Gordon C. Tucker

Herbs, subshrubs, shrubs, or trees, (rarely vines), perennial, deciduous or evergreen, usually autotrophic, sometimes mycotrophic (subfam. Monotropoideae), usually chlorophyllous and autotrophic, sometimes achlorophyllous and heterotrophic (subfam. Monotropoideae), aromatic compounds (e.g., methyl salicylate) sometimes present (Gaultheria). Stems (absent in some Monotropoideae) erect or decumbent to prostrate, glabrous or hairy, (aerial stems sometimes produced from suckers, rhizomes, or corms), pith solid (hollow, with diaphragms in Agarista). Leaves (reduced or absent in some Monotropoideae), usually cauline, sometimes in basal rosettes (subfam. Monotropoideae), usually alternate or pseudoverticillate, sometimes opposite or, rarely, whorled, simple; stipules absent; petiole present or absent; blade plane or acicular, often coriaceous, margins entire or toothed, plane or revolute. Inflorescences terminal or axillary racemes, umbels, corymbs, panicles, fascicles, spikes, or solitary flowers. Flowers usually bisexual, rarely unisexual (subfam. Ericoideae), radially symmetric (sometimes slightly bilaterally symmetric in subfam. Monotropoideae and subfam. Ericoideae); perianth and androecium hypogynous (epigynous in some Vaccinioideae); hypanthium absent; sepals absent or (2-)4-5(-7), distinct or connate basally; petals (2-)4-5(-8), rarely absent or highly reduced, connate or distinct, not sticky (covered with sticky exudate in Bejaria), corolla absent or rotate to crateriform, campanulate, cylindric, globose, or urceolate (salverform in Epigaea); intrastaminal nectary disc present or absent; stamens (2-)5-8(-10) [14, 16, 20]; filaments distinct; anthers inverted during development, often with awns, dehiscent by pores or short slits (at apparent apex) or slits (lateral); pistils 1, 4-5-carpellate; ovary superior (inferior in some Vaccinioideae), incompletely (2-)5-10-locular (1-locular in some Monotropoideae), often furrowed or lobed externally; placentation axile or parietal; ovules anatropous, unitegmic, tenuinucellate; styles 1, straight or declinate (curved in Elliottia), hollow; stigmas 1, capitate or peltate to funnelform, usually 5-lobed. Fruits capsular and dehiscent (loculicidal, septifragal, or septicidal), or drupaceous (axis fibrous or soft in some Monotropoideae) or baccate (rarely each surrounded by accrescent or fleshy calyx in Gaultheria) and indehiscent. Seeds 1-10(-1000+), tan to yellowish brown or brown, ellipsoid, ovoid or spheroidal, or fusiform to flattened, or oblong (sometimes 3-sided); testa thin (bony in subfam. Arbutoideae and subfam. Vaccinioideae); embryo usually straight, fusiform, rarely minute and undifferentiated; endosperm abundant, cellular, fleshy.

Genera ca. 120, species ca. 4100 (46 genera, 212 species in the flora): nearly worldwide.

The closest relatives of the broadly defined Ericaceae are Clethraceae and Cyrillaceae. Some phylogenies show Cyrillaceae as sister to Ericaceae; other analyses have Clethraceae and Cyrillaceae as closest relatives to each other, together forming the sister group to Ericaceae. Monotropa and related genera (genera 5-12 of this treatment), and Pyrola and related genera (genera 1-4 of this treatment) have been treated as families Monotropaceae and Pyrolaceae. Not all botanists agreed with this, as summarized by G. H. M. Lawrence (1951): "Many botanists (including Hutchinson) have held the view that the Pyrolaceae are not sufficiently distinct from the Ericaceae to be treated as a separate family." Differences in habit, floral features, and pollen have helped maintain family status for Pyrolaceae and Monotropaceae in regional floras. Molecular and morphological analyses (K. A. Kron et al. 2002) show these lineages embedded within Ericaceae. Similarly, Empetraceae has been demonstrated to be nested within Ericaceae and is here included in the Ericaceae.

P. F. Stevens (2004) recognized eight subfamilies within Ericaceae; six of these are represented in the flora area. Subfamily Enkianthoideae, basal in recent phylogenies of the family, forms a sister clade to the remaining subfamilies. The subfamily includes only the single genus Enkianthus Loureiro (12 species), native to temperate eastern Asia. Enkianthus campanulatus (Miquel) G. Nicholson is cultivated occasionally in the northeastern and northwestern United States (M. A. Dirr 1998). Subfamily Styphelioideae Sweet (subfam. Epacridoideae Arnott) of the Southern Hemisphere (especially diverse in Australia with such genera as Astroloma R. Brown, Epacris Cavanilles, and Styphelia Smith), long considered a close relative of the Ericaceae, has been demonstrated as embedded within the Ericaceae. As G. H. M. Lawrence (1951) noted, distinctions between the two families are weak.

Studies in the last several decades, especially since 1990 including molecular data, have resulted in rearrangements of generic limits in the Ericaceae. These are discussed under the various genera; for the reader’s convenience they are summarized here. Ledum is included in Rhododendron; Leiophyllum and Loiseleuria are included in Kalmia; and Hypopitys is included in Monotropa. Arctous is separated from the much larger Arctostaphylos, to which it is inferred to form a sister clade. Eubotrys is segregated from Leucothoe, with which it has often been combined. Vaccinium is treated in a broad sense, to include segregates such as Oxycoccus; although Vaccinium is decidedly polymorphic, this seems a workable approach until generic limits in the Vaccinieae Reichenbach are better understood.

Most Ericaceae are evergreen shrubs. Some species are deciduous, notably in Rhododendron and Vaccinium. The propensity of members of the family to grow in acidic soils is well known. Although the family Ericaceae is generally regarded as exclusively growing on acidic substrates, some members of the family do occur in neutral or alkaline soils in North America and elsewhere.

Ericaceae are widely distributed in the Northern Hemisphere, almost ubiquitous except in desert areas. In the tropics, especially in South America, the family is diverse in upland and montane areas, and notably diverse in such genera as Bejaria and Cavendishia Lindley. Rhododendron, with centers of diversity in the Himalayas, New Guinea, and eastern North America, and Erica, diverse in southern Africa and Europe, are the largest genera in the family. The largest genus in the flora area is Arctostaphylos, with most species endemic to California and bordering states.

Species among some genera of the family enrich the human condition with edible fruits. In North America, by far the most important of these is Vaccinium. The high-bush blueberry, V. corymbosum, is cultivated in some states, notably Michigan, New Jersey, and North Carolina, and the low-bush blueberry, V. angustifolium, in Maine, Quebec, and the Canadian Maritime Provinces. The fruits of V. macrocarpon, the cranberry, are cultivated commercially in some provinces, including British Columbia, Nova Scotia, and Quebec, and some states including Massachusetts, Oregon, Rhode Island, Washington, and Wisconsin. Vaccinium vitis-idaea, lingonberry, is collected and sold in Newfoundland and Labrador as fresh fruits and preserves, and is an important addition to diet and health in the more northern areas of Canada. The leaves of Rhododendron groenlandicum (Ledum groenlandicum), Labrador tea, are used for a beverage in parts of its transcontinental range. The foliage of some genera, notably Leucothoe, Lyonia, and Rhododendron, contains andromedotoxins and is occasionally implicated in poisonings of humans, domestic pets, and livestock (J. M. Kingsbury 1964; S. D. Mancini and J. M. Edwards 1979). Kalmia also is reportedly toxic, perhaps why it is called sheep laurel, in addition to probably being allelopathic and thus detrimental to reforestation in some situations in the eastern boreal forest. Lyonia ferruginea is a valuable "forest product" in Florida. It is harvested and the stems are used in interior decoration; once silk leaves have been added, they are marketed as "artificial" plants.

Some species of Ericaceae, both native and exotic, are cultivated and of importance to the horticultural industry (M. A. Dirr 1998). Chief among these are Kalmia and Rhododendron (including many deciduous species known as "azaleas"). Other cultivated genera include Arbutus, Elliottia, Enkianthus, Leucothoe, Menziesia, Oxydendrum, and Pieris. Rock garden plants include Arctostaphylos uva-ursi, Kalmia buxifolia, K. procumbens, and Rhododendron lapponicum, as well as species of the Old World genera Calluna and Erica. Shrubs of some genera, including Gaultheria, Gaylussacia, and Vaccinium, are prominent in the understories of deciduous and evergreen forests, especially in regions of acidic soil, such as the southeastern United States. Wetlands in much of Canada and the northern United States support dense populations of ericaceous shrubs, notably Andromeda polifolia and Chamaedaphne calyculata; Kalmia spp., Rhododendron canadense, and R. groenlandicum may be as prominent depending on the region.

SELECTED REFERENCES Anderberg, A. A. 1993. Cladistic interrelationships and major clades of Ericaceae. Pl. Syst. Evol. 184: 207-231. Cipollini, M. L. and E. W. Stiles. 1992. Antifungal activity of ripe ericaceous fruits: Phenolic acid interactions and palatability for dispersers. Biochem. Syst. & Ecol. 20: 501-514. Harborne, J. B. and C. A. Williams. 1973. A chemotaxonomic survey of flavonoids and simple phenols in leaves of the Ericaceae. Bot. J. Linn. Soc. 66: 37-54. Judd, W. S. and K. A. Kron. 1993. Circumscription of Ericaceae (Ericales) as determined by preliminary cladistic analyses based on morphological, anatomical, and embryological features. Brittonia 45: 99-114. Kron, K. A. et al. 2002. Phylogenetic classification of Ericaceae: Molecular and morphological evidence. Bot. Rev. (Lancaster) 68: 335-423. Luteyn, J. L. et al. 1996. Ericaceae of the southeastern United States. Castanea 61: 101-144. Small, J. K. 1914. Ericaceae. In: N. L. Britton et al., eds. 1905+. North American Flora.... 47+ vols. New York. Vol. 29, pp. 33-102. Stevens, P. F. 1969. Taxonomic Studies in the Ericaceae. Ph.D. thesis. University of Edinburgh. Stevens, P. F. 1970. Calluna, Cassiope and Harrimanella: A taxonomic and evolutionary problem. New Phytol. 69: 1131-1148. Stevens, P. F. 1971. A classification of the Ericaceae: Subfamilies and tribes. Bot. J. Linn. Soc. 64: 1-53. Stevens, P. F. et al. 2004. Ericaceae. In: K. Kubitzki et al., eds. 1990+. The Families and Genera of Vascular Plants. 7+ vols. Berlin, etc. Vol. 6, pp. 145-194. Wood, C. E. Jr. 1961. The genera of Ericaceae in the southeastern United States. J. Arnold Arbor. 42: 10-80.