Difference between revisions of "Smilax auriculata"

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==Ecology==
 
==Ecology==
 
===Habitat=== <!--Natural communities, human disturbed habitats, topography, hydrology, soils, light, fire regime requirements for removal of competition, etc.-->
 
===Habitat=== <!--Natural communities, human disturbed habitats, topography, hydrology, soils, light, fire regime requirements for removal of competition, etc.-->
It can be found in xeric areas with well-drained, sandy soils (Menges and Kohfeldt 1995; Foster and Schmalzer 2003).
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In the Coastal Plain in Florida and Georgia, ''S. auriculata'' can be found bordering mesic woodlands, longleaf pine turkey oak sand ridges (FSU Herbarium), palmetto flatwoods (FSU Herbarium; Olano et al. 2006), oak-saw palmetto scrubs (Foster and Schmalzer 2003), sandhill communities (FSU Herbarium; Reinhart et al. 2004), xeric longleaf pine woodlands (Peet and Allard 1993), and unburned scrubby flatwoods (Menges and Kohfeldt 1995). It can also be found along railroads, powerline corridors, and disturbed longleaf pine restoration sites (FSU Herbarium). Soil types include loamy sand (FSU herbarium; Foster and Schmalzer 2003) and sandy, siliceous, hyperthermic Ultic haplaquod of the Pomona series (Moore et al. 1982).
Oak-saw palmetto scrub (Foster and Schmalzer 2003).  
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Scrubby flatwoods (which include oaks, dwarf palmettos and ericads)-Olano et al 2006.
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In habitats that include ''Pinus palustris, Quercus laevis, Q. incana, Sporobolus junceus'' and ''Licania michauxii'', ''S. auriculata'' accounts for most of the groundcover density (Rodgers and Provencher 1999).
“Fire is the primary ecological disturbance in this ecosystem…”(Olano et al 2006).
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“Southern Xeric Longleaf Pine Woodlands” classification according to Peet and Allard 1993, states Provencher et al 2001, where it includes ''P. palustris, Q. laevis, Q. incana, Sporobolus junceus'', and ''Licania michauxii'' – where ''Smilax auriculata'' is accounted for most of the groundcover density (Rodgers and Provencher 1999) – Provencher et al 2001.
 
Occurred in a mixed stand of slash and longleaf pine; soils were mainly sandy, siliceous, hyperthermic Ultic haplaquod of the Pomona series (Moore et al 2982).
 
It can be found in scrub and sandhill communities (Menges and Kohfeldt 1995; Reinhart et al 2004).
 
 
===Phenology=== <!--Timing off flowering, fruiting, seed dispersal, and environmental triggers.  Cite PanFlora website if appropriate: http://www.gilnelson.com/PanFlora/ -->
 
===Phenology=== <!--Timing off flowering, fruiting, seed dispersal, and environmental triggers.  Cite PanFlora website if appropriate: http://www.gilnelson.com/PanFlora/ -->
 
“is a woody vine with large specializes storage organs enabling rapid postfire recovery.” – Olano et al 2006.
 
“is a woody vine with large specializes storage organs enabling rapid postfire recovery.” – Olano et al 2006.

Revision as of 13:24, 7 October 2015

Smilax auriculata
Smilax auriculata Gil.jpg
Photo taken by Gil Nelson
Scientific classification
Kingdom: Plantae
Division: Magnoliophyta – Flowering plants
Class: Liliopsida – Monocotyledons
Order: Liliales
Family: Smilacaceae
Genus: Smilax
Species: S. auriculata
Binomial name
Smilax auriculata
Walter
SMIL AURI dist.jpg
Natural range of Smilax auriculata from USDA NRCS Plants Database.

Common name: earleaf greenbrier

Taxonomic notes

Description

A description of Smilax auriculata is provided in The Flora of North America.

Distribution

Ecology

Habitat

In the Coastal Plain in Florida and Georgia, S. auriculata can be found bordering mesic woodlands, longleaf pine turkey oak sand ridges (FSU Herbarium), palmetto flatwoods (FSU Herbarium; Olano et al. 2006), oak-saw palmetto scrubs (Foster and Schmalzer 2003), sandhill communities (FSU Herbarium; Reinhart et al. 2004), xeric longleaf pine woodlands (Peet and Allard 1993), and unburned scrubby flatwoods (Menges and Kohfeldt 1995). It can also be found along railroads, powerline corridors, and disturbed longleaf pine restoration sites (FSU Herbarium). Soil types include loamy sand (FSU herbarium; Foster and Schmalzer 2003) and sandy, siliceous, hyperthermic Ultic haplaquod of the Pomona series (Moore et al. 1982).

In habitats that include Pinus palustris, Quercus laevis, Q. incana, Sporobolus junceus and Licania michauxii, S. auriculata accounts for most of the groundcover density (Rodgers and Provencher 1999).

Phenology

“is a woody vine with large specializes storage organs enabling rapid postfire recovery.” – Olano et al 2006.

Seed dispersal

Seed bank and germination

It can reproduce by resprouting, clonal spreading, and seeding (Menges and Kohfeldt 1995).

Fire ecology

It increases in abundance after fire (Menges and Kohfeldt 1995). Its rapid recovery post-fire can be attributed to large specialized storage organs (Olano et al 2006). However, Greenberg found out that S. auriculata decreased to almost nonexistent following a May fire (2003). This suggests that season of burning is important for this species.

Pollination

The following Hymenoptera families and species were observed visiting flowers of Smilax auriculata at Archbold Biological Station (Deyrup 2015):

Apidae: Apis mellifera

Halictidae: Augochlora pura

Megachilidae: Coelioxys dolichos, Megachile mendica, M. xylocopoides

Use by animals

S. auriculata was found in 5.5% of the Gopherus polyphemus scat observed by Carlson and her team (2003). Thus, the gopher tortoise can serve as an agent of seed dispersal. Deyrup (2002) observed these bees, Augochlora pura, Coelioxys dolichos, Megachile mendica, M. xylocopoides, Apis mellifera, Xylocopa micans, X. virginica krombeini, on S. auriculata.

Diseases and parasites

Conservation and Management

Cultivation and restoration

Photo Gallery

References and notes

Carlson, J. E., E. S. Menges, et al. (2003). "Seed dispersal by Gopherus polyphemus at Archbold Biological Station, Florida." Florida Scientist 66: 147-154.

Deyrup, M.A. and N.D. 2015. Database of observations of Hymenoptera visitations to flowers of plants on Archbold Biological Station, Florida, USA.

Deyrup, M. and L. Deyrup (2012). "The diversity of insects visiting flowers of saw palmetto (Arecaceae)." Florida Entomologist 95(3): 711-730.

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.

Menges, E. and N. Kohfeldt (1995). "Life History Strategies of Florida Scrub Plants in Relation to Fire." Bulletin of the Torrey Botanical Club 122(4): 282-297

Menges, E. S. and N. M. Kohfeldt (1992). Life history strategies of scrub plants in relation to fire [abstract]. History and Ecology of the Florida scrub, Lake Placid, FL, Archbold Biological Station.

Moore, W. H., B. F. Swindel, et al. (1982). "Vegetative response to prescribed fire in a north Florida flatwoods forest." Journal of Range Management 35: 386-389.

Olano, J. M., E. S. Menges, et al. (2006). "Carbohydrate storage in five resprouting Florida scrub plants across a fire chronosequence." New Phytologist 170: 99-105.

Provencher, L. M., B. J. Herring, et al. (2001). "Effects of hardwood reduction techniques on longleaf pine sandhill vegetation in northwest Florida." Restoration Ecology 9: 13-27.

Reinhart, K. O. and E. S. Menges (2004). "Effects of re-introducing fire to a central Florida sandhill community." Applied Vegetation Science 7: 141-150.

Schmalzer, P. A., S. R. Turek, et al. (2002). "Reestablishing Florida scrub in a former agricultural site: survival and growth of planted species and changes in community composition." Castanea 67: 146-160.