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, carinal, 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]; 2C genome size 1-8.2 pg [1 pg = 109 base pairs], 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.
[MONOCOTS [CERATOPHYLLALES + EUDICOTS]]: (veins in lamina often 7-17mm/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 scattered, asarone 0 [unknown in some groups, + in some asterids]; root epidermis derived from root cap [?Buxaceae, etc.]; nodes 3:3; stomata anomocytic; flowers (dimerous), cyclic; 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 [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?; 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 developing internally/adaxially to the corolla whorl and successively 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.
[DILLENIALES [SAXIFRAGALES [VITALES + ROSIDS s. str.]]]: nodes 3:3; stipules + [usually apparently inserted on the stem].
[SAXIFRAGALES [VITALES + ROSIDS]] / ROSANAE Takhtajan / SUPERROSIDAE: ??
[VITALES + ROSIDS] / ROSIDAE: anthers articulated [± dorsifixed, transition to filament narrow, connective thin].
ROSIDS: (mucilage cells with thickened inner periclinal walls and distinct cytoplasm); embryo long; genome duplication; chloroplast infA gene defunct, mitochondrial coxII.i3 intron 0.
ROSID I / FABIDAE / [ZYGOPHYLLALES [the COM clade + the nitrogen-fixing clade]]: endosperm scanty.
[the COM clade + the nitrogen-fixing clade]: ?
[FABALES [ROSALES [CUCURBITALES + FAGALES]]] / the nitrogen-fixing clade: (N-fixing by associated root-dwelling bacteria); tension wood +; seed exotestal.
[ROSALES [CUCURBITALES + FAGALES]]: ovules 1-2/carpel, apical.
ROSALES Perleb Main Tree, Synapomorphies.
(Frankia infection via intercellular penetration); (isoflavonoids, dihydroflavonols +); mucilage cells +; roots diarch [lateral roots 4-ranked]; prismatic crystals in ray cells [not Barbeyaceae, Elaeagnaceae]; (sieve element with non-dispersive protein bodies; sieve element plastids lacking starch [Rhamnaceae, Dirachmaceae?]); inflorescence cymose; hypanthium +, nectariferous, K valvate, C clawed; styles branched, stigma dry; ovule 1/carpel, epitropous, micropyle endostomal; K and/or hypanthium persistent in fruit; (polyembryony +). - 9 families, 261 genera, 7725 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 for many characters, with with variation within and between clades. Furthermore, 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. Wikström et al. (2001) date stem Rosales to (90-)88(-86) m.y., crown Rosales at (79-)76(-73) m.y. Most other estimates are rather older. Crown Rosales were estimated as (96-)93, 88(-85) m.y. (two penalized likelihood dates), the stem at (110-)105(-100) or (94-)89(-84) m.y.; Bayesian relaxed clock estimates were slightly older, to 103 or 111 m.y. respectively (Wang et al. 2009: relationships - [Rosales [Fabales [Cucurbitales + Fagales]]]), while Magallón and Castillo (2009: relationships - [[Fabales + Rosales] [Cucurbitales + Fagales]]) estimated ages of ca 101.15 m.y. for stem Rosales, and 94 m.y. for the crown group.
Rosales contain ca 1.9% of eudicot diversity (Magallón et al. 1999).
Ronse De Craene (2003, see also 2010) suggested that loss of petals might characterise Rosales, with apparent "petals" occupying the position of stamens and their evolution allowing e.g. Rosaceae to diversify. If Rosales are sister to Fabales, as Ronse de Craene (2003) suggested, they are not a notably diverse group in terms of species numbers, the more so since almost 4,000 species of Rosales - about half - are in the Ulmaceae-Urticaceae group, which lack petals of any sort. This latter group forms a single clade, and the wind pollination that is so common there cannot be considered basic to Rosales as a whole (c.f. Ronse de Craene 2010). Even with the relationships [Rosales [Cucurbitales + Fagales]] (see above) it seems that no argument connecting petals in Rosales with diversity can be made (see also Ronse de Craene & Brockington 2013).
Plant-Animal Interactions. Quite a number of butterfly larvae - especially caterpillars of "basal" groups and Lycaeninae - feed here (Fiedler 1995; Janz & Nylin 1998).
Bacterial/Fungal Associations. Some taxa in at least Rosaceae, Rhamnaceae, Elaeagnaceae and Ulmaceae are ectomycorrhizal (see Malloch et al. 1980; S. E. Smith and Read 1997).
Chemistry, Morphology, etc. Roots are commonly diarch in Rosaceae, but are also tetrarch, etc.; sampling elsewhere is poor, although less so in Ulmaceae and relatives, and diarch roots are found throughout the order. Tracheary members in Rosaceae commonly have pseudotori (thickenings in pit membranes associated with plasmodesmata), while true tori also occur in Rosaceae (Cercocarpus) and also Cannabaceae and Ulmaceae (Jansen et al. 2007), although these tori are formed in two different ways (Dute et al. 2010a). Sieve tube plastids lacking both starch and protein inclusions are rare outside Rosales, although they have been found in some parasites as well as Crassulaceae and Malpighiaceae (Behnke 1991a). A granular layer below the tectum may be a synapomorphy for the clade. For polyembryony, sporadic in the clade, see G. Dahlgren (1991).
For wood anatomy, esp. of Elaeagnaceae, see Jansen et al. (2000b) and Baas et al. (2001: fibre pits not bordered). Kubitzki (2004) provides a summary of the order; there is much useful information in Thulin et al. (1998).
Phylogeny. In early molecular studies Rosaceae appeared to be sister to the rest of the order (strong support: Savolainen et al. 2000a; Wang et al. 2009), while Ulmaceae and relatives (the old Urticales) and Rhamnaceae and relatives formed two clades (also Thulin et al. 1998; Savolainen et al. 2000b; Richardson et al. 2000b; Sytsma et al. 2002: position of Rosaceae, etc., uncertain; Wang et al. 2009; Soltis et al. 2011), as in the tree below. The position of Elaeagnaceae was sometimes rather labile (Richardson et al. 2000b: successive approximation weighting), even being embedded in Rhamnaceae in a rbcL analysis, and there was quite strong support for a clade [Barbeyaceae + Dirachmaceae]. The tree found by S.-D. Zhang et al. (2011) is based on an analysis of twelve genes from 25 taxa of Rosales, and the major relationships within the order are very well supported, although somewhat less so in the subclade that includes Rhamnaceae (see below); their relationships are followed here.
There is also the issue of the placement of the holoparasitic Cynomoriaceae. Z.-H. Zhang et al. (2009; see also Moore et al. 2011) placed Cynomoriaceae in Rosales and sister to Rosaceae based on analyses of chloroplast inverted repeat sequences; support was strong, but Moraceae were the only other family in the order examined. Cynomoriaceae certainly were to be excluded from Saxifragales (good sampling) where they had sometimes been included, albeit with modest support (see Saxifragales page for further details). S.-D. Zhang et al. (2011) did not include Cynomoriaceae in their study; 10/12 genes they sequenced were plastid genes. Cynomoriaceae are placed both here and in Saxifragales for now, although there is little in their morphology to suggest relationships with Rosales.
Previous Relationships. In the past, Urticales (Urticaceae, Moraceae, etc.) were kept well separate from Rosaceae, largely because their very reduced and usually wind-pollinated flowers suggested relationships to the old Amentiferae.
Includes Barbeyaceae, Cannabaceae, Cynomoriaceae, Dirachmaceae, Elaeagnaceae, Moraceae, Rhamnaceae, Rosaceae, Ulmaceae, Urticaceae.
Synonymy: Rhamnineae Shipunov - Amygdalales Link, Artocarpales Martius, Barbeyales Takhtajan & Reveal, Cannabales Döll, Dryadales Link, Elaeagnales Berchtold & J. Presl, Ficales Dumortier, Frangulales Wirtgen, Morales Martius, Rhamnales Link, Sanguisorbales Link, Spiraeales Link, Ulmales Link, Urticales Berchtold & J. Presl
ROSACEAE Jussieu, nom. cons. Back to Rosales
Triterpenes +, alkaloids 0; cork deep seated; (vessel elements with scalariform perforation plates); (true) and fibre tracheids +; sieve tubes with non-dispersive protein bodies; petiole vasculature of arcuate or annular bundles, or annular; leaves spiral (opposite), lamina vernation usu. conduplicate, (secondary veins palmate), stipules often petiolar; inflorescences racemose; (C 0); A (1-)15-many [ca 20 common - 10 + 5 + 5, centripetal, in groups], (latrorse); (pollen porate); G free, stigmas punctate to expanded or down stylulus; ovules with parietal tissue 2-4 cells across, nucellar cap ca 4 cells across; megaspore mother cells several; fruit aggregate of achenes; exotestal cells periclinally elongated, radial walls thickened, or palisade or tabular, walls with spiral or reticulate thickenings, outer wall often becoming mucilaginous, endotegmic cells slightly thickened, or seed coat undistinguished; chalazal endosperm haustorium +; x = 9; duplication of GBSSI [granule bound starch synthase I] gene.
90[list]/2520. World-wide, but esp. N. hemisphere, often not deserts or tropical rainforest (map: from Vester 1940 [overly optimistic - or inc. Chrysobalanaceae?]; Hultén 1971; Trop. Afr. Fl. Pl. Ecol. Distr. 2. 2006; FloraBase i.2013; Australia's Virtual Herbarium i.2013). [Photos - [Collection, Collection.]
1. Rosoideae Arnott
Herbs to shrubs; 2-pyrone-4,6dicarboxylic acid, ellagic acid +; rays often narrow; cuticle waxes as narrow ribbons and triangular rodlets; leaves usu. compound; (epicalyx +), carpels many; fruits usu. achenes or drupelets; ovule (straight), unitegmic; x = 7; plant with phragmidiaceous rusts.
Especially temperate (to Arctic) areas.
1A. Filipendula - Plant herbaceous; receptacle enlarged; ovules 2/carpel. - 1/10. Eurasia.
Synonymy: Ulmariaceae Gray
Rosodeae T. Eriksson, Smedmark, & M. S. Kerr (= all other Rosoideae): ?
1B. Rubus - Prickly scrambling shrub; receptacle enlarged; ovules 2/carpel [Rubus], integument ca 6 cells across; fruit an aggregate of drupelets. - 1/± 250. ± Worldwide, esp. N. temperate.
Synonymy: Chamaemoraceae Lilja
1C. Colurieae Rydberg
Ovule apotropous [Geum].
3/42: Geum (40). Temperate, inc. montane tropics, Chile.
[Sanguisorbeae [Rosa + Potentilleae]]: ?
1D. Sanguisorbeae Candolle
G 1-5; integument 6-8 cells across; phragmidiaceous rusts 0.
Within Sanguisorbeae are two subtribes. Agrimoniinae J. Presl - 5/20: Agrimonia (15). N. Temperate, Africa. Sanguisorbineae Torrey & A. Gray - 7/360: Cliffortia (115), Acaena (100). ± Worldwide, few Indo-Malesia, tropical America.
Synonymy: Agrimoniaceae Gray[?], Fragariaceae Nestler, Poteriaceae Rafinesque, Sanguisorbaceae Berchtold & J. Presl
[Rosa + Potentilleae]: ?
1E. Rosa - Prickly arching shrub; hypanthium fleshy, urn-shaped; integument ca 8 cells across. - 1/100-150. N. temperate; 1/3 spp. in Europe.
1F. Potentilleae Sweet
(Epicalyx +); receptacle enlarged; integument ca 4 cells across. Potentillineae: style often lateral/gynobasic. 5-6/540: Potentilla + Argentina et al. N. temperate to Arctic (montane tropics to S. temperate). Fragariinae + Alchemillinae: anther thecae more or less confluent; parietal tissue ca 2 cells across, nucellar cap ca 7 cells across. Fragariinae Torrey & A. Gray: (leaves simple); (G 1); phragmidiaceous rusts 0 (Fragaria +). 10/60. Alchemillinae 3/960-1100: Alchemilla (1000+). N. temperate, esp. Europe, tropical mountains (S. temperate).
Synonymy: Alchemillaceae Martinov, Potentillaceae Berchtold & J. Presl, Tormentillaceae Martynov
[Dryadoideae + Spiraeoideae]: sugar alcohol sorbitol + [transport carbohydrate], cyanogenic glycosides +.
2. Dryadoideae Juel
Association with N-fixing Frankia; leaves usu. simple; G 1-many; ovules straight (anatropous, apotropous - Dryas); fruits achenes with hairy styles.
4/19: Cercocarpus (8). W. North America, Dryas circumboreal.
Synonymy: Cercocarpaceae J. Agardh, Dryadaceae Gray
3. Spiraeoideae C. Agardh
Plant woody, (ectomycorrhizal); flavones +, ellagic acid 0; cuticle waxes as tubules or platelets; leaves simple (compound); G <5, opposite petals, 2< ovules/carpel, papillate funicular obturator +, stigma usu. wet; fruit a follicle.
3A. Lyonothamnus - Cyanogenic glycosides 0; leaves opposite, compound, stipules deciduous; G seminferior, placentation apical; ovules 4-6/carpel. - 1/1: Lyonothamnus floribundus. California Islands, off S. California.
3B. Niellieae Maximowicz
Cyanogenic glycosides?; leaf teeth colleter-like; ovule 1/carpel, apical, apotropous (-5, pleurotropous); fruitlets hard, shiny, indehiscent.
2/24: Niellia (14). E. and W. North America.
Synonymy: Neilliaceae Miquel
3C. Amygdaleae Jussieu
(Plant ectomycorrhizal); cork superficial; true tracheids 0; lamina vernation laterally or vertically conduplicate, extrafloral nectaries +, on petiole, towards base of the margin, or abaxial lamina; leaf teeth colleter-like; G 1; outer integument 6-8 cells across, inner integument 3-6 cells across, obturator from ovary wall; fruit a drupelet; seed coat mostly pachychalazal; n = 8.
1/200. Temperate and tropical montane.
Synonymy: Amygdalaceae Marquand, Prunaceae Martinov
Kerriodae D. Potter, S. H. Oh, & K. R. Robertson [= Osmaronieae + Kerrieae]: phragmidiaceous rusts 0.
3D. Osmaronieae Rydberg
Cork superficial; pith chambered; stipules deciduous; styles lateral; obturator from ovary wall; fruit a drupe, or septicidal capsule, the carpels also opening adaxially [Exochorda]; n = 8.
3/9: Exochorda (4), Prinsepia (4). Central to East Asia, W. North America.
3E. Kerrieae Focke
Wart-like projections on lamina; G 1-5; ovule ?obturator; fruit an aggregate, nut-like units, (achenes: Neviusia); n = ?
4/4. East Asia, W. North America, Alabama.
Synonymy: Coleogynaceae J. Agardh, Rhodotypaceae J. Agardh
3F. Sorbarieae Rydberg
Leaves compound (simple: Adenostoma); (G 1, Adenostoma), placentation apical; (fruit an achene: Adenostoma).
4/8: Spiraeanthus (4). Central to East Asia, W. North America
3G. Spiraeeae Candolle
Vestured pits +; nodes 1:1 [?all]; stipules 0; ovules 6-8/carpel, unitegmic; (fruit an achene - Holodiscus).
8/106: Spiraea (80-100). N. temperate, to Columbia, (S. and) E. Africa, West Malesia.
Synonymy: Spiraeaceae Bertuch
Pyrodeae C. S. Campbell, R. C. Evans, D. R. Morgan, & T. A. Dickinson
Flavone C-glycosides +; cork superficial [?Gillenia]; rays often narrow; colleters + [probably elsewhere]; G ± connate, adnate to base of hypanthium, opposite sepals or odd member abaxial, gynoecial ring primordium +; ovules two/carpel, ± apotropous, (micropyle bistomal); exotesta ± thickened, often mucilaginous, mesotesta thick, sclerotic; Gymnosporangium rust common.
3H. Gillenia - Leaves compound. - 1/2. E. North America.
3I. Pyreae Baillon
N = 17; four copies of GBSSI [granule bound starch synthase I].
[Kageneckia + Lindleya]
(Plant dioecious); 4-many pleurotropous ovules/carpel; Gymnosporangium rust 0.
2/5. Mexico, Peru, Chile. [Kageneckia Flower, Fruit.]
Synonymy: Lindleyaceae J. Agardh
Vauquelinia - Tannin-containing cells pervasive; fruit septicidal, carpels opening adaxially (and partially abaxially as well). - 1/3. S.W. North America.
(Plant ectomycorrhizal); (leaves compound), stipules deciduous; G at least half inferior, (carpels laterally free); outer integument 5-14 cells across, inner integument 3-6 cells across; hypanthium fleshy in fruit ["pome"], (endocarp +).
30/1000: Sorbus (260), Crataegus (260, inc. Mespilus), Cotoneaster (260), Pyrus (75), Malus (55). Largely north Temperate.[Photo - Flower]
Synonymy: Cydoniaceae Schnizlein, Malaceae Small, nom. cons., Mespilaceae Schultz-Schultzenstein, Pyraceae Vest, Sorbaceae Brenner
Floral formula: * ⚥ K 5; C 5; A (10-)15<; N; G (1-)10< / [3-5].
Evolution. Divergence & Distribution. Turonian fossils some 90 m.y. old are assignable to Rosaceae (Crepet et al. 2004 for references); other estimates are younger, e.g. stem group ca 76 m.y., crown group 47-46 m.y. (Wikström et al. 2001: Rosoideae not included]). Prunus endocarps have been found in the early Eocene of China ca 55 m.y.a., and there was considerable diversification of the family in the Eocene (Wehr & Hopkins 1994; Benedict et al. 2011; Li et al. 2011 and references).
The inferior-ovaried Pyreae may represent a rapid but ancient radiation (Campbell et al. 2007). Stem group Pyrinae have been dated to (64-)58, 53(-43) m.y., with subsequent divergence in the Eocene and Oligocene, a substantial amount of movement around the northern hemisphere, probably via the Beringian land bridge, and much heterogeneity in clade size that is independent of age (Lo & Donoghue 2012). There are about 34 species of Lachemilla (= Alchemilla) growing in the páramo (Gehrke et al. 2008; Sklenár et al. 2011).
Optimisation of characters on the tree presents problems. Potter et al. (2007) used DELTRAN, and so being host to Gymnosporangium rusts is not an apomorphy of Pyrodeae; using ACCTRAN (as here) it is. Along the same lines, they reasonably divided up the presence of sorbitol into two states; it might be present in only small amounts (Dryadoideae), or it was more abundant (Spiraeaoideae); presence of at least some sorbitol characterizes the larger clade.
Ecology & Physiology. Some, but not all, Dryadoideae, are N-fixers, but the widespread Dryas integrifolia appears to be unable to fix nitrogen (Markham 2009); Dryas is prominent in tundra vegetation. Nodules and association with Frankia have also been reported from other Rosaceae, e.g. from Rubus ellipticus (Markham 2009). Species of the N-fixing (Cowania (Dryadoideae) and the non N-fixing Fallugia (Rosoideae-Colurieae) can form successful grafts; when Fallugia is the stock the combination will not fix nitrogen (Kyle et al. 1986).
Pollination Biology. There is a period of about 19 days between pollination and fertilization in Prunus persica (Herrera & Arbeloa 1989).
Plant-Animal Interactions. Galls caused by cecidomyid midges are quite common in North American Rosaceae (Gagné 1989). Cynipid gall wasps of the tribe Diplolepidini are notably common on Rosa, Diplolepis rosae forming the well-known robin's pincushion or bedeguar gall (Csoka et al. 2005; Redfern 2011).
Bacterial/Fungal Associations. At least some Dryadoideae and Spiraeaoideae are ectomycorrhizal. Geopora (Pezizales, an ascomycete) is the fungus involved in the mycorrhizae of Cercocarpus (Dryadoideae), and it also forms associations with Quercus and Arctostaphylos (Ericaceae, with a subtype of the distinctive mycorrhizae of that family), the result being a complex mycorrhizal network; ascomycetes are associated with other ectomycorrhizal members of the family (McDonald et al. 2010).
Savile (1979b; see also Jackson 2004b: possible codivergence) discusses the distribution of phragmidiaceous rusts within Rosaceae-Rosoideae; they occcur on no other Rosaceae, and only rarely on plants from other families. Most of these rusts are autoecious, that is, their entire life cycle occurs on the one species. Gymnosporangium rusts, found scattered on Spiraeaoideae-Pyrodeae, are heteroecious. Here the telial stage (the teliospore is a thick-walled resting spore that germinates to produce basidisospores) is common on some Cupressaceae, the aecial stage, which produces thinner-walled binucleate aeciospores, is found on Pyrodeae (Lo & Donoghue 2012 for "gains" and "losses" of infestation). Interestingly, Rosaceae rarely produce phytoalexins, protective compounds induced by e.g. fungal infection (Harborne 1999).
Genes & Genomes. The basic chromosome number of the family may be x = 7 (Shulaev et al. 2010). It has long been suspected that Pyreae were of wide hybrid origin, as their chromosome number might suggest (n = 9 [Rosoideae] x n = 7 [Spiraeaoideae] = n = 16 [some Maloideae]), see Evans et al. (1998), however, Evans and Campbell (2002) suggest that this is unlikely. Polyploidisation with subsequent aneuploidy (9 x 9 -> 18, 18 - 1 -> 17) of the diploid Gillenia (herbaceous, with compound leaves) or something similar is more likely; Gillenia is sister to Pyreae (Potter et al. 2002; Evans & Dickinson 2002). Gillenia is host to the same rusts that are found on other Pyrodeae, but it has only two copies of GBSSI, as is the condition in the rest of the family. Within Pyrodeae, there is some evidence of wide crosses in the Oligocene (Lo & Donoghue 2012).
For the relationship between polyploidy and diversification in Rosaceae - perhaps direct - see Vamosi and Dickinson (2006). Allopolyploidy in Fragariinae and its taxonomic implications were studied by Lundberg et al. (2009). Within Fragaria itself, the only taxon known to have one of the parental genomes of F. magellanica grows in eastern Japan (Rousseau-Gueutin et al. 2009). Apomixis is common, as in Rubus and Alchemilla (Rosoideae) and Amelanchia, Sorbus, Cotoneaster and Crataegus (Spiraeaoideae-Pyrodeae). Hybridisation occurs in Crataegus, and the hybrids are triploid and apomictic. There were ca 17 North American species of Crataegus in 1896, while 30 years later there were over 1000 species, and at least some were triploid apomictic hybrids; C. S. Sargent described many of these. Within Crataegus clades are linked with geography, yet, as in Fragaria, parents of genomes may have very disparate geographic origins (Lo et al. 2009). In general, apomixis seems to have preceded hybridisation (Dickinson et al. 2007).
Chemistry, Morphology, etc. For general chemistry, see Hegnauer (1973, 1990), and for 2-pyrone-4,6dicarboxylic acid distribution, see Wilkes and Glasl (2001). Okuda et al. (1992) discuss tannin distribution in the family; chlorogenic acid was found in nearly all taxa examined. A polyderm is common, although perhaps not occurring in Pyreae (Mylius 1913). 1:1 nodes occur in Spiraea, a genus that also lacks stipules, although normally Rosaceae have stipulate leaves and 3:3 nodes (see e.g. Sinnott & Bailey 1914). There are extensive data on cuticle waxes in the family (Fehrenbach & Barthlott 1988), but they are recorded only as summaries in the context of conventional subfamilies; Barthlott (pers. comm.) kindly provided a more detailed breakdown. Chin et al. (2013) surveyed nectaries and nectary-like structures on the leaves of Prunus and optimized them on a phylogenetic tree. Interestingly, leaf teeth in several species of the genus, as well as in Niellia and Physocarpus, are colleter-like both in terms of their structure and what they secrete (mucilage); other species of Spiraeoideae, at least, should be surveyed for such teeth.
The epicalyx that occurs in some Rosaceae seems to represent stipules associated with the calyx members. For hypanthium development, see Rauh and Reznik (1951). Ronse de Craene (2007) wondered whether the petals were modified staminodes. There are often five traces to each carpel. Even in taxa with inferior ovaries, there is great variation in whether or not the carpels are connate, or what parts are connate, and in whether or not the carpels are adnate to the axial tissue enveloping the carpels/hypanthium. Thus Cotoneaster has an inferior ovary in which the carpels are more or less separate although adnate to the hypanthium, c.f. also Pyracantha. The odd genus Dichotomanthes, also included in Pyreae, has a single carpel that is superior in position (Rohrer et al. 1994); its distinctive gynoecial morphology must represent a reversal. The single, basal ovule of Chamaebatia (Dryadoideae) lacks an obturator (Evans & Dickinson 2002). Ovules of Rhodotypos have a protruding nucellus (c.f. Rhamnaceae). The lignified exotesta common in the family can be found even in the seeds of the drupaceous Prunus.
Some general information is taken from Robertson (1974), Kalkman (2004), Judd et al. (2002), and especially Potter et al. (2007). There is information on cork initiation and bark anatomy in Lotova and Timonin (e.g. 1998, 1999, 2002) and Weiss (1890), on wood anatomy in Zhang (1992), on petiole vasculature in Morvillez (1917), on carpel orientation and general morphology in Focke (1888), Schäppi (1951: peltate and plicate carpels), Schäppi and Steindl (1950), Sterling (1969 and references), Kania (1973: also androecium) and Weberling (1989), androecial diversity is discussed in Murbeck (1941: also vasculature, Neurada etc. "basal") and Lindenhofer and Weber (2000 and references), pollen morphology in Sanguisorbeae in Chung et al. (2010), carpel development in van Heel (1981, 1983), ovule morphology in Péchoutre (1902: quite comprehensive, also seeds) and Schäppi and Steindl (1950: Rosoideae), exotesta in Frohne and Jensen (1992), and floral development in Evans and Dickinson (1999a, 1999b, 2005); for information on Vauquelinia, see Hess and Henrickson (1987), for that on Geum, see Kajewski (1957: classic cytological work) and Smedmark and Eriksson (2006: development of stylar hook).
Phylogeny. Rosoideae and a number of clades within it, Spiraeoideae, Spiraeoideae minus Lyonothamnus, [Pyrodeae + Sorbarieae] and Pyrodeae are all well-supported, but little can yet be said of other larger patterns of relationship (e.g. Morgan et al. 1994; Potter et al. 2002; Potter 2003; Potter et al. 2007). The position of Dryadoideae is uncertain, other than being a rather "basal" branch in the tree (Potter et al. 2002: Evans et al. 2002), hence perhaps the lack of obturators. Potter (2003: several genes) found that Dryadoideae were fairly well supported as sister to remaining Rosaceae, but their position was not secure in Potter et al. (2007), although a sister group relationships with Spiraeaoideae was indeed perhaps most likely.
Eriksson et al. (2003) provide a phylogeny of Rosoideae: Alchemilla, Fragaria, and other genera form a well-supported clade outside Potentilla and relatives (see also Dobes & Paule 2010). Filipendula is sister to other Rosoideae. "Intergeneric" hybridisation seems to occur (Smedmark et al. 2003). Within Potentilleae, Potentilla is sister to the rest (see Eriksson et al. 2003), or, more precisely, Potentilla (including a few genera) is sister to a small clade including Argentina (Potentilla sect. Anserina), the two forming a clade sister to the other Potentilleae (all relationships with strong support: Dobes & Paule 2010). Fragariinae are sister to Alchemillinae; for relationships within Alchemilla s.l., which have a strong geographic signal, see Gehrke et al. (2008). The current infrageneric classification of Rubus does not reflect relationships there (Alice & Campbell 1999). For Rosa, see Bruneau et al. (2007), Wissemann and Cox (2007) and Koopman et al. (2008); relationships here are not easy to disentangle.
Aldasoro et al. (2005) suggest morphological and biogeographic relationships in the inferior-ovaried Spiraeaoideae-Pyreae. Exochorda forms a small clade along with Oemleria and Prinsepia (Evans & Dickinson 1999a for information); they have been placed near Prunus (Potter et al. 2002, see also Lee & Wen 2001) to which they do show some morphological similarity. Amygdaleae are circumscribed narrowly here (one genus, Prunus, from which there have previously been segregates), following Potter et al. (2002, 2006). For phylogenies of Prunus, see Lee and Wen (2001) and Wen et al. (2008: some conflict between ITS and ndhF); the distribution and nature of calcium oxalate crystals correlate quite well with relationships (see Lersten & Horner 2000). In the recent past Maddenia (dioecious, apetalous) has been placed near Prunus; it is a member of . Generic limits in Pyreae-Pyrineae have been difficult, there being little molecular divergence between many of them (but considerable divergence within them (Dickinson et al. 2007; Lo et al. 2007, esp. Crataegus s.l.; Q.-Y. Li et al. 2012: little support for most of the relationships discussed). Cotoneaster forms grafts with Crataegus. However, recent work including over 330 species and large amounts of data has provided substantial resolution of relationships in Pyrineae, although support along the backbone could still be improved (Lo & Donoghue 2012).
Classification. Fruit types are certainly not as good indicators of relationships within Rosaceae as was for a long time thought, but chemistry, chromosomes, and fungi all support the realignments suggested by molecular data (especially Morgan et al. 1994), as does developmental work by Evans and Dickinson (1999a, b, 2002). Thus the old Spiraeoideae, characterised by follicular fruit, are strongly paraphyletic, and include both Prunoideae/Amygdaloideae and Maloideae; Prunoideae were characterized by drupaceous fruits, and Maloideae by their pomes (a pretty useless term). In the past Spiraeoideae had been considered a very natural group (e.g. Kalkman 1988), however, tribes in Spiraeaoideae may represent clades (especially Evans et al. 2002; Potter et al. 2006).
Generic limits in Pyrinae may reflect the European origin of taxonomy and the fact that the group is common in Europe (e.g. Walters 1961). However, there is now support for many of the main clades there and one can now aspire to a stable taxonomy; Sorbus and some other genera have turned out to be polyphyletic (Lo & Donoghue 2012). Generic limits in Potentilleae are becoming clearer (Dobes & Paule 2010, but see Soják 2008 for an alternative); Alchemilla is to include Aphanes and Lachemilla (Gehrke et al. (2008).
Previous Relationships. Rosaceae as circumscribed above are holding together very well despite their morphological heterogeneity, but there have been departures. Chrysobalanaceae, often associated with Rosaceae in the past, are well embedded within Malpighiales, Quillaja rather unexpectedly is an isolated clade within Fabales, while Guametala is correspondingly isolated in Crossosomatales (Oh & Potter 2006).
Botanical Trivia. Trees of Polylepis tarapacana grow at some 5,100 m in Bolivia, the highest known altitude for all trees (Hoch & Körner 2005).
[[Rhamnaceae [Elaeagnaceae [Barbeyaceae + Dirachmaceae]]] [Ulmaceae [Cannabaceae [Moraceae + Urticaceae]]]]: ovules apotropous, trans-spliced intron in nad1 gene [cis-spicing elsewhere].
Evolution. Diversification in this clade may begin 64-62 m.y.a. (Wikström et al. 2001: Rhamnaceae sister to the rest).
Chemistry, Morphology, etc. For nad1 intron splicing, see Qiu et al. (1998).
[Rhamnaceae [Elaeagnaceae [Barbeyaceae + Dirachmaceae]]]: petiole bundle arcuate; stamens = and opposite C/alternate with P; capsule septicidal; ovule basal, parietal tissue 5-6 cells across; coat multiplicative, exotesta palisade, thick-walled; cotyledons large.
Evolution. Divergence & Distribution. Note that most of the apomorphies mentioned above are those of the [Dirachmaceae + Rhamnaceae + Elaeagnaceae] clade for the pre vi.2011 version of the site; they must now reverse - or be uncertain - in the poorly-known Barbeyaceae... Dense, curly hairs on the abaxial surface of the leaf blade could be an apomorphy here (Sytsma et al. 2002), but Qiu et al. (1998) put this feature at a higher node. For changes in infratectum morphology on the tree (see also Doyle 2009).
Chemistry, Morphology, etc. The wood anatomy of Dirachmaceae is particularly similar to that of Rhamnaceae (Baas et al. 2001)
A granular layer below the tectum is more or less developed in both Rhamnaceae and Dirachmaceae - I am unsure of its distribution elsewhere in the clade. The flattened seed with an antiraphal vascular bundle of Dirachmaceae is similar to seeds in Rhamnaceae (Boesewinkel & Bouman 1997); the distribution of testal and tegmic epidermal cells with sinuous anticlinal walls could be interesting.
Phylogeny. This grouping is suggested by Campbell (pers. comm. 2003), Sytsma et al. (2002: support weak) and especially Zhang et al. (2011). Rhamnaceae, Barbeyaceae and Dirachmaceae may form a clade (Richardson et al. 2000a). However, this was not confirmed by S.-D. Zhang et al. (2011), but the maximum parsimony bootstrap values for the relationships here are not strong, nor is the maximum likelihood support for [Elaeagnaceae [Barbeyaceae + Dirachmaceae]], although posterior probabilities are all 1.0.
RHAMNACEAE Jussieu, nom. cons. Back to Rosales
Woody (lianes); leaves much reduced and whole plant thorny); chelidonic acid +; saponins, biflavonyls, benzylisoquinoline alkaloids +, myricetin, ellagic acid 0; (vessel elements with scalariform perforation plates); libriform fibres +; lysigenous mucilage cavities +; leaves opposite or spiral, lamina vernation conduplicate(-plicate) or involute, (margins entire), (stipules 0), colleters +; (plant dioecious); flowers small, 4-5(-6)-merous; K (connate), with a longitudinal median ridge adaxially, C cucullate, enfolding A (0); tapetal cells multinucleate; infratectum granulate-intermediate, (nectary as disc; on ovary); G [2-3(-5)], ± inferior, opposite sepals or odd member adaxial, style + or styles separate, with canals as many as carpels (one; 0), stigma papillate; ovules (2; median), (apotropous), (bistomal), outer integument 4-10 cells across, inner integument 3-4 cells across, parietal tissue 4-7 cells across, nucellar cap to 6 cells across, nucellus ± protruding through micropyle, hypostase +, funicular obturator +; often several megaspore mother cells, (embryo sac bisporic, 8-nucleate - Allium type), antipodals degenerate; K often deciduous; seeds often laterally flattened, (arillate); testa with median integumentary antiraphe bundle +/0, (mesotesta with a few sclerotic cells), endotegmen of cuboid cells, with scalariform thickenings (slightly lignified); endosperm +/0, (starchy), (perisperm +?), polyembryony common, embryo green.
52[list]/925 - three groups below. World-wide, especially tropics and warm temperate regions (map: see van Steenis & van Balgooy 1966; Meusel et al. 1978; Frankenberg & Klaus 1980; Richardson et al. 2003; Australia's Virtual Herbarium xii.2012; Trop. Afr. Fl. Pl. Ecol. Distr. 5. 2010: C. Asia?). [Photo - Flower, Dry fruit, Fleshy fruit.]
G inferior; fruit a drupe or samara; n = 6, 10, 12.
Rhamnus (125). Tropical, north temperate.
Synonymy: Frangulaceae de Candolle
Lamina with secondary venation palmate; fruit a drupe; n = ?
3/4. Cuba, north South America, Madagascar.
(Herbs), (plant thorny); (roots with N-fixing Frankia); (indumentum stellate); (axillary buds superposed); (lamina with secondary venation palmate); stipules also petiolar [Colletia]; (hypanthium long and tubular); nectary position variable; G semi-inferior to inferior (superior); (embryo sac bisporic, eight celled [Allium type]); fruit a drupe, (winged), also partly loculicidal capsule; (seed arillate); n = 6, 8, 11.
Phylica (150), Ziziphus (100-170), Ceanothus (55), Gouania (50). Pantropical, warm temperate.
Synonymy: Gouaniaceae Rafinesque, Phylicaceae J. Agardh, Ziziphaceae Adanson
Floral formula: * ⚥ K 5; C 5; A 5 opp. C; G  / .
The capsules are rather similar to those of Euphorbiaceae, Phyllanthaceae and Putranjivaceae where the capsule also falls to bits as dehiscence, which can be explosive, occurs; there, too, the fruit wall often separates into two layers; the inner, woody, twists as dehiscence occurs so helping to eject the seed. However, since the seeds are basal in Rhamnaceae, there is usually no columella, as is so typical of these families, but they lack a hypanthium; Phyllanthaceae and Putranjivaceae have two seeds per carpel.
Evolution. Divergence & Distribution. Wikström et al. (2001), followed by Richardson et al. (2004), date stem Rhamnaceae to some 64-62 m.y. However, fossils from the Cretaceous-Cenomanian, some 94 m.y. before present, have been identified as Rhamnaceae (Crepet et al. 2004 for references). Calvillo-Canadell and Cevallos-Ferriz (2007) describe Mexican fossils in Rhamnaceae from the late Campanian onwards; those from the late Campanian have tiny spathulate petals ca 0.7 mm long... Apparent rhamnaceous fossils with puzzling fruits and leaves from the Cretaceous-Maastrichtian some 68 mya are in serious conflict with dates of diversification within the family if assigned to tribes, but not if they are placed incertae sedis (Correa et al. 2010).
Crown Rhamneae are some (31.2-)28.5, 27.6(-24.9) m.y. old and Paliureae (34.7-)31.6, 30.6(-27.5) m.y. (Richardson et al. 2004). Richardson et al. (2004, see also Richardson et al. 2001a) discuss the evolution and historical biogeography of the family in detail, noting i.a. the rapid diversification of the speciose Phylica within the last ca 8 m.y.. However, how the genus gets around is unclear; 8,000 km separates P. arborea on Gough and Amsterdam islands (Richardson et al. 2003). Most diversification within Ceanothus has been within the last ca 6 m.y., and it started well before the origin of the Mediterranean-type vegetation the genus now favours (Burge et al. 2011). There seems to have been three origins of the climbing habit in the family (Richardson et al. 2000a), and in two of these the plants have winged fruits.
Bacterial/Fungal Associations. The North American Ceanothus has N-fixing actinomycetes, as do many Colletieae; N-fixing genera may form a monophyletic group, although there is no strong evidence for this yet (Richardson et al. 2000b).
For the complex ansmycin maytasinoids found in Colubrina and - the precursors, at least - probably synthesized by a bacterium, see references in Cassady et al. (2004). Ectomycorrhizae have been reported from Rhamnus and Pomaderris (Malloch et al. 1980). Quite a few species are xeromorphic.
Pollination Biology & Seed Dispersal. The nectary position is particlarly variable in Colletieae, members of which have a long hypanthial tube, sometimes with a ligule; the nectary can be on the inside of the tube or on the underside of the ligule (Medan & Aagesen 1995).
Perhaps a third of the family, all in the ziziphoid group, has myrmecochorous seeds (Lengyel et al. 2010).
Chemistry, Morphology, etc. New World species of Gouania have glands at the base of the lamina; Karwinskia has pellucid dots in the leaves.
For pollen tube growth in the hollow styles of Colletieae, which is sometimes through the cells, see Gotelli et al. (2012); hollow styles have been reported elsewhere (Medan 1985: list; Medan & Hilger 1992: Colubrina) and may be an apomorphy for all or part of the family, but they may also be single, or even absent. Is there some kind of chalazal haustorium (see Srinivasachar 1940)? The outer epidermis of the outer integument of the ovule can have rather large cells (Juel 1929).
General information is taken from Brizicky (1964) and Medan and Schirarend (2004); Vikhireva (1952: not read) described fruit anatomy, Hegnauer (1973, 1990) summarized chemistry, Nair and Sarma (1961) floral anatomy, Medan (1985, 1988) discussed gynoecial development, Medan and Aagesen (1995) and Medan and Hilger (1992) comparative floral and fruit morphology, and Juel (1929) and Arora (1953) ovules, etc.
Phylogeny. There are three main clades in the family. There is weak support for the relationships [rhamnoids [ziziphoids + ampeloziziphoids], however, relationships between the major clades in the ziziphoid group in particular are poorly understood (Richardson et al. 2000b). For relationships in Pomaderreae, one of these tribes, see Kellermann et al. (2005) and Kellermann and Udovicic (2008), and for the phylogeny and morphology of Colletieae, see Aagesen et al. (2005). Ziziphus is paraphyletic (Islam & Simmons 2006).
Classification. For a phylogeny-based classification of the family, see Richardson et al. (2000a). The rhamnoids include three tribes, [Ventilagineae [Maesopsideae + Rhamneae]]. The ziziphoids are made up of five tribes, Phyliceae, Pomaderrieae, Gouanieae, Colletieae, and Paliureae, as well as unplaced genera like Ceanothus and Alphitonia, and include most of the rest of the family. The ampeloziziphoids include three tribes, three genera, and four species (Richardson et al. 2000b).
[Elaeagnaceae [Barbeyaceae + Dirachmaceae]]: ?
ELAEAGNACEAE Jussieu, nom. cons. Back to Rosales
Trees or shrubs; roots with N-fixing Frankia; dihydroflavonols?, 0-methyl flavonoids, ellagic acid +, myricetin 0; no mucilage cells in leaves; hairs lepidote or stellate; cambium storied; phloem stratified; pits vestured; true and fibre tracheids +; fibre pits bordered; wood with broad rays; sieve tubes with non-dispersive protein bodies, plastids lacking starch grains; nodes 1:1; petiole bundles arcuate or annular; mucilage cells?; leaves spiral or opposite, lamina vernation conduplicate-flat, margins entire, stipules 0; (plant dioecious - Hippophae); inflorescence a raceme, or flowers axillary; flowers (2-)4(-6)-merous; hypanthium long to short; P +; A also 2 x P, borne in throat of tube; pollen 3-nucleate; G 1, stylulus long, stigma decurrent or capitate; ovule orientation?, micropyle?, outer integument 5-16 cells across, inner integument 3-4 cells across, funicular obturator +; megaspore mother cells several; hypanthium accrescent, fleshy, closely investing fruit; pericarp thin [Hippophae]; testa very thick, exotesta with sinuous anticlinal walls at least in part, (not palisade), mesotesta ± thick-walled; endosperm with chalazal haustorium, wall formation delayed, (starchy), cotyledons usu. unequal; n = 6, 10, 11, 13, 14.
3[list]/45: Elaeagnus (20-45). North Temperate, warm tropical; Malesia and Australia - also quite widely cultivated and/or escaped (map: from Meusel et al. 1978; Hultén & Fries 1986). [Photos - Collection, Shepherdia Fruit © R. Kowal.]
Floral formula: * ⚥ P (5); A 5 alt. P, 10; G 1.
Evolution. Ecology & Physiology. All genera are associated with N-fixing Frankia, and cluster roots have been reported from Hippophae (Shane & Lambers 2005); carboxylate exudation may help in phosphorous acquisition (Lambers et al. 2012b). For the host preferences of rust host, see Savile (1979).
Bacterial/Fungal Associations. For the host preferences of rusts found here, see Savile (1979).
Chemistry, Morphology, etc. The androecium is obdiplostemonous according to Huber (1963). When stamens are equal in number to the perianth, they alternate with the lobes; this is consistent with an interpretation of P = K, with antepetalous stamens... Seed anatomy is rather like that of Rhamnaceae (Corner 1976); for fruit and seed anatomy of Hippophae, see Harrison & Beveridge (2002), for general information, see Bartish and Swenson (2004).
Previous Relationships. Elaeagnaceae have been difficult to place. They were included in Proteales by Cronquist (1981) because of superficial floral similarities, and in Elaeagnales - Rhamnanae, next to Proteanae, in Rosidae, by Takhtajan (1997).
Synonymy: Hippophaeaceae G. Meyer
[Barbeyaceae + Dirachmaceae]: connective produced; ovule with outer integument 3-5 cells across, parietal tissue 5-6 cells across.
Chemistry, Morphology, etc. In both families the embryo sac is quite deep seated, and in Dirachma socotrana in particular, the nucellar tissue at the chalazal end of the seed is very well developed.
BARBEYACEAE Rendle, nom. cons. Back to Rosales
Trees; ellagic acid +; libriform fibres +; nodes 1:1; no mucilage cells in leaves; stomata laterocytic; hairs unicellular, spirally twisted; leaves opposite, lamina vernation supervolute-curved, margins entire, stipules 0; plant dioecious; inflorescence fasciculate, bracts and bracteoles 0; hypanthium 0; P +, 3-4; A (6-)9-12; pollen infratectum granulate-intermediate; nectary 0; G 1-2(-3), ± separate, styluli long, stigma long-clavate, decurrent, ?type; ovule subapical, micropyle long-endostomal, inner integument 5-6 cells across, nucellar cap ca 5 cells across, hypostase +; fruit a nutlet, P accrescent, wing-like; seed coat undistinguished, exotesta perforated, not palisade, anticlinal walls sinuous, endotegmen tanniniferous, anticlinal walls sinuous; n = ?
1[list]/1: Barbeya oleoides. N.E. Africa, Arabia (map: from Aubréville 1974; Trop. Afr. Fl. Pl. Ecol. Distr. 5. 2010).
Floral formula: * [♂] [♀] P 3-4; A 9-12. /// P 3-4; G 1-2<.
Chemistry, Morphology, etc. The sieve tubes have compound perforations, unlike Ulmaceae and its immediate relatives and other Rosales. The perforated seed coat is rather like that common in the Ulmaceae group (Bouman & Boesewinkel 1997).
Additional information is taken from Dickison and Sweitzer (1970: morphology), Tobe and Takahashi (1990: hairs and pollen), Friis (1993: general), and Bouman and Boesewinkel (1997: ovule and seed); Hegnauer (1990) has a little information on chemistry.
Previous Relationships. The monotypic Barbeyales were placed in Hamamelididae-Urticales by Cronquist (1981) and in Hamamelididae-Barbeyanae by Takhtajan (1997).
DIRACHMACEAE Hutchinson Back to Rosales
Shrub; stalked glands +/0; chemistry?; phloem stratified; nodes ?lacunar; leaves spiral, stipules subulate, persistent; flowers single, terminal; flowers 5-8-merous; epicalyx of 4-8 lobes (in middle of pedicel); K basally connate, C contorted, vasculature fan-shaped; nectaries on base of C, or on subbasal appendages, lacking stomata; anthers extrorse, long, opening from apex; G , deeply longitudinally ridged, opposite the K, style +, stigma clavate or punctate, elongated; ?ovule orientation, micropyle zig-zag, inner integument ca 2 cells across, nucellar cap 0, hypostase ?+; fruit beaked, segments opening from the base, wooly inside, columella +, K deciduous above the "hypanthium"; seeds laterally flattened, tegmen multiplicative?, median integumentary antiraphe bundle +, exotesta with anticlinal walls thickened, endotegmen tanniniferous; endosperm slight, embryo color?; n = ?
1/2. Socotra, Somalia (map: from Link 1991b).
Floral formula: * ⚥ K (5-8); C 5-8; A 5-8 opp. C; G .
Chemistry, Morphology, etc. The single flowers may represent a reduced, cymose inflorescence (Ronse De Craene & Miller 2004). A "hypanthium" is described as involving either the sepals and petals and also the petals and stamens (Ronse De Craene & Miller 2004); there does not seem to be a conventional hypanthium. Petal initiation is later than that of the stamens, as is common is rosids, and until quite late in development they are very much shorter than the stamens. There is a lot of starch in the pollen grains (Boesewinkel & Bouman 1997). The presence of an antiraphal vascular bundle means that the outer integument is very thick (6-9 cells or more) when viewed in the abaxial median plane; integument measurements are taken from the sides of the ovule (see Boesewinkel & Bouman 1997). There is a structure on the seed described as a small, funicular aril, perhaps similar to that found in some Rhamnaceae (Ronse De Craene & Miller 2004).
For additional information, see Link (1991b [c.f. 1990], 1994), Boesewinkel and Bouman (1997: ovule and seed), Baas et al. (2001), Ronse De Craene and Miller (2004: floral morphology), and Bayer (2004: general).
Previous Relationships. The exotestal seeds with straight embryos suggest that Dirachma is not close to Geraniaceae (Geraniales), with which Dirachma had been linked, as by Cronquist (1981) - see e.g. Boesewinkel (1985) and Boesewinkel and Bouman (1997). Takhtajan (1997) included Dirachmaceae in his Malvales because of its similarity in gross morphology.
[Ulmaceae [Cannabaceae [Moraceae + Urticaceae]]]: flavonols and their glycosides, myricetin [some Ulmaceae, Cannabaceae] +, ellagic acid 0; plant with ± watery exudate; hairs unicellular and multicellular-glandular; cambium ± storied; libriform fibres +; phloem stratified; sieve tubes with non-dispersive protein bodies (some Cannabaceae - 0), (plastids lacking starch grains); cystoliths [globose; usu. CaCO3] and epidermal and hair cell wall silicification and calcification common; at least one prominent prophyllar bud; lamina with secondary veins proceeding straight to non-glandular teeth and higher-order veins convergent on those teeth [urticoid], stipules cauline; flowers small [7³ mm across]; hypanthium?, P +; stamens equal and opposite P; pollen porate, infratectum granular; nectary 0; G , abaxial only fertile, stigmas sessile, spreading, receptive area extending down adaxial surface and ± confluent; ovule single, apical; fruit a drupe; testa perforated [rare in Ulmaceae]; endosperm scanty, polyembryony common; x = 14, centromeres both median and subterminal.
Evolution. Divergence & Distribution. This clade may be some 67-65 m.y. old, Ulmaceae diverging 57-55 m.y.a., the rest ca 48-42 m.y.ago (Wikström et al. 2001).
The copious information on the four families awaits synthesis; Sytsma et al. (2002) should be consulted for details of character evolution. Sytsma et al. (2002) note that inflexed stamens and their dehiscence, fruit type, and laticifers need detailed study; hypanthium presence and other characters can be added to this list. Two-ranked leaves may be an additional synapomorphy (or pegged at a still higher level), as well as urticoid teeth.
Ecology & Physiology. 12/42 of the commoner species in west Amazonian rainforests are members of Urticales (Pitman et al. 2001).
Plant-Animal Interactions. Some Nymphalinae-Nymphalini butterflies and their immediate outgroups like Apaturinae have larvae on members of these families (see also under Urticaceae) - but also on the immediately unrelated Euphorbiaceae (Malpighiales: see Ehrlich & Raven 1964); the ancestor of Nymphalinae may have fed on Urticaceae and relatives (Nylin & Wahlberg 2008). Members of the clade shifted to Lamiales some time around the K/T boundary (Nylin & Wahlberg 2008). Caterpillars of Acraea (Acraeinae, also Nymphalidae) are quite common on Urticaceae (including Cecropia), and also on Moraceae, etc.; this particular genus is also particularly common on Passifloraceae and their relatives.
Chemistry, Morphology, etc. Raffinose and stachyose are common oligosaccharides in phloem exudate in Ulmaceae, Moraceae and Cannabaceae sampled (Zimmermann & Ziegler 1975). The group has homogeneous wood anatomy: Rays are relatively broad, pits are simple, intervessel pitting is alternate, fibres are septate, and parenchyma is paratracheal (Baas et al. 2000). Furthermore, at least some members (Celtis, Ulmus) have a torus-bearing pit membrane (Coleman et al. 2004) that is only weakly lignified. Because of the well-developed prophyllar bud(s), the inflorescences are often paired, with a bud between them, and/or the branches may have a bud on one or both sides at the base; Ulmus does not show this arrangement. The "stipular buds" of Cannabis (Miller 1970 and references) are really prophyllar buds.
It is not clear which taxa have a hypanthium; at least some species of Ulmus and Pilea do, but other species of Ulmus, Zelkova and Trema show no obvious signs of one (see also Bechtel 1921). Staedler (1923) discussed the absence of an anther epidermis, although it is present in Ficus (other Rosales?); there is no obvious link with dehiscence mechanism. Starchy pollen is common, but apparently not in Urticaceae. Bechtel (1921) and Eckardt (1937) described gynoecial morphology in considerable detail. Mohan Ram and Nath (1964) noted that the chalazal megaspore was the functional one, but I do not know how important this is. Taxa with a perforated testa are quite common, although this feature may have arisen more than once (Kravtsova & Oskolski 2007).
For further information, see Satake (1931: spodograms), Tippo (1938) and Sweitzer (1971), both anatomy, Giannasi (1978, 1986: chemistry), Behnke and Barthlott (1983: hairs), Takaso and Tobe (1990: testa), Omoron and Terabayashi (1991: phylogeny), Terabayashi (1991: vernation), Hennig et al. (1994: cuticle waxes), and Tobe and Takaso (1996: hairs).
Phylogeny. The phylogenies suggested by Sytsma et al. (2000) and Song et al. (2001) place Cannabis within Celtidaceae (see also e.g. Ueda et al. 1997b); Cannabaceae is the earliest name for the combined group and Cecropia within Urticaceae, and this set of relationships was strongly supported by a more comprehensive analysis (Sytsma 2002). See Judd et al. (1994) for a morphological phylogeny and Zavada and Kim (1996) for a molecular phylogeny focussed on the old paraphyletic Ulmaceae s.l.
ULMACEAE Mirbel, nom. cons. Back to Rosales
Trees, (growth symopodial, apex of innovation aborts); (ectomycorrhizae +); lignans +; (wood fluoresces); unicellular hairs smooth; sieve tube plastids often with protein crystalloids; cystoliths usu. pegless; leaves two-ranked, lamina vernation laterally (vertically) conduplicate-plicate, secondary veins going into teeth, stipules extrapetiolar; flowers perfect and mixed; P spiral, (connate); A extrorse, (2 x P); pollen 4-7-porate, exine rugulose; at least one stigma with 3(-5) vascular bundles; ovule (with bistomal micropyle), outer integument 4(-6 - Holoptelea) cells across, inner integument ca 4 cells across; fruit also a samara; seeds flattened, coat undistinguished, exotestal cells elongated, unthickened; (embryo curved - Zelkova); often terminal/subterminal diffuse-complex centromeres; 69bp ndhF deletion.
6[list]/35: Ulmus (20-30, species limits uncertain). Mostly N. temperate, esp. Asian, few species tropical, not in Australia and the Pacific (map: from Soepadmo 1977; Hultén & Fries 1986; Fl. N. Am. 3. 1997; Todzia 1989, 1992: Trop. Afr. Fl. Pl. Ecol. Distr. 5. 2010). [Photos - Collection]
Evolution. Divergence & Distribution. Ulmus is known as leaves and fruits from Early Eocene deposits of northeastern China some 50 m.y. old (Wang et al. 2010).
Chemistry, Morphology, etc. There are distinctive fatty acids in the seeds of some Ulmaceae, but not in those of Cannabaceae or Moraceae (Badami & Patil 1981: sampling). Ulmus lacks well-developed prophyllar buds and has one of the two stipules intrapetiolar, they are both intrapetiolar in seedlings of some species, and the leaves may also be opposite, as in seedlings. Hemiptelea has pegged cystoliths. The breeding system in the family is variable, but at least some flowers are perfect. Nawaschin (1895) suggested that chalazogamy occurred in Ulmus. Holoptelea has a thick-walled exotesta.
For gynoecial morphology, see Okamoto et al. (1992).
Phylogeny. The poorly-known Ampelocera is to be included here (see Ueda et al. 1997b; also Wiegrefe et al. 1998); although its hairs are smooth, its leaves have ascending veins. The family has two main clades, the largely tropical Ampelocera, Phyllostylon and Holoptelea, and the rest, north temperate in distribution (Neubig et al. 2012b).
[Cannabaceae [Moraceae + Urticaceae]]: C-glycoflavones also +; (sieve tube plastids with starch grains); unicellular hairs usu. micropapillate; secondary veins palmate; stipules cauline-intrapetiolar; flowers imperfect; stigmas with single vascular bundle; fuits not or barely flattened; embryo curved.
Evolution. Seed Dispersal. Members of all threee families are quite often dispersed by bats in the New World (Lobova et al. 2009). Trema, Ficus and Cecropia are all important food sources for frugivorous birds (Snow 1981).
CANNABACEAE Martynov, nom. cons. Back to Rosales
Trees or ± herbaceous, erect or twining; sesquiterpene lactones +; true tracheids +; cystoliths usu. with pegs [distribution?]; leaves (spiral; opposite), lamina vernation (laterally) conduplicate-plicate (conduplicate; supervolute); (strongly palmately lobed or compound, veins proceeding to the apex of lobes - Cannabis, Humulus), secondary veins ascending, stipules connate or not; pollen 2-3(-5) porate, exine scabrate to verrucate; micropyle bistomal, outer integument 2-4(-8) cells across, inner integument 2-3 cells across, parietal tissue ca 6 cells across, nucellar cap ca 2 cells across; embryo sac haustorium +; (fruit an achene); exotestal cells tangentially elongated, with arms, unthickened; endosperm +, embryo also coiled; (n = 8-11, 13, 15), centromeres medial/submedial, simple.
11[list]/170: Celtis (ca 100). Worldwide, but not Arctic, distribution of Humulus lupulus in Asia is unclear (map: from Wickens 1976; Soepadmo 1977; Hultén & Fries 1986; Fl. Austral. 3. 1989; Fl. N. Am. III 1997; Trop. Afr. Fl. Pl. Ecol. Distr. 5. 2010). [Photos - Collection, Celtis Flower.]
Evolution. Divergence & Distribution. For the early Tertiary fossil history of Cannabaceae that are now East Asian endemics, see Manchester et al. (2009).
Plant-Animal Interactions. Caterpillars of most Apaturinae (Nymphalidae) are found on Cannabaceae, although those of Hestinalis eat Urticaceae, Sephisa, Fagaceae, and Apatura, the spectacular purple emperor, has moved on to salicin-containing Salicaceae (Salix and Populus: Ohshima et al. 2010).
Bacterial/Fungal Associations. Parasponia is the only non-legume nitrogen fixer that is associated with other than actinomycetes, and its rhizobia remain in infection threads like those of some Fabaceae, especially "Caesalpinioideae". Infection of the plant is by entry through cracks in the epidermis. The nodules are modified lateral roots and have central vascular tissue, the bacteria being in the cortex; this is unlike the nodules of Fabaceae but like those found elsewhere in the N-fixing clade that are Frankia-induced (Streng et al. 2011 for some literature). Gironniera is reported to be ectomycorrhizal (Smits 1994).
Genes & Genomes. Cannabis and Humulus have an X-autosome balance system determining the 'sex' of the plant.
Chemistry, Morphology, etc. Humulus, with its opposite leaves, has split laterals/a commissural vascular bundle (Colomb 1887). The "distinctive" camptodromous (to semicraspedodromus) venation of Celtidaceae s. str. is disturbed both by the inclusion of Cannabis, etc., in this clade, but also by the occurrence of strictly craspedodromous venation in Palaeocene Celtis (Manchester et al. 2002).
Whether the laticifers of Cannabis etc., are really similar to those of Urticaceae and Moraceae must be confirmed; there is no milky exudate and they occur throughout the plant. Only the "basal" Aphananthe and Gironniera have flavonols. Lozanella, with its opposite leaves and boxy venation, looks rather like Urticaceae, but it has a bilobed stigma. The anticlinal walls of the testa of Humulus are sinuous and its embryo is green. n = 10 is common in Cannabaceae.
For general information, see Grudzinskaya (1967), Mohan Ram and Nath (1964: Cannabis ovules and seeds), Leins and Orth (1979: Cannabis flowers), Todzia (1993: general, as Ulmaceae), and Kubitzki (1993b: general, as Cannabaceae), for chemistry, see Hegnauer (1973, 1990, as Ulmaceae; also 1964, 1989).
Phylogeny. Pteroceltis, Humulus, and Cannabis are close, and they and some other members of this clade have sieve tube plastids with starch grains (Behnke 1989). Lozanella is sister to Aphananthe or sister to the rest of the family (Wiegrefe et al. 1998; Soltis et al. 2002).
Synonymy: Celtidaceae Link, Humulaceae Berchtold & J. Presl, Lupulaceae Link
[Moraceae + Urticaceae]: latex system +; (calcium carbonate crystals); (lamina with pinnate secondary veins); staminate flowers: stamens incurved in bud; pistillode +; seed coat undistinguished; polyembryony 0.
Evolution. Genes & Genomes. Rates of molecular evolution are likely to have increased at least twice in this clade, e.g. in most Urticaceae and also in Dorstenia, the increase being associated with the adoption of the herbaceous habit (Smith & Donoghue 2008).
There is a group of genera of Moraceae with explosive pollen dispersal, and inflexed stamens may be a synapomorphy for [Moraceae + Urticaceae] (Datwyler & Weiblen 2004), although where stamen dehiscence changes on the tree of the former family depends very much on how it is optimized (Clement & Weiblen 2009). The moraceous genera with such stamens are in the paraphyletic Moreae that was part of a basal polytomy within Moraceae in early reconstructions.
Chemistry, Morphology, etc. Scattered in the group are taxa in which the tepals are persistent (e.g. Pilea) or accrescent (e.g. Morus), i.e. the fruits are anthocarps in the strict sense.
Phylogeny. For a morphological phylogeny focussing on Urticaceae s.l., i.e. Moraceae and Urticaceae here, see Kravtsova and Oskolski (2007).
Classification. The two families have much in common, and Corner (1952) even included Moraceae in Urticaceae.
MORACEAE Gaudichaud, nom. cons. Back to Rosales
Largely woody; (isoflavonoids +); (cork in outer cortex); laticifers throughout the plant, latex milky; (stomata aniso- and cyclocytic); leaves spiral, lamina vernation variable, stipule also ensheathing stem, (0 - Fatoua); dioecious [plesiomorphously so]; inflorescence congested, spicate [staminate] or ± globose [carpellate); flowers 4-merous, (P 0-10); staminate flower: bracts peltate; P free; carpellate flower: P connate; (G inferior), styles 1 or 2, often unequal; ovule (subapical; campylotropous), outer integument 3-4 cells across, inner integument ca 3 cells across, nucellar cap ca 5 cells across [nucellar beak]; fruits an achene, (drupe; P accrescent), receptacle often accrescent; exotesta ± tanniniferous, (several thickened layers - Prainea); (endosperm +); (n = 12 upwards, esp. 13, 14), both terminal and median centromeres.
39[list]/1125 - six groups below. Mostly tropical to warm temperate (map: from Jalas & Suominen 1976; Wickens 1976; Frankenberg & Klaus 1980; Fl. Austral. 3. 1989; Fl. N. Am. III 1997; Wilmott-Dear & Brummit 2007: Asia and South America only approximate).
[Artocarpeae + Moreae]: carpellate flowers: bracts peltate.
1. Artocarpeae Lamarck & de Candolle
(P connate, that of adjacent flowers adnate in the middle portion [completely]); staminate flowers: 2 merous; A 1(-3), filaments straight.
3/67: Artocarpus (61). Largely tropical, Indo-Malesia (Artocarpus) and America. Photo: Fruit].
Synonymy: Dorsteniaceae Chevallier
2. Moreae Dumortier
Staminate flower: (bracts not peltate; filaments straight).
7/56. Tropical, some temperate.
[Maclureae [Dorstenieae [Ficeae + Castilleae]]]: ?
3. Maclureae Clement & Weiblen
Habit various, axillary thorns +; inflorescence with golden dye; staminate flowers: bracts not peltate, (filaments straight); pistillate flower: (bracts peltate).
1/11. Tropical to Temperate. [Photo - Inflorescence.
[Dorstenieae [Ficeae + Castilleae]]: radial latex tubes +; plant monoecious, inflorescence bisexual; inflorescence axis expanded; pistillode conical.
4. Dorstenieae Dumortier
(Herbs); inflorescence disciform; staminate flowers: (3-merous; P connate; filaments straight); carpellate flowers: (2-merous; embedded in receptacle.
13/145: Dorstenia (105). Pantropical. Photo: Fruit.
Synonymy: Dorsteniaceae Chevallier
[Ficeae + Castilleae]: insect pollination +; staminate flowers: filaments straight; carpellate flowers: bracts not peltate; P free.
5. Ficeae Dumortier
Lianes, stranglers, etc.; (latex 0); (leaves opposite), ensheathing stipules open in leaf axil; inflorescence axis urceolate; flowers 3-merous: staminate flowers: bracts not peltate; A 2; carpellate flowers: style branches unequal or not; fruit a syconium.
1/800. Pantropical. Photo: Fruit.
Synonymy: Ficaceae Berchtold & J. Presl
6. Castilleae C. C. Berg
(Branches spreading), (cladoptosis +); (cystoliths 0); infloresence involucrate, unisexual, disciform to urceolate; staminate flower: bracts 0, pistillode 0; carpellate flowers: (bracts 0).
11/62. Pantropical, esp. America.
Evolution. Divergence & Distribution. Berg (2005) suggests that diversification in Moraceae occurred on a still physically coherent tropical supercontinent. Zerega et al. (2005) advance a more complex hypothesis to explain the distribution and diversification of the family; they date the crown group to at least 79 m.y.a., and the stem group to at least 89 m.y.
Within Moraceae, there are suggestions for the ages of some clades. Berg and Hijman (1999) suggested that the distribution of Dorstenia, found in both Africa and South America, could be explained by continental drift; Zerega et al. (2005), however, estimated the crown-group age of the genus to be a mere 18.4-3.5 m.y.a. However, in a more complete analysis, Misiewicz and Zerega (2012) dated the crown age at (132.0-)112.3(-84.8) m.y., with the age of the New World crown group, (44.8-)30.3(-16.5) m.y. - and in fact the latter was the age that Zerega et al. (2005) had estimated, given their sampling. The age of crown group Ficus was estimated to be (101-9-)74.9(-60.0) m.y., its origin being Eurasia, while most diversification was in the Tertiary, dispersal rather than vicariance best explaining details of the current distribution of the genus (Cruaud et al. 2012b). Subgenus Pharmosycea is restricted to the New World, as is Urostigma section Americana, the latter being sister to the African section Urostigma, while Urostigma-Malvanthera is Australasian (Cruaud et al. 2012b).
Ecology. Moraceae, and in particular Ficus, includes a number of (hemi)epiphytes, stranglers and lianes, and they are often the second most speciose family in lowland tropical rainforest in both America and Africa (Gentry 1988). Figs in particular are a very important and dependable source of food for frugivores, both birds and mammals, throughout the tropics, and the diversity of their growth forms means they are encountered throughout the forest. Figs are perhaps surprisingly nutritious (Herre et al. 2008 for references), and individuals of many species will be in fruit throughout the year. The species richness of Ficus is correlated with that of their avian frugivores, particularly specialised frugivores, and the frugivores also select on particular aspects of the morphology of the fig species (Shanahan et al. 2001; Kissling et al. 2007; Herre et al. 2008). Some bats also eat figs, and, depending on whether the bats are New or Old World, they search for food in different ways and have selected figs with different qualities - thus in the New World Artibeus phyllostomid bats are the predominant frugivores and the figs tend to be greenish and odoriferous (Compton 1996 [a whole series of papers]; Korine et al. 2000; Shanahan et al. 2001; Harrison 2005).
Plant-Animal Interactions. The beginning of the fig wasp/fig association/co-divergence dates to 100-60 m.y.a.; Lopez-Vaamonde et al. (2009) discuss dating and biogeography of the wasps, suggesting that the ancestor of the wasps lived in Asia, dispersal rather than Gondwanan break-up being important for their subsequent distribution (see also Cruad et al. 2012b: Xu et al. 2012 suggested a Gondwanan ancestry, but with much subsequent dispersal). Recent estimates of the age of crown group Ficus, (101.9-)74.9(-60.0) m.y., and that of the fig wasps, (94.9-)75.1(-56.2) m.y., are quite similar (Cruaud et al. 2012b); interestingly, comparing the ages of figs and pollinators at 36 nodes, in 8/36 of the nodes the estimates of the ages of the figs were older, in the rest, those of the wasps, and in general the numbers were often quite different.
The parasites of the agaonid wasps and and also galling wasps are part of the fig-fig wasp system (e.g. Lopez-Vaamonde et al. 2001; Jousselin et al. 2003; Jackson 2004a; Kjellberg et al. 2005; Rønsted et al. 2005b, 2008a for references). The parasitoid wasps that parasitize the fig wasps may be of considerable importance in preserving the relationship between the agaonid wasp and fig (Dunn et al. 2008). Galling chalcid wasps (Hymenoptera-Chalcidoidea) belong to five separate groups and gall individual flowers; they may have have moved on to figs some 50-40 m.y.a., with subsequent dispersal to other groups (Cruaud et al. 2011); as many as 36 species of chalcids may be found on a single species of fig (Cruaud et al. 2011). Part of this microcosm are drosophilid flies that in Africa, at least, have a very close association with figs and oviposit either on the stomium or the exit holes made by the male fig wasps (Harry et al. 1996, 1998). For more information on figs and wasps, as well as gallers and parasitioids, see also Kjellberg et al. (2005), the papers in Symbiosis 45, 1-3 (2008); Silvieus et al. (2008), and especially Herre et al. (2008).
Bombyx mori (the silkworm) caterpillars can eat quite a number of species of Moraceae, but not those of most other members of the Ulmaceae group - although they will grow on Ulmus itself (Fraenkel 1959). Caterpillars of danaine butterflies quite commonly eat Moraceae; both they and their usually preferred Apocynaceae are rich in latex, although Moraceae do not often have cardenolides (Ackery & Vane-Wright 1984).
Pollination Biology & Seed Dispersal. Basic details of the association between figs and their agaonid fig-wasp pollinators (Agaonidae) may be summarized as follows. Female wasps are fertilized by flightless males inside the fig, and many actively pick up pollen from the male flowers - at least sometimes aggregated around the ostiole - before leaving the fig via exit holes prepared by the males. They then enter a receptive fig via the ostiole, having specialised jaws and a head that is shaped to allow them to get between the bracts protecting the ostiole, although they often lose their wings and antennae in the process (van Noort " Compton 1996). They then lay eggs in the female flowers inside, pollinating the flowers at the same time. They cannot lay eggs in ovaries of flowers with long styles, their ovipositors being too short, and these flowers develop into fruits; they can lay eggs in shorter-styled flowers, and these develop into the next generation of wasps. The life cycle in dioecious figs is slightly more complex, but follows the same basic principles (see Janzen 1979 for a good early account).
Details of the early evolution of this association are unclear. It is not known whether the active pollination described above, or passive pollination, in which the wasp simply becomes coated with pollen before it leaves the fig, is ancestral for Ficus (Cruaud et al. 2012b). Ficus is sister to Castilleae (which include some errant ex-Artocarpeae). Female inflorescences of Castilleae such as Antiaropsis are urceolate. The pollinators (thrips) breed among the flowers of the male inflorescences, eating pollen, etc., pollination occurs when the thrips visit female inflorescences (Datwyler et al. 2003; Datwyler & Weiblen 2004; esp. Zerega et al. 2004; Clement & Weiblen 2009). Insect pollination here is a reversal from wind pollination.
The fig/fig wasp association has been touted as a classic example of an obligate one-on-one association of plant and wasp pollinator (e.g. Herre 1996 and references). Some recent work suggests that there is sometimes rather little specificity in the association between fig and wasp (Machado et al. 2005; Jackson et al. 2008; Yang et al. 2012), so questioning both the classic idea of an obligate association and also the frequency of occurrence of strict co-speciation. Nevertheless, there is at least a general association between figs and wasps, and in groups like section Ficus sect. Galoglychia cospeciation is likely, even in the non-pollinating wasps that are members of the system (Jousselin et al. 2008; Cruaud et al. 2012a, b). Pollinator sharing between fig species seems to be more common in monoecious neotropical figs than in dioecious palaeotropical figs (Moe et al. 2011); it also occurs in some African taxa, where the insect can reproduce in a number of closely related figs, as well as lineage duplication, wasp speciation occuring within the one species of fig (McLeish & van Noort 2012); see papers in J. Biogeog. 23(4). 1996, also Plant-Animal Relationships (above) for further details.
Fig development is often more or less synchronized within trees and asynchronous between trees, so favouring out-crossing (Ahmed et al. 2009). Although fig pollen is dispersed by agaonid wasps, which are tiny, this does not mean that the population sizes of figs are small. The wasps can be transported up by air currents for to 14 km even in the rainforest, and so the breeding units of figs may be an order of magnitude larger - covering some 100 square kilometres or more - than those of other plants there (Herre 1996; Nason et al. 1998). Indeed, pollen is transported by female wasps for distances over 160 km in riparian popularions of Ficus sycomorus in the Namib desert (Ahmed et al. 2009).
Seed dispersal in Moraceae is often by animals, but just what part of the plant contributes to the fleshiness that attracts the disperser varies. In Morus the fruits, achenes, are surrounded by the fleshy perianth and are closely packed on an erect inflorescence axis. In Artocarpus - it includes the bread and jack fruits - the more or less elongated infructesences can weigh up to 50 kg, and the fleshy part comes both from perianth members and the inflorescence axis itself (see Zerega et al. 2010: phylogeny and morphology). Broussonetia papyrifera has heads of bright red, dangling drupes, while Dorstenia, etc., have "dehiscent" drupes; there the stone is shot out of the turgid mesocarp, the separation following a line of weakness in the tissue; in both cases the developing fruits appear to be extruded by the closely-packed perianth members. In Antiaropsis (Castilleae) the inflorescence axis is concave at first, but spreading ("dehiscing") when ripe, when the drupes contrast in colour with the bracts, etc. (e.g. Zerega et al. 2004).
In Ficus the fruits are borne on the inside of the fleshy, invaginated axis, and are commonly dispersed by bats (Muscarella & Fleming 2008). Overall fig morphology is quite diverse. The fig may be dull coloured and scented; in the New World some 21 species of Artibeus bats (phyllostomids) commonly disperse the tiny achenes; they also often eat Cecropia (Urticaceae), particularly in Mexico (Lobova et al. 2009). The bats are slow feeders and spit out seeds, fibre, etc.; like other bat-dispersed taxa in the New World, species of Ficus can be found in early successional communities (Muscarella & Fleming 2008). The altitudinal ranges of the bats and figs are similar (Fleming 1986). Figs that are eaten by birds are often small and red, and although bat-dispersed fruits are often green, in the Old World bat fruits often yellow, etc., and are sometimes quite large (Kalko et al. 1996; Harrison & Shanahan 2005; Lomáscolo et al. 2008, 2010). Bat-dispersed figs in Malesia, also dull-coloured, may not smell; pteropodids (fruit bats) are the dispersers there (Hodgkinson et al. 2003).
Ficus is a major food resource in terms both of quantity and nutritional quality (although there is some argument about the latter - see Fleming 1986; Shanahan et al. 2001) for frugivorous animals in the tropics, being especially important when other plants are not fruiting; whether or not fruits on individual plants ripen synchronously, individual species do not fruit synchronously. Figs are important in both the New (e.g. Cocha Cashu, Peru) and Old (Borneo) Worlds, although perhaps less in Africa and India, and they have considerable local diversity - for example, there are 77 species in Lambir Hills National Park in Sarawak alone (Shanahan et al. 2001). Harrison & Shanahan 2005). Leighton and Leighton (1983) called the relationship between Ficus and its frugivores a keystone mutualism, since the loss of the figs would deplete the populations of animals that dispersed both Ficus and the fruits of other plants. Similarly, Terborgh (1986: p. 339) observed, "[s]ubtract figs from the ecosystem and one could expect to see it collapse"; in some New World ecosystems figs, less than 1% of the species (12 out of ca 2,000), sustained nearly the entire frugivore community for three months of the year. Janzen (1979) had calculated that seven species of figs on Barro Colorado Island produced 200,000 ± 75,000 figs ha-1/yr - maybe 195 kg dry weight. Although it is debatable to what extent figs really are keystone species, they are certainly eaten by a great variety of vertebrates (Shanahan et al. 2001).
Chemistry, Morphology, etc. Laticiferous cells elongate and branch and intrude between other cells, the nuclei divide, but cell walls are not formed. Some species of Dorstenia have small, cauline stipules that do not overlap the petiole.
For fig/syconium development, see Rauh and Reznik (1951). Chromosome numbers in Dorstenia are very variable, and ovule morphology and embryology there need examination (Berg & Himan 1999).
Some information is taken from Rohwer (1993a); for embryology, see Johri and Konar (1956: Ficus), for chemistry, see Hegnauer (1969, 1990); for pollen, see Burn and Mayle (2008); chromosomes, see Oginuma and Tobe (1995).
Phylogeny. For phylogeny, see Datwyler et al. (2003), Datwyler and Weiblen (2004) and especially Clement and Weiblen (2009). Some of the old and paraphyletic Moreae with their incurved stamens are now placed in Maclureae, Castilleae are sister to Ficeae, and relationships between the other tribes are on the whole well supported (Clement & Weiblen 2009). Analyses of morphological characters alone provided little resolution, only Ficeae (one genus!) being well supported, although most Castilleae formed a clade, albeit with very little support (Clement & Weiblen 2009). Zerega et al. (2010) provided a detailed phylogeny of Artocarpeae, which they recircumscribed. Cruad et al. (2012b) also found that relationships along the backbone of Ficus were still rather poorly supported, although section Pharmacosycea was likely to be sister to the rest.
Classification. See Clement and Weiblen (2009) for tribal delimitation (note likely position of Treculia); they also discuss one or two problems with generic limits.
Botanical Trivia. The straightening stamens and reflexing tepals of Morus alba are reported to show the fastest movement of any plant parts known, over half the speed of sound (Taylor et al. 2006).
URTICACEAE Jussieu, nom. cons. Back to Rosales
Herbs to shrubs (trees; lianes); dihydroflavonols?, (furanocoumarins) +; cork cortical [Urtica]); (wood fluoresces); (wood parenchyma not lignified); laticifers in bark only, latex not milky (milky); petiole bundle(s) annular or arcuate; bundle sheath extensions 0; cystoliths often elongated (0); stomata often anisocytic (paracytic, etc.); leaves two-ranked or spiral; lamina base often asymmetric, vernation laterally or vertically conduplicate, stipule also intrapetiolar or sheathing [open on stem opposite leaf] (0 - Soleirolia); (plant dioecious); P (1-)4, 5(-6), valvate, (connate), staminate flowers: filaments explosively straightening, (not explosive - Poikilospermum), endothecium 0, pistillode +; carpellate flower: staminodes +; G 1, stylulus +, or stigma sessile, penicillate; ovule basal, ± straight, both integuments often 2 cells across, (protruding into the stylar canal; inner integument obturator, of several 1-celled thick projections in t.s.), parietal tissue 4-6 cells across, nucellar cap 2-4 cells across; fruit often a nut or achene; seed coat perforated, ± crushed, but various testal/tegmic layers persisting; chalazal endosperm haustorium +, (endosperm +; starchy), embryo straight, (cotyledons thick, radicle short - Pouruma, Myrianthus); n = 7-14 [x = 14 is unlikely to be basal], protein bodies in nuclei.
54[list]/2625: Pilea (500-600), Elatostema (300), Urtica (80). World-wide, but mainly tropical (map: from Frankenberg & Klaus 1980; Hultén & Fries 1986; Fl. Austral. #. 1989; Fl. N. Am. 3. 1997: ??Arabia, Central Asia). [Photo - Shoot, Flower, Fruit.]
Evolution. Plant-Insect Relationships. It has been suggested that caterpillars of Nymphalini butterflies have a plesiomorphic association with Urticaceae as food plants (Janz et al. 2001); caterpillars in a clade of Nymphalidae-Heliconiinae-Acraeini utilise members of this family, probably switching from host plants in the Passifloraceae area (Silva-Brandão et al. 2008; see also Nylin & Wahlberg 2008).
Cecropia is a fast-growing pioneer tree that is associated with Azteca and some other ants that live in the stems and eat glycogen-rich food bodies (Müllerian bodies) produced by the plant at the abaxial base of the petiole (for a phylogeny, see Treiber & Weiblen 2009); beetles also eat these food bodies, as well as ant eggs, etc. (Jolivet 1991; Longino 1991; Yu & Davidson 1997). The association between plant and ant can break down, especially on islands and at high altitudes (Janzen 1973); Musanga, e.g. M. cecropioides, from Africa, also lacks ants but is otherwise very similar to Cecropia. Species of Macaranga (Euphorbiaceae, q.v.) are ecological analogues of Cecropia in Malesian forests.
Pollination Biology & Seed Dispersal. Explosive dispersal of the pollen as the filaments abruptly straighten is common in Urticaceae. In Pilea the achenes are similarly dispersed by the abrupt straightening of the fleshy, inflexed filaments of the staminodes.
In Mexico in particular, the phyllostomid bat Artibeus eats Cecropia (Lobova et al. 2009 for records). Cecropia dominates succession after clearing in South America, but the forest soon changes composition (Mesquita et al. 2001)
Chemistry, Morphology, etc. Groups of cells in the vascular tissue may be unlignified and the pericyclic sheath may also be late in lignifying; the presence of unlignified apotracheal parenchyma was used to divide the family (minus Cecropiaceae) into two main groups (Bonson & ter Welle 1984); Cecropia et al. have lignified parenchya (Bonson & ter Welle 1983). The different leaf types of aniosphyllous Pellionia are very differently vascularized and have different nodal anatomies (Dengler & Donnelly 1987).
Boehmeria has a fleshy perianth. For the absence of an endothecium, see Staedtler (1923); this character needs more extensive sampling. The gynoecium is basically bicarpellate, but one carpel is highly reduced (Eckardt 1937). Shamrov (2004) shows the inner integument of Leucosyke becoming much elaborated and functioning as an obturator. The seeds of Dendrocnide may lack holes in the exotesta, and the whole seed coat is relatively well developed, while Kravtsova (2006) found ingrowths in cell walls of both the pericarp and seed coat, observations that should be extended.
See also Bigalke (1933: cystoliths and hairs), Fagerlind (1944a: Elatostema - embryology, apomixis, quite a lot of variation in ovule), Miller (1971: general), Hegnauer (1973, 1990: chemistry), Berg (1978), Kubitzki (1993b: general), Friis (1993: general) and Kravtsova (2003: seed coat anatomy) for additional information.
Phylogeny. Urticaceae minus Cecropiaceae are paraphyletic (Sytsma et al. 2000, 2002 - three genes; Monro 2006 - two genes); the latter are polyphyletic and heterogeneous. Hadiah et al. (2008) found similar relationships, Poikilospermum being in a well-supported clade with Urtica, etc. However, Datwyler & Weiblen (2004 - one gene) and Zerega et al. (2005) find the reverse relationship, and strong support for Poikilospermum (map below - green) as sister to the rest of the family - [Poikilospermum [Cecropiaceae s. str. [rest of Urticaceae]]]. Either way, Cecropiaceae are best included in Urticaceae; I characterise Cecropieae briefly below.
Pellionia should probably be included in Procris (Hadiah et al. 2008). For a preliminary phylogenetic study of Elatostema, see Hadiah et al. (2003); Tseng et al. (2012) found Pellionia to be embedded in Elatostema, with Procris sister to Elatostema s.l. See Monro (2006) for suggestions as to how to proceed with the phylogenetic analysis of the large genus Pilea.
Trees (hemiepiphytes); cystoliths spherical/0; bundle sheath extensions +; stomata anomocytic; hairs arachnoid, unicellular; leaves deeply lobed or compound; filaments straight.
5/147: Cecropia (61), Coussapoa (50). African and esp. New World tropics (Map: red, see Bonsen & ter Welle 1963; Trop. Afr. Fl. Pl. Ecol. Distr. 5. 2010).
Synonymy: Cecropiaceae C. C. Berg
CYNOMORIACEAE Lindley, nom. cons. Back to Saxifragales
Echlorophyllous, root parasite; vessel elements?; cork?; plant glabrous; leaves spiral; plant monoecious, inflorescence capitate; flowers minute; P +, (1)4-5(-8), basally connate or not; staminate flowers: A 1, adnate to P; pollen colporate; ?nectary-stylodium +; carpellate flowers: staminodia 0; G 1, inferior, style long, channeled; ovule 1/carpel, apical, pendulous, straight, unitegmic, integument 5-7 cells across, nucellar cap +?; fruit an achene; testa ca 7 cells across, persistent, cells little thickened; endosperm cellular, copious, thick-walled, embryo undifferentiated; n = 12, size strongly bimodal.
1[list]/2. Mediterranean to C. Asia (map: from Jalas & Suominen 1976; Jäger et al. 1985; Hansen 1986). [Photo - Habit © D. L. Nickrent.]
Evolution. In the Mediterranean area the host is often a member of Cistaceae or Amaranthaceae, elsewhere Cynomorium parasitizes Amaranthaceae, Tamaricaceae, Nitrariaceae, etc. (Jäger at al. 1985).
Chemistry, Morphology, etc. The root has root hairs. Perfect flowers are also known. The perianth is less well developed in pistillate than in staminate flowers, and there is debate as to its morphological nature. The pistillode in staminate flowers may be superior or inferior, according to Hooker (1856), clearly a matter that should be cleared up. The channeled style has two vascular bundles, together a rather odd combination.
For details of seed anatomy, see Takhtajan (2000), for morphology, see Weddell (1860), for ovule, etc., see Juel (1902) and Teryokhin et al. (1975), for some chemistry, see references in Zhang et al. (2009), and for general information, see the Parasitic Plants website (Nickrent 1998 onwards) and also Heide-Jørgensen (2008).
Previous relationships. Cynomoriaceae have usually been included in Balanophoraceae or Balanophoranae (e.g. Cronquist 1968; Takhtajan 1997), or their position has seemed to be completely uncertain (see above).