Difference between revisions of "Krigia virginica"
Sp. Pl. 3: 1618. 1803.
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|common_names=Virginia dwarfdandelion | |common_names=Virginia dwarfdandelion | ||
| − | |basionyms={{Treatment/ID/ | + | |special_status={{Treatment/ID/Special_status |
| + | |code=E | ||
| + | |label=Endemic | ||
| + | }} | ||
| + | |basionyms={{Treatment/ID/Basionym | ||
|name=Hyoseris virginica | |name=Hyoseris virginica | ||
|authority=Linnaeus | |authority=Linnaeus | ||
| + | |rank=species | ||
| + | |publication_title=Sp. Pl. | ||
| + | |publication_place=2: 809. 1753 | ||
}} | }} | ||
|synonyms= | |synonyms= | ||
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|elevation=0–1200 m | |elevation=0–1200 m | ||
|distribution=B.C.;Ala.;Ark.;Conn.;Del.;Fla.;Ga.;Ill.;Ind.;Iowa;Ky.;La.;Maine;Md.;Mass.;Mich.;Minn.;Miss.;Mo.;N.H.;N.J.;N.Y.;N.C.;Ohio;Okla.;Pa.;R.I.;S.C.;Tenn.;Tex.;Vt.;Va.;W.Va.;Wis. | |distribution=B.C.;Ala.;Ark.;Conn.;Del.;Fla.;Ga.;Ill.;Ind.;Iowa;Ky.;La.;Maine;Md.;Mass.;Mich.;Minn.;Miss.;Mo.;N.H.;N.J.;N.Y.;N.C.;Ohio;Okla.;Pa.;R.I.;S.C.;Tenn.;Tex.;Vt.;Va.;W.Va.;Wis. | ||
| − | |discussion=<p>Krigia virginica is introduced in British Columbia. It grows in the Eastern deciduous forest biome, tallgrass prairie, and southeastern Coastal Plain. Its weedy habit may lead to introductions outside the present range.</p><!-- | + | |discussion=<p><i>Krigia virginica</i> is introduced in British Columbia. It grows in the Eastern deciduous forest biome, tallgrass prairie, and southeastern Coastal Plain. Its weedy habit may lead to introductions outside the present range.</p><!-- |
| − | --><p>The tetraploid populations of Krigia virginica are believed to have arisen through autoploidy; they are morphologically indistinguishable from the diploids. A single origin for this autoploid event is suggested by the chloroplast DNA studies by K. J. Kim et al. (1992b, 1992c), with marked genetic divergence of the tetraploids having occurred since their origination. Plants collected late in the season have a branching habit remarkably unlike the scapiform vernal form.</p> | + | --><p>The tetraploid populations of <i>Krigia virginica</i> are believed to have arisen through autoploidy; they are morphologically indistinguishable from the diploids. A single origin for this autoploid event is suggested by the chloroplast DNA studies by K. J. Kim et al. (1992b, 1992c), with marked genetic divergence of the tetraploids having occurred since their origination. Plants collected late in the season have a branching habit remarkably unlike the scapiform vernal form.</p> |
|tables= | |tables= | ||
|references= | |references= | ||
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-->{{#Taxon: | -->{{#Taxon: | ||
name=Krigia virginica | name=Krigia virginica | ||
| − | |||
|authority=(Linnaeus) Willdenow | |authority=(Linnaeus) Willdenow | ||
|rank=species | |rank=species | ||
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|publication title=Sp. Pl. | |publication title=Sp. Pl. | ||
|publication year=1803 | |publication year=1803 | ||
| − | |special status= | + | |special status=Endemic |
| − | |source xml=https:// | + | |source xml=https://bitbucket.org/aafc-mbb/fna-data-curation/src/2e0870ddd59836b60bcf96646a41e87ea5a5943a/coarse_grained_fna_xml/V19-20-21/V19_581.xml |
|tribe=Asteraceae tribe Cichorieae | |tribe=Asteraceae tribe Cichorieae | ||
|genus=Krigia | |genus=Krigia | ||
Latest revision as of 19:53, 5 November 2020
Annuals, 4–30 cm; taprooted. Stems 1–50+, initially scapiform, later elongate and leafy (after rosette leaves wither), erect, eglandular or stipitate-glandular, especially near heads. Leaves initially produced basally (rosettes); later leaves cauline; sessile or petiolate; blades oblanceolate to spatulate, 1.5–18 cm, usually irregularly pinnately lobed, terminal lobes often denticulate, faces glabrous, eglandular or loosely glandular-villous; cauline (appearing opposite on late-season stems), narrowly oblanceolate to linear, mostly entire. Heads borne singly. Peduncles from rosettes (early) or axillary or terminal on stems (later). Involucres 4.5–8 mm. Phyllaries 9–15, reflexed in fruit, lanceolate, midveins obscure, apices acute. Florets 8–35; corollas yellow, often purplish abaxially, 5–12 mm. Cypselae dark reddish brown, narrowly obconic, 1.5–2.3 mm, 15–20-ribbed; pappi of 5, hyaline, rounded outer scales 0.5–1 mm plus 5, scabrous inner bristles 4–6 mm. 2n = 10, 20.
Phenology: Flowering Feb–Nov.
Habitat: Sandy, silty, or loam soils, rock outcrops, open mixed mesophytic, northern hardwoods, beach-maple, oak-pine, and oak-hickory woods, pastures, prairies, and roadsides, often in disturbed, weedy sites
Elevation: 0–1200 m
Distribution
B.C., Ala., Ark., Conn., Del., Fla., Ga., Ill., Ind., Iowa, Ky., La., Maine, Md., Mass., Mich., Minn., Miss., Mo., N.H., N.J., N.Y., N.C., Ohio, Okla., Pa., R.I., S.C., Tenn., Tex., Vt., Va., W.Va., Wis.
Discussion
Krigia virginica is introduced in British Columbia. It grows in the Eastern deciduous forest biome, tallgrass prairie, and southeastern Coastal Plain. Its weedy habit may lead to introductions outside the present range.
The tetraploid populations of Krigia virginica are believed to have arisen through autoploidy; they are morphologically indistinguishable from the diploids. A single origin for this autoploid event is suggested by the chloroplast DNA studies by K. J. Kim et al. (1992b, 1992c), with marked genetic divergence of the tetraploids having occurred since their origination. Plants collected late in the season have a branching habit remarkably unlike the scapiform vernal form.
Selected References
None.