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This description provides characteristics that may be relevant to fire ecology and is not meant for identification. Keys for identification are available (e.g., [42,47,56,57,85,150]). Yellow salsify hybrids are described in a review by Clements and others [25].
Yellow salsify grows as an annual, biennial, or monocarpic perennial [25,51,56,106,121]. Plants grow between 12 and 39 inches (30-100 cm) tall [47,155]. In its first year(s), yellow salsify produces an erect rosette of grass-like leaves. Plants may remain vegetative for up to 10 years before flowering. After flowering, yellow salsify dies [25,51].
Yellow salsify produces ascending, leafy, and sometimes branched stems that exude a milky latex sap when broken [7,56,121,123]. Alternate leaves are narrow, measure 0.4 to 12 inches (1-30 cm) long, and are tapered from base to tip [35,107,121]. Young leaves can be hairy [121], but mature leaves are waxy [149]. Head flowers occur at the stem ends on inflated peduncles [63]. Heads measure up to 2.2 inches (5.5 cm) in diameter and are comprised of only ray flowers [121,145]. Flowers open early in the day and close by early afternoon and may not open during cloudy or rainy days [74,121].
Yellow salsify produces achenes that measure 1 to 1.6 inches (25-40 mm) long. Achenes are attached to a large feathery pappus that may reach 4 inches (10 cm) in diameter at maturity [12,44,57,121]. When achenes mature, the base of the flower reflexes, forming a dandelion-like ball of fruits [35,47]. Seeds produced in abandoned fields in Michigan weighed an average of 6.5 mg [50]. Seed placement within the flower affects its weight; mass gradually increases from the center to the periphery of the flower head [88,94].
© Kenneth Chamberlain, Ohio State Weed Lab Archive, Ohio State University
Yellow salsify taproots are described as stout, fleshy, thick, and long [44,47,107,145]. On disturbed sites in Utah, yellow salsify roots were often "heavily" infected with mycorrhizae [118]. As of this writing (2008), no excavation studies reported taproot size or rooting depth for yellow salsify rosettes or flowering plants.
© Michael Shephard, USDA Forest Service, Bugwood.org
Yellow salsify occurs as a nonnative species throughout most of the United States and Canada. Extreme northwestern and southeastern distributions are tentative. Yellow salsify occurs in Alaska according to maps presented by the United States Department of Agriculture [147] but not according to the distribution map presented by the Flora of North America [39]. In Canada, yellow salsify occurs in all provinces and territories except Nunavut [39]. In the lower 48 US states, yellow salsify occupies all but Mississippi, Alabama, South Carolina, Florida, and maybe Georgia [39,147]. Yellow salsify does not occur in Hawaii [147].
Throughout most of its range, yellow salsify is described as infrequent, occasional, locally common, or scattered [17,56,63,123,155,159]. There are also reports of yellow salsify as common and widespread (Mahler 1988, as cited in [35]),[74,104], and large populations are reported from the southern Kootenay, Thompson-Nicola, and Okanagan regions of British Columbia [148].
According to a review by Clements and others [25], yellow salsify was introduced to North America as a garden plant in the early 1900s. Spread was likely from east to west, as this is was the pattern in the Pacific Northwest [40]. Plants Database provides a distributional map of yellow salsify and its hybrids.
Fire adaptations: Yellow salsify is common in early postfire communities [32,59,80,111]. Because yellow salsify does not produce a persistent seed bank [20,25,51], establishment on burned sites is primarily from off-site seed. However, in a controlled study, yellow salsify seeds emerged from soil heated for 1 hour at 120 °F (50 °C), suggesting that seed in the litter or soil may survive a low-severity fire [22]. For additional information, see Plant Response to Fire.
FIRE REGIMES: The prevailing fire regime in which yellow salsify evolved is not described in the available literature. FIRE REGIMES in North American yellow salsify habitats are difficult to characterize, since it is possible in nearly any vegetation type. Because yellow salsify is a rapidly reproducing, early-seral species, it is unlikely that frequent fire would eliminate it. Elimination of the seed source is the only way yellow salsify could be lost from a community, and any disturbance by animals or extreme weather events has the potential of providing conditions for yellow salsify establishment, and with successful establishment a potential seed source. It is not likely that fire is necessary for the maintenance of yellow salsify habitats. Likely both short and long fire-return intervals would be tolerated.
Yellow salsify fuel characteristics were not described in the reviewed literature. However, dense populations are extremely rare, suggesting that yellow salsify has little effect on fuels or FIRE REGIMES where it occurs. Find fire regime information for the plant communities in which this species may occur by entering the species name in the FEIS home page under "Find FIRE REGIMES".
Fire is not a likely control method for yellow salsify. While fire would likely kill yellow salsify plants and most of its recently shed seed, dispersal and establishment from an off-site seed source is probable. It is possible that postfire seeding and/or grazing could be used to decrease yellow salsify abundance on burned sites. Yellow salsify frequency was lower on unseeded than on seeded burned sites in Daggett County, Utah. Mature Colorado pinyon-Utah juniper woodlands burned in 1976 were dominated by cheatgrass by 1986. The cheatgrass-dominated site was burned in June of 1990. A portion of burned sites was seeded with mixed grasses and forbs. Six years later, frequency values for yellow salsify were nearly double on unseeded than on seeded burned areas [45].
Grazing on burned sites with yellow salsify is likely to occur. In the foothills of Oregon's Wallowa Mountains, yellow salsify made up 25% of mule deer and elk diets from March to July. Yellow salsify was predominant in an area clearcut and burned 4 years prior to the study [100]. In the Sun River area of west-central Montana, yellow salsify was important in elk, mule deer, and bighorn sheep winter diets. Yellow salsify was consumed most in 40- to 50-year-old burn sites dominated by snowberry (Symphoricarpos spp.) and bluebunch wheatgrass [132]. Yellow salsify was utilized extensively by mule deer and domestic sheep on a very disturbed site in the Tahoe National Forest that was burned in a 1978 wildfire, logged in 1979, slash burned in 1980, and planted to ponderosa pine in 1981. By 1989, yellow salsify was nearly restricted to fenced areas [91].
Throughout its range, yellow salsify is most often described in disturbed areas such as roadsides, fields, and vacant lots [47,63,104,144,150]. However it is also described in open, dry sites that may or may not have been recently disturbed [42,57,152,153,155].
Climate: The ubiquitous distribution of yellow salsify suggests a broad tolerance of climatic conditions. Optimal growing conditions in yellow salsify's native European habitats include long days, cool temperatures, and moderate moisture. In Europe, yellow salsify reaches its maximum abundance between 40 and 50° N latitude [1]. In North America, yellow salsify occurs in similar habitats but also much harsher environments. Yellow salsify occurs on glacial moraine mounds in Powell County, Montana, where microsites can be hot and dry or cool and mesic. In microsites occupied by yellow salsify, soil moisture content averages ranged from 7.2% to 20.3%, and the highest soil surface temperature was 109 °F (42.5 °C) in August [11]. Yellow salsify leaves have a wax coating nearly identical to that of Jack-go-to-bed-at-noon. In a controlled study, the abundance and size of Jack-go-to-bed-at-noon wax crystals increased with soil moisture stress and decreased with decreased light intensity [149]. Yellow salsify may also regulate the size and abundance of its wax crystals to minimize water loss in harsh environments.
Elevation: In North America, yellow salsify primarily occupies habitats at elevations from 30 to 8,200 feet (10-2,500 m) [39].
Elevation range for yellow salsify in parts of the western United States State, region Elevation range (feet) Arizona 3,500-7,500 [66]Grand Canyon region
2,800-8,200 [138] California 0-8,860 [56] Colorado 4,500-10,500 [54] Nevada 3,900-9,500 [63] New Mexico 4,500-7,500 [85] Utah 4,490-10,500 [155]Uinta Basin
4,700-8,000 [44]Soil: Yellow salsify grows on a wide variety of soil types, but likely cannot tolerate saturated or anaerobic soil conditions. Textures from sand to clay loam are tolerated [148]. In central and eastern Canada, yellow salsify occurs on limestone soils [148]. In Park City, Utah, yellow salsify grows on silver, lead, and zinc mine dumps [3].
Anaerobic conditions induced secondary dormancy in yellow salsify seeds collected from the Canoe and Williams lake areas of British Columbia. After 3 to 4 days in deaerated water, almost no seed germinated. After 12 days seed viability was lost completely [122]. Along the Loup Rivers of central Nebraska, yellow salsify occupied sites where the water table was 0 to 4 inches (10 cm) deep and sites with a water table over 40 inches (101 cm) deep [109].
Impacts: Yellow salsify is rarely abundant in any vegetation type. While yellow salsify may be persistent in open grassland and shrubland habitats, it rarely occupies much cover. Impacts on native vegetation and/or ecosystem processes were not noted in the available literature. In a Montana flora, yellow salsify was referred to as a "harmless" introduced species [74].
In many cases, yellow salsify is restricted to disturbed sites. In a survey of roadsides and disturbed sites in Yellowstone National Park and the Gallatin National Forest, yellow salsify occurred on roadsides and in clearcuts but abundance decreased from disturbed sites to the interior lodgepole pine (Pinus contorta)/antelope bitterbrush forests [117]. In Glacier National Park, yellow salsify occurred on roadsides but not at distances 7 feet (2 m) into rough fescue-Idaho fescue grasslands [146]. However, yellow salsify was 1 of 3 nonnative species in remote, open, old-growth ponderosa pine stands on the North Rim of Grand Canyon National Park that were protected from logging and grazing since the mid-1930s [78]. Large yellow salsify populations are reported from British Columbia's southern Kootenay, Thompson-Nicola, and Okanagan regions [148].
Control: Limiting disturbances may be the most successful and most economical method of yellow salsify control. Some suggest that yellow salsify is not "aggressive" and that "control is seldom necessary" [145]. In any control or management plans, yellow salsify's importance to wildlife should be considered. Potential control methods are discussed below.
Prevention: Studies and observations suggest that yellow salsify's survival, growth, and reproduction may be reduced by the presence of neighboring vegetation. After 10 years of observations in Swift Current, Saskatchewan, researchers noted that yellow salsify spread in "overgrazed" sites with "weakened" grasses [18]. In a wind tunnel experiment, the number of yellow salsify seeds dispersing beyond neighboring vegetation decreased significantly (P<0.01) with the increasing height of neighboring vegetation [33]. In another experiment, the presence of neighboring vegetation affected yellow salsify survival, growth, and reproduction moreso than disturbances by plains pocket gopher activities. Survival, growth, and reproduction were all significantly greater (P<0.05) when yellow salsify grew without other vegetation [127].
Integrated management: Upadhyaya and others suggest that herbicides and grazing can be used together to control yellow salsify [148].
Physical/mechanical: Yellow salsify is not a likely problem in cultivated fields but could persist in no-till systems [108].
Fire: See Fire Management Considerations.
Biological: Livestock and wildlife utilize yellow salsify, sometimes extensively. Flower and/or seed heads are consumed by sage-grouse [119], dusky grouse [29], pronghorn [16], and white-tailed deer [128]. Native and nonnative herbivores may have played a role in limiting yellow salsify's abundance. However, the effects of grazing on yellow salsify are inconsistent. While herbivores likely eliminated portions of the season's seed, they also create disturbances and openings in canopy cover and may aid in seed dispersal. Grazing animal, intensity, and timing may all affect the usefulness of grazing to reduce yellow salsify abundance. In simulated grazing trials, 3 years of intense, early-season grazing decreased yellow salsify density by 25% to 50% (Blumenauer, personal communication, cited in [25]),[148].
Chemical: Herbicide effectiveness on yellow salsify is discussed in these references: [99,148].
Cultural: See Prevention. No additional information is available on this topic.
Yellow salsify provides forage for native ungulates, small mammals, birds, and livestock and may also be consumed by bears. Seeds, flowers, foliage, and roots are eaten [74,87,145].
Native ungulates: Although rarely abundant, yellow salsify is often found in elk, deer, bighorn sheep, pronghorn, and wild horse diets. Yellow salsify received consistent low levels of use by elk and mule deer in Montana's Missouri River Breaks, although its cover was less than 2% in all vegetation types studied [82]. In the Sun River area of west-central Montana, yellow salsify was important in elk, mule deer, and bighorn sheep winter diets. It was consumed most in 40- to 50-year-old burned sites dominated by snowberry and bluebunch wheatgrass [132]. Yellow salsify was utilized extensively by mule deer on a very disturbed site in the Tahoe National Forest. The site was burned by a wildfire in 1978, logged in 1979, slash burned in 1980, and planted to ponderosa pine in 1981. By 1989, yellow salsify was nearly restricted to fenced areas [91]. On low-elevation winter range in north-central New Mexico, yellow salsify made up only a trace of the available forage but made up 9% of elk, 16% of mule deer, 17% of pronghorn, and 6% of wild horse diets [136]. In the same area, pronghorn diets contained significantly (P<0.05) more yellow salsify (16% by weight) in a year when precipitation was 49% of normal than in a year when precipitation was 197% of normal (4% by weight) [137].
Elk: Yellow salsify made up 25% of elk diets from March to July in the foothills of Oregon's Wallowa Mountains. From mid-May to June, yellow salsify was 1 of the 2 most important forage species. Yellow salsify was dominant on the site clearcut and burned 4 years prior to the study [100]. In June in Montana's Sapphire Mountains, yellow salsify had an elk preference index of 38. An index value of 1 or more indicated preference [83]. On the Blacktail Plateau in northern Yellowstone National Park, yellow salsify was found significantly more often (P<0.05) on protected than on grazed sites; however, it was not eliminated from sites where elk density averaged 15 individuals/km² [134].
Deer: Studies from Oregon to Minnesota report yellow salsify in deer diets. Yellow salsify made up 25% of mule deer diets from March to July in the foothills of the Wallowa Mountains [100]. In the Bridger Mountains of southwestern Montana, yellow salsify averaged 12% of the volume of 6 mule deer rumen samples [157]. From 6 mule deer rumens collected in the summer from the Snowy Mountains of central Montana, yellow salsify made up 17% of rumen contents. In 3 fall-collected mule deer rumens, composition was 33% yellow salsify. White-tailed deer rumens collected in the same seasons contained almost no yellow salsify [61]. In the Bear Paw Mountains of north-central Montana, yellow salsify was 41% of the total volume of mule deer summer diets. Yellow salsify made up only a trace of the volume of fall and winter diets [86]. Yellow salsify was the most heavily used spring forb by white-tailed deer in the Missouri River bottomlands of north-central Montana. Yellow salsify volume averaged 15% in 13 spring-collected rumen samples [2]. In an old field in Minnesota's Cedar Creek Natural History Area, white-tailed deer often consumed yellow salsify flowers [128].
Pronghorn: Pronghorn diets often include yellow salsify in the summer. In south-central Alberta, the volume of yellow salsify averaged 9% in summer pronghorn diets. In other seasons, yellow salsify volume was less than 1% [102]. The volume of yellow salsify reached a maximum of 18% in pronghorn rumens collected from central Montana in August [156]. In Petroleum County, Montana, the maximum volume of yellow salsify was 21.5% in summer-collected rumens [26]. Yellow salsify was one of the most important pronghorn forages in 1 of the 2 years of observations made in South Dakota's Wind Cave National Park. Pronghorn consumed flower buds; by late summer, some plants were missing up to 6 flower stalks. Yellow salsify cover was less than 10.5% in the area [16].
Other mammals: Small and large mammals may feed on yellow salsify. Yellow salsify made up a minor component of grizzly bear scat collected in the Greater Yellowstone ecosystem [87]. In laboratory feeding trials, plains pocket gophers trapped from east-central Minnesota's Cedar Creek Natural History Area consumed large quantities of yellow salsify [9]. In a 10-year-old field in southwestern Michigan, between 3.1% and 8.4% of seeds were removed/dish/day by primarily deer mice. Differences in vegetation cover resulted in different amounts of seed removal [103].
Birds: Yellow salsify is important in the diets of juvenile and adult sharp-tailed grouse, sage-grouse, and dusky grouse. In northeastern Montana, the occurrence of yellow salsify was as high as 9% in the crops of juvenile and adult sharp-tailed grouse collected in September [101]. In the summer on the Valentine National Wildlife Refuge in north-central Nebraska, the occurrence of goatsbeard averaged 13% in young and 34.1% in adult sharp-tailed grouse diets [70]. Near Savery, Wyoming, yellow salsify occurred in all potential sage-grouse and sharp-tailed grouse habitats surveyed, but was more abundant in habitats selected by sage-grouse broods [68].
In Idaho and Montana, yellow salsify is an important juvenile sage-grouse food. In southeastern Idaho, yellow salsify made up the greatest volume (27%) and frequency (56%) in 6-week-old sage-grouse diets. Flower buds were preferred over stems and leaves [67]. In the Medicine Lodge Area of Clark County, Idaho, the frequency of yellow salsify in the diets of sage-grouse chicks was 23% [46]. Yellow salsify flower buds were the most preferred food of juvenile sage-grouse in central Montana. Yellow salsify made up a maximum average frequency and volume of 83% and 30%, respectively, in the crops of chicks 5 to 8 weeks old. In the rest of the juvenile age classes, the average yellow salsify frequencies were 41% to 60%. Yellow salsify frequency was 60% in the crops of adult sage-grouse killed in August [119]. In another sage-grouse study in central Montana, the frequency of yellow salsify was 39% to 71%, and the volume was 20% to 25% in June to August sage-grouse diets. Spring and fall diets had much lower amounts of yellow salsify [151].
In Wallowa County, Oregon, yellow salsify was frequent in the fall diets of dusky grouse. Dusky grouse fed primarily on seed heads, and of the 145 crops analyzed, yellow salsify frequency averaged 41%. Yellow salsify was more frequent in mature and immature female crops than in mature and immature male crops [29].
Livestock: Cattle and domestic sheep will consume yellow salsify. In the Missouri River Breaks of Montana, yellow salsify received consistent, low-level use by cattle, although its cover was less than 2% in all vegetation types studied [82]. In prairie and sagebrush habitats of north-central Montana, yellow salsify was a common forb in summer cattle diets [37]. Yellow salsify was utilized extensively by domestic sheep on a site in the Tahoe National Forest that was highly disturbed. Within 8 years of the last disturbance, yellow salsify was nearly restricted to fenced areas [91]. In north-central New Mexico, yellow salsify was more prevalent in cattle and domestic sheep diets during a drought year than an above-average precipitation year. Cattle diets were 12% yellow salsify in the drought year and 2% in the wet year. Domestic sheep diets were 7% yellow salsify in the drought year and only a trace in the wet year. Yellow salsify was rare in pastures but averaged 4% cover along roadsides [137].
Given a seed source and a canopy opening, yellow salsify is a potential
inhabitant of nearly any vegetation or community type. It has been described on
open beaches and in grasslands, shrublands, woodlands, and coniferous forests
throughout North America [63,77,78,79,148,160]. Yellow salsify is common in
abandoned agricultural fields and many studies have been conducted
in this environment. Throughout this review, the age of old fields
refers to time since abandonment or time since last cultivation.
For example, "1-year-old fields" have been out of
cultivation or left fallow for 1 year.
Disturbed areas are typical yellow salsify habitats, but in open forests
and woodlands, shrublands, and grasslands yellow salsify may be persistent.
In a survey of disturbed sites in Yellowstone National Park and the adjacent
Gallatin National Forest, yellow salsify occurred on roadsides and in clearcuts,
but abundance decreased from disturbed sites to the forest interior [117]. In
Glacier National Park, yellow salsify occurred adjacent to roadsides but not at
sites 7 feet (2 m) into intact rough fescue-Idaho fescue (Festuca altaica-F.
idahoensis) grasslands [146]. However, yellow salsify was 1 of 3 nonnative species
noted in remote, open, old-growth ponderosa pine (Pinus ponderosa) stands
in Grand Canyon National Park, which were closed to grazing and protected from
logging by the mid-1930s [78].
While often frequent in disturbed or open habitats, yellow salsify rarely
occupies much of the total vegetation cover, regardless of the habitat type or
disturbance regime. Yellow salsify was the second most frequent nonnative
species in Utah's Grand Staircase-Escalante National Monument, but
average cover was less than 1% [21]. In a survey of disturbed sites in Utah,
yellow salsify occurred on just 2 of 7 disturbed sites, and maximum average cover
on the sites was 0.01% [118].
Yellow salsify reproduces solely by seed [25].
Pollination and breeding system: Yellow salsify produces perfect flowers [47,155]. Self pollination and cross pollination are possible [25,28]. Yellow salsify flowers on the Palouse Prairie of Idaho and Washington were visited by a variety of generalist bees and flies (Cook, personal observation, cited in [28]).
Seed production: Generally yellow salsify is highly fertile; typically 97% or more of its flowers produce fruits [115]. Flower and seed production can be affected by rosette size, temperature, day length, season, time since last disturbance, herbivory, and predation.
In eastern Washington and western Idaho, yellow salsify plants averaged more than 100 ray flowers/head [115]. In old fields in Michigan, yellow salsify produced an average of 90 seeds/plant [50]. In an abandoned pasture in Peterborough County, Ontario, plants produced 35 to 88 seeds/flower head [88]. In the foothills above Salt Lake City, Utah, yellow salsify produced 1 to 14 flower heads and 20 to 127 seeds/head [94]. In North Dakota, average-sized yellow salsify produced 150 seeds in outer flowers and 330 seeds in inner flowers. Seeds produced by outer flowers were heavier than those from inner flowers, but seed weight did not affect germination. The study plant in North Dakota produced just 5 flower heads [140].
Seed production may be greater from larger plants, during long days, and in very early-seral habitats. Probability of yellow salsify flowering increased with increased rosette size in old fields in Michigan. The minimum root crown diameter for flowering was 0.11 cm. The maximum probability of flowering was 0.87 for plants with a root crown diameter greater than 0.7 cm; however, flowering probability decreased when rosette diameters exceeded 0.7 cm. Yellow salsify plants grown in a greenhouse failed to flower although they surpassed the minimum root crown diameter required for flowering. A vernalization period may be required for flowering in temperate climates [48,51]. Day length can also affect yellow salsify flowering. Flowering increased with increasing day lengths from 10 to 14.5 hours. As day length decreases, yellow salsify is more likely to remain a rosette and potentially delay flowering to the next year [1]. For yellow salsify populations near Salt Lake City, Utah, the number of seeds produced/flower head decreased significantly (P<0.01) as the season progressed [94]. In old fields in southwestern Michigan, yellow salsify seed production decreased with increasing old field age. The 3 flowering yellow salsify in 15-year-old fields produced an average of 73 seeds each. In 1-year-old fields, 21 yellow salsify plants flowered and produced an average of 127 seeds each [50].
Herbivory/predation: Effects of herbivory on yellow salsify are variable, but the presence of seed predators will reduced the number of yellow salsify seeds. In an old field in Minnesota's Cedar Creek Natural History Area, researchers simulated herbivory on yellow salsify leaves and roots. Treatments included leaf removal of 25% and 75%, root removal of 25% and 75%, and leaf and root removal of 25%. Flower production was greatest for control plants and least for any treatments involving root removal. Plants with 1 or more flowers removed by herbivores, primarily white-tailed deer, were larger and produced more flowers than those without flowers removed, regardless of the simulated herbivory treatment [128]. In the Bison Flats area of South Dakota's Wind Cave National Park, yellow salsify was one of the most important pronghorn forages in 1 of 2 observed feeding years. By late summer, some plants lost up to 6 flower heads [16]. Pronghorn and deer are not the only yellow salsify herbivores. For more on this topic, see IMPORTANCE TO LIVESTOCK AND WILDLIFE.
Predation on yellow salsify seeds can be as high as 100%. Presence of neighboring vegetation has been shown to affect predation rates, but not consistently. In southwestern Michigan old fields, 73% of yellow salsify seeds were removed within 24 hours when dishes of seeds were randomly arranged [50]. In a 10-year-old southwestern Michigan old field, more yellow salsify seeds were removed from undisturbed than disturbed sites. In plowed fields, areas of small disturbances, and in undisturbed vegetation 3.1%, 5.5%, and 8.4% of seeds were removed/dish/day, respectively. Through comparisons of visual evidence at feeding sites and during controlled laboratory studies, researchers concluded that deer mice were the primary seed predators. At most feeding sites, there were seed coats present, suggesting that seeds were not cached. Predation patterns were patchy and once a feeding source was located it was exploited, which may allow for pockets of seed survival and a patchy distribution of seedlings on the landscape [103]. However, if seeds do not germinate rapidly, seed predation may exceed 95% regardless of the presence of neighboring vegetation. In old fields abandoned for 20 years or more near Guelph, Ontario, yellow salsify seeds glued to fish line were left available to predators for 10 months. After this time, 95% of yellow salsify seeds were removed in areas with intact vegetation, and 100% of seeds were removed in areas of cleared vegetation [126].
Seed dispersal: Yellow salsify achenes break easily from the flower and can travel long distances in the wind [44]. Under controlled conditions, yellow salsify achenes had a slow descent velocity, which relates to a high potential dispersal ability [4]. While 65% to 90% of yellow salsify seeds typically fall within 16 feet (5 m) of the parent plant, seeds may travel more than 820 feet (250 m) in upward wind gusts [51]. On the tallgrass Cayler Prairie in Dickinson County, Iowa, yellow salsify seeds were found "several hundred meters" from the nearest parent plant [120]. In the South Platte River Basin of north-central Colorado, 12% of all seeds caught in aerial seed traps were yellow salsify or dandelion (Taraxacum officinale). Yellow salsify seeds were not collected from samples taken from the water or channel bed, suggesting that dispersal in water is unlikely [97].
Dispersal of yellow salsify seed by animals was not mentioned in the available literature. Dispersal in fur or feathers is possible, and if seeds survive passage through the digestive tract, dispersal through animal waste is possible as well. A large variety of animals feed on yellow salsify flowers and seeds. For more on this, see IMPORTANCE TO LIVESTOCK AND WILDLIFE.
Seed size, plant height, and neighboring vegetation can affect seed dispersal. For populations of yellow salsify in foothills above Salt Lake City, pappus radius decreased significantly (P<0.01) over the season. Although the pappus area was larger on heavier seeds, heavier seeds had a lower dispersal potential than lighter seeds. Seed release height may, however, compensate some for the dispersal of heavy seeds, since flower heads producing heavier seeds occurred higher above the ground than those producing lighter seeds (P<0.001) [93,94]. In a controlled wind tunnel experiment, as the height of neighboring vegetation increased the number of yellow salsify seeds dispersing beyond the neighboring vegetation decreased (P<0.01). Increased wind speeds and increased release distance from established vegetation, however, increased the percentage of seeds dispersing beyond the established vegetation [33].
Seed banking: Yellow salsify does not produce a large and/or persistent seed bank. Successful establishment and persistence of yellow salsify populations depends on the dispersal and germination of newly produced seed (Qi and Upadhyaya, unpublished data, cited in [148]),[25]. Seeds do not likely survive more than 1 to 2 years in the soil [51]. In a controlled study, yellow salsify seed germinated the first year soil was left fallow but did not germinate in any of the following years when soil was cultivated. The researcher concluded that yellow salsify seed dormancy is typically less than 1 year [20]. Yellow salsify seeds did not germinate after 3 or more months in the water of Washington's Chandler Power Canal. After 60 months of dry storage, yellow salsify seed germination was 55% [27].
A low density of yellow salsify emergents or seeds was recovered from grassland, shrubland, and forested sites in the Greater Yellowstone Ecosystem and British Columbia. A maximum of 13 yellow salsify seedlings/m² emerged from unburned soil samples collected in Idaho fescue/bluebunch wheatgrass (Pseudoroegneria spicata) habitats in Yellowstone. Although present in the aboveground vegetation, there were no yellow salsify emergents from burned or unburned soil samples collected in bluebunch wheatgrass/Sandberg bluegrass-needle-and-thread grass (Poa secunda-Hesperostipa comata) or subalpine fir/pinegrass (Abies lasiocarpa/Calamagrostis rubescens) habitats. For the effects of heating on soil-stored yellow salsify seed, see Plant response to fire [22]. In ungrazed to heavily grazed sites dominated by antelope bitterbrush (Purshia tridentata) in British Columbia's Okanogan Valley, the density of yellow salsify was 9 plants/m² in aboveground vegetation, and 1.8 seeds/m² were extracted from soil samples. Soils were sampled from 24 May to 4 June [24], which likely preceded substantial yellow salsify seed dispersal.
Germination: Yellow salsify seeds germinate best in moderate temperatures (59-72 °F (15-22°C)) [88,122], in full light conditions [49], and with burial in litter or soil up to 0.8 inch (2 cm) deep [49,122].
Yellow salsify seed dormancy is variable. Yellow salsify seeds collected from old fields in Michigan required 60 days of afterrippening to germinate in controlled conditions [51]. Upadhyaya and others [148] also reported short-term primary dormancy; however, yellow salsify seeds collected from an abandoned pasture in Peterborough County, Ontario, germinated at over 90% immediately after harvest [88]. Secondary dormancy in yellow salsify seeds can be induced by low-oxygen environments [148]. Anaerobic conditions induced secondary dormancy in yellow salsify seeds collected from the Canoe and Williams Lake areas of British Columbia. After 3 to 4 days in deaerated water, almost no seed germinated. Stratification treatments successfully broke the secondary dormancy. After 12 days in water, yellow salsify seed viability was lost [122].
Studies have shown that germination of yellow salsify decreases with extreme temperatures, increased depth of burial, decreased light availability, and with established vegetation and litter. Seed size and moisture did not restrict germination.
The optimum germination temperature for yellow salsify seeds collected from British Columbia's Canoe and Williams lake areas was 59 °F (15 °C). Seeds did not germinate at temperatures of 41 °F (5 °C) or 86 °F (30 °C). Seed exposed to 41 °F (5 °C) retained their viability, but those exposed to 86 °F (30 °C) showed high levels of decay. Emergence was 80% for seeds planted 0.8 inch (2 cm) deep; no seedlings emerged when planting depths exceeded 2 inches (5 cm). Seeds at 3 inches (8 cm) deep germinated but failed to emerge [122]. Dark conditions decreased germination, and seed size did not affect germination of yellow salsify seeds collected from populations in Michigan and/or Ohio [49].
Germination of small, medium, and large yellow salsify seeds in dark and light conditions at 25/15 °C [49] Seed size Average weightGermination rates of over 90% were obtained from yellow salsify seeds collected from old fields in Peterborough County, Ontario, immediately after and up to 2 months after seed harvest in late June or early July. Seeds were kept at 72 °F (22 °C) and given 16 hours of light. Seed size and moisture conditions did not affect germination [88].
Number of yellow salsify germinants and number of days to half emergence in moist, normal, and dry conditions [88] Parameter evaluated MoistIn a greenhouse study, yellow salsify emergence was reduced when both established vegetation and litter were present. Emergence of yellow salsify was greatest in trays with a straw litter cover and lowest in trays with established Kentucky bluegrass (Poa pratensis) and litter. Emergence in established Kentucky bluegrass without litter was similar to that in trays of bare soil. The fate of seedlings in this study is discussed below [49].
Seedling establishment/growth: Predictions regarding yellow salsify's survival and flowering success can be made from the diameter of its root crown as a rosette [48,51]. Successful yellow salsify seedling establishment and growth, however, are affected by temperature, litter, neighboring vegetation, seed predation, and herbivory. In a controlled study, yellow salsify seedling shoot biomass increased with increasing nighttime temperatures. Seedlings were grown from seed collected in Utah's Uinta National Forest and subjected to nighttime temperatures from 36 to 68 °F (2-20 °C). After 8 weeks of growth, seedling shoots averaged 0.48 g at the highest and 0.15 g at the lowest nighttime temperatures [92]. Moisture conditions in a controlled study did not dramatically affect seedling height or weight [88].
Probability of yellow salsify survival and flowering generally increase as the rosette root crown diameter increases. A minimum root crown diameter of 0.1 cm was required in the previous year for flowering to occur; however, the flowering probability was low, 0.19, for root crown diameters of 0.1 to 0.3 cm. The maximum probability of flowering, 0.87, occurred when root crown diameters were 0.7 cm, but the flowering probability decreased when root crown diameters exceeded 0.7 cm. The probability of yellow salsify dying before flowering was low, 0 to 0.16, regardless of root crown diameter. Non-flowering plants did not typically die but remained vegetative until the next year. The researcher predicted that yellow salsify could remain vegetative for up to 10 years before flowering [48,51].
Presence of established vegetation has been shown to decrease yellow salsify seedling size and seedling survival in greenhouse and field studies. In a greenhouse study, yellow salsify seedling biomass was greatest in trays with straw litter or with bare soil and lowest in trays with established Kentucky bluegrass. Initial seed size did not substantially affect seedling biomass in trays with established Kentucky bluegrass. Seedling growth in areas with litter or vegetation cover may be better predicted by early seedling weight than seed weight [49].
Mean final dry weights (mg after 78 days) of yellow salsify seedlings* in greenhouse trays with differing types of cover [49] Seed size Ground cover type Bare Litter Vegetation Vegetation and litter Small 247 440 14.4 10.9 Medium 196 353 12.2 12.6 Large 133 268 10.6 13.9 *Seedlings were thinned to maximum density of 10 seedlings/tray (19 Ã 9 Ã 6 cm)In southwestern Michigan old fields, yellow salsify seedling emergence increased but the probability of survival and flowering decreased with increasing old field age. Researchers monitored yellow salsify emergence in seeded and in control plots in 1-year-old, 5-year-old, and 15-year-old fields. Yellow salsify established in open and vegetated patches of 1- and 15-year-old fields. In 15-year-old fields, the average probability of seedling survival was 0.17. The survival probability was greatest, 0.67, on bare ground and lowest on vegetated areas, 0.14. Yellow salsify reproductive output was lowest in the 15-year-old fields, a pattern likely to lead to the eventual local extinction of yellow salsify. Researchers reported that because yellow salsify does not produce a persistent seed bank and relies on seed dispersal to occupy disturbed sites, it is not typical in old fields until 4 to 10 years after abandonment [50,51]. Seed production was also affected by old field age.
Yellow salsify emergence, seedling survival, and flowering in old fields of increasing age in Michigan [50,51] 1-year-old 5-year-old 15-year-old Emerging seedlings/0.25 m²Seed predation affected seedling emergence more than the presence of neighboring vegetation in an abandoned pasture near Guelph, Ontario. When yellow salsify seeds were sown in an abandoned pasture, cages to reduce predation significantly (P<0.05) increased emergence [125].
Number of yellow salsify seedlings emerging/1000 seeds sown on sites with and without vegetation and/or predation [125] Vegetation/predation characteristics Ground cover intact/caged Ground cover removed/caged Ground cover intact/no cage Ground cover removed/no cage Average number of seedlings 800c 790c 20a 89b Values followed by different letters are significantly different (P<0.05).Yellow salsify is somewhat sensitive to defoliation and more sensitive to root damage. In simulated herbivory experiments on an old field in Minnesota's Cedar Creek Natural History Area, researchers removed 25% and 75% of leaves, 25% and 75% of roots, and 25% of both leaves and roots. Mortality of untreated plants and plants with 25% of leaves removed were not different; however, all other treatments led to mortality of ≥80% [128]. Information on flower production by experimental plants is available in Seed production.
Vegetative regeneration: Yellow salsify does not reproduce vegetatively [25].
Although yellow salsify is often found on open, disturbed sites, it is also found in relatively undisturbed sites and on sites with moderate canopy cover. Long-distance seed dispersal from more disturbed to less disturbed sites may play a role in yellow salsify's persistence.
Shading: While often most abundant in open sites, yellow salsify is somewhat shade tolerant and occurs in woodlands and forests [77,148]. In Theodore Roosevelt National Park, yellow salsify was most frequent in grasslands with little or no shrub or tree cover but occurred on some transects in all 11 vegetation types, including those dominated by sagebrush (Artemisia spp.), rubber rabbitbrush (Ericameria nauseousa subsp. nauseousa var. nauseousa), Rocky Mountain juniper (Juniperus scopulorum), and eastern cottonwood (Populus deltoides) [77]. At Point of the Mountain, near Salt Lake City, Utah, yellow salsify seedlings were observed under the canopy of 9-year-old big sagebrush (A. tridentata) [154].
In a ponderosa pine/common snowberry (Pinus ponderosa/Symphoricarpos albus) community type in the foothills of eastern Oregon's Wallowa Mountains, trenching to reduce root competition increased yellow salsify density whereas thinning reduced yellow salsify density. Thinning treatments reduced tree density by about half. Yellow salsify increased significantly on trenched plots (P<0.05) [129].
Yellow salsify density (number of plants/m²) one year after treaments [129] Control Thinned only Trenched only Thinned and trenched 0.8 0.2 7.9 1.1Disturbances: Disturbed sites are common yellow salsify habitats, but persistence on disturbed sites is indefinite, and long-distance seed dispersal from disturbed sites into relatively open, undisturbed sites is common.
Yellow salsify is common on severely disturbed sites. In north-central New Mexico, yellow salsify made up only a trace of vegetative cover in pastures, but cover was 4% along roadsides [137]. In Utah, yellow salsify is a disturbance indicator on rangelands [116]. In southwestern Montana mining towns abandoned 45 to 77 years earlier, yellow salsify occurred on severely disturbed old roads and moderately disturbed areas near abandoned buildings. It did not occur in relatively undisturbed sites outside of the towns [69]. In Billings County, North Dakota, yellow salsify occurred in 3 of 4 surveyed prairie dog towns. Towns are continually disturbed by prairie dog digging and burrowing, and by prairie dog and livestock grazing [143].
Relatively undisturbed sites, however, are also potential yellow salsify habitat. Yellow salsify occurred on both recently disturbed and relatively undisturbed portions of big sagebrush and antelope bitterbrush shrublands on the Columbia River Plain of Washington. Researchers were unsure if yellow salsify would persist on undisturbed sites without seed input from disturbed sites [15]. In the Upper South Platte Watershed of central Colorado, yellow salsify occurred in both disturbed and relatively undisturbed ponderosa pine/Douglas-fir (Pseudotsuga menziesii) forests. Yellow salsify occurred on 3 of 30 plots within the Turkey Creek site that had been logged, grazed, burned, and used for recreation. On the relatively undisturbed Cheesman Lake plots, yellow salsify occurred on 9 of 30 plots [41]. On the North Rim of Grand Canyon National Park, yellow salsify was 1 of the 3 nonnative species noted in remote, open, old-growth ponderosa pine stands, although the area was closed to grazing and protected from logging since the mid-1930s [78].
Grazing: Yellow salsify is often considered an indicator or invader of heavily grazed sites in the West [73,95,105]. However, in several studies, yellow salsify was either absent or less abundant on grazed than ungrazed sites. Grazing pattern may affect changes in yellow salsify abundance. For more on the use of yellow salsify by livestock and wildlife, see IMPORTANCE TO LIVESTOCK AND WILDLIFE.
In mixed prairie vegetation in southeastern Alberta, yellow salsify cover was greatest on sites protected from large animal livestock grazing. On Chernozemic soils, yellow salsify cover was 0.2% on grazed and 1.2% on protected sites. On sites with Solonetzic soils, yellow salsify was absent from grazed sites and had 0.4% cover on protected sites. Litter biomass was greater on ungrazed than grazed sites but significantly greater (P<0.05) only on Chernozemic soils. Increased litter may have favored yellow salsify establishment on protected sites [158]. Yellow salsify was absent from Letterman's needlegrass (Achnatherum lettermanii)-Kentucky bluegrass grasslands southeast of Cedar City, Utah, subjected to long-term (over 90 years) domestic sheep grazing. Aboveground biomass of yellow salsify was 7 kg/ha on late-seral grasslands opposite the fence of the sheep-grazed area [14]. In semiarid western wheatgrass-bottlebrush squirreltail (Pascopyrum smithii-Elymus elymoides) grasslands of north-central Arizona, yellow salsify cover increased from 0% to 2% after 8 years of short-duration, high-impact cattle grazing [81].
Old field succession: Yellow salsify is typical in abandoned fields and pastures. Rarely is yellow salsify present and/or abundant in the first fallow year. In the early secondary succession of old fields, yellow salsify abundance commonly increases with increasing old field age. Yellow salsify has been observed in fields as old as 41 years. In southeastern Washington, yellow salsify was present in nearly all old fields sampled 1 to 52 years since abandonment. Cover and frequency were low (<1%) in the 1-year-old field. Cover and frequency of yellow salsify were 3% and 40%, respectively, 5 years after abandonment. In the 41-year-old field, cover was 2% and frequency 35%. In relatively undisturbed, presettlement habitats cover was 1% or less and frequency reached 12% [32]. In eastern South Dakota's Lake Andes National Wildlife Refuge, corn and soybean fields were seeded to native grasses in 1971; the importance of yellow salsify increased in each successive year from 1973 to 1975 [10]. Yellow salsify was abundant on old fields that averaged 26.7 years old in the Cedar Creek Natural History Area, southeastern Minnesota. The study evaluated 22 old fields 5 to 60 years old [43]. In Ottertail County, Minnesota, yellow salsify occurred in a 30-year-old field. Abundance was not reported [55].
Secondary succession in forests and woodlands: Logged and/or burned forests and woodlands are likely habitat for yellow salsify, often within 3 years of the disturbance. In the Wallowa Mountains, researchers named Kentucky bluegrass-yellow salsify the early-seral community present 4 years after cutting and burning in a ponderosa pine-common snowberry habitat type [100]. Yellow salsify was the most abundant nonnative 7 years after mixed-conifer forests were logged or logged and burned in California's Plumas National Forest. Yellow salsify did not occur in undisturbed, old-growth forests [65]. In California's Tahoe National Forest, yellow salsify occurred on sites visited in 1989 that were burned by a wildfire in 1978, logged in 1979, slash burned in 1980, and planted to ponderosa pine in 1981 [91]. Yellow salsify occurred on clearcuts in a mixed-conifer forest on the Challenge Experimental Forest in north-central California. Density was 33 plants/ha in the 3rd year after logging and 17 plants/ha 4 and 5 years after logging [90]. In central Idaho, yellow salsify occurred in early-seral communities within the western redcedar/Oregon boxwood (Thuja plicata/ Paxistima myrsinites) habitat type. Yellow salsify frequency was 4% on a site burned 3 years earlier and 12% in more mature communities dominated by mature shrubs and young conifers. Yellow salsify did not occur in mid-seral to near-climax communities [130]. Yellow salsify density increased dramatically in each of the 3 successive posttreatment years after anchor chaining in Colorado pinyon-Utah juniper (Pinus edulis-Juniperus osteosperma) woodlands near Ephraim, Utah. Chaining reduced the density of Utah juniper from 2,230 trees/ha to 186 trees/ha and Colorado pinyon trees from 620 trees/ha to 62 trees/ha [34].
The scientific name of yellow salsify is Tragopogon dubius Scop.
(Asteraceae) [39,62]. Within the Asteraceae family, yellow salsify
belongs to the Cichorieae or chicory tribe [7].
Hybrids:
Tragopogon miscellus Ownbey, Moscow salsify [31,115]
Tragopogon ÃÂ crantzii Dichlt. [62,150]
Tragopogon mirus Ownbey, remarkable salsify [31,115]
Moscow salsify is the name used for yellow salsify ÃÂ
Jack-go-to-bed-at-noon (Tragopogon lamottei)
hybrids that occur in parts of Washington, Idaho,
Montana, and Wyoming [31]. Tragopogon ÃÂ crantzii is
the name used for yellow salsify ÃÂ Jack-go-to-bed-at-noon
hybrids in the Great Lakes area [62,150]. Remarkable
salsify is the yellow salsify ÃÂ salsify (Tragopogon
porrifolius) hybrid. These hybrids are possible anywhere
the distributions of parent species overlap [31,115]. For
more on goatsbeard (Tragopogon spp.) hybrids, see the
following references: [38,110,115].
La barbaja mariella (Tragopogon dubius) ye una planta de la familia de les asteracees.
Planta compuesta, añal o bienal de 20-60 cm, de tarmu simple, mychas vegaes con fueyes del añu anterior na base; fueyes alternes, llanceolaes, estreches y largamente apuntaes, ensin dientes, abrazando siquier la metá del tarmu cola so base. Flores en primavera y branu, toes con llámina o lígula, mariella y estilos escuros, surdiendo d'una "copa" o receptáculu formáu por 8-12 hojitas o bráctees, muncho más llargues que les flores, triangulares y largamente apuntiaes, bien carauterístiques. Los frutos, casi cilíndricos, non peludos, porten un miriguanu de pelos plumosos, a la fin d'un rabillu finu.[1]
N'Austria, Bulgaria, República Checa, Francia, Alemaña, Grecia, Suiza, España, Hungría, Italia, ex Yugoslavia, Portugal, Rumanía, Rusia, Ucrania, Turquía. Introducida en Bélxica.[2] Na Península Ibérica en Castiella y Llión. Crez esvalixada en terrenes soleyeros de meruxes y nitrificaos pol home o animales. Montes secos, praderíes, comunidaes rurales.
Esta páxina forma parte del wikiproyeutu Botánica, un esfuerciu collaborativu col fin d'ameyorar y organizar tolos conteníos rellacionaos con esti tema. Visita la páxina d'alderique del proyeutu pa collaborar y facer entrugues o suxerencies. La barbaja mariella (Tragopogon dubius) ye una planta de la familia de les asteracees.
Tragopogon dubius és una espècie de planta composta nativa d'Europa meridional i Àsia central i occidental que habita tan al nord i al nord-oest de França. Encara que s'ha informat la seva presència al Caixmir i l'Índia, les últimes dades indiquen que les mostres d'aquestes àrees poden ser una espècie diferent. T. dubius ha estat introduïda a Amèrica del Nord, on s'ha generalitzat, s'informa de tot el territori continental dels Estats Units amb excepció d'uns pocs a l'extrem sud-est, i totes les províncies del Canadà, excepte Terranova i els territoris del nord.
Tragopogon dubius creix com a planta herbàcia anuals o biennals a vegades, aconseguint una altura de 20 a 60 cm en general, però de vegades gairebé un metre. Creix generalment en llocs càlids i protegits amb terra humida. La seva flor groga és de 4-6 cm de diàmetre, i és probable que sigui vist a finals de primavera o principis de l'estiu. Les flors s'obren al matí d'hora i amb freqüència de prop a la tarda. Més tard, la planta forma un cap de la llavor que s'assembla a la de la dent de lleó, però és clarament més gran. Les llavors pròpies (aquenis) són de 2-4 cm de llarg, però de pes ploma, pes aproximat de 8 mg cadascuna de mitjana. Hi ha alguna variació natural entre els aquenis centrals i perifèrics en la formació de llavors, amb els perifèrics sent generalment més fosc i més pesat, i que té una major concentració de compostos fenòlics, el que pot millorar el seu potencial de supervivència.
T. dubius és força semblant a la comuna T. pratensis, però té més bràctees i més vistoses darrere de la flor, una característica distintiva del gènere. Encara que no és molt estretament relacionat amb Tragopogon pratensis o T. porrifolius, T. dubius hibrida amb facilitat amb les dues, i a Amèrica del Nord els seus híbrids han donat lloc als híbrids T. mirus i T. miscellus.
A diferència d'altres espècies de Trapogon com Tragopogon porrifolius, T. dubius no és generalment considerada comestible, encara que l'arrel es pot menjar (crua o cuita) i també les tiges joves. No se'n coneixen usos medicinals. És considerada invasora en la majoria dels estats dels EUA i en algunes províncies canadenques com Ontàrio, Colúmbia Britànica i Alberta.
Tragopogon dubius és una espècie de planta composta nativa d'Europa meridional i Àsia central i occidental que habita tan al nord i al nord-oest de França. Encara que s'ha informat la seva presència al Caixmir i l'Índia, les últimes dades indiquen que les mostres d'aquestes àrees poden ser una espècie diferent. T. dubius ha estat introduïda a Amèrica del Nord, on s'ha generalitzat, s'informa de tot el territori continental dels Estats Units amb excepció d'uns pocs a l'extrem sud-est, i totes les províncies del Canadà, excepte Terranova i els territoris del nord.
Tragopogon dubius creix com a planta herbàcia anuals o biennals a vegades, aconseguint una altura de 20 a 60 cm en general, però de vegades gairebé un metre. Creix generalment en llocs càlids i protegits amb terra humida. La seva flor groga és de 4-6 cm de diàmetre, i és probable que sigui vist a finals de primavera o principis de l'estiu. Les flors s'obren al matí d'hora i amb freqüència de prop a la tarda. Més tard, la planta forma un cap de la llavor que s'assembla a la de la dent de lleó, però és clarament més gran. Les llavors pròpies (aquenis) són de 2-4 cm de llarg, però de pes ploma, pes aproximat de 8 mg cadascuna de mitjana. Hi ha alguna variació natural entre els aquenis centrals i perifèrics en la formació de llavors, amb els perifèrics sent generalment més fosc i més pesat, i que té una major concentració de compostos fenòlics, el que pot millorar el seu potencial de supervivència.
T. dubius és força semblant a la comuna T. pratensis, però té més bràctees i més vistoses darrere de la flor, una característica distintiva del gènere. Encara que no és molt estretament relacionat amb Tragopogon pratensis o T. porrifolius, T. dubius hibrida amb facilitat amb les dues, i a Amèrica del Nord els seus híbrids han donat lloc als híbrids T. mirus i T. miscellus.
A diferència d'altres espècies de Trapogon com Tragopogon porrifolius, T. dubius no és generalment considerada comestible, encara que l'arrel es pot menjar (crua o cuita) i també les tiges joves. No se'n coneixen usos medicinals. És considerada invasora en la majoria dels estats dels EUA i en algunes províncies canadenques com Ontàrio, Colúmbia Britànica i Alberta.
Kozí brada pochybná (Tragopogon dubius) je dvouletá, žlutě kvetoucí, planě rostoucí rostlina slunných a suchých míst. Je jedním ze tří druhů rodu kozí brada, které v české přírodě rostou, je považována za zdomácnělý archeofyt.[1]
Tento druh se vyskytuje jako původní téměř v celé Evropě, jen do Skandinávie a Pobaltí se dostala až druhotně. Dále východním směrem sahá její původní areál přes Malou Asii, Kavkaz, Ural, západ Sibiře a oblasti Střední Asie až po severozápad Číny. Kozí brada pochybná byla také hojně zavlečena do místa mimo Evropu, např. do Severní a Jižní Ameriky, Jižní Afriky, Indie, Austrálie i na Nový Zéland. V České republice je poměrně hojná v teplých oblastech na jihu Moravy a ve středních a severozápadních Čechách.[1][2][3]
Tato dvouletá rostlina vypouští v prvém roce přízemní růžici listů, ze které ve druhém roce vyrůstá jedna nebo více květných lodyh. Obvykle ji nalezneme na osluněných suchých stanovištích, na travnatých stráních, pastvinách, mezích, v příkopech, na náspech okolo cest a tratí, v lomech i na rumištích, kde je písčitá až kamenitá půda. Ráda vyrůstá na místech s narušovaným povrchem, kde ve slabě zapojeném drnu semena snáze vyklíčí.[1][4][5][6]
Bylina s 30 až 60 cm vysokou lodyhou, která je obvykle jednoduchá a mívá jediný úbor, pod kterým je kyjovitě ztlustlá; někdy bývá také vidličnatě rozvětvená. Oblá, dutá lodyha je porostlá střídavými, přisedlými až objímavými listy s paralelní žilnatinou, které jsou kopinaté či čárkovité, až 35 cm dlouhé a 15 mm široké, po obvodě jemně pilovitě zubaté a někdy vlnovitě zprohýbané. Přezimující přízemní růžice je tvořena obdobnými listy, jež jsou v době kvetení již suché. Rostlina vyrůstá z vřetenovitého, dužnatého, vně hnědého a uvnitř bílého kořene obsahujícího hořké mléko, stejně jako lodyhy a listy.
Na konci lodyhy nebo větví vyrůstají 2,5 cm velké květné úbory s bezplevým lůžkem, ve kterém je 20 až 50 pouze jazykovitých, oboupohlavných kvítků s tmavě fialovými až černými vrcholy trubkovitých prašníků a se sírově až citrónově žlutými ligulami zakončenými pěti zuby. Jednořadý zákrov má nejčastěji dvanáct vespod srostlých, dlouhých, kopinatých listenů, jež o polovinu liguly přečnívají. Úbor se rozvíjí v ranních hodinách a obrací se ke slunci, ale ještě před polednem květy uzavírá. Rostlina kvete hlavně v červnu a červenci, květy poskytují pyl i nektar a přitahují mnohé opylovače, včely i mouchy.
Plody jsou světlé, měkce osténkaté nažky s ostrými hranami. Před deštěm jsou chráněné uzavřením úboru, který se po uzrání ohrnuje nazpět. Nažka je zakončena kyjovitě rozšířeným zobánkem a věnčena paprsčitým chmýrem. Ten je bílý až nahnědlý a jehož postranní chloupky jsou spolu spleteny, tím je chmýr pevnější a nažka může být větrem zanášena dále od mateřské rostliny. Odkvétající rostliny jsou výrazné bílými koulemi nažek o průměru až 9 cm, jednotlivé nažky s paprsčitým chmýrem jsou dlouhé 2,5 až 4 cm.
Rozmnožují se výhradně semeny, která mají krátkou dobu dormance a vyklíčí ještě téhož roku, co dozrály. Listy obsahují hořkou latexovou šťávu, a proto rostliny obvykle nebývají býložravci spásány.[1][3][4][5][6]
Kozí brada pochybná často vyrůstá na podobných stanovištích jako kozí brada luční, která má podobný vzhled. Morfologicky se odlišují hlavně tím, že kozí brada luční nemá listeny delší než liguly a mívá jich míň, obvykle jen osm.[6]
Nákres rostliny
Úbor
Nažky s chmýrem
Nažky
Obrázky, zvuky či videa k tématu kozí brada pochybná ve Wikimedia Commons
Kozí brada pochybná (Tragopogon dubius) je dvouletá, žlutě kvetoucí, planě rostoucí rostlina slunných a suchých míst. Je jedním ze tří druhů rodu kozí brada, které v české přírodě rostou, je považována za zdomácnělý archeofyt.
Der Große Bocksbart (Tragopogon dubius), auch Groß-Bocksbart genannt, ist eine Pflanzenart aus der Unterfamilie der Cichorioideae innerhalb der Familie der Korbblütler (Asteraceae).
Die ausdauernde Pflanze wird 20 bis 60 Zentimeter hoch. Am Grunde des Stängels finden sich häufig Reste vorjähriger Blätter. Die Blätter sind schmal lanzettlich, lang zugespitzt und ganzrandig. Die Stiele der Blütenkörbchen sind hohl und oberwärts keulig verdickt. Der Große Bocksbart blüht von Mai bis Juli. Die hellgelben Blütenstände (Korb) haben einen Durchmesser von 4 bis 6 Zentimeter. Sie öffnen sich morgens um acht Uhr und schließen sich bereits mittags wieder. Die acht bis zwölf Hüllblätter sind über dem Grund nicht eingeschnürt und deutlich länger als die Zungenblüten. Die Körbchenstiele sind zur Fruchtzeit stark vergrößert. Die lang geschnäbelten Früchte sind 20 bis 40 Millimeter lang; der Pappus ist fedrig.
Die Chromosomenzahl beträgt 2n = 12.[1]
Die kalk- und wärmeliebende Art wächst auf Ruderalstellen, Wegen, Dämmen,[2] in sonnigen Staudenfluren, auf Trockenrasen, beispielsweise in gestörten Trespen-Halbtrockenrasen, in mesophilen, halbruderalen Quecken-Trockenfluren, in Honigklee- und Natternkopf-Fluren und auf Eisenbahngelände. Sie kommt in Mitteleuropa besonders in Gesellschaften des Verbands Dauco-Melilotion, aber auch des Mesobromion oder Convolvulo-Agropyrion vor.[1] Das ursprüngliche Verbreitungsgebiet umfasst Mitteleuropa, Südeuropa, Osteuropa, die Türkei, das Kaukasusgebiet, Kasachstan, Sibirien und Xinjiang.[3] In Belgien, in den Niederlanden, in Schweden, Litauen, Indien, Bhutan, im südlichen Afrika, Australien, Neuseeland, Argentinien, Kanada und in den Vereinigten Staaten ist die Art ein Neophyt.[3]
In Deutschland ist die Art recht selten und es werden vor allem wärmebegünstigte Regionen im mittleren Teil besiedelt, beispielsweise im Rhein-Main-Gebiet und im Thüringer Becken. Im norddeutschen Tiefland fehlt der Große Bocksbart über weite Strecken.
In Österreich tritt der Groß-Bocksbart in den Bundesländern Wien, Niederösterreich, dem Burgenland, Oberösterreich sowie unbeständig in der Steiermark, Kärnten, Salzburg und Tirol in der kollinen bis untermontanen Höhenstufe auf. Im pannonischen Gebiet Österreichs ist die Art häufig anzutreffen, sonst selten und nur unbeständig (z. B. neben Bahnstrecken) oder lokal eingebürgert.[2]
Man kann folgende Unterarten unterscheiden:[4]
Der in Mitteleuropa häufig anzutreffende Wiesen-Bocksbart (Tragopogon pratensis) hat ebenfalls gelbe Blüten, jedoch keine deutlich keulig verdickten Korbstiele.
Dagegen hat die ursprünglich aus dem Mittelmeergebiet stammende Haferwurz (Tragopogon porrifolius) ähnlich wie der Große Bocksbart einen keulig verdickten Korbstiel, blüht jedoch weinrot und weist mehr blaugrüne Blätter auf.
Blütenkopf
Der typische "Bocks-Bart" des Großen Bocksbarts
Korb kurz vor der Samenreife (aufgeschnitten)
Blüte mit reifen Samen, die vom Wind verbreitet werden
Pappus mit Fiedern, diese sind miteinander verwoben
Reife Achänen (aufgeschnitten)
Der Große Bocksbart (Tragopogon dubius), auch Groß-Bocksbart genannt, ist eine Pflanzenart aus der Unterfamilie der Cichorioideae innerhalb der Familie der Korbblütler (Asteraceae).
Tragopogon dubius (yellow salsify,[1] western salsify, western goat's-beard, wild oysterplant, yellow goat's beard, goat's beard, goatsbeard, common salsify, salsify) is a species of salsify native to southern and central Europe and western Asia and found as far north and west as northern France. Although it has been reported from Kashmir and India, recent evidence suggests that specimens from these areas may be a different species. Western salsify has been introduced into North America where it has become widespread, being reported from all the continental United States except for a few in the far south-east, and all provinces of Canada except Newfoundland and the northern territories.
Like most salsifies, the western salsify grows as an annual or occasionally biennial forb, reaching a height of typically 20–60 cm but sometimes almost a metre. It grows typically in warm, sheltered spots with moist soil. Its yellow flower head is 4–6 cm in diameter and is likely to be seen in late spring or early summer. Buds are blue-green, tall, and tapered. The inflorescence opens early in the morning and often closes up by late afternoon. Later the plant forms a seed head that resembles that of the dandelions but is distinctly larger. The seeds themselves (known as achenes) are 2–4 cm long but featherweight, weighing about 8 mg each on average. There is some natural variation between the central and peripheral achenes in the seedhead, with the peripheral ones being generally darker and heavier, and having a higher concentration of phenolic compounds; this may enhance their survival potential.
Western salsify is quite similar to the generally more common meadow salsify, T. pratensis, but the bracts which show behind the flower head, a distinctive feature of salsifies, are longer and more noticeable. Although not particularly closely related to meadow salsify or the common salsify or oyster plant (T. porrifolius), the western salsify hybridises readily with both, and in North America its hybrids have given rise to the new alloploid hybrid species T. mirus and T. miscellus.
Because western salsify is a widespread plant, it has a large number of alternative common names. They include western goat's beard, wild oysterplant, yellow salsify, yellow goat's beard, meadow goat's beard, goat's beard, goatsbeard, common salsify, or salsify. Some of these are also, or more commonly, used for other species, and are better avoided. A synonym, Tragopogon major, may also be encountered.
The basal leaves can be eaten raw or cooked.[2] Native Americans ate the roots, which are best cooked,[3] and are said to taste like oysters.[4]
Tragopogon dubius (yellow salsify, western salsify, western goat's-beard, wild oysterplant, yellow goat's beard, goat's beard, goatsbeard, common salsify, salsify) is a species of salsify native to southern and central Europe and western Asia and found as far north and west as northern France. Although it has been reported from Kashmir and India, recent evidence suggests that specimens from these areas may be a different species. Western salsify has been introduced into North America where it has become widespread, being reported from all the continental United States except for a few in the far south-east, and all provinces of Canada except Newfoundland and the northern territories.
Like most salsifies, the western salsify grows as an annual or occasionally biennial forb, reaching a height of typically 20–60 cm but sometimes almost a metre. It grows typically in warm, sheltered spots with moist soil. Its yellow flower head is 4–6 cm in diameter and is likely to be seen in late spring or early summer. Buds are blue-green, tall, and tapered. The inflorescence opens early in the morning and often closes up by late afternoon. Later the plant forms a seed head that resembles that of the dandelions but is distinctly larger. The seeds themselves (known as achenes) are 2–4 cm long but featherweight, weighing about 8 mg each on average. There is some natural variation between the central and peripheral achenes in the seedhead, with the peripheral ones being generally darker and heavier, and having a higher concentration of phenolic compounds; this may enhance their survival potential.
T. dubius, large seedhead Western salsify is quite similar to the generally more common meadow salsify, T. pratensis, but the bracts which show behind the flower head, a distinctive feature of salsifies, are longer and more noticeable. Although not particularly closely related to meadow salsify or the common salsify or oyster plant (T. porrifolius), the western salsify hybridises readily with both, and in North America its hybrids have given rise to the new alloploid hybrid species T. mirus and T. miscellus.
Because western salsify is a widespread plant, it has a large number of alternative common names. They include western goat's beard, wild oysterplant, yellow salsify, yellow goat's beard, meadow goat's beard, goat's beard, goatsbeard, common salsify, or salsify. Some of these are also, or more commonly, used for other species, and are better avoided. A synonym, Tragopogon major, may also be encountered.
The basal leaves can be eaten raw or cooked. Native Americans ate the roots, which are best cooked, and are said to taste like oysters.
Tragopogon dubius, conmúnmente llamada barba, escorzonera, piñones,[1] es una especie de planta bienal herbácea del género Tragopogon de la familia de las asteráceas.
Se trata de una planta herbácea bienal, con tallo erecto simple o ramificado en su parte inferior, de 40-100 cm de altura. Las hojas, basales —no organizadas en roseta— y caulinares, tienen unos 5-30 cm de largo por medio centímetro de ancho y son de forma linear a lanceolada —con los márgenes no ondulados— y eventualmente recurvadas en el ápice. El pedúnculo floral está fuertemente hinchado por debajo del involucro del capítulo. Dicho involucro mide unos 4-5 cm en la antesis y hasta 7 cm en la fructificación y está constituido por 8-14 largas y agudas brácteas. Las lígulas, de color amarillo y en número de 100-180, engendran cipselas con cuerpo de 10-15 mm de largo por 1,5 mm de diámetro, más o menos curvado y ornamentado de 5 costillas tuberculadas, acabado gradualmente en un largo y fino pico liso apicalmente inflado; soporta un vilano de pelos plumosos de 2-3 cm de largo implantados en un disco densamente pubescente.[2]
Es planta nativa en casi toda Europa y extendida hasta Pakistán; introducida y naturalizada en Europa septentrional (Suecia) y los Países bálticos, África del Sur, Norteamérica y, localmente en América del Sur (Argentina), Australia y Nueva Zelanda,[2] En la península ibérica, se encuentra dispersa en todo el territorio, sobre todo en la mitad norte; prácticamente ausente en el suroeste (solo en Portugal (Evora)) y totalmente ausente en Baleares y Canarias.[1]
Crece dispersa en terrenos soleados de malas hierbas y nitrificados por el hombre o animales, bosques secos, estepas pedregosas y praderas desde 500 hasta 2000 m de altitud.
La especie ha sido creada y descrita por primera vez por Giovanni Antonio Scopoli como Tragopogon Dubium y publicada, sin ilustración, en Flora Carniolica, Editio Secunda, vol. 2, nº947, p. 95, 1772[1].[3]
₳: Especies consideradas aceptadas o meros sinónimos según los autores contemporáneos.
La especie, introducida en Estados Unidos donde se volvió localmente maleza invasore, ha dado lugar a híbridos alopoliploides (2n=24) fértiles endémicos de zonas limitadas de Estados Unidos (Estados de Washington y de Idaho): Tragopogon mirus (Tragopogon dubius × Tragopogon porrifolius) y Tragopodon miscellus (Tragopogon dubius × Tragopogon pratensis) y que, a su vez, se híbridan entre ellos[10]
Otro híbrido entre las especies introducidas T. dubius y T. pratensis está citado del Estado de Míchigan en el norte de Estados Unidos y la región limítrofe del vecino Canadá Provincia de Manitoba: Tragopogon × crantzii Dichtl.[11]
Había sido descrito originalmente de Baja Austria por Alois Dichtl como Tragopogon Crantzii (T. orientalis × T. major) y publicado en Deutsche Botanische Monatsschrift : Organ für Floristen, Systematiker und alle Freunde der heimischen Flora, vol 1, p. 171, 1883[2]. Es sinónimo de Tragopogon interjectus Waisb., especie descrita también, algo más tarde, de Austria[3].
Además de estos híbridos citados, están aceptados (o solo provisionalmente aceptados a la espera de estudios complementarios), los siguientes:
Tragopogon dubius, conmúnmente llamada barba, escorzonera, piñones, es una especie de planta bienal herbácea del género Tragopogon de la familia de las asteráceas.
Tragopogon dubius, le Salsifis pâle[2], est une plante de la famille des Astéracées.
L'espèce n'est pas encore évaluée à l'échelle mondiale et européenne par l'UICN. En France elle est classée comme non préoccupante [3].
Toutefois localement l'espèce est considérée comme vulnérable (VU) en Picardie, Haute-Normandie, Basse-Normandie, Champagne-Ardennes ; quasi menacée (NT), proche du seuil des espèces menacées ou qui pourraient l'être si des mesures de conservation spécifiques n'étaient pas prises, en Limousin.
Selon The Plant List (27 mai 2016)[1] :
Tragopogon dubius, le Salsifis pâle, est une plante de la famille des Astéracées.
Il barba di becco a tromba (nome scientifico Tragopogon dubius (Scop., 1772) è una specie di pianta angiosperma dicotiledone della famiglia delle Asteraceae.[1][2]
Da Dioscoride sappiamo che il nome della pianta (e quindi del genere Tragopogon) deriva dal greco τραγος (tragos = caprone) e πὠγων (pogon = barba) per la somiglianza delle setole del pappo con la barba di un caprone.[3][4] L'epiteto specifico (dubius) in botanica viene usato nel senso di "incerto" o "di non conforme a un modello".[5]
Il nome scientifico di questa pianta è stato definito per la prima volta dal medico e naturalista italiano Giovanni Antonio Scopoli (Cavalese, 3 giugno 1723 – Pavia, 8 maggio 1788) nella pubblicazione "Flora Carniolica Exhibens Plantas Carniolae Indigenas et Distributas in Classes Naturales cum Differentiis Specificis, Synonymis Recentiorum, Locis Natalibus, Nominibus Incolarum, Observationibus Selectis, Viribus Medicis. Editio Secunda Aucta et Reformata. Viennae - 2: 95." del 1772.[6]
Habitus. La forma biologica è emicriptofita bienne (H bienn), ossia sono piante a ciclo biologico bienne, con gemme svernanti al livello del suolo e protette dalla lettiera o dalla neve, spesso sono dotate di un asse fiorale eretto e privo di foglie.[4][7][8] Gli organi interni di queste piante contengono lattoni sesquiterpenici.[9][10][11][12][13][14][15]
Fusto. La parte aerea del fusto è eretta, semplice o poco ramosa; la superficie è striata e più o meno arrossata; è ingrossata sotto il capolino. Le radici sono costituite da un fittone. L'altezza di queste piante varia da 20 a 60 cm (massimo 80 – 100 cm in America).
Foglie. Le foglie lungo il caule sono disposte in modo alternato e in genere hanno un aspetto graminiforme; quelle inferiori hanno una forma conduplicato-lineare e sono amplissicauli. Le foglie superiori sono più piccole ed hanno la base rigonfia; la superficie è percorsa da 7 nervi. Dimensioni delle foglie inferiori: larghezza 5 mm; lunghezza 2 - 3 dm. Dimensione delle foglie superiori: larghezza (alla base) 15 mm; lunghezza 1 dm.
Infiorescenza. Le infiorescenze sono composte da un capolino isolato su un peduncolo allungato (l'infiorescenza emerge dalla foglie superiori). Il capolino è formati da un involucro a forma cilindrica composto da brattee (o squame) disposte su una (due) serie all'interno delle quali un ricettacolo fa da base ai fiori tutti ligulati. L'infiorescenza è sottesa da una brattea lineare larga 1 mm e lunga 10 – 14 mm. Le squame si allungano alla fruttificazione. Il ricettacolo è nudo, ossia è privo di pagliette a protezione della base dei fiori. Diametro del capolino: alla base 2 – 5 cm; all'apice 4 – 5 mm; alla fruttificazione più di 10 mm. Dimensioni dell'involucro: larghezza 8 mm; lunghezza 15 mm. Dimensioni delle squame: larghezza 3 mm; lunghezza 40 mm.
Fiore. I fiori sono tutti del tipo ligulato[16] (il tipo tubuloso, i fiori del disco, presente nella maggioranza delle Asteraceae, qui è assente), sono tetra-ciclici (ossia sono presenti 4 verticilli: calice – corolla – androceo – gineceo) e pentameri (ogni verticillo ha 5 elementi). I fiori sono ermafroditi e zigomorfi.
, [C (5), A (5)], G 2 (infero), achenio[17]
Frutti. I frutti sono degli acheni con pappo. L'achenio, ristretto all'apice, è lungo 20 – 40 mm ed è provvisto di un lungo becco lungo come l'achenio o più corto. Il pappo è formato da setole piumose.
Dal punto di vista fitosociologico alpino la specie di questa voce appartiene alla seguente comunità vegetale:[21]
La famiglia di appartenenza di questa voce (Asteraceae o Compositae, nomen conservandum) probabilmente originaria del Sud America, è la più numerosa del mondo vegetale, comprende oltre 23.000 specie distribuite su 1.535 generi[23], oppure 22.750 specie e 1.530 generi secondo altre fonti[24] (una delle checklist più aggiornata elenca fino a 1.679 generi)[25]. La famiglia attualmente (2021) è divisa in 16 sottofamiglie.[1][12][13]
Il genere della specie di questa voce appartiene alla sottotribù Scorzonerinae della tribù Cichorieae (unica tribù della sottofamiglia Cichorioideae). In base ai dati filogenetici la sottofamiglia Cichorioideae è il terz'ultimo gruppo che si è separato dal nucleo delle Asteraceae (gli ultimi due sono Corymbioideae e Asteroideae).[1] La sottotribù Scorzonerinae è il secondo clade che si è separato dalla tribù.[13]
All'interno della sottotribù sono stati individuati diversi cladi, alcuni in posizione politomica. Il genere di questa voce, da un punto di vista filogenetico, si trova in una posizione centrale e con il genere Geropogon forma un "gruppo fratello" (differiscono soprattutto per gli acheni e il pappo). Il genere Tragopogon come è descritto attualmente è monofiletico.[15]
I caratteri distintivi per la specie di questa voce sono:[26]
Il numero cromosomico della specie è: 2n = 12.[26]
La specie di questa voce è variabile nel diametro del peduncolo che in alcuni casi è fortemente ingrossato (oltre a un centimetro di diametro). Alcuni Autori hanno preferito creare una nuova specie (Tragopogon major Jacq.) per questa varietà. Ma attualmente la maggior parte delle checklist considera questa entità un sinonimo della specie principale.
Per questa specie sono riconosciute le seguenti sottospecie:[2]
Secondo la divisione fatta da Pignatti[26] questa specie, nell'ambito del genere, fa parte del gruppo a fiori completamente gialli. In questo gruppo sono comprese alcune specie che si distinguono per i seguenti caratteri:
Nella medicina popolare le radici sono usate per i suoi effetti aperitivi e pettorali.[4]
Secondo le usanze popolari le parti commestibili sono le basi delle foglie più basse e i giovani steli, cotti o crudi in salata.[27]
Questa pianta può essere coltivata in terreni da giardino comuni (in preferenza con argille pesanti).[27]
Il barba di becco dubbia in altre lingue è chiamato nei seguenti modi:
Il barba di becco a tromba (nome scientifico Tragopogon dubius (Scop., 1772) è una specie di pianta angiosperma dicotiledone della famiglia delle Asteraceae.
De bleke morgenster (Tragopogon dubius) is een kruidachtige, tweejarige plant uit de composietenfamilie (Asteraceae). De soort komt van nature voor van Europa tot West-Azië. De plant is ingevoerd in Noord-Amerika.
De plant wordt 40-80 cm hoog en heeft een grote penwortel. De plant bevat veel melksap. De tot 25 cm lange bladeren zijn lancetvormig en op dwarsdoorsnede driehoekig. Aan de basis zijn de bladeren 2,5 cm breed en lopen naar boven spits toe. Bleke morgenster bloeit van mei tot juli met alleenstaande, bleekgele lintbloemen, waarbij de 3 cm lange en 3 mm brede omwindselbladen langer zijn dan de lintbloemen. De bloemstengel is naar boven sterk verbreed en net onder het bloemhoofd hol. De stijlen zijn paars.
De vrucht is een tot 3 cm lang nootje met 1 cm lang gesteeld wit vruchtpluis. Als zodanig vormt zich een "pluizenbol".
De bleke morgenster komt voor op open, tamelijk droge zandgrond, op spoordijken en industrieterreinen.
De wortel van bleke morgenster is eetbaar en meegenomen door de emigranten uit Europa naar Noord-Amerika, waar het tot een onkruid is verworden.
De namen in andere talen kunnen vaak eenvoudig worden opgezocht met de interwiki-links.
De bleke morgenster (Tragopogon dubius) is een kruidachtige, tweejarige plant uit de composietenfamilie (Asteraceae). De soort komt van nature voor van Europa tot West-Azië. De plant is ingevoerd in Noord-Amerika.
De plant wordt 40-80 cm hoog en heeft een grote penwortel. De plant bevat veel melksap. De tot 25 cm lange bladeren zijn lancetvormig en op dwarsdoorsnede driehoekig. Aan de basis zijn de bladeren 2,5 cm breed en lopen naar boven spits toe. Bleke morgenster bloeit van mei tot juli met alleenstaande, bleekgele lintbloemen, waarbij de 3 cm lange en 3 mm brede omwindselbladen langer zijn dan de lintbloemen. De bloemstengel is naar boven sterk verbreed en net onder het bloemhoofd hol. De stijlen zijn paars.
De vrucht is een tot 3 cm lang nootje met 1 cm lang gesteeld wit vruchtpluis. Als zodanig vormt zich een "pluizenbol".
De bleke morgenster komt voor op open, tamelijk droge zandgrond, op spoordijken en industrieterreinen.
Kozibród wielki (Tragopogon dubius Scop.) – gatunek rośliny z rodziny astrowatych.
Jest szeroko rozprzestrzeniony na kuli ziemskiej. Występuje na wszystkich kontynentach (poza Antarktydą)[3]. Do Ameryki Północnej został sprowadzony wraz z żywnością i roślinami ozdobnymi na przełomie XIX i XX wieku przez osadników europejskich. Obecnie jest tam szeroko rozprzestrzeniony. W wielu regionach na pastwiskach wypiera rodzimą roślinność i staje się gatunkiem inwazyjnym[4]. W Polsce jest średnio pospolity[5]. Najczęściej występuje w południowej części niżu, ku północy po Mazowsze i Pomorze. Często jest zawlekany[6].
Kozibród wielki (Tragopogon dubius Scop.) – gatunek rośliny z rodziny astrowatych.
Tragopogon dubius é uma espécie de planta com flor pertencente à família Asteraceae.
A autoridade científica da espécie é Scop., tendo sido publicada em Flora Carniolica, Editio Secunda 2: 95. 1772.[1]
Trata-se de uma espécie presente no território português, nomeadamente em Portugal Continental.
Em termos de naturalidade é nativa da região atrás indicada.
Não se encontra protegida por legislação portuguesa ou da Comunidade Europeia.
Tragopogon dubius é uma espécie de planta com flor pertencente à família Asteraceae.
A autoridade científica da espécie é Scop., tendo sido publicada em Flora Carniolica, Editio Secunda 2: 95. 1772.
Stor haverrot (Tragopogon dubius) är en växtart i familjen korgblommiga växter.
Wikimedia Commons har media som rör Stor haverrot.
Stor haverrot (Tragopogon dubius) är en växtart i familjen korgblommiga växter.
Tragopogon dubius là một loài thực vật có hoa trong họ Cúc. Loài này được Scop. miêu tả khoa học đầu tiên năm 1772.[1]
Tragopogon dubius là một loài thực vật có hoa trong họ Cúc. Loài này được Scop. miêu tả khoa học đầu tiên năm 1772.
Tragopogon dubius Scop.
Синонимы
Козлоборо́дник сомни́тельный (лат. Tragopógon dúbius) — двулетнее растение, вид рода Козлобородник (Tragopogon) семейства Астровые (Asteraceae).
Стебли высотой 30—70 (150) см, простые или слабо разветвлённые, ребристые, голые или слабоопушённые у основания листьев.
Листья линейные или линейно-ланцетные, многочисленные, средние 6—20 см длиной и 5—20 мм шириной, полустеблеобъемлющие, верхние короче.
Цветки жёлтые. Цветоносы полые, 6—12 мм в диаметре. Соцветия — крупные, длиной 50—60 мм корзинки, обёртки 8—12-листочковые, листочки значительно превышают длину цветков. Ножки цветочных корзинок вздутые при плодах.
Цветёт с мая по август, плодоносит с июля по сентябрь.
Встречается в степях, на степных склонах, иногда на сорных местах.
В пищу употребляются корни и молодые стебли с листьями. При варке в солёной воде свойственный сырым корням горький вкус исчезает[2].
Вид Козлобородник сомнительный входит в род Козлобородник (Tragopogon) семейства Астровые (Asteraceae) порядка Астроцветные (Asterales).
Козлоборо́дник сомни́тельный (лат. Tragopógon dúbius) — двулетнее растение, вид рода Козлобородник (Tragopogon) семейства Астровые (Asteraceae).
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