Plant a shrub or tree; true roots +, origin endogeneous, root cap +, apex multicellular; endodermis +; shoot apical meristem multicellular; lateral meristems +, cork cambium producing cork abaxially, vascular cambium producing phloem abaxially and xylem adaxially; lamina with mean venation density 1.8 mm/mm2 (to 5 mm/mm2).
EXTANT SEED PLANTS/SPERMATOPHYTA
Plant woody, 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 derived from (some) sinapyl and particularly coniferyl alcohols, thus containing p-hydroxyphenyl and guaiacyl lignin units, so no Maüle reaction; root xylem exarch, cork cambium deep seated; arbuscular mycorrhizae +; shoot apical meristem interface specific plasmodesmatal network; stem with vascular tissue around central pith [eustele], vascular bundles with interfascicular tissue, ectophloic, endodermis 0, xylem endarch; 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 +; stem cork cambium superficial; branches exogenous; leaves with single trace from vascular sympodium ["nodes 1:1"]; vascular bundles collateral [stem: phloem external; leaf: phloem abaxial]; stomata morphology?, pore opening controlled by abscisic acid; leaves with petiole and lamina, spiral, development basipetal, blade simple; axillary buds +, not associated with all leaves; prophylls two, lateral; plant heterosporous, sporangia borne on sporophylls; microsporophylls aggregated in indeterminate cones/strobili; true pollen +, grains mono[ana]sulcate, exine and intine homogeneous; ovules unitegmic, parietal tissue 2+ cells across, megaspore tetrad tetrahedral, only one megaspore develops, megasporangium indehiscent; male gametophyte development first endo- then exosporic, tube developing from distal end of grain, to ca 2 mm from receptive surface to egg, gametes two, developing after pollination, with cell walls, flagellae numerous; ovules increasing considerably in size between pollination and fertilization, female gametophyte endosporic, initially syncytial, walls then surrounding individual nuclei; seeds "large" [ca 8 mm3], but not much bigger than ovule, with morphological dormancy; embryo cellular ab initio, endoscopic, plane of first cleavage of zygote transverse, suspensor +, short-minute, embryo straight, shoot and root at opposite ends [allorrhizic], white, cotyledons 2; plastid transmission maternal; ycf2 gene in inverted repeat, 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 nad1 intron 2 and coxIIi3 intron and trans-spliced introns present.
Lignans, O-methyl flavonols, dihydroflavonols, triterpenoid oleanane, non-hydrolysable tannins, quercetin and/or kaempferol +, apigenin and/or luteolin scattered, [cyanogenesis in ANITA grade?], S [syringyl] lignin units common, positive Maüle reaction [syringyl:guaiacyl ratio more than 2-2.5:1], and 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, 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 unilacunar [1:?]; stomata brachyparacytic [ends of subsidiary cells level with ends of pore], outer stomatal ledges producing vestibule; lamina formed from the primordial leaf apex, margins toothed, development of venation acropetal, secondary veins pinnate, overall growth ± diffuse, venation hierarchical, fine venation reticulate, veins (1.7-)4.1(-5.7) mm/mm2, endings free; most/all leaves with axillary buds; flowers perfect, pedicellate, ± haplomorphic, parts spiral [esp. the A], free, numbers unstable, development in general centripetal; P not sharply differentiated, with a single trace, outer members not enclosing the rest of the bud, often smaller than inner members; A many, filament not sharply distinguished from anther, stout, broad, with a single trace, anther introrse, tetrasporangiate, sporangia in two groups of two [dithecal], ± embedded in the filament, with at least outer secondary parietal cells dividing, each theca dehiscing longitudinally, 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 columellar, endexine thin, compact, lamellate only in the apertural regions; nectary 0; G superior, free, several, ascidiate, with postgenital occlusion by secretion, stylulus short, hollow, cavity not lined by distinct epidermal layer, stigma ± decurrent, dry [not secretory]; 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, megaspore tetrad linear, functional megaspore chalazal, lacking sporopollenin and cuticle; female gametophyte 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 binucleate at dispersal, male gametophyte trinucleate, germinating in less than 3 hours, pollination siphonogamous, tube elongated, growing between cells, growth rate 20-20,000 µm/hour, outer wall pectic, inner wall callose, 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, flagellae 0, double fertilization +, ovules aborting unless fertilized; P deciduous in fruit; seed exotestal, becoming much larger than ovule at time of fertilization; endosperm diploid, cellular [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; embryogenesis cellular; germination hypogeal, seedlings/young plants sympodial; Arabidopsis-type telomeres [(TTTAGGG)n]; whole genome duplication, 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]]]]]: vessels +, elements with elongated scalariform perforation plates; 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]]]]: essential oils in specialized cells [lamina and P ± pellucid-punctate]; tension wood 0; 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 +; 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 positiion]; embryo sac bipolar, 8 nucleate, antipodal cells persisting; endosperm triploid; ?germination.
I largely follow Ronse De Craene et al. (2003) on the insertion of floral organs. To add where?: A whorled, carpel fusion by congenital occlusion.
Evolution. Divergence & Distribution. The divergence of magnoliids, i.e. the age of this branching point, is estimated at (190-)167(-47) m.y. (95% HPD, Smith et al. 2010, Table S3), while a fossil-based estimate is ca 100 m.y. (Crepet et al. 2004).
Phylogeny. Relationships between the lineages immediately above the basal pectinations in the main tree, the ANITA grade - Amborellales, Nymphaeales and Austrobaileyales here - have been for some time unclear. The positions of Ceratophyllales and Chloranthaceae have been particularly uncertain. Indeed, Graham et al. (2005) found that the inclusion of Ceratophyllum and Chloranthaceae in analyses could destabilise relationships among other early branching clades, e.g., the position of the monocots became labile.
There has been weak support for an (eu)magnoliid clade being sister to the eudicots (e.g. D. Soltis et al. 2000; P. Soltis et al. 2000; Wu et al. 2007; Qiu & Estabrook 2008 [compatibility analysis]); in the first study Chloranthales, monocots, and Piperales were successively sister to the remaining taxa, but these relationships also had little support. Hilu et al. (2003: a matK analysis alone), suggested that Ceratophyllaceae were sister to eudicots (see also D. Soltis et al. 2000; Borsch et al. 2005: three rapidly evolving genes, 62% jacknife, 96% posterior probabilities; Müller et al. 2006: 96% posterior probability; some analyses in Saarela et al. 2007; Qiu & Estabrook 2008). However, Zanis et al. (2002) analysed 11 genes from all genomes and found some support for the magnoliids (strong support for this clade) as being sister to eudicots, with Chloranthaceae, and [monocots + Ceratophyllaceae] occurring as successively more basal branches; below these were the ANITA grade (see also Graham & Olmstead 2000; Borsch et al. 2003). Support for some of these nodes depended on the method of analysis (see also Borsch et al. 2000; Graham & Olmstead 2000; Hilu et al. 2001; Whitlock et al. 2001; Zanis et al. 2002) or the particular gene studied (see Duvall & Bricker 2002: nuclear 18s; Hilu et al. 2003: matK; Duvall et al. 2006: nuclear 18S in particular causes problems). Parkinson et al. (1999) found some evidence for a [Piperales + eudicot] clade, but support was weak. Davis et al. (2004) found the magnoliids to be sister to monocots, with Chloranthaceae and Ceratophyllaceae successively sister to a clade including the few eudicots in the analysis, but support was not exactly overwhelming (the best supported topology in Duvall et al. 2006 is somewhat similar). There was fairly good support for a clade [monocots + Ceratophyllaceae] in a compartmentalised 6-gene analysis (Zanis et al. 2003; see also Qiu et al. 1999; some analyses in Saarela et al. 2007). Müller et al. (2006) found very poorly supported relationships between Chloranthaceae and monocots, which together linked with the magnoliids. In work by Whitlock et al. (2002) largely similar groupings were recognised, but support was only moderate; the exact position of Chloranthaceae remained unclear. Some analyses suggested the possibility of a sister taxon relationship between Chloranthaceae and eudicots (Borsch et al. 2003), while Hilu et al. (2003) in a matK analysis, suggested that they were sister to monocots. Although the support was weak in parsimony analyses, there were 100% posterior probabilities in Bayesian analyses, furthermore, in the latter case only, [Chloranthacaeae + monocots] were sister to magnoliids, although the probabilities there were low. Qiu et al. (2005; see also Löhne & Borsch 2005) found initial rather strong bootstrap support for an association between monocots and Ceratophyllaceae in a 9-gene analysis being vitiated by the failure to obtain much support in any of the subanalyses and by details of the topology obtained in the 9-gene analysis itself (e.g. Acorus sister to the Alismatales that were included) that are rather improbable. Other studies also show no clear pattern (e.g. Jansen et al. 2006a; Qiu et al. (2006b). Interestingly, Piper has the "monocot" pattern of PHY genes (A, B, C genes only), while Ceratophyllum has PHYE (Mathews et al. 1995). Jansen et al. (2006b) and Hansen et al. (2007) found support for a sister-group relationship between Chloranthales and the magnoliids, although the analyses in Mathews (2006a) preferred an unresolved position for Chloranthales and Ceratophyllales above the Austrobaileyales. Duvall et al. (2006) and Qiu et al. (2010: chloroplast data, support weak) found a relationship between Chloranthales and Ceratophyllales, as did N. Zhang et al. 92012), that clade being successively sister to the magnoliids and monocots. Soltis et al. (2007a) found weak support for [Ceratophyllum + eudicots]; relationships of Chloranthaceae were unclear and there was very weak support for monocots as sister to [magnoliids, Chloranthaceae, eudicots, etc.]. Although relationships between basal angiosperms were not their focus, Xue et al. (2012) found the relationships [monocots [[Ceratophyllaceae + Piperaceae] + eudicots]] in a ML analysis of whole chloroplast dataD. Soltis et al. (2005b) had very reasonably summarized their discussion on relationhips in this area by showing a pentatomy (see also P. Soltis et al. 1999).
Morphology in particular has quite often suggested that more or less herbaceous clades like Piperales, Chloranthaceae, and Nymphaeales might be related to monocots, the pal(a)eoherb hypothesis (see e.g. Donoghue & Doyle 1989; Taylor & Hickey 1992; Endress 2000). Analysis of combined morphological and molecular data found that Piperales were sister to monocots (Doyle & Endress 2000, support weak). Although quite popular in the latter years of the last century, its support comes from homoplasies associated with the adoption of the herbaceous habit. Indeed, Piperales are now firmly (usually!) embedded in the magnoliid clade, Nymphaeales are very near the base of the whole angiosperm clade, etc.
Some resolution may be on the way. Thus Graham et al. (2005) found a rather weakly supported (73% bootstrap) [monocot + eudicot] grouping, but this was weaker when Chloranthaceae and Ceratophyllaceae were included. However, evolution of some floral developmental genes, e.g. in the C and D lineages, are also consistent with such a relationship (Kramer et al. 2004). The positional relationships between members of the androecium and the perianth, the stamens being individually opposite perianth members, and perhaps some other characters (trimery of some floral whorls is fairly widespread within Ranunculales) are also consistent with such relationships. (There is the same perianth member/stamen relationship in magnoliids like Lauraceae.) Variation in how calcium oxalate is synthesized may also be of phylogenetic interest, although sampling is very poor; neither members of the ANITA grade nor magnoliids have been examined. Vacuolar crystal formation associated with membranes and paracrystalline bodies with widely spaced subunits are found in eudicots (crystals seem also to be formed in other ways here), while in monocots there are no membrane complexes and the paracrystalline bodies have closely spaced subunits (Horner & Wagner 1995; Evert 2006). Some patterns of RNA editing may be phylogenetically informative at this level (Logacheva et al. 2008).
Other studies have found this [monocot + eudicot] grouping; Jansen et al. (2006b: 37 whole chloroplast genomes, see also Zhengqiu et al. 2006), Cai et al. (2006: 35 whole chloroplast genomes, neither Chloranthales, Ceratophyllales, nor any member of Austrobaileyales included), and Duvall et al. (2006: four genes, three compartments, nuclear PHYC gene, 18S being excluded; overall, a relationships between magnoliids and monocots was preferred), Mathews (2006a: three PHY genes, 105 taxa), and Hansen et al. (2007: 61 protein-coding chloroplast genes). When sequences of complete chloroplast genomes are analysed, an association between monocots and eudicots is more strongly suggested. Thus Jansen et al. (2007) found good support for a [monocot + eudicot] grouping, a number of alternative topologies being excluded, but support in Moore et al. (2007) was somewhat less strong. Ceratophyllum, with quite a long branch, was sister to eudicots (in some reconstructions, Piper, with a very long branch, was also involved), and Chloranthus was sister to the magnoliids with moderate to strong support (Jansen et al. 2007), a position also found by Saarela et al. (2007), many analyses in Moore et al. (2007, 2010), and Smith et al. (2010).
However, in Moore et al. (2010) there were a variety of other "minority" relationships - Ceratophyllum or [Ceratophyllum + Piper] as sister to monocots, and Chloranthaceae sister to a clade including magnoliids, monocots, and eudicots; the latter pair of relationships with moderate jacknife support were found by Davis et al. (2013) in their comprehensive chloroplast analysis focussing on monocots. Goremykin et al. (2009b) recently found a [Ceratophyllum + magnoliid] clade (Chloranthaceae were not included) after removing 2,500 highly variable positions from the analysis of chloroplast genome data; with the removal of 1,000 positions Ceratophyllum was sister to a [monocot + eudicot] clade. Analyses of morphological data gave a grouping [Ceratophyllum + Chloranthaceae] with quite strong support (Endress & Doyle 2009; see also Huang et al. 2010, weak support using the ycf2 gene; Moore et al. 2011, very weak support). Finally, in the massive parsimony analysis of Goloboff et al. (2009) a set of relationships [Ceratophyllum [[Amborella + Nymphaeales]....[[Chloranthaceae + monocots] eudicots]]] was retrieved, Duarte et al. (2010) found the relationships [monocots [magnoliids + eudicots]], and Tamura et al. (2011: 6 plastid, 7 mitochondrial, and 1 nuclear genes sequenced) found some support for a [Piperales + monocot] clade, as did Barrett and Davis (2011: or [Piperales + Ceratophyllales] the sister group). For another study, see Fiz-Palacios et al. (2011).
A further complication was introduced by Lee et al. (2011) who found that monocots were sister to all angiosperms minus Nymphaeales and Amborellales. Although this may be a sampling problem (no Austrobaileyales, Chloranthales or Ceratophyllales were included), Lee et al. (2011) initially looked at almost 23,000 sets of orthologues from nuclear genomes of 101 genera of land plants (most taxa represented by ESTs, genes included if represented in as few as 4 taxa).
Nevertheless, pending further studies, the relationships [[Chloranthales + magnoliids] [monocots [Ceratophyllales + eudicots]]] are used as a basis for further discussion, rather different from the relationships suggested in the first six editions of this site and also from the tree in A.P.G. II (2003) and Soltis et al. (2005b). Direct links are provided to the pages where the clades just mentioned are discussed further; this discussion will generally be just above or below where the link takes you: Ceratophyllales, Chloranthales, eudicots, and monocots.
[CHLORANTHALES [[MAGNOLIALES + LAURALES] [CANELLALES + PIPERALES]]]: sesquiterpenes +; seed endotestal.
[[MAGNOLIALES + LAURALES] [CANELLALES + PIPERALES]] / MAGNOLIIDS / MAGNOLIANAE Takhtajan: (neolignans +); vessels solitary and in radial multiples; (sieve tube plastids with polygonal protein crystals); lamina margins entire; A many, spiral [possible position here], extrorse; ovules with hypostase, nucellar cap +, raphal bundle branches at the chalaza; antipodal cells soon die. Back to Main Tree
4 orders, 20 families, 9900 species.
Evolution. Divergence & Distribution. Crown group magnoliids diverged 134.5-125.7 m.y.a. (Moore et al. 2007), while Bell et al. (2010) suggested ages of (138-)122(-108) or (130-)125(-121) m.y. depending on the method used. Magallón and Castillo (2009) estimated crown group divergence at ca 201.7-198.2 and 128-127.7 m.y.a. - relaxed and constrained penalized likelihood datings respectively. An earlier fossil-based estimate for both stem and crown divergence is ca 98 m.y. (Crepet et al. 2004: magnoliids sister to monocots). Other estimates range from (181-)155(-136) m.y. old (with eudicot calibration) to (198-)163(-138) m.y. (without: Smith et al. 2010), to (144-)116(-89) m.y. (N. Zhang et al. 2012) or 132-122 m.y. (Wikstöm et al. 2001), while Magallón et al. (2013: with temporal constraints) suggested an age of around (167.2-)147.7-142.6(-128.5) m.y. for this clade.
For summaries of the fossil history of the group, espeacially prominent in the Mid Cretaceous and later, see Friis et al. (1997, 2006, 2011).
Plant-Animal Interactions. Caterpillars of Papilionidae-Papilioninae butterflies are notably common (almost 33% of the records) on members of this group; they are, however, not known on Myristicaceae, in Laurales they predominate on Lauraceae, and in Piperales on Aristolochiaceae (see Scriber et al. 1995 for references; Zakharov et al. 2004). They are also commonly found on Rutaceae, which have similar alkaloids.
Chemistry, Morphology, etc. Hegnauer (1990) discussed the chemistry of the Polycarpicae, which includes Austrobaileyales and Ranunculales; similar isoflavonoids are found in Magnoliaceae, Lauraceae and Chloranthaceae.
For a convenient summary of a number of features of wood anatomy, see Herendeen et al. (1999b). Magnolioid roots are scattered through the clade, being recorded from a number of woody members of Laurales and Magnoliales. These roots are stout, often ³3 mm across, lack root hairs (?always), and are endomycorrhizal - associated conditions (see Baylis 1975; St John 1980). Taxa with broadly lobed leaf blades are scattered throughout this clade (but not in the small Canellales). See Erbar (1983, inc. Illicium) for carpel morphology and Ronse Decraene and Smets (1992b) for androecial morphology.
Phylogeny. Although the sister group relationship of Piperales with Canellales in particular is at first sight unexpected, the magnoliid clade as a whole and the relationships within the group are turning out to be quite robust. There was not much morphological support for this grouping (Doyle & Endress 2000); features like tectum structure, etc., show considerable variation (J. A. Doyle 2005). However, molecular support for the clade has been increasing in successive studies (e.g. Qiu et al. 1999, 2000, 2005: support levels depend on the analysis, the node sometimes collapses], 2006b, 2010; Zanis et al. 2002; Jansen et al. 2006b; Zhengqiu et al. 2006; Cai et al. 2006; Müller et al. 2006: support for [Canellales + Piperales] poor; Jansen et al. 2007: little maximum parsimony support; Moore et al. 2007: group not in all analyses; Soltis et al. 2007a; Soltis et al. 2011). Support includes the possession of unique indels (Löhne & Borsch 2005). Soltis et al. (2007a) found weak support for a grouping [Magnoliales + Canellales]; relationships in Bell et al. (2010) are [Piperales [Laurales [Canellales + Magnoliales]]], although they have little support. As can be seen, the clade now has some morphological support.
[MAGNOLIALES + LAURALES]: cuticle waxes as annularly-ridged rodlets, palmitol the main wax; A whorled; pollen 1-2 nexine foliations, outer member massive, lamellate endexine; carpel cross-zone initiated late; ovules 1(-2)/carpel, basal, erect, apotropous; fruitlets 1-seeded.
Evolution. Divergence & Distribution. Magallón and Castillo (2009) suggest that the two clades diverged ca 198.2 and 127.7 m.y.a. - relaxed and constrained penalized likelihood datings, while Magallón et al. (2013) suggested an age of around 137.2 m.y..
There is considerable variation as to how the androecium is initiated; it would not take much for "flowers with inner staminodes" to be an apomorphy at this level. Seed size is notably large in this clade (Moles et al. 2005a; Sims 2012).
MAGNOLIALES Bromhead Main Tree, Synapomorphies.
Vessels in multiples; secondary phloem stratified; pith septate [with sclerenchymatous diaphragms]; nodes 3:3; petiole vasculature an arc with an adaxial plate; branching from the current innovation; leaves two-ranked, lamina vernation conduplicate; "bract" sheathing; P whorled; G occluded by fusion and secretion; ovule with outer integument 5-10 cells across, obturator +; seeds medium-sized, testa vascularized, multiplicative; endosperm ?type, irregularly ruminate. - 5 families, 154 genera, 2929 species.
Note: Possible apomorphies are now being added throughout the site; they 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 because there is very considerable homoplasy, with variation within and between clades, for most characters. Furthermore, the basic information for all too many characters is very incomplete, often coming from taxa well embedded in the clade of interest and so making the position of any putative apomorphy uncertain. Then there is the not-so-trivial issue of how ancestral states are reconstructed...
Evolution. Divergence & Distribution. Magallón and Castillo (2009: relaxed and constrained penalized likelihood datings) suggest possible ages for the crown group of 171.5 and 116.6 m.y..
There is extensive discussion on character evolution in Sauquet et al. (2003), and much of the character hierarchy here is based on this paper. However, where characters like extrorse/introrse anther dehiscence and ruminate/non-ruminate testa are placed on the tree depends on how the characters are optimised, or even defined (e.g. ruminate endosperm). There is also some conflict with the positions of characters as they are optimised on a more extensive tree for basal angiosperms, although less detailed for Magnoliales (c.f. Ronse De Craene et al. 2003, also Judd et al. 2003). Doyle and Endress (2000) and Soltis et al. (2005) suggest additional characters for the clade, including reduced fibre pit borders, palisade parenchyma, foliar astrosclereids, and pollen with continuous tectum; Doyle and le Thomas (2012) outline pollen evolution. More characters may well need to be added to the apomorphy scheme for the order.
Chemistry, Morphology, etc. Intra- and interfamilial variation of morphological characters that are frequently used to reconstruct phylogenies is considerable, in particular, Furness et al. (2002) emphasize the variability of microsporogenesis in the order.
The "bracts" with sheathing bases that have been reported for a number of Magnoliales (Endress & Armstrong 2011: condition in Degeneriaceae?), are perhaps a little unexpected since the leaf bases in the clade tend to be quite narrow - except for the stipulate Magnoliaceae. Deroin (2010) noted a tendency for the vasculature of the perianth and/or androecium in some Annonaceae and Magnoliaceae to be pentamerous.
For additional information, see Sugiyama (1976a, b, 1979: esp. considerable variation in cotyledonary nodal morphology), Hiepko (1964b: perianth vasculature), Endress (1977b, 1986a, 1994a: floral morphology), van Heel (1981, 1983: carpel development), Erbar and Leins (1983: floral development), Metcalfe (1987: general anatomy), Taylor and Hickey (1995: general), Ronse Decraene and Smets (1996a: androecium), Kimoto and Tobe (2001: embryology), and Kim et al. (2003, 2004: AP3 and P1 genes: Myristicaceae not sampled).
Phylogeny. Molecular data suggested that Myristicaceae are sister to the rest of the order, but support was only moderate (D. Soltis et al. 2000); the addition of morphological data strengthened that position, and also placed Magnoliaceae as sister to the remaining taxa (Doyle & Endress 2000), although the latter position had only moderate support (c.f. P. Soltis et al. 2000; see also Sauquet et al. 2001). The family pairs [Annonaceae + Eupomatiaceae] and [Degeneriaceae + Himantandraceae] are both well supported (D. Soltis et al. 2000; P. Soltis et al. 2000; Doyle & Endress 2000). Other studies confirm these relationships (Sauquet et al. 2003; Müller et al. 2006), and they are followed here.
Hilu et al. (2003: matK analysis alone, ?sampling) found a somewhat different but poorly supported set of relationships, and Qiu et al. (2010: mitochondrial genes) also recovered a somewhat different topology, Degeneriaceae being sister to the rest of the order minus Myristicaceae, although again support was weak. Soltis et al. (2011) found that Magnoliaceae were sister to the rest of the order, the clade [Degeneriaceae + Myristicaceae] had good support although otherwise support was weak; this unexpected topology was ascribed to signal from rDNA sequences. Finally, Morton (2011: nuclear gene Xdh) found a set of relationships [Himantandraceae [Myristicaceae [Degeneriaceae [the rest]]]].
Includes Annonaceae, Degeneriaceae, Eupomatiaceae, Himantandraceae, Magnoliaceae, Myristicaceae.
Synonymy: Annonales Berchtold & Presl, Degeneriales C. Y Wu et al., Eupomatiales Reveal, Himantandrales Doweld & Shevyryova, Myristicales Berchtold & Presl - Magnoliineae, Myristicineae Chatrou - Annonanae Doweld, Magnolianae Takhtajan - Magnoliidae Takhtajan - Magnolipsida Brongniart - Magnoliid I group (Nandi et al. 1998).
MYRISTICACEAE R. Brown Back to Magnoliales
Tree, branches plagiotropic, pseudowhorled; exudate +, red; isoflavonoids, flavonoids diverse [flavones +], polyketide [acetogenins], (tryptamine) alkaloids +, isoquinoline alkaloids 0; cork also in outer cortex; primary stem ± with continuous cylinder; vessel elements with simple or scalariform(-reticulate) perforations; tannin-containing tubes in the xylem; sieve tubes with non-dispersive protein bodies, (plastids with protein crystalloids and starch); petiole bundles bicollateral; (branched) sclereids or fibres +; (acicular) crystals +; hairs branched, arbuscular to stellate (T-shaped); cuticle waxes as platelets; (leaves spiral), (lamina lobed - some Knema); plants dioecious; flowers small (<1 cm across), receptacle small; P (2-)3(-5), uniseriate, connate; staminate flowers: A whorled (spiral), 2-40, connate (not), (anthers unithecate); (pollen inaperturate, ulceroid, spiraperturate, ektexine granular), pollen aperture membrane sculpted; pistillode 0; carpellate flowers: staminodes 0; G 1; (stylulus ± long), stigma 2-lobed to peltate; ovule 1/carpel, subbasal, inner integument (3-)7-10 cells across; fruit a follicle, dehiscing abaxially as well, (indehiscent); seed large [³1 cm across], pachychalazal, aril +, micropylar-funicular, vascularized, (aril small); exotesta thick-walled, endotesta palisade, lignified, crystalliferous, tegmen multiplicative or not, exotegmen with fibres or sclerotic or tracheidal cells, chalaza massive, with a lignified counter-palisade; endosperm nuclear, with (starch and) oil; embryo with hypocotyl not developed; n = 20, 22, 25, 26; germination hypogeal.
20[list]/475: Myristica (175), Horsfieldia (100), Knema (95), Virola (60). Pantropical, few mainland Africa (map: from de Wilde 2000 [Indo-Malesia]; Heywood 2007; Trop. Afr. Fl. Pl. Ecol. Distr. 1. 2003).[Photo - Carpellate flower, Fruit].
Floral formula: * P ; A [2-40]: * P ; G 1.
Evolution. Divergence & Distribution. Diversification within the family may be very recent, within the last 21-15 m.y., very recent indeed given the age of the family (c. 171.5 and 116.6 m.y., Magallón & Castillo 2009), its distribution throughout the humid tropics, and its apparently low dispersability (J. A. Doyle et al. 2004). Unfortunately, the discovery of fossil seeds apparently of Myristicaceae from the Eocene (London Clay) does not bear on this issue because they cannot be placed precisely on the tree of the family (J. A. Doyle et al. 2008a). There is a long branch leading to crown Myristicaceae and little molecular divergence between its extant members (Sauquet et al. 2003), and this might indeed suggest recent diversification. In this respect Myristicaceae can be compared with Annonaceae, also pantropical but a little younger; there diversification may have begun mid-Cretaceous or slightly later (Doyle et al. 2004; Scharaschkin & Doyle 2005; esp. Couvreur et al. 2011a; Doyle et al. 2012).
See Chatrou (2003) for possible apomorphies.
Genes & Genomes. Isozyme duplication (in Myristica) suggests ancient polyploidy (Soltis & Soltis 1990).
Chemistry, Morphology, etc. There are free phloem strands in the center of the midrib bundle. The wood rays are not notably broad.
Inflorescence morphology is a little confusing. Ronse de Craene (2010; see also Armstrong & Tucker 1986) shows a large, abaxial "bracteole" in addition to paired lateral prophyllar/bracteolar-like structures that may (staminate inflorescence) or may not subtend buds. The "bract" immediately below the staminate flower of Myristica fragrans has a very broad base.
There are three traces per perianth lobe (Siddiqui & Wilson 1976). The synandrium of Myristica has a sterile apex, probably axial (Armstrong & Tucker 1986), and judging from the vasculature, the unithecal anthers found in some species of Myristica represent half of a divided bithecal anther (Wilson & Maculans 1967; Armstrong & Tucker 1986); anthers in Knema are tetrasporangiate (Xu & Ronse de Craene 2010a). For the complex vascularisation of the carpel in Myristica, see Wilson and Maculans (1967), and for the vascularization of the ovule in Myristica fragrans, see Dickison (2000). A small structure developing between the two integuments is reported by Nair (1972). Corner (1976) commented on the complexity of the seed coat in Myristicaceae which is as elaborate as that of any other angiosperm. Not all taxa appear to have a multiplicative testa, and some have a multiplicative tegmen; the ruminations may develop best in the pachychalazal part of the seed.
For more information, see Hegnauer (1969, 1990: chemistry), Mauritzon (1939a) and Endress (1973), both seed, Kerster and Baas (1981: anatomy), Kühn and Kubitzki (1993: general), de Wilde (2000: Malesian Myristicaceae), Jiménez-Rojas et al. (2002: growth patterns - Massart's model), Sauquet (2003: androecium), Sauquet and Le Thomas (2003: pollen) and Oginuma et al. (2012: chromosome numbers, a few South East Asian-Malesian taxa only known).
Phylogeny. Relationships within the family are unclear. The African and Madagascan taxa may form a clade, possibly sister to Compsoneura (but perhaps long branch attraction), overall, geography and relationships may be summarized as [[Asia + America] [Madagascar and Africa]]. Within Asian/Malesian Myristicaceae, Knema and Myristica may be sister taxa. Sauquet et al. (2001, 2003), Sauquet (2003) and Sauquet and Le Thomas (2003) suggest that the free stamens (in some species they are numerous and apparently spirally inserted) and small aril of Mauloutchia, apparently plesiomorphic features, are in fact more likely to be derived.
[Magnoliaceae [[Degeneriaceae + Himantandraceae] [Eupomatiaceae + Annonaceae]]]: primary stem with distinct bundles [eustele]; wood with broad rays; flowers solitary, large [.1.5 cm across]; receptacle with cortical vascular system; P = K + C; A many, spiral [possible position here], filaments with three veins, anther thecae separate, embedded in the broad connective, connective prolonged [one position]; tectum imperforate; G spiral; ovule with funicular obturator; ³1 seeds/fruitlet; 10-aa deletion in PI-derived motif in AP3 gene.
Evolution. Divergence & Distribution. This clade may have started to diversify 120-100 m.y.a. (Doyle et al. 2004) or as little as ca 71.1 m.y.a. (Magallón et al. 2013).
Chemistry, Morphology, etc. There is more than one kind of cortical vascular system here, and what parts of the flower are supplied by which system varies (Ronse De Craene et al. 2003, see also Deroin 1991, 1999a).
MAGNOLIACEAE Jussieu Back to Magnoliales
(Deciduous); (silicon concentration high), sesquiterpene lactones +; vessel elements with simple and scalariform perforation plates, (walls vestured - Liriodendron); wood fluorescing; (secondary phloem ± stratified, rays broad); (sieve tube plastids with polygonal protein crystalloids and starch - Magnolia); ³6:³6; secretory cells 0; petiole also with medullary bundles (strictly annular - Liriodendron); leaves also spiral, lamina vernation laterally or vertically conduplicate (supervolute-curved), stipules +, sheathing stem, open opposite petiole; (dioecious); flowers terminal or axillary; receptacle much elongated; P 2, 3 + 3 or 3 + many, K and C ± distinguishable; (A introrse - Magnolia), (filament vein single), tapetal cells multinucleate; pollen grains boat-shaped; G 1-many, fusion complete, but secretory canal +, stigma (terminal), dry, elongate (not); ovules(1-)2-12(-16)/carpel, micropyle exo/bistomal/zig-zag, outer integument 4-10 cells across, inner integument 2-3(-4) cells across, parietal tissue 2-8 cells across; fruit dehiscing abaxially (circumscissile; indehiscent, winged); sarcotesta +, endotesta lignified [fibres], (tegmen ± tanniniferous), (testa inconspicuous - Liriodendron); endosperm not ruminate, (nuclear - "Magnolia" septentrionalis); n = 19.
2[list]/227: Magnolia (ca 225). The Americas (but not W. North America), and South East Asia to Malesia (map: from Good 1974; Lozana-Contreras 1994).[Photo - Collection]
Evolution. Divergence & Distribution. Archaeanthus, a Cenomanian fossil of some 98 m.y. in age from North America, may be assignable to Magnoliaceae (Dilcher & Crane 1984); it is placed sister to the family in the constrained morphological analysis of Doyle and Endress (2010). It has follicular fruits with 10-18 seeds per carpel. Lesqueria, from about the same period, may also belong around here; it has similar fruits (Crane & Dilcher 1984). The fruits of Protomonimia, in Turonian deposits from Japan ca 91 m.y. old, have several carpels borne in spirals on a concave axis; there is a stigmatic crest. The young seeds have a thick testa, the exotesta being palisade and with sinuous anticlinal cell walls (Nishida & Nishida 1988); they may be of a taxon somewhere near Magnoliaceae, although i.a. the shape of its receptacle is very different.
Liriodendron was widely distributed in the Northern Hemisphere in the early Tertiary (Ferguson et al. 1997). For divergence ages of and within Magnolia, see Azuma et al. 92001) and Nie et al. (2008).
Pollination Biology. Beetles are common pollinators, and the flowers of species like Magnolia ovata, pollinated by dynastid scarab beetles, are thermogenic (Seymour 2001; Gottsberger et al. 2012). Floral scents of the family have been extensively studied (Azuma et al. 1999; Gottsberger et al. 2012).
Genes & Genomes. Both isozyme duplication and stomatal size increase over time suggest ancient polyploidy (Soltis & Soltis 1990; Masterson 1994).
Chemistry, Morphology, etc. Sclerenchymatous diaphragms are particularly conspicuous in the Michelia group of Magnolia. Terminal tracheids are commonly silicified, forming distinctive phytoliths (Piperno 2006).
The endexine is lamellate and the columellae fused-granular (Xu & Kirchoff 2008). Nectar is secreted from the exposed surfaces of the carpels in some species of Magnolia. The micropyle is exostomal in the Michelia group of Magnolia. The seed of Magnolia may dangle from the open fruitlet attached by extended annular thickenings of the protoxylem vessels.
Liriodendron: leaves lobed, with palmate secondary veins; petiole bundle strictly annular; fruit a samara, single-seeded; seeds lack a sarcotesta, mesotesta more or less sclerotic; endosperm slight and not ruminate. Magnolia: leaves entire; anthers introrse; ovule lacks a funicular obturator(?); fruit dehiscent. but not adaxial (so the fruit is not a follicle in the strict sense); sarcotesta +, scleroendotesta with crystals and lignified fibrils in the cells; endosperm copious. There is also a simple or tubular pore in the seed coat that marks the passage of the vascular bundle through the sclerotesta (Xu 2003).
Some information is also taken from Hegnauer (1969, 1990: chemistry), Bouman (1977: ovules and seeds of Liriodendron), Nooteboom (1993: general), Yamada et al. (2003b: ovules), Pan et al. (2003) and especially Fu et al. (2012 and references), both embryology, Xu (2006) and Xu and Rudall (2006: floral development), and Xu and Kirchoff (2008: pollen morphology); see Azuma et al. (2000), Ueda et al. (2000) and Wang et al. (2006) for molecular phlogenies, Figlar (2000) for branching patterns, Charlton (1994) and Liao and Xia (2007) for phyllotaxis and vernation.
Phylogeny. Magnolia s. str. is pretty wildly paraphyletic, and section Talauma is sister to the rest of Magnolia (Qiu et al. 1995; Kim et al. 2001a, b; Azuma et al. 2001, 2011: support along the backbone weak; Nie et al. 2008: again support along the backbone poor).
Classification. It seems best to expand Magnolia to encompass the whole of the current Magnolieae; the family thus includes only two genera and tribes are superfluous. See also Nooteboom (2000) for suggestions about classification, and Xia (2012) and Sima and Lu (2012) for a reclassification in which Magnolia is divided into 16 genera placed in two tribes... For a checklist and bibliography (under some old generic names), see Frodin and Govaerts (1996).
Synonymy: Liriodendraceae F. Barkley
[[Degeneriaceae + Himantandraceae] [Eupomatiaceae + Annonaceae]]: flower haplomorphic; anthers valvate, inner staminodes +, secretory; pollen smooth, exine thin, [0.2-1.3 µm across], nexine foliations?, infratectum granular; style with differentiated transmission tissue; seed ruminations irregular, mesotesta fibrous.
Evolution. Divergence & Distribution. Endressinia brasiliana, from the Brazilian Crato formation of some 113 m.y.a. has i.a. distinctive glandular staminodia. It is placed sister to this clade by Doyle and Endress (2010), largely confirming the position suggested by Mohr and Bernardes-de-Oliviera (2004).
Chemistry, Morphology, etc. Doyle (2007) noted that the venation here is often poorly differentiated and so of low rank (but c.f. many Annonaceae, albeit not "basal" members) - I have not placed this character on the tree. For the inner staminodes that are often so conspicuous in the flowers, and their function in pollination - food for pollinators, attractants - see Endress (1984).
[Degeneriaceae + Himantandraceae]: flowers axillary; nexine foliations absent; outer integument with annular opening; x = 12.
DEGENERIACEAE I. W. Bailey & A. C. Smith Back to Magnoliales
Alkaloids 0; cork ?; vessel elements with scalariform perforation plates; sieve tube plastids with polygonal protein crystalloids and starch; nodes 5:5; petiole also with medullary bundles; secretory cells 0; cuticle waxes as platelets; leaves spiral; bracts?; K 3, C many, whorled; pollen boat-shaped; G 1, basally ascidiate, occluded by fusion only, stigmatic crest much elongated; ovules many/carpel, outer integument 7-8 cells across, inner integument ca 3 cells across, funicle long; fruit a follicle; exotestal cells palisade, thin-walled, sarcomesotesta +, endotesta with lignified internal fibrils; suspensor massive, embryo with 3 (4) cotyledons.
1[list]/2. Fiji, Viti Levu (map: original!).
Chemistry, Morphology, etc. Some information is taken from Hegnauer (1973, 1990, as Winteraceae: chemistry) and Kubitzki (1993b: general).
HIMANTANDRACEAE Diels Back to Magnoliales
Polyketide alkaloids only; vessel elements with simple (and scalariform) perforations; sieve elements with non-dispersive protein bodies; trichomes peltate; cuticle wax crystalloids 0; branching?; P or bract + bracteoles enclosing the flower in 2 series, caducous, or 2 connate + 4 connate; "C" 3-23 [staminodial]; pollen scabrate; additional staminodes with glands; G 6-30, (1) 2 pendulous ovules/carpel; fruit ± syncarpous, drupaceous, with several stones; seeds laterally flattened, ?ruminations; testa not multiplicative, endotesta aerenchymatous; endosperm development?; seedling?
1 (Galbulimima)[list]/2. The Celebes, New Guinea and N.E. Australia (map: from Hoogland 1972; Endress 1983). [Photo - Flower, Fruit, Buds, Habit]
Chemistry, Morphology, etc. For the testa, see Doweld and Shevyryova (1997); the ruminations are at best obscure. The perianth may be staminodial in origin; according to Johri et al. (1992) the outer integument is not vascularized. Some other information is taken from Hegnauer (1966, 1989: chemistry) and Endress (1993: general).
[Eupomatiaceae + Annonaceae]: sieve tube plastids also with polygonal protein crystalloids; rays 8-15-seriate; petiole bundles arcuate; trunk leaves spiral; prophyll single, adaxial; inflorescence +; nexine foliations undifferentiated; fruit ± berry-like.
Chemistry, Morphology, etc. Optimisation of prophyll position on the tree is uncertain. Adaxial prophylls are common in Annonaceae, including Anaxagorea, although some taxa have paired, lateral prophylls (Fries 1911).
EUPOMATIACEAE Orban, nom. cons. Back to Magnoliales
Also rhizomatous, with xylopodium or root tubers; pith not septate; vessel elements with scalariform perforation plates; secondary phloem stratification?; sieve tubes with non-dispersive protein bodies [check], plastids also with protein rods; nodes (5-)7(-11):(5-)7(-11); secretory cells +; (stomata anomocytic); branching?; inflorescence fasciculate; receptacle concave, calyptra +, thick, deciduous, with sclereids, phyllotaxis spiral; P 0; A introrse; pollen with encircling equatorial sulcus; petal-like staminodes 15+, connate basally and with fertile stamens, with many glands; G many, ± connate, ascidiate, occluded by fusion only, placentation sublaminar, stigma flat, papillate; ovules 2-11/carpel; aggregate fruit +; testa ?not vascularized, exotestal cells with thickened unlignified walls, endotesta unlignified, exotegmic cells cuboid, slightly lignified, endotegmic cells enlarged, crushed; n = 10; germination epigeal/phanerocotylar.
1[list]/3. New Guinea and E. Australia (map: from Hoogland 1972; Endress 1983). [Photos - Flower, Flower]
Chemistry, Morphology, etc. The main axes are mixed, initially being orthotropic and bearing spirally-arranged leaves, later becoming more or less plagiotropic and with distichous leaves. There are about three two-ranked bracts on the pedicel; the calyptra itself is often interpreted as being a modified, amplexicaul bract (e.g. Endress 2003b; esp. Kim et al. 2005b). There is no evidence of isozyme duplication (Soltis & Soltis 1990).
Some information is taken from Hegnauer (1966, 1989: chemistry), Endress (1983, 1993: general) and Rix and Endress (2007: an easy account).
ANNONACEAE Jussieu Back to Magnoliales
Vessel elements with simple perforation plates; parenchyma in bands joining rays; sieve tube plastids also with protein filaments; epidermal cells with single crystals [?level]; flowers with open development, 6-merous; P very thick, 3, ± calycine, often? valvate, + 3 + 3, ± corolline, open to valvate; A whorled, filaments with a single vein; G plicate; funicle short; monocarp abscission at the base; endotestal plug +, mesotesta with several layers of longitudinal and internally of transverse fibres, aerenchyma internal; vascular bundle in antiraphe.
129/2220 [list] - four groups below. Largely tropical.
1. Anaxagoreoideae Chatrou, Pirie, Erkens & Couvreur
Ray cells with druses; uniseriate hairs terminate in a rounded cell, other hairs ± stellate; trunk leaves distichous; (petiole vascular tissue ± annular; with adaxial bicollateral plate; small arcuate bundles variously arranged); stomata allelocytic; inner staminode secretions 0; pollen with granular infratectum; orbicules +; G 3, receptacular vascular system 0; ovules 2/carpel; fruit an explosively dehiscent follicle; seed asymmetric; endotesta aerenchymatous, tegmen alone involved in ruminations, with oil globules; n = 8.
1/21. Tropical America, Sri Lanka to West Malesia, also Halamahera and Ceram (map: from Maas & Westra 1984, 1985). [Photo - Flower, Fruit, Fruit.]
[Ambavioideae [Malmeoideae + Annonoideae]]: ray cells lacking druses; (outer staminodes +), inner staminodes 0; ovules with outer integument 4-6 cells across, inner integument 2-4 cells across; fruit berrylets, (monocarp abscission at the apex); seed symmetric, with perichalazal ring; amyloid [xyloglucans] in endosperm +. (map: from Aubréville 1974a; Trop. Afr. Fl. Pl. Ecol. Distr. 1. 2003.)
2. Ambavioideae Chatrou, Pirie, Erkens & Couvreur
Anther connective ± tongue-like to peltate truncate; orbicules ?; carpels 3-8, stipe articulated, (extragynoecial compitum + - Cananga), ovules (1)2-16/carpel, middle integument + (0), 4-6 cells across; (seed arillate), (endosperm ruminations lamelliform); n = 7, 8.
9/50: Drepananthus (26). Tropical, inc. Madagascar.
[Malmeoideae + Annonoideae]: (polyacetylenes +), petioles short; (pollen inaperturate), tectum retiperforate, infratectum columellate, outer foliation of nexine massive; ovules 1-many/carpel,
3. Malmeoideae Chatrou, Pirie, Erkens & Couvreur / The Short Branch Clade
(Pollen globose, ± spiny, disulcate); orbicules + (0); (tegmen with oil globules); endosperm ruminations spiciform (lamelliform); (mesotesta with transverse fibres only - Polyalthia).
Polyalthia (100), Monoon (56), Pseuduvaria (50), Unoniopsis (45). Lowland tropics.
4. Annonoideae Rafinesque / The Long Branch Clade
(Lianes), (deciduous); (C 3); (anthers locellate), (outer staminodes +); pollen (in tetrads or polyads), (inaperturate), (exine foliations numerous), (orbicules +); (G connate); (middle integument + - Artabotrys); (fruit follicle/dehiscing abaxially); endosperm ruminations lamelliform (irregular); n = 7-9.
Guatteria (280), Annona (120-175, soursop, sweetsop: inc. Rollinia), Xylopia (100-160), Uvaria (110-150), Artabotrys (100), Goniothalamus (50-120), Duguetia (70-95), Fissistigma (60), Monanthotaxis (55), Friesodielsia (50-60). Predominantly lowland tropics, rarely temperate.
To be assigned to the above two subfamilies.
acetogenins [antimicrobial] +, neolignans 0?; terminal cell of uniseriate hairs pointed (hairs stellate); (primary stem with continuous cylinder); cambium storied; (sieve tube plastids also with protein fibres); petiole bundle also annular; branched sclereids or fibres common; secretory cells +; (prophyll single, adaxial); inflorescence cymose (leaf opposed), or flowers axillary; flowers A (³3), (latrorse, introrse), tapetal cells plasmodial, multinucleate; (microsporogenesis successive); (pollen with circular sulcus), (trinucleate); G (3-)many (syncarpous; parietal placentation), when 3 opposite outer P, stigma capitate to U-shaped, wet, extragynoecial compitum common; (nucellar cap 0); (sarcotesta +), endotesta crystalliferous, (with thin walled, longitudinal fibres); germination epigeal/crypto- or phanerocotylar.
Synonymy: Hornschuchiaceae J. Agardh, Monodoraceae J. Agardh [where?]
Floral formula - Anaxagoreoideae: * K 3; C 3 + 3; A many, + severalo; G 3.
Everything Else: * K 3; C 3 + 3; A many; G (1-)many.
Evolution. Divergence & Distribution. Estimates of the age of stem Annonaceae vary considerably: (110.4-)106.3(-102.0) m.y. (Couvreur et al. 2011a: HPD estimates), (110.4-)101.7(-99.4) m.y. old (Surveswaran et al. 2010: HPD estimates), (101.5-)98.0(-94.9) m.y. (Su & Saunders 2009), 91-82 ± 4 m.y. old (Wikström et al. 2001), or somewhere between 84.7 and 62.6 m.y. (Erkens et al. 2009: a variety of estimates); see also Pirie and Doyle (2012). Crown group diversification may have occurred 92-89 m.y. (Su & Saunders 2009) or 82-57 m.y.a. (Doyle et al. 2004; Scharaschkin & Doyle 2005 [84 m.y. before present]; Couvreur et al. 2011a: additonal estimates).
Futabanthus, based on fossil flowers from the late Cretaceous (Early Coniacian, ca 89 m.y.a.) of Japan, can perhaps also be assigned to crown-group Annonaceae (Takahashi et al. 2008b).
The biogeography and diversification of the family has been much studied (see also Doyle et al. 2004; Richardson et al. 2004). Erkens et al. (2012b; ?program) found little in the way of changes in diversification rates in the family, speciation behaving as if it were a random branching process, and so there was little need to invoke key innovations. Divergence within Anaxagorea may have begun ca 44 m.y.a. (Scharaschkin & Doyle 2005). Diversification of the rest of the family may also be Tertiary, figures of (76.6-)68, 64.5(-53.0) m.y. for the divergence between the Ambavioideae and the rest being suggested by Erkens et al. (2009), or some time between 84.4-63.6 m.y.a. (Su & Saunders 2009; see Couvreur et al. 2011a for other estimates). Crown group Ambavioideae themselves diversified perhaps (80.9-)57.0(-52.3 m.y.a. (Surveswaran et al. 2010: q.v. for other dates, HPD estimates) or (78-)69.4(-60.2) m.y. (Couvreur et al. 2011a: HPD estimates).
The divergence of [Annonoideae and Malmeoideae] may date to 70-65 m.y.a. and the crown node to 66.7-56.6 ± 2.3 m.y. ([78.08-]67.33[-55.22] m.y. - see Su & Saunders 2009; Couvreur et al. 2011a; estimates of this and other clade divergence times). In any event, divergence largely happened after the break-up of the continents and is Tertiary in age. Couvreur et al. (2011a) contrast the diversification in Annonoideae and Malmeoideae. The former began to diversify ca 66 m.y.a. and the latter much later, ca 33 m.y.a.; the former has about twice as many species as the latter, even if rather paradoxically the latter may have a higher diversification rate - once it got going (see Couvreur et al. 2011a; Thomas et al. 2012, older, but similar diparity, both give other ages). However, although stem age estimates are in the 70 million year range, crown ages vary widely, Couvreur et al.'s age being the youngest, and Piries and Doyle (2012) the oldest, a crown group estimate of (70-)66(-62) my. Su and Saunders (2009) offer dates for additional splits in the family, focusing on Pseuduvaria, and Thomas et al. (2012) give many dates for divergences within both main subfailies.
The Old World Uvaria may have originated (38.4-)31.6(-25.1) m.y.a. in Africa, whence it dispersed to other parts of the Old World (Zhou et al. 2012: HPD). The large New World genus Guatteria has undergone much speciation in (Amazonian) South America perhaps 8.8-4.9 m.y. before present, having moved to South America from Central America, perhaps from Africa via Europe (Erkens 2007; Erkens et al. 2007a, b, 2009).
Ecology. Annonaceae are important lianes of the tropical South East Asian forests (Gentry 1991), and there have been several origins of this habit within Annonoideae (Meinke et al. 2011). Artabotrys, one of these lianes, has curved hooks on the ultimate branches; these are modified inflorescences. The orthotropic stems may have stout, paired and rather vicious thorns. The other lianes do not have hooks or thorns, and development of the liane habit varies.
Pollination Biology & Seed Dispersal. Saunders (2010: good photographs) summarizes variation in floral morphology in the context of pollination. Flowers in which the stamens are enclosed in some sort of bowl-shaped structure are common, and there are often floral rewards on the inner surfaces of the inner perianth whorl. Pollination of the more or less odoriferous flowers is predominantly - and perhaps ancestrally - by small beetles, but there is also fly pollination (e.g. Su et al. 2008) and pollination by thrips, bees, cockroaches, etc. (Saunders 2012; Gottsberger 2012); a variety of scents is produced (Goodrich 2012 and references). The tough, apically expanded connective that predominates in stamens of flowers of Annonoideae and Malmeoideae may protect the pollen from the depradations of unwanted visitors (Gottsberger 1999, 2012; Silberbauer-Gottsberger et al. 2003). The flowers of some Annonaceae show thermogenesis (Seymour 2001), and some kind of extracarpellary compitum is common (Deroin 1991). The internal staminodes of Anaxagorea cover the gynoecium in the staminate floral phase, apparently preventing selfing (Gottsberger 2012; Saunders 2012). For pollen evolution, see Doyle et al. (2000) and especially Doyle and le Thomas (2012).
Dispersal of fruit is predominantly by mammals and birds. The lianes of tropical South East Asia are notably important food resouces for frugivores because they fruit more or less continually (Leighton " Leighton 1983).
Vegetative Variation. The main axes of Annonaceae are often mixed (?Troll's model), initially being orthotropic and with spirally-arranged leaves, later being more or less plagiotropic with two-ranked leaves (see also Eupomatia). Taxa such as Asimina and Annona have orthotropic axes with distichous leaves. In general, axillary branches depart from the stem slightly to one side of the axil. Branches generally have plagiotropic leaves, and in some Xylopia, etc., the plagiotropic branch systems are frondose and very beautiful.
Chemistry, Morphology, etc. Protoberberidine alkaloids are reported from Annonaceae (Wink 2008). Cork in the roots of Goniothalamus may be superficial (Blunden & Kyi 1974). The wood occasionally fluoresces. Terminal tracheids are fairly commonly silicified (Piperno 2006). For the petiolar anatomy of Anaxagorea, see Jovet-Ast (1942) and Maas and Westra (1984); it is unlikely that there are annular petiolar bundles, although the midrib anatomy can be complex. Tetrameranthus sometimes seems to have opposite leaves; according to George Schatz (pers. comm.) it lacks plagiotropic branches and has all branches with spirally-arranged leaves.
There are reports that the pollen grains of both Annona and Asimina may germinate via the proximal pole (Hesse et al. 2009a), although in the former (and some other genera) individual grains of the tetrad may rotate during development (Tsou & Fu 2002, 2006; Lora et al. 2009b). Xylopia, like Anaxagorea also with follicles, has micropylar-arillate seeds (Corner 1976); other genera may also have reduced arils (Svoma 1997). Reports that the micropyle is formed by both integuments need to be confirmed (c.f. Svoma 1998b). Monodora (derived) has a rather thin outer integument, and anatomy of the seed coat of Ambavioideae with a third integument (Zwischenintegument) can be complex (Christmann 1986).
For an introduction to Annonaceae and much more besides, see the papers in Bot. J. Linnean Soc. 169(1). 2012, including Erkens et al. (2012a) for a comprehensive bibliography. Additional information is taken from Fries (1919: inflorescence morphology), Jovet-Ast (1942: indumentum and anatomy), Corner (1949: seed anatomy), van der Wyck and Canright (1956: anatomy), Hegnauer (1964, 1989: chemistry), Okada and Ueda (1984: cytology), Morawaetz (1986, 1988: esp. cytology), Deroin (1991b: stigmatic surface and carpel morphology), Kessler (1993: general), Steinecke (1993: esp. flower and fruit), Rudall and Furness (1997: tapetum), Svoma (1998a: seeds), van Setten and Koek-Noorman (1992: fruits and seeds), Endress (2011b), ovules, Deroin (1999a: receptacular vascular system), Bakker (2000a, b: general); Johnson (2003: leaf insertion), Junikka and Koek-Noorman (2007: bark anatomy), Koek-Noorman and Westra (2012: wood anatomy), van Setten and Koek-Noorman (1986: leaf anatomy), Couvreur et al. (2008a: evolution of syncarpy, etc.), Couvreur et al. (2008b: pollen in the Monodora group), Sun et al. (2008: epidermal anatomy), and Lora et al. (2009: infraspecific variation in number of pollen nuclei in Annona cherimola). For floral (developmental) morphology, see van Heusden (1992), Ronse Decraene and Smets (1990b), Leins and Erbar (1980, 1982, 1996, 2010), Xu and Ronse De Craene (2010b), Endress (1975: carpel and stamen development), and Endress and Armstrong (2011: Anaxagorea).
Phylogeny. See Doyle and le Thomas (1994, 1996) for morphological phylogenies and character evolution, and for a molecular phylogeny of Anaxagorea that is integrated with morphological variation, see Scharaschkin and Doyle (2005, 2006). The position of Unonopsis on the tree has been somewhat erratic, probably because of ancient paralogy (Pirie et al. 2007). For relationships in Ambavioideae, see Surveswaran et al. (2010).
Two major clades make up the rest of the family (see also Richardson 2004). Malmeoideae include a polyphyletic Polyalthia (Richardson et al. (2004). This clade is not very speciose, mostly lacking large genera aside from Polyalthia, and has relatively little internal molecular divergence (hence its early name, the short-branch clade: Mols et al. 2008a; Xue et al. 2011). New World members of this clade form a monophyletic group (Pirie et al. 2006). For Pseuduvaria, see Su and Saunders (2006) and Su et al. (2008, 2010), while for the relationships and dimemberment of Polyalthia, see Xue et al. (2011, 2012). Mols et al. (2008b) explore character evolution within Malmeoideae. Annonoideae include the inaperturate pollen clade; here there is more molecular divergence (hence its name, the long branch clade: see also J. A. Doyle et al. 2004; Pirie et al. 2005). Uvaria is polyphyletic (Mols et al. 2004), and Zhou et al. (2009a, esp. b, 2010) suggested that its limits be extended; geography and phylogeny correlate quite well. The limits of genera like Dasymaschalon and Friesodielsia are also unclear (Wang et al. 2012: indepdendent loss and subsequent parallel evolution in taxa that have lost their inner petals). )For Guatteria, see Erkens (2007) and Erkens et al. (2007a, b).
Classification. The classification outlined by Chatrou et al. (2012) is followed here, although they also recognize tribes; their principles of classification are clearly explained. The limits of genera and hence the numbers of their included species in Annonoideae seem particularly uncertain. Zhou et al. (2010) clarify the limits of Uvaria, Xue et al. (2011, 2012) those of Polyalthia, while Surveswaran et al. (2010) discuss generic limits in the ambavioid clade. For a checklist of the New World species of the genus, see Maas et al. (2011); Annonbase should also be consulted.