Difference between revisions of "Centrosema virginianum"

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(Seed bank and germination)
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===Fire ecology===<!--Fire tolerance, fire dependence, adaptive fire responses-->  
 
===Fire ecology===<!--Fire tolerance, fire dependence, adaptive fire responses-->  
It thrives under fire.<ref name="cushwa"/> Hendricks observed that the Piedmont National Wildlife Refuge plots, which had been under a 4-year burning regime since 1966, each contained more than 10 times more ''C. virginianum'' individuals per ha than the Oconee National Forest plots, which had no burning history.<ref name="hendricks">Hendricks, J. J. and L. R. Boring (1999). "N2-fixation by native herbaceous legumes in burned pine ecosystems of the southeastern United States." Forest Ecology and Management 113: 167-177.</ref> Seasonal burning does not seem to negatively affect nitrogen fixation.<ref name="hiers2003">Hiers, J. K., R. J. Mitchell, et al. (2003). "Legumes native to longleaf pine savannas exhibit capacity for high N2-fixation rates and negligible impacts due to timing of fire." New Phytologist 157: 327-338</ref> ''C. virginianum'' showed increased flowering synchrony in response to lightning-season burns.<ref name="hiers2000"/> It responded the best to March burns with respect to annual tissue inputs as well as nitrogen contribution.<ref name="hiers2003"/> ''C. virginianum'' showed robust flowering response to late winter/ early spring burns, supporting the response to March burns noted earlier. It has a mid-summer flowering peak.<ref name="hiers2000"/> Also, Hiers found no evidence that increased flowering affects nitrogen-fixing capability.<ref name="hiers2003"/>
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It thrives under fire.<ref name="cushwa"/> Hendricks observed that the Piedmont National Wildlife Refuge plots, which had been under a 4-year burning regime since 1966, each contained more than 10 times more ''C. virginianum'' individuals per ha than the Oconee National Forest plots, which had no burning history.<ref name="hendricks">Hendricks, J. J. and L. R. Boring (1999). "N2-fixation by native herbaceous legumes in burned pine ecosystems of the southeastern United States." Forest Ecology and Management 113: 167-177.</ref> Seasonal burning does not seem to negatively affect nitrogen fixation.<ref name="hiers2003">Hiers, J. K., R. J. Mitchell, et al. (2003). "Legumes native to longleaf pine savannas exhibit capacity for high N2-fixation rates and negligible impacts due to timing of fire." New Phytologist 157: 327-338</ref> ''C. virginianum'' showed increased flowering synchrony in response to lightning-season burns.<ref name="hiers2000"/> It responded the best to March burns with respect to annual tissue inputs as well as nitrogen contribution.<ref name="hiers2003"/> ''C. virginianum'' showed robust flowering response to late winter/ early spring burns, supporting the response to March burns noted earlier. It has a mid-summer flowering peak.<ref name="hiers2000"/> Also, one study found no evidence that increased flowering affects nitrogen-fixing capability.<ref name="hiers2003"/>
  
 
===Pollination===  
 
===Pollination===  

Revision as of 13:04, 7 November 2016

Centrosema virginianum
Centrosema virginianum Gil.jpg
Photo by Gil Nelson
Scientific classification
Kingdom: Plantae
Division: Magnoliophyta - Flowering plants
Class: Magnoliopsida – Dicotyledons
Order: Fabales
Family: Fabaceae ⁄ Leguminosae
Genus: Centrosema
Species: C. virginianum
Binomial name
Centrosema virginianum
(L.) Benth.
CENT VIRG dist.jpg
Natural range of Centrosema virginianum from USDA NRCS Plants Database.

Common name: Spurred butterfly pea

Taxonomic notes

Synonyms: Centrosema virginianum var. virginianum; C. virginianum var. ellipticum Fernald; Bradburya virginiana (Linnaeus) Kuntze; C. virginianum var. angustifolium (A.P. de Candolle) Grisebach

Description

Centrosema virginianum is a perennial herbaceous vine. It grows as a twining vine, climbing on Smilax vines and low vegetation, frequently appearing among grasses.[1]

Centrosema virginianum is seen growing in a tailing, climbing, and twining fashion. The plant is a perennial herbaceous vine that grows 0.5-1.5 m long, and is more or less minutely pubescent throughout. The leaves are 3-foliolate; the leaflets are widely to narrowly ovate, ovate-lanceolate or oblong to elliptic, are conspicously reticulate, mostly growing 2-7 cm long, and are stipellate. The stipules are ovate-lanceolate to lanceolate, striate, persistent, 1.5-4 mm long. The racemes are with peduncles usually growing 1-5 cm long, the zig-zag rachis bears 1-4 nodes each with an ovate bract growing up to 1.5-3 cm long subtending a pedicel (growing 2-10 cm long) surmounted by 2 ovate bractlets growing 0.8-1.2 cm long. The calyx is somewhat hidden by the braclets, the tube is broadly hemispheric, growing 4-5 mm long, the lobes are linear-subulate, growing 0.6-1.4 cm long, the lowermost longest. The petals are pale blue-violet to lavender in color, growing 2.5-3.5 cm long, is spurred near the base, the wigs and keel are nearly equal in size, ca. 2 cm long. The stamens are diadelphous, 9 and 1. The legume is linear, flattened, and grows 7-14 cm long and ca. 4 mm broad, is subsessile, many seeded with an elongate, persistent, beak-like style, valves longitudinally twisting after dehiscence.[2]

Distribution

Ecology

It is a legume that has one of the highest nitrogen-fixing potentials.[3] Because of this, it may be able to help restore N lost from fire.[4] By mid-season in June and July, a maximum nitrogen-fixing rate was observed.[3]

Habitat

It is found in a wide range of natural and disturbed conditions, including frequently burned sandhills, upland longleaf-wiregrass and old-field pinelands[4][5] and flatwoods, coastal island dunes and shorelines, open areas within mangrove swamps, wooded floodplains and edges of hardwood forests, and bogs . It can be found in loblolly pine communities.[5] It can also be found in longleaf pine-wiregrass communities.[4] It is tolerant of overstory canopies that decrease the light level to about half the ambient (i.e., it can live in partially shaded areas and its nitrogen-fixing capability won't be significantly affected).[3] It grows in highly disturbed areas, but it is also ubiquitous in high quality native longleaf pine uplands and sandhills. It occurs in soils ranging from deep sands (Entisols) to sandy loams (Ultisols).

Associated species includes Blackberry Bramble, turkey oak, longleaf pine, Galactia, Strophostyles, Smilax, Penstemon, Lechea, Chrysopsis, Brumelia, Centrosema, Euphorbia, Cassia, Serenoa repens, Quercus incana, Quercus chapmanii, Diospyros, Aristida, Andropogon, bahia grass, Rubus, cloverleaf, Pinus taeda, Liquidambar styraciflua, and others.[1]

Phenology

It flowers in April through October and fruits primarily in June thorugh September.[1]

Seed dispersal

According to Kay Kirkman, a plant ecologist, this species disperses by explosion mechanisms or by ants. [6]

Seed bank and germination

In Hier's study, changes in flowering did not seem to affect seed germination[7]. It spreads clonally by production of rhizomes.[8] Seed coats are hard and viable seed can persist in the seed bank for at least two years. [9]

Fire ecology

It thrives under fire.[5] Hendricks observed that the Piedmont National Wildlife Refuge plots, which had been under a 4-year burning regime since 1966, each contained more than 10 times more C. virginianum individuals per ha than the Oconee National Forest plots, which had no burning history.[10] Seasonal burning does not seem to negatively affect nitrogen fixation.[11] C. virginianum showed increased flowering synchrony in response to lightning-season burns.[7] It responded the best to March burns with respect to annual tissue inputs as well as nitrogen contribution.[11] C. virginianum showed robust flowering response to late winter/ early spring burns, supporting the response to March burns noted earlier. It has a mid-summer flowering peak.[7] Also, one study found no evidence that increased flowering affects nitrogen-fixing capability.[11]

Pollination

Its flower is highly specialized for pollination by large Hymenoptera.[12] It requires bees for pollination to "trip" the pollen delivery mechanism. Pollinator-plant relationships appear to be robust to alteration in flowering phenology resulting from variation in season of burn.[7]

Use by animals

Because C. virginianum is a legume, and legumes are high in protein and mineral content, a number of herbivores including but not limited to Gopherus polyphemus, white-tailed deer, and bob-white quail, consume it.[4]

Conservation and management

Cultivation and restoration

Photo Gallery

References and notes

  1. 1.0 1.1 1.2 Florida State University Robert K. Godfrey Herbarium database. URL: http://herbarium.bio.fsu.edu. Last accessed: June 2014. Collectors: Loran C. Anderson, John C. Ogden, Gwynn W. Ramsey, R.K. Godfrey, R. S. Mitchell; R. C. Phillips, K. Craddock Burks, Gary R. Knight, D. W. Mather, C. Jackson, D. B. Ward, Mary Margaret Williams, O. Lakela, Brenda Herring, Jame Amoroso, Gwynn W. Ramsey, Richard Mitchell, Gail A. Steverson, Grady W. Reinert, George R. Cooley, R. J. Eaton, R. Kral, Cecil R Slaughter, Andre F. Clewell, R. Komarek, R. F. Doren, Kevin Oakes, Richard Gaskalla, Lisa Keppner, Clarke Hudson, Wilbur H Duncan, Jean Wooten, H. R. Totten, R. L. Wilbur, C. Ritchie Bell, Delzie Demaree, F. S. Earle, A. B. Seymour, Samuel B. Jones, Jr., H. R. Reed, A. B. Seymour, Michael B. Brooks, Sidney McDaniel, D. C. Bain, D. S. Correll, H. B. Correll, Lloyd H. Shinners, Geo M. Merrill, and H J Hamby. States and Counties: Alabama: Baldwin. Arkansas: Little Rock. Florida: Bay, Citrus, Collier, Duval, Escambia, Franklin, Gadsden, Gulf, Hillsborough, Jackson, Jefferson, Leon, Liberty, Manatee, Marion, Okaloosa, Polk, St Johns, St. Lucie, Suwannee, Wakulla, and Washington. Georgia: Bartow, Grady, Madison, and Thomas. Mississippi: Forrest, Harrison, Jackson, Pearl River, and Pike. North Carolina: Alamance, Orange, and Wilkes. Texas: Angelina, Bastrop, Freestone, Harris, Morris, Tarrant, and Van Zandt.
  2. Radford, Albert E., Harry E. Ahles, and C. Ritchie Bell. Manual of the Vascular Flora of the Carolinas. 1964, 1968. The University of North Carolina Press. 635-6. Print
  3. 3.0 3.1 3.2 Cathey, S. E., L. R. Boring, et al. (2010). "Assessment of N2 fixation capability of native legumes from the longleaf pine-wiregrass ecosystem." Environmental and Experimental Botany 67: 444-450.
  4. 4.0 4.1 4.2 4.3 Hainds, M. J., R. J. Mitchell, et al. (1999). "Distribution of native legumes (Leguminoseae) in frequently burned longleaf pine (Pinaceae)-wiregrass (Poaceae) ecosystems." American Journal of Botany 86: 1606-1614.
  5. 5.0 5.1 5.2 Cushwa, C. T. (1966). The response of herbaceous vegetation to prescribed burning. Asheville, USDA Forest Service.
  6. Kay Kirkman, unpublished data, 2015.
  7. 7.0 7.1 7.2 7.3 Hiers, J. K., R. Wyatt, et al. (2000). "The effects of fire regime on legume reproduction in longleaf pine savannas: is a season selective?" Oecologia 125: 521-530.
  8. Hiers, J. K. and R. J. Mitchell (2007). "The influence of burning and light availability on N-2-fixation of native legumes in longleaf pine woodlands." Journal of the Torrey Botanical Society 134: 398-409.
  9. Coffey, K. L. and L. K. Kirkman (2006). "Seed germination strategies of species with restoration potential in a fire-maintained pine savanna." Natural Areas Journal 26: 289-299.
  10. Hendricks, J. J. and L. R. Boring (1999). "N2-fixation by native herbaceous legumes in burned pine ecosystems of the southeastern United States." Forest Ecology and Management 113: 167-177.
  11. 11.0 11.1 11.2 Hiers, J. K., R. J. Mitchell, et al. (2003). "Legumes native to longleaf pine savannas exhibit capacity for high N2-fixation rates and negligible impacts due to timing of fire." New Phytologist 157: 327-338
  12. Spears, Jr. E. E. 1987. Island and mainland pollination ecology of Centrosema virginianum and Opuntia s trie ta. J. Ecol. 75: 351-362.