The green links below add additional plants to the comparison table. Blue links lead to other Web sites.
enable glossary links

wavy bitter-cress, wood bitter-cress, woodland bitter-cress

forkleaf toothwort

Habit Annuals or biennials; sparsely to densely hirsute basally or throughout, or glabrous. Perennials; glabrous throughout.
Rhizomes

absent.

(tuberiform, fragile), moniliform, segments oblong, 3–5 mm diam., (fleshy).

Stems

erect, ascending, or decumbent, branched or unbranched, (0.6–)1–5 dm, (slightly flexuous).

erect, unbranched, 1–3.5 dm.

Basal leaves

(often withered by anthesis), not rosulate, 5–15-foliolate, (2.7–)4–14(–19) cm, leaflets petiolulate;

petiole 0.7–5 cm, (ciliate or not);

lateral leaflet blade oblong, ovate, or elliptic, smaller than terminal, margins entire, repand, crenate, or 3 (or 5)-lobed;

terminal leaflet (petiolule 0.3–1.7 cm), blade reniform, broadly ovate, or suborbicular, 0.5–2.5 cm × 4–30 mm, margins repand, crenate, or 3 or 5-lobed.

Rhizomal leaves

palmately compound (biternate), 7–20 cm, leaflets petiolulate;

petiole 4–13 cm;

lateral leaflets similar to terminal, blade sometimes smaller;

terminal leaflet (petiolule 1–3(–4) cm), blade ternately or pinnately lobed, (distal segment) linear, 0.7–3.5 cm × 0.6–3 mm, base attenuate to cuneate, margins entire (apiculate).

Cauline leaves

3–15, 5–15-foliolate [leaves (2–)3.5–5.5(–7) cm, including petiole], petiolate, leaflets petiolulate;

petiole base not auriculate;

lateral leaflets similar to basal, (0.4–2.5 mm wide).

(2 or) 3, palmately compound (biternate, similar to rhizomal leaves, alternate to subopposite), petiolate, leaflets petiolulate;

petiole (0.5–)1–4(–5.5) cm, base not auriculate;

lateral leaflets similar to terminal;

terminal leaflet (petiolule (0.3–)0.7–1.5(–2.5) cm), blade (ternate, distal segment) linear, (0.4–)1.5–5(–6.5) cm × 0.7–4(–6) mm, base cuneate to attenuate, margins entire.

Racemes

ebracteate.

ebracteate.

Flowers

sepals oblong, 1.5–2.5 × 0.7–1 mm, lateral pair not saccate basally;

petals white, spatulate, 2.5–4(–5) × 1–1.7 mm; (stamens rarely 4, lateral pair absent);

filaments 2–3 mm;

anthers ovate, 0.3–0.5 mm.

sepals oblong, 4–6 × 1.5–2 mm, lateral pair not saccate basally;

petals white to pale pink, oblanceolate, 9–15 × 2–4 mm, (not clawed, apex rounded);

filaments: median pairs 6–7.5 mm, lateral pair 3–5 mm;

anthers linear, 1.5–2.5 mm.

Fruiting pedicels

divaricate or ascending, (5–)6–14(–17) mm.

ascending to divaricate, 10–25(–35) mm.

Fruits

linear, (torulose), (0.8–)1.2–2.8 cm × 1–1.5 mm;

ovules 18–40 per ovary;

style 0.3–1(–1.5) mm.

linear-lanceolate, 2–3.5 cm × 1.5–2 mm;

ovules 10–14 per ovary;

style 4–7(–10) mm.

Seeds

brown, oblong or subquadrate, 0.9–1.5 × 0.6–1 mm, (narrowly margined or not).

brown, oblong, 1.5–2.5 × 1–1.5 mm.

2n

= 32.

= 64, 112.

Cardamine flexuosa

Cardamine dissecta

Phenology Flowering Apr–Jul. Flowering Mar–May.
Habitat Disturbed areas, fields, nurseries, plantations, gardens, flower beds, lawns, roadsides Oak-hickory woods, moist loamy areas, floodplain woods, bluffs, rocky calcareous woods, limestone slopes, along streams
Elevation 0-1100 m (0-3600 ft) 0-300 m (0-1000 ft)
Distribution
from FNA
AL; CA; FL; GA; IL; IN; LA; MD; MI; NC; NY; OH; OR; RI; TX; VA; WA; BC; NF; ON; Europe; e Asia [Introduced in North America; introduced also in Mexico, Central America, South America, Australia]
[WildflowerSearch map]
[BONAP county map]
from FNA
AL; GA; IN; KY; NC; OH; TN
[WildflowerSearch map]
[BONAP county map]
Discussion

According to J. Lihová et al. (2006), the populations referred to Cardamine flexuosa in North America comprise two taxa of different polyploid origins and evolutionary histories: tetraploid C. flexuosa (2n = 32), native to Europe, and the octoploid taxon informally called “Asian C. flexuosa” (2n = 64), native to eastern Asia. For the latter, the name C. flexuosa subsp. debilis can be used. Nevertheless, these two taxa should be recognized at species level and the correct name for the Asian species should be sought. Based on available data, both taxa occupy the same habitats in North America, but the Asian taxon is much more widespread. The occurrence of European C. flexuosa was, until now, confirmed only for Washington, where both taxa have been recorded. More detailed studies of the North American distributions of both these weeds are needed.

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

Source FNA vol. 7, p. 474. FNA vol. 7, p. 473.
Parent taxa Brassicaceae > tribe Cardamineae > Cardamine Brassicaceae > tribe Cardamineae > Cardamine
Sibling taxa
C. angulata, C. angustata, C. bellidifolia, C. blaisdellii, C. breweri, C. bulbosa, C. californica, C. clematitis, C. concatenata, C. constancei, C. cordifolia, C. digitata, C. diphylla, C. dissecta, C. douglassii, C. flagellifera, C. hirsuta, C. holmgrenii, C. impatiens, C. longii, C. macrocarpa, C. maxima, C. micranthera, C. microphylla, C. nuttallii, C. nymanii, C. occidentalis, C. oligosperma, C. pachystigma, C. parviflora, C. pattersonii, C. penduliflora, C. pensylvanica, C. pratensis, C. purpurea, C. rotundifolia, C. rupicola, C. umbellata
C. angulata, C. angustata, C. bellidifolia, C. blaisdellii, C. breweri, C. bulbosa, C. californica, C. clematitis, C. concatenata, C. constancei, C. cordifolia, C. digitata, C. diphylla, C. douglassii, C. flagellifera, C. flexuosa, C. hirsuta, C. holmgrenii, C. impatiens, C. longii, C. macrocarpa, C. maxima, C. micranthera, C. microphylla, C. nuttallii, C. nymanii, C. occidentalis, C. oligosperma, C. pachystigma, C. parviflora, C. pattersonii, C. penduliflora, C. pensylvanica, C. pratensis, C. purpurea, C. rotundifolia, C. rupicola, C. umbellata
Synonyms C. flexuosa subsp. debilis, C. flexuosa var. debilis, C. hirsuta subsp. flexuosa, C. scutata subsp. flexuosa Dentaria dissecta, C. angustata var. multifida, C. laciniata subsp. multifida, Dentaria furcata, Dentaria heterophylla var. multifida, Dentaria laciniata var. multifida, Dentaria multifida
Name authority Withering: Arr. Brit. Pl. ed. 3, 3: 578. (1796) (Leavenworth) Al-Shehbaz: J. Arnold Arbor. 69: 82. (1988)
Web links