Difference between revisions of "Stillingia sylvatica"
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===Fire ecology=== <!--Fire tolerance, fire dependence, adaptive fire responses--> | ===Fire ecology=== <!--Fire tolerance, fire dependence, adaptive fire responses--> | ||
− | + | ''S. sylvatica'' seems to respond positively to burning. In an experiment by Greenberg (2003), and he noted that the percent cover of ''S. sylvatica'' was highest 16 months after a May burn.<ref name="g03"> Greenberg, C. H. 2003. Vegetation recovery and stand structure following a prescribed stand-replacement burn in sand pine scrub. Natural Areas Journal 23:141-151.</ref> | |
− | + | ===Pollination and use by animals=== | |
− | + | ''S. sylvatica'' has been observed to host ''Perdita obscurata'' (family Andrenidae). The seeds of ''S. sylvatica'' contain elaiosomes and have been found in middens of Florida harvester ants, ''Pogonomyrmex badius''.<ref name="sl"/> | |
− | The seeds of ''S. sylvatica'' contain elaiosomes and have been found in middens of Florida harvester ants, ''Pogonomyrmex badius''.<ref name="sl"/> | ||
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Revision as of 09:37, 18 June 2021
Stillingia sylvatica | |
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Photo taken by Michelle M. Smith | |
Scientific classification | |
Kingdom: | Plantae |
Division: | Magnoliophyta – Flowering plants |
Class: | Magnoliopsida – Dicotyledons |
Order: | Euphorbiales |
Family: | Euphorbiaceae |
Genus: | Stillingia |
Species: | S. sylvatica |
Binomial name | |
Stillingia sylvatica L. | |
Natural range of Stillingia sylvatica from USDA NRCS Plants Database. |
Common name: Queen's-delight
Contents
Taxonomic notes
Synonyms: S. spathulata (Müller of Aargau) Small.[1]
Description
"Glabrous, monoecious, perennial herbs or shrubs with alternate leaves. Leaves finely crenate, the teeth with pointed, callous spicules, sessile or short-petiolate. Spike terminal, rachis with numerous large glands, the lower portion pistillate flowered, the upper staminate. Calyx 2-3 parted, yellow; petals none; stamens 2; stigmas 3, red. Capsules as long as broad, leaving a 3-lobed disc upon falling from plant. Seeds grayish white, ovoid; caruncle small."[2]
"Herbaceous perennial, to 8 dm tall, with few to numerous stems arising from a crown; stems branching only immediately below an inflorescence with 2-4 branches. These usually terminated in an inflorescence. Leaves elliptic, 3.5-9 cm long, 1-4.5 cm wide; petioles 0-4 mm long, base glandular-stipulate. Spike 5-12 cm long. Capsules 8-10 mm long. Seeds nearly smooth, 5-6 mm long."[2]
The root system of Stillingia sylvatica includes stem tubers which store non-structural carbohydrates (NSC) important for both resprouting following fire and persisting during long periods of fire exclusion.[3] Diaz-Toribio and Putz (2021) recorded this species to have an NSC concentration of 413.9 mg/g (ranking 3 out of 100 species studied) and water content of 62.3% (ranking 50 out of 100 species studied).[3]
Distribution
Stillingia sylvatica var. tenuis is endemic to subtropical Florida from Lake Okeechobee southward. The Miami Rocklands and Big Pine Key seem to be key speciation areas.[4]
Ecology
Habitat
In the Coastal Plain in Florida and Georgia, S. sylvatica can be found in sandhills (FSU Herbarium),[5] pine flatwoods, open pine-oak woodlands, recently burned pine-oak scrubs, longleaf pine-wiregrass stands, longleaf pine-turkey oak-wiregrass, and annually burned pinelands (FSU Herbarium). Substrate types include loamy sand, sand (FSU Herbarium), and siliceous, hypothermic Ultic haplaquod of the Pomona series.[6] S. sylvatica does not respond to soil disturbance by clearcutting and chopping in North Florida flatwoods forests.[7]
Associated species include Stillingia aquatica, Phlox floridana, Asimina longifolia var. spathulata, Lactuca graminifolia, Pterocaulon undulatum, Asclepias humistrata and Quercus hemisphaerica (FSU Herbarium).
Stillingia sylvatica is frequent and abundant in the Peninsula Xeric Sandhills and North Florida Subxeric Sandhiils community types as described in Carr et al. (2010).[8]
Phenology
S. sylvatica has been observed flowering April through August with peak inflorescence in April and May (FSU Herbarium).[9]
Seed dispersal
This species is thought to be dispersed by ants and/or explosive dehiscence.[10] It is dispersed explosively (up to 3 meters); seeds are forcefully expelled after the fruit matures and dries.[5]
Though seeds may be dispersed in part by ants, studies show the seeds were attractive to fire ants but rarely moved by them.[11]
Fire ecology
S. sylvatica seems to respond positively to burning. In an experiment by Greenberg (2003), and he noted that the percent cover of S. sylvatica was highest 16 months after a May burn.[12]
Pollination and use by animals
S. sylvatica has been observed to host Perdita obscurata (family Andrenidae). The seeds of S. sylvatica contain elaiosomes and have been found in middens of Florida harvester ants, Pogonomyrmex badius.[5]
Conservation, cultivation, and restoration
Cultural use
Historically, the plant's roots were mashed and boiled and given to native women after giving birth, and it was used to treat menstrual irregularity. In the south, it was used to treat constipation and induce vomiting. It was also used as a treatment for syphilis, skin diseases, pulmonary issues, and liver problems.[13] This species should be used with caution, as cyanide has been detected within the plant.[14]
Photo Gallery
References and notes
- ↑ Weakley, A.S. 2015. Flora of the southern and mid-atlantic states. Working Draf of 21 May 2015. University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
- ↑ 2.0 2.1 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. 667. Print.
- ↑ 3.0 3.1 Diaz-Toribio, M.H. and F. E. Putz 2021. Underground carbohydrate stores and storage organs in fire-maintained longleaf pine savannas in Florida, USA. American Journal of Botany 108: 432-442.
- ↑ Sorrie, B. A. and A. S. Weakley 2001. Coastal Plain valcular plant endemics: Phytogeographic patterns. Castanea 66: 50-82.
- ↑ 5.0 5.1 5.2 Stamp, N. E. and J. R. Lucas. 1990. Spatial patterns and dispersal distances of explosively dispersing plants in Florida sandhill vegetation. Journal of Ecology 78:589-600.
- ↑ Moore, W. H., B. F. Swindel and W. S. Terry. 1982. Vegetative response to prescribed fire in a north Florida flatwoods forest. Journal of Range Management 35:386-389.
- ↑ Moore, W.H., B.F. Swindel, and W.S. Terry. (1982). Vegetative Response to Clearcutting and Chopping in a North Florida Flatwoods Forest. Journal of Range Management 35(2):214-218.
- ↑ Carr, S.C., K.M. Robertson, and R.K. Peet. 2010. A vegetation classification of fire-dependent pinelands of Florida. Castanea 75:153-189.
- ↑ Nelson, G. PanFlora: Plant data for the eastern United States with emphasis on the Southeastern Coastal Plains, Florida, and the Florida Panhandle. www.gilnelson.com/PanFlora/ Accessed: 14 DEC 2016
- ↑ Kirkman, L. Katherine. Unpublished database of seed dispersal mode of plants found in Coastal Plain longleaf pine-grasslands of the Jones Ecological Research Center, Georgia.
- ↑ Cumberland, M.S. and Kirkman, L.K. 2013. The effects of the red imported fire ant on seed fate in the longleaf pine ecosystem. Springer Science+Business Media Dordrecht. Plant Ecol 214: 717-724.
- ↑ Greenberg, C. H. 2003. Vegetation recovery and stand structure following a prescribed stand-replacement burn in sand pine scrub. Natural Areas Journal 23:141-151.
- ↑ Korchmal, Arnold & Connie. 1973. A Guide to the Medicinal Plants of the United States. The New York Times Book Company, New York.
- ↑ Burrows, G.E., Tyrl, R.J. 2001. Toxic Plants of North America. Iowa State Press.