Difference between revisions of "Dicentra cucullaria"
Linnaea 8: 457, 468. 1833.
FNA>Volume Importer |
imported>Volume Importer |
||
(7 intermediate revisions by 2 users not shown) | |||
Line 13: | Line 13: | ||
}}{{Treatment/ID/Special_status | }}{{Treatment/ID/Special_status | ||
|code=F | |code=F | ||
− | |label= | + | |label=Illustrated |
}} | }} | ||
− | |basionyms={{Treatment/ID/ | + | |basionyms={{Treatment/ID/Basionym |
|name=Fumaria cucullaria | |name=Fumaria cucullaria | ||
|authority=Linnaeus | |authority=Linnaeus | ||
+ | |rank=species | ||
+ | |publication_title=Sp. Pl. | ||
+ | |publication_place=2: 699. 1753 | ||
}} | }} | ||
|synonyms={{Treatment/ID/Synonym | |synonyms={{Treatment/ID/Synonym | ||
|name=Bicuculla cucullaria | |name=Bicuculla cucullaria | ||
|authority=(Linnaeus) Millspaugh | |authority=(Linnaeus) Millspaugh | ||
− | }}{{Treatment/ID/Synonym | + | |rank=species |
+ | }} {{Treatment/ID/Synonym | ||
|name=Bicuculla occidentalis | |name=Bicuculla occidentalis | ||
|authority=Rydberg | |authority=Rydberg | ||
− | }}{{Treatment/ID/Synonym | + | |rank=species |
+ | }} {{Treatment/ID/Synonym | ||
|name=Dicentra cucullaria var. occidentalis | |name=Dicentra cucullaria var. occidentalis | ||
|authority=(Rydberg) M. Peck | |authority=(Rydberg) M. Peck | ||
+ | |rank=variety | ||
}} | }} | ||
|hierarchy=Fumariaceae;Dicentra;Dicentra cucullaria | |hierarchy=Fumariaceae;Dicentra;Dicentra cucullaria | ||
Line 36: | Line 42: | ||
}}<!-- | }}<!-- | ||
− | --><span class="statement" id="st- | + | --><span class="statement" id="st-undefined" data-properties=""><b>Plants </b>perennial, scapose, from short rootstocks bearing pink to white, teardrop-shaped bulblets. <b>Leaves</b> (10-)14-16(-36) × (4-)6-14(-18) cm; petiole (5-)8-16(-24) cm; blade with 4 orders of leaflets and lobes; abaxial surface glaucous; ultimate lobes linear to linear-elliptic or linear-obovate, (2-)5-15(-23) × (0.4-)2-3(-4.2) mm, usually minutely apiculate. <b>Inflorescences</b> racemose, 3-14-flowered, usually exceeding leaves; bracts minute. <b>Flowers</b> pendent; pedicels (2-)4-7(-12) mm; sepals broadly ovate, 1.8-5 × 1.3-4 mm; petals white, frequently suffused pink, apex yellow to orange-yellow; outer petals (10-)12-16(-20) × (3-)6-10(-13) mm, reflexed portion 2-5 mm; inner petals (7.5-)9-12(-14) mm, blade 1.8-4 mm, claw linear, 4-8 × less than 1 mm, crest prominent, ca. 2 mm diam.; filaments of each bundle connate from base to shortly below anthers; nectariferous tissue forming 1-3(-4.5) mm spur diverging at angle from base of bundle; style 2-4 mm; stigma 2-horned with 2 lateral papillae. <b>Capsules</b> ovoid, attenuate at both ends, (7-)9-13(-16) × 3-5 mm. <b>Seeds</b> reniform, ca. 2 mm diam., very obscurely reticulate, elaiosome present. <b>2n</b> = 32.</span><!-- |
-->{{Treatment/Body | -->{{Treatment/Body | ||
Line 43: | Line 49: | ||
|elevation=0-1500 m | |elevation=0-1500 m | ||
|distribution=N.B.;N.S.;Ont.;P.E.I.;Que.;Ala.;Ark.;Conn.;Del.;D.C.;Ga.;Idaho;Ill.;Ind.;Iowa;Kans.;Ky.;Maine;Md.;Mass.;Mich.;Minn.;Mo.;Nebr.;N.H.;N.J.;N.Y.;N.C.;N.Dak.;Ohio;Okla.;Oreg.;Pa.;R.I.;S.C.;S.Dak.;Tenn.;Vt.;Va.;Wash.;W.Va.;Wis. | |distribution=N.B.;N.S.;Ont.;P.E.I.;Que.;Ala.;Ark.;Conn.;Del.;D.C.;Ga.;Idaho;Ill.;Ind.;Iowa;Kans.;Ky.;Maine;Md.;Mass.;Mich.;Minn.;Mo.;Nebr.;N.H.;N.J.;N.Y.;N.C.;N.Dak.;Ohio;Okla.;Oreg.;Pa.;R.I.;S.C.;S.Dak.;Tenn.;Vt.;Va.;Wash.;W.Va.;Wis. | ||
− | |discussion=<p>Dicentra cucullaria is occasionally confused with D. canadensis, with which it is sympatric. It is distinguished from that species by its basally pointed (versus rounded) outer petal spurs, by its flowers lacking a fragrance, by flowering 7-10 days earlier, and by its pink to white, teardrop-shaped (versus yellow, pea-shaped) bulblets.</p><!-- | + | |discussion=<p><i>Dicentra cucullaria</i> is occasionally confused with <i>D. canadensis</i>, with which it is sympatric. It is distinguished from that species by its basally pointed (versus rounded) outer petal spurs, by its flowers lacking a fragrance, by flowering 7-10 days earlier, and by its pink to white, teardrop-shaped (versus yellow, pea-shaped) bulblets.</p><!-- |
− | --><p>After fruit set, the bulblets of both Dicentra cucullaria and D. canadensis remain dormant until fall, when stored starch is converted to sugar. At this time also, flower buds and leaf primordia are produced below ground; these then remain dormant until spring (P. G. Risser and G. Cottam 1968; B. J. Kieckhefer 1964; K. R. Stern 1961). Pollination of both species is effected by bumblebees (Bombus spp.) and other long-tongued insects (L. W. Macior 1970, 1978; K. R. Stern 1961).</p><!-- | + | --><p>After fruit set, the bulblets of both <i>Dicentra cucullaria</i> and <i>D. canadensis</i> remain dormant until fall, when stored starch is converted to sugar. At this time also, flower buds and leaf primordia are produced below ground; these then remain dormant until spring (P. G. Risser and G. Cottam 1968; B. J. Kieckhefer 1964; K. R. Stern 1961). Pollination of both species is effected by bumblebees (Bombus spp.) and other long-tongued insects (L. W. Macior 1970, 1978; K. R. Stern 1961).</p><!-- |
− | --><p>Flavonoid components indicate that Dicentra canadensis and D. cucullaria are more closely related to each other than to any other member of the genus (D. Fahselt 1971). Even so, species purported to be hybrids between them probably are not. There is considerable variation in floral morphology within D. cucullaria, which can have flowers superficially resembling those of D. canadensis. However, when all characters of the plants are examined, these putative hybrids almost always are clearly assignable to one species or the other.</p><!-- | + | --><p>Flavonoid components indicate that <i>Dicentra canadensis</i> and <i>D. cucullaria</i> are more closely related to each other than to any other member of the genus (D. Fahselt 1971). Even so, species purported to be hybrids between them probably are not. There is considerable variation in floral morphology within <i>D. cucullaria</i>, which can have flowers superficially resembling those of <i>D. canadensis</i>. However, when all characters of the plants are examined, these putative hybrids almost always are clearly assignable to one species or the other.</p><!-- |
− | --><p>The western populations of Dicentra cucullaria appear to have been separated from the eastern ones for at least a thousand years. The western plants are generally somewhat coarser, which apparently led Rydberg to designate the western populations as a separate species. Plants from the Blue Ridge Mountains of Virginia, however, are virtually indistinguishable from those of the West, and much of the variation (which is considerable) within the species probably involves phenotypic response to the environment, or represents ecotypes within the species.</p><!-- | + | --><p>The western populations of <i>Dicentra cucullaria</i> appear to have been separated from the eastern ones for at least a thousand years. The western plants are generally somewhat coarser, which apparently led Rydberg to designate the western populations as a separate species. Plants from the Blue Ridge Mountains of Virginia, however, are virtually indistinguishable from those of the West, and much of the variation (which is considerable) within the species probably involves phenotypic response to the environment, or represents ecotypes within the species.</p><!-- |
− | --><p>The Iroquois prepared infusions from the roots of Dicentra cucullaria for a medicinal liniment (D. E. Moerman 1986).</p> | + | --><p>The Iroquois prepared infusions from the roots of <i>Dicentra cucullaria</i> for a medicinal liniment (D. E. Moerman 1986).</p> |
|tables= | |tables= | ||
|references= | |references= | ||
Line 56: | Line 62: | ||
-->{{#Taxon: | -->{{#Taxon: | ||
name=Dicentra cucullaria | name=Dicentra cucullaria | ||
− | |||
|authority=(Linnaeus) Bernhardi | |authority=(Linnaeus) Bernhardi | ||
|rank=species | |rank=species | ||
Line 70: | Line 75: | ||
|publication title=Linnaea | |publication title=Linnaea | ||
|publication year=1833 | |publication year=1833 | ||
− | |special status=Endemic; | + | |special status=Endemic;Illustrated |
− | |source xml=https:// | + | |source xml=https://bitbucket.org/aafc-mbb/fna-data-curation/src/2e0870ddd59836b60bcf96646a41e87ea5a5943a/coarse_grained_fna_xml/V3/V3_230.xml |
|genus=Dicentra | |genus=Dicentra | ||
|species=Dicentra cucullaria | |species=Dicentra cucullaria | ||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
}}<!-- | }}<!-- | ||
-->[[Category:Treatment]][[Category:Dicentra]] | -->[[Category:Treatment]][[Category:Dicentra]] |
Latest revision as of 21:47, 5 November 2020
Plants perennial, scapose, from short rootstocks bearing pink to white, teardrop-shaped bulblets. Leaves (10-)14-16(-36) × (4-)6-14(-18) cm; petiole (5-)8-16(-24) cm; blade with 4 orders of leaflets and lobes; abaxial surface glaucous; ultimate lobes linear to linear-elliptic or linear-obovate, (2-)5-15(-23) × (0.4-)2-3(-4.2) mm, usually minutely apiculate. Inflorescences racemose, 3-14-flowered, usually exceeding leaves; bracts minute. Flowers pendent; pedicels (2-)4-7(-12) mm; sepals broadly ovate, 1.8-5 × 1.3-4 mm; petals white, frequently suffused pink, apex yellow to orange-yellow; outer petals (10-)12-16(-20) × (3-)6-10(-13) mm, reflexed portion 2-5 mm; inner petals (7.5-)9-12(-14) mm, blade 1.8-4 mm, claw linear, 4-8 × less than 1 mm, crest prominent, ca. 2 mm diam.; filaments of each bundle connate from base to shortly below anthers; nectariferous tissue forming 1-3(-4.5) mm spur diverging at angle from base of bundle; style 2-4 mm; stigma 2-horned with 2 lateral papillae. Capsules ovoid, attenuate at both ends, (7-)9-13(-16) × 3-5 mm. Seeds reniform, ca. 2 mm diam., very obscurely reticulate, elaiosome present. 2n = 32.
Phenology: Flowering early–late spring.
Habitat: Deciduous woods and clearings, in rich loam soils
Elevation: 0-1500 m
Distribution
N.B., N.S., Ont., P.E.I., Que., Ala., Ark., Conn., Del., D.C., Ga., Idaho, Ill., Ind., Iowa, Kans., Ky., Maine, Md., Mass., Mich., Minn., Mo., Nebr., N.H., N.J., N.Y., N.C., N.Dak., Ohio, Okla., Oreg., Pa., R.I., S.C., S.Dak., Tenn., Vt., Va., Wash., W.Va., Wis.
Discussion
Dicentra cucullaria is occasionally confused with D. canadensis, with which it is sympatric. It is distinguished from that species by its basally pointed (versus rounded) outer petal spurs, by its flowers lacking a fragrance, by flowering 7-10 days earlier, and by its pink to white, teardrop-shaped (versus yellow, pea-shaped) bulblets.
After fruit set, the bulblets of both Dicentra cucullaria and D. canadensis remain dormant until fall, when stored starch is converted to sugar. At this time also, flower buds and leaf primordia are produced below ground; these then remain dormant until spring (P. G. Risser and G. Cottam 1968; B. J. Kieckhefer 1964; K. R. Stern 1961). Pollination of both species is effected by bumblebees (Bombus spp.) and other long-tongued insects (L. W. Macior 1970, 1978; K. R. Stern 1961).
Flavonoid components indicate that Dicentra canadensis and D. cucullaria are more closely related to each other than to any other member of the genus (D. Fahselt 1971). Even so, species purported to be hybrids between them probably are not. There is considerable variation in floral morphology within D. cucullaria, which can have flowers superficially resembling those of D. canadensis. However, when all characters of the plants are examined, these putative hybrids almost always are clearly assignable to one species or the other.
The western populations of Dicentra cucullaria appear to have been separated from the eastern ones for at least a thousand years. The western plants are generally somewhat coarser, which apparently led Rydberg to designate the western populations as a separate species. Plants from the Blue Ridge Mountains of Virginia, however, are virtually indistinguishable from those of the West, and much of the variation (which is considerable) within the species probably involves phenotypic response to the environment, or represents ecotypes within the species.
The Iroquois prepared infusions from the roots of Dicentra cucullaria for a medicinal liniment (D. E. Moerman 1986).
Selected References
None.