Taxonomic name: Cirsium arvense (L.) Scop.
Synonyms: Carduus arvensis (L.) Robson, Cirsium arvense var. argenteum (Vest) Fiori, Cirsium arvense var. horridum Wimmer & Grab., Cirsium arvense var. integrifolium Wimmer & Grab., Cirsium arvense var. mite Wimmer & Grab., Cirsium arvense var. vestitum Wimmer & Grab., Cirsium incanum (Gmel.) Fisch., Cirsium setosum (Willd.) Bess. ex Bieb., Serratula arvensis L.
Common names: Californian thistle (English), Canada thistle (English), Canadian thistle (English), creeping thistle (English), field thistle (English), perennial thistle (English)
Organism type: herb
Cirsium arvense is an herbaceous perennial in the Aster family. It occurs in nearly every upland herbaceous community within its range, and is a particular threat in grassland communities and riparian habitats. C. arvense is shade intolerant and can tolerate soils with up to 2% salt content. It grows on all but waterlogged, poorly aerated soils, including clay, clay loam, silt loam, sandy loam, sandy clay, sand dunes, gravel, limestone, and chalk, but not peat. It spreads primarily by vegetative means, and secondarily by seed. The seeds spread as a contaminant in agricultural seeds in hay and in cattle and horse droppings and on farm machinery. It produces an abundance of bristly-plumed seeds that are easily dispersed by the wind and they may also be transported by water.
Thunhorst and Swearingen (1997) report that C. arvense is a herbaceous perennial of the aster family with erect stems 0.5 - 1.0m tall, prickly leaves, and an extensive creeping rootstock. Stems are branched, often slightly hairy, and ridged. Leaves are lance-shaped, irregularly lobed with spiny, toothed margins and are borne singly and alternately along the stem. Rose-purple, lavender, or sometimes white flower heads appear from June through October, generally, and occur in rounded, umbrella-shaped clusters. The small, dry, single-seeded fruits, called achenes, are 0.3 - 0.5m long and have a feathery structure attached to the seed base. Nuzzo (1997) states that the plant is usually dioecious, with male and female flowers produced on separate plants. Female (pistillate) flowers can be readily distinguished from male (staminate) flowers by the absence of pollen (abundant in male flowers) and presence of a distinct vanilla-like fragrance.
Carduus spp., Cirsium vulgare
agricultural areas, riparian zones, ruderal/disturbed, urban areas, wetlands
Nuzzo (1997) cites that C. arvense occurs in nearly every upland herbaceous community within its range, and is a particular threat in prairie communities and riparian habitats. Throughout its range it is common on roadsides, in oldfields, croplands, and pastures, in deep, well-aerated, mesic soils. In eastern North America, it occasionally occurs in relatively dry habitats, including sand dunes and sandy fields, as well as on the edges of wet habitat, including stream banks, lakeshores, cleared swamps, muskegs and ditches. It is shade intolerant. It grows on all but waterlogged, poorly aerated soils, including clay, clay loam, silt loam, sandy loam, sandy clay, sand dunes, gravel, limestone, and chalk, but not peat. Zouhar (2001) reports that it can tolerate soils with up to 2% salt content. It grows best between 0 - 32 °Celsius. It tolerates annual precipitation ranging from 305-1015mm per year and grows best with 400-750mm of precipitation per year.
Nuzzo (1997) states that C. arvense threatens natural communities by directly competing with and displacing native vegetation, decreasing species diversity, and changing the structure and composition of some habitats. Species diversity in an "undisturbed" Colorado grassland was inversely proportional to the relative frequency of C. arvense. It presents an economic threat to farmers and ranchers. Infestations reduce crop yield through competition for water, nutrients and minerals, and through interference with harvest. In Canada, the major impact of C. arvense is in agricultural land, and in natural areas that have been disturbed or are undergoing restoration. In the United States, it is a host for bean aphid and stalk borer, insects that affect corn and tomatoes, and for sod-web worm, which damages corn. In Bulgaria, C. arvense is a host for the cucumber mosaic virus. In addition to reducing forage and pasture production, it may scratch grazing animals, resulting in small infections. Zouhar (2001) reports that it has been identified as a management problem in many national parks and on TNC (The Nature Conservancy) preserves in the upper Midwest, the Great Plains states, and the Pacific Northwest. Infestations of C. arvense may contribute to the elimination of endangered and/or endemic plant species, such as the Colorado butterfly plant in Wyoming.
Nuzzo (1997) reports that American Indians purportedly used an infusion of C. arvense roots for mouth diseases. The Chippewa considered it to be a "tonic, diuretic, and astringent". Young shoots and roots "can be used in the same ways as asparagus," and were eaten in Russia and by Native Americans. The nectar of its flowers is also said to make good honey. Zouhar (2001) reports that the weed has been used by native people in the northeastern United States in remedies for worms and poison-ivy (Toxicodendron radicans) and was used to make a mouthwash for children, a treatment for tuberculosis, and a tonic for gastrointestinal ailments.
In the United States native species of thistle, some of which are rare, can be confused with C. arvense so it should be accurately identified before any control is attempted.
Native range: Nuzzo (1997) reports that it is native to southeastern Europe, the eastern Mediterranean, and possibly northern Europe, western Asia, and northern Africa.
Known introduced range: It now has a near global distribution between 37 and 58-59 degrees N in the northern hemisphere, and at latitudes greater than 37 degrees S in the southern hemisphere, exclusive of Antarctica. It occurs throughout Europe, northern Africa, western and central Asia, northern India, Japan, China, northern North America, South Africa, New Zealand, Tasmania, and southeastern Australia.
Introduction pathways to new locations
Ship: Cirsium arvense is native to southeastern Europe and the eastern Mediterranean area, and was probably introduced to North America in the 1600's as a contaminant of crop seed and/or ship's ballast (Zouhar, 2001).
Local dispersal methods
Agriculture (local): Cirsium arvense seeds are spread as a contaminant in agricultural seeds and in hay (Nuzzo, 1997).
Consumption/excretion: C. arvense seeds may also be dispersed in cattle and horse droppings (Nuzzo, 1997).
Natural dispersal (local): Nuzzo (1997) reports that Cirsium arvense spreads primarily by vegetative growth of its roots. The root system can be extensive, growing horizontally as much as 6 m in one season. Most patches spread at the rate of 1-2 m/year.
On animals (local): Cirsium arvense produces an abundance of bristly-plumed seeds that are easily dispersed by the wind (Thunhorst and Swearingen, 1997).
Translocation of machinery/equipment (local): Cirsium arvense seeds can also be dispersed on farm machinery (Nuzzo, 1997).
Water currents: Cirsium arvense seeds may also be transported by water (Nuzzo, 1997).
Nuzzo (1997) states that the weed spreads primarily by vegetative means (by its root), and secondarily by seed. The root system can be extensive, growing horizontally as much as 6m in one season, and individual roots live up to two years. Most patches spread at the rate of 1-2 m/year. Under good growing conditions, female plants produce an average of 29 flowering shoots/square metre, each with an average of 41 heads/shoot and 59 seeds/head. A single plant produces an average of 1500 and up to 5300 seeds. Multiple plants produced 100-64,300 viable seeds/m2 in Australia and up to 30,200/m2 in Holland.
Germination may be affected by ecotype, temperature, day length, depth of seed burial, substrate stratification, and seed freshness. Seeds from "male" plants are smaller and percent germination is lower. Seeds germinate best in warm temperatures 20 - 40 degrees Celsius, with alternating light and dark periods. At lower temperatures germination is aided by high light intensity. Germination at higher temperatures can help ensure that maximum germination takes place during warmer periods of the year. Seeds are somewhat tolerant of heat, and some were still viable after 10 minutes at 102 degrees Celsius and 2 minutes at 262 degrees Celsius, although viability was decreased at these temperatures compared to unheated controls. The seeds germinate over a wide range of soil moisture.
Compiled by: National Biological Information Infrastructure (NBII) & IUCN/SSC Invasive Species Specialist Group (ISSG)
Last Modified: Monday, 16 August 2010