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David J. Keil, except as noted

Annual to tree. Leaf: basal and/or cauline, alternate, opposite, rarely whorled, simple to 2+ × compound. Inflorescence: 1° inflorescence a head, resembling a flower, of several types (see below), 1–many in generally ± cyme-like cluster; each head generally with ± calyx-like involucre of 1–many series of phyllaries (involucre bracts); receptacle of head flat to conic or columnar, paleate (bearing paleae = receptacle bracts) or epaleate; flowers 1–many per head. Flower: bisexual, unisexual, or sterile, ± small, of several types (see below); calyx 0 or modified into ± persistent pappus of bristles, scales, and/or awns; corolla radial or bilateral (0), lobes generally (0)3–5; stamens 4–5, filaments generally free, generally fused to corolla at tube/throat junction, anthers generally fused into cylinder around style, anther base generally rounded or cordate (deeply sagittate or with tail-like appendages), tip (= flattened appendage) generally projecting beyond pollen sac; pistil 1, 2-carpeled, ovary inferior, 1-chambered, 1-seeded, placenta basal, style 1, tip generally ± 2-branched (except in some staminate disk flowers), branch tips truncate or generally bearing ± brush-like appendages; stigmas 2, generally on adaxial faces of style branches. Fruit: achene (also called a cypsela) (drupe in Chrysanthemoides), cylindric to ovoid, sometimes compressed, generally deciduous with pappus attached.
± 1500 genera, 23000 species: worldwide, many habitats. Flower and head types differ in form and sexual condition. A disk flower has a generally radial corolla, with a cylindric tube, expanded throat, and generally 5 lobes. Disk flowers are generally bisexual and fertile but occasionally staminate with reduced ovaries. Discoid heads comprise only disk flowers. A radiant head is a variant of a discoid head, with peripheral disk flower corollas expanded, often bilateral. A ray flower corolla is bilateral, generally with a slender tube and flattened petal-like ray (single lip composed of generally 3 lobes). Ray flowers are generally pistillate or sterile (occasionally lacking styles). Radiate heads have peripheral ray flowers and central disk flowers. Disciform heads superficially resemble discoid heads, with pistillate or sterile flowers that lack rays, together with or separate from disk flowers. A ligulate flower is bisexual, with a bilateral, generally ephemeral corolla and 5-lobed ligule. Liguliflorous heads comprise only ligulate flowers. See glossary p. 31 for illustrations of family characteristics. Echinops sphaerocephalus L., Gaillardia aristata Pursh, Gaillardia pulchella Foug., Hymenothrix loomisii S.F. Blake, Tagetes erecta L., Thelesperma megapotamicum (Spreng.) Kuntze are waifs. Melampodium perfoliatum Kunth, historic urban waif. Ageratum conyzoides L., Guizotia abyssinica (L. f.) Cass., Santolina chamaecyparisus L., orth. var. are rare or uncommon escapes from cultivation. Dyssodia papposa, Ismelia carinata (Schousb.) Sch. Bip. [Chrysanthemum carinatum Schousb.], Mantisalca salmantica (L.) Briq. & Cavill. are historical or extirpated waifs in California. Inula helenium L. not documented in California. Taxa of Aster in TJM (1993) treated here in Almutaster, Eucephalus, Eurybia, Ionactis, Oreostemma, Sericocarpus, Symphyotrichum; Chamomilla in Matricaria; Cnicus in Centaurea; Conyza in Erigeron and Laennecia; Dugaldia in Hymenoxys; Erechtites in Senecio; Hymenoclea in Ambrosia; Lembertia in Monolopia; Osteospermum ecklonis in Dimorphotheca; Picris echioides in Helminthotheca; Prionopsis in Grindelia; Raillardiopsis in Anisocarpus and Carlquistia; Schkuhria multiflora in Bahia; Trimorpha in Erigeron; Venidium in Arctotis; Whitneya in Arnica. Taxa of Arida in TJM2 (2012) treated here in Leucosyris. —Scientific Editors: David J. Keil, Bruce G. Baldwin.
Unabridged note: Largest family of vascular plants in California and of eudicots globally.

Key to Asteraceae


David J. Keil & G. Ledyard Stebbins

Annual, biennial [perennial herb] from strong taproot; herbage ± glabrous in California; sap milky. Stem: branches few, stiffly ascending. Leaf: basal and cauline, alternate, sessile, sheathing, entire, grass-like. Inflorescence: heads liguliflorous, 1, generally closed by mid-day; peduncle long, bractless; involucre cylindric, urn-shaped, or narrowly conic in bud, ± bell-shaped in flower; phyllaries in 1 series, linear to lanceolate, acute, reflexed in fruit; receptacle flat to convex, pitted, epaleate. Flower: corolla yellow to bronze or purple; ligules readily withering. Fruit: 2.5–3 cm, cylindric or ± fusiform, 5–10-ribbed, ribs generally roughened; beak stout, > body; pappus of stout plumose bristles, 2° bristles tangled, tips of a few 1° bristles exceeding others, unbranched; fruits spreading, forming spheric ball 4–5 cm diam.
± 150 species: Eurasia, Mediterranean, northern Africa, widely naturalized (hybrid species have evolved from aliens in western North America). (Greek: goat's beard) [Soltis 2006 FNANM 19:303–306]
Unabridged references: [Soltis et al. 2004 Biol J Linn Soc 82:485–501]
Unabridged note: Allotetraploid hybrid species Tragopogon mirus Ownbey (Tragopogon dubius × Tragopogon porrifolius) and Tragopogon miscellus Ownbey (Tragopogon pratensis × Tragopogon dubius) have originated (apparently multiple times) in western North America. Neither has yet been reported from California, but may be expected, especially where parental species co-occur. Hybrids variably combine features of parents.

Key to Tragopogon

T. dubius Scop. YELLOW SALSIFY
Annual, biennial, 3–10 dm. Leaf: 2–5 dm, tips straight, faces ± minutely tomentose, soon glabrous. Inflorescence: peduncle much wider distally in flower; involucre conic in bud, phyllaries 8–13, 2.5–4 cm in flower heads, much exceeding flowers, 4–7 cm in fruit heads. Flower: ligule pale lemon-yellow. Fruit: 25–35 mm; pappus ± white.
2n=12. Uncommon. Disturbed places; < 2700 m. Klamath Ranges, High Cascade Range, Sierra Nevada, Great Central Valley, Central Western California, South Coast, Transverse Ranges, Peninsular Ranges, Great Basin Floristic Province; native to Europe. May–Sep [Online Interchange]

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Next taxon: Tragopogon porrifolius


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Citation for the whole project: Jepson Flora Project (eds.) 2013. Jepson eFlora,, accessed on Nov 28 2015
Citation for this treatment: [Author of taxon treatment] 2013. Tragopogon, in Jepson Flora Project (eds.) Jepson eFlora,, accessed on Nov 28 2015

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click for enlargement Tragopogon dubius
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1995 Saint Mary's College of California

Geographic subdivisions indicated for the distribution of Tragopogon dubius Markers link to CCH specimen records. If the markers are obscured, reload the page [or change window size and reload]. Yellow markers indicate records that may provide evidence for eFlora range revision or may have georeferencing or identification issues.
map of distribution 1
(Note: any qualifiers in the taxon distribution description, such as 'northern', 'southern', 'adjacent' etc., are not reflected in the map above, and in some cases indication of a taxon in a subdivision is based on a single collection or author-verified occurence).

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Data provided by the participants of the Consortium of California Herbaria.
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CCH collections by month

Duplicates counted once; synonyms included.
Species do not include records of infraspecific taxa.
Blue line denotes eFlora flowering time.