, white inflorescence bracts of Cornus, an heterotopic shift that has occurred at least twice (Maturen et al. 2005; Xiang et al. 2010; W.-H. Zhang et al. 2008: extensive PI-like gene duplication; Feng et al. 2012). For inflorescence architecture in Cornus, in particular for the role of CorLFY genes there, see J. Liu et al. (2013), while Ma et al. (2017) looked at the effect of the amount and timing of expression of CorTRL1 and CorAP1 on inflorescence architecture.

Chemistry, Morphology, etc. Blue-fruited dogwoods have lost iridoids (Xiang et al. 1997). In nodes of Alangium the central vascular trace may immediately divide into three (nodes 3:5). Mabberley (1997) describes Alangiaceae as having spiral leaves; they are often two-ranked.

Alangium has very little vascular tissue in the center of the ovary. There is considerable variation in embryo sac development in Cornus in particular (Johri et al. 1992 for references).

For further information, see Kubitzki (2004b: general), Jensen et al. (1975a: iridoids), Adams (1949: anatomy), Mittal (1961) and Neubauer (1978), both petiole anatomy, Feng et al. (2011: inflorescence morphology and evolution), Reidt and Leins (1994: corolla of Alangium), Eyde (e.g. 1968, 1988: flower and fruit in particular), Ferguson (1977: pollen), Fagerlind (1939c: embryo sac), and Manchester et al. (2010b: fruit morphology).

Phylogeny. For relationships within Cornus, c.f. Murrell (1993) and Xiang et al. (1993, 2006), Xiang and Thomas (2008) and Feng et al. (2011), and for relationships within Alangium, see Feng et al. (2009).

Botanical Trivia. The anthers of Cornus canadensis have explove dehiscence; the maximum acceleration rate of the pollen grains has been estimated at 24,000 m/s2 (Edwards et al. 2011).

Synonymy: Alangiaceae Candolle, nom. cons.

[Grubbiaceae + Curtisiaceae]: style short, lobed; ovules epitropous, parietal tissue 0; endosperm copious.

Age. The age of this clade is ca 90 m.y., suggesting that it is very much a relict in the Cape flora (Warren & Hawkins 2006); ca 59.4 m.y. is the age in Magallón et al. (2015).

Chemistry, Morphology, etc. For characters holding these two families together, see in part Xiang et al. (2002).

Classification. Xiang et al. (2002) suggested that Grubbiaceae and Curtisiaceae might be combined, but they are kept separate here because they are rather different in appearance (see also A.P.G. III 2009).

GRUBBIACEAE Meisner, nom. cons.  - Back to Cornales


Evergreen ericoid shrubs; iridoids 0?; sieve tube plastids?; subepidermal collenchyma +; hairs unicellular; cuticle waxes as long narrow platelets; leaves ± ericoid, lamina margins revolute; inflorescences axillary, capitate or cone-like; flowers also 6-merous; K valvate, C 0; A 8 (12), anthers inverting, bisporangiate, monothecal; pollen surface ± smooth, ?endapertures; G [2], transverse, placentation axile at base, becoming free-central; nectary hairy; ovule integument "thick" [4-6 cells?], micropyle "long", hypostase +; fruit a syncarp; ?endocarp, stone ?grooving; 1 seed/fruit proper; coat thin; micropylar and chalazal endosperm haustoria +, embryo long; n = ?

1[list]/3. Cape Floristic Province, South Africa (map: from Vester 1940).

Chemistry, Morphology, etc. The family is poorly known. The inversion of the anther is very comprehensive in Grubbiaceae, and for some (e.g. Fagerlind 1947b) this has suggested relationships with Ericaceae. Carlquist (1978a) found Grubbiaceae to be anatomically identical to Bruniaceae (Bruniales, a campanulid), c.f. also Geissolomataceae (rosid-Crossosomatales).

Some information is taken from Dahlgren in Dahlgren and van Wyk (1988) and Kubitzki (2004b), both general, Schnizlein (1843-1870: fam. 18 - carpel orientation), and Fagerlind (1948b: embryology).

Synonymy: Ophiraceae Arnott

CURTISIACEAE Takhtajan  - Back to Cornales


Evergreen trees; route I secoiridoids +, ?ellagic acid; ?nodes; petiole bundle annular, with medullary strands; single crystals +; lamina vernation ± flat, margins serrate; inflorescence terminal; K small, open; stamens = and opposite sepals; pollen with complex endaperture [a pore joining two lateral thinnings parallel to the colpus]; G [2-4], with axial/central vascular bundles; fruit usu. 4-seeded, mesocarp with sclereids, endocarp of large sclereidal cells with horizontally-elongated digitate-interlocking walls, germination valve elongated, septum with isodiametric sclereids; endotesta tanniniferous, rest ± collapsed; ?endosperm haustoria, embryo minute; n = 13.

1[list]/1: Curtisia dentata. Southern Africa (map: from Palgrave 2002; Yembaturova et al. 2009; fossil [blue] from Manchester et al. 2007a]). [Photo - Fruit]

Age. Manchester et al. (2007a) recognised the distinctive fruits of Curtisia from the early Eocene London Clay ca 55 m.y.o.; the fossils were originally placed in Epacridaceae (= Ericaceae-Styphelioideae)!

Evolution: Divergence & Distribution. Curtisia is known fossil from southern England (Manchester et al. 2007a, 2015); see also Ericales-Roridulaceae for a comparable extant/fossil distribution.

Chemistry, Morphology, etc. Takhtajan (1997) described the hairs of the branchlets, petioles and inflorescences of Curtisia as being stellate; they are simple and curled. The "plications" (Cullen 1978) in the young leaves are in fact only prominent veins.

Curtisia is embryologically unknown, but it lacks transseptal bundles, having the "normal" central bundles.

For general information, see Kubitzki (2004b), for pollen, see Ferguson (1977).

Classification. See Yembaturova et al. (2009).

[Nyssaceae [Hydrostachyaceae [Hydrangeaceae + Loasaceae]]]: ?

NYSSACEAE Dumortier, nom. cons. - Back to Cornales


Trees and shrubs;(Al accumulators); route I secoiridoids, triterpenoid saponins, (resin), +, tanniniferous, (mucilage +); (laticifers +); (leaf traces running along the stem - Mastixia), (sclereids +), pith septate or not; petiole bundles arcuate or with adaxial plate; (stomata paracytic); hairs T-shaped, unicellular; leaves spiral (opposite), lamina vernation conduplicate [Nyssa], margins serrate or entire; plants andromonoecious, dioecious, etc., or flowers perfect; inflorescences various, racemose, (capitate); flowers usu. (4-)5-merous, small; P 0, or K notably small, C ± imbricate, or valvate and inflexed at apex and with an adaxial median ridge; A 4-26 [often diplostemonous]; pollen with complex endaperture [a pore joining two lateral thinnings parallel to the colpus], tectum perforate [?all]; (nectary 0 - Davidia); G [1(-3), (6-10)-locular], style short, (long - Nyssa; styles +); ovules epitropous, micropyle long, integument ca 8-10(-15+) cells across, parietal tissue 1-3 cells across, (nucellar cap ca 2 cells across), suprachalazal zone much elongated, hypostase +, supraraphal chalaza massive, (pachychalazal), (endothelium +); (megaspore mother cells several); fruits 1-5-seeded, drupe walls with intertwining fibres; germination valve short, at apex of loculus, or elongate, septum with fibres (sclereids), (vasculature as longitudinal rows - Davidia), septal ridge on stone [?all], (seed U-shaped in t.s. because of intrusive germination valve - Mastixia); testa multiplicative, exotesta lignified, cells polygonal; (endosperm also nuclear), embryo long or short; n = 11, 13 [both Nyssa], 21, 22.

5 [list]/22. Mainly East Asia, also Indo-Malesia and E. North America (map: see van Steenis & van Balgooy 1966; Matthew 1977). [Photo - Nyssa Flower, Fruit © H. Wilson.]

Age. Hironoia fusiformis, from Cretaceous-early Coniacian deposists in Japan ca 89 m.y.o., may be best placed here (Takahashi et al. 2002; see also Manchester et al. 2015), while Eydeia hokkaidoensis, some 84 m.y.o., has i.a. the distinctive septal vasculature of Davidia (Stockey et al. 2016a). Atkinson (2015) placed an 82 m.y.o. fossil in this area although, as he noted, it has a novel combination of characters - the fruits are very large and the seed is described as being orthotropous. Indeed, a number of fossils are placed as crown- or stem-group Nyssaceae by Atkinson (2018), although Hironoia is stem [Curtisiaceae [Nyssaceae + Cornaceae]] and placed sister to Amersinia, also initially thought to be close to Nyssaceae (Manchester et al. 1999), albeit with little support.

Evolution: Divergence & Distribution. Manchester et al. (2009 and references, 2015) discuss the early Caenozoic fossil history of what are now East Asian endemic genera of Nyssaceae. Fossils of mastixioid fruits in particular are widespread in the northern hemisphere in the Late Cretaceous and Caenozoic-Palaeogene in particular, some being 3- or 4-carpellate; they are placed in 8 genera and 33 species (Eyde & Qiuyun 1990; Eyde 1997, for details). Mastixia was especially abundant in Europe and Siberia 65-70 m.y.a. (Manchester 2002). See also Kvacek (2008).

Pollination Biology. Davidia has numerous perianth-less flowers in capitulae that are subtended by 2 large white bracts. Expression of B-class floral genes in these bracts is implicated (Vekemans et al. 2011), and overall each staminate flower is very highly reduced, the inflorescence meristem having many features of a floral meristem (Claßen-Bockhoff & Arndt 2018).

Plant-Animal Interactions. For the indole alkaloid camptothecin, see Lorence and Nessler (2004). The enzyme that camptothecin targets is in the plant, but the plant is probably protected by changes in its amino acid sequence, one of which (serine in position 722) is the same as is found in camptothecin-resistant tumours in humans (Sirikantaramas et al. 2009). Camptothecin is sequestered in glandular hairs although not in the laticifers (Hagel et al. 2008).

Chemistry, Morphology, etc. Diplopanax contains petroselenic acid (Zhu et al. 1998). Although Zhu et al. did not find petroselenic acid in Fatsia (Araliaceae) or Aucuba (Garryaceae), it is found in a number of Apiales, and relationships between Cornaceae and some Apiales have been suggested in the past...

Mohana Rao (1973a) described the integument of Nyssa as being ca 5 cells across and the ovules as being tenuinucellate. However, the integument is much thicker when the embryo sac is mature (ibid: Fig. 5G), and a single subepidermal layer of cells is shown between the embryo sac and epidermis (ibid.: Fig 3D, E); epidermal cells on occasion divide periclinally, but such divisions seem not to account for this subepidermal layer.

Davidia lacks a perianth and may have bitegmic ovules (but c.f. Horne 1914). Diplopanax has recently been placed in Mastixiaceae s. str. (Eyde & Quiyun 1990; c.f. Xiang et al. 1997). It has five lobes on the disc opposite the corolla and a single-seeded fruit the embryo of which is C-shaped in transverse section (Ying et al. 1993); see above for chemistry.

For general information, see Kubitzki (2004), for floral development, see Gong et al. 2018 (Camptotheca, also family summary), for pollen, see Ferguson (1977: Mastixia), for some embryology, see also Horne (1909, 1914), Tandon and Herr (1971), and for cytology, see He et al. (2004). For Mastixia, see Matthew (1976); embryological details are unknown for it, Diplopanax, etc.

Phylogeny. Z.-D. Chen et al. (2016) obtained the relationships [Diplopanax + Mastixia] [Davidia [Camptotheca + Nyssa]]], with good support.

Synonymy: Camptothecaceae Chen, Davidiaceae H.-L. Li, Mastixiaceae Calestani

[Hydrostachyaceae [Hydrangeaceae + Loasaceae]]: ovary with intrusive parietal placentation; ovules many/carpel, parietal tissue 0; micropylar endosperm haustorium +.

HYDROSTACHYACEAE Engler, nom. cons.  - Back to Cornales


Annual to perennial herbs; submerged aquatics; primary root 0, "adventitious" roots +; kaempferol +, iridoids 0; vessels present, ?type; nodes ?; stomata 0; leaves spiral, deeply and complexly divided, surface with small enations, stipule single, intrapetiolar (two, lateral); inflorescence spicate, plants di(mon)oecious; P 0; nectary 0; staminate flowers: A 2, extrose, monothecal; pollen in tetrads, inaperturate; carpellate flowers: G superior, [2], transverse, placentation parietal, style branches separate, filiform, impressed; ovules with integument ca 5 cells across, ?endothelium; fruit a septicidal capsule; seeds minute, exotestal, outer cell walls much thickened, mucilaginous; endosperm scanty or 0; n = 10-12.

1 [list]/20. C. and S. Africa, Madagascar (map: from Rauh & Jäger-Zürn 1966b; Trop. Afr. Fl. Pl. Ecol. Distr. 5. 2010).

Chemistry, Morphology, etc. The caffeoyl ester chlorogenic acid is found here and in the Loasaceae-Hydrangeaceae clade (Rønsted et al. 2002). Another interpretation of the androecium is that is consists of one tetrasporangiate stamen. Vessels are reported (Jäger-Zürn 1998), but are not described. There seems not to be an endothelium. The styles are more or less impressed into the apex of the ovary, a feature that Leins and Erbar (1988) noted was common in Lamiales, although I do not know the general distribution of this feature.

For floral development, see Leins and Erbar (1988), for general information, see Erbar and Leins (2004a), and for chemistry, Rønsted et al. (2002).

Previous Relationships. Hydrostachyaceae have variously been suggested to be sister to Decumaria (Hydrangeaceae) (Albach et al. 2001), or close to Crassulaceae (Saxifragales), or - perhaps - close to Podostemaceae (sister to Hypericaceae, in Malpighiales). However, Takhtajan (1997) included Hydrostachyales in his Lamiidae, Cronquist (1981) also put Hydrostachyaceae in that general area, and Burleigh et al. (2009) also suggested they might be in Lamiales.

[Hydrangeaceae + Loasaceae]: similar route I secoiridoids and route II decarboxylated iridoids [C-8 iridoid glucosides +; C-9 iridoids, keeping the C-11, e.g. deutzioside, +], flavonols +, ellagic acid 0; cork cambium deep-seated; hairs tuberculate, walls calcified, with basal cell pedestals; leaves opposite, lamina (lobed), margins with glandular teeth; A (initiated as antesepalous triplets), (2x C-)many; ovary with axial/central vascular bundles, stigma dry; ovules with endothelium; fruit septicidal, (persistent placental strands +); exotestal cells variously elongated, inner walls thickened; chalazal endosperm haustorium +; mitochondrial coxII.i3 intron 0.

Age. A possible age for this node is (64-)50, 49(-36) m.y. (Bell et al. 2010), ca 70.4 m.y. (Tank et al. 2015: Table S2; ca 36.8 m.y. Table S1), while Wikström et al. (2001) suggest an age of (96-)91, 82(-77) m.y., Schenk and Hufford (2010) an age of 91.6-58 m.y., while around 90.5 m.y.a. is the age in Magallón et al. (2015).

Chemistry, Morphology, etc. For some distinctive iridoids found in this family pair, see Frederiksen et al. (1999) and Gousiadou et al. (2016).

The androecium of both families is very variable in development (Hufford 1990, 1998). It is possible that diplostemony is plesiomorphic, with polystemony derived. The antisepalous androecial triplets sometimes found here are also found in Rosaceae and Zygophyllaceae (Hufford 2001b, see also Ronse Decraene & Smets 1996a). The embryology of the group is poorly studied. Fruits are sometimes septicidal and sometimes loculicidal; this variation has not been integrated with the phylogeny.

Classification. Takhtajan (1997) included Hydrangeales in Cornidae-Cornanae, but Loasales-Loasanae were part of his Lamiidae.

HYDRANGEACEAE Dumortier, nom. cons.  - Back to Cornales

Shrubs, vines, or herbs; (plants Al accumulators); kaempferol, flavonols +, tanniniferous; (hairs stellate or branched); cork inner cortical or outer pericyclic; (vessel elements with simple perforation plates); true tracheids +; (stomata paracytic); leaves opposite, bases joined by lines across the stem, lamina vernation conduplicate or supervolute, (secondary veins palmate); inflorescence cymose; flowers 4-5(-10)-merous; anthers with basal pit; tapetal cells 1-4-nucleate; nectary vascularized; G [(2-)3-5(-12)] to inferior, ovary ribbed, arrangement variable, stigma linear to capitate; ovules apotropous, integument (3-)5-7(-10 - Hydrangea) cells across; embryo sac protruding into micropyle, antipodal cells persist; seed winged or not; endosperm moderate, micropylar endospermal cells elongated; n = 13-18.

9 [list]/270 (223) - two subfamilies below. Warm temperate, some species in tropics. [Photo - Flower] [Photos - Collection]

Age. The age for crown Hydrangeaceae may be (87-)83, 69(-65) m.y.a. (Wikström et al. 2001) or (58-)44, 43(-30) m.y. (Bell et al. 2010); both include Hydrostachyaceae. Ca 52 m.y.a. is the age in C. Kim et al. (2015b)[and ca 45 m.y. (C. Kim et al. 2015)?].

Some of the Late Cretaceous fossils assigned to Esgueiria and placed in Combretaceae may end up here - c.f. style, hair surface, etc. (see Takahashi et al. 1999). The Late Cretaceous Scandianthus from Sweden, has also been linked with Hydrangeaceae (see Friis & Pedersen 2012 for references). Tylerianthus crossmanensis, in Late Cretaceous deposits from eastern North America of ca 90 m.y. age, has been linked with Hydrangeaceae; it has nectaries on the upper part of the inferior ovary, five sepals, five stamens opposite the sepals that alternate with five long, linear staminodes. It has been mostly compared with Hydrangeaceae (see also Crepet et al. 2004) or Saxifragaceae s. str. (well, sort of, also including Parnassiaceae, Gandolfo et al. 1998b: also compared with Grossulariaceae, see Friis et al. 2014).


1. Jamesioideae Hufford

(Myricetin +), iridoids 0 [Jamesia]; leaf buttresses prominent after leaves fall; K valvate, C free, (clawed - Fendlera); A 10, filaments flattened, ± forming tube; G (3-)4-5, style branches separate or almost so; endothelium 0, basal part of nucellus persists [Fendlera]; endosperm nuclear [Fendlera]; n = 16.

2 (Jamesia, Fendlera)/ca 5. W. North America (map: from Holmgren & Holmgren 1989).

Age. Crown-group Jamesioideae are around 25 m.y.o. (C. Kim et al. 2015b).

2. Hydrangeoideae Burnett


Phloem loading via intermediary cells [specialized companion cells with numerous plasmodesmata, raffinose etc. involved]; nodes also 5:5, 7(+):7(+); petiole bundles (arcuate [+ inverted bundles])/annular, often with medullary bundles; raphide sacs + (0); stomata variable; (hairs stellate); K valvate, (C contorted); microsporogenesis simultaneous [Platycrater]; (archesporial cells several), embryo sac long [inc. long chalazal half], grows out of micropyle; (placentation axile).

15/185 - two tribes below. Warm temperate, esp. South East Asia and North America, S. to Chile and Malesia (map: from Hu 1955; Zaikonnikova 1966; McClintock 1957; van Balgooy 1984; Mai 1985; Hong 1993).

Age. The age of crown Hydrangeoideae is estimated at (82-)78, 67(-63) m.y.a. (Wikström et al. 2001: note position of Hydrostachys!) or ca 43 m.y.a. (C. Kim et al. 2015).

2a. Philadelpheae Duby

(Stomata laterocytic); (K connate), C imbricate; A 10, (filaments flattened, forming tube), or many and initiation as five common primordia; style ± branched or not; ovule with 1 lateral layer of nucellar tissue; embryo sac ± protruding from the nucellus.

6/130: Philadelphus (65 or fewer), Deutzia (60). Warm temperate, esp. South East Asia to the Philippines, SW North America, also Central America, Philadelphus coronarius in Europe.

Age. The age of the clade [Kirengeshoma + the rest] is 70.6-33.9 m.y. (Guo et al. 2013).

Synonymy: Philadelphaceae Martynov

2b. Hydrangeeae de Candolle

Myricetin + [sect. Decumaria]; raphides +; inflorescence often with conspicuous marginal flowers [= large petal-like K]; C valvate; style +, short to long, stigmas ± separate; fruits loculicidal, endocarp of large cells with horizontally-elongated digitate-interlocking walls, (baccate).

1/65. Warm N. temperate, esp. East Asia, S. to Chile and Malesia, Hawaii.

Chemistry, Morphology, etc. Species of Deutzia have stamens in a single whorl with strongly flattened filaments that may form a tube around the ovary and style (see also C. Kim et al. 2015), and a similar arrangement occurs elsewhere in the family (e.g. see also Jamesia). Philadelphus has centrifugal androecial development. In Philadelphus, Deutzia, and Hydrangea sect. Dichroa the four carpels alternate with the sepals, or there are three carpels with the odd member adaxial; in other species of Hydrangea the odd carpel is abaxial or there are five carpels opposite the sepals. There is considerable variation in the degree of fusion of the styles, but transitions between the extremes are easy to envisage (Roels et al. 1997). In a number of taxa the embryo sac more or less protrudes into the micropyle or beyond (Maheshwari 1950; Hufford 2004). The presence of chalazal haustoria needs confirmation; Mauritzon (1933) noted that the antipodal cells might persist, as in Kirengeshoma, and talks of an "Antipodenhaustorium". The base of the endosperm is lignified; Fendlera has nuclear endosperm (Mauritzon 1939a). The endocarp of Hydrangea consists of large cells with horizontally digitate-interlocking anticlinal walls, as in Curtisia, but not in Cornus (Manchester et al. 2007).

For iridoids, see Frederiksen et al. (1999) and Gousiadou et al. (2016) and for flavonoids, see Bohm et al. (1985), for vegetative anatomy, see Watari (1939), Styer and Stern (1979 and references) and Gregory (1998), for variation in the position of the carpels when the gynoecium is bicarpellate, see Eichler (1878; also Eckert 1966), for floral anatomy and morphology, see Klopfer (1971, 1973) and Bensel and Palser (1975c), for androecial development, Gelius (1967) and Hufford (1998, 2001a), for floral morphology of Hydrangeae, see Hufford (2001), for some embryology, etc., see Gaümann (1919: Philadelphus), Mauritzon (1933, 1939a) and Ao (2008), for seeds, see Hufford (1995, 1997) and Nemirovich-Danchenko and Lobova (1998), and for general information, see Hufford (2004).

Phylogeny. For relationships within the family, see Hufford (1997b), Hufford et al. (2001: support for its monophyly is not overwhelming), Soltis et al. (1995a) and C. Kim et al. (2015b). Rleationships in C. Kim et al. (2015) are [Philadelphoideae [Jamesioideae + Hydrangeoideae]].

Z.-D. Chen et al. (2016) show relationships within Chinese Hydrangeoideae, quite diverse. Samain et al. (2010b) and Granados Mendoza et al. (2012) discuss relationships in Hydrangeeae, where Hydrangea is polyphyletic, and relationships there were further clarified by de Smet et al. (2015: quite good support for many deeper branches). Guo et al. (2013) studied relationships around Philadelphus, within which Carpenteria may be embedded. The couple of species of Deutzia from Mexico are sister to the rest of the genus (C. Kim et al. 2015b).

Classification. For a classification of Hydrangeaceae, see Hufford et al. (2001). Generic limits around Hydrangea were a mess - Platycrater and seven other genera are embedded in Hydrangea s. str. - but although the circumscription of Hydrangea has been extended and a sectional classification provided (de Smet et al. 2015), some prefer narrower generic limits (Ohba & Akiyama 2016).

Previous Relationships. Hydrangeaceae were part of the old woody Saxifragaceae/Saxifragales, or included with members of this group in Rosales (e.g. Cronquist 1981).

Synonymy: Hortensiaceae Martinov, Kirengeshomaceae Nakai

LOASACEAE Jussieu, nom. cons.  - Back to Cornales


Often coarse herbs (shrubs); myricetin, tannins 0; cork inside pericycle; vessel elements with simple perforation plates; petiole bundles arcuate or annular, with wing bundles; indumentum complex, trichomes unicellular, glochidiate, stinging (0), also with calcium phosphate (0), silicification +/0; leaves spiral (opposite), (compound), lamina (margins lobed), secondary veins pinnate-palmate; flowers (4-)5(-7)-merous; K connate, "large" [usu. enclosing bud], C with three traces; C-A synorganisation, C-A plate formed, filaments terete; pollen tectum striate; G [5], (± superior), opposite sepals, (3, odd member adaxial), style hollow, lobed, stigma narrow or clavate; ovules epitropous, integument 12-17 cells across; (fruit spirally twisted); (testa with hypodermal layer thickened); endosperm copious to none.

20 [list]/265 (308) - five clades below. Mostly American, but also Africa and the Marquesas Islands (map: from Heywood 1978).

Age. Possible crown-group ages for Loasaceae are (44-)33, 31(-21) m.y. (Bell et al. 2010) or (73-)67, 63(-57) m.y. (Wikström et al. 2001).

1. Eucnideae Gilg

Shrublet; C quincuncial, (connate), A (adnate to C), centripetal, connate basally; fruit a septicidal capsule; n = (?19-)21.

1/15. S.W. North America. [Photo - Eucnide Flower © J. Reveal.]

2. Schismocarpus S. F. Blake

Shrublet; A 10, filaments shorter than the anthers; G opposite petals, stigma capitate; n = ?

1/1: Schismocarpus pachypus. Mexico.

[Loaseae [Mentzelieae + Gronovieae]]: (wood rayless); G [3-5], when [3], odd member adaxial.

3. Loaseae Reichenbach

Herbs to (deciduous) shrubs; (iridoids 0); K and C shed separately, petals cymbiform, clawed; A centripetal and centrifugal, stamens in 5 groups opposite petals, antesepalous staminodes + [outer whorl connate, as complex nectariferous scales, inner whorl separate]; pollen ?not striate; n = 6.

Nasa (105). America, but also Africa (Kissenia) and the Marquesas Islands (Plakothira). [Photo - Flower, Flower, Flower, Fruit, Flower.]

[Mentzelieae + Gronovieae]: loss of C-A synorganisation.

4. Mentzelieae Gilg

K and C quincuncial, shed as a unit; A centripetal, connate basally, (forked staminodes +); n = 7.

Mentzelia (60). [Photo - Flower © S. Wolf.]. America.

5. Gronovieae Horaninow

(Hypanthium +), C valvate, petals with a single vascular trace; A 5, opposite sepals (2, three staminodes), anthers bifacial; G [3]; ovule 1/carpel, apical, crassinucellate [Petalonyx, Gronovia], funicular obturator +; fruit a cypsela; testa none; endosperm haustoria 0.

[Photo - Gronovia Flower.] America.

Synonymy: Cevalliaceae Grisebach, Gronoviaceae Endlicher

Evolution: Divergence & Distribution. Schenk and Hufford (2008) suggest dates for some of the main clades in the family.

The distribution of the [Plakothira + Klaprothia + Kissenia] clade (Hufford et al. 2005) is remarkable - the Marquesas, South America, N.E. and S.W. Africa and Arabia...

Pollination Biology. There are some very distinctive floral morphologies in the family. Weigend and Gottschling (2006) discuss pollination in Nasa; there are revolver flowers in this genus (see also Weigend et al. 2003 for nectaries, etc.). Pollination of some South American taxa by small mammals is likely, and in general nectar amount and sugar concentration increase with altitude (Ackermann & Weigend 2006).

Plant-Animal Interactions. Loasaceae from drier environments and in danger of being eaten by mammals tend to contain a diversity of iridoids; interestingly, genera like Nasa that can be defoliated by pyralid caterpillars have little in the way of iridoids, but Nasa in particular has a great diversity of leaf shape (Weigend et al. 2000).

Chemistry, Morphology, etc. There is variation in the composition of fatty acids in the seeds, but its systematic significance is unclear - of the taxa studied by Weigend et al. (2004b), Nasa (Loasoideae) was most distinct; it is well embedded in the family.

For the morphology and mineral composition of the stinging hairs of Blumenbachia and other taxa, see Mustafa et al. (2017: hairs in general in the family, 2018b; also Ensikat et al. 2017).

In some species of Petalonyx (Gronovoideae) there is postgenital fusion of the corolla, this forces the stamens outside the corolla. For the complexities of androecial initiation, see Hufford (1990); antepetalous stamens arise from the flanks of primordia of antisepalous stamens. Hufford (2003) described staminode evolution in detail; see also Weigend et al. (2003) for the staminodes of Nasa, = nectar scales. The stigma is at least sometimes very long (Loasa triphylla - see Hanf 1935). Garcia (1962) found the chalazal endosperm to be very variable - single- to many-celled, much branched or not, while the micropylar haustorium is coenocytic and branched.

Additional information is taken from Moody and Hufford (2000a) and Weigend (2004: general), Thompson and Ernst (1967: Eucnide), Rodriguez et al. (1997, 2002) and Weigend et al. (2000), all iridoids, and Leins and Winhard (1973), Brown and Kaul (1981), Weigend (1996), Hufford (1988, 1989, 1990), all floral morphology/development.

Phylogeny. Strongly supported relationships suggested by Moody and Hufford (2000a), Moody et al. (2001), Hufford et al. (2003) and Hufford (2003) are Eucnide [Schismocarpus [Loasoideae [Mentzelioideae + Gronovioideae]]]. Within Loasoideae, the clade [Plakothira + Klaprothia + Kissenia] may be sister to the rest, but that relationship has little support (Hufford et al. 2005), or the clade may be part of a major polytomy (see also Weigend et al. 2004a). Acuña et al. (2017) discuss relationships in southern Andean Loaseae.

Classification. For generic limits in Loaseae from the southern Andes, see Acuña et al. (2017).

Previous Relationships. In older classification Loasaceae were often grouped with other families that had parietal placentation (e.g. Cronquist 1981).