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

common sheep sorrel, field sorrel, oseille, petite oseille, red sorrel, sheep dock, sheep sorrel, sour weed, sûrette

curled dock, curly dock, patience crépue, reguette, rumex crépu, sour dock, yellow dock

Habit Plants perennial, glabrous, with vertical rootstock and/or creeping rhizomes. Plants perennial, occasionally biennial, glabrous or very indistinctly papillose normally only on veins of leaf blades abaxially, with fusiform, vertical rootstock.
Stems

erect or ascending, several from base, branched in distal 1/2 (in inflorescence), 10–40(–45) cm;

shoots variable.

erect, branched distal to middle, 40–100(–150) cm.

Leaves

ocrea brownish at base, silvery and lacerated in distal 1/2;

blade normally obovate-oblong, ovate-lanceolate, lanceolate-elliptic, or lanceolate, occasionally, linear-lanceolate to almost linear, 2–6 × 0.3–2 cm, base hastate (with spreading, entire or sometimes multifid, dissected lobes), occasionally without evident lobes, then base broadly cuneate, margins entire, flat or nearly so, apex acute or obtuse.

ocrea deciduous, rarely partially persistent at maturity;

blade lanceolate to narrowly lanceolate or lanceolate-linear, normally 15–30(–35) × 2–6 cm, base cuneate, truncate, or weakly cordate, margins entire to subentire, strongly crisped and undulate, apex acute.

Inflorescences

terminal, usually occupying distal 1/2–2/3 of stem, usually lax and interrupted to top, broadly or narrowly paniculate.

terminal, occupying distal 1/2 of stem, dense or interrupted at base, narrowly to broadly paniculate, branches usually straight or arcuate.

Pedicels

1–3 mm.

articulated in proximal 1/3, filiform, (3–)4–8 mm, articulation distinctly swollen.

Flowers

(3–)5–8(–10) in whorls;

inner tepals not or slightly enlarged, normally 1.2–1.7(–2) × 0.5–1.3 mm (free wing absent or barely visible), base cuneate, apex obtuse or subacute.

10–25 in whorls;

inner tepals orbiculate-ovate or ovate-deltoid, 3.5–6 × 3–5 mm, base truncate or subcordate, margins entire or subentire to very weakly erose, flat, apex obtuse or subacute;

tubercles normally 3, rarely 1 or 2, unequal, at least 1 distinctly larger, more than (1–)1.5 mm wide.

Achenes

brown or dark brown, 0.9–1.5 × 0.6–0.9 mm.

usually reddish brown, 2–3 × 1.5–2 mm.

2n

= 14, 28, 42.

= 60.

Rumex acetosella

Rumex crispus

Phenology Flowering spring–summer. Flowering late spring–early fall.
Habitat Roadsides, cultivated fields, waste places, disturbed areas, lawns, meadows, railroad gravels, sandy and muddy shores: usually in acidic soils Very broad range of ruderal, segetal, and seminatural habitats, disturbed soil, waste places, cultivated fields, roadsides, meadows, shores of water bodies, edges of woods
Elevation 0-2700 m (0-8900 ft) 0-2500 m (0-8200 ft)
Distribution
from FNA
AK; AL; AR; AZ; CA; CO; CT; DC; DE; FL; GA; IA; ID; IL; IN; KS; KY; LA; MA; MD; ME; MI; MN; MO; MS; MT; NC; ND; NE; NH; NJ; NM; NV; NY; OH; OK; OR; PA; RI; SC; SD; TN; TX; UT; VA; VT; WA; WI; WV; WY; AB; BC; MB; NB; NF; NS; ON; PE; QC; SK; YT; SPM; Greenland; Europe; w Asia [Introduced in North America; introduced almost worldwide]
[WildflowerSearch map]
[BONAP county map]
from FNA
AK; AL; AR; AZ; CA; CO; CT; DC; DE; FL; GA; IA; ID; IL; IN; KS; KY; LA; MA; MD; ME; MI; MN; MO; MS; MT; NC; ND; NE; NH; NJ; NM; NV; NY; OH; OK; OR; PA; RI; SC; SD; TN; TX; UT; VA; VT; WA; WI; WV; WY; AB; BC; MB; NB; NF; NS; NT; ON; PE; QC; SK; YT; SPM; Eurasia [Introduced in North America; introduced almost worldwide]
[WildflowerSearch map]
[BONAP county map]
Discussion

Rumex acetosella in the broad sense is an extremely variable and taxonomically complicated polyploid complex, which includes diploids, tetraploids, hexaploids, and octoploids. This complex (excluding more distantly related arctic-montane R. graminifolius and its allies) probably originated and developed mostly in southern Europe and southwestern Asia. Some races of R. acetosella now are distributed almost worldwide as introduced and often completely naturalized aliens.

Á. Löve (1941, 1983) assumed that in this group chromosome numbers are strictly correlated with morphology. In his opinion, every chromosome race represents a distinct species: diploid Rumex angiocarpus Murbeck [= Acetosella angiocarpa (Murbeck) Á. Löve]; tetraploid R. multifidus Linnaeus [= R. tenuifolius (Wallroth) Á. Löve = Acetosella multifida (Linnaeus) Á. Löve]; hexaploid R. acetosella in the narrow sense [= A. vulgaris (W. D. J. Koch) Fourreau, with gymnocarpous A. vulgaris subsp. vulgaris and angiocarpous A. vulgaris subsp. pyrenaica (Pourret ex Lapeyrouse) Á. Löve]; hexaploid R. graminifolius Rudolph ex Lambert [= A. graminifolia (Rudolph ex Lambert) Á. Löve]. However, the distribution given by Löve for these taxa seems unnatural. Studies by J. C. M. den Nijs and collaborators (den Nijs 1974, 1976, 1984; den Nijs and T. Panhorst 1980; den Nijs et al. 1980, 1985; see also W. Harris 1969, 1973) indicate that the situation is more complicated. They postulated the development of two major evolutionary lines into two ploidy complexes: a primary western Mediterranean one and a secondary eastern Mediterranean one. According to this scheme, polyploid races independently and spontaneously emerged (and still are emerging) within different ancestral populations.

The most widespread, almost cosmopolitan race, presumably native to the southwestern Mediterranean region, including southwestern and Atlantic Europe, which is common in North America, is characterized by a hexaploid chromosome set (2n = 42), nonmultifid lateral lobes of basal leaves, and angiocarpy (fruits are not easily separable from accrescent inner tepals). It was commonly and erroneously referred to as Rumex angiocarpus Murbeck, or R. acetosella subsp. angiocarpus (Murbeck) Murbeck. According to J. R. Akeroyd (1991), who in general followed the taxonomic revision of the group by J. C. M. den Nijs (1984), the correct name for this taxon is R. acetosella subsp. pyrenaicus (Pourret ex Lapeyrouse) Akeroyd (=Acetosella vulgaris subsp. pyrenaica (Pourret ex Lapeyrouse) Á. Löve). Gymnocarpous nonmultifid and multifid forms (R. acetosella subsp. acetosella and R. acetosella subsp. acetoselloides (Balansa) den Nijs, respectively) also occur in North America, but evidently rarely. The distributions of subspecies of R. acetosella in North America are poorly known. Keys and detailed descriptions for the subspecies were provided by den Nijs and Akeroyd. However, the tempting simplicity of the keys is somewhat suspicious. The alternative point of view (and an alternative key) may be found in Á. Löve (1983).

Rumex acetosella subsp. arenicola Mäkinen ex Elven was recently described from Greenland and reported for Scandinavia and arctic Russia (R. Elven et al. 2000). This entity seems to be morphologically transitional toward Rumex graminifolius (see discussion under that species below). According to Elven et al., it differs from other infraspecific entities of R. acetosella in having the following characters: leaves usually without basal lobes (as in R. graminifolius), with revolute margins; inflorescence sparsely branched; tepals and pedicels densely covered with red papillae (as in R. graminifolius). From R. graminifolius and related taxa (R. beringensis and R. krausei) it can be distinguished by narrower inner tepals (similar in size to those in other subspecies of R. acetosella). The distribution of subsp. arenicola and its relations to other taxa are in need of further study.

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

Rumex crispus (belonging to subsect. Crispi Rechinger f.; see K. H. Rechinger 1937) is the most widespread and ecologically successful species of the genus, occuring almost worldwide as a completely naturalized and sometimes invasive alien. It has not been reported from Greenland, but it probably occurs there.

Rumex crispus hybridizes with many other species of subg. Rumex. Hybrids with R. obtusifolius (Rumex ×pratensis Mertens & Koch) are the most common in the genus, at least in Europe, and have been reported for several localities in North America. Rumex crispus × R. patientia (Rumex ×confusus Simonkai) was reported from New York. According to R. S. Mitchell (1986, p. 47), “this hybrid is now spreading along highway shoulders, and it has replaced R. crispus in some local areas.” However, that information should be confirmed by more detailed studies since spontaneous hybrids between species of sect. Rumex usually are much less fertile and ecologically successful than the parental species. Hybrids of Rumex occuring in North America need careful revision.

Numerous infraspecific taxa and even segregate species have been described in the Rumex crispus aggregate. Many seem to represent minor variation of little or no taxonomic significance, but some are geographically delimited entities that may deserve recognition as subspecies or varieties. The typical variety has inner tepals with three well-developed tubercles; the less common var. unicallosus Petermann, with one tubercle, occurs sporadically in North America.

Some eastern Asian plants differ from typical Rumex crispus is having somewhat smaller inner tepals, longer pedicels, lax inflorescences with remote whorls, and narrower leaves that are almost flat or indistinctly undulate at the margins. These plants, originally described as R. fauriei Rechinger f., are now treated as R. crispus subsp. fauriei (Rechinger f.) Mosyakin & W. L. Wagner; the subspecies was recently reported from Hawaii (S. L. Mosyakin and W. L. Wagner 1998) and may be expected as introduced in western North America.

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

Source FNA vol. 5, p. 498. FNA vol. 5, p. 522.
Parent taxa Polygonaceae > subfam. Polygonoideae > Rumex > subg. Acetosella Polygonaceae > subfam. Polygonoideae > Rumex > subg. Rumex > sect. Rumex
Sibling taxa
R. acetosa, R. alpinus, R. altissimus, R. arcticus, R. beringensis, R. britannica, R. brownii, R. bucephalophorus, R. californicus, R. chrysocarpus, R. confertus, R. conglomeratus, R. crassus, R. crispus, R. cristatus, R. cuneifolius, R. densiflorus, R. dentatus, R. ellipticus, R. fascicularis, R. floridanus, R. fueginus, R. graminifolius, R. hastatulus, R. hesperius, R. hymenosepalus, R. kerneri, R. krausei, R. lacustris, R. lapponicus, R. longifolius, R. maritimus, R. mexicanus, R. nematopodus, R. obovatus, R. obtusifolius, R. occidentalis, R. orthoneurus, R. pallidus, R. palustris, R. paraguayensis, R. patientia, R. paucifolius, R. persicarioides, R. praecox, R. pseudonatronatus, R. pulcher, R. pycnanthus, R. salicifolius, R. sanguineus, R. sibiricus, R. spiralis, R. stenophyllus, R. subarcticus, R. thyrsiflorus, R. tomentellus, R. transitorius, R. triangulivalvis, R. utahensis, R. venosus, R. verticillatus, R. violascens
R. acetosa, R. acetosella, R. alpinus, R. altissimus, R. arcticus, R. beringensis, R. britannica, R. brownii, R. bucephalophorus, R. californicus, R. chrysocarpus, R. confertus, R. conglomeratus, R. crassus, R. cristatus, R. cuneifolius, R. densiflorus, R. dentatus, R. ellipticus, R. fascicularis, R. floridanus, R. fueginus, R. graminifolius, R. hastatulus, R. hesperius, R. hymenosepalus, R. kerneri, R. krausei, R. lacustris, R. lapponicus, R. longifolius, R. maritimus, R. mexicanus, R. nematopodus, R. obovatus, R. obtusifolius, R. occidentalis, R. orthoneurus, R. pallidus, R. palustris, R. paraguayensis, R. patientia, R. paucifolius, R. persicarioides, R. praecox, R. pseudonatronatus, R. pulcher, R. pycnanthus, R. salicifolius, R. sanguineus, R. sibiricus, R. spiralis, R. stenophyllus, R. subarcticus, R. thyrsiflorus, R. tomentellus, R. transitorius, R. triangulivalvis, R. utahensis, R. venosus, R. verticillatus, R. violascens
Synonyms Acetosa acetosella, Acetosa hastata, Acetosa vulgaris, R. acetosella var. vulgaris Lapathum crispum
Name authority Linnaeus: Sp. Pl. 1: 338. (1753) Linnaeus: Sp. Pl. 1: 335. (1753)
Web links