Veronica copelandii |
Veronica sublobata |
|
---|---|---|
Copeland's speedwell |
false ivy-leaf speedwell |
|
Habit | Perennials. | Annuals. |
Stems | ascending, unbranched, 5–15 cm, densely glandular-hairy. |
decumbent to ascending, sometimes erect in young plants, 5–40(–50) cm, eglandular-hairy. |
Leaves | blade oblong-elliptic, (5–)10–15(–35) × 4–8 mm, base cuneate, margins entire, apex short-acuminate, surfaces hairy. |
blade ovate to broadly ovate, 5(–7)-lobed, central lobe longer than wide and broadest, (7–)9–15(–25) × (7–)9–17(–27) mm, base truncate, margins 5(–7)-lobed, apex obtuse to rounded, surfaces sparsely eglandular-hairy. |
Racemes | 1, terminal, distalmost leaves often with 1 or 2 axillary flowers, 10–80 mm, (3–)5–15-flowered, axis glandular-hairy; bracts lanceolate, 3–5 mm. |
1–10, terminal, 50–400(–500) mm, 5–20-flowered, axis eglandular-hairy; bracts broadly ovate, 5(–7)-lobed, central lobe longer than wide and broadest, (7–)9–15(–25) mm. |
Pedicels | erect, 5–8 mm, equal to ± longer than subtending bract, densely glandular-hairy. |
patent or deflexed, (7–)10–18(–24) mm, ± longer than subtending bract, length 3–4(–6) times calyx, eglandular-hairy (densely adaxially). |
Flowers | calyx 4(or 5)-lobed, lobes (1–)2–3 mm, apex obtuse, glandular-hairy; corolla pale blue to purple, rotate, 8–10 mm diam.; stamens 4–5 mm; style 7 mm. |
calyx lobes 3–4 mm, apex acute, sparsely hairy on abaxial surface or glabrous, ciliate with 25–35 hairs per side; corolla pale violet to whitish, 4–5(–6) mm diam.; stamens pale violet, 0.4–0.8 mm; style 0.2–0.7 mm. |
Capsules | compressed in cross section, broadly oblong, 5–6 × 3.5 mm, longer than wide, apex emarginate, glandular-hairy. |
± round in cross section, ovoid, 2–3 × 3.5–5 mm, apex ± emarginate, glabrate. |
Seeds | number unknown, brown, ovoid, flat, 1–1.2 × 0.7–1.1 mm, thickness and texture unknown. |
1–4, bright reddish brown, broadly ovoid to subglobular, urn-shaped, 2.2–2.7 × 2–2.4 mm, 1–1.8 mm thick, transverse ribs inconspicuous, thinner towards margin, margins strongly involute. |
2n | = 18. |
= 36 (Europe). |
Veronica copelandii |
Veronica sublobata |
|
Phenology | Flowering Jul–Aug. | Flowering Mar–May. |
Habitat | Subalpine meadows, alpine slopes. | Moist forests, damp, shady ruderal places, thickets, gardens, montane fields. |
Elevation | 1900–2500 m. (6200–8200 ft.) | 0–1000 m. (0–3300 ft.) |
Distribution |
CA |
AL; KY; MD; MO; OH; UT; VA; Europe [Introduced in North America] |
Discussion | Veronica copelandii is sister to V. cusickii in the phylogenetic analysis by D. C. Albach et al. (2006). It occurs in the Klamath Ranges of northwestern California. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Veronica sublobata is closely related to V. hederifolia and has been frequently synonymized with or treated as a subspecies of the latter. It has rarely been reported in the flora area and is surely more widespread than indicated above. It seems to be more rare than V. hederifolia with only about a dozen verified records from seven states. However, its frequent occurrence in cultivated habitats in Europe makes it likely that it has been introduced to the flora area on multiple occasions. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 17, p. 310. | FNA vol. 17, p. 315. |
Parent taxa | ||
Sibling taxa | ||
Synonyms | V. hederifolia subsp. lucorum, V. hederifolia var. lucorum | |
Name authority | Eastwood: Bot. Gaz. 41: 288, fig. 2. (1906) — (as copelandi) | M. A. Fischer: Oesterr. Bot. Z. 114: 201, 227, figs. 3c, 4c. (1967) |
Web links |