Cao and Ma (Taxon 55: 233. 2006) proposed the name Elaeodendron fortunei Turczaninow (1863) for conservation against the senior taxonomic synonym Euonymus hederaceus Champion ex Bentham (Hooker’s J. Bot. Kew Gard. Misc. 3: 333. 1851). Conservation as proposed was subsequently recommended by the Committee for Vascular Plants (Brummitt, Taxon 56: 1291. 2007).
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., [22,46,73]).
Winter creeper is a perennial, typically evergreen, trailing or climbing (by aerial, adventitious roots) liana, subshrub, or shrub [1,3,22,30,46,52,73,76]. Stems are narrow [52] and minutely warty [1,52,73]. Winter creeper leaves are densely arranged on branches [76], opposite, ovate to elliptic, leathery, and vary from 1 to 2.5 inches (2.5-6.5 cm) long [1,3,46,52,54]. Leaves may be petiolate [22], with a petiole 2 to 9 mm long, but are sometimes sessile [76].
According to reviews, winter creeper seldom flowers [73], and flowers occur only on adult types [17]. Observations in Kentucky, however, indicate that winter creeper flowers and fruits consistently and prolifically from year to year (personal communication [63]). See Flower and seed production for further details. Flowers are inconspicuous [1,17,52], perfect [17,22,46], and occur in cymes [1,22,46,52] with few to several flowers [3]. Winter creeper fruits are smooth, dehiscent capsules [3,22,46], about 5 to 6 mm in diameter [76]. Its seeds are enclosed in a fleshy, colorful aril [3,17,22,73].
Winter creeper stems have abundant aerial rootlets or trailing roots [1,52] that form at nodes [46]. Aerial rootlets aid winter creeper plants in climbing vertical surfaces [1,3,73] or form independent plants by sprouting along the ground surface [1]. Stem with aerial roots in MayThe numerous cultivars of winter creeper vary mostly in leaf size and color (reviews by [12,17,29]) but may also vary in plant size, growth form, and fruit production (review by [17]).
Growth form and population structure: Winter creeper plants can form dense groundcover [1,29,43,52] trailing to 20 or more feet (6 m) [1,29], climb 40- to 70-foot-tall (12-21 m) vertical surfaces with the aid of aerial roots [17,43,52], or grow as shrubs up to 3 feet (1 m) tall [1,29,43,52].
When growing as a groundcover, independent winter creeper plants originate from rootlets at short intervals along procumbent stems. Established populations appear as a dense mat of vegetation (reviews by [1,12,52]) that may impede the growth of native seedlings. As a liana, winter creeper may climb rocks, trees, or other supporting structures. It may overtop trees, covering tree leaves and preventing photosynthesis (review by [52]). See Impacts for additional information. Photo by Chris Evans, River to River CWMA, Bugwood.orgWinter creeper growth and architecture may be altered after plants are damaged. Winter creeper cultivar 'Coloratus' plants damaged by rabbits in a nursery in Arkansas in fall and winter had lower canopy cover in March than the previous November; however, plants damaged by rabbits saw a considerable regrowth of stems and leaves from March through May. New spring growth nearly tripled previous growth percentages due to the unique architecture of second-year growth, which produced lateral stems with additional leaves on existing nodes [58].
Winter creeper is native to China ([76], reviews by [1,62,73]) and was introduced to North America as an ornamental ground cover in 1907 (reviews by [1,29,52,54]). It has escaped cultivation and established in scattered areas in the central and eastern United States (reviews by [1,52,54]). According to distribution maps provided by Plants Database, in Canada winter creeper occurs only in Ontario, and in the United States it occurs from Maryland to Wisconsin, south to Georgia and Mississippi (with the exception of West Virginia), and west to Missouri and Nebraska. The distribution of E. f. var radicans is identical to that of the species; while E. f. var fortunei occurs only in Maryland and Illinois [69]. Winter creeper, along with several other horticultural plant species, is susceptible to attack by a fungal parasite that is native to and occurs only in the southwestern United States and adjacent Mexico (Duffield and Jones 1998 as cited by [40]). This fungus, Texas root rot (Phymatotrichum omnivorum), may exert a strong influence on plant invasions in that region [40].
Local floras and other references report varying frequency of escape from cultivation among areas where winter creeper occurs, suggesting a scattered and disjunct pattern of distribution. Winter creeper occasionally escapes in the northeastern United States [22,42]. It was observed and described as "naturalized" along the west bank of Rock Run near Plummers Island in Maryland around 2003 [56]. It appeared "sporadically" as escapes in Ohio as of 1961 [3] and "seldom" escaped in Michigan as of 1985 [73]. It was a newly reported component of the flora in Illinois sometime between 1956 and 1978 [27], listed in only 1 county there in 1978 [47], and described as "infrequently escaped from cultivation and scattered" in 1986 [46]. A 1990 review by Hutchison [29] reports that winter creeper occurred mostly near urban centers in Illinois, with reports from several sites in the East St Louis area. It was common throughout Giant City State Park and Fern Rocks Nature Preserve in Jackson County, Illinois, and near Karnak in Pulaski County [29]. Winter creeper was not described the flora of the Carolinas (1968), but the flora states that various horticultural species of Euonymus (including winter creeper) "may persist around old homesites or may rarely escape from cultivation" [50].
Forest Inventory and Analysis (FIA) data from forests in 12 southern states indicate that winter creeper was detected in only 5 states and was most common in Kentucky and Tennessee [44]:
Estimated acres covered by winter creeper in forests in the southern United States, summed from subplots within each state using the Southern Research Station's Forest Inventory and Analysis database from 15 March 2008 [44] AL AR FL GA KY LA MS NC SC TN TX VA 0 82 0 0 6,644 0 0 164 0 4,328 0 7Preventing postfire establishment and spread: If fire occurs in an area where winter creeper is already established, it is likely to survive and sprout after fire. If fire occurs in an area where winter creeper does not occur on site, but flowering populations are known to occur in the vicinity, the site should be monitored for winter creeper establishment, because seeds are readily spread by birds and other animals (see Seed dispersal). Winter creeper seedlings should be removed immediately upon detection.
During fire suppression and postfire management activities in areas where winter creeper occurs, preventing its establishment and further spread may be accomplished through early detection and eradication, careful monitoring and follow-up, and limiting dispersal of winter creeper plant material or seed into burned areas. General recommendations for preventing establishment and spread of invasive plants in burn areas include:
For more detailed information on these topics see the following publications: [4,23,68].
Use of prescribed fire as a control agent: In areas where winter creeper has become a major component of the ground cover, prescribed fire is not likely to carry in the dense winter creeper fuels, and is unlikely to control winter creeper unless used in combination with other treatments (personal communications [38,63]). See Integrated management for details of a management approach that includes burning of winter creeper using a propane torch.
In some forest ecosystems in which winter creeper occurs, fire is either unlikely to burn (personal communication [9]) or is not desirable (review by [29]) due to potential negative impacts on native species.
Fuels: Winter creeper leaves have a thick cuticle, so it is difficult to get the moisture content low enough to burn. Using a 500,000 BTU propane torch it took approximately 35 to 40 minutes to burn 100 square feet of winter creeper at 100% cover. Winter creeper can carry fire in areas where bur oak (Quercus macrocarpa) leaves have accumulated on top of the winter creeper. Patches of winter creeper where leaves have been scorched with a propane torch and allowed to desiccate in warm, dry weather for 3 days may also carry fire (personal communication [38]).
FIRE REGIMES: As of 2009, no information was available regarding FIRE REGIMES where winter creeper is native. In North America, winter creeper typically occurs in forests where presettlement FIRE REGIMES probably varied. For example, it occurs in oak forests that likely experienced relatively frequent, low-severity fires; and it occurs in mixed mesophytic and northern hardwood forests that probably burned less frequently but with greater severity (reviews by [15,74]). Once established, winter creeper is likely to survive and persist under any of these FIRE REGIMES (see Fire adaptations and plant response to fire). See the Fire Regime Table for summaries of fire regime characteristics for vegetation communities in which winter creeper may occur.
Winter creeper may alter fuel properties in invaded areas; however, no data are available on this topic. In areas where winter creeper replaces plants with similar fuel properties, it may alter overall fuel biomass, which has the potential to influence fire intensity. In invaded areas where winter creeper introduces novel fuel characteristics to the invaded system, it may have the potential to alter both fire intensity and fire frequency (sensu [13]). Several reviews (e.g., [5,6,14]) discuss effects of nonnative species invasions on FIRE REGIMES.
Much of the information regarding site tolerances of winter creeper comes from reviews [1,12,17,30,52,54,62] in which the source of the original information is not given or not clear, and it appears that they mostly cite one another. Very little primary information from field observations was found in the available literature as of 2009. No information was found describing invasive populations: on sites where winter creeper occurred it was typically described as occasional or rare. Thus the following description does not necessarily describe sites where winter creeper is most likely to be invasive.
Disturbance: As a popular ornamental plant, winter creeper is usually associated with human habitation and disturbance. Winter creeper was scarce and occurred only in disturbed areas including park facilities, clearings, and old homesteads at Fall Creek Falls State Park in Tennessee [19]. It occurred in an urban woodland surveyed in 1987 at the Wave Hill Natural Area in Bronx, New York [77], and in disturbed woodlots in Indianapolis that had evidence of extensive human impact and supported several other nonnative and invasive plant species [53]. One of two collections of winter creeper in Michigan was from a gravel pit on dumped roadside debris in Benzie County, in 1982 [73]. From home sites where it was planted, winter creeper sometimes escapes cultivation and establishes, persists, and spreads in surrounding forests, woodlands [1,29,30], riparian communities [1,26,39], and other natural areas (see Habitat Types and Plant Communities). In central Kentucky, winter creeper is most abundant in older neighborhoods and along country roads, where it frequently covers the trunk and lower third of the crown of old roadside trees (personal communication [63]).
Landforms and climate: As of 2009, no information describing landform preferences or climate tolerances was found in the available literature. According to Schwegman [54] winter creeper has spread into forests and rocky bluffs in the eastern and central parts of the United States from Chicago southward, although it also occurs in Michigan [73]. Detrended correspondence analysis suggests an association of winter creeper with floodplains in the eastern United States [39]. Winter creeper is listed as occurring in coastal plain habitats on hydric and mesic sites in Virginia [72]. In a field study of old-growth forests in central Indiana, winter creeper occurred on 2 of 14 edges surveyed and was somewhat more common on warm (south- or west-facing) edges than on cool (north or east-facing) edges [7]. Winter creeper is occasional in deciduous forest and edge habitat in Rock Creek Park in Washington, DC, where the climate is continental, with warm, humid summers and mild to cold winters. The lowest average monthly temperature is 43.5 °F (6.4 °C) in January, and the highest average monthly temperature is 88.2 °F (31.2 °C) in July [20]. Dirr [17] indicates that winter creeper can grow in USDA Hardiness Zone 4, where the average minimum temperature reaches -30 to -20 °F (-34 to -29 °C), but it is not "happy" there unless provided snow cover or winter shade. It better fits USDA Hardiness Zone 5 (average annual minimum teperature of -20 to -10 °F (-29 to -23 °C)) to Zone 8 or 9 (average annual minimum teperature of 20 to 30 °F (-7 to -1 °C)) [17].
No information on winter creeper's elevational range in North America was found in the available literature as of 2009. In its native China, winter creeper occurs from near sea level to 11,155 feet (3,400 m) [76].
Soils: According to reviews, winter creeper is a popular landscape plant due to its rapid growth [1,17] and its ability to tolerate a variety of environmental conditions including heavy shade [1,12,17,30,52], poor soils, and variable pH [1,12,17,52,62]; it apparently does not do well in extremely wet conditions [12,17,30,52]. At Stones River National Battlefield, winter creeper occurs on flat to gently sloping, rocky upland woods on soils derived from limestones or other basic substrates [49]. In Rock Creek Park in Washington, DC, winter creeper occurs on low-fertility, fine-textured soils with pH ranging from 3.6 to 5.5 [20]. Winter creeper occurred on sandy beach berms on the Potomac River lowland that were "occasionally overwhelmed by high tide" [59].
Impacts: As of this writing (2009), no studies were found in the available literature on the impacts of winter creeper invasion; however, several reviews [12,29,35,52,54,62,64,67] and personal communications [9,38,63] indicate that winter creeper is persistent,competitive, and difficult to control in some areas. A review by Remaley [52] suggests that the traits that make it a desirable ornamental plant, such as rapid growth, evergreen nature, and tolerance of variable site conditions, also make it a threat to natural areas. Reviews suggest that winter creeper outcompetes and displaces native groundlayer plants (e.g., [12,52,62]) and may form single-species stands (review by [54]). Decreased native plant diversity may negatively impact native fauna (e.g., butterflies) [54]. Based on observations in Illinois, Hutchison [29] states that winter creeper is a serious potential threat because it spreads rapidly and replaces spring ephemerals. In mesic and dry-mesic woods at Fern Rocks Nature Preserve, winter creeper covered the ground and eliminated native groundcover species in many places [29]. Reviews suggest that winter creeper may overtop and block sunlight to trees [12,52], possibly smothering and killing them [54], especially smaller trees (up to about 20 feet (6 m) tall) (personal communication [63]).
Winter creeper liana in an ice-felled black cherry (Prunus serotina), approximately 40 feet (12 m) from the root collar. Photos, courtesy of David Taylor, taken 6 March 2009.Rankings by the USDA, Forest Service [66,67], local exotic pest plant councils [21,35,45,57,64], and the Virginia Department of Conservation and Recreation [72] suggest that as of 2009, winter creeper may be most invasive and have the greatest impact in the Southern Region, especially in Kentucky, Tennessee, and Missouri:
Invasiveness rankings by state and region in order of threat level Area Rank Rank definition States Kentucky Severe threat Nonnative plant species that possess characteristics of invasive species and spread easily into native plant communities and displace native vegetation. Includes species which are or could become widespread in Kentucky [35] Tennessee Rank 1, severe threat Nonnative plant species that possess characteristics of invasive species and spread easily into native plant communities and displace native vegetation [64]. Missouri Category A-2 Plant species that are invading and disrupting native plant communities in more than 10 counties in Missouri [45] Virginia Moderately invasive Nonnative plants that may have minor influence on ecosystem processes, alter plant community composition, and affect community structure in at least one layer. They may become dominant in the understory layer without threatening all species found in the community. Usually require a minor disturbance to establish [72] South Carolina Watch A Nonnative plants found in South Carolina in limited infestations that are a potential threat to natural areas. They exhibit invasive characteristics such as high reproductive rate, high growth rate, and independent establishment of new populations [57]. Georgia Category 3 Plants that are a minor problem in Georgia, or not yet known to be a problem in Georgia, but known to be a problem in adjacent states [21]. Regions Forest Service, Southern Region Category 1 Nonnative plant species that are prohibited and must be controlled. These species are known to be invasive and persistent throughout all or most of their range within the Southern Region. They can spread into and persist in native plant communities and displace native plant species and therefore pose a demonstrable threat to the integrity of the natural plant communities in the region. Their use is prohibited on National Forest lands. Efforts to control these species are encouraged [67]. Forest Service, Eastern Region Category 2 These plants are less invasive than those in Category 1. If these species are significantly replacing native species, they are doing so only in local areas [66].Control: Probably the most effective way to control winter creeper is to prevent its establishment by minimizing its use as a landscape plant and preventing further seed dispersal (see Prevention). Once established, control of winter creeper requires complete removal of plants and roots, because it can spread vegetatively (see Vegetative regeneration). According to Hutchison [30], the most effective management of winter creeper is to totally eradicate it from natural areas and the surrounding vicinity by pulling and removing individuals as soon as possible after recognition.
Fire: For information on the use of prescribed fire to control this species see Fire Management Considerations.
Prevention: It is commonly argued that the most cost-efficient and effective method of managing invasive species is to prevent their establishment and spread by maintaining "healthy" natural communities [41,55] and by conducting monitoring several times each year [31]. Managing to maintain the integrity of the native plant community and to mitigate the factors enhancing ecosystem invasibility is likely to be more effective than managing solely to control the invader [28].
Weed prevention and control can be incorporated into many types of management plans, including those for logging and site preparation, grazing allotments, recreation management, research projects, road building and maintenance, and fire management [68]. See the Guide to noxious weed prevention practices for specific guidelines in preventing the spread of weed seeds and propagules under different management conditions.
The simplest way to prevent winter creeper establishment is to not plant it. Winter creeper is commonly sold as a groundcover for landscaping [12]. Native creeping or climbing vines that may make good alternatives to winter creeper in the eastern United States include trumpet creeper (Campsis radicans), Dutchman's pipe (Aristolochia macrophylla), crossvine (Bignonia capreolata), trumpet honeysuckle (Lonicera sempervirens), American bittersweet (Celastrus scandens), and American wisteria (Wisteria frutescens) [52,62]. If bittersweet and wisteria are used, make sure they are native species, as nonnative species in these genera (C. orbiculatus, W. floribunda, and W. sinensis) are also invasive.
Prevention of fruiting is critical to prevent further spread of winter creeper once it is established. This is accomplished by cutting climbing stems to prevent flowering and fruiting (see Flowering and seed production), and repeating cutting to keep stems from climbing again (personal communication [63]).
Cultural control: According to Hutchison [29], no native species are known that can compete with winter creeper in Illinois. However, planting competitive, desirable native species may help suppress winter creeper as part of an integrated management plan (personal communication [38]).
Physical or mechanical control: Hand-pulling or grubbing using a pulaski or similar digging tool may control small populations of winter creeper (reviews by [1,52]). In order to be effective, the entire plant, including the roots, stem fragments, and fruits, must be bagged and removed from the site to prevent reestablishment. Any portion of the remaining root system may sprout (reviews by [1,30,52,54]). Young plants with small root systems are likely easiest to control in this manner. Hand-pulling is easiest when soils are moist (reviews by [1,52]). Hand-pulling may be impractical for large infestations (review by [29]).
Cutting is not recommended as a control method except to prevent fruiting (personal communication [63], reviews by [43,54]) or in combination with herbicide application (see Chemical control). Cutting alone may lead to sprouting from roots, root crowns, and cut stems (personal communications [38,63], review by [52]). Mowing is similarly ineffective without chemical treatment and not practical in natural areas (review by [29]).
In an area of Kentucky where winter creeper grew in monoculture (no native plants were visible), it was effectively suppressed when light was excluded by covering the population with 6 mil black plastic for an entire growing season (personal communication [38]); however, winter creeper may require 2 years of covering to die (personal communication [9]).
Biological control: Biological control of invasive species has a long history that indicates many factors must be considered before using biological controls. Refer to these sources: [71,75] and the Weed control methods handbook [65] for background information and important considerations for developing and implementing biological control programs.
As of this writing (2009), no effective biological controls were known for winter creeper. However, winter creeper is one of the top 10 invasive plants of Asian origin in the United States that is being studied for future biological control opportunities, and scientists are looking for host-specific natural enemies in China [16]. Dirr [17] lists several diseases and insects that impact winter creeper in North America. It is especially susceptible to damage and mortality from the Asian euonymus scale (Unaspis euonymi), which is not native to but does occur in North America [70]. The euonymus scale has been lethal to winter creeper on many plantings, especially those containing the cultivars 'Vegetus', 'Coloratus', and Euonymus tree species such as European spindletree (E. europaeus), winterberry euonymus (E. bungeanus), and Hamilton's spindletree (E. hamiltonianus subsp. sieboldianus) (review by [17]). This same scale is also showing up on native Euonymus species, burningbush (E. atropurpurea) and bursting-heart (E. americanus), and it is causing mortality in populations of Canby's mountain-lover (Paxistima canbyi), a rare subshrub, in Kentucky (personal communication [63]). At least 5 organisms (2 insect predators and 3 aphelinid parasitoids) have been collected in Asia and released in southern New England as biological control agents against the euonymus scale. Releases were made in Massachusetts, Connecticut, and Rhode Island on winter creeper and European spindletree plants infested with medium to large populations of euonymus scale in urban and suburban locations from 1991 to 1995 [70].
Intense seasonal browsing with domestic goats and/or sheep is being investigated as a potential control for winter creeper in Kentucky. This approach shows some promise because winter creeper is reportedly a frequent favorite for most livestock under the right conditions, and it is much browsed by white-tailed deer in the winter (personal communication [9]).
Chemical control: On winter creeper populations that are too large to control by hand-pulling or digging, foliar or cut-stem applications of herbicides may be effective (reviews by [1,12,30,52,54]). Cut stem application of herbicides is effective in areas where lianas are well established on or around nontarget plants or where they have grown into tree canopies or other vertical surfaces. Subsequent foliar application of herbicides will likely be required for adequate control [1,52]. Foliar applications of herbicide may be used to control large populations of winter creeper. It may be necessary to precede foliar sprays with cut stem treatments to reduce the risk of damage to nontarget plants [1,52]. Whichever method is used, multiple herbicide treatments are needed to control winter creeper (personal communications [38,63]) because it sprouts following top-kill.
Recommended timing of herbicide treatment for winter creeper is late fall, when most native vegetation is dormant, or in spring prior to emergence of spring ephemerals (reviews by [12,30]). Herbicide use is not recommended during the growing season, when native species are likely to be impacted. Care should be taken to avoid contacting nontarget species with herbicide (review by [30]).
Herbicides may be effective in gaining initial control of a new invasion or a severe infestation, but they are rarely a complete or long-term solution to weed management [8]. See the Weed control methods handbook [65] for considerations on the use of herbicides in natural areas and detailed information on specific chemicals. See these sources: [1,43,52] for details on specific chemicals, timing, rates, and methods used for controlling winter creeper.
Integrated management: Intensive management of winter creeper monocultures, integrating burning with a propane torch and/or spot spraying with glyphosate followed by planting of desirable species, may effectively suppress winter creeper and promote desirable plant communities. Monocultures in Kentucky were sprayed with glyphosate in spring, when there were about 6 newly-formed leaves without a thick cuticle. Leaves turned red and dropped off in the fall. Any new winter creeper sprouts that emerged the following spring were spot sprayed with glyphosate, and where the native seed bank was slow to respond, wild rye (Elymus villosus and E. macgregori) was seeded. Areas with dense wild rye stands had no rebound of winter creeper populations (personal communication [38]). An intensively managed swale that was once 100% winter creeper. Treatments were: burning with propane torch, followed by spot spraying of glyphosate and hand pulling of sprouts the 1st year; and planting swamp milkweed (Asclepias incarnata), wild rye and fowl manna grass (Glyceria striata) plugs the 2nd year. Photo taken in year 3 (personal communication [38]).Winter creeper was the most heavily browsed of more than 50 ornamental plant species studied during the winters of 1982 to 1984 at the Greenwich Landscaping Company in Connecticut. An average of 97.3% of winter creeper shoots were browsed, substantially more than the congeneric, deciduous shrub winged burning bush (E. alatus) (10% browsed), another nonnative invasive plant [11]. 'Coloratus' plants in a nursery in northwestern Arkansas were damaged by rabbits in fall and winter, presumably because the rabbits were eating it [58].
Palatability/nutritional value: No information is available on this topic.
Cover value: No information is available on this topic.
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 relationships, and
nonnative species may still be expanding their North American range. Therefore,
winter creeper may occur in plant communities other than those discussed here
and listed in the Fire Regime Table.
Winter creeper is most commonly reported as occurring near homesites and
disturbed areas (see Site Characteristics)
and in forests and woodlands. In its native China, winter creeper is common in
woodlands, scrub, and forests [76]. In North America, it has spread into
upland and lowland forests in the eastern and central parts of the United States (review by [54]).
A review by Grese [24] lists winter creeper as a problem species in forest
communities in the United States but not in open or wetland communities; however,
it may also occur in open communities (personal communication [32], [59])
such as savannas and grasslands (personal communication [63]).
Winter creeper occurs in forests and woodlots in the Great Lakes states. It was
collected in an oak woods west of Marshall, Michigan in 1984, where
it evidently (based on juvenile foliage) had established from seed [73].
Winter creeper occurred in forests dominated by sugar maple and American
beech in central Indiana [7], and it occurred in disturbed woodlots in
Indianapolis that were dominated by maples (Acer spp.), oaks,
elms (Ulmus spp.), ashes (Fraxinus spp.), and hickories.
These woodlots had evidence of extensive human impact and supported several
other nonnative and invasive plant species [53]. According to a
review by Hutchison [30], winter creeper has spread into many
types of forest in Illinois, including floodplain, mesic, and dry-mesic forests.
In the mid-Atlantic region, winter creeper may occur in oak-pine (Quercus-Pinus),
oak-hickory (Quercus-Carya), and mixed mesophytic forests
characterized by tree species such as American beech (Fagus grandifolia),
yellow-poplar (Liriodendron tulipifera), yellow buckeye (Aesculus
flava), sugar maple (Acer saccharum), white oak (Quercus alba),
northern red oak (Q. rubra), and black walnut (Juglans nigra) among others
(personal communication [63]). Winter creeper was occasional in
mature, second-growth oak-hickory forest and edge habitat in Rock Creek Park in
Washington, DC, where common canopy species included a variety of oaks (Quercus spp.),
American beech, yellow-poplar, hickories (Carya spp.), and red maple
(Acer rubrum) [20]. Winter creeper did not occur in Strounds
Run State Park in southern Ohio in 1957, but was listed as a "naturalized
alien" there in a study published in 2006. It was described as "rare":
occurring in only 1 or 2 locations. It occurred on mesic ravines and/or stream
terraces that were generally occupied by mixed mesophytic forests dominated by
red maple, silver maple (A. saccharinum), shagbark hickory (C. ovata),
American beech, green ash (Fraxinus pennsylvanica), yellow-poplar,
black cherry (Prunus serotina), and northern red oak [26].
At Stones River National Battlefield in Tennessee, winter creeper occurs in
the Interior Plateau chinquapin oak-Shumard oak (Quercus muehlenbergii-Quercus
shumardii) forest association. These dry-mesic forests are codominated by
varying proportions of shagbark hickory, Carolina shagbark hickory (Carya
carolinae-septentrionalis), eastern redcedar (Juniperus virginiana var.
virginiana), and sugarberry (Celtis laevigata). In addition to
winter creeper, other nonnative plant species occurring in this community include
Amur honeysuckle (Lonicera maackii), Japanese honeysuckle (Lonicera
japonica), privets (Ligustrum sinense, Ligustrum vulgare), and
tree-of-heaven (Ailanthus altissima). This forest association is considered
globally rare, and most, if not all, high-quality examples have been eliminated
or severely impacted by timber removal, grazing, soil erosion, and fire exclusion.
Other threats include windthrow, microclimate modification from intensive
silvicultural practices on adjacent uplands, forest type conversion, and herbicide
use [49].
A review by Stocker and Hupp [61] suggests that winter creeper is potentially
invasive in oak-hickory woodland in the southeastern United States.
Winter creeper may also occur in more open plant communities (personal
communications [32,63]). Winter creeper occurred but was rare on the
Potomac River Lowland in Piscataway and Fort Washington National Parks
in Maryland. Here it occurred on sandy beach berms in communities dominated
by calamus (Acorus calamus), narrow-leaved cattail (Typha
angustifolia), and other marsh species, in areas where silver maple,
green ash, and poison-ivy (Toxicodendron radicans) also occurred [59].
According to a review by Bean and McClellan [1], because winter creeper is evergreen and begins growing before other vegetation emerges, it outcompetes existing vegetation for available space and resources.
In North America, winter creeper generally flowers in the summer (June to July) and produces mature fruits by fall (reviews by [12,17,43,52,54]), though flowering and fruiting may occur earlier at lower latitudes (see table below). According to a review by Dirr [17], fruits mature October to November and often persist.
Flowering and fruiting dates for winter creeper by area Area Flowering dates Fruiting dates Illinois July-August [46] ---* Tennessee May-June June-July [1] Northeastern United States and adjacent Canada June or July [22] --- China April-July September-December [76] *No data.Winter creeper may abscise a few leaves throughout the year, but most abscission occurs in early spring (unpublished data cited by [10]).
Winter creeper regenerates sexually by producing fruits that are readily dispersed by birds, and vegetatively through long branches and lateral shoots that root at the nodes and form independent plants (reviews by [1,12,52]).
Pollination and breeding system: Winter creeper flowers are perfect [17,22,46]. No additional information is available on this topic.
Flower and seed production: As of 2009 very little published information was available regarding seed production in winter creeper. According to reviews, winter creeper seldom flowers [73], and flowers occur only on adult types [17]. Observations in Kentucky, however, indicate that winter creeper flowers and fruits consistently and prolifically from year to year (personal communication [63]). In order to flower and produce seed, winter creeper must climb trees or other objects to get more sunlight. If no uprights are present, it does not obtain the liana diameter (approximately 1cm or greater) that triggers flowering (personal communication [63]). Climbing stems of winter creeper typically flower in summer and produce mature fruit in fall (see Seasonal Development). Groundcover populations seldom, if ever, flower and fruit (reviews by [12,17,54]). Because it can form extensive groundcover without developing upright, climbing stems, it probably appears that it does not readily flower in many areas (personal communication [63]).
Seed dispersal: Winter creeper seeds are equipped with arils that are readily eaten by birds and other wildlife, which then disperse the seed (reviews by [12,30,52], personal communication [63]), possibly many miles away [54]. Muhlenbach [48] recorded the occurrence of a few specimens of winter creeper (E. f. var. radicans) on one site along the railroad in St Louis, Missouri, in 1969. He notes that although this species was often cultivated as a ground cover in St Louis, there were no gardens in the vicinity [48], suggesting long-distance dispersal. Similarly, winter creeper's presence in fragmented old-growth forests in Indiana suggests some form of long-distance dispersal because it is not an agricultural weed, and these forests were bordered mostly by corn and soybean fields [7].
On an old farm site in Kentucky with large scattered trees, the understory is covered by dense growth of the nonnative invasive species multiflora rose (Rosa multiflora), winged burning bush (Euonymus alatus), winter creeper, and Oriental bittersweet (Celastrus orbiculatus). All of these species have bird-dispersed seed, suggesting that birds using the large old trees as perches "planted" seeds of the invasives (personal communication [63]).
Winter creeper may also be dispersed by water. A review by Remaley [52] states that it "escapes from neglected gardens and is carried by water to undisturbed forest and riparian areas".
Seed banking: No information is available regarding occurrence or longevity of winter creeper seed in the seed bank.
Germination: As of 2009, no information was available regarding germination of winter creeper in the field; however, a review by Dirr [17] suggests that winter creeper seeds have dormant embryos and recommends moist stratification at cold temperatures for propagation.
Seedling establishment: No information is available on requirements for winter creeper seedling establishment, but it is capable of establishing on disturbed, relatively inhospitable sites (see photo below).
Winter creeper plant growing from crack in pavement, at least 0.5 mile (km) from the nearest established, fruiting plants.Plant growth: A review by Dirr [17] suggests that winter creeper has a "fast" growth rate. A nursery study in northwestern Arkansas using the cultivar 'Coloratus' reported that winter creeper covered almost 75% of its plots with dense foliage within 1 year when grown in beds prepared with mushroom compost and watered from June to September (during establishment) [58]. Winter creeper growth may be affected by a number of factors, including degree of shading (see Shade tolerance) and damage caused by vertebrates, insects, or water stress.
Winter creeper cultivar 'Coloratus' plants damaged by rabbits in fall and winter showed "considerable" regrowth of stems and leaves from March through May, nearly tripling previous growth percentages [58].
Insect damage and water stress can both influence winter creeper growth. Field experiments using the winter creeper cultivar 'Coloratus' suggest that euonymus scales, primarily the males feeding on the leaves, damage the leaf tissue so that the leaves have a higher than normal diffusive resistance and a lower transpiration rate, which eventually leads to increased leaf abscission and impaired growth of root tissue, especially when compounded by water stress [10]. The euonymus scale is native to eastern Asia and is associated with Euonymus spp. throughout most of their native and cultivated range (review by [10]). A greenhouse and field study found that both scale-infested and water-stressed winter creeper plants abscised leaves whereas uninfested, unstressed plants did not; and there was a synergistic effect on leaf abscission from the 2 stresses combined [10]. Winter creeper may abscise a few leaves throughout the year, but most abscission occurs in early spring (unpublished data cited by [10]). Greenhouse experiments using the winter creeper cultivar 'Emerald and Gold' found that leaves began to abscise from water-stressed plants 61 days after infestation and 2 days after the soil water potential reached -1.7 MPa. Feeding by 2 generations of scales on non-water-stressed plants did not reduce total stem growth or significantly reduce intact leaf tissue, but infested plants had lower mean root weight than controls (P=0.05). Water-stressed plants—both infested and uninfested— were shorter, had lower mean root weight, and lower mean intact leaf weight than unstressed plants. Scale infestation significantly decreased the amount of leaf tissue remaining on water-stressed plants (P=0.05). Plants subjected to both water stress and scale infestation abscise more leaves than those exposed to either stress alone, apparently because scale feeding damage causes a heightened sensitivity to other stresses [10].
Vegetative regeneration: Winter creeper spreads vegetatively by producing lateral shoots along the main branches and establishing new, independent plants that emerge from rootlets occurring along procumbent stems at short intervals (reviews by [1,12,52]). When cut, winter creeper sprouts from roots (review by [52]), root crowns, and/or cut stems (review by [17], personal communication [63]). In a nursery study, 'Coloratus' plants damaged by rabbits in fall had considerable regrowth of lateral stems and additional leaves from existing nodes the following spring [58]. Stem with distinctive buds in MayAs of this writing (2009), very little information was available regarding successional relationships of winter creeper. Some authors suggest that it can establish in relatively undisturbed habitats (e.g., [12,30]), and others suggest that populations of winter creeper may establish in forest openings caused by windthrow, insect defoliation, or fire [1,30,52,62]. Records of field observations to support these suggestions were lacking in the available literature. A field study of old-growth forests in central Indiana, which were mostly small woodlots surrounded by agricultural fields, found that winter creeper was at least as frequent in the forest interior as on the forest edge [7].
Observations by Hutchison [29,30] in Illinois suggest that invasive populations of winter creeper may alter successional trajectories because it spreads rapidly and replaces spring ephemerals. In mesic and dry-mesic woods at Fern Rocks Nature Preserve, winter creeper covered the ground and eliminated native groundcover species in many places [29]. Observations by managers in Kentucky indicate that invasive, groundcover populations of winter creeper can establish monocultures in which native species are excluded (personal communication [38]).
Shade tolerance: Several reviews suggest that winter creeper tolerates heavy shade [1,12,17,30,52], and a few of these also suggest that it also tolerates full sun [12,17,30,52]; empirical evidence of winter creeper's shade tolerance is limited and somewhat contradictory. Shade tolerance may vary among cultivars. In a nursery experiment, the cultivar 'Variegata' was grown indoors in containers for 5 months under 1 of 3 conditions: 1) full sun, 2) 47% shade, 3) 64% shade. Growth indices (height + width + width/3, in cm) were significantly different (P≤0.05) among treatments, with growth in full sun the lowest and in 47% shade the highest. Indices were 21.0, 25.0, and 22.9, respectively [34]. A nursery study in northwestern Arkansas using the cultivar 'Coloratus' reported that after fertilizer treatments and 6 months of growth, winter creeper canopy cover was similar and total shoot dry weight was somewhat higher in full sun than in 60% shade. After an additional fertilizer treatment and 6 months of additional growth, shoot and whole plant dry weights for winter creeper were greater under full sun than 60% shade. Statistical comparisons were not made due to lack of replication [58].
The scientific name of winter creeper is Euonymus fortunei (Turcz.)
Hand.-Maz. (Celastraceae) [3,18,22,33,42,46,73,76].
Although not distinguished in local floras, Kartesz [33] recognizes 2 varieties in North America:
Euonymus fortunei (Turcz.) Hand.-Maz. var. fortunei
Euonymus fortunei (Turcz.) Hand.-Maz. var. radicans (Sieb. ex Miq.) Rehd.
A review by Dirr [17] describes another variety in the United States, E. f. var. coloratus, which he says is often listed as the cultivar 'Coloratus'. Dirr [17] describes 51 cultivars of E. fortunei. A review by Blakelock [2] describes several varieties and forms of E. fortunei, occurring mostly in Asia or as cultivars, distinguished primarily by leaf characteristics. The Flora of China states "Numerous taxa have been named within the E. fortunei complex but many of these refer to cultivated plants and are best treated as cultivars" [76]. In this review, E. fortunei is referred to as "winter creeper", varieties are referred to by scientific name, and cultivars, when identified as such in the literature, are referred to by cultivar name in single quotation marks (e.g., 'Emerald and Gold').
Euonymus fortunei (lat. Euonymus fortunei) - gərməşovkimilər fəsiləsinin gərməşov cinsinə aid bitki növü.[1]
İkiləpəlilər ilə əlaqədar bu məqalə qaralama halındadır. Məqaləni redaktə edərək Vikipediyanı zənginləşdirin.
Euonymus fortunei (lat. Euonymus fortunei) - gərməşovkimilər fəsiləsinin gərməşov cinsinə aid bitki növü.
Brslen Fortunův (Euonymus fortunei) je stálezelená rostlina (keř) z čeledi jesencovité (Celastraceae), která pochází z Východní Asie.
Brslen Fortunův je keř s dlouhými zakořeňujícími větvemi.
Listy jsou jemně zubaté, oválné, mají světlejší žilnatinu a jsou lesklé.[1]. Jsou uspořádány v protilehlých párech. Jsou cca 2-6 cm dlouhé a 1-3 cm široké. Existují i kultivary s barevnými listy (žlutě skvrnité, bílé nebo červené).[1]
Květy jsou nevýrazné. Mají v průměru 5 mm. Kvete od května do června.[2]
Existují tři odrůdy této rostliny:
Plody
Kultivar „Emerald`n Gold“
Obrázky, zvuky či videa k tématu brslen Fortunův ve Wikimedia Commons
Brslen Fortunův (Euonymus fortunei) je stálezelená rostlina (keř) z čeledi jesencovité (Celastraceae), která pochází z Východní Asie.
Krybende benved (Euonymus fortunei) er en stedsegrøn busk med en fladt krybende eller klatrende og tæt forgrenet vækstform. Hele planten, inklusive frugterne, er giftig.
Barken er grøn, og det bliver den ved med at være meget længe. Gamle grene kan dog få grå og opsprækkende bark. Knopperne sidder modsat, og de er glatte, spidse og lysegrønne. Bladene er ægformede til ovale med rundtakket rand. Oversiden er blank og friskt grøn, mens undersiden er lysegrøn og mat. Enkelte blade farves orangerøde om efteråret. Blomsterne er grønne, og man lægger ikke mærke til dem. Frugterne, derimod, er koralrøde kapsler, der åbner sig i fire klapper, så man kan se ind til de orangerøde kerner. Frøene modner sjældent her i landet.
Rodnettet består af talrige, ret tynde hovedrødder og et tæt net af finrødder.
Højde x bredde og årlig tilvækst: 1 x 3 m (10 x 45 cm/år). Højden bliver dog væsentligt større, hvis busken får lov til at klatre! 4 planter dækker 1 m² på 3 år.
Krybende benved vokser som bunddækkende eller klatrende underskov i blandede løvskove og i krat samt på overdrev fra havniveau til 3.400 m højde over størstedelen af Kina og i Indien, Pakistan, Myanmar, Korea, Japan, Sydøstasien og Indonesien. Arten er meget variabel, men foretrækker fugtig, porøs og næringsrig jord[1].
På øen Lamma i den tidligere, britiske kronkoloni Hongkong findes en åben, blandet skovbevoksning. Her vokser arten sammen med bl.a. Almindelig Ildkrone, almindelig sukkerrør, galæblesumak, guineagræs, hvid morbær, kinesisk elefantgræs, kinesisk liguster, litchi, mango, stillehavsskruepalme, Vitex negundo (en art af kyskhedstræ) og Zanthoxylum avicennae (en art af tandved)[2]
I handlen findes en varitet af krybende benved, nemlig Euonymus fortunei var. vegetus. Den kendes også under synonymerne E. fortunei var. radicans og E. fortunei f. carrierei. Varieteten udmærker sig ved at være rigt frugtbærende med gule kapsler, der åbner sig i fire klapper og viser de orangerøde frøkapper[3].
Desuden sælges der nogle sorter af arten under navnene:
Blade
Skudbygning
Blomster
Frugt
Vækstform
Krybende benved (Euonymus fortunei) er en stedsegrøn busk med en fladt krybende eller klatrende og tæt forgrenet vækstform. Hele planten, inklusive frugterne, er giftig.
Der Kletter-Spindelstrauch (Euonymus fortunei), auch Kriechspindel genannt, ist eine Pflanze aus der Gattung der Spindelsträucher.
Der Kletter-Spindelstrauch wächst als immergrüner, aufsteigender oder kriechender Halbstrauch, wobei die Größe von Zwergformen bis zu etwa 10 Meter Höhe variiert. Die Zweige sind rund, braun bis braungrün, manchmal gestreift und dicht mit Blättern besetzt. Diese sind unbehaart und eiförmig bis eiförmig-elliptisch mit leicht gekerbtem bis gesägtem Rand, stumpfer bis keilförmiger Basis und stumpfer bis zugespitzter Spitze. Sie sind 2 bis 5,5 Zentimeter lang, 2 bis 3,5 Zentimeter breit und entweder sitzend oder mit einem 2 bis 9 Millimeter langen Blattstiel versehen. Die Blütenstände tragen wenige vierzählige Blüten mit etwa 5 Millimeter Durchmesser, die an 5 Millimeter langen Stielen sitzen. Die Kelchblätter sind halbrund, die weißlichen oder grünlichen Kronblätter fast kugelförmig. Als Früchte werden braune bis rotbraune Kapseln mit rotem Arillus gebildet.[1]
Wenn eine Klettermöglichkeit vorhanden ist, kann der Spindelstrauch bis zu 20 m hoch klimmen. Wie der Efeu bildet der Spindelstrauch als immergrüne Kletterpflanze Haftwurzeln aus und existiert zunächst in einer sterilen Jugend- bzw. Kletterphase. Wenn eine Höhe mit ausreichenden Lichtverhältnissen erreicht wird, beginnt die fruchttragende Phase und es werden keine Haftwurzeln mehr gebildet.
Die Frosthärte beträgt −20 °C.[2]
Die Art kommt in Wäldern und Buschland in Süd- und Südostasien von Pakistan bis Japan, Indonesien und auf den Philippinen vor, wo sie auf Erde oder felsigem Untergrund wächst und in Höhenlagen bis 3400 m vorkommt.[1]
In gärtnerischer Kultur ist die Art und insbesondere ihre dem jeweiligen Klima angepassten Kulturformen weltweit verbreitet, mit Ausnahme arktisch-kontinentaler und arider Klimagebiete.
Ähnlichkeit besteht zum Euonymus japonicus, der ebenfalls häufig als Zierstrauch gepflanzt wird, jedoch keine Kletterwurzeln ausbildet.[3] Eine Verwandtschaft besteht zu ähnlichen Arten wie Euonymus theifolius und Euonymus vagans.
Der Kletter-Spindelstrauch wird als Bodendecker, in Hecken oder zur Fassadenbegrünung verwendet.[2] Es sind zahlreiche Cultivare mit verschiedenem Aussehen und unterschiedlichen Klimaansprüchen gezüchtet worden. In Mittel- und Westeuropa bilden Formen mit weißbunten und gelbbunten (panaschierten) Blättern (z. B. Euonymus fortunei 'Emerald Gold', Euonymus fortunei 'Gracilis') den Schwerpunkt der Produktion, da sie in großen Stückzahlen zur Grabbepflanzung eingesetzt werden.[4]
Euonymus fortunei 'Emerald Gaiety'
Euonymus fortunei 'Emerald Gaiety'
Euonymus fortunei 'Emerald Gold'
Euonymus fortunei
Euonymus fortunei Beeren
Euonymus fortunei Frucht
Der Kletter-Spindelstrauch (Euonymus fortunei), auch Kriechspindel genannt, ist eine Pflanze aus der Gattung der Spindelsträucher.
Euonymus fortunei, the spindle, Fortune's spindle, winter creeper or wintercreeper, is a species of flowering plant in the family Celastraceae, native to east Asia, including China, Korea, the Philippines and Japan.[1] It is named after the Scottish botanist and plant explorer Robert Fortune. E. fortunei is highly invasive and damaging in the United States, causing the death of trees and forest in urban areas.[2]
It is an evergreen shrub which grows as a vine if provided with support. As such it grows to 20 m (66 ft), climbing by means of small rootlets on the stems, similar to ivy (an example of convergent evolution, as the two species are not related). Like ivy, it also has a sterile non-flowering juvenile climbing or creeping phase, which on reaching high enough into the crowns of trees to get more light, develops into an adult, flowering phase without climbing rootlets.
The leaves are arranged in opposite pairs, elliptic to elliptic-ovate, 2–6 cm long and 1–3 cm broad, with finely serrated margins. The flowers are inconspicuous, 5 mm in diameter, with four small greenish-yellow petals. The fruit is a smooth, dehiscent capsule with reddish arils.[3]
There are two or three varieties:
It has an extensive native range, including many parts of China (from sea level to 3400 m elevation), India, Indonesia, Japan, Korea, Laos, Myanmar, Philippines, Thailand, and Vietnam.[1] It resembles Euonymus japonicus, which is also widely cultivated but is a shrub, without climbing roots.[4] It also is related to a variety of similar species, including Euonymus theifolius, or Euonymus vagans and also a number of named "species" which are found only in cultivation and better treated as cultivars.[1] Its habitats include woodlands, scrub, and forests.[5]
Euonymus fortunei is widely cultivated as an ornamental plant, with numerous cultivars selected for such traits as yellow, variegated and slow, dwarfed growth. It is used as a groundcover or a vine to climb walls and trees. The following cultivars have gained the Royal Horticultural Society's Award of Garden Merit:[6]
Plants propagated from mature flowering stems (formerly sometimes named "f. carrierei") always grow as non-climbing shrubs. Some popular cultivars such as 'Moon Shadow' are shrub forms.
Most of the cultivated plants belong to var. radicans (Huxley 1992). It is generally considered cold hardy in USDA zones 5 to 9, and is considered an invasive species in some parts of the world, notably the eastern United States[12][13] and Canada.[14]
The fruit
Flowers on a mature vine
The variegated cultivar 'Emerald 'n Gold'
Cultivar 'Emerald Gaiety'
Winter Creeper, Euonymus fortunei, showing its orange berries
Euonymus fortunei, the spindle, Fortune's spindle, winter creeper or wintercreeper, is a species of flowering plant in the family Celastraceae, native to east Asia, including China, Korea, the Philippines and Japan. It is named after the Scottish botanist and plant explorer Robert Fortune. E. fortunei is highly invasive and damaging in the United States, causing the death of trees and forest in urban areas.
Euonymus fortunei, el huso de la fortuna, es una especie natural de China, Corea y Japón.
Es una vid perenne arbolada que alcanza 20 metros de longitud, trepando apoyada en pequeñas raicillas en los tallos, similares a la hiedra (ejemplo de evolución convergente, pues las dos especies no están relacionadas). Como la hiedra, tiene una fase juvenil que no florece hasta alcanzar la corona de los árboles para conseguir más luz, una vez allí, entra en la fase adulta, florece y deja de tener raicillas en esa parte.
Las hojas son pareadas y opuestas, elípticas de 2-6 cm por 1-3 cm de ancho con bordes finamente serrados. Las flores son discretas, tienen cuatro pétalos pequeños de color amarillo verdoso. La fruta es una vaina como una baya de color verde pálido con cuatro lóbulos, en parte abiertos para mostrar las semillas carnosas de color anaranjado.
Hay tres variedades:
Se diferencia de la especie Euonymus japonicus en que esta solo es un arbusto sin raíces que le permitan elevarse.
Se cultiva como planta ornamental y se utiliza para cubrir paredes.
Euonymus fortunei fue descrita por (Turcz.) Hand.-Maz. y publicado en Symbolae Sinicae 7(3): 660. 1933.[1]
Euonymus: nombre genérico que viene de las palabras griegas eu = "bueno", y onoma = "nombre".[2]
fortunei: epíteto otorgado en honor del explorador Robert Fortune.
Euonymus fortunei, el huso de la fortuna, es una especie natural de China, Corea y Japón.
Euonymus fortunei, jatorriz Txina, Korea eta Japoniakoa den espezie naturala da.
Hosto-iraunkorreko mahatsondo zuhaitza, 20 metrorainoko luzera har lezakeena, huntzaren gisan, zurtoinetako sustrai txikietan bermatuz gora egiten duena.
Hiru aldaera daude:
Euonymus japonicus-ekin daukan ezberdintasuna, hau zuhaixka bat dela da, gora egiteko beharrezko diren sustrairik gabekoa.
Landare apaingarri gisa landatzen da, paretak estaltzeko helburuarekin.
Euonymus fortunei, jatorriz Txina, Korea eta Japoniakoa den espezie naturala da.
Wijaty kapralc (Euonymus fortunei) je rostlina ze swójby kapralcowych rostlinow (Celastraceae).
Wijaty kapralc je kerk, kotryž móže kaž błušć na murje hač do wysokosće wot 6 m horje lězć. Ale rozšěrjene sorty su zwjetša bóle kompaktne.
Kćěje wot nalěća hač do srjedźneho lěća. Kćenja su nazeleń běłe a steja na njelězucych starowurostkach.
Wijaty kapralc (Euonymus fortunei) je rostlina ze swójby kapralcowych rostlinow (Celastraceae).
Trzmielina Fortune’a, trzmielina pnąca (Euonymus fortunei (Turcz.) Hand.-Mazz.) – gatunek krzewu z rodziny dławiszowatych (Celastraceae). Pochodzi z Japonii, Chin i Korei[2]. W Europie zaczęto go uprawiać w 1907 r. W Polsce jest uprawiany jako roślina ozdobna. Nazwa pochodzi od Roberta Fortune’a, który przywiózł tę roślinę z Chin do Europy.
Roślina ozdobna. Jest dość często uprawiana, ze względu na swój ładny pokrój, ale przede wszystkim ozdobne liście. Rośnie wolno. Nadaje się na rabaty, gdyż tworzy ładne zestawienia kolorystyczne z innymi roślinami, bywa też używana jako roślina okrywowa, może też rosnąć samotnie na strzyżonym trawniku. Często jest uprawiana w dużych donicach i skrzynkach, zwykle w zestawieniu z innymi roślinami, szczególnie iglakami.
Trzmielina Fortune’a, trzmielina pnąca (Euonymus fortunei (Turcz.) Hand.-Mazz.) – gatunek krzewu z rodziny dławiszowatych (Celastraceae). Pochodzi z Japonii, Chin i Korei. W Europie zaczęto go uprawiać w 1907 r. W Polsce jest uprawiany jako roślina ozdobna. Nazwa pochodzi od Roberta Fortune’a, który przywiózł tę roślinę z Chin do Europy.
扶芳藤（学名：Euonymus fortunei）为卫矛科卫矛属的植物。分布在中国大陆的江苏、安徽、江西、四川、湖北、浙江、陕西、湖南等地，生长于海拔300米至2,200米的地区，见于山坡丛林中，多個栽培品種。
这是一篇與植物相關的小作品。你可以通过编辑或修订扩充其内容。 扶芳藤（学名：Euonymus fortunei）为卫矛科卫矛属的植物。分布在中国大陆的江苏、安徽、江西、四川、湖北、浙江、陕西、湖南等地，生长于海拔300米至2,200米的地区，见于山坡丛林中，多個栽培品種。
Euonymus fortunei (Turcz.) Hand.-Mazz. var. radicans (Miq.) Rehder
和名 ツルマサキ（蔓柾）ツルマサキ（蔓柾、学名：Euonymus fortunei）は、ニシキギ科ニシキギ属の常緑つる性木本。別名、リュウキュウツルマサキ、ナガバツルマサキ、マルバツルマサキ。
種小名は、幕末に来日したイギリスのプラントハンター、ロバート・フォーチュンへの献名。
緑色の枝の各所から多数の気根をだして他の樹木をよじ登るか、地上を這う。葉は革質で長さ0.3-1cmの葉柄をもって年茎ごとに1-5対、対生する。葉の形は、楕円形、長楕円形、ときに円形で、縁には低鋸歯がある。葉身は長さ1.5-6cm、幅0.7-3cmになる。
花期は6-7月、今年枝の下部の葉腋や芽鱗痕わきから集散花序を付ける。花は4弁花で淡緑色、花弁の長さは2mm、花の径5mmになる。雄蕊は4本つく。果期は10-12月、果実は蒴果で径5-6mm、割れると橙赤色の仮種皮を持つ種子が現れる。
日本では、北海道、本州、四国、九州、沖縄に分布し、林内に自生する。東アジアでは朝鮮、中国、フィリピンにも分布する。
キョウチクトウ科のテイカカズラとはよく似ている。以下のような点は共通する特徴である。
花が咲けば全く違うのでわかるが、若い枝では悩ましい場合がある。区別点についてはテイカカズラ#類似の植物の項を参照のこと。
葉は対生する
果実
枝と気根
高木を這い登る
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