Lespedeza angustifolia
| Lespedeza angustifolia | |
|---|---|
| |
| Photo by Guy Anglin, Atlas of Florida Vascular Plants | |
| Scientific classification | |
| Kingdom: | Plantae |
| Division: | Magnoliophyta - Flowering plants |
| Class: | Magnoliopsida – Dicotyledons |
| Order: | Fabales |
| Family: | Fabaceae ⁄ Leguminosae |
| Genus: | Lespedeza |
| Species: | L. angustifolia |
| Binomial name | |
| Lespedeza angustifolia (Pursh) Elliott | |
| |
| Natural range of Lespedeza angustifolia from USDA NRCS Plants Database. | |
Common name: narrowleaf lespedeza
Contents
Taxonomic notes
Description
“Annual or perennial herbs or shrubs. Leaves pinnately 3-folioate; leaflets entire, estipellate; stipules persistent, setaceous to ovate-lanceolate. Inflorescence usually few-to-many-flowered, loose to compact, sessile to long-pedunculate, axillary or terminal, spictate, racemose, capitate or rarely paniculate cluster; pedicels subtended by a bract and with a pair of inconspicuous bractlets immediately beneath the flower. Both apetalous (cleistogamous) and petaliferous (Chasmogamous) flowers present in most species, but the apetalous flower are more readily detected and more abundant in some species than others. Calyx persistent in fruit, the tube campanulate to cylindric with 5 nearly equal lobes or the upper 2 partly united and shorter; corolla papilionaceous, violet, purplish, roseate, yellow or whitish; stamens diadelphous, 9 and 1. Legume 1-seeded, indehiscent, sessile or stalked, flattened, elliptic, ovate or orbicular.” – Radford et al 1964
“Erect perennial 0.3-1.2 (1.8) m tall, above usually densely strigillose or weakly to strongly spreading, short-pubescent or even short-pilose. Densely strigillose to glabrate below. Leaflets narrowly oblong-elliptic to linear, (1.2) 2-6 cm long, 4-12X as long as wide, glabrous to more commonly densely appressed short-pubescent or strigillose above and densely strigillose beneath; stipules very narrowly linear to linear-subulate. Racemes spicate, or rarely globose, numerous, loose to compact, 0.7-3 cm long; peduncles ca. (0.5) 1-5 cm long, typically equaling or longer than the subtending leaves; peduncles and axes densely spreading short-pubescent; pedicels 1-2 mm long. Calyx densely spreading puberulent, lobes 4-6 mm long and nearly as long on the calyx; petals yellowish, the standard 5-7 mm long bearing a purplish spot. Legume densely spreading short-pubescent, broadly elliptic to oblong-obovate, 4-6 mm long, nearly equaling the calyx in length.” - Radford et al 1964
Distribution
Ecology
Habitat
Lespedeza angustifolia habitats include sandhills, pine flatwoods, and oldfield pinelands, as well as dry pond margins and open flood plains on areas that are mesic to excessively well drained (FSU Herbarium). It has been strongly associated with hydric habitats (Hainds et al. 1990) because of a higher tolerance for periodically inundated soil conditions (Hainds et al. 1997). It has been documented to occur in dried up bottoms of sinkhole ponds (FSU Herbarium). Soils include sand and sandy loams, including Ultisols, Entisols, and dry Spodosols .[1]. Other soil types includes red sandy clay hills and sandy peat (FSU Herbarium).
L. angustifolia is prevalent along eroded roadsides and railroads and in disturbed high pine habitats (FSU Herbarium).
Plants associated include Aristida, Ctenium, Andropogon, Sporobolus and Panicum hemitomon (FSU Herbarium).
Phenology
Blooms September to November (FSU Herbarium). Frequent where present by populations tend to be separated from one another.[2]
Seed dispersal
Seed bank and germination
Lespedeza and other legume species have a hard seed coat. Species with hard seed coats are likely capable of forming long-term persistent seed banks and continuation of the buried seed bag portion of this study will yield long-term data on this subject (Coffey and Kirkman 2006). Although perennial species found in longleaf pine ecosystems, such as Lespedeza, persist through frequent fire, fire exposes seeds in soil to higher temperature and high amplitudes of temperature fluctuation (Grime 1989) leading in some cases to germination (Coffey and Kirkman 2006).
Fire ecology
Frequent dormant season burning increased legume populations in southern pine forests, although fires during the growing season at the same frequency tended to reduce legume abundance (White et. al 1990).
Presence of Imperata cylindrica (cogan grass), an invasive plant found in the southeastern United States, did not deter the occurrence of L. angustifolia in plots that had been burned every 1 to 2 years in southeastern Mississippi (Brewer and Cralle 2003). In its natural habitat it requires frequent fire for persistence. It is primarily located in undisturbed sites and sometimes colonizes frequently burned old-field pinelands.[2]
Pollination
Bee and Lepidopteran pollinated in chasmogamous flowers afc
Use by animals
Diseases and parasites
Conservation and Management
Cultivation and restoration
Photo Gallery
References and notes
Brewer, J. S. and S. P. Cralle (2003). "Phosphorus addition reduces invasion of a longleaf pine savanna (southeastern USA) by a non-indigenous grass (Imperata cylindrica)." Plant Ecology 167: 237-245.
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.
Florida State University Robert K. Godfrey Herbarium database. URL: http://herbarium.bio.fsu.edu. Last accessed: July 2015. Collectors: Loran C. Anderson, Wilson Baker, A. F. Clewell, James R. Coleman, Delzie Demaree, William B. Fox, J. P. Gillespie, Robert K. Godfrey, Gary R. Knight, R. Komarek, R. Kral, T. MacClendon, John Morrill, A. E. Radford, John K. Small. States and Counties: Alabama: Baldwin. Florida: Franklin, Jackson, Jefferson, Leon, Liberty, Madison, Nassau, Wakulla, Washington. Georgia: Appling, Baker, Camden, Clinch, Grady, Lowndes, Miller, Seminole, Thomas, Walton, Wilcox. North Carolina: Cumberland, Harnett, Pitt. South Carolina: Sumter. Compiled by Tall Timbers Research Station and Land Conservancy.
Grime, J.P. 1989. Seed banks in ecological perspective. Pp. xv-xxii in M.A. Leck, V.T.Parker, and R.L. Simpson, eds., Ecology of Soil Seed Banks. Academic Press, San Diego, Calif.
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.
Hainds, M. J., R. J. Mitchell, et al. (1997). "Legume population dynamics in frequently burned longleaf pine-wiregrass fire ecosystem." Proceedings Longleaf Alliance Conference: Longleaf Alliance Report 1: 82-86.
