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Emory's Rock daisy

Warnock's Rock daisy

Habit Annuals (sometimes persisting), 2–60 cm (delicate or robust, stems relatively few to many, erect or spreading); puberulent to hirsute, glandular-pubescent. Perennials or subshrubs, 2–10 cm; densely scabrous-pubescent.
Leaves

petioles 3–45 mm;

blades ovate, cordate, suborbiculate, or triangular, 17–60 × 10–50 mm, margins deeply toothed, lobed, cleft, or divided, lobes indented to irregularly dissected.

petioles 2–5(–8) mm;

blades lance-ovate, ovate, or suborbiculate, 6–10 × 4–8(–10) mm, margins serrate.

Peduncles

1–70 mm.

1–7 mm.

Involucres

campanulate to hemispheric.

campanulate.

Ray florets

usually 8–14, rarely rudimentary or 0;

corollas white, laminae oblong, 1–4(–6) × 1–3 mm.

0.

Disc florets

40–100+;

corollas yellow, tubes 0.7–1.3 mm, throats tubular to tubular-funnelform, 0.8–1.3 mm, lobes 0.1–0.2 mm.

9–12;

corollas bright white, tubes 0.6–1 mm, throats subfunnelform, 2–2.5 mm, lobes 1–1.6 mm.

Phyllaries

10–20, lanceolate or oblanceolate to ovate-lanceolate, 4–6 × 1–2 mm.

9–10, linear to lanceolate, 5–7 × 1.2–2.2 mm.

Heads

borne singly or in corymbiform arrays, 4–10 × 4–10 mm.

borne singly (often partially obscured by leaves), 7–10 × 4–7 mm.

Cypselae

suboblong, oblanceolate, or subcuneate, (1.5–)2–3 mm, margins thin (not calloused), long- or short-ciliate;

pappi 0 or of 1 antrorsely to retrorsely barbellate bristles 1–3 mm plus crowns of hyaline, laciniate scales.

oblong to oblanceolate, 2.2–2.8 mm, margins notably calloused, glabrous;

pappi callous crowns, bristles 0.

2n

= 65–72 or 100–116.

= 34.

Perityle emoryi

Perityle warnockii

Phenology Flowering year round (depending on latitude). Flowering spring–fall.
Habitat Coastal bluffs, desert plains, slopes, washes Limestone
Elevation 10–1500 m (0–4900 ft) 500–700 m (1600–2300 ft)
Distribution
from FNA
AZ; CA; NV; UT; Mexico; South America (Chile, Peru)
[WildflowerSearch map]
[BONAP county map]
from FNA
TX
[BONAP county map]
Discussion

Perityle emoryi is a widespread polyploid of diverse habitats and is often weedy. It is variable; none of the variation appears to have population significance and does not require taxonomic recognition. The range of P. emoryi appears to be gradually expanding.

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

Of conservation concern.

Perityle warnockii is known only from the type locality in Val Verde County. The relationship of P. warnockii to P. bisetosa is evidenced by its similar though often reduced vegetative and floral morphology. The two species may have been derived separately from a common ancestor, perhaps a white-flowered member of sect. Pappothrix such as P. vitreomontana.

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

Source FNA vol. 21, p. 321. FNA vol. 21, p. 325.
Parent taxa Asteraceae > tribe Heliantheae > subtribe Peritylinae > Perityle > sect. Perityle Asteraceae > tribe Heliantheae > subtribe Peritylinae > Perityle > sect. Laphamia
Sibling taxa
P. aglossa, P. ajoensis, P. ambrosiifolia, P. angustifolia, P. bisetosa, P. cernua, P. ciliata, P. cinerea, P. cochisensis, P. congesta, P. coronopifolia, P. dissecta, P. fosteri, P. gilensis, P. gracilis, P. huecoensis, P. intricata, P. inyoensis, P. lemmonii, P. lindheimeri, P. megalocephala, P. microglossa, P. parryi, P. quinqueflora, P. rupestris, P. saxicola, P. specuicola, P. stansburyi, P. staurophylla, P. tenella, P. vaseyi, P. villosa, P. vitreomontana, P. warnockii
P. aglossa, P. ajoensis, P. ambrosiifolia, P. angustifolia, P. bisetosa, P. cernua, P. ciliata, P. cinerea, P. cochisensis, P. congesta, P. coronopifolia, P. dissecta, P. emoryi, P. fosteri, P. gilensis, P. gracilis, P. huecoensis, P. intricata, P. inyoensis, P. lemmonii, P. lindheimeri, P. megalocephala, P. microglossa, P. parryi, P. quinqueflora, P. rupestris, P. saxicola, P. specuicola, P. stansburyi, P. staurophylla, P. tenella, P. vaseyi, P. villosa, P. vitreomontana
Name authority Torrey: in W. H. Emory, Not. Milit. Reconn., 142. (1848) A. M. Powell: Sida 3: 177, fig. 1. (1966)
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