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Wisteria floribunda, W. sinensis


Chinese wisteria
Photo by Ted Bodner, Southern Weed Science Society,

Stone, Katharine R. 2009. Wisteria floribunda, W. sinensis. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: /database/feis/plants/vine/wisflo/all.html [].



Japanese wisteria
Chinese wisteria

The genus name for wisteria is Wisteria Nutt. (Fabaceae). This review summarizes information on the following wisteria species:

Wisteria floribunda (Willd.) DC., Japanese wisteria [13,28]
Wisteria sinensis (Sims) DC., Chinese wisteria [1,13,28,47]

In this review, species are referred to by their common names, and "wisteria" refers to both species.

Hybrids: In the southeastern United States, the majority of wisteria plants growing outside of cultivation were hybrids of Chinese and Japanese wisteria [35,36].

for Wisteria floribunda (Willd.) DC.:
Rehsonia floribunda (Willd.) Stritch [24]

for Wisteria sinensis (Sims) DC.:
Rehsonia sinensis (Sims) Stritch [24]



Information on state-level noxious weed status of plants in the United States is available at Plants Database.


SPECIES: Wisteria floribunda, W.sinensis

As their names imply, Japanese and Chinese wisteria are native to Japan and China, respectively [34]. Chinese wisteria was brought to the United States for horticultural purposes in 1816 [45], while Japanese wisteria was introduced around 1830 [30]. Wisterias are used extensively in the southern and mid-Atlantic states to adorn porches, gazebos, walls, gardens and parks, and most infestations in natural areas are the result of plants escaping from such settings [34]. As of 2009, distributional maps of the United States show wisterias concentrated in the southeast, with spotty distributions to the north and west. Japanese wisteria is found as far west as Texas, east to Florida, north to Maine, and west to Illinois. Chinese wisteria is found as far west as Texas, east to Florida, north to Vermont, and west to Michigan. Chinese wisteria also occurs in Hawaii. The high rate of hybridization in wisteria plants in the southeastern states [35,36] may make distribution maps for the individual species suspect. Plants Database provides current distribution maps for both Japanese and Chinese wisteria.

Plant community associations of nonnative species are often difficult to describe accurately because detailed survey information is lacking, there are gaps in understanding of nonnative species' ecological characteristics, and nonnative species may still be expanding their North American range. Though known to have a broad distribution, as of 2009 there were very few published descriptions of plant communities in which either wisteria species occurs. Therefore, wisterias likely occur in plant communities other than those discussed here and listed in the Fire Regime Table.

Chinese wisteria was found at the forest edge at Mt. Vernon, Virginia, where most of the forest was described as mature oak-hickory (Quercus spp.-Carya spp.) [45]. Similarly, it occurred in the North Carolina Piedmont of Durham and Orange Counties in undisturbed sites dominated by a temperate cold-deciduous forest mixture of oaks and hickories. In this same region, Chinese wisteria also occurred in areas of disturbed forest and abandoned agricultural land dominated by an overstory of loblolly pine (Pinus taeda). It was found with a number of other nonnative species, including tree-of-heaven (Ailanthus altissima), mimosa (Albizia julibrissin), princesstree (Paulownia tomentosa), multiflora rose (Rosa multiflora), Chinese privet (Ligustrum sinense), and Japanese honeysuckle (Lonicera japonica) [18].

In a Washington D.C. park, Chinese wisteria occurred with the overstory tree species yellow-poplar (Liriodendron tulipifera), American beech (Fagus grandifolia), American elm (Ulmus americana), black locust (Robinia psuedoacacia), northern red oak (Q. rubra), and sycamore (Platanus occidentalis). It was itself being climbed by western poison-ivy (Toxicodendron rydbergi) and Virginia creeper (Parthenocissus quinquefolia) [26].

The presence of Chinese wisteria is listed as a problem in the restoration of bottomland hardwood forests in Mississippi [32], which may be part of the southern floodplain forest type, with dominant species such as black tupelo (Nyassa sylvatica), sweetgum (Liquidambar spp.), oaks, baldcypress (Taxodium distichum), and pines (Pinus spp.) [9]. Chinese wisteria also occurred in an old-growth forest remnant stand dominated by longleaf pine (P. palustrus), a particularly rare southeastern forest type [40].

The only published record of plant community associations for Japanese wisteria noted that it was found alongside other nonnative species in a New Jersey forest preserve dominated by oaks, American beech, and sugar maple (Acer saccharum) [41].


SPECIES: Wisteria floribunda, W. sinensis
Chinese wisteria infestation
Photo by Randy Westbrooks, U.S. Geological Survey,


Botanical description: This description provides characteristics that may be relevant to fire ecology and is not meant for identification. Keys for identification are available (e.g., [24]).

Both Japanese and Chinese wisteria are showy, ornamental perennial lianas that commonly climb, twine, or trail on the ground [21,34]. Chinese wisteria is also occasionally described as a shrub [8,19]. Both species have been observed 65 feet (20 m) high in the canopy [34], and there are records of vines 70 feet (21 m) long [21]. The species look similar to each other and can be difficult to distinguish because they hybridize [21,35]. One way to differentiate the species is by examining the direction of vine twining; Chinese wisteria vines twine clockwise, while Japanese wisteria vines twine counter-clockwise [22].

Roots: One flora describes Chinese wisteria roots as few but "deeply penetrating" [41].

Stems: Stems of older wisteria plants can grow 15 inches (38 cm) in diameter, and have infrequent, alternate branches [34].

Leaves: Compound leaves of wisterias are about 1 foot (0.3 m) in length and alternate along the stem. Japanese wisteria leaves consist of 13 to 19 leaflets, while Chinese wisteria leaves consist of 7 to 13 leaflets [34].

Flowers: Wisteria flowers are dangling and showy, blue-violet, and are borne on racemes. Racemes are 4 to 20 inches (10-50 cm) long and 3 to 4 inches (7-10 cm) wide. All Chinese wisteria flowers bloom at the same time, while Japanese wisteria flowers bloom in sequence, starting at the base [21].

Fruits: Wisteria fruits are velvety brown seed pods, 4 to 6 inches (10-15 cm) long, narrowed toward the base, with constrictions in the pods that separate the seeds [34]. Each pod contains 1 to 8 flat, round, brown seeds, each 0.5 to 1 inch (1.2-2.5 cm) in diameter [21].

Raunkiaer [27] life form:

For both species, flowering occurs in spring (April-May) [34] and fruits are formed from July to November [21].


There is very little information available about the reproductive and regeneration strategies of wisterias. The information available suggests that although seeds are produced in favorable conditions, vegetative growth from rooting of vines and stolons is the main method of wisteria spread [17,30]. Following injury, Japanese wisteria sprouts from the stump and from root fragments [30].

Pollination and breeding system: Hummingbirds were observed visiting Chinese wisteria [25].

Seed production: No information is available on this topic.

Seed dispersal: Wisteria pods and seeds are large and heavy, which limits dispersal by birds and mammals [21,22]. Seeds are water-dispersed along riparian areas and can travel great distances this way [21,22,30,34].

Seed banking: No information is available on this topic.

Germination: No information is available on this topic.

Seedling establishment and plant growth: Canopy gap formation which occurs when wisteria topples a large tree favors the growth of wisteria seedlings [34] and existing wisteria plants [17]. Once established in an area, wisteria patches can potentially cover several acres (see Impacts). One review states that Japanese wisteria plants can grow for more than 50 years [30], while another paper states that individual vines of both species can live for more than100 years [35].

Vegetative regeneration: Although seeds are produced in favorable conditions, vegetative growth is the main method of wisteria spread [17,30]. Reviews describe vines [21,22] and stolons [21,34] rooting at nodes. One review also notes the ability of Japanese wisteria to sprout repeatedly after mechanical damage, either from the stump or from any fragment of root system left in the ground [30]. Rates and distances of spread are not known, though individual vines have been documented at over 70 feet (21 m) long [21].

Wisterias form dense infestations that spread from horticultural plantings [21,35]. They tend to establish and spread in forest edges, disturbed areas, and riparian zones [35], as well as roadsides, ditches, and rights-of-way [30]. Wisterias grow best in full sun but are tolerant of shade [17,30].

Soil: One review states that wisterias tolerate a variety of soil and moisture levels in the southeastern United States [35]. In Virginia, both species are listed as occurring on mesic sites [42]. In the southeastern United States, Japanese wisteria tolerates a variety of soil and moisture regimes but prefers loamy, deep, and well-drained soil [30]. One flora from the Southwest indicates that Chinese wisteria prefers deep, rich soil [41]. At Fire Island National Seashore, Suffolk County, New York, an isolated Chinese wisteria shrub was found growing in moist sand along a bayshore [8].

Climate: Two studies offered limited climate data for locations with Chinese wisteria. At Fire Island National Seashore, Suffolk County, New York, the mean annual temperature was 50 °F (10 °C) and annual precipitation was approximately 45 inches (1143 mm) [8]. In Durham and Orange Counties in North Carolina, mean daily maximum temperatures of 88.7 °F (31.5 °C) occurred in July, and mean daily minimum temperatures of 29.8 °F (-1.2 °C) occurred in January. Annual precipitation was 41 inches (1,052 mm) [18].

Elevation: Chinese wisteria occurs at 3,000 to 3,500 feet (900-1,000 m) in Bolivia [12]. Elevation ranges for wisterias in North America were not found in the available literature (2009).

Flooding: Chinese wisteria is considered problematic in bottomland hardwood forests, a plant community which experiences frequent flooding [32].

Wisterias grow best in full sun but are capable of tolerating and reproducing in partial shade [30,35,42]. While Chinese wisteria has been observed on the edge of mid- and late-successional forests [45], occurrence within the forest interior is not well-documented. The ability of wisterias to spread vegetatively suggests that they could move into the forest interior if favorable light conditions were created through disturbances. Observations of Japanese wisteria climbing surrounding vegetation in the direction of sunlight [30] suggest that this vine may spread and fill in canopy gaps as they are created.

Once established in an area, wisterias may persist for a long time and eventually alter successional pathways for the area they inhabit. It has been repeatedly noted that infestations of wisteria are so dense that they strangle or shade out existing vegetation and displace native species [30,34,35]. Heavy infestations that topple large canopy trees and increase sunlight to the forest floor could favor colonizing species, including wisteria seedlings [34].

Because wisterias typically use other vegetation as support, it is not clear what their response would be following a disturbance that removed all potential supporting vegetation.


SPECIES: Wisteria floribunda, W. sinensis
Immediate fire effect on plant: As of this writing (2009), there was no available literature that described the immediate effects of fire on either wisteria species. It is possible that severe fire may kill entire mature plants, although this response has not been documented. Because Japanese wisteria sprouts from the stem and root fragments after mechanical treatments [30], wisteria plants might also sprout after fire. As of 2009, no information was available on fire effects on or heat tolerance of wisteria seeds.

Postfire regeneration strategy [33]:
Prostrate woody plant, stem growing in organic soil
Initial off-site colonizer (off site, initial community)

Fire adaptations and plant response to fire: There was very little information (as of 2009) regarding specific adaptations of wisterias to fire. The ability of Japanese wisteria to sprout repeatedly from the stem and root fragments following mechanical treatments [30] (see Physical and/or mechanical control) suggests that either species would have the ability to sprout after fire if those parts were not subjected to lethal temperatures.

The dispersal characteristics of wisteria seeds suggest that seedlings would be unlikely to establish in postfire habitats unless there was an immediately adjacent riparian area or a source population of wisteria. Because seed bank information is lacking for wisterias, it is not known whether they might establish from a seed bank after fire.

Fuels: As of 2009, no studies specifically addressed fuel characteristics of wisterias. One review suggests that Chinese wisteria, along with a number of other invasive vines, has the potential to alter the fuel characteristics of invaded communities. Specifically, invasive vines could increase fuel loading and continuity, and contribute to the likelihood of crown fire by acting as a ladder fuel [7]. The density, spatial extent, and climbing nature of wisteria populations suggest that they may alter fuel characteristics in invaded communities.

Fire regimes: It is not known what type of fire regime wisterias are best adapted to. In North America, they are found in plant communities that experience both long (e.g., northern hardwood, southern floodplain forests) and short (e.g., oak-hickory-pine communities) fire-return intervals (see the Fire Regime Table). In many areas where wisterias occur, historic fire regimes have been dramatically altered due to fire exclusion and massive disturbances associated with human settlement, and the potential natural vegetation may be difficult to discern.

It is unclear how the presence of wisterias may affect fire regimes in invaded communities. In ecosystems where wisterias replace plants with similar fuel characteristics, they may alter fire intensity or slightly modify an existing fire regime. If wisteria spread introduces novel fuel properties to the invaded ecosystem, fire behavior, and potentially fire regime, may be altered (see: [4,6]). This topic warrants additional study.

Potential for postfire establishment and spread: As of 2009, no studies documented the establishment or spread of either wisteria species after fire. The large seed size and consequent lack of long-distance dispersal suggest that it would be difficult for wisterias to establish by seed unless the fire occurred near a riparian area or a source population of wisteria. However, the ability for the species to spread vegetatively, combined with a preference for sunny environments [17,30], suggests that wisterias may be problematic in postfire habitats if intact populations are nearby.

Preventing postfire establishment and spread: Preventing invasive plants from establishing in weed-free burned areas is the most effective and least costly management method. This can be accomplished through early detection and eradication, careful monitoring and followup, and limiting dispersal of invasive plant propagules into burned areas. Specific recommendations include:

For more detailed information on these topics see the following publications: [2,5,10,38].

Use of fire as a control agent: As of 2009, there were no studies that tested the efficacy of using fire to control wisteria populations.


SPECIES: Wisteria floribunda, W. sinensis
As of 2009, there was very little information on the importance of wisteria to wildlife or livestock.

Palatability and/or nutritional value: A number of reviews list wisteria flowers, leaves, fruits, and seeds as poisonous [3], and one further indicates that seed ingestion causes symptoms such as nausea, vomiting, stomach pains, and diarrhea [17]. Japanese wisteria was listed as a minor winter plant food for bobwhite quail in Alabama [31], and hummingbirds have been observed feeding on the nectar of Chinese wisteria [25].

Cover value: No information is available on this topic.

One review describes uses for lectins and resins derived from Chinese wisteria [3].

Impacts: Information regarding the impacts of wisterias on invaded communities includes evidence that both species displace existing vegetation by strangling or shading out native plants and trees [17,21,30,34,35]. The death of large trees from wisteria establishment results in breaks in closed canopy forest, which favors further growth and spread of wisteria [17]. Once established in an area, wisteria patches can potentially cover several acres; one herbicide experiment in Alabama was conducted in a Chinese wisteria patch that covered 2 to 3 acres (1 ha) [22]. The presence of Chinese wisteria was listed as a problem in the restoration of bottomland hardwood forests in Mississippi [32] and threatens old-growth remnant stands of longleaf pine in the Southeast [40]. Chinese wisteria is also listed as occurring on National Wildlife Refuges in Florida [16].

While both wisteria species are listed as invasive species of concern in a number of states, information as of 2009 suggests that they are less of a perceived threat than other, co-occurring invasive species [23,29,37,44]. For example, in a paper describing woody invaders of eastern forests, Japanese and Chinese wisteria are not considered as much of a threat as other woody vines, including Oriental bittersweet (Celastrus orbiculatus), Japanese honeysuckle (Lonicera japonica), or kudzu (Pueraria montana) [44]. However, that status may change in the future.

Control: In all cases where invasive species are targeted for control, the potential for other invasive species to fill their void must be considered, no matter what method is employed [5]. Information presented in the following sections may not be comprehensive and is not intended to be prescriptive in nature. It is intended to help managers understand the ecology and control of wisterias in the context of fire management. For more detailed information on control of Japanese or Chinese wisteria, consult the references cited here or local extension services.

Fire: For information on the use of prescribed fire to control this species see Fire Management Considerations.

Prevention: No information is available on this topic.

Cultural: No information is available on this topic.

Physical and/or mechanical: One review outlines strategies for cutting climbing or trailing vines of Japanese wisteria. Wisteria can sprout numerous times after cutting, so the treatment must be repeated until root stores are exhausted. If done approximately every 2 weeks from spring until autumn, cutting prevents seed production and strangulation of surrounding vegetation. This type of treatment is appropriate for small populations, as a pre-treatment for large, impenetrable sites, or in areas where herbicides are not appropriate [30].

It is also possible to try to control juvenile or isolated Japanese wisteria plants using a pulaski or similar digging tool to remove the entire plant, including all roots and runners. Any portions of the root system not removed are capable of sprouting. This treatment is appropriate for small initial populations or areas where herbicide use is not feasible [30].

Biological: No information is available on this topic.

Chemical: A range of foliar spray herbicides has been effectively used for wisteria control [22,30], though high rates and repeated applications were needed to produce near-eradication [22] and it was possible to damage non-target species with treatment. Cut-stump application of glyphosate or triclopyr 2 inches (5 cm) above ground level was also found to be effective for Japanese wisteria control, though foliar spray treatments may be needed afterward to compensate for the stimulation of wisteria seedlings after large vine removal [30]. Care must be taken when other invasive species are present; in one herbicide treatment, the reduction in Chinese wisteria cover released the invasive Chinese privet (Ligustrum sinense), which was not impacted by the herbicides [22].

Integrated management: No information is available on this topic.


SPECIES: Wisteria floribunda, W. sinensis

This Fire Regime Table summarizes characteristics of fire regimes for vegetation communities in which Japanese or Chinese wisteria may occur based on descriptions in available literature and from inferences based on county distribution records found in the Plants Database. Follow the links in the table to documents that provide more detailed information on these fire regimes. This table does not include plant communities across the entire range of either wisteria. Find further fire regime information for the plant communities in which these species may occur by entering the species' names in the FEIS home page under "Find Fire Regimes".

Fire regime information on vegetation communities in which Japanese and Chinese wisteria may occur. This information is taken from the LANDFIRE Rapid Assessment Vegetation Models [15], which were developed by local experts using available literature, local data, and/or expert opinion. This table summarizes fire regime characteristics for each plant community listed. The PDF file linked from each plant community name describes the model and synthesizes the knowledge available on vegetation composition, structure, and dynamics in that community. Cells are blank where information is not available in the Rapid Assessment Vegetation Model.
Southeast Great Lakes Northeast South-central US Southern Appalachians
Great Lakes
Vegetation Community (Potential Natural Vegetation Group) Fire severity* Fire regime characteristics
Percent of fires Mean interval
Minimum interval
Maximum interval
Great Lakes Forested
Northern hardwood maple-beech-eastern hemlock Replacement 60% >1,000    
Mixed 40% >1,000    
Oak-hickory Replacement 13% 66 1  
Mixed 11% 77 5  
Surface or low 76% 11 2 25
Vegetation Community (Potential Natural Vegetation Group) Fire severity* Fire regime characteristics
Percent of fires Mean interval
Minimum interval
Maximum interval
Northeast Woodland
Pine barrens Replacement 10% 78    
Mixed 25% 32    
Surface or low 65% 12    
Northeast Forested
Northern hardwoods (Northeast) Replacement 39% >1,000    
Mixed 61% 650    
Appalachian oak forest (dry-mesic) Replacement 2% 625 500 >1,000
Mixed 6% 250 200 500
Surface or low 92% 15 7 26
South-central US
Vegetation Community (Potential Natural Vegetation Group) Fire severity* Fire regime characteristics
Percent of fires Mean interval
Minimum interval
Maximum interval
South-central US Grassland
Bluestem-sacahuista Replacement 70% 3.6 1  
Mixed 30% 7.7 2  
South-central US Forested
Southern floodplain Replacement 42% 140    
Surface or low 58% 100    
Southern Appalachians
Vegetation Community (Potential Natural Vegetation Group) Fire severity* Fire regime characteristics
Percent of fires Mean interval
Minimum interval
Maximum interval
Southern Appalachians Forested
Appalachian oak-hickory-pine Replacement 3% 180 30 500
Mixed 8% 65 15 150
Surface or low 89% 6 3 10
Appalachian oak forest (dry-mesic) Replacement 6% 220    
Mixed 15% 90    
Surface or low 79% 17    
Vegetation Community (Potential Natural Vegetation Group) Fire severity* Fire regime characteristics
Percent of fires Mean interval
Minimum interval
Maximum interval
Southeast Shrubland
Pocosin Replacement 1% >1,000 30 >1,000
Mixed 99% 12 3 20
Southeast Woodland
Longleaf pine/bluestem Replacement 3% 130    
Surface or low 97% 4 1 5
Longleaf pine (mesic uplands) Replacement 3% 110 40 200
Surface or low 97% 3 1 5
Longleaf pine-Sandhills prairie Replacement 3% 130 25 500
Surface or low 97% 4 1 10
Southeast Forested
Coastal Plain pine-oak-hickory Replacement 4% 200    
Mixed 7% 100    
Surface or low 89% 8    
Mesic-dry flatwoods Replacement 3% 65 5 150
Surface or low 97% 2 1 8
Loess bluff and plain forest Replacement 7% 476    
Mixed 9% 385    
Surface or low 85% 39    
Southern floodplain Replacement 7% 900    
Surface or low 93% 63    
*Fire Severities
Replacement: Any fire that causes greater than 75% top removal of a vegetation-fuel type, resulting in general replacement of existing vegetation; may or may not cause a lethal effect on the plants.
Mixed: Any fire burning more than 5% of an area that does not qualify as a replacement, surface, or low-severity fire; includes mosaic and other fires that are intermediate in effects.
Surface or low: Any fire that causes less than 25% upper layer replacement and/or removal in a vegetation-fuel class but burns 5% or more of the area [11,14].


SPECIES: Wisteria floribunda, W. sinensis

1. Ali, S. I.; Qaiser, M. 2001. Flora of Pakistan, [Online]. In: Karachi, Pakistan: University of Karachi; St. Louis, MO: Missouri Botanical Garden (Producers). Available:°Flora_id=5 [2009, February 26]. [73152]
2. Asher, Jerry; Dewey, Steven; Olivarez, Jim; Johnson, Curt. 1998. Minimizing weed spread following wildland fires. Proceedings, Western Society of Weed Science. 51: 49. [40409]
3. Austin, Daniel F. 1999. Ethnobotany of Florida's weedy vines. In: Jones, David T.; Gamble, Brandon W., eds. Florida's garden of good and evil: Proceedings of the 1998 joint symposium of the Florida Exotic Pest Plant Council and the Florida Native Plant Society; 1998 June 3-7; Palm Beach Gardens, FL. West Palm Beach, FL: South Florida Water Management District: 171-179. [54024]
4. Brooks, Matthew L.; D'Antonio, Carla M.; Richardson, David M.; Grace, James B.; Keeley, Jon E.; DiTomaso, Joseph M.; Hobbs, Richard J.; Pellant, Mike; Pyke, David. 2004. Effects of invasive alien plants on fire regimes. BioScience. 54(7): 677-688. [50224]
5. Brooks, Matthew L.; Pyke, David A. 2001. Invasive plants and fire in the deserts of North America. In: Galley, Krista E. M.; Wilson, Tyrone P., eds. Proceedings of the invasive species workshop: The role of fire in the control and spread of invasive species; Fire conference 2000: 1st national congress on fire ecology, prevention, and management; 2000 November 27 - December 1; San Diego, CA. Misc. Publ. No. 11. Tallahassee, FL: Tall Timbers Research Station: 1-14. [40491]
6. D'Antonio, Carla M. 2000. Fire, plant invasions, and global changes. In: Mooney, Harold A.; Hobbs, Richard J., eds. Invasive species in a changing world. Washington, DC: Island Press: 65-93. [37679]
7. Dibble, Alison C.; Zouhar, Kristin; Smith, Jane Kapler. 2008. Chapter 5: Fire and nonnative invasive plants in the Northeast bioregion. In: Zouhar, Kristin; Smith, Jane Kapler; Sutherland, Steve; Brooks, Matthew L., eds. Wildland fire in ecosystems: fire and nonnative invasive plants. Gen. Tech. Rem. RMRS-GTR-42-vol. 6. Ogden, UT: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station: 61-90. [70902]
8. Dowhan, Joseph J.; Rozsa, Ron. 1989. Flora of Fire Island, Suffolk County, New York. Bulletin of the Torrey Botanical Club. 116(3): 265-282. [22041]
9. Garrison, George A.; Bjugstad, Ardell J.; Duncan, Don A.; Lewis, Mont E.; Smith, Dixie R. 1977. Vegetation and environmental features of forest and range ecosystems. Agric. Handb. 475. Washington, DC: U.S. Department of Agriculture, Forest Service. 68 p. [998]
10. Goodwin, Kim; Sheley, Roger; Clark, Janet. 2002. Integrated noxious weed management after wildfires. EB-160. Bozeman, MT: Montana State University, Extension Service. 46 p. Available online: [2003, October 1]. [45303]
11. Hann, Wendel; Havlina, Doug; Shlisky, Ayn; [and others]. 2008. Interagency fire regime condition class guidebook. Version 1.3, [Online]. In: Interagency fire regime condition class website. U.S. Department of Agriculture, Forest Service; U.S. Department of the Interior; The Nature Conservancy; Systems for Environmental Management (Producer). 119 p. Available: [2008, September 03]. [70966]
12. Jorgensen, Peter Moller. 2004. Bolivia checklist, [Online]. In: St. Louis, MO: Missouri Botanical Garden; Cambridge, MA: Harvard University Herbaria (Producers). Available:°Flora_id=40 [2009, February 26]. [73151]
13. Kartesz, John T. 1999. A synonymized checklist and atlas with biological attributes for the vascular flora of the United States, Canada, and Greenland. 1st ed. In: Kartesz, John T.; Meacham, Christopher A. Synthesis of the North American flora (Windows Version 1.0), [CD-ROM]. Chapel Hill, NC: North Carolina Botanical Garden (Producer). In cooperation with: The Nature Conservancy; U.S. Department of Agriculture, Natural Resources Conservation Service; U.S. Department of the Interior, Fish and Wildlife Service. [36715]
14. LANDFIRE Rapid Assessment. 2005. Reference condition modeling manual (Version 2.1), [Online]. In: LANDFIRE. Cooperative Agreement 04-CA-11132543-189. Boulder, CO: The Nature Conservancy; U.S. Department of Agriculture, Forest Service; U.S. Department of the Interior (Producers). 72 p. Available:°File=RA_Modeling_Manual_v2_1.pdf [2007, May 24]. [66741]
15. LANDFIRE Rapid Assessment. 2007. Rapid assessment reference condition models, [Online]. In: LANDFIRE. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Lab; U.S. Geological Survey; The Nature Conservancy (Producers). Available: [2008, April 18] [66533]
16. Maffei, Mark D. 1994. Invasive non-indigenous species on national wildlife refuges in Florida. In: Schmita, Don C.; Brown, Tom C., eds. An assessment of invasive non-indigenous species in Florida's public lands. Technical Report No. TSS-94-100. Tallahassee, FL: Florida Department of Environmental Protection, Division of Environmental Resource Permitting, Bureau of Aquatic Plant Management: 179-185. [55880]
17. Martin, Tunyalee. 2002. Weed notes Wisteria sinensis (Chinese wisteria) Wisteria floribunda (Japanese wisteria. The Nature Conservancy. Available: [1-29-2009]. [72841]
18. McDonald, Robert I.; Urban, Dean L. 2006. Edge effects on species composition and exotic species abundance in the North Carolina Piedmont. Biological Invasions. 8: 1049-1060. [68821]
19. Miller, J. H. 1995. Exotic plants in southern forests: their nature and control. In: Street, J. E., ed. Herbicide-resistant crops: a bitter or better harvest; 1995 January 16-18; Memphis, TN. In: Proceedings, Southern Weed Science Society 48th annual meeting. Champaign, IL: Southern Weed Science Society; 48: 120-126. [51347]
20. Miller, J. H. 1998. Primary screening of forestry herbicides for control of Chinese privet (Ligustrum sinense), Chinese wisteria (Wisteria sinensis), and trumpetcreeper (Campsis radicans). In: Dusky, Joan A., ed. Preparing for a new millenium; 1998 January 26-28; Birmingham, AL. In: Proceedings, Southern Weed Science Society 51st annual meeting. Champaign, IL: Southern Weed Science Society; 51: 161-162. [43440]
21. Miller, James H. 2003. Nonnative invasive plants of southern forests: A field guide for identification and control. Gen. Tech. Rep. SRS-62. Asheville, NC: U.S. Department of Agriculture, Forest Service, Southern Research Station. 93 p. Available: hhtp:// [2004, December 10]. [50788]
22. Miller, James H. 2006. Non-native wisteria control with herbicides. Wildland Weeds. [Volume unknown] 19-21. [72465]
23. Missouri Botanical Garden. 2002. Missouri exotic pest plants: Category B, [Online]. Missouri Botanical Garden (Producer). Available: [2004, December 23]. [51511]
24. Mohlenbrock, Robert H. 1986. [Revised edition]. Guide to the vascular flora of Illinois. Carbondale, IL: Southern Illinois University Press. 507 p. [17383]
25. Pickens, A.L. 1931. Some flowers visited by birds. The Condor. 33(1): 23-28. [72445]
26. Putz, Francis E. 1995. Relay ascension of big trees by vines in Rock Creek Park, District of Columbia. Castanea. 60(2): 167-169. [40214]
27. Raunkiaer, C. 1934. The life forms of plants and statistical plant geography. Oxford: Clarendon Press. 632 p. [2843]
28. Royal Botanic Garden Edinburgh. 2009. Flora Europaea, [Online]. Edinburgh, UK: Royal Botanic Garden Edinburgh (Producer). Available: [41088]
29. Southeast Exotic Pest Plant Council, Tennessee Chapter. 2001. Invasive exotic pest plants in Tennessee, [Online]. Athens, GA: University of Georgia; Southeast Exotic Pest Plant Council (Producer). Available: [2004, February 12]. [46747]
30. Southeast Exotic Pest Plant Council. 2003. Southeast Exotic Pest Plant Council invasive plant manual, [Online]. Southeast Exotic Pest Plant Council (Producer). Available: [2005, August 10]. [54193]
31. Speake, Dan W. 1967. Effects of controlled burning on bobwhite quail populations and habitat of an experimental area in the Alabama piedmont. Proceedings, Annual Conference of the Southeastern Association of Game and Fish Commission. 20: 19-32. [14649]
32. Stanturf, J. A.; Conner, W. H.; Gardiner, E. S.; Schweitzer, C. J.; Ezell, A. W. 2004. Recognizing and overcoming difficult site conditions for afforestation of bottomland hardwoods. Ecological Restoration. 22(3): 183-193. [51278]
33. Stickney, Peter F. 1989. Seral origin of species comprising secondary plant succession in Northern Rocky Mountain forests. FEIS workshop: Postfire regeneration. Unpublished draft on file at: U.S. Department of Agriculture, Forest Service, Intermountain Research Station, Fire Sciences Laboratory, Missoula, MT. 10 p. [20090]
34. Swearingen, J.; Reshetiloff, K.; Slattery, B.; Zwicker, S. 2002. Plant invaders of mid-Atlantic natural areas. [Washington, DC]: U.S. Department of the Interior, National Park Service; Fish and Wildlife Service. 82 p. Available online: [2005, September 9]. [54192]
35. Trusty, J. L.; Lockaby, B. G.; Zipperer, W. C.; Goertzen, L. R. 2007. Identity of naturalised exotic Wisteria (Fabaceae) in the south-eastern United States. Weed Research. 47: 479-487. [70352]
36. Trusty, Jennifer L.; Goertzen, Leslie R.; Zipperer, Wayne C.; Lockaby, B-Graeme. 2007. Invasive Wisteria in the southeastern United States: genetic diversity, hybridization, and the role of urban centers. Urban Ecosystems. 10(4): 379-395. [72451]
37. U.S. Department of Agriculture, Forest Service, Eastern Region. 2004. Eastern Region invasive plants ranked by degree of invasiveness, [Online]. In: Noxious weeds and non-native invasive plants. Section 3: Invasive plants. Milwaukee, WI: Eastern Region (Producer). Available: /r9/wildlife/range/weed/Sec3B.htm [2004, February 16]. [46748]
38. U.S. Department of Agriculture, Forest Service. 2001. Guide to noxious weed prevention practices. Washington, DC: U.S. Department of Agriculture, Forest Service. 25 p. Available online: /rangelands/ftp/invasives/documents/GuidetoNoxWeedPrevPractices_07052001.pdf [2005, October 25]. [37889]
39. U.S. Department of Agriculture, Natural Resources Conservation Service. 2009. PLANTS Database, [Online]. Available: /. [34262]
40. Varner, J. Morgan, III; Kush, John S. 2004. Remnant old-growth longleaf pine (Pinus palustris Mill.) savannas and forests of the southeastern USA: status and threats. Natural Areas Journal. 24(2): 141-149. [50968]
41. Vines, Robert A. 1960. Trees, shrubs, and woody vines of the Southwest. Austin, TX: University of Texas Press. 1104 p. [7707]
42. Virginia Department of Conservation and Recreation, Division of Natural Heritage. 2003. Invasive alien plant species of Virginia, [Online]. Virginia Native Plant Society (Producer). Available: [2005, June 17]. [44942]
43. Webb, Sara L.; Dwyer, Marc; Kaunzinger, Christina K.; Wyckoff, Peter H. 2000. The myth of the resilient forest: case study of the invasive Norway maple (Acer platanoides). Rhodora. 102(911): 332-354. [42443]
44. Webster, Christopher R.; Jenkins, Michael A.; Jose, Shibu. 2006. Woody invaders and the challenges they pose to forest ecosystems in the eastern United States. Journal of Forestry. 104(7): 366-374. [65270]
45. Wells, Elizabeth Fortson; Brown, Rebecca Louise. 2000. An annotated checklist of the vascular plants in the forest at historic Mount Vernon, Virginia: a legacy from the past. Castanea. 65(4): 242-257. [47363]
46. Woodcock, E. F. 1925. Observations on the poisonous plants of Michigan. American Journal of Botany. 12(2): 116-131. [62183]
47. Yatskievych, George. 1999. Flora of Missouri, [Online]. In: St. Louis, MO: Missouri Botanical Garden (Producer). Available:°Flora_id=11 [2009, February 26]. [73153]