EMBRYOPSIDA Pirani & Prado
Gametophyte dominant, independent, multicellular, thalloid, with single-celled apical meristem, showing gravitropism; rhizoids +, unicellular; acquisition of phenylalanine lysase [PAL], phenylpropanoid metabolism [lignans +, flavonoids + (absorbtion of UV radiation)], xyloglucans +; plant [protoplasm dessication tolerant], ectohydrous [free water outside plant physiologically important]; cuticle +; cell wall also with (1->3),(1->4)-ß-D-MLGs [Mixed-Linkage Glucans]; chloroplasts per cell, lacking pyrenoids; glycolate metabolism in leaf peroxisomes [glyoxysomes]; centrioles in vegetative cells 0, metaphase spindle anastral, predictive preprophase band of microtubules, phragmoplast + [cell wall deposition spreading from around the spindle fibres], plasmodesmata +; antheridia and archegonia jacketed, stalked; spermatogenous cells monoplastidic; blepharoplast, bicentriole pair develops de novo in spermatogenous cell, associated with basal bodies of cilia [= flagellum], multilayered structure [4 layers: L1, L4, tubules; L2, L3, short vertical lamellae] + 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 dependent on gametophyte, embryo initially surrounded by haploid gametophytic tissue, plane of first division horizontal [with respect to long axis of archegonium/embryo sac], suspensor/foot +, cell walls with nacreous thickenings; sporophyte multicellular, with at least transient apical cell [?level], sporangium +, single, dehiscence longitudinal; meiosis sporic, monoplastidic, microtubule organizing centre associated with plastid, cytokinesis simultaneous, preceding nuclear division, sporocytes 4-lobed, with a quadripolar microtubule system; spores in tetrads, sporopollenin in the spore wall, initially laid down in association with several trilamellar layers [white-line centred layers, i.e. walls multilamellate]; nuclear genome size <1.4 pg, LEAFY and KNOX1 and KNOX2 genes present, ethylene involved in cell elongation; chloroplast genome with close association between trnLUAA and trnFGAA genes.
Many of the bolded characters in the characterization above are apomorphies of subsets 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.
Abscisic acid, ?D-methionine +; sporangium - tapetum +, columella + [developing from endothecial cells], seta developing from basal meristem [between epibasal and hypobasal cells]; stomata +, anomocytic, cell lineage that produces them with symmetric divisions [perigenous]; underlying similarities in the development of conducting tissue and in rhizoids/root hairs; spores trilete; polar transport of auxins and class 1 KNOX genes expressed in the sporangium alone; shoot meristem patterning gene families expressed; MIKC, MI*K*C* and class 1 and 2 KNOX genes, post-transcriptional editing of chloroplast genes; gain of three group II mitochondrial introns.
[Anthocerophyta + Polysporangiophyta]: archegonia embedded/sunken in the gametophyte; sporophyte long-lived, chlorophyllous; sporophyte-gametophyte junction interdigitate, sporophyte cells showing rhizoid-like behaviour.
Sporophyte branched, branching apical, dichotomous; sporangia several, each opening independently; spore walls not multilamellate [?here].
EXTANT TRACHEOPHYTA / VASCULAR PLANTS
Photosynthetic red light response; plant homoiohydrous [water content of protoplasm relatively stable]; control of leaf hydration passive; (condensed or nonhydrolyzable tannins/proanthocyanidins +); sporophyte soon independent, dominant, with basipetal polar auxin transport; lignins +; vascular tissue +, G- and S-type tracheids, sieve cells + [nucleus degenerating], tracheids +, in both protoxylem and metaxylem, plant endohydrous [physiologically important free water inside plant]; endodermis +; leaves spirally arranged, blades with mean venation density 1.8 mm/mm2 [to 5 mm/mm2]; sporangia adaxial on the sporophyll, derived from periclinal divisions of several epidermal cells, wall multilayered [eusporangium]; columella 0; tapetum glandular; gametophytes exosporic, green, photosynthetic; basal body 350-550 nm long, stellate array in transition region initially joining microtubule triplets; placenta with single layer of transfer cells in both sporophytic and gametophytic generations, root lateral with respect to the longitudinal axis of the embryo [plant homorhizic].[MONILOPHYTA + LIGNOPHYTA]
Sporophyte branching ± indeterminate; root apex multicellular, root cap +, lateral roots +, endogenous; endomycorrhizal associations + [with Glomeromycota]; G-type tracheids +, with scalariform-bordered pits; leaves with apical/marginal growth, venation development basipetal, growth determinate; sporangia borne in pairs and grouped in terminal trusses, dehiscence longitudinal, a single slit; cells polyplastidic, microtubule organizing centres not associated with plastids, diffuse, perinuclear; blepharoplasts +, paired, with electron-dense material, centrioles on periphery, male gametes multiciliate; chloroplast long single copy ca 30kb inversion [from psbM to ycf2]; LITTLE ZIPPER proteins.
Sporophyte woody; lateral root origin from the pericycle; branching lateral, meristems axillary; cork cambium + [producing cork abaxially], vascular cambium bifacial [producing phloem abaxially and xylem adaxially].
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].
EXTANT SEED PLANTS / SPERMATOPHYTA
Plant evergreen; nicotinic acid metabolised to trigonelline, (cyanogenesis via tyrosine pathway); primary cell walls rich in xyloglucans and/or glucomannans, 25-30% pectin [Type I walls]; lignins particularly with guaiacyl and p-hydroxyphenyl [G + H] units [sinapyl units uncommon, no Maüle reaction]; root stele with xylem and phloem originating on alternate radii, cork cambium deep seated; mitochondrial density in whole SAM 1.6-6.2[mean]/μm2 [interface-specific mitochondrial network]; stem with vascular cylinder around central pith [eustele], phloem abaxial [ectophloic], endodermis 0, xylem endarch [development centrifugal]; 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; leaves with single trace from vascular sympodium [nodes 1:1]; stomatal pore with active opening in response to leaf hydration, control by abscisic acid, metabolic regulation of water use efficiency, etc.; axillary buds exogenous, (none; not associated with all leaves); prophylls two, lateral; leaves with petiole and lamina, development basipetal, blade simple; plant heterosporous, sporangia borne on sporophylls, sporophylls spiral; 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; megasporangium indehiscent; ovules with parietal tissue 2+ cells across, megaspore tetrad linear, functional megaspore single, chalazal, sporopollenin 0; gametophyte development initially endosporic, dependent on sporophyte, apical cell 0, rhizoids 0, development continuing outside the spore; 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, endoscopic, plane of first cleavage of zygote transverse, suspensor +, short-minute, embryonic axis straight [shoot and root at opposite ends; plant allorhizic], cotyledons 2; plastid transmission maternal; ycf2 gene in inverted repeat, whole nuclear genome duplication [ζ - zeta - duplication], two copies of LEAFY gene, PHY gene duplications [three - [BP [A/N + C/O]] - copies], nrDNA with 5.8S and 5S rDNA in separate clusters; mitochondrial trans- nad2i542g2 and coxIIi3 introns present.
ANGIOSPERMAE / MAGNOLIOPHYTA
Lignans, O-methyl flavonols, dihydroflavonols, triterpenoid oleanane, apigenin and/or luteolin scattered, [cyanogenesis in ANITA 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 apical meristem intermediate-open; root vascular tissue oligarch [di- to pentarch], lateral roots arise opposite or immediately to the side of [when diarch] xylem poles; origin of epidermis with no clear pattern [probably 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; reaction wood ?, associated gelatinous fibres [g-fibres] with innermost layer of secondary cell wall rich in cellulose and poor in lignin; 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, cytoplasm not occluding pores of sieve plate, companion cell and sieve tube from same mother cell; sugar transport in phloem passive; nodes 1:?; stomata brachyparacytic [ends of subsidiary cells level with ends of pore], outer stomatal ledges producing vestibule, reduction in stomatal conductance to increasing CO2 concentration; lamina formed from the primordial leaf apex, margins toothed, development of venation acropetal, overall growth ± diffuse, venation hierarchical-reticulate, secondary veins pinnate, veins (1.7-)4.1(-5.7) mm/mm2, endings free; most/all leaves with axillary buds; flowers perfect, pedicellate, ± haplomorphic; protogynous; parts spiral [esp. the A], free, numbers unstable, development in general centripetal; P +, members 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], sporangium pairs dehiscing longitudinally by a common slit, ± embedded in the filament, walls with at least outer secondary parietal cells dividing, endothecium +, endothecial cells elongated at right angles to long axis of anther; (tapetum glandular), 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; nectary 0; carpels present, superior, free, several, ascidiate, with postgenital occlusion by secretion, stylulus at most short [shorter than ovary], hollow, cavity not lined by distinct epidermal layer, stigma ± decurrent, carinal, stigma wet, 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 [crassinucellate], nucellar cap?; megasporocyte single, hypodermal, functional megaspore chalazal, lacking cuticle; female gametophyte lacking chlorophyll, not photsynthesising, 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 land on stigma, bicellular at dispersal, mature male gametophyte tricellular, germinating in less than 3 hours, pollen tube elongated, unbranched, growing 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 gametes lacking cell walls, cilia 0, siphonogamy; double fertilization +, ovules aborting unless fertilized; P deciduous in fruit; mature seed much larger than ovule when fertilized, small , dry [no sarcotesta], exotestal; endosperm diploid, cellular, heteropolar [micropylar and chalazal domains develop differently, 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; dark reversal Pfr → Pr; Arabidopsis-type telomeres [(TTTAGGG)n]; nuclear genome size <1.4 pg [1 pg = 109 base pairs], whole nuclear genome duplication [ε - epsilon - duplication]; protoplasm dessication tolerant [plant poikilohydric]; 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, paleo AP3 and PI genes [paralogous B-class genes] +, with "DEAER" motif, SEP3/LOFSEP and three copies of the PHY gene, [PHYB [PHYA + PHYC]].
[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]]]]: vessel elements with scalariform perforation plates in primary xylem; essential oils in specialized cells [lamina and P ± pellucid-punctate]; tension wood +; tectum reticulate; anther wall with outer secondary parietal cell layer dividing; carpels plicate; 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 [possible position]; pollen tube growth intra-gynoecial [extragynoecial compitum 0]; embryo sac bipolar, 8 nucleate, antipodal cells persisting; endosperm triploid.
[MONOCOTS [CERATOPHYLLALES + EUDICOTS]]: (extra-floral nectaries +); (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.
EUDICOTS: (Myricetin, delphinidin +), 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 few, (polyandry widespread, initial primordia 5, 10, or ring, ± centrifugal), 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, SABIACEAE [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]: ?
CORE EUDICOTS / GUNNERIDAE: (ellagic and gallic acids +); leaf margins serrate; compitum + [one place]; micropyle?; whole nuclear genome duplication [palaeohexaploidy, gamma triplication], 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 = calyx + corolla, the calyx enclosing the flower in bud, sepals with three or more traces, petals with a single trace; stamens = 2x K/C, in two whorls, internal/adaxial to the corolla whorl, alternating, (numerous, but then usually fasciculate and/or centrifugal); pollen tricolporate; G , G  also common, when [G 2], carpels superposed, compitum +, placentation axile, style +, stigma not decurrent; 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).
[SANTALALES [BERBERIDOPSIDALES [CARYOPHYLLALES + ASTERIDS]]] / ASTERIDS ET AL. / SUPERASTERIDS : ?
[BERBERIDOPSIDALES [CARYOPHYLLALES + ASTERIDS]]: ?
[CARYOPHYLLALES + ASTERIDS]: seed exotestal; embryo long.
ASTERIDS / ASTERIDAE / ASTERANAE Takhtajan: 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?; (nectary gynoecial); G , style single, long; ovules unitegmic, integument thick, endothelium +, nucellar epidermis does not persist; exotestal [!: even when a single integument] cells lignified, esp. on anticlinal and/or inner periclinal walls; endosperm cellular.
[ERICALES [ASTERID I + ASTERID II]]: (ovules lacking parietal tissue) [tenuinucellate].
[ASTERID I + ASTERID II] / CORE ASTERIDS: ellagic acid 0, non-hydrolysable tannins not common; sugar transport in phloem active; inflorescence basically cymose; A = and opposite sepals or P, (numerous, usu. associated with increased numbers of C or G); style short[?]; duplication of the PI gene.
ASTERID II / CAMPANULIDAE: myricetin 0; vessel elements with scalariform perforation plates; endosperm copious, embryo short/very short.
[ASTERALES [ESCALLONIALES [BRUNIALES [APIALES [PARACRYPHIALES + DIPSACALES]]]]] / APIIDAE: iridoids +; C forming a distinct tube, tube initiation early; A epipetalous; ovary inferior, [2-3], style long[?].
[ESCALLONIALES [BRUNIALES [APIALES [PARACRYPHIALES + DIPSACALES]]]]: ?
[BRUNIALES [APIALES [PARACRYPHIALES + DIPSACALES]]]: ?
[APIALES [PARACRYPHIALES + DIPSACALES]] / DIPSAPIIDAE: nodes 3:3.
[PARACRYPHIALES + DIPSACALES] / DIPSIDAE: true tracheids +; lamina serrate; inflorescence terminal.
DIPSACALES Berchtold & J. Presl Main Tree.
Route I secoiridoids +; vessel elements with scalariform perforation plates; petiole bundles arcuate; colleters 0; buds perulate; leaves opposite, margins gland-toothed, bases ± confluent, (leaves amplexicaul); inflorescence cymose; pollen grains tricellular; G , at least partly inferior; ovules apotropous, with parietal tissue ca 1 cell across; fruit indehiscent, K persistent, endocarp with fibrous layers perpendicular to each other and thick walled sclereids, containing crystals; seed coat 1-21 µm thick, testa vascularized, exotestal cells enlarged, cuboid/rectangular, variously thickened and lignified; endosperm without haustoria, cells thin-walled, not differentiated. - 2 families, 46 genera, 1090 species.
Age. The first split within crown-group Dipsacales may have occurred in the mid-Cretaceous, some 111-102 m.y.a., the oldest of the estimates (Bell & Donoghue 2005a and references). The age has also been estimated at (90-)62(-32) m.y. in Lemaire et al. (2011b), who also unaccountably note "more recent stem node ages" of 31 m.y. for Dipsacales, which in the context of their tree would be the age of the [Apiales [Paracryphiales + Dipsacales]] clade, and which they dated at (105-)84(-58) m.y. ago. K. Bremer et al. (2004) date the beginning of diversification here at 101 m.y.a., Wikström et al. (2001) at (87-)82, 78(-73) m.y., Beaulieu et al. (2013a: 95% HPD) at (94-)80(-87) m.y., Magallón et al. (2015) at around 70.9 m.y., Bell et al. (2010) at (74-)60, 57(-46) m.y., and N. Zhang et al. (2012), (82-)68(-45) m.y.; ca 77.5 m.y. is the age in Nicolas and Plunkett (2014; ?sampling), around 75.6-62.0 m.y. (Nylinder et al. 2012: suppl.) and (94-)80(-65) m.y. in Wikström et al. (2015).
Note: (....) denotes a feature common in the clade, exact status uncertain, [....] includes explanatory material. Possible apomorphies are in bold. However, the actual level at which many of these features, particularly the more cryptic ones, should be assigned is unclear. This is partly because many characters show considerable homoplasy, in addition, basic information for all too many 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).
Evolution. Divergence & Distribution. The origin of Dipsacales was probably in the northern hemisphere (Beaulieu et al. 2013a). Major diversification within both Dipsacoideae and Valerianoideae - and hence a major part number-wise of diversification of the whole clade - is relatively recent, occurring within perhaps ca 10 m.y. (Bell & Donoghue 2005a); diversification in Dipsacales as a whole has often seemed to increase as plants moved into new geographical areas, especially if these were mountainous (Moore & Donoghue 2007).
For a very detailed discussion of morphological evolution here, see Donoghue et al. (2003); Jacobs et al. (2010b) discussed the evolution of characters of fruit anatomy, while Xu et al. (2011) optimised some pollen characters on the tree. Howarth and Donoghue (2004, esp. 2005, 2008, 2009) and Howarth et al. (2011) noted intriguing correlations between gene duplications with possible neofunctionalisation of e.g. Cycloidea-like genes and changes in floral form in the order, with concomitant restriction of expression of some genes in the petaline whorl and resultant changes in the symmetry of the flowers. Nevertheless, direct connections to diversification rates remain to be established.
Genes & Genomes. For cytological variation, see Benko-Iseppon and Morowaetz (2000a); the two families are rather different. There is considerable variation in the presence of the mitochondrial coxII.i3 intron. Rates of molecular evolution vary considerably in Dipsacales, and this is usually associated with changes in the life style, woody plants usually having lower rates of change than herbaceous (Smith & Donoghue 2008).
Chemistry, Morphology, etc. Anthocyanin variation does not allow a sharp distinction between Caprifoliaceae and Adoxaceae (Jordheim et al. 2006).
Involute vernation of the lamina is more common in Adoxaceae than in Caprifoliaceae (Cullen 1978). For the morphology of the stipule-like structures and amplexicaul leaves in Caprifoliaceae and Adoxaceae see Weberling (1957); amplexicaul leaves, perhaps most common in the inflorescence, are scattered throughout the order. Split-lateral bundles and a girdling vascular trace occur in taxa with perfoliate leaves (e.g. Colomb 1887) as well as in the Morinoideae-Dipsacoideae area (see below). Glands at the base of the leaf in Sambucus and Viburnum may be vascularized (see also Colomb 1887).
Troll and Weberling (1966) and Weberling (1961, 1989) described the inflorescence structure of the woody Dipsacales in particular in considerable detail; inflorescence structure is notably complex in Caprifoliaceae. The morphology of the basic nectary type for the order is unclear, although Wagenitz and Laing (1984) suggest that most Caprifoliaceae s.l. lack terminal flowers. In Viburnum it is a disc-like structure on top of the inferior ovary, in Adoxa it consists of multicellular hairs on the corolla, and in Caprifoliaceae, unicellular hairs (Wagenitz & Laing 1984, Takhtajan 1997; Leins & Erbar 2010). For variation in floral anatomy, which clearly separates two groups of genera in the old Caprifoliaceae, see Wilkinson (1949 and references), interestingly, taxa in both families may have one or more locules infertile, the fertile locule(s) having but a single ovule, however, the reduced loculi may have two to six or so ovules. For more on the inferior/superior ovary distinction in the asterid II clade, see e.g. the Asterales page.
Phylogeny. For the relationships of Dipsacales, see the asterid IIclade. The order has strong support in D. Soltis et al. (2000: see also Wagenitz 1997; Bremer et al. 2001; c.f. A.P.G. 1998). The phylogeny here is based especially on work by Donoghue et al. (2001b, 2003), W.-H. Zhang et al. (2003), Davis et al. (2001), Bell (2003) and Moore and Donoghue (2007). There are some (not major) disagreements with the phylogeny in Pyck and Smets (2001), while Judd et al. (1994) provide an early morphological analysis which gives a similar topology.
Previous Relationships. This grouping has often been recognised. Takhtajan (1997) included Dipsacales, Adoxales and Viburnales in his Dipsacanae, while Cronquist 1981) recognised four families in his Dipsacales.
Thanks. I am very grateful to Volker Bittrich for catching a number of mistakes on this page.
Includes Adoxaceae, Caprifoliaceae.
Synonymy: Dipsacineae Shipunov - Adoxales Nakai, Caprifoliales Berchtold & J. Presl, Lonicerales T. Leibe, Sambucales Berchtold & J. Presl, Valerianales Berchtold & J. Presl, Viburnales Dumortier
ADOXACEAE E. Meyen, nom. cons. Back to Dipsacales
0-methylated flavonols only +; true tracheids?; pericyclic sheath poorly developed; (nodes 1:1, 5:5); (stomata paracytic); (petiole also with adaxial inverted bundles; closed C-shaped and with wing bundles); palisade mesophyll with arm cells; glandular hairs common; (buds not perulate); (extrafloral nectaries +); lamina vernation involute or conduplicate (plicate), secondary veins palmate to pinnate, (stipules on leaf base); flowers small [<5 mm across], (4-merous); K open, usu. very small, sepals with one trace, C rotate; pollen reticulate; G not entirely inferior, lateral and dorsal carpellary bundles free, ventral bundles move from axis to ovary septae, style short, stigma (long-)lobed, dry or wet; ovule 1/carpel, median, parietal tissue ca 2 cells across, endothelium +; fruit drupaceous, stone compressed; seed single, exotestal cells palisade or not, not lignified; endosperm often ruminate; n = (8-)9, chromosomes large, 2.6-10 µm long, centromeres , interphase nucleus (semi)reticulate, euchromatic granules coarse, chromocentres large, distribution irregular, mitotoic condensing behaviour continuous, telomeric areas in particular of mitotic chromosomes condensed when cold.
5[list]/200. North temperate, tropical montane, S.E. Australia, rare in Africa (map: from Hultén 1958, 1971; Meusel & Jäger 1992). 2 groups below. [Photos - Collection]
Age. Crown Adoxaceae are around (67-)60, 57(-50) m.y.o. (Wikström et al. 2001), 85-70.5 m.y. old (Bell & Donoghue 2005a), or (54-)33, 31(-13) m.y.o. (Bell et al. 2010).
1. Viburnum L.
Shrubs (trees); hairs stellate and variants; G , odd member abaxial, 2 abort, nectary on top of G, epithelial; endocarp with layers of fibres oriented parallel to each other, 1+ layers of sclereids; seed coat 21-100 µm thick; outer layer of endosperm differentiated, endosperm with crystals, cell walls ± thickened.
1/175. North temperate, tropical montane, but not in Africa. [Photo - Flower.]
Synonymy: Tinaceae Martynov, Viburnaceae Rafinesque
2. Adoxoideae Syme
Shrubs or herbs; (cambium storied - Sambucus); vessel elements with simple perforation plates; (nodes 1:1), (+ split laterals - Sambucus); leaves compound (deeply lobed); anthers extrorse (8, monothecal); nectary on stigma, on C associated with multicellular hairs, or 0; G 1, [(4), 5], opposite petals, [all fertile], styles separate, stigmas capitate; integument ca 4 cells across, (ovules lacking parietal tissue - Adoxa); embryo sac tetrasporic, eight nucleate [Adoxa-type]; endocarp with three layers of cells, 2 layers of fibres, 1 layer of sclereids; (embryo large - Sambucus).
4/23. Mainly north temperate, esp. China, also tropical montane (few in Africa), S.E. Australia.
Age. Crown Adoxoideae are around 35.5-32.5 m.y. old (Bell & Donoghue 2005a).
Synonymy: Sambucaceae Borkhausen
Evolution. Divergence & Distribution. The devolution and diversification of Viburnum has been much studied. A number of deep branches within Viburnum are occupied by taxa that are currently tropical in distribution (ex section Megalotinus - polyphyletic); the Malesian V. clemensiae is sister to the rest of the genus (Clement & Donoghue 2011; Clement et al. 2014). There may have been several shifts from evergreen leaves with elliptical blades and entire margins to deciduous leaves with more rounded blades and serrate margins (Schmerler et al. 2012), while Jacobs et al. (2008) discuss variation in endocarp and seed. Clement et al. (2014: no out-group) discuss the evolution of these and other such traits, while Spriggs et al. (2015) suggest that diversification in the genus has been driven by extrinsic traits such as the occupation of mountainous regions (in South America and the eastern Himalayas) and shifts between cooler and warmer temperate forests rather than by intrinsic traits.
The evolution of one-seeded fruits in Viburnum seems to be connected with increased speciation rates (Moore & Donoghue 2009), while Weber and Agrawal (2014) suggested that the evolution of extra-floral nectaries was associated with an increase in diversification rate.
For more details of possible apomorphies within the family, see Donoghue et al. (2001b, 2003) and Jacobs et al. (2010b: fruit and seed characters).
Genes & Genomes. Cycloidea gene duplication has occurred within Adoxaceae, e.g. in Viburnum plicatum (Howarth et al. 2011), with its monosymmetric marginal flowers that serve as "petals" for the inflorescence.
Chemistry, Morphology, etc. Tannin-secreting tubes in Sambucus are coenocytic and up to 32.8 cm long, they span the length of an entire internode, but do not extend into the nodal region (Zobel 1986). A fibrous pericyclic sheath in Viburnum may be absent, and that of Sambucus interrupted; that of Caprifoliaceae is better developed, and the cells in the latter are also longer, except those of Linnaea (Cooper 1939). Sambucus has crystal sand.
There is considerable variation in Adoxa and its immediate relatives. Adoxa itself lacks any obvious corolline ring primordium and it has eight stamens with monothecate anthers, nectary on the petal lobes, tenuinucellate ovules, weak endothelium, etc. (Erbar 1994). There are five semi-superior carpels with five styles/styluli (Leins 2000) and there are initially five stamen primordia. The leaves at the bases of the rosettes and on the rhizomes are spiral and there are no extrafloral nectaries (c.f. Sambucus). Reports of an amoeboid tapetum are incorrect (e.g. Wangenitz & Laing (1984). In the recently-described Sinadoxa the stamens appear to be divided into two half stamens, each with a separate filament and a monothecal anther; it is molecularly close to Adoxa (Liu et al. 2000). Donoghue et al. (2003) describe the flowers of Sinadoxa as having three corolla lobes and a single carpel. In another curious genus, Tetradoxa, the half anthers are peltate, there are separate styles (= styluli), the ovary was described as being superior, and the sepals are persistent (Ying et al. 1993).
The ovules in Sambucus may be attached to the axis below the level of insertion of the sepals, etc (Roels & Smets 1994), although they are also shown as being attached slightly above (Thomé 1889, pl. 555). In both Sambucus and Adoxa there are small groups of meristematic cells above the ovules which may represent aborted ovules (Roels & Smets 1994).
For some embryology, see Lagerberg (1909: Adoxa), (Horne 1914) and Moissl (1941), for nectaries in some Adoxaceae, see Vogel (1997), for information about arm cells, see Wagenitz and Laing (1984), for fruits and seeds, see Jacobs et al. (2010b), and for general information about Japanese taxa, see Hara (1983).
Phylogeny. For a phylogeny of Viburnum, see Winkworth and Donoghue (2005), Schmerler et al. (2012), Clement et al. (2014), and references.
CAPRIFOLIACEAE Jussieu, nom. cons. Back to Dipsacales
Bark papery-flaky; O-methylated flavones, flavonols +; cork cambium deep-seated; wood often fluorescing; (pith diaphragms +); pericyclic fibres moderately developed; inflorescence axis racemose, (branched), with ultimate units cymes; flowers rather weakly monosymmetric [K ± polysymmetric]; C 2 + 3, tubular, main petal veins laterally connected [transpetalar veins] nectary of unicellular hairs, on C; anthers sagittate; tapetum amoeboid; pollen grains spheroid, echinate; ovary inferior, lateral and dorsal carpellary bundles 0, ventral bundles in axis, stigma capitate, wet; (testa hypodermis also differentiated, fibrous or not); chromosomes small, 0.6-4.2 µm long, centromeres median or submedian, no C-banding, interphase nucleus semireticulate, euchromatic granules fine, chromocentres small, regular or polarized, mitotic condensing behaviour (continuous to ) proximal-early, no condensation of mitotic chromosomes when cold; duplication of dipsCYC2 and dipsCYC3 genes, horizontal transfer of mitochondrial rps11 gene [?Morinoideae and upwards in the tree].
42/890. Largely temperate/warm temperate in the northern hemisphere, some montane tropics (exp. Valerianoideae), but neither the Antipodes nor the Pacific.
Age. An estimate of the crown-group age is ca 86-68 m.y. (Bell & Donoghue 2005a); K. Bremer et al. (2004: c.f. topology, Lonicera sister to rest) suggested an age of around 75 m.y., Bell et al. (2010: again, c.f. topology) an age of (40-)37, 36(-35) m.y., and Wikström et al. (2015) an age of (76-)62(-49) m. years.
Evolution. Divergence & Distribution. Endress (2011a) suggested that monosymmetric flowers might be a key innovation here, but, as noted above, understanding diversification in Dipsacales is not simple.
Chemistry, Morphology, etc. The glandular leaf teeth have a main vein plus two accessory veins, or one accessory vein proceeding above the tooth.
For paired flowers as inflorescence units, esp. in Linnaeoideae and Zabelia, see Landrein and Prenner (2013). Transpetal veins, branch veins linking adjacent median veins, occur in the upper part of the corolla in at least Diervilla, Kolkwitzia and some Valerianoideae and Dipsacoideae (Gustafsson 1995). The calyx often persists, characteristically remaining small and perched on top of the fruit, which may be narrowed towards the apex. Biparental plastid transmission occurs in some taxa, but sampling is poor.
Some information is taken from Magócsy-Dietz (1899: pith diaphragms, woody members only) Carlquist (1982: wood anatomy), Verlaque (1984: relationships), Ogata (1988, 1991: wood anatomy), Hoffmann and Göttmann (1990: general), Backlund and Donoghue (1996: general), Backlund and Nilsson (1997: pollen), Backlund and Pyck (1998: general), Benko-Iseppon and Morawetz (2000a: general), Nilova (2001: bark anatomy), Donoghue et al. (2001b) and especially Bell et al. (2001) and Jacobs et al. (2011), all general.
Phylogeny. The position of Heptacodium was initially somewhat uncertain (Pyck & Smets 2000, 2001), although there are suggestions that it be included in Caprifolioideae (e.g. Donoghue et al. 2001a, 2003; Soltis et al. 2011 [support weak]; Landrein et al. 2012). However, its flowers have several bracteoles and only one of the three carpels develops, the fruit having a single seed; these are not features characteristic of Caprifolioideae. It may well be a hybrid between members of Caprifolioideae and Linnaeoideae (Z.-Y. Zhang et al. 2002; Landrein & Prenner 2013).
Recently much attention has been paid to the circumscription of Linnaeoideae. Jacobs et al. (2010c) found that Zabelia (ex Abelia) might be in the [Morinoideae [Dipsacoideae + Valerianoideae] clade, although support was only moderate (see also Soltis et al. 2011); pollen morphology was perhaps consistent with this position (Jacobs et al. 2010d). There was weak support for the relationships [Zabelia [Morinoideae [Dipsacoideae + Linnaeoideae]]] in the analysis of H.-F. Wang et al. (*2015). Landrein and Prenner (2013) suggested that Zabelia and Diabelia (Linnaeoideae) had similar "primitive" (their scare quotes) inflorescences.
In other analyses Zabelia and Morinoideae formed a clade, although support for this was only moderate (Jacobs et al. 2011). Landrein et al. (2012: useful table of characters, topology of some trees difficult to interpret) suggested that Zabelia was sister to the whole [Morinoideae [Valerianoideae + Dipsacoideae]] clade. Soltis et al. (2007a) found that the position of Valerianoideae was unstable in some analyses; analyses of mitochondrial data are perhaps particularly challenging (Winkworth et al. 2008b). Morinoideae migrated basally in an analysis by Beaulieu et al. (2013a), but only 4 genes were in that analysis, and they were sister to Linnaeoideae in Wikström et al. (2015: taxon sampling).
Classification. The circumscription and number of families in the area of the Caprifoliaceae and Dipsacaceae sensu versions 12 and before (see also A.P.G. II 2003) was the direct result of deciding to maintain the well known Dipsacaceae and Valerianaceae in their old circumscriptions - the small clades resulting from the break-up of the old, broadly-circumscribed and strongly paraphyletic Caprifoliaceae had to be accounted for (Backlund & Bremer 1997; Backlund & Pyck 1998; c.f. Stevens 1998). The whole lot are usefully be combined in a Caprifoliaceae s.l. (see also A.P.G. III 2009), since similarities between the families are considerable and differences are mostly slight. There is still (as of iv.2013) instability in the backbone of the tree, furthermore, because of the possible hybrid origin of Heptacodium - Caprifolioideae x Linnaeoideae - it is characterized separately below.
Shrubs; lamina vernation involute [Weigela]; (K monosymmetric); nectary at base of C; filaments hairy; pollen pororate, membrane granulose; G ; ovules many/carpel, ?marginal; fruit beaked, dehiscing laterally, septicidal; (seeds winged); n = 9.
1-2[list]/16. East Asia, S.E. U.S.A. (map: from Li 1952, approximate).[Photo - Flowers © M. Clayton]
Age. For the early Caenozoic fossil history of Weigela, see Manchester et al. (2009).
Chemistry, Morphology, etc. The large nectary at the base of the corolla in Diervilla (perhaps including Weigela) is a swelling covered by nectar-secreting hairs similar to those in Lonicera, etc. Only one carpel may be fertile, and in some species there may be an "epicalyx" (see below) immediately below the ovary.
Phylogeny. For relationships in Diervilloideae, see Kim and Kim (1999). Weigela maximowiczii is of uncertain position at the base of the tree, while W. middendorffiana is weakly supported as sister to Diervilla.
Synonymy: Diervillaceae Pyck
[Caprifolioideae [Linnaeoideae [Morinoideae [Valerianoideae + Dipsacoideae]]]]: inflorescence lacking terminal flower.
Age. The age of this node is ca 84-66.5 m.y. (Bell & Donoghue 2005a); Wikström et al. (2001: c.f. scrambled topology) suggested an age of (62-)58, 54(-50) m.y., while an age of ca 40.7 m.y. is suggested by Naumann et al. (2013).
2. Caprifolioideae Eaton
Shrubs (trees); vessel elements usu. with simple perforation plates; lamina vernation supervolute or conduplicate (involute - Heptacodium), margins entire, secondary veins pinnate to palmate; K small; A (4-)5, filaments glabrous; G [3(-4)], all, 3/4 or 2/4 fertile, odd member adaxial (opposite petals - Leycesteria); ovules 1-8/carpel; fruit baccate [Lonicera] or drupaceous [Symphoricarpus]; n = 9; deletion in the chloroplast gene clpP.
5[list]/220: Lonicera (180). Mostly N. temperate, esp. East Asia and E. North America (map: see Hultén 1971; Hultén & Fries 1986; Meusel et al. 1992). [Photo - Flower.]
Age. The age of crown Caprifolioideae is ca 79-64 m.y. (Bell & Donoghue 2005a: note position of Heptacodium). Another estimate of their age is 51-36 m.y.a. (Smith 2009).
Evolution. Divergence & Distribution. Diversification of this clade possibly began in Asia (Smith 2009).
Chemistry, Morphology, etc. There is no stem endodermis.
Triosteum seems to lack dorsal carpellary bundles only and has apotropous ovules (Wilkinson 1949). The drupes of Symphoricarpus have a thick outer layer of narrow, vertical fibres and an layer of horizontal fibres; the seed coat itself is crushed.
For the morphology of Japanese taxa, see Hara (1983).
Phylogeny. Relationships in Caprifolioideae - [Heptacodium [Triosteum *[Lonicera [Leycesteria + Symphoricarpos]]]] - are suggested by Theis et al. (2008); the node with the asterisk has a poor posterior probability, but a good bootstrap value.
Synonymy: Loniceraceae Vest
Cork mid-cortical; fibres in cortex; lamina tripli-nerved; inflorescences with flowers in whorls of 6; 2 carpels abort, 1 fertile; fertile ovule 1/carpel; fruit a cypsela; n = 14, centromeres submedian and (sub)terminal.
1/1: Heptacodium miconioides. E. China, uncommon (Map: FoC vol. 19. 2011).
Chemistry, Morphology, etc. For cytology, etc., see Z.-Y. Zhang et al. 2001.
[Linnaeoideae [Morinoideae [Valerianoideae + Dipsacoideae]]]: epicalyx + [from aborted flowers, etc.]; A 4, didynamous; 1 carpel fertile, 2 carpels abort; fertile ovule 1/carpel; fruit a cypsela; seed coat flattened, exotesta not lignified.
Age. Magallón and Castillo (2009: note topology) offer an estimate of ca 59 m.y. for the age of this node; Bell and Donoghue 2005) an age of 71.5-49.5 m.y..
Evolution. Divergence & Distribution. For fruit characters perhaps apomorphic at this level, see Jacobs et al. (2010b, 2011).
Chemistry, Morphology, etc. The morphological nature of structures variously described as supernumerary bracts, bracteoles, epicalyx, and involucel that are associated with flowers in this clade has occasioned much and complex discussion - see Troll and Weberling (1966), Weberling (1992), Roels and Smets (1996), Donoghue et al. (2003), Pyck and Smets (2004), Landrein et al. (2012), Landrein and Prenner (2013) and H.-F. Wang et al. (2015) . The epicalyx is sometimes described as consisting of four fused bracts and having nothing to do with bracteoles (Hofmann & Göttmann 1990; Mayer 1998); the individual flower that it surrounds may then be the terminal flower of a partial thyrsoid inflorescence (esp. Roels & Smets 1996; see also Landrein et al. 2012, Landrein & Prenner 2013). But perhaps some of the bracts presumed to signify "things" like aborted flowers, missing inflorescence branches, etc, may simply be developmentally duplicated structures... In the characterisations below, the particular condition of the epicalyx for each subfamily is described in general terms; what the epicalyx might "be" morphologically is a separate issue.
Where there are only two stamens, it is usually the adaxial pair that persists. Of the three carpels, it is an adaxial lateral carpel that remains fertile (Donoghue et al. 2003). If the flower has four carpels, two are fertile (Landrein et al. 2012).
3. Linnaeoideae Rafinesque
Shrubs (prostrate, ± herbaceous); vessel elements with scalariform perforation plates; stomata paracytic [Abelia]; lamina vernation supervolute(-curved); epicalyx with 4 or 6 members, accrescent or not; (K foliaceous), nectariferous petal abaxial, bulging, (nectary as 1-3 lines of compact hairs between abaxial filaments); filaments hairy; (pollen 3-4-colpate, surface spiny - Abelia); (G , 2 fertile - Dipelta); ovule ?apotropous; K and/or bracts often modified, enlarged, in fruit; fruits dorsiventrally compressed; ?embryo length [small - Abelia]; n = 8, 9.
6 [list]/32. Circumboreal (Linnaea), Mexico (Abelia), China to Japan (five genera), Mexico (map [Zabelia not included]: from Hultén & Fries 1986; Meusel & Jäger 1992; Villareal-Quintanilla 2013; see also H.-F. Wang et al. 2015). [Photo - Habit, Flower.]
Age. The crown-group age of Linnaeoideae has been estimated at 48.5-37.5 m.y.a. (Bell & Donoghue 2005a) and (60.2-)50.9(-42.8) m.y. (H.-F. Wang et al. 2015).
Evolution. Divergence & Distribution. For distinctive late Eocene fruits (Diplodipelta, ca 37 m.y.o.) assignable to this group and their implications for biogeography and evolution, see Manchester and Donoghue (1995); H.-F. Wang et al. (2015) offer a somewhat different interpretation and place them within Linnaeoideae. Manchester et al. (2009) discussed the fossil distribution of Dipelta, which is known from Eocene/Oligocene rocks in southern England.
H.-F. Wang et al. (2015, q.v. for dates) discussed the biogeography and evolution of the subfamily in detail.
Pollination Biology & Seed Dispersal. Wind-dispersed fruits predominate in the subfamily (H.-F. Wang et al. 2015).
Chemistry, Morphology, etc. For general information, see Hara (1983) and Landrein et al. (2012), also Villarreal-Quintanilla et al. (2014: Abelia). For details of inflorescence morphology, see Landrein and Prenner (2013), although they did not interpret the variation that they found in the context of phylogeny.
Phylogeny. For relationships, see Jacobs et al. (2010c, 2011) and Landrein et al. (2012); the basic phylogenetic structure may be [Linnaea [Vesalea + The Rest]], but H.-F. Wang et al. (2015) found quite good support for the relationships [[Linnaea + Vesalea] The Rest].
Classification. For generic limits and groupings, see Landrein (2010) and Landrein et al. (2012) and for characterisations of the genera, see H.-F. Wang et al. (2015).
Synonymy: Linnaeaceae Backlund
[Zabelia, Morinoideae [Valerianoideae + Dipsacoideae]]: vessel elements with simple perforation plates; petioles connate basally/leaves amplexicaul; nectary at base of C.
Evolution. Divergence & Distribution. The inclusion of Zabelia will affect character optimizations. I have suggested some characters the whole group has in common; given that the petioles of Zabelia are basally connate, I would not be surprised to find that its nodal vascular architecture was like that of other members of this group. However, Zabelia is poorly known, and until there is more certainty over its position in the tree, it is characterized separately below, and characters for [Morinoideae [Valerianoideae + Dipsacoideae]] are also listed separately.
Chemistry, Morphology, etc. For flank-bridges, see Neubauer (1979); it is as if two bundles on each side form split laterals, and one branch from each bundle fuses, so forming the bridging bundle. Bundles innervating the petiole arise from the bridging bundle, except in Morina.
Both Zabelia and Morinoideae have smooth pollen grains with endocinguli (Jacobs et al. 2011; Landrein et al. 2012).
For pollen size, see Xu et al. (2011), and for relationships suggested by some morphological characters, see Peng et al. (1995).
4. Zabelia Makino
Shrubs; ?chemistry; wood ring porous; lamina entire, petiole bases swollen, enclosing axillary bud; epicalyx with 6 or 14 members, not accrescent; nectary pouched abaxially, with four lines of compact hairs; pollen grains smooth, with endocinguli; ovule?; seed?; n = 9.
1/4: Central Asia (Tian Shan) to the Far East (Map: from Meusel & Jäger 1992; FoC vol. 19. 2011).
Chemistry, Morphology, etc. For general information, see Hara (1983), Landrein et al. (2012) and Landrein and Prenner (2013).
[Morinoideae [Valerianoideae + Dipsacoideae]]: perennial rosette herbs with taproot; monoterpenoids, cathecolic tannins, alkaloids +, ellagic acid 0; libriform fibres +; nodes 5:5; vascular flank-bridge in stem between lateral bundles; buds not perulate; filaments glabrous, anthers dorsifixed; pollen "large"; G with sterile loculi much reduced,; ovule apical, endothelium prominent, with crystal layer; chalazal nuclei variously proliferating; exotesta not thickened; endosperm scanty, embryo large; distinctive expansion of the chloroplast inverted repeat.
Age. The age of this node is around 69-48 m.y. (Bell & Donoghue 2005a: Zabelia not included).
Chemistry, Morphology, etc. For a comparison of Morinoideae, Valerianoideae and Dipsacoideae, see Cannon and Cannon (1984). Zabelia and Morinoideae have smooth pollen grains with endocinguli (Jacobs et al. 2011; Landrein et al. 2012).
Phylogeny. For relationships suggested by some morphological characters, see Peng et al. (1995).
For embryology, see Johri et al. (1991).
Ethereal oils +, iridoids 0; stems hollow; lamina vernation involute, margins spinose to pinnatifid (entire), secondary veins palmate; inflorescence of sessile cymes [verticels], epicalyx 12-ribbed; flowers strongly monosymmetric; K 4, monosymmetric; A pairs inserted at different heights on the C tube (A 2, + 2 staminodes); tapetum ?glandular; pollen binucleate, (turret-like triporate), surface smooth, with endocinguli [extra thickened layer of pollen wall], exine columellae reduced, intine-covered tubular extrusions; embryo with hypostase; embryo sac with chalazal cells producing multicellular structures; integument multiplicative, not vascularized, outer layer only persisting; endosperm ruminate; n = 17; duplication of dipsCYC2 and dipsCYC3 genes.
2-3[list]/13. Balkans to China (map: see Cannon & Cannon 1984). [Photo - Morina Inflorescence, Acanthocalyx Inflorescence.]
Age. Crown-group Morinoideae are estimated to be around 46-31 m.y.o. (Bell & Donoghue 2005a).
Evolution. Divergence & Distribution. Bell and Donoghue (2003) discuss biogeographic relationships within the clade.
Chemistry, Morphology, etc. Remarkable intine-covered structures like pollen tubes are produced in all taxa before pollen germination (Blackmore & Cannon 1983), and sometimes also in also Dipsacoideae (Hesse et al. 2009b). The integument is 14-18 cells across when the embryo sac is mature, becoming ca 25 cells across later (Vijayaraghavan & Sarveshwari 1968).
For tables of differences between Morinoideae and Dipsacoideae, see Vijayaraghavan and Sarveshwari (1968), Cronquist (1981), Cannon and Cannon (1984) and Johri et al. (1992). There seems to be total confusion as to the nature of the tapetum of Morina: Vijayaraghavan and Sarveshwari (1968) describe it as being polyploid, multinuclear and secretory, Kamelina (1983) as cellular, binuclear and glandular, and Johri et al. (1992) as being amoeboid (and that of Dipsacoideae as being glandular).
For embryology, see Vijayaraghavan and Sarveshwari (1968: Morina longifolia only), for pollen, Verlaque (1984, 1986), and for a monograph of the subfamily, Cannon and Cannon (1984: as Morinaceae).
Phylogeny. Acanthocalyx is sister to the rest of the family, Morina may be paraphyletic (Bell & Donoghue 2003).
Synonymy: Morinaceae Rafinesque
[Dipsacoideae + Valerianoideae]: (annual herbs); saccharose +, quercetin 0; (nodes 5 or more:5 or more); leaves simple to ± pinnate, lamina vernation conduplicate, (margins entire); flowers rather small; A ± equal in length; tapetal cells 4 or more nucleate [?level]; pollen with prominent and branched exine columellae; stigma dry; embryo sac with 2-4-nucleate chalazal cells; embryo green; centromeres metacentric to subtelocentric, no C bands.
Age. The age of this node is estimated to be ca 62.5-44.5 m.y. (Bell & Donoghue 2005a) or (41-)31(-22) m.y. (Wikström et al. 2015).
6. Dipsacoideae Eaton
(Shrubby); (vessel elements with scalariform perforation plates); starch almost 0; (stomata anisocytic); lateral abaxial C lobes overlapping adaxial lobes; ovule apotropous, micropyle very long, hypostase +; chalazal nuclei polyploid; stigma entire or 2-lobed.
11[list]/290. Eurasia, Africa, esp. Mediterranean region, to Malesia.
Age. Crown Dipsacoideae can be dated to ca 52.5-39.5 m.y. (Bell & Donoghue 2005a).
6a. Triplostegia de Candolle
Valpotriate-type iridoids +; flowers with bracteoles and double epicalyx; C ± polysymmetric; pollen aperture with a halo, colpus granulose; fruit surrounded by capitate-glandular outer epicalyx, the tips hooked; endosperm slight; n = ?
1/2. Southeast Asia, East Malesia (map: from van Steenis 1951).
Synonymy: Triplostegiaceae Airy Shaw
6b. The Rest.
Inflorescence a capitulum, with involucral bracts; epicalyx single, 8-ribbed; (C with 4 lobes); (A 2-3); (pollen 3-porate); G ; ovule with integument 10-15 cells across; fruit with calycine awns or bristles; endosperm +; n = 5, 7-9(-10).
10/290: Scabiosa (80), Cephalaria (65), Knautia (60). Eurasia, Africa, esp. Mediterranean region. [Photo - Habit, Inflorescence, Flower.]
Synonymy: Dipsacaceae, Juss., nom. cons., Scabiosaceae Martinov
Evolution. Divergence & Distribution. For large-scale migration within Scabiosa, including north to south movement in Africa, see Carlson et al. (2012).
Seed Dispersal. Caputo et al. (2004) examined the evolution of seed dispersal syndromes. The well-developed epicalyx suggests that the fruits are often wind-dispersed, but myrmecochory may occur in almost half of the subfamily, especially in the large genera Knautia and Scabiosa (Lengyel et al. 2009, 2010).
Genes & Genomes. In Knautia it was found that genome size increased towarsd the periphery of the range of the genus, although why was unclear; the distribution of polyploidy, etc., was also studied (Frajman et al. 2015).
Chemistry, Morphology, etc. The cork of Knautia may be superficial (Metcalfe & Chalk 1950).
For embryology, see Kamelina (1983), and for fruit, see Verlaque (1977), for a general study, see Verlaque (1985, 1986).
Phylogeny. Triplostegia, which has a double epicalyx and valepotriates, seems best assigned to Dipsacoideae (e.g. 100% support in a 30 taxon-5 gene analysis - Davis et al. 2001; see also Bell & Donoghue 2000, 2005a; W.-H. Zhang et al. 2001; Bell 2004; Soltis et al. 2011). However, Pyck and Smets (2004) showed that although a two-gene analysis places Triplostegia in this position, morphological data alone and when combined with the molecular data place it sister to Valerianoideae. As they note, the clade [Triplostegia + Valerianoideae] has valpotriate-type iridoids, a pollen aperture with a halo, a granulose colpus, and also endosperm reduction in common, and possibly even epicalyx/bracteole similarities. Avino et al. (2009) found that Triplostegia might be sister to [Valerianoideae + Dipsacoideae], and used this topology in their character state reconstruction. Indeed, where Triplostegia ends up will substantially affect apomorphy positions, and the characters that Triplostegia and Valerianoideae have in common may be either paralellisms, or apomorphies for the larger clade, but with reversals.
The position of Triplostegia aside, Pterocephalodes, a recent segregate from Pterocephalus (Mayer & Ehrendorfer 2000), and Bassecoia together form a clade that is sister to the rest (Avino et al. 2009; Carlson et al. 2009). For other phylogenetic studies, see Caputo et al. (2004) and Carlson et al. (2012: Scabiosa); Resetnik et al. (2014) look at relationships between diploid species of Knautia.
Classification. Mayer and Ehrendorfer (2013: much morphology) provide a classification of the subfamily.
7. Valerianoideae Rafinesque
Foetid monoterpenoids and sesquiterpenoids, valpotriates +; (root with superficial cork - Valeriana); true tracheids ?; (leaves bijugate), (leaf bases not sheathing); (plant dioecious); flowers small, corolla ± polysymmetric, bracteoles +, epicalyx 0; K small, abaxial C basally spurred (or not); A (1-)3(4-5), (anthers bisporangiate, ?thecae - Valeriana subg. Phyllactis); pollen colpate; (G with sterile loculi absent); K + (very large; a pappus; reduced); testa 1-layered; (endosperm 0); n = (7-)8(9-12).
17[list]/315: Valeriana (200), Valerianella (80). N. temperate, especially Mediterranean, and Andean South America (half the subfamily) (map: from Hultén 1958; Meusel et al. 1978). [Photo - Habit, Flower, Flower.]
Age. Crown-group Valerianoideae may be 56-34.5 m.y. old (Bell & Donoghue 2005a), ca 50 m.y. (Moore & Donoghue 2007) and (54-)42(-33) m.y. (Beaulieu et al. (2013a: 95% HPD).
Synonymy: Valerianaceae Batsch
Evolution. Divergence & Distribution. There were around four migrations of Valerianoideae to South America about (20-)15.7(-12) m.y.a. (Bell et al. 2012a), and diversification in the Andean paramo, where ca 1/7 of the subfamily grow, happened less than 5 m.y.a. (Bell & Donoghue 2005b). Further diversification - ca 1/6 of the species - occurred south of 33oS (Kutschker & Morone 2012).
Seed Dispersal. For fruit and seed evolution, see Jacobs et al. (2010a: Nardostachys not included). The fruits are very variable in their morphology, and dispersal is by a variety of mechanisms.
Chemistry, Morphology, etc. Valepotriates are triesters of route I secoiridoids; for their distribution - they are also found in Nardostachys and Triplostegia - see Backlund and Moritz (1998). The anatomy of some of the high-Andean Valerianoideae will repay further investigation (e.g. see Weberling & Uhlarz); they may have unilacunar nodes and distinctive secondary vascular tissue, lack girdling bundles, etc..
The calyx in Patrinia and in particular Nardostachys is well-developed. Evident sterile loculi, a well developed calyx, an androecium with either four or five stamens, presence of endosperm, etc., are likely to be plesiomorphic here. The corolla tube of Centranthus is divided vertically into two by a septum. The extra "bracteole" of Patrinia may be an interpolated structure that develops into a fruit wing (Hoffmann & Göttmann 1990).
For general morphology, see Eriksen (1989), for anatomy, see Vidal (1903), and for ovule morphology (no vascular tissue?), see Guignard (1893).
Phylogeny. Patrinia may be sister to the rest of the subfamily (Pyck 2002), with Nardostachys sister to the remaining taxa (Bell 2004; Bell & Donoghue 2005a, b: both with very strong support), or the two together form a well-supported clade sister to other Valerianoideae (Hidalgo et al. 2004); the former topology is more likely. Valeriana celtica, Valerianella and Centranthus may be successively sister to Valeriana (Bell & Donoghue 2005b, for which see for further details); Valerianamay indeed be para- or polyphyletic (Hidalgo et al. 2004). For other phylogenies, see Bell (2004) and Bell et al. (2015).