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pine mat

buckbrush, buckthorn, California-lilac, ceanothus, wild-lilac

Habit Shrubs, evergreen, 0.2–0.3(–0.5) m, matlike. Shrubs, rarely arborescent, armed with thorns or unarmed; bud scales present.
Stems

spreading, sometimes rooting at nodes;

branchlets green, sometimes tinged red, not thorn-tipped, usually round, sometimes angled, in cross section, flexible, puberulent.

Leaves

petiole 3–11 mm;

blade flat, elliptic to widely ovate, 12–45 × 6–20 mm, base obtuse to rounded, margins serrulate to denticulate, not revolute, usually not wavy, sometimes wavy, teeth 27–42, apex ± obtuse to rounded, abaxial surface pale green, pilosulous, adaxial surface green, pilosulous; usually pinnately veined, rarely 3-veined from base.

persistent or deciduous, alternate or opposite, sometimes fascicled on short shoots;

blade not gland-dotted; pinnately veined or 3-veined from base (acrodromous).

Inflorescences

axillary, umbel-like to racemelike, 1.3–4 cm.

terminal or axillary, cymes aggregated into umbel-like clusters, or latter aggregated into racemelike or paniclelike thyrses;

peduncles and pedicels not fleshy in fruit.

Pedicels

present.

Flowers

sepals, petals, and nectary usually blue to pale blue, rarely white.

bisexual;

hypanthium shallowly cupulate to hemispheric, less than 0.5 mm wide;

sepals 5 (or (5–)6(–8) in C. jepsonii), usually incurved, sometimes becoming spreading, usually white to cream, blue, or purple, rarely pink, lanceolate to deltate, keeled adaxially;

petals 5 (or (5–)6(–8) in C. jepsonii), usually white to cream, blue, or purple, rarely pink, hooded, spatulate or obovate, clawed;

nectary fleshy, free from hypanthium;

stamens 6(–8);

ovary 1/2-inferior, 3-locular;

styles 3 (sometimes 4 in C. jepsonii), connate basally.

Fruits

capsules, leathery exocarp sloughing off prior to dehiscence.

Capsules

4–5 mm wide, weakly lobed near apex;

valves smooth, crested.

x

= 12.

Ceanothus diversifolius

Ceanothus

Phenology Flowering Apr–Jun.
Habitat Well-drained slopes and canyons, open to shaded sites, mixed evergreen and conifer forests.
Elevation 700–2300 m. (2300–7500 ft.)
Distribution
from FNA
CA
[WildflowerSearch map]
[BONAP county map]
from USDA
North America; Mexico; Central America (Costa Rica, Guatemala, Panama)
[BONAP county map]
Discussion

Ceanothus diversifolius occurs in the North Coast Ranges and the western slopes of the Cascade Range and the Sierra Nevada; it often forms mats to two meters wide. Marginal teeth on young leaves are notable in having more or less persistent, narrowly conic glands, not seen elsewhere in Ceanothus.

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

Species 58 (51 in the flora).

Among the Ceanothus species found in the flora area, only three occur entirely east of the Rocky Mountains. Among the remaining species, a few of which are widespread in western North America, 42 are endemic to the California Floristic Province. Four species are entirely restricted to ultramafic (serpentine, gabbro) soils, while others occur on a diversity of substrates. Several widespread species are co-dominant shrubs in chaparral, or are important understory shrubs in woodlands and forests, especially in western North America. In addition to reproduction by seeds, many species of subgenus Ceanothus respond to fire by developing sprouts from the root crown, whereas all species in subgenus Cerastes reproduce strictly from seeds (F. I. Pugnaire et al. 2006). Many species form mycorrhizal associations (subterranean coralloid root clusters) with actinomycete symbionts (Frankia) and thus are capable of nitrogen fixation (S. L. Rose 1980; S. G. Conard et al. 1985).

Hybridization is widespread in the genus, with at least 44 interspecific combinations reported in the literature (H. McMinn 1944; D. Fross and D. H. Wilken 2006), resulting from a common diploid chromosome number of 2n = 24 and the absence of strong isolating mechanisms. At least one putative hybrid swarm has been documented to include four species, Ceanothus cuneatus, C. divergens, C. gloriosus, and C. sonomensis (J. T. Howell 1940; M. A. Nobs 1963). The widespread occurrence of some hybrids often contributes to difficulty in identifying specimens, and in some cases may have contributed to complex local and regional patterns of variation in flower color or leaf morphology. Most hybrids are between taxa within the same subgenus. Intersubgeneric hybrids are few, and characterized by high levels of sterility. Ceanothus is a popular source of horticultural cultivars, with over 200 named selections (Fross and Wilken). One of the first and most popular hybrids in the 1830s was C. ×delilianus Spach, which was developed in France from a cross between C. americanus (eastern North America) and C. caeruleus Lagasca (Mexico).

Some species and varieties of Ceanothus are considered difficult to identify. Some identification problems result from both local and geographical variation within species and intergradation following hybridization (M. Van Rensselaer and H. McMinn 1942; M. A. Nobs 1963). The dependence on both flower color and mature fruit morphology for accurate identification is exacerbated by a delay in fruit maturation following a short duration of flowering. Careful attention to life form, flower color, and fruit morphology is critical to identification. Knowledge of geographic distribution and edaphic substrate preference, especially in the California Floristic Province, can be helpful in determining a number of species.

In the keys and descriptions that follow, tooth number is per leaf.

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

Key
1. Stipules thin, deciduous; leaves alternate, blades usually herbaceous, sometimes leathery, pinnately veined or 3-veined from base; inflorescences usually racemelike to paniclelike, sometimes umbel-like; capsules not horned, sometimes crested.
subg. Ceanothus
1. Stipules thick, persistent, wartlike; leaves opposite (alternate in C. verrucosus and C. megacarpus), blades leathery, pinnately veined; inflorescences usually umbel-like, rarely racemelike; capsules horned or not, usually not crested (crested in C. divergens and C. gloriosus).
subg. Cerastes
Source FNA vol. 12, p. 94. FNA vol. 12, p. 77. Authors: Clifford L. Schmidt†, Dieter H. Wilken.
Parent taxa Rhamnaceae > Ceanothus > subg. Ceanothus Rhamnaceae
Sibling taxa
C. americanus, C. arboreus, C. arcuatus, C. confusus, C. cordulatus, C. crassifolius, C. cuneatus, C. cyaneus, C. dentatus, C. divergens, C. fendleri, C. ferrisiae, C. foliosus, C. fresnensis, C. gloriosus, C. griseus, C. hearstiorum, C. herbaceus, C. impressus, C. incanus, C. integerrimus, C. jepsonii, C. lemmonii, C. leucodermis, C. maritimus, C. martini, C. masonii, C. megacarpus, C. microphyllus, C. oliganthus, C. ophiochilus, C. otayensis, C. palmeri, C. papillosus, C. parryi, C. parvifolius, C. pauciflorus, C. perplexans, C. pinetorum, C. prostratus, C. pumilus, C. purpureus, C. roderickii, C. sanguineus, C. sonomensis, C. spinosus, C. thyrsiflorus, C. tomentosus, C. velutinus, C. verrucosus
Subordinate taxa
C. subg. Ceanothus, C. subg. Cerastes
Synonyms C. decumbens
Name authority Kellogg: Proc. Calif. Acad. Sci. 1: 58. (1855) Linnaeus: Sp. Pl. 1: 195. (1753): Gen. Pl. ed. 5, 90. (1754)
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