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desert tansy-aster

small-flower tansy-aster

Habit Annuals, perennials, or subshrubs, 10–60(–90) cm; usually taprooted, sometimes rhizomatous. Annuals or short-lived perennials, 10–50 cm; taproots slender to ± thickened.
Stems

erect to ascending or sprawling, often much branched, glabrous or hairy, sometimes stipitate-glandular or gland-dotted.

1–15+, mostly erect to ascending, rarely reclining, slender, much branched distally or throughout, glaucous, glabrous or sparsely gland-dotted from midstem distally.

Leaves

basal (sometimes withering by flowering) and cauline; alternate;

petiolate (basal) or sessile (cauline; sometimes succulent);

basal blades 1-nerved, linear to lanceolate, oblanceolate or obovate;

cauline lanceolate to scalelike (bases tapered to clasping), margins entire, dentate, lacerate to deeply pinnatifid, or 2-pinnatifid (apices, including of lobes and teeth, apiculate to bristle-tipped, bristles 0.1–1 mm), faces glabrous or densely hairy, sometimes stipitate-glandular.

mostly cauline;

sessile;

blades lanceolate to oblong, reduced distally, 10–30 × 2–7 mm, bases often clasping, margins shallowly or deeply pinnatifid to 2-pinnatifid, toothed, or entire, apices apiculate to rounded, faces glabrous to sparsely stipitate-glandular;

distal ascending to appressed.

Involucres

turbinate to depressed-hemispheric, (3–12 ×) 4–16 mm.

hemispheric, 3–5 × 4–6 mm (fresh).

Receptacles

convex, indistinctly pitted (pit borders ± chartaceous, laciniate 0.1–0.5 mm, in A. blepharophylla), epaleate.

Ray florets

0 (A. carnosa) or 8–80+, pistillate, fertile;

corollas light to dark blue.

10–30+;

laminae violet-blue to lavender, rarely whitish, 6–8 mm, coiled after flowering.

Disc florets

12–100+, bisexual, fertile;

corollas yellow, tubes 1/4–1/2 times ± funnelform throats (usually glabrous), lobes 5, erect, triangular (glabrous to minutely hairy).

18–40+;

corollas yellow, 4–5 mm.

Phyllaries

40–150+ in 4–8 series, appressed, spreading, or reflexed, 1-nerved (flat to rounded or weakly keeled), linear-lanceolate to oblong-lanceolate, unequal, bases indurate to herbaceous, apices herbaceous, margins sometimes scarious, faces glabrous or moderately to densely hairy, sometimes stipitate-glandular.

in 3–4 series, ± appressed, lanceolate to oblanceolate, 1–4 mm, bases whitish, margins ± entire, apices green or purple, mostly acute, minutely glandular.

Heads

radiate or discoid (A. carnosa), borne singly (terminal), or in cymiform or corymbiform arrays.

borne singly (terminal), in loose, leafy, corymbiform arrays.

Cypselae

± dimorphic, narrowly oblong (thin-walled), 8–13-nerved per face (nerves filiform), sparsely to densely sericeous;

ray cypselae (if present) obscurely 3-sided, rounded abaxially, disc ones slightly compressed laterally;

pappi persistent, of 20–40, white or whitish (tawny in A. blepharophylla), barbellulate, apically attenuate bristles in 2–3 series (at most ± flattened and wider near sometimes slightly overlapping bases);

ray lengths 1/3 to ± equaling disc.

oblanceolate, 1.5–2 mm, 8–10 per face, faces moderately sericeous;

pappi setose;

ray 0 or white, 1–1.5 mm;

disc whitish, 4–5.5 mm.

x

= 5.

2n

= 10.

Arida

Arida parviflora

Phenology Flowering Jul–Oct.
Habitat Saline flats, playas, swales, sandy areas, river margins
Elevation 1100–1700 m (3600–5600 ft)
Distribution
sw United States; n Mexico; Desert regions
from FNA
AZ; CO; NM; TX; UT; Mexico (Chihuahua, Coahuila)
Discussion

Species 9 (6 in the flora).

Arida belongs to a group of taxa once included within a broadly circumscribed Machaeranthera containing more than 36 species. This genus was generally distinguished by its taproots, spiny-toothed pinnatifid leaves, bristly-tipped phyllaries, blue ray corollas, epappose ray florets, and chromosome numbers of n = 4, 5, or 6 (A. Cronquist and D. D. Keck 1957; R. L. Hartman 1990; L. H. Shinners 1950b; B. L. Turner 1987b; Turner and D. B. Horne 1964). Arida was recognized as a section of Machaeranthera with epappose ray florets, unequal phyllaries, and a chromosome number of n = 5. Studies incorporating data from cpDNA restriction site analysis (D. R. Morgan and B. B. Simpson 1992) indicated that section Psilactis was not closely related to the other taxa and it was removed (Morgan 1993). Further studies utilizing DNA sequence data (Morgan 1997) suggested that other genera, such as Oönopsis, Pyrrocoma, and Xanthisma, were closely related to various parts of Machaeranthera. The combined phylogenetic information from molecular, morphologic, cytologic, and flavonoid analyses did not support recent taxonomies, so a new one was proposed by Morgan and Hartman (2003). Machaeranthera was reduced to two species, and the remaining taxa were distributed in Xanthisma, Dieteria, and Arida.

Data from chloroplast DNA restriction sites and nuclear ETS sequences support a close relationship between Arida parviflora, A. turneri, both with pinnate or 2-pinnate leaves, A. riparia, and A. blepharophylla (D. R. Morgan 2003; Morgan and B. B. Simpson 1992). Conflicts between the two data sets were attributed to reticulate evolution resulting from occasional intergeneric crosses. Arida blepharophylla is somewhat unusual within the genus in being a short-lived perennial with rhizomes, basal rosettes of leaves, and receptacular scales (Morgan and R. L. Hartman 2003). These characters are similar to those found in Xanthisma and with these morphologic features as well as chloroplast versus nuclear DNA data, it may have evolved through intergeneric hybridization (Morgan 2003).

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Arida parviflora is recognized by its wiry stems, small, deeply pinnatifid leaves, rather small involucres, and ray cypselae usually with pappi. This species is often described as being an annual; however, some specimens have a large, woody root and well-developed branching crown like a perennial plant.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Key
1. Ray cypselae epappose (except in occasional plants)
→ 2
1. Ray cypselae pappose or ray florets 0 (in A. carnosa)
→ 4
2. Midstems densely hispiduloso-glandular; s Arizona, s California, s Nevada, n Sonora (Mexico)
A. arizonica
2. Midstems glabrous or sparsely gland-dotted
→ 3
3. Cauline leaf blades entire or toothed; w Texas
A. mattturneri
3. Cauline leaf blades deeply pinnatifid; e Arizona, s Colorado, New Mexico, Utah, Chihuahua and Coahuila (Mexico)
A. parviflora
4. Leaves (at least some) pinnatifid to 2-pinnatifid
A. parviflora
4. Leaves entire or toothed
→ 5
5. Ray florets 0
A. carnosa
5. Ray florets present.
→ 6
6. Perennials, rhizomatous, forming vegetative rosettes; leaf margins entire with 8–20 cilia per side (cilia 0.4–1.5 mm); involucres broadly turbinate, 5–8 mm wide (fresh); phyllaries oblong to oblanceolate or obovate, broadly acute to short-acuminate
A. blepharophylla
6. Annuals; leaf margins entire, eciliate or with 1–8 cilia per side; involucres hemispheric, 10–16 mm wide (fresh); phyllaries linear-lanceolate, acute to acuminate
A. riparia
Source FNA vol. 20, p. 401. Authors: Ronald L. Hartman, David J. Bogler. FNA vol. 20, p. 405.
Parent taxa Asteraceae > tribe Astereae Asteraceae > tribe Astereae > Arida
Sibling taxa
A. arizonica, A. blepharophylla, A. carnosa, A. mattturneri, A. riparia
Subordinate taxa
A. arizonica, A. blepharophylla, A. carnosa, A. mattturneri, A. parviflora, A. riparia
Synonyms Machaeranthera section A. Machaeranthera parviflora
Name authority (R. L. Hartman) D. R. Morgan & R. L. Hartman: Sida 20: 1410. (2003) (A. Gray) D. R. Morgan & R. L. Hartman: Sida 20: 1414. (2003)
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