This description provides characteristics that may be relevant to fire ecology and is not meant for identification. Keys for identification are available (e.g., [63,145,214]).
Chinese tallow is a quick-growing, deciduous tree capable of root and basal sprouting [52,63,67,112,126,170]. It typically grows from 24 to 35 feet (7-11 m) tall [125,210], but individuals up to 65 feet (20 m) tall and over 3 feet (1 m) in diameter have been reported [69]. Chinese tallow leaves are alternate, simple, and typically oval to round [112,113], but they may also be rhombic [112]. They range from 1.4 to 3.3 inches (3.5-8.5 cm) long and from 1.4 to 3.5 inches (3.5-9.0 cm) wide [112,145]. The length of petioles ranges from 0.6 to 3.5 inches (1.5-9.0 cm) [112]. Sharma and others [174] found a maximum leaf area of 2.7 inches² (SD 0.2) (17.36 cm² (SD 1.23)) and mature leaf moisture content of 66.3% (SD 1.3) before leaf fall. Trunks may be gnarled [112] with fissured bark [126] that thickens as the tree grows [67]. Tiny, imperfect flowers occur in terminal spikes 2.4 to 7.9 inches (6-20 cm) long, with fascicles of up to 5 pistillate flowers near the base and fascicles of up to 15 staminate flowers along the spike [52,62,63,112,126,145]. Fruits are capsules about 9.5 to 19 mm in diameter [112,126]. They contain 3 wax-coated seeds about 6 to 10 mm long and 4.3 to 6.1 mm wide [112,126].
Little information regarding belowground features of Chinese tallow is available. However, Nijjer and others [134] observed greater colonization of Chinese tallow roots with arbuscular mycorrhizae than native tree species such as black tupelo and water oak.
The lifespan of Chinese tallow stems seems to be less than 100 years, although roots may live longer [89]. Scheld and others [169] report that Chinese tallow is short-lived, surviving 40 to 50 years. Grace and others [69] state that Chinese tallow over 50 years old become "somewhat senescent".
Allelopathy: Allelopathic effects of Chinese tallow appear limited. Chinese tallow extracts have not been shown to have an allelopathic effect on little bluestem [95,164], black willow [39], baldcypress [39,42], or sweetgum [86,164]. Effects of exposure to Chinese tallow extracts on sweetgum, little bluestem, King ranch bluestem (Bothriochloa ischaemum var. ischaemum), and perennial ryegrass (Lolium perenne) did not differ from effect of exposure to extracts from sweetgum, silver maple (Acer saccharinum), and sycamore [86]. Little bluestem exposed to Chinese tallow extracts exhibited significantly (P<0.05) larger mass [95]. Baldcypress exposed to Chinese tallow extracts exhibited increased germination rates and/or growth, although variation was observed across seasons and source of extracts (leaves, litter, and soil). Chinese tallow also had consistently higher germination and growth rates in Chinese tallow-exposed treatments, which suggests that at least in some communities, increased performance of tallow itself may be more important in the species’ success than limiting the success of other species [42]. There is some evidence that Chinese tallow extracts have a negative effect on loblolly pine germination and seedling growth [71].
Light availability, ambient temperature, water immersion, burial, and site characteristics likely influence Chinese tallow germination.
The effect of time of planting and associated light conditions on Chinese tallow germination differs between studies. Nijjer and others [133] note that germination of Chinese tallow seeds in the field peaks in April and May [133]. Similarly, seeds planted at Lake Jackson began germinating in February, and germination peaked in mid-March and in mid-April [21]. In contrast, germination of Chinese tallow seeds collected near the Pakistan-India border and planted either in February or in May was about 60% after 60 days [191]. In a greenhouse with "natural" photoperiod and temperature, average germination rates (58%-59%) observed 120 days after planting in January and February were significantly (P<0.001) greater than rates seeds buried in early spring or late fall (21%-46%). Several benefits of winter germination are suggested, including decreased activity of possible seed predators, increased light due to a more open canopy, and decreased interspecific competition for nutrients or light due to fewer annuals and dormancy in perennials [25]. However, about 15% germination was observed in light and dark treatments, significantly (P<0.05) higher than Chinese tallow germination [133].
Chinese tallow germination is likely greater under variable temperature regimes than with constant temperatures [133]. Given that temperature fluctuations occur more often in open areas, such as canopy gaps, it is suggested that Chinese tallow may have higher germination in disturbed habitats [133]. In the coastal prairie of eastern Texas, Chinese tallow seedling emergence was significantly higher (P<0.05) in experimental plots without mulch than on sites with 2 inches (5 cm) of Chinese tallow mulch. Cumulative seedling emergence on sites with 2 inches of mulch was greater (P<0.05) than on sites with 4 inches (10 cm) or 6 inches (15 cm) of mulch. From 9 April to 14 April, soil temperatures on sites with no mulch varied about 16 to 23 °F (11-13 °C) daily; temperatures on sites with 2 inches of Chinese tallow mulch varied about 5 to 10 °F (3-4 °C) daily; and those on sites with 4 or 6 inches of Chinese tallow mulch varied about 1 to 6 °F (1-3 °C) daily [49]. A complementary laboratory study found greater germination of Chinese tallow seeds subject to fluctuating temperature regimes compared to seeds exposed to constant temperatures, with no consistent trends related to mulch depths within temperature treatments (Donahue 2004 cited in [49]).
Studies investigating the impact of water immersion on Chinese tallow germination in which seeds were soaked for 192 hours or less did not find significant effects [40,192]. In contrast, Chinese tallow seeds soaked in water for 30 days and either placed in a shade-house or in prairie habitat in northern Florida had significantly (P<0.001) greater germination rates than acid-treated seeds in the shade-house or prairie habitat [167].
Burial increases germination of Chinese tallow seeds [152,167]. In a greenhouse experiment, seeds buried to a depth of 0.4 inch (1 cm) exhibited a 56% germination rate, while only 17.5% of seeds placed on the soil surface germinated (P<0.0001). Buried seeds began germinating after about 7 days, significantly (P<0.05) faster than digested surface-sown seeds (13.1 days) or unmanipulated surface-sown seeds (42.2 days) [152]. For information on the interaction of digestion and burial, see the paragraph on effects of digestion. Germination of Chinese tallow seeds placed on the soil or litter surface following acid treatment ranged from 0% to 20%, depending on the habitat or soil source [167].
Several site factors likely influence Chinese tallow germination rates including elevation, soil temperature and moisture, community composition, and litter characteristics. In a central California riparian area, Chinese tallow germination was significantly (P<0.05) greater at elevations less than 7.5 feet (2.3 m) above water level compared to 15 feet (4.6 m) above water level. Soil temperature (P=0.045) and electrical conductivity (P=0.039) had significant positive effects on germination. Germination rates were lower (P=0.042) on south facing slopes, possibly due to drier soils [15]. In the Lake Jackson area of northern Florida, germination rates differed significantly (P<0.001) over a 3-foot (1 m) elevational gradient, with higher germination rates at high and intermediate portions of this gradient compared to the low end of the gradient. Although germination rates on sites with Chinese tallow in this area were slightly higher than those without Chinese tallow, the difference was not significant [21]. Chinese tallow germination was lower (P=0.07) on herbaceous marsh substrates than on soil from southern bayberry thickets from Barataria Preserve just south of New Orleans, Louisiana [11]. In a shade house, acid-treated seeds had significantly (P<0.05) higher germination in soils from prairie than in mixed pine-hardwood or oak hammock habitats of northern Florida. Acid-treated seed placed in shaded wet prairie had significantly (P<0.05) greater germination than acid-treated seeds placed on the litter in mixed pine-hardwood or oak hammock habitats. Samuels [167] suggested that the general trend of greater germination in prairie soil was primarily due to forest litter providing a drier germination substrate. Watering frequency had no significant effect on germination in a greenhouse experiment [18].
Potential for postfire establishment and spread: The overall ability of Chinese tallow to establish in the postfire environment is unclear. Germination of Chinese tallow may be reduced by burning in certain circumstances [21]. However, in regions already experiencing high rates of Chinese tallow invasion, risk of invasion increased in stands where 25% of trees were damaged by fire [58]. Due to its ability to establish following other types of disturbance [35,132,193,214], Chinese tallow establishment following fire is a concern.
Preventing postfire establishment and spread: To some extent, repeated burning mitigates the risk of postfire colonization of Chinese tallow. Monitoring burned sites in areas where Chinese tallow occurs is recommended, especially in areas prone to invasion such as sites that are near water, naturally regenerated, and/or in areas with abundant seed sources [58].
Preventing invasive plants from establishing in weed-free burned areas is the most effective and least costly management method. This may be accomplished through early detection and eradication, careful monitoring and follow-up, and limiting dispersal of invasive plant propagules into burned areas. General recommendations for preventing postfire establishment and spread of invasive plants include:
For more detailed information on these topics, see the following publications: [4,16,17,65,206].
Use of prescribed fire as a control agent: Use of frequent prescribed fire in communities with short presettlement fire-return intervals is probably fire's most practical use in controlling Chinese tallow, since fire is most effective when used repeatedly and frequently. In addition to burning sprouts from Chinese tallow top-killed in previous fires and possibly causing increased damage to older trees [67,68], the susceptibility of young Chinese tallow [68] and the potential for lower germination rates [21] means repeated fires may decrease recruitment. However, the lack of fine fuel biomass and continuity in Chinese tallow-invaded sites may make prescribed burning difficult, and decrease fire intensity in the immediate vicinity of the trees such that they are not damaged by fire (personal communication [149]). Chemical and/or mechanical treatments may be used initially to increase fuels so prescribed fires can be conducted [48,49]. If conditions conducive to burning do not occur often enough to allow for a fire frequency that will reduce Chinese tallow dominance, other control methods are required. This will likely be the case in relatively mature Chinese tallow stands, wet areas, and sites where production of herbaceous fuels is low and/or patchy ([15,75,138], personal communication [149]). For example, repeated burning is used in combination with herbicides and mowing in the coastal prairie of the Armand Bayou Nature Center ([75,138], personal communication [149]). Occurrence of Chinese tallow in urban settings also limits the use of fire as a control method [15].
Altered fuel characteristics: Invasive populations of Chinese tallow may reduce the amount of fine fuels on a site, and Chinese tallow woodlands rarely burn (see FIRE REGIMES). Due to these factors, prescribed fire may not be an effective control agent in established Chinese tallow woodlands.Fire adaptations: Chinese tallow has the potential to respond positively to fire, given its ability to sprout following damage (see Vegetative regeneration), its association with disturbed areas (see Plant communities), and its response to increased sunlight (see Shade tolerance) and nutrients (see nutrient supplementation).
Chinese tallow has several adaptations to survive and persist after fire, even at frequent intervals. Bark that thickens with age insulates older trees. Chinese tallow top-killed by fire may produce vigorous basal sprouts, and roots are capable of sprouting up to 16 feet (5 m) from the original stem [67]. Chinese tallow has been observed sprouting after several years of annual burning (personal communication [149]). In addition, it is not prone to crown fires and typically ignites only when fires are intense. This and the lack of herbaceous fuels under Chinese tallow stands (see Fuels, below) result in woodlands that are resistant to burning [67].
Information regarding colonization of burned sites is lacking. Surviving Chinese tallow trees are the most likely source of seed. However, no data address the ability of seeds in the seed bank to survive fire, and information is sparse regarding the ability of Chinese tallow seeds to establish on burned sites (see below).
Plant response to fire: In some instances fire in forested habitats may enhance Chinese tallow invasiveness. Chinese tallow was not invading a mixed-hardwood pine site in northern Florida where fire was excluded, but it was invading a similar habitat in South Carolina burned every 3 to 5 years. The unburned site had significantly (P=0.03) greater litter depths than the South Carolina site, which was thought to reduce access to moist soil and impede Chinese tallow germination [167]. In counties already highly invaded by Chinese tallow, probability of invasion of forested areas was significantly greater (P<0.047) where fire had damaged at least 25% of trees within the previous 5 years. Conversely, in counties that were not yet highly invaded, there was a negative relationship between fire damage and the probability of invasion, although the relationship was not significant (P=0.176) [58].
Fire may reduce Chinese tallow recruitment in some circumstances. At Lake Jackson in northern Florida, Chinese tallow germination from February to May averaged 7.4% in unburned areas, which was significantly (P<0.001) more than the average 1.0% germination rate in areas that were burned in early to mid-March [21]. According to an abstract from a conference proceedings, annual spring burning reduced survival and growth of Chinese tallow seedlings in a coastal prairie in eastern Texas. A single spring fire had no impact on Chinese tallow invasion three years after burning [162].
Circumstantial evidence suggests that Chinese tallow density may be lower on burned than unburned sites. Smith and others [193] found more Chinese tallow in unburned than burned plots following prescribed burning in maritime forests in Cape Romain National Wildlife Refuge, South Carolina. Burns were conducted in winter and were of low severity, with most of the duff layer remaining unburned [193]. In a tallgrass coastal prairie of Texas with encroaching woody species, primarily Chinese tallow and Rio Grande dewberry, a late February fire had a significant (P=0.03) negative impact on percentage of woody species [80]. Relative density of Chinese tallow was 41.5% on a site that was burned after clearcutting, compared to relative densities of 85% and 80% on larger tracts that had different postharvest treatments [85]. It is important to note that confounding factors, such as Chinese tallow seed availability or differences in site characteristics, were not eliminated as possible explanations for these observations.
Stage of development of a Chinese tallow stand is possibly the most important factor influencing its long-term response to fire, due the effects of tree size and fuel characteristics [67,68]. Repeated burning of stands with enough fuel to carry a fire may eventually lead to declines in Chinese tallow dominance [67,68]. However, as Chinese tallow stands age they become increasingly resilient due to increased ability of older trees to recover after fire (see IMMEDIATE FIRE EFFECT ON PLANT) and reduced severity of burns in woodlands with little fuel [67] (see Fuels). Grace and others [69] report that repeated fires performed with adequate herbaceous fuel near Chinese tallow trunks killed large, isolated individuals. However, once a "critical stand density" is reached, burning will have little to no long-term impact on Chinese tallow stands [69]. This critical threshold is likely affected by season of burning and other fire and site characteristics [67,68,69].
Season of burning influences Chinese tallow's response to fire. Prescribed burns conducted during the growing season had greater long-term negative effects on growth and survival of Chinese tallow basal sprouts than those conducted when Chinese tallow was dormant [67]. Chinese tallow generally recovers more slowly from burning during the growing season [67,68].
Site conditions are likely to influence Chinese tallow's response to fire. The amount of clay in soils may affect Chinese tallow response by increasing water retention and insulating roots from the heat of a fire (personal communication [194]). In general, soil moisture influences the impact a fire has on plants [78,175,190].
Fuels: In established Chinese tallow stands, fine fuel loads have been observed to decrease over time as Chinese tallow shades out understory grasses ([19,67,68], personal communication [149]). According to a comprehensive review [211], forbs increase in dominance in Chinese tallow stands compared to native wetland or upland grassland vegetation. This results in a patchier, discontinuous fuel layer comprised of less flammable species than the original community. Sometimes Chinese tallow seedlings establish at such high densities that fine fuels are lacking even in a stand of smaller trees (personal communication [149]). These changes in fuel characteristics result in patchier and/or less severe fires, which are less likely to impact Chinese tallow [67,211]. According to Grace [67], "it is common to watch a prescribed fire burn right up to the edge of a tallow stand and simply go out because of a lack of fuel."
Chinese tallow woodlands may generate or retain less litter than native woodlands. Areas with high densities of Chinese tallow in the understory and overstory had significantly lower daily litterfall (P≤0.038) and lower cumulative litterfall (P≤0.035) than areas of a bottomland hardwood forest with little Chinese tallow in the overstory [82]. There are exceptions, however. The average amount of leaf fall observed in a Chinese tallow woodland in coastal Texas, 382.6 g/m²/year, is typical for southern deciduous trees [27]. Chinese tallow litter decays quickly compared to that of native species [27,82,109] (see Impacts).
FIRE REGIMES: There is a wide range of fire frequencies and severities in habitats where Chinese tallow occurs. Many of these habitats have evolved with short fire-return intervals. Observations suggest that sites with relatively infrequent or irregular fire frequencies may be more easily colonized by Chinese tallow [67,68,153,163], although data are lacking. Frequent burning may decrease Chinese tallow recruitment or prevent establishment of Chinese tallow woodlands in coastal prairies [67]. Burning or mowing at 1- to 3-year intervals has been effective at maintaining native prairie vegetation at Armand Bayou Nature Center in southern Texas [75]. Reintroduction of fire into native plant communities adapted to a regime of frequent fires may help slow establishment and spread of Chinese tallow while promoting native species.
In Chinese tallow woodlands, the moisture and fuel conditions necessary to ignite and carry a fire rarely occur [67]. The lack of fine fuel biomass and patchiness of fuels on sites invaded by Chinese tallow (see Fuels, above) likely reduce the probability of ignition and spread on those sites. Grace [67] suggests that "it is possible for tallow to render the ecosystem nonflammable".
See the Fire Regime Table for further information on FIRE REGIMES of vegetation communities in which Chinese tallow is important. That table is not inclusive for all plant communities in which Chinese tallow occurs. Find further fire regime information for the plant communities in which this species may occur by entering the species name in the FEIS home page under "Find FIRE REGIMES".
Chinese tallow germination and time to germination are influenced by season of planting, digestion by birds, site characteristics, and seed characteristics. This results in a wide range of reported germination rates both across and within studies. For instance, Conway and others [40] did not obtain germination rates higher than 10% from ripe seeds collected in fall that were either soaked in cold water, soaked and chilled, or not subject to any pretreatments, while germination rates observed by Cameron and others [25] ranged from 0% to 94%. Chinese tallow germination rates ranged from about 13% to 80% in a greenhouse experiment investigating the effects of bird consumption and seed burial on Chinese tallow germination [152]. Germination of Chinese tallow seeds in various treatments and at varying elevations above water level at a riparian site in central California ranged from 6.1% to 68.3%. Sixty-five percent of ungerminated seeds were viable at the end of the experiment, suggesting a longer experimental period would have resulted in greater germination rates [15].
Germination of native species is typically similar to or higher than Chinese tallow germination and may occur over a broader range of conditions [18,133]. However, regardless of comparatively low germination rates, including rates below 10% [40,41] or 15% [133], high seed production may cause difficulties in controlling Chinese tallow invasions [40]. In areas where Chinese tallow is already present, the possibility of increased germination of Chinese tallow seeds [39,42] compared to germination of seeds of native species causes additional concern. However, success of Chinese tallow seedlings in closed-canopy Chinese tallow woodlands may be low [18,186].
Digestion by birds likely enhances germination of Chinese tallow seeds [15,152,167,192]. In a greenhouse experiment, 51% of seeds that passed through an avian digestive tract germinated, significantly (P<0.0001) more than the 22.5% germination rate of seeds that had no evidence of being manipulated by birds. There was an interaction between burial and digestion (P<0.0005), with digested seeds that were buried exhibiting 81% germination compared to about 15% to 30% germination rates in other treatment combinations. Cumulative emergence of digested seeds was 76.5%, significantly (P≤0.0003) greater than the 39.5% cumulative emergence of unmanipulated seeds [152]. Lack of a difference in germination between uneaten seeds collected after yellow-warbler feeding activities and those collected from trees [41] indicates that digestion of the seed, not manipulated by the birds, results in enhanced germination. Effects of digestion by birds on Chinese tallow seeds collected from areas around Davis, California was simulated by soaking in sulfuric acid. The germination rate of these seeds was significantly (P<0.05) higher than germination of seeds removed from trees [15]. Sulfuric acid treatment also exhibited the fastest mean time for germination (36.4 days) of all treatments. However, exposure to sulfuric acid for more than 10 minutes resulted in significant (P<0.05) decreases in germination compared to a 10-minute treatment. A 62.3% germination rate was observed in seeds that had their tallow coating completely removed, while seeds in the treatment where the coating was split exhibited 17.3% germination [192].
Chinese tallow is most successful in wet, open habitats. It is flood tolerant [126] and is often found along the shores of water bodies, in floodplains, and in swampy areas [47,62,63,126,132,214]. However, it also occurs in drier, upland habitats [62,63,126,152,214]. Chinese tallow invades intact habitats and is successful in disturbed areas [35,132,193,214]. Thin woodlands, canopy gaps, and open understory appear more easily colonized by Chinese tallow than closed-canopy forests [52,77,132,138,183]. Although Chinese tallow has been reported to withstand some exposure to freezing temperatures [154], substantial damage has been observed after 36 hours of below-freezing temperatures [20]. Chinese tallow distribution is likely limited by cold temperatures in the north [20,93].
Chinese tallow typically occurs at low elevations [52,62,63,212] but does grow at higher elevations. In forests of the southern United States, Chinese tallow is most common on low and flat lands. About 80% of invasive Chinese tallow populations in southern forests occur on sites below 165 feet (50 m) and with slopes less than 2°, and all invasive populations occur on sites below 540 feet (165 m) and with slopes of 18° or less [58]. In the Lake Jackson area of northern Florida, Chinese tallow cover was greatest, typically about 10%, at elevations of 84 to about 89 feet (25.5-27 m) above sea level, and cover was less than 5% outside of this elevational range [21]. In a southern New Mexico experimental planting, Chinese tallow survived and grew at 3,770 feet (1,150 m) [100]. Chinese tallow plantations occur at elevations from 1,300 to 2,300 feet (400-700 m) in Taiwan [112] and from 4,000 to 5,000 feet (1,200-1,600 m) in northern India [174].
Water Chinese tallow has been reported on sites with average annual precipitation ranging from 9.6 to 147 inches (243-3,733 mm). Average annual precipitation in Chinese tallow-invaded habitats near Houston ranged from 42.1 to 55.9 inches (1,070-1,420 mm) [183]. In Taiwan average annual precipitation ranges from 52.6 inches to 147 inches (1,336-3,733 mm) in habitats where Chinese tallow occurs [112]. In plantations in New Mexico that receive average annual precipitation of 9.6 inches (243 mm), Chinese tallow that were irrigated for 2 months after transplanting exhibited 90.6% survival and grew to an average height of 55 inches (140 cm) over 2 growing seasons [100].Chinese tallow apparently prefers wet sites, although it does grow in drier areas. Based on logistic regression from sites throughout the Southeast, the probability of invasion of forests by Chinese tallow increases with decreased distance to water. This is likely due to movement of seeds by water, occurrence of bird habitat around water, and soil moisture levels favorable for Chinese tallow establishment [58]. Chinese tallow exhibited significantly (P<0.01) lower seedling survival in treatments with 23% soil moisture compared to treatments with ≥31% soil moisture [18]. Chinese tallow near the border of India and Pakistan grew taller, had larger stem diameters, and produced seed at an earlier age when planted on a waterlogged site compared to those planted on an agricultural site [191]. In central California, all Chinese tallow that had established on their own at North Davis Pond occurred within 23 feet (7 m) of the water's edge. Chinese tallow planted ≥3.7 feet (1.1 m) above the water level of Putah Creek did not survive more than 132 days, while 80% of those planted at water level survived a summer drought [15]. Chinese tallow was less abundant on dry sites in Gulf Coast forests [77] and in a dry pine-turkey oak community in coastal South Carolina [152] than on more moist sites or communities nearby.
Chinese tallow can survive dry periods, although growth may be impacted. In eastern Texas coastal prairies, Chinese tallow that received ambient precipitation survived significantly (P<0.05) longer than Chinese tallow in plots where pumps removed surface water following large rain events [189]. Chinese tallow in a greenhouse survived and grew when watered monthly. However, significantly (P=0.0001) larger total plant biomass was observed in more frequently watered plants [8]. In another greenhouse experiment, an intermittent drought treatment did not have significant impacts on growth rate or the total mass of Chinese tallow [22]. Scheld and Cowles [170] attribute Chinese tallow survival during dry periods to rapid taproot development.
Chinese tallow survives and grows in most flooding conditions, although Chinese tallow in drained soils generally have significantly (P<0.05) smaller root biomass and significantly (P<0.05) larger heights, stem diameters, and leaf biomass [31,32,34,91]. Chinese tallow may produce hypertrophied lenticels, adventitious roots, and thicker feeder roots when flooded [31,91]. Flooding duration did not have a significant effect on Chinese tallow survival (P>0.31) or mass (P>0.35) in a floodplain forest where flooding depths ranged from 8 to 20 inches (20-52 cm) and flooding duration ranged from 14 to 61 days [183]. Chinese tallow trees in drained soil exhibit significantly (P=0.0001) increased photosynthesis compared to flooded (to 2.0 inches (5 cm) above the soil surface) plants [122]. The reduction in Chinese tallow size due to flooding to 1.0 inch (2.5 cm) above the soil surface was significantly (P<0.0001) larger than the reduction in water tupelo under 100% light but not under 20% light (P>0.03) [91]. In a greenhouse experiment, flooding to 0.4 to 1 inch (1-3 cm) for 16 weeks significantly (P<0.05) decreased Chinese tallow growth rate. This and a treatment consisting of daily watering for 2 weeks followed by flooding for 2 weeks repeated over 16 weeks resulted in significant (P<0.05) declines in Chinese tallow mass [22]. Greenhouse experiments in coastal Texas and east-central China showed that Chinese tallow seedling growth rate, leaf, shoot, and total biomass were significantly greater in soils that were not flooded compared to soils flooded to 0.4 inch (1 cm) above the soil surface [219].
Chinese tallow tolerates moderate levels of salinity [31,33,122], with younger plants [31,122], plants exposed for longer periods [31,33,122], and plants exposed to greater salinities the most negatively impacted [31,122]. All 4-month-old Chinese tallow trees died after 6 weeks exposure to 10 ppt saline water, while no mortality occurred over an 8-week period in a group of 5.5-month-old Chinese tallow trees exposed to the same conditions [31]. Chinese tallow was only slightly affected by saline (20-27 ppt) flooding of up to 2 days, and after 5 days survival was 60% [33]. No Chinese tallow mortality was reported following simulated storm surge treatments of 21 ppt salinity lasting 48 hours. Tip dieback did occur, mainly in plants that were flooded with freshwater before the simulation [31,32]. Chinese tallow watered with 10 ppt saline water had significantly (P<0.05) reduced height [32], photosynthesis [122], and stem and root biomass [31] than those watered with less saline water (2 ppt) or freshwater.
Temperature: Chinese tallow establishment and persistence are restricted by freezing temperatures in the north [20,58,93]. The average extreme minimum January temperature was associated with the probability of invasion of southern forests, with no Chinese tallow invasion detected on sites with average extreme minimum January temperatures below 10 °F (-12 °C) [58]. In open-canopy habitats and closed-canopy uplands along the east coast, germination rates of Chinese tallow were positively correlated with mean minimum temperature in January 2001 (P<0.05) [141]. Seeds from North Carolina planted in fall had higher germination rates than seed from South Carolina planted in fall. Seedlings from North Carolina were more likely to survive extended periods (6-384 hours) of freezing temperatures ((19 °F) -7 °C) (P=0.04) and had significantly less height loss from November to April (P=0.02) than Chinese tallow seedlings from South Carolina. However, seedlings from North Carolina and South Carolina did not differ in survival or date of budbreak. About 70% to 80% of Chinese tallow seedlings from North Carolina and South Carolina survived exposure to 23 °F (-5 °C) for 6 hours [139]. Rockwood and Geary [154] report Chinese tallow survival after a December 1983 freeze, and Grace and others [69] note Chinese tallow growth after damage from exposure to cold temperatures. However, Chinese tallow suffered substantial damage after exposure to freezing temperatures for 36 hours. From these observations and a distributional map, the authors conclude that the northern boundary of Chinese tallow spread is in the 7b zone (average minimum winter temps of 5 °F to 10 °F (-12 to -15 °C)) of the USDA Plant Hardiness Zone map [69].
A warming climate is expected to increase the range and severity of Chinese tallow invasion, especially if coupled with increased occurrence and intensity of disturbance. Based on Forest Inventory and Analysis data from southern forests, a 4 °F (2 °C) increase in temperature was projected to result in low levels of invasion into central and northern Alabama and Mississippi and further east into Texas and increased invasion rates in most of southern Louisiana and parts of southern Mississippi and southeastern Texas [58]. Based on the climate in Chinese tallow's native and introduced range and results of seeding and planting trials in the eastern United States, a CLIMEX model predicts that Chinese tallow's potential distribution would extend from New Jersey west through southern portions of Pennsylvania, Ohio, Indiana, and Illinois to central Missouri and southeastern Kansas with a 2 °C increase in maximum and minimum daily temperatures [140].
Soil: Chinese tallow occurs in a wide range of soil types. It occupies sites with acidic to slightly basic soils. Soil pH ranged from 3.9 to 8.5 in Chinese tallow plantations in Taiwan [112]. Values of pH on sites with Chinese tallow in India [116,131], Texas [200], and soil used in an experiment [34] where within this range. Chinese tallow grows on a wide range of soil textures from clays [18,170] to loams [18,131] to sandy [84,145] soils. Nutrient levels in soil from Chinese tallow plantations in Taiwan [112] and India [116,131] are available.
Chinese tallow is tolerant of slightly saline soils [112,126,170]. Chinese tallow was present in a southeastern Louisiana community type with significantly (P<0.05) greater soil salinity in 4 years of a 5-year study than in 3 community types where Chinese tallow did not occur. Salinity ranged from just over 1 ppt to over 4 ppt in a drought year [83]. In field experiments, Chinese tallow had lower mortality and better growth on eastern and central coastal prairie sites with electrical conductivities from 139.5 µS to 634 µS compared to Chinese tallow on western sites with mean electrical conductivity of 3,070 µS. Although other factors may have influenced this pattern, a likely cause is high salinity on the western sites [8].
Nutrient supplementation: Fertilizer may increase Chinese tallow survival, occurrence, and size, which may facilitate establishment in areas where nutrients have been added [187,189]. In a tallgrass coastal prairie of Texas with encroaching woody species such as Chinese tallow and Rio Grande dewberry (Rubus riograndis), addition of fertilizer was positively associated (P=0.09) with percentage of woody species [80]. In eastern Texas coastal prairie, Chinese tallow in plots fertilized with nitrogen, phosphorus, and potassium survived longer (P<0.05) than in plots that were not fertilized [189]. However, in another study in the same area, nitrogen addition did not affect Chinese tallow survival [182,187]. Chinese tallow height [157,158,189], diameter [157], aboveground biomass [134,189], shoot mass [157,158], root mass [157], and individual plant mass [157,182] have been shown to increase with nutrient supplementation. Mean leaf area (P≤0.0006) [156,158] and individual leaf mass (P<0.0001) [156] were significantly increased with increased nitrogen. In contrast, in 2 greenhouse studies Chinese tallow shoot mass [158,159], root mass [159], diameter growth [158], and stem growth [159] were not significantly influenced by addition of fertilizer. The effects of nitrogen and shade have been the topic of several studies [157,158,182], and their results regarding the effect of shade and the interaction of nitrogen addition and shade are summarized in the Shade tolerance section.
IMMEDIATE FIRE EFFECT ON PLANT: Mature Chinese tallow typically survives or is top-killed by fire. Small trees are more vulnerable than large trees [67,148]. As of 2010, there was no information regarding the effect of fire on Chinese tallow seed viability.
Chinese tallow seedlings are more susceptible to fire than adult trees. Observations at Armand Bayou Nature Center suggest that trees larger than 1 inch (2.5 cm) in diameter are difficult to top-kill with fire (personal communication [149]). The only immediate mortality Grace [67] observed after prescribed fire was that of 4-inch (10 cm) tall transplanted seedlings. Grace and others [68] reported generally decreasing mortality and decreasing top-kill with increasing height after prescribed fires in Texas coastal prairies [68]:
Approximate postfire mortality and top-kill rates of Chinese tallow as a function of tree size [68] Chinese tallow height class Died (%) Top-killed (%) Survived (%) <0.1 m 100 0 0 0.1-1.0 m 40 ~25 ~35 1-2 m ~15 ~60 ~25 2-3 m ~3 ~36 ~61 3-4 m 0 ~8 ~92Fuel biomass and continuity influence the direct fire effects on Chinese tallow. More Chinese tallow trees were burned in a prairie site (73-100%) than in an abandoned rice field (24-73%) because fuel load and continuity were greater on the prairie site [67]. Observations at Armand Bayou Nature Center indicate that Chinese tallow trees of any size are more likely top-killed by fire when they have substantial fine fuels around the base of the tree (Regmund 2005 personal communication [149]). See the Research Paper by Grace and others [68] for further details.
Impacts: Invasion of coastal prairie and longleaf pine communities by Chinese tallow is a major concern, given the already limited distribution of these habitats [67,209]. The degree to which Chinese tallow establishes in these and other communities (Distribution and Occurrence), its probable impact on some wildlife species (see Cover value), and its potential to alter fuels and FIRE REGIMES have been addressed in previous sections of this review. A summary of the literature investigating allelopathic effects of Chinese tallow is also discussed.
Chinese tallow leaf litter decomposes quickly and potentially increases nutrient availability. Litter bags with either 0.7 or 1.2 ounces (20 or 35 g) of Chinese tallow leaf litter placed in the main channel of Abita Creek in southeastern Louisiana had decomposition rates 2.6 to 14.5 times that of red maple leaves, and litter bags with 35 g of leaf litter placed in 3 ephemeral ponds near Florenville, Louisiana, had average decomposition rates 16.5 times that of laurel oak leaves. In all experiments Chinese tallow leaf litter had completely broken down after no more than 64 days [109]. Chinese tallow leaves decay rapidly in terrestrial habitats [27,82]. On sites within a bottomland hardwood forest with varying degrees of Chinese tallow invasion, only 8% of 0.35-ounce (10-g) samples of Chinese tallow litter remained after 16 weeks on the forest floor, and none remained after 32 weeks. This decomposition rate was faster than that observed for sugarberry, red maple, sweetgum, live oak, or a mixture of sugarberry, red maple, and sweetgum litter. Chinese tallow litter was considered "high quality" based on nitrogen and phosphorus content [82]. The lignin to initial nitrogen concentration ratio was lower in Chinese tallow than in native southern trees, which may partially explain Chinese tallow's rapid leaf decay. Concentrations of several nutrients, such as phosphorus, potassium, and zinc, were significantly (P<0.05) higher in Chinese tallow woodland soil than in nearby prairie soil, while manganese and sodium concentrations were significantly (P<0.05) lower [27]. In the Jackson Lake area of northern Florida, Chinese tallow was associated with sites with high soil magnesium content, possibly due to decomposition of Chinese tallow leaves increasing magnesium levels [21]. Cameron and Spencer [27] conclude that rapid leaf decay resulting in the release of nutrients may cause increased productivity in areas with Chinese tallow. Greater aboveground net primary productivity has been observed in Chinese tallow woodland (1,264 g/m² (SD 27 g/m²)) compared to unburned (462 g/m² (SD 49 g/m²)) and burned (624 g/m² (SD 63 g/m²)) grassland [76].
Control: Several reviews summarize different Chinese tallow control options [13,20,92,93,197]. Bruce and others [20] suggest that Chinese tallow control efforts should be maintained for 3 to 5 years, and managed sites must be monitored. Due to Chinese tallow's ability to sprout following top-kill [67,154,170], continued control and monitoring are recommended regardless of the method used. McCormick [121] provides a comprehensive review of control techniques and case studies of Chinese tallow removal. Ramsey and others [146,147] describe techniques for mapping Chinese tallow stands using remote sensing techniques.
Fire: For information on the use of prescribed fire to control this species, see Fire Management Considerations.
Prevention: Fire and mowing are used to prevent Chinese tallow establishment in prairies. For details regarding the effects of fire on Chinese tallow, see the Fire Effects section. Regular mowing is used to prevent Chinese tallow invasion in the coastal prairie of Texas [75,138,183]. Chinese tallow seedlings did not occur on sites near Natchitoches, Louisiana, that were regularly mowed but did occur in adjacent edges and ditches that were not regularly mowed [5].
Monitoring can be focused in areas where Chinese tallow is likely to establish, such as areas downstream from Chinese tallow seed sources where water is likely to deposit seeds and seedlings are likely to survive [15]. Results of logistic regression of data from forested sites throughout the Southeast suggest that monitoring should focus on low, flat areas near water or roads that were recently disturbed or are vegetated by young, naturally regenerated forests. Prompt restoration of harvested or disturbed sites that incorporates Chinese tallow control would likely be a cost-effective way to prevent invasions [58]. Monitoring may also include fertilized lands (see Nutrient supplementation).
General recommendations to prevent the spread of invasive species in Florida included strengthening legislation that prohibits the sale of invasive species, having a mandatory quarantine period for livestock moved from infested to uninfested areas, and implementing public education programs [66]. Gan and others [58] recommend efforts to educate public landowners and encourage their participation in Chinese tallow control efforts and prevention of Chinese tallow establishment because Chinese tallow establishment is more common on private than public lands.
Educating the public about the consequences of using Chinese tallow as an ornamental, encouraging planting of native species, and removing Chinese tallow from nurseries are important steps to reduce seed sources [120,144]. Langeland [106] includes a list of ornamental species that are good alternatives to Chinese tallow in areas with an annual minimum temperature of 15 °F (-9.4 °C) or higher.
Cultural control: No information is available on this topic.
Physical or mechanical control: As mentioned in Prevention, mowing may prevent establishment of Chinese tallow. High-impact mechanical control techniques are practical only in certain situations [92]. They are typically used on heavily impacted sites, such as rights-of-way [13,93] and canal banks [208]. Mulching live Chinese tallow trees in invaded prairies may be a viable method of restoration in some areas and allow for future management through mowing or prescribed burning [49]. In central Louisiana, small (<1 foot (0.3 m)) Chinese tallow trees cut in autumn had higher mortality than small, uncut trees (P<0.05). No mortality was observed in larger Chinese tallow trees, regardless of cutting treatment [5]. In sensitive areas, mechanical treatment typically involves manual removal of seedlings and felling trees in place [20]. Due to the ability of Chinese tallow to sprout, mechanical techniques have the potential to exacerbate Chinese tallow invasions [92] and are almost always accompanied by herbicide application. Conway and others [44] conclude that mechanical harvest is best done during seed formation because this is when total nonstructural carbohydrate concentrations in Chinese tallow roots are the lowest. Cutting during flowering [197] and removing fruit from fallen trees [13] would help minimize seed left on newly cleared sites.
Flooding is not typically used to control Chinese tallow, given its tolerance. However, cutting below the water level may kill Chinese tallow [13]. Smith (personal communication [194]) has observed successful control of Chinese tallow with constant flooding for 36 months.
Biological control: Only preliminary surveys of the feasibility of biological control of Chinese tallow had been undertaken as of 2010 [45,143,197,213].
Grazing has been noted to prevent establishment of Chinese tallow [138]. However, in a personal communication cited by Bruce and others [20], Kramer reports that short-term rotation of high-density cattle herds is less successful in controlling Chinese tallow than in controlling groundsel-tree, despite cattle eating Chinese tallow less than 2.4 inches (6.1 cm) tall.
Chemical control: Herbicides are widely used for controlling Chinese tallow [20,46,67,101,197], and guidance specifically for property owners is available [106]. Application of herbicide following cutting is a typical application method [54,107,208]. Langeland and others [107] provide direction on the application of herbicides to cut Chinese tallow. Basal bark applications are preferred by many organizations including The Nature Conservancy and the Florida Department of Environmental Protection [13,20,208]. Conway and others [44] conclude that the period from "seed maturation until leaf fall" is the best time for foliar herbicide application, since the chemicals would be moved downward into the root system during this time, resulting in a higher probability of the death of the entire plant. McCormick [121] provides detailed descriptions of herbicide treatments for small- and large-scale Chinese tallow control projects.
Integrated management: No information is available on this topic.Although Chinese tallow leaves, fruit and sap are toxic to many animals including cattle, several bird species eat the fruits, and insects eat a limited amount of various parts.
Palatability and/or nutritional value: Chinese tallow is toxic to several species including humans [52,62,113,197]. Compounds from Chinese tallow roots may irritate skin and produce tumors [172]. The toxic effect of Chinese tallow leaves and fruit on cattle was demonstrated by Russell and others [165]. However, cattle have been reported to eat seedlings <2.4 inches (6.1 cm) tall (Kramer personal communication in [20]). Domestic sheep and goats are much less affected by Chinese tallow [165]. They have been reported to eat the leaves [3], although Sharma and others [174] note that domestic goats in northern India do not eat Chinese tallow.
Several bird species eat Chinese tallow seeds [41,124,150,151] and are important dispersal agents. Winter residents eat Chinese tallow seeds more often than other birds (P<0.001) [41,150]. Species commonly observed eating Chinese tallow seeds include northern cardinals, red-winged blackbirds, gray catbirds, and red-bellied woodpeckers [41,150,151]. Baltimore orioles and yellow-rumped warblers comprised 72% of the foraging observations in coastal Texas [41], while northern flickers and American robins were important in South Carolina [150,151]. Chinese tallow met the energy requirements of yellow-rumped warblers and American robins, but not northern cardinals in feeding trials. Chinese tallow occurrence may influence local winter distributions of yellow-rumped warblers [7]. Hermit thrushes ate Chinese tallow seeds in loblolly pine plantations that were 12 to 14 years old and 21 to 23 years old [201]. Given the importance of birds as dispersal agents and the possibility of competition with native plant species for dispersal agents [151], more research is needed on birds' preference for Chinese tallow seeds compared to native foods. Mammalian seed predators of Chinese tallow were observed in a prairie habitat of northern Florida and included marsh rabbit, eastern cottontail, and marsh rice rat [167].
Little information on the nutritional content of Chinese tallow is available. However, seeds have been reported to contain crude fat in quantities >25% of dry matter [177]. According to a review of nutritional content of edible plants of the Sikkim Himalaya, Chinese tallow is high in fat and protein [202].
Nutritional data (% dry matter) for Chinese tallow collected by Rockwood and included in a literature review by Rockwood and others [155] Organic matter Neutral detergent fiber, ash free Digestibility by rumen microbes Acid detergent fiber Lignin Nitrogen Phosphorus 98.5 85.7 19.1 69.5 20.2 0.49 0.04Insect herbivory: Few insects typically feed on Chinese tallow in the field. For example, much lower herbivory was observed in Chinese tallow (mean 3.3%; range 0-5% of total leaf area) than in green ash (mean, 25.8%; range 5-75%) [91]. Insect damage on Chinese tallow in coastal Texas was low, averaging 0.67% of leaf area removed [189]. In southeastern Texas, maximum loss of Chinese tallow to insect herbivores was significantly (P=0.002) less than maximum loss of willows [28]. Chinese tallow woodland in this area had fewer insects [28] and a lower proportion of insect herbivores than native species [28,79]. Only 7% of arthropods collected in a Chinese tallow woodland near Houston, Texas, were herbivores, while predators and detritivores comprised 70% of arthropods collected. Herbivores comprised 49% to 67% of arthropods in several native communities surveyed in previous studies, including prairies, riparian habitats, and pastures [79]. In bottomland hardwood forest in southeastern Louisiana with high densities of Chinese tallow in the understory and overstory, primary and secondary terrestrial invertebrate consumers were less abundant than in less invaded areas [82]. See Impacts for more information on Chinese tallow's effects on invertebrates.
Experiments suggest that behavioral avoidance, as opposed to strong Chinese tallow defenses, may result in low herbivory. Siemann and Rogers [185] found increased grasshopper growth rates with increased amounts of Chinese tallow foliage consumed (P<0.05). In laboratory trails, Lankau and others [108] found that grasshoppers preferred Chinese tallow over 3 native species (P<0.05). Invasive Chinese tallow experienced greater herbivory than native Chinese tallow in a common garden in China [220], possibly due to lower levels of tannins in invasive Chinese tallow [28]. Several insects feed on Chinese tallow including leaf-footed bugs [87], leaf-cutting ants [171], fire ants [167], termites [99], yellow-striped army worms, and eri silkworms [173]. Insect loads in Chinese tallow woodlands have been shown to increase with time since establishment [28,188]. Despite this and other evidence for reduced defenses compared to Chinese tallow from China [28,181,184,185,220], Chinese tallow occurring in the southeastern United States do have some herbivory defense [119,161]. For instance, one terrestrial reducer ate leached and ground Chinese tallow leaves faster than unprocessed leaves [26], and terrestrial isopods ate Chinese tallow leaves once tannins were leached [109].
Much of the research on insect foraging on Chinese tallow has investigated the hypothesis that the evolution of reduced defenses in response to low herbivory has allowed Chinese tallow to allocate more resources to increasing performance [181,183,184,185,218,220]. Several studies show that invasive Chinese tallow has faster growth rates compared to Chinese tallow from its native range [216,217,218,219] (see Plant growth). Increased growth allows Chinese tallow in the United States to recover from herbivore damage faster than native Chinese tallow. Thus, invasive Chinese tallow has become less resistant to and more tolerant of herbivory than native Chinese tallow [160,218,220].
Chinese tallow response to herbivore exclusion is variable. Despite having lower herbivore damage than sugarberry, application of insecticide in coastal prairie, mesic forest, and floodplain forest in Texas resulted in greater increases in Chinese tallow survival and growth than observed in sugarberry [183]. Exclusion of invertebrate herbivores did not impact Chinese tallow seedling growth in open coastal prairies of eastern Texas [162] but resulted in significant increases in Chinese tallow seedling growth (P=0.01) in an established Chinese tallow woodland [186]. Although Chinese tallow shows high tolerance to short-term herbivory, the amount of herbivory in the 1st year was negatively correlated with survival from the start to the end of the 2nd growing season [183]. Greenhouse experiments investigating the effect of herbivory have consistently found no effect of simulated insect herbivory on Chinese tallow from the southeastern United States under varying nutrient conditions [157,158,159].
Cover value: The value of Chinese tallow as cover is uncertain. Small mammals such as cotton rats and harvest mice in coastal Texas preferred other habitats over those containing Chinese tallow [97,98]. Chinese tallow woodlands had lower avian species diversity than bottomland hardwood forest in southwestern Louisiana. Only 3 species, American robin, gray catbird, and yellow-rumped warbler, were more common in Chinese tallow woodland than bottomland hardwood forest [7]. Use of specific layers of Chinese tallow forests by species of migrant birds, such as black-throated warblers and black and white warblers, suggest that Chinese tallow provides adequate cover for some bird species [43]. On coastal prairie sites in southeastern Texas, sedge wrens and swamp sparrows were more common in areas where Chinese tallow was present, while savanna sparrows were more common in areas where it was absent [6]. Of 45 American woodcock roost points in the Alazan Bayou Wildlife Management Area in eastern Texas, 29 occurred under sapling-sized Chinese tallow trees that had been treated with herbicide the previous summer [61]. In a tallgrass coastal prairie of Texas with encroaching woody species, primarily Chinese tallow and Rio Grande dewberry, arthropod diversity was negatively associated with woody species cover and percent woody vegetation [80].
Chinese tallow leaf fall may affect terrestrial and aquatic invertebrate communities and aquatic vertebrates. Stress from tannin input from Chinese tallow leaves may be responsible for changes in microbial community characteristics [129]. Chinese tallow woodlands typically have fewer herbivores than native communities [28,79,82] (see Palatability and/or nutritional value), suggesting that Chinese tallow invasion alters litter food webs [82]. In the laboratory, 2 common aquatic invertebrates showed significantly (P<0.05) higher mortality in treatments with sufficient food and Chinese tallow tannin than controls with sufficient food and distilled water [26]. In southeastern Louisiana, Chinese tallow impacted aquatic invertebrate community composition and negatively (P<0.001) affected survival of Cajun chorus frog and southern toad tadpoles. In tallow litter, Cajun chorus frog tadpole survival was 0%, and southern toad tadpole survival was 2.2%. In litter from native trees, survival of Cajun chorus frog tadpoles ranged from 89.1% to 95.3%, and survival of southern toad tadpoles ranged from 51.3% to 61.1%. In contrast, survival of green treefrog tadpoles was not affected by Chinese tallow leaf litter. Effects of Chinese tallow litter on water quality included significantly lower dissolved oxygen than treatments with native litter (P<0.001), and dissolved oxygen in Chinese tallow treatments did not increase over the course of the experiment as it did in native litter treatments (P=0.031). The effect of leached tannins is likely to have a persistent effect on aquatic organisms and seasonal effects on terrestrial invertebrates [109].
Feral hogs use Chinese tallow woodlands, and their effects on Chinese tallow are equivocal. In a mixed pine-hardwood forest with abundant feral hogs in the Big Thick National Preserve in Texas, Chinese tallow was twice as numerous in areas affected by feral hogs than in areas where they were excluded (P<0.05). Feral hogs disturbed an average of 22% of ground area within control plots [180]. In contrast, Chinese tallow saplings outside enclosures experienced 90% mortality over a 103-day experiment on a barrier island of the Georgia coast with high feral hog densities (24.7 hogs/km²). On a site near Jesup, Georgia, with a stable or increasing feral hog population, Chinese tallow saplings outside enclosures experienced 34.6% mortality. Mortality within enclosures was negligible at both sites [121].
Chinese tallow invades several plant communities including Gulf coastal prairies and many types of forests in the southeastern United States. It commonly occurs on disturbed sites such as spoilbanks [9,10,137], roadsides [2,118,215], agricultural lands [146], urban areas [115], and storm-damaged forests [36,96,117]. Chinese tallow is also known to occur in riparian areas of central California [15,124].
Chinese tallow woodland may establish in several habitats. Cameron and Spencer [27] report scattered sugarberry (Celtis laevigata) and black willow (Salix nigra) within a Chinese tallow woodland in the coastal prairie region about 35 miles (56 km) southeast of Houston, Texas. Outside of nearby Alvin, Texas, the most common species in Chinese tallow woodland sites of the coastal prairie were sugarberry, yaupon (Ilex vomitoria), stiff dogwood (Cornus foemina), and American elm (Ulmus americana) [19]. However, their density and cover were much lower (maximum 93 stems/ha, combined covers <2% for all stands) than that of Chinese tallow (up to 4,432 stems/ha, several stands with cover >80%) [18,19]. In forested habitat of South Carolina's Bull Island, Chinese tallow, cabbage palmetto (Sabal palmetto), loblolly pine (Pinus taeda), redbay (Persea borbonia), and in some areas southern bayberry (Morella cerifera) were codominants. Chinese tallow dominated-stands had a dense shrub layer (9,689 stems/ha), of which 79% (7,656 stems/ha) were Chinese tallow stems. American beautyberry (Callicarpa americana) (625 stems/ha) and dwarf palmetto (S. minor) (469 stems/ha) were the next most common shrubs [81]. Jubinsky [92] reported high densities of Chinese tallow in wetlands and along the shore of Lake Jackson in Florida. Despite it only being present at the site for approximately 20 years, Chinese tallow had the highest density (0.452/m²), the highest relative frequency (0.636), and the second highest mean DBH-based cover (6.69 cm²/m²) of woody species. The only species with more cover was sweetgum (Liquidambar styraciflua), and neither sweetgum nor any other woody species present, which included American black elderberry (Sambucus nigra subsp. canadensis), oaks (Quercus spp.), black willow, and stiff dogwood, had densities greater than 0.055/m² [92]. The extent to which Chinese tallow invades other wet [92,132] and riparian [138] forests is discussed below.
Chinese tallow invades grassland communities [199] and is especially successful in coastal prairies [19,67]. In these areas bluestems (Andropogon spp. and Schizachyrium spp.), blazing stars (Liatris spp.), coneflowers (Echinacea spp.), and prairie coneflowers (Ratibida spp.) occur with cordgrasses (Spartina spp.), morning glories (Ipomoea spp.), pine lilies (Alophia drummondii spp.), and sundews (Drosera spp.) [67]. As
Chinese tallow invades, graminoid cover declines [19]. Kincaid and Cameron [97] reported Chinese tallow in 2 categories of coastal prairie. In one type it occurred with goldenrods (Solidago spp.). The second type included little bluestem (Schizachyrium scoparium), groundsel-tree (Baccharis halimifolia), southern dewberry (Rubus trivialis), blue mistflower (Conoclinium coelestinum), gulf cordgrass (Spartina spartinae), and bushy bluestem (Andropogon glomeratus), in addition to goldenrods [97]. Density of Chinese tallow trees larger than 1.6 feet (0.5 m) tall in a grass-sedge (Carex spp.) meadow typical of southern bogs was 13 stems/ha [200]. Trees were sparse and included longleaf pine (P. palustris), loblolly pine, black tupelo (Nyssa sylvatica), sweetgum, and sweetbay (Magnolia virginiana). The dominant grass was little bluestem. Sundews, tenangle pipewort (Eriocaulon decangulare), clubmosses (Lycopodium spp.), coastal plain yelloweyed grass (Xyris ambigua), and sedges such as beaksedge (Rhynchospora spp.) and hairy umbrella-sedge (Fuirena squarrosa) were common [200]. Examples of dominant species of coastal interdunal swales in Florida that are invaded by Chinese tallow include southern umbrella-sedge (F. scirpoidea), Atlantic St Johnswort (Hypericum reductum), Carolina redroot (Lachnanthes caroliana), spadeleaf (Centella asiatica), Elliott's yelloweyed grass (Xyris elliottii), and broomsedge bluestem (A. virginicus) [57].
Chinese tallow invades several woodland types in southeastern United States, including bottomland hardwood [146,212], floodplain [73,77,153], riparian [138], pine [146,163] and mixed [77,81,146,151,163] woodlands. Typical associated species include baldcypress (Taxodium distichum) [37,47,77,136,146], water tupelo (N. aquatica) [37,47,77,146], red maple (Acer rubrum) [47,77,146,212], sugarberry, black willow [132,136,212], hawthorns (Crataegus spp.) [132,136,163], sweetgum [73,77,138,151,163], and loblolly pine [77,81,146,151,163]. In a Louisiana bottomland forest [212] and in forests on Cheniers of southwestern Lousiana [132], Chinese tallow occurred with several species including live oak (Quercus virginiana), sugarberry, black willow, and common persimmon (Diospyros virginiana). In the floodplain of the Neches River in Texas, Chinese tallow, water tupelo, river birch (Betula nigra), water oak (Q. nigra), and redbay were establishing in a longleaf pine/bluestem stand where fire had been excluded in Village Creek State Park [153], and Chinese tallow occurred with sweetgum, deciduous holly (Ilex decidua), swamp chestnut oak (Q. michauxii), water oak (Q. nigra), and American hornbeam (Carpinus caroliniana) in the Big Thicket National Preserve [73,77]. In oak-elm (Ulmus spp.) riparian forests at the Armand Bayou Nature Center in Texas, Chinese tallow, sweetgum, yaupon, and American beautyberry were more likely to occur in western plots than eastern plots [138]. Chinese tallow trees from 0.4 to 4.0 inches (1-10 cm) in diameter occurred with baldcypress,
black willow, sugarberry, sycamore (Platanus occidentalis), green ash (Fraxinus pennsylvanica), common persimmon, planertree (Planera aquatica), water hickory (Carya aquatica), and/or hawthorns in 3 communities along the Trinity River in Texas [136]. In the Big Branch March National Wildlife Refuge, Chinese tallow occurred with Jesuit's bark (Iva frutescens), saltwater false willow (B. angustifolia), southern bayberry, dwarf palmetto, and groundsel-tree in areas of the slash pine/saltmeadow cordgrass-black rush-switchgrass (Pinus elliottii var. elliottii/Spartina patens-Juncus roemerianus-Panicum virgatum) association with infrequent fire [163]. In mixed woodlands, Chinese tallow commonly occurs with loblolly pine [77,151,163], sweetgum [77,151,163], and oaks such as live oak, laurel oak (Q. laurifolia) [151], water oak, white oak (Q. alba) [77], southern red oak (Q. falcata), and/or bottomland post oak (Q. similis) [163]. Renne and others [151] observed few Chinese tallow trees in a longleaf pine-turkey oak (Q. laevis) forest of Georgetown County, South Carolina. Although rare, Chinese tallow was present in an oak-hickory-pine forest of Big Thicket National Preserve in Texas [77].
Chinese tallow occurred in southern bayberry floating marsh thickets in coastal Louisiana. Common species in the understory included bryophytes, eastern marsh fern (Thelypteris palustris), and maidencane (Panicum hemitomon) [10,137]. Chinese tallow occurrence was significantly (P<0.0001) positively associated with southern bayberry in a floating marsh community dominated by bulltongue arrowhead (Sagittaria lancifolia) and maidencane with areas of dense southern bayberry [11].
Imperfect flowers of both sexes occur in the same inflorescence [52,62,63,112,126,145]. There are 2 inflorescence types, called "grape-like" and "eagle claw", which differ in morphology and development [20,112].
Mechanisms of Chinese tallow pollination are uncertain. A fact sheet asserts that Chinese tallow is wind pollinated [54]. However, Chinese tallow is a honey tree used by beekeepers [126] and was the dominant pollen in 1 of 7 samples examined in Louisiana [110]. The extent to which bees, other insects, and/or wind pollinate Chinese tallow has not been investigated.
Seed characteristics Seed source has been shown to have a large effect on Chinese tallow germination rates. Seeds from 3 areas of northern India exhibited significant (P=0.001) differences in germination [192]. Germination rate of Chinese tallow seeds from Florida was significantly higher than seeds from the 4 other source locations investigated, while germination rates of seeds from Houston, Taiwan, and Georgia were significantly higher than those of seeds from South Carolina. Differences in developmental stage of seeds from plants at different latitudes and/or site factors are possible explanations for these trends. The following table displays total germination rates for seeds from these areas [25].
Germination rates (SE) of Chinese tallow seed from different locations after 120 days [25] Locality n Total percent germinated Florida 9 52.4 (5.9) Houston 53 24.3 (2.7) Taiwan 36 28.8 (3.3) Georgia 9 30.9 (6.3) South Carolina 15 5.7 (3.1)Chinese tallow seed size and length of time in storage also affect germination. Large seeds had significantly (P<0.05) higher germination rates (≥0.15 g = 87.1%) than medium (0.1-0.14 g = 35.4%) and small seeds (<0.1 g = 10.4%) [192]. In a greenhouse experiment, 75.3% of freshly collected Chinese tallow seeds emerged, significantly (P=0.0001) more than the 44.5% cumulative emergence of 1-year-old seeds that had been stored in a paper bag in a sheltered outdoor location in northwestern South Carolina [152]. In another greenhouse experiment, length of seed storage has significant (P<0.0001) negative effects on Chinese tallow germination. After 4 to 5 years cold, dry, storage, mean germination rate started falling and by 7 years was 12% or less. The following table shows Chinese tallow germination rates for seeds of varying ages planted at different times of the year in a greenhouse; the interaction between these variables was significant (P<0.0004) [25].
Germination rates (SE) for Chinese tallow seed stored for 0 to 7 years 120 days after planting date [25]
Age (years) of seeds
Date of Planting
Nov 2 Nov 30 Jan 2 Feb 1 Mar 6 Apr 5 7 0 0 12 (3.7) 6 (2.5) 2 (2.0) 0 5 18 (8.0) 48 (5.8) 52 (13.6) 36 (22.3) 20 (3.2) 20 (5.5) 4 36 (9.3) 60 (8.4) 64 (5.1) 80 (4.5) 40 (5.5) 28 (7.3) 2 44 (9.3) 82 (3.7) 94 (2.5) 84 (4.0) 76 (7.5) 46 (7.5) 0 8 (5.8) 40 (4.5) 66 (6.8) 92 (5.8) 40 (8.4) 14 (4.0)Seedling establishment: Chinese tallow seedlings are capable of quick growth and are able to survive in a variety of conditions. Seedlings that emerged up to 15 weeks after planting exhibited survival rates from 80% to 100% [34].
Presence of Chinese tallow on a site may influence Chinese tallow seedling success. Chinese tallow seedling emergence in the understory of Chinese tallow woodlands of coastal Texas averaged 4.3% of sown Chinese tallow seeds, and average survival of these seedlings was 19%, which was less than sugarberry [186]. In a pot experiment, survival and biomass of Chinese tallow seedlings were significantly (P<0.05) lower in soil collected near conspecifics in the Big Thicket National Preserve than in soil collected near different species in the same area. Success of Chinese tallow in Chinese tallow soil that was sterilized or had fungicide applied suggests that fungi in soil from Chinese tallow woodland reduced seedling performance [135]. Jones [88] found that after 42 days, the species growing with Chinese tallow had a significant (P<0.01) effect on Chinese tallow seedling biomass, with seedlings in Chinese tallow-only pots smaller than those in grown in mixed-species pots. After 96 days there was no longer a significant difference between Chinese tallow seedlings in inter- and intraspecific treatments [88]. In the Lake Jackson area of northern Florida, seedling survival was not significantly influenced by the presence of Chinese tallow [21]. Chinese tallow had consistently higher germination and growth rates when exposed to Chinese tallow extracts in a laboratory experiment [42].
Planting Chinese tallow from Texas with Italian ryegrass (Lolium multiflorum) had no significant effect on shoot growth, shoot mass, or root mass of Chinese tallow seedlings [159]. Roots of nearby plants invading the area containing Chinese tallow roots resulted in a significant (P<0.05) decrease in total Chinese tallow seedling mass, total height, and leaf area [91]. Chinese tallow seedling growth rates in greenhouses were significantly greater on substrates collected from southern bayberry thickets of southeast Louisiana than substrates from edges of these thickets (P=0.01) or herbaceous marsh areas (P=0.05) [11].
Timing of planting did not have a significant effect on seedling emergence or survival [152]. Chinese tallow seedlings emerged throughout the growing season in coastal forests with established Chinese tallow. Seeds planted in December and those planted in February showed no significant difference in total emergence (P=0.5308) or number of Chinese tallow seedlings emerged by sampling date (P>0.10). Similarly, there was no significant effect of planting date on seedling survival either across habitats (P=0.8851) or within habitats (P>0.20) [152].
In the Lake Jackson area of northern Florida, seedlings that germinated from seeds planted 82 feet (25 m) above sea level survived for significantly (P<0.03) shorter periods than seedlings from seed planted 2 to 3 feet (0.6-1 m) higher. Significantly (P<0.017) higher soil moisture at low elevation sites may have contributed to this trend [21].
Root damage (roots cut 2 inches (5 cm) below the soil surface) did not significantly affect stem growth, root mass, or shoot mass of 3- to 5-month-old Chinese tallow seedlings from Texas that were grown in a laboratory [159].
Information on the effects of site characteristics such as water and soil conditions on establishment of Chinese tallow are discussed in the Site Characteristics section below, while the effect of light is addressed in the Shade tolerance section.
Plant growth: Growth rate of Chinese tallow seedlings has been reported as equal to or greater than many native seedlings in most conditions [18,89,90] and is a factor in its success invading coastal prairies [18]. Growth rates of 0.03 inch (0.08 cm) per day were recorded in canopy gaps of Chinese tallow forest and coastal prairie, and up to 0.13 inch (0.33 cm) per day in cleared grassland plots. In all water treatments, Chinese tallow had one of the highest growth rates and one of the greatest total masses of the 5 species investigated [22]. Average height of Chinese tallow seedlings at the end of the 1991 growing season was 8.7 inches (22 cm) [18]. Chinese tallow planted on a southern Florida site when 10 to 12 inches (25-30 cm) tall grew to 13 feet (4 m) 1.7 years after planting. Coppiced Chinese tallow on the site grew over 26 feet (8 m) in 24 months [154]. Maximum heights of coppiced Chinese tallow in coastal Texas were 11 to 12 feet (3-4 m) 1 year after cutting and over 18 feet (>5.5 m) 2 years after cutting [170].
Invasive Chinese tallow may grow faster than Chinese tallow from its native range. Chinese tallow seedlings from the United States, grown in pot experiments in China, had greater total biomass (P<0.003) after 120 days [217] and greater shoot biomass (P<0.0001) after about 4 months [218] than Chinese tallow seedlings from China.
The following table shows the mean annual mortality and recruitment rates of small and large Chinese tallow saplings in a 10-acre (4 ha) floodplain forest site along the Neches River in the Big Thicket Preserve, Texas, over 14 years [73].
Mean annual mortality and recruitment rates (fraction of saplings/year) of small and large Chinese tallow saplings in the Big Thicket Preserve, Texas [73] Small saplingsVegetative regeneration: Chinese tallow spreads locally by root sprouts [69,126] and has strong sprouting capabilities following damage [20,38,69,126]. Root sprouting up to 16 feet (5 m) from the tree trunk has been reported [67]. Near the coast in eastern Texas, Chinese tallow sprouted prolifically within a month of cutting [170]. On an abandoned agricultural field in southern Florida, experimentally planted Chinese tallow coppiced consistently and exhibited 37% survival after 36 months [154].
Chinese tallow seeds are dispersed by water ([167], reviews by [20,92]) and birds [15,41,150,151,167]. Chinese tallow seeds soaked in water for 30 days had higher germination rates than unsoaked seeds. Chinese tallow germination rates in flooded northern Florida prairies were greater than those in nearby forested habitats that were not flooded, suggesting that water dispersal of Chinese tallow seeds may have contributed to Chinese tallow invasion of the prairie habitat [167]. Birds removed an estimated 675,000 (SD 56,000) Chinese tallow seeds (about 40% of the total seed crop) in a South Carolina study area [151].
Conway and others [41] observed 24 different bird species eating Chinese tallow seeds in coastal Texas; Renne and others [151] saw 14 species feeding on Chinese tallow seeds in South Carolina; and Samuels [167] reported 21 bird species dispersing Chinese tallow seeds away from parent trees in northern Florida. Red-bellied woodpeckers, northern cardinals, northern flickers, and red-winged blackbirds are common dispersal agents in the Southeast [41,150,151,167]. Eight species were observed consuming Chinese tallow fruits in riparian areas of central California, including American robins, European starlings, cedar waxwings, and northern flickers [15].
Chinese tallow likely begins producing seed when 3 to 8 years old [51,171,208]. Scheld and others [168] noted that about 50% of Chinese tallow populations developed flowers in their third growing season. Some Chinese tallow seeds planted in a greenhouse reached maturity in a year (Grace 1977 personal communication in [208]). Near the border of Pakistan and India, 16% of a population of Chinese tallow in waterlogged conditions flowered in their 3rd year, while those on agricultural land flowered in their 4th year [191].
Chinese tallow can produce large amounts of seed. Tree age, inflorescences type, and habitat influence seed production. Average yields of Chinese tallow in Taiwan were approximately 1 pound (0.5 kg) for 5-year-old trees, 7.4 pounds (3.4 kg) for 10-year-old trees, and a maximum of approximately 26.4 pounds (12.0 kg) for 20-year-old trees. Mean seed weight over all sites for seeds from "eagle claw" inflorescences was 0.112 g and from "grape like" inflorescences was 0.121 g, giving an approximate average seed production of 100,000 seeds from a 20-year-old tree [112]. In northern India seed production ranged from 3,276 seeds in a tree with a diameter of 2.4 inches (6 cm) to 45,276 seeds in a tree with a diameter of 8.0 inches (20.4 cm) [174].
Mean Chinese tallow seed crop in a 16,900-foot² (1,570 m²) area of coastal South Carolina was estimated at 1,681,000 seeds [151]. In a Chinese tallow-dominated forest in southeastern Texas, estimated Chinese tallow seed production was 327,670 seeds/year or 273 seeds/m²/year. Dominance in seed input may explain Chinese tallow's dominance in the understory, since Chinese tallow had a lower seedling establishment rate (seedling:seed) than native species [186]. In 2007, Chinese tallow trees on a riparian site in central California had fruit loads similar to those of horticultural trees in Davis, Woodland, and West Sacramento, California, averaging 39,538 seeds/tree. Viability of evaluated seeds from horticultural trees was 95% [15]. According to the Woody Plant Seed Manual, Chinese tallow seed viability is 90% (Bonner 1974 cited in [14]).
Although Chinese tallow occurs in undisturbed areas, it is more common on disturbed sites. In forests of the southern United States, Chinese tallow is common adjacent to roadways, recently harvested sites, and sites disturbed by animals or wind. Based on logistic regression from sites throughout the Southeast, Chinese tallow is more likely to invade young than mature forests in that region [58].
It is probable that in some instances, high seed input of Chinese tallow maintains its dominance rather than seedling performance. Chinese tallow seedling emergence was lower than that of sugarberry in the understory of Chinese tallow woodlands in an area of coastal Texas that was previously dominated by coastal prairie. Native tree species may establish and increase in the understory of invasive Chinese tallow woodlands. However, distance to seed sources can be restrictive and creation of canopy openings would likely favor Chinese tallow [186].
Shade tolerance: Although Chinese tallow survives and grows in shade, it generally performs better in sunlight. In a floodplain forest in eastern Texas, Chinese tallow mortality increased from about 0.05% at 10% full sunlight to 5.3% at 0.1% full sunlight [111]. In a grassland field experiment, Chinese tallow seedling survival was significantly (P<0.01) reduced in shade treatments and significantly (P<0.05) increased in increased-light treatments [182]. Chinese tallow dry mass [89,90,91], height [90,91], basal diameter [91], root mass [158], and growth rate [11,90,219] have all shown increases with increasing light availability. Significant (P<0.0001) increases in stomal conductance [156] and root to shoot ratios [158] have been observed with increasing light. Leaf area (P<0.0001) and number (P≤0.019) declined with increasing light [156,158]. In greenhouse experiments, Chinese tallow from Texas showed greater positive responses to higher light levels than Chinese tallow from China, including greater increases in leaf area, leaf biomass, and shoot biomass [219]. Net photosynthesis and dry mass of Chinese tallow were significantly greater than those of sycamore and cherrybark oak under 5% full sunlight [89], and absolute growth was greater than Carolina ash (Fraxinus caroliniana) under 5% and 100% full sunlight [90].
Chinese tallow's response to light may be moderated by other site characteristics. Siemann and Rogers [183] found a significant (P<0.05) effect of light availability on Chinese tallow survival and growth in prairie sites, but not in mesic (P>0.16) or floodplain (P>0.61) forests.
Chinese tallow height growth may decrease at high light levels. Jones and McLeod [90] found that the tallest Chinese tallow trees occurred in the intermediate (53% and 20%) light treatments (P<0.05). In greenhouse experiments, Chinese tallow seedling shoot and total biomass were significantly lower in ambient light than under an 87% shade cloth [219]. Chinese tallow grown in 37% and 12% sunlight had significantly (P<0.0001) greater height growth than those grown in full sunlight. They suggest this may have been caused by photo inhibition or by temperature or water stress [157].
In the field, Chinese tallow seedlings perform much better in open than shaded habitats. Bruce [18] observed 100% mortality of Chinese tallow seedlings in a closed-canopy Chinese tallow forest, while Chinese tallow seedlings survived and grew, in some cases rapidly, in canopy gaps, grassland, and cleared sites. Chinese tallow was prevalent on the edges of Chenier woodland sites in Louisiana [132]. In southeastern Louisiana, Chinese tallow was present in a community type with significantly (P<0.05) lower basal area, stem density, standing wood biomass, and bulk density than 3 other community types where Chinese tallow did not occur [83]. Increases in Chinese tallow were associated with canopy gaps in relatively closed-canopy, mixed-bottomland hardwood forest on the border of southern Louisiana and Mississippi following Hurricane Katrina in 2005 [29] and maritime forest on Bulls Island, South Carolina, following Hurricane Hugo in 1991 [36]. Chinese tallow basal area growth increased significantly following a large die-off of American hornbeam (Carpinus caroliniana) trees in a bottomland hardwood forest in eastern Texas. The authors suggest that increased light due to a more open canopy following American hornbeam mortality resulted in increased Chinese tallow growth [117]. Average relative growth rate was significantly greater (P=0.01) in open herbaceous marsh than in sparse and dense southern bayberry thickets of southeastern Louisiana, despite greater growth of Chinese tallow in substrates from southern bayberry thickets in greenhouse experiments (see Seedling establishment) [11]. In several Atlantic coast and inland sites, Chinese tallow germination was greatest in open-canopy habitats where Chinese tallow had established and lowest in closed-canopy lowland habitats were Chinese tallow had not yet established. Growth rates of Chinese tallow seedlings were generally higher in open-canopy habitats than closed-canopy habitats, and Chinese tallow grew in all open areas, even those outside its current distribution [141]. Oliver [138] suggests that Chinese tallow dominance in part of her Harris County, Texas, study area may be explained by the relatively open canopy and/or greater moisture availability. In contrast, Chinese tallow typically occurred on transects that corresponded with high canopy cover and moderate soil moisture in an ordination of sites in the Lake Jackson area of northern Florida [21].
Chinese tallow's response to shade may vary with nitrogen availability. Chinese tallow growth was significantly (P<0.05) greater in a shaded and nitrogen-added treatment than in other treatments. This result may be attributable to better performance of Chinese tallow than prairie vegetation under shaded, nitrogen-added conditions [182]. Petiole length showed a significant (P=0.0089) nitrogen × shade interaction, with more shade and nitrogen resulting in longer petioles [156]. Significant (P<0.05) shade × nitrogen interactions were also observed for Chinese tallow in pots placed on a rooftop. Increased nitrogen and intermediate shade were associated with increased stem diameter growth, and increased shade and nitrogen were associated with decreasing root:shoot ratio [157]. No significant interactions between nitrogen and shade were found in a paired greenhouse and field experiment on a coastal prairie site in eastern Texas [158]. Results regarding the effect of nutrient addition are discussed in the nutrient supplementation section.
Flood tolerance may vary with shading. Reduction of Chinese tallow growth due to flooding under 20% sunlight was not significantly different from that of water tupelo, while Chinese tallow growth reductions due to flooding under full light were significantly larger than those of water tupelo [91]. Quick seedling growth of flood-tolerant species may allow them to inhabit areas that would typically be occupied by more shade tolerant species [72,111].Triadica sebifera, comúnmente llamada árbol de sebu, Florida aspen, árbol popcorn ye nativu del este d'Asia, acomuñáu col este de China, Taiwán y Xapón. Foi introducíu a América. Nes rexones de distribución natural, la cubierta sebosa de les granes ye usada para veles y manufactura de xabón, y les fueyes para medicina yerbácea pa tratar forúnculos. La planta y n'especial les fueyes tán reputaes de tóxiques, les mesmes fueyes caduques cayíes, son tóxiques a otres especies de plantes. Los epítetos específicos sebifera y sebiferum signifiquen "ceroso" y refiérense al sebu vexetal que cubre granes.
Les fueyes simples, decidues d'esti árbol, son alternaes, anches, rómbiques a ovales y con nidios cantos, de forma acorazonada, dacuando con una cola estendida que recuerda al Ficus relixosa. Les fueyes son verde brillantes nel fexe, y más pálides nel viesu. Na seronda tomen tonos brillosos mariellos, naranxes, púrpures, colloraos. Ye una especie diclina monoica, produciendo flores machu y fema nel mesmu fuste.
Les fueyes verde cerosas pasen a verde-amarellentaes, y tien flores blanques. Les flores tán n'inflorescencies terminales de 2 decímetros de llargu. Verde clares, eses flores son bien conspicuas na primavera. Cada pistilu de flor fema ye solitariu y tien un ovariu trilobuláu, tres estilos, y nun tien pétalos. Tán en curties cañes na base de la punta. Los estames (machu) en grupos nel estremu de la inflorescencia.
Los frutos son trilobulaos, cápsules trivalvaes. Cuando una cápsula madura, el so color camuda de verde a pardu escuru. Les parés de la cápsula cayen y lliberen cada cápsula tres granes globoses con una cerosidad blanca que la anubre. Les granes usualmente cuelguen de les plantes per delles selmanes. En Norteamérica, les flores maurecen d'abril a xunu y la fruta maduro de setiembre a ochobre.
Apaez nel sudeste d'EE. XX.. Foi introducida en laépoca colonial y se naturalizó en Carolina del Sur, a lo llargo del océanu Atlánticu y tol Golfu de Méxicu, onde crez profusamente.
Anque la planta ta llistada como una maleza tóxica en munchos estaos, entá se viende en xardinería como árbol ornamental. Nun ye bien d'escoyer tipos de suelos o drenaxe, pero nun puede vivir a la solombra. Crez en tou Xapón, y ye razonablemente duru. Ye apreciáu pol so abondosu y espectacular xamasca serondiega.
La cera de les granes ye collechada asitiándoles n'agua caliente, y bañando les sos superficies cola agua. Anque otres partes de la sp. son tóxiques, la cera non, y puede usase en reemplazu d'aceite vexetal pa cocer.
El néctar tampoco ye tóxicu, y ye bien bonu como flora apícola para apicultura. El miel nun ye d'alta calidá, siendo vendida como grau de panadería, pero produz copiosamente en dómines maneres del añu, cuando la mayoría de los floriamientos de primavera cesaron. Nos estaos de la mariña del Golfu, el apicultores migren colos sos setues p'allugar bonos árboles cerca del mar.
Ye un árbol bien ornamental, de rápida crecedera y de bona solombra.
Triadica sebifera describióse por (L.) Small y espublizóse en Florida Trees 59. 1913.[1]
Esta páxina forma parte del wikiproyeutu Botánica, un esfuerciu collaborativu col fin d'ameyorar y organizar tolos conteníos rellacionaos con esti tema. Visita la páxina d'alderique del proyeutu pa collaborar y facer entrugues o suxerencies. Triadica sebifera, comúnmente llamada árbol de sebu, Florida aspen, árbol popcorn ye nativu del este d'Asia, acomuñáu col este de China, Taiwán y Xapón. Foi introducíu a América. Nes rexones de distribución natural, la cubierta sebosa de les granes ye usada para veles y manufactura de xabón, y les fueyes para medicina yerbácea pa tratar forúnculos. La planta y n'especial les fueyes tán reputaes de tóxiques, les mesmes fueyes caduques cayíes, son tóxiques a otres especies de plantes. Los epítetos específicos sebifera y sebiferum signifiquen "ceroso" y refiérense al sebu vexetal que cubre granes.
Triadica sebifera és un arbre natiu de l'est d'Àsia, associat amb l'est de la Xina, Taiwan i Japó. Ha estat introduït a Amèrica. A les regions de distribució natural, la coberta greixosa de les llavors és usada per la fabricació d'espelmes i la manufactura de sabó, i les seves fulles poden ser usades per a tractar furóncols com a planta medicinal. La planta i, especialment, les fulles, són tòxiques, fins i tot les mateixes fulles caduques caigudes ho són. Els epítets específics sebifera i sebiferum signifiquen "cerós" i fa referència al sèu vegetal que cobreix llavors.
Les fulles simples i caduques d'aquest arbre, són alternes, amples, de forma ròmbica a oval i amb vores suaus, en forma de cor, i a vegades amb una cua estesa que recorda a l'espècie Ficus religiosa. Les fulles són verd brillants al feix, i més pàl·lides al revers. A la tardor prenen tons brillants grocs, taronges, porpres i vermells. És una espècie diclina monoica, que produeix flors mascle i femella al mateix fust.
Les fulles verd ceroses passen a verd groguenc, i tenen flors blanques. Les flors es troben disposades en inflorescències terminals de 2 dm de llarg. Verd clares, aquestes flors són molt conspícues a la primavera. Cada pistil de les flors femelles és solitari i té un ovari trilobulat, tres estils, i no té pètals. Estan en curtes branques a la base de la punta. Els estams (mascle) es troben en grups a l'extrem de la inflorescència.
Els fruits són trilobulats i les càpsules són trivalvades. Quan una càpsula madura, el seu color canvia de verd a marró fosc. Les parets de la càpsula cauen i allibera cada càpsula tres llavors globoses amb un sèu blanc que la recobreix. Les llavors normalment pengen de les plantes durant diverses setmanes. A Amèrica del Nord les flors maduren d'abril a juny i la fruita madura de setembre a octubre.
Apareix al sud-est dels EUA. Va ser introduïda a l'època colonial i es va naturalitzar a Carolina del Sud, al llarg de l'oceà Atlàntic i tot el Golf de Mèxic, on creix profusament.
Tot i que la planta està llistada com una mala herba tòxica a molts estats, encara es ven a jardineria com a arbre ornamental. No té una preferència específica en relació al tipus de sòl o drenatge, però no pot viure a l'ombra. Creix a tot Japó, i és raonablement dur.
La cera de les llavors és collida col·locant-les en aigua calenta, i banyant les seves superfícies amb l'aigua. Encara que altres parts de la planta són tòxiques, la cera no, i pot usar-se com a reemplaçament de l'oli vegetal per a coure.
El nèctar tampoc és tòxic, i és molt bo com a flora apícola per a l'apicultura. La mel no és d'alta qualitat, sent venuda com a grau de forn de pa, però produeix copiosament en èpoques estèrils de l'any, quan la majoria de les floracions de primavera han cessat. Als estats de la costa del Golf els apicultors migren amb les seves bresques de cera per ubicar bons arbres prop del mar.
És un arbre molt ornamental, de ràpid creixement i de bona ombra. És apreciat pel seu abundant i espectacular fullatge de tardor.
Triadica sebifera és un arbre natiu de l'est d'Àsia, associat amb l'est de la Xina, Taiwan i Japó. Ha estat introduït a Amèrica. A les regions de distribució natural, la coberta greixosa de les llavors és usada per la fabricació d'espelmes i la manufactura de sabó, i les seves fulles poden ser usades per a tractar furóncols com a planta medicinal. La planta i, especialment, les fulles, són tòxiques, fins i tot les mateixes fulles caduques caigudes ho són. Els epítets específics sebifera i sebiferum signifiquen "cerós" i fa referència al sèu vegetal que cobreix llavors.
Triadica sebifera (někdy též kožokvět lojonosný[1] nebo Sapium sebiferum) je malý strom z čeledi pryšcovité (Euphorbiaceae). Pochází z Číny.
Triadica sebifera dorůstá do výšky 15 m. Je jednodomý. Listy jsou střídavé. Plodenství může být až 28 cm dlouhé a obsahuje 3 černá semena. Roste pouze ve výšce 100 m n. m. Jeden strom může za rok vyprodukovat až 100 000 semen.[2] Květy jsou zelenožluté až bílé. Kvete od dubna do června. Dozrává od září do října.
Původně tento strom rostl jen poblíž čínské řeky Chuang-che. Později byl rozšířen do Jižní Asie, na Tchaj-wan a do Vietnamu. Poté byl zavlečen do Japonska, Indie, do východní části Austrálie a také do amerických států Georgie, Jižní Karolína, Louisiana a Texas.
Na jihu USA je tento druh považován za invazivní. Za dovlečení tohoto druhu se většinou viní státník a přírodovědec Benjamin Franklin, který poslal koncem 18. století z Londýna do Georgie balíček semen tohoto stromu. Druh ho zaujal hlavně velkou produkcí semen a jejich následovným využitím. Genetické zkoumání tohoto druhu však ukázalo, že stromy ze semen, které zaslal, rostou jen na několika čtverečních kilometrech. Většina ostatních stromů pochází ze semen z roku 1905 od federálních biologů.[3]
Ze semen tohoto stromu se po vylisování získá lůj, který lze využít např. k výrobě svíček nebo mýdla. V Číně se pro komerční využití pěstuje již více než 1500 let.[2] Kořeny se v tradiční čínské medicíně používají k léčbě hadího uštknutí. V Asii se začal hojně pěstovat kvůli výrobě bionafty.
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Triadica sebifera (někdy též kožokvět lojonosný nebo Sapium sebiferum) je malý strom z čeledi pryšcovité (Euphorbiaceae). Pochází z Číny.
Der Chinesische Talgbaum (Triadica sebifera) ist eine Pflanzenart in der Familie der Wolfsmilchgewächse (Euphorbiaceae). Er ist in Asien heimisch und kommt vor allem in der Volksrepublik China, Taiwan und Japan vor. Mittlerweile ist diese Art auch in den Vereinigten Staaten verbreitet, wo sie als invasive Pflanze angesehen wird.
Triadica sebifera wächst als laubabwerfender Baum und erreicht Wuchshöhen von bis zu 15 m. Es ist ein weißer Milchsaft vorhanden. Alle Pflanzenteile sind unbehaart. Die Rinde ist anfangs dunkelgrün mit Längsstreifen, später hellbraun.
Die wechselständig an den Zweigen angeordneten Laubblätter sind in Blattstiel und Blattspreite gegliedert. Am 2,5 bis 6 cm langen Blattstiel befinden sich ein oder zwei Drüsen. Die einfache, meist rhombische bis breit eiförmige oder etwas herzförmige Blattspreite ist häutig, 3 bis 13 cm lang und 3 bis 9 cm breit mit einer breit gerundeten Basis und einem spitzen Ende. Es liegt Fiedernervatur mit sechs bis zwölf Seitennerven vor, wobei das unterste Blattnervenpaar den unteren Blattrand bildet, und die Mittelrippe etwas erhaben ist. Der Blattrand ist glatt. Die Nebenblätter sind 1 bis 1,5 mm lang. Die Herbstfärbung ist orange-rötlich.
Triadica sebifera ist einhäusig getrenntgeschlechtig (monözisch). Endständig werden 3 bis 35 cm lange einfache, traubenähnliche traubige, mehr oder weniger hängende (also kätzchenartige) Blütenstände gebildet. Im unteren Bereich des Blütenstandes sitzen weibliche im oberen Bereich männliche Blüten. Alle Tragblätter besitzen an ihrer Basis zwei große, fast nierenförmige Drüsen. Den kleinen, gelben, eingeschlechtigen Blüten fehlen immer Kronblätter und Diskus. In den Achsen von breit-eiförmigen, 1,5 bis 2 × 1,5 bis 2 mm großen Tragblättern stehen an 1 bis 4 mm langen, schlanken Stielen, in kleinen Bündeln 10 bis 15 männliche Blüten und drei ungleiche Deckblätter zusammen. Die männlichen Blüten besitzen becherförmig verwachsene häutige Kelchblätter und der Kelch ist nur undeutlich dreilappig oder gezähnt. Ein rudimentäres Gynoeceum fehlt. Die zwei bis drei Staubblätter überragen den Kelch. Die freien Staubfäden sind fast gleich lang wie die kugeligen Staubbeutel. Nur eine weibliche Blüte steht auf einem 2 bis 5 mm langen Stiel über einem dreiteiligen Tragblatt. Die weiblichen Blüten sind größer als die männlichen. Manchmal stehen auch einige männliche Blüten über dem gleichen Tragblatt. Bei den weiblichen Blüten ist der becherförmige Blütenkelch meist dreiteilig. Drei Fruchtblätter sind zu einem ei- bis kugelförmigen, glatten, dreifächerigen Fruchtknoten verwachsen. Jedes Fruchtknotenfach enthält nur eine Samenanlage. Die drei freien Griffel enden jeweils in einer zurückgebogen Narbe. Die Blütezeit reicht von April bis August.
Die Fruchtstände sind bis zu 28 cm lang. Die kugel-, birnenförmigen, dreifächerigen, anfänglich grünen Kapselfrüchte werden zur Reife schwärzlich, sie weisen einen Durchmesser von 11 bis 13 mm auf und enthalten drei Samen. Die 8 × 6 bis 7 mm großen, dunkelbraunen Samen sind von einem weißlichen, wachsigen Arillus bedeckt und besitzen ein hartes Exokarp und ein fleischiges Endosperm. Die Früchte reifen zwischen August und Dezember.
Der Chromosomensatz beträgt 2n = 44.
In Asien wird der wachsartige Überzug der Samen (Stillingiaöl, Stillingiatalg oder Pflanzen-, Chinesischer Talg) zur Herstellung von Kerzen und Seife verwendet. Die Blätter werden in der Medizin zur Behandlung von Furunkeln eingesetzt. Der Saft und die Blätter der Pflanze gelten als giftig. Die Epitheta sebifera und sebiferum bedeuten wachshaltig und beziehen sich auf das Wachs, das die Samen überzieht.
Die Pflanze kann zur Produktion von Biodiesel verwendet werden und gilt als die drittertragsreichste Öl-produzierende Pflanze nach Algen und Ölpalmen.
Das Wachs der Samen, im chemischen Sinne ein Triglycerid, wird durch Kochen der Samen in heißem Wasser gewonnen. Das Wachs schwimmt dabei auf der Oberfläche und wird dort abgeschöpft. Obwohl andere Teile der Pflanze giftig sind, ist das Wachs ungiftig und kann als Pflanzenöl zum Kochen benutzt werden.
Aus den Blättern kann ein dunkler Farbstoff gewonnen werden.
Der Pflanzennektar ist ebenfalls ungiftig. Die Pflanze ist daher bei Imkern als Honigpflanze beliebt. Der daraus gewonnene Honig gilt jedoch als niederqualitativ und wird als Bäckereihonig genutzt. Die Pflanze gilt auch als ergiebig nachdem die Blütezeit anderer Pflanzen vorbei ist.
Der frostharte Chinesische Talgbaum gilt als dekorativ, schnell wachsend und schattenspendend. In Gegenden mit hohen saisonalen Temperaturunterschieden weist er im Herbst ein farbenprächtiges Laub auf.
Die natürliche Heimat von Triadica sebifera liegt auf Taiwan und den südlichen Teilen Japans und Chinas (von Yunnan und Hainan bis Gansu, Shandong und Henan). Sie gedeiht in vielen Waldtypen und auf unterschiedlichen Böden von trockenen bis feuchten Bedingungen und toleriert sogar kurzzeitige Überflutungen. Sie erreicht Höhenlagen von bis zu etwa 1700 Meter.
Triadica sebifera wurde von Benjamin Franklin in den Südstaaten der USA eingeführt und ist verwildert. Sie wächst gut auf verlassenem Farmland wo sie teilweise Dominanzbestände bildet. Sie gilt in weiten Teilen der USA als invasive Pflanze.[1]
Diese Art wurde 1753 von Carl von Linné als Croton sebifer oder Croton sebiferum in Species Plantarum, 2, 1004 erstveröffentlicht. Der heute gültige botanische Name Triadica sebifera wurde 1913 von John Kunkel Small in Florida Trees, 59 veröffentlicht. Diese Art wurden oft von einer zur anderen Gattung verschoben und so gibt es eine Vielzahl von Synonymen. Weitere Synonyme sind: Excoecaria sebifera (L.) Müll.Arg., Sapium chihsinianum S.K.Lee, Sapium pleiocarpum Y.C.Tseng, Sapium sebiferum (L.) Roxb., Sapium sebiferum var. cordatum S.Y.Wang, Sapium sebiferum var. dabeshense B.C.Ding & T.B.Chao, Sapium sebiferum var. multiracemosum B.C.Ding & T.B.Chao, Sapium sebiferum var. pendulum B.C.Ding & T.B.Chao, Triadica sinensis Lour., Stillingia sebifera (L.) Michx., Stillingia sinensis (Lour.) Baill.
Der Chinesische Talgbaum (Triadica sebifera) ist eine Pflanzenart in der Familie der Wolfsmilchgewächse (Euphorbiaceae). Er ist in Asien heimisch und kommt vor allem in der Volksrepublik China, Taiwan und Japan vor. Mittlerweile ist diese Art auch in den Vereinigten Staaten verbreitet, wo sie als invasive Pflanze angesehen wird.
Triadica sebifera is a tree native to eastern China (Chinese 乌桕, wū jiù) . It is commonly called Chinese tallow,[1] Chinese tallowtree, Florida aspen, chicken tree, gray popcorn tree,[2] or candleberry tree.[3]
The seeds (as well as from those of Triadica cochinchinensis) are the sources of stillingia oil, a drying oil used in paints and varnishes. The fatty coat of the seeds, used for candle and soap making, is known as stillingia tallow; hence its common name. It is relevant to biodiesel production because it is the third most productive vegetable oil producing crop in the world, after algae and oil palm. The leaves are used as herbal medicine to treat boils. The plant sap[4] and leaves are reputed to be toxic, and decaying leaves from the plant are toxic to other species of plants. The species is classified as a noxious invader in the southern U.S.[5][6]
This species and T. cochinchinensis were formerly classified in the genus Stillingia, as Stillingia sebifera and Stillingia discolor (hence the name still used for the oil and tallow). The specific epithet sebifera is derived from Latin sebum (meaning "tallow"[7]) and fero (meaning "to bear"[8]), thus "tallow-bearing". At some time before 1950, this tree was reclassified into the genus Sapium as Sapium sebiferum, and many papers about the oil still refer to the tree by this name. In 2002 or so it was reclassified again into the genus Triadica with its present name.[9]
The simple, deciduous leaves of this tree are alternate, broad rhombic to ovate in shape and have smooth edges, heart shaped and sometimes with an extended tail often resembling the bo tree, Ficus religiosa. The leaves are bright green in color and slightly paler underneath. They become bright yellows, oranges, purples and reds in the autumn. The tree is monoecious, producing male and female flowers on the same plant.
The waxy green leaves set off the clusters of greenish-yellow and white flowers at bloom time. The flowers occur in terminal spike-like inflorescences up to 20 cm long. Light green in color, these flowers are very conspicuous in the spring. Each pistillate (female) flower is solitary and has a three-lobed ovary, three styles, and no petals. They are located on short branches at the base of the spike. The staminate (male) flowers occur in clusters at the upper nodes of the inflorescence.
Fruits are three-lobed, three-valved capsules. As the capsules mature, their color changes from green to a brown-black. The capsule walls fall away and release three globose seeds, about 12 mm in diameter and weighing about 0.15 g,[10] with a white, tallow-containing covering. Seeds usually hang on the plants for several weeks. In North America, the flowers typically mature from April to June and the fruit ripens from September to October.
Triadica sebifera is native to China and Taiwan, and was introduced to Japan during the Edo period. It is also found in the southeastern United States, Puerto Rico, Costa Rica, India, Martinique, Sudan, and southern France.[11]
Thought to have been introduced in colonial times by Benjamin Franklin,{[12]} the tree has become naturalized from North Carolina southward along the Atlantic and the entire Gulf coast, where it grows profusely along ditchbanks and dikes. It grows especially well in open fields and abandoned farmland coastal prairie regions featuring disturbed ground—such as abandoned farmland, spoil banks, roadsides, and storm-damaged forests—and along the edges of the Western Gulf coastal grasslands biome, sometimes forming monocultures.[13] The Chinese Tallow Tree is listed as an invasive species to the state of South Carolina.[14]
The seed's white waxy aril is used in soap making. The seed's inner oil ("stillingia oil") is toxic but has industrial applications.
The nectar is non-toxic, and it has become a major honey plant for beekeepers. The honey is of high quality, and is produced copiously during the month of June, on the Gulf Coast. In the Gulf coast states, beekeepers migrate with their honey bees to good tallow locations near the gulf.[15]
The tree is ornamental, fast growing, and a provides shade. It is especially noteworthy if grown in areas that have strong seasonal temperature ranges with the leaves becoming a multitude of colours rivaling maples in the autumn. It is not choosy about soil types or drainage, but will not grow in deep shade. It has naturalized all over in Japan, and is reasonably hardy. It should not be planted outside of its native range due to its invasive tendencies.
The tallow tree is a non-native species to many places around the world. Its introduced status in North America along with the harm it causes to ecosystems makes the tree considered an invasive species there. Tallow trees present a danger of expansion that can hurt local ecosystems by out-competing native vegetation and creating a monoculture. The monoculture lowers species diversity and overall resilience of the area.[16] The tree's tenacious nature, high growth rates, and high reproductive ability contribute to its invasive success. According to the U.S. Department of Agriculture, tallow trees begin producing viable seed in as soon as three years.[16] They can spread by root sprouts and cuttings and are quick to invade after a disturbance occurs in an area, due to the clearing out of land.[11] A single tallow tree can produce nearly 100,000 viable seeds annually that can remain in the soil for several years before sprouting. A mature stand can produce 4,500 kilograms of seeds per hectare per year.[16] These seeds are easily carried to different places by birds and water. Tallow trees can remain productive for 100 years.[16] It is also extremely hard to kill—its poisonous features in its leaves and berries leave it with few to no predators, and its short generation time means even freshly cut trees can quickly regrow.[11] Currently, herbicides and prescribed fire are the only effective treatments available to contain and control Chinese tallow.[11] The USDA is evaluating the flea beetle (Bikasha collaris) as a natural control agent.[17]
In the Houston area, Chinese tallow trees account for a full 23 percent of all trees, more than any other tree species and is the only invasive tree species in the 14 most common species in the area.[18] The Texas Department of Agriculture lists Chinese Tallow as one of the 24 most invasive plants, and includes Chinese Tallow in a list of Noxious and Invasive Plants which are illegal to sell, distribute or import into Texas.[19][20] Herbivores and insects have a conditioned behavioral avoidance to eating the leaves of Chinese tallow tree, and this, rather than plant toxins, may be a reason for the success of the plant as an invasive.[21]
In Europe, the species features on the Union list of invasive alien species.[22] This means it is now illegal to import or sell this plant in the European Union.[23]
In parts of the USA biological control of the Chinese tallow tree has been considered, using the flea beetle Bikasha collaris, whose larvae attack the roots, and the moth Gadirtha fusca, whose caterpillars attack the leaves. In those areas, the resulting prospect of losing the Chinese tallow as a honey source has caused concern in beekeepers.[24]
The species has several synonyms and former names:[9]
{{cite web}}: CS1 maint: url-status (link) {{cite web}}: CS1 maint: url-status (link) Triadica sebifera is a tree native to eastern China (Chinese 乌桕, wū jiù) . It is commonly called Chinese tallow, Chinese tallowtree, Florida aspen, chicken tree, gray popcorn tree, or candleberry tree.
The seeds (as well as from those of Triadica cochinchinensis) are the sources of stillingia oil, a drying oil used in paints and varnishes. The fatty coat of the seeds, used for candle and soap making, is known as stillingia tallow; hence its common name. It is relevant to biodiesel production because it is the third most productive vegetable oil producing crop in the world, after algae and oil palm. The leaves are used as herbal medicine to treat boils. The plant sap and leaves are reputed to be toxic, and decaying leaves from the plant are toxic to other species of plants. The species is classified as a noxious invader in the southern U.S.
This species and T. cochinchinensis were formerly classified in the genus Stillingia, as Stillingia sebifera and Stillingia discolor (hence the name still used for the oil and tallow). The specific epithet sebifera is derived from Latin sebum (meaning "tallow") and fero (meaning "to bear"), thus "tallow-bearing". At some time before 1950, this tree was reclassified into the genus Sapium as Sapium sebiferum, and many papers about the oil still refer to the tree by this name. In 2002 or so it was reclassified again into the genus Triadica with its present name.
Triadica sebifera,[1] comúnmente llamado árbol de sebo,[2] árbol de la cera[2] o álamo de Florida, es un árbol originario del Lejano Oriente, particularmente el valle del Yangtsé en la China central, así como Taiwán, Japón y la isla de Java en Indonesia. Introducido en América desde el siglo XVIII, donde es considerado una especie invasora. En las regiones de distribución natural, la cubierta sebosa de las semillas es usada para velas y manufactura de jabón, y las hojas para medicina herbal para tratar forúnculos. La planta y en especial las hojas están reputadas de tóxicas, las mismas hojas caducas caídas, son tóxicas a otras especies de plantas. Los epítetos específicos sebifera y sebiferum significan "ceroso" y se refieren al sebo vegetal que cubre semillas. Llega a alcanzar una altura de 12 metros.
Las hojas simples, deciduas de este árbol, son alternadas, anchas, rómbicas a ovales y con suaves bordes, de forma acorazonada, a veces con una cola extendida que recuerda al Ficus religiosa. Las hojas son verde brillantes en el haz, y más pálidas en el envés. En el otoño toman tonos brillantes amarillos, naranjas, púrpuras, rojos. Es una especie diclina monoica, produciendo flores macho y hembra en el mismo fuste.
Las hojas verde cerosas pasan a verde-amarillentas, y tiene flores blancas. Las flores están en inflorescencias terminales de 2 decímetros de largo. Verde claras, esas flores son muy conspicuas en la primavera. Cada pistilo de flor hembra es solitario y tiene un ovario trilobulado, tres estilos, y no tiene pétalos. Están en cortas ramas en la base de la punta. Los estambres (macho) en grupos en el extremo de la inflorescencia.
Los frutos son trilobulados, cápsulas trivalvadas. Cuando una cápsula madura, su color cambia de verde a pardo oscuro. Las paredes de la cápsula caen y liberan cada cápsula tres semillas globosas con una cerosidad blanca que la recubre. Las semillas usualmente cuelgan de las plantas por varias semanas. En Norteamérica, las flores maduran de abril a junio y la fruta madura de septiembre a octubre.
El árbol parece originario del valle del Yangtsé en la provincia central china de Sichuan.[3][4] Crece asimismo en Taiwán y por todo el Japón.
Aparece en el sudeste de EE. UU.. Fue introducida en el siglo XVIII y se naturalizó en Carolina del Sur, a lo largo del océano Atlántico y todo el Golfo de México, donde crece profusamente.
Aunque la planta está clasificada como una maleza tóxica en muchos estados de los Estados Unidos, aún se vende en jardinería como árbol ornamental. No es muy selectivo con los tipos de suelos o drenaje, pero no puede vivir a la sombra. Es un árbol razonablemente duro y apreciado por su abundante y espectacular follaje otoñal.
En Australia el árbol fue asimismo introducido en la era colonial y en la actualidad le puede encontrar especialmente alrededor de las costas en Nueva Gales del Sur.
La cera de las semillas es cosechada colocándolas en agua caliente, y bañando sus superficies con el agua. Aunque otras partes de la sp. son tóxicas, la cera no, y puede usarse en reemplazo de aceite vegetal para cocer.
El néctar tampoco es tóxico, y es muy bueno como flora apícola para apicultura. La miel no es de alta calidad, siendo vendida como grado de panadería, pero produce copiosamente en épocas estériles del año, cuando la mayoría de las floraciones de primavera han cesado. En los estados de la costa del Golfo, los apicultores migran con sus panales para ubicar buenos árboles cerca del mar.
Es un árbol muy ornamental, de rápido crecimiento y de buena sombra.
Triadica sebifera fue descrita por (L.) Small y publicado en Florida Trees 59. 1913.[5]
Triadica sebifera, comúnmente llamado árbol de sebo, árbol de la cera o álamo de Florida, es un árbol originario del Lejano Oriente, particularmente el valle del Yangtsé en la China central, así como Taiwán, Japón y la isla de Java en Indonesia. Introducido en América desde el siglo XVIII, donde es considerado una especie invasora. En las regiones de distribución natural, la cubierta sebosa de las semillas es usada para velas y manufactura de jabón, y las hojas para medicina herbal para tratar forúnculos. La planta y en especial las hojas están reputadas de tóxicas, las mismas hojas caducas caídas, son tóxicas a otras especies de plantas. Los epítetos específicos sebifera y sebiferum significan "ceroso" y se refieren al sebo vegetal que cubre semillas. Llega a alcanzar una altura de 12 metros.
Arbre à suif
Triadica sebifera ou Gluttier[a], Arbre à suif chinois[b] (ou Arbre à beurre, Croton, Suiffier)[1],[2], est une espèce d’arbres de la famille des Euphorbiaceae, originaire du sud de la Chine, de Taiwan, du Vietnam et du Japon. L’espèce a été mise en culture dans de nombreuses régions tropicales, subtropicales et tempérées chaudes où elle a pu se naturaliser et parfois devenir envahissante.
En Chine, depuis le VIIe siècle, l’arbre est exploité pour ses graines oléagineuses avec lesquelles on fabrique des savons, des chandelles et des peintures. Actuellement, il est aussi planté comme arbre d’ornement le long des routes et dans les parcs.
Toutes les parties de l’arbre sont toxiques, c’est d’ailleurs pourquoi elles ont été employées dans la pharmacopée chinoise traditionnelle.
Le nom de genre Triadica vient du grec τριάς trias « trois » (Bailly) via le latin trias, adis, « triade » en référence aux fleurs trimères (3 sépales, 3 carpelles, 3 styles).
L’épithète spécifique sebifera est un terme latin composé de sebum « suif » et fero « porter » soit « qui porte du suif ».
En 1753, Linné donne dans Species Plantarum (2:1004), une description de l’espèce sous le nom de Croton sebiferum[3]. En 1913, le botaniste américain Small dans Florida Trees (59), avec le nom de Triadica sebiferum, la reclasse dans le genre Triadica[4] (créé en 1790 par João de Loureiro, un botaniste portugais).
L’espèce possède de multiples noms en chinois. Actuellement, le nom vulgaire qui s’est imposé est wujiu 乌桕, nom composé des morphèmes wu: « noir, sombre » et jiu: « espèce d’arbre ». Pour expliquer l’origine du premier caractère wu, le naturaliste du XVIe siècle Li Shizhen, indique que « les corbeaux aiment manger ses graines » (wuxishiqizi 乌喜食其子), avec wu 乌, une abréviation de wuya 乌鸦 « corbeau »[5]; l'étymologie serait en quelque sorte « l’arbre à corbeaux », comme le synonyme contemporain de l'espèce, yājiù 鸦桕, l’atteste d’ailleurs. En effet, les oiseaux sont friands de ses fruits en hiver, ainsi qu'on peut le voir sur une photo ci-dessous.
D’après Tropicos, les synonymes
Triadica sebifera est un petit arbre à feuilles caduques, pouvant atteindre 15 m de haut en Chine[7]. Il devient fertile quand il atteint 1 m de haut[8]. C’est une espèce monoïque, avec des fleurs mâles et femelles distinctes sur le même pied.
Les feuilles simples sont portées par un pétiole de 2–7 cm de long, avec 2 glandes discoïdes, à l’apex et des stipules persistantes, elliptiques. Le limbe est de forme ovale à largement elliptique ou rhomboïde, de 3,5–10 cm de long sur 3–9,5 cm de large, à base largement cunéiforme à presque tronquée et apex acuminé. Des glandes laminaires, elliptiques, de 0,3 × 0,2 mm, sont généralement placées sur la moitié distale du limbe. En automne, les feuilles deviennent jaunes, oranges et écarlates[9].
L’inflorescence terminale en épi peut atteindre 20 cm. La plante étant monoïque, l’épi comporte des fleurs mâles et femelles distinctes. Sur sa moitié distale, il porte des cymules (petites cymes) avec 10-20 fleurs staminées (♂), à bractées ovales de 1,5 mm, sous-tendues par 2 (-4) glandes ellipsoïdes, 2-3 étamines de 1,3–3 mm. Les fleurs femelles pistillées (♀) sont au nombre de 0 à 6 par inflorescence, avec 1 ovaire trilobé, 3 styles connées (soudés) à la base et aucun pétale. Les fleurs staminées sont jaunes, les fleurs pistillées sont vert jaunâtre[8].
Les fruits sont des capsules de 1 à 1,3 cm de diamètre, subglobuleuses, trifides, charnues[10]. La capsule comporte 3 graines (ou plus), à tégument extérieur blanc, cireux, et poils intérieurs ligneux, brun. Durant l’hiver, les 3 valves noires de la capsule s’ouvrent et tombent, laissant apparaitre les graines blanches qui vont rester dans l’arbre tout dénudé de ses feuilles.
En Chine la floraison va d’avril à août et la fructification suit jusqu’en octobre. La floraison aux États-Unis a lieu d’avril à juin, la fructification d’août à novembre[8].
Parc de T. sebifera, près du Temple du Grand Bouddha, Japon
Feuilles d’automne
Feuilles et fruits
Inflorescence en fleurs
Infrutescence de fruits triloculaires mûrs, avant ouverture de la capsule
Graines, avec son tégument blanc, cireux
Le Zosterops japonicus mange les graines
L’espèce est originaire d’Asie : du sud de la Chine, de Taïwan, du Japon, du Vietnam et en Inde[7]. En Chine, elle croit particulièrement dans la région du sud du Fleuve jaune en allant au nord jusqu’au Shaanxi et au Gansu[5]. Elle pousse dans les espaces ouverts, près des étangs ou dans les forêts clairsemées.
L’espèce a été introduite et cultivée dans les régions tropicales, subtropicales et tempérées chaudes (à hiver doux) du monde. Elle s’est naturalisée en de multiples endroits d’Asie, d’Afrique, des États-Unis, d’Australie, de Polynésie française et d’Hawaï.
Elle pousse dans les zones où la température moyenne annuelle est supérieure à 15 °C et les précipitations moyennes annuelles sont supérieures à 750 mm. Les feuilles commencent à jaunir à des températures inférieures à 20 °C. L'arbre cherche la lumière et ne tolère pas l’ombre[11]. Il préfère les sols alluviaux profonds, humides et fertiles des rives de cours d’eau. Mais il est capable de s’adapter à un large éventail de types de sol, allant des sols acides à légèrement basiques, et même ceux légèrement salins (jusqu’à 0,3 %). Il tolère pendant une courte période les eaux stagnantes.
Il fut introduit aux États-Unis en 1776 par Benjamin Franklin[12], à Charleston (Caroline du Sud) puis en Californie, S. Arizona, Louisiane, Mississippi, Texas, et Floride. Il fut aussi importé dans le sud la France, au Jardin Botanique de Marseille, (où il porte le nom en provençal de Kresto de Gaou) et en Algérie. L’espèce a été aussi introduite en Martinique, en Polynésie française, où elle est cultivée et non établie[10]. On retrouve des mentions de plantations historiques et d’introductions dans les jardins du sud de la France depuis le 19ème siècle (Société nationale d’horticulture de France, 1832). L’espèce survivrait bien dans le Grand Jardin de La Valette-du-Var, à proximité de Toulon, et pourrait manifestement produire des graines, mais aucune mention de l’espèce n’a été faite en dehors du jardin[13].
L’arbre à suif chinois peut proliférer dans les milieux naturels et former des peuplement monospécifiques capables de déplacer les espèces végétales indigènes en modifiant les écosystèmes envahis. Actuellement, cette espèce est répertoriée comme envahissante aux États-Unis, en Inde, en Australie (Queenland)[14] et même en France métropolitaine (Arrêté du 10 mars 2020)[2].
En Europe, Triadica sebifera est inscrite depuis 2019 dans la liste des espèces exotiques envahissantes préoccupantes pour l’Union européenne[15]. Cela signifie qu'elle ne peut pas être importée, cultivée, commercialisée, plantée, ou libérée intentionnellement dans la nature, et ce nulle part dans l’Union européenne[16].
En Chine, il existe une longue et riche histoire des matières médicales (bencao) qui a ressemblé au cours des siècles des informations sur l’utilisation médicinale des substances naturelles minérales, végétales et animales. Elle produisit un nombre substantiel d’ouvrages de materia medica - sans équivalent en Europe durant la même période - qui fournit une source précieuse d’informations sur l’histoire de l’utilisation des plantes.
Les premières matières médicales ne mentionnent pas l’arbre à suif, sous aucune de ses multiples dénominations: 乌桕 / 烏桕 wūjiù, 乌木 / 烏木 wūmù, 乌槔 wūgāo, 乌臼 wūjiù, 鸦臼 yājiù, 乌桖 wūxuè, 桊子树 juànzǐshù, 桕树 jiùshù. Nom vulgaire: 木蜡树 mùlàshù, 桩仔 zhuāngzǐ, 琼仔/橩仔树 qióngzǐ/qióngzǐshù etc.
Au VIIe siècle, à l’époque de la dynastie Tang, la publication en 659 de la « Nouvelle révision de la matière médicale » 《新修本草》 Xinxiu bencao de Su Jing 苏敬 / 蘇敬, apporte un accroissement important du nombre de drogues médicinales. Parmi celles-ci, se trouve une fiche intéressante sur le 乌臼 wūjiù (dont la graphie deviendra 乌桕 avec la même prononciation[c]) « arbre à suif ». Son écorce est une drogue caractérisée par sa nature « amère, légèrement tiède, toxique » et ses propriétés thérapeutiques[17]. Quatre-vingts ans plus tard, le médecin Chen Cangqi 陳藏器 (681-757) dans sa matière médicale《本草拾遺》Bencao shiyi (739) donne des informations complémentaires sur ses utilisations « avec les feuilles on peut colorer le savon. La graine pressée donne de l’huile, enduite sur la tête, les cheveux blancs deviennent noir. Pour les lampes, elle est très lumineuse ».
Au XVIe siècle, l’ouvrage réputé le Bencao gangmu 《本草綱目》de Li Shizhen 李时珍, publié en 1593 l’année de sa mort, fut comme un point culminant de la tradition des bencao. En compilant toutes les anciennes données, il apporte des informations plus complètes sur l’arbre à suif et ses usages[18] (voir section médicale ci-dessous).
Le « Traité complet sur l’agriculture » Nongzheng quanshu 《农政全书》, publié 1639 par Xu Guangqi 徐光启 a offert un article enthousiaste sur la culture de l’arbre à suif. Il indique que le « suif » des graines sert à faire des bougies. L’huile qui en est extraite est aussi idéale pour les lampes d’éclairage. De plus, l’huile peut aussi servir à teindre les cheveux en noir, à diluer la laque, et à faire des papiers huilés. Les feuilles sont une source de teinture noire et l’arbre est très rustique. Il met en garde toutefois de ne pas le planter trop près d’un étang à poissons, parce que si les feuilles tombent dans l’eau, elles la noircissent et rendent les poissons malades[19].
Pour troisième source d’informations sur les arbres à suif, le regard extérieur et curieux des missionnaires jésuites en Chine est des plus instructifs. Grâce à Matteo Ricci (1552-1610), les portes de la Chine s’entre-ouvrirent aux jésuites, en particulier aux missionnaires français à partir de la fin du XVIIe siècle. Ceux-ci envoyèrent régulièrement à leurs supérieurs en France des lettres sur l’évangélisation et la culture chinoise. À Paris, le père Jean-Baptiste Du Halde en tire un ouvrage encyclopédique qui deviendra la principale source des représentations de la Chine en Europe au XVIIIe siècle[20],[21].
Voici quelques extraits instructifs de sa description de l'arbre à suif et de ses usages:
Suit une description du tronc, des feuilles, des fruits et des graines[d]
Toutes les parties de l’arbre sont toxiques.
Le feuillage vert de T. sebifera provoque de sévères irritations des voies digestives et a des effets purgatifs sur les bovins mais apparemment pas sur les ovins et caprins[22].
Le feuillage contient de l’acide gallique et de l’astragaline, mais les principales molécules toxiques sont du type tigliane, des diterpènes que l’on trouve chez les autres Euphorbiacées[22].
En Chine, il existe de nombreux rapports d’intoxication, indiquant après absorption, des douleurs abdominales, diarrhées, vertiges, engourdissement des membres et des lèvres, acouphènes, palpitations, pâleur, et membres froids[23].
Les feuilles contiennent acide gallique et acide ellagique, isoquercitrine et tanin (5,5 %)[24].
Actuellement, l’arbre à suif a une valeur horticole et économique.
En Chine, l’arbre à suif est exploité au sud du Fleuve Jaune, depuis la dynastie Tang, ce qui fait environ 14 siècles. Jadis, les gens plantaient des arbres à suif dans leurs cours et leurs jardins. Au cours des saisons, ils pouvaient profiter du jeu des changements de couleurs, les feuilles passant du vert émeraude au printemps puis après avoir connu le vert foncé, le jaune et l’orange, atteindre un rouge chatoyant à l’automne. L’hiver, les capsules des fruits d’un brun-noir éclataient pour révéler de petites graines d’un blanc très pur comme autant de « boutons blancs » de cire qui demeuraient sur l’arbre dénudé[26].
De nos jours, les régions touristiques prennent soin d’entretenir et de planter des arbres ornementaux capables d’attirer les touristes pour leurs odeurs ou bien leurs couleurs, comme les osmanthes parfumés qui exhalent de douces senteurs, les Gingkos au feuillage jaune d'or, et les arbres à suif pour leur feuillage rouge rutilant etc.[11] Les aménageurs du paysage plantent les arbres à suif le long des pelouses, sur le bord des lacs, le long des rues et des routes et dans les parcs[23]. Dans les plantations de thé, il sert d’essence d’ombrage[27].
Aux États-Unis, l’arbre séduit aussi par ses belles couleurs rouges d’automne, sa croissance rapide et sa résistance aux ravageurs. Malgré les risques de prolifération, il est toujours vendus et plantés dans ce pays pour l’ornement[28]. Il est cultivé dans les jardins le long des côtes atlantique et du Golfe du Mexique de la Caroline du Sud au Texas[22].
La couche de cire blanche qui couvre les graines de T. sebifera s’appelle jiuzhi 桕脂 « graisse de jiu, suif végétal chinois » (ou baixi 白蜡 « cire blanche », piyou 皮油)[29]. Elle sert en Chine et au Japon, à fabriquer des chandelles, des savons et des savonnettes et du papier ciré. Le point de fusion de cette cire blanche est plus élevé que celui de la cire d’abeille jaune. Sous les Song, des chandelles spéciales pour brûler cette cire blanche ont été conçues[e]. Les chandelles obtenues en mélangeant dix doses de suif végétal chinois et trois doses de cire d’abeille, ont la réputation de conserver leur blancheur et de se consumer avec une flamme claire et lumineuse, sans odeur ni fumée[27]. En savonnerie, le suif végétal est utilisé pour renforcer la consistance des graisses alimentaires molles.
Les graines peuvent être pressées pour en extraire une huile (nommée en chinois jiuyou 桕油 « huile de jiu » ou qingyou 青油 « huile bleu-vert » et dans le commerce « huile de stillingia »[27]) qui peut entrer dans la fabrication de savons et de cosmétiques typiquement chinois. La dénomination d’huile de stillingia vient de ce que Stillingia sebifera (L.) Michaux soit un synonyme de Triadica sebifera. Cette huile est toxique et ne peut être consommée. Le point de fusion de ses acides gras est élevé. L’huile de T. sebifera représente 55 % du contenu des savons pour la lessive et 25 % des savons de toilette[30]. Elle entre aussi dans les peintures, les vernis et les encres[5]. Jadis l’huile servait à l’éclairage avec des lampes à huile.
Les graines ont un contenu en cire-huile de 42,2 %[22].
Au lendemain de la seconde Guerre mondiale, il y eut une pénurie d’huile siccative pour les peintures, ce qui provoqua la vogue de l’huile de stillingia. Des plantations expérimentales furent créées dans plusieurs pays, mais à l’exception de la Chine les essais ne furent pas à la hauteur des espérances. Le travail considérable que représentait la récolte manuelle des fruits mûrs constitua un obstacle de taille à l’exploitation commerciale de l’arbre. À cette époque-là, la Chine exportait 4000–5000 t par an. Actuellement, seule la Chine continue a produire un peu de suif végétal et d’huile de stillingia[27].
Les feuilles contiennent un colorant, utilisé en Indochine et en Chine à teindre la soie en noir. Elles servaient aussi à fabriquer un insecticide[23]. Le bois dense et très dur peut servir à faire des meubles et des sculptures.
L'espèce est utile à la production de biodiesel, car c'est le troisième végétal le plus productif d'huile végétale après les algues et le palmier à huile. Tant le suif végétal que l’huile de stillingia servent à allonger les carburants sur une petite échelle[27].
Un regain d’intérêt a vu le jour depuis les années 1980 pour cette espèce qui pourrait se transformer en carburant et en producteur de biomasse sur les sols marginaux, en particulier dans le sud-est des Etats-Unis, mais elle y est considérée actuellement comme une espèce envahissante nuisible.
Le principal avantage de choisir T. sebifera comme matière première du biodiesel est son rendement élevé en huile pour une parcelle de terrain donnée. Un hectare d'arbres à suif chinois peut produire environ 12 500 kg de graines, ce qui pourrait potentiellement produire 5 500 kg d'huile. Cette quantité d'huile par hectare est près de 15 fois celle de l'huile de soja, qui est l'huile la plus couramment utilisée pour fabriquer du biodiesel aux États-Unis[31]. Les recherches continuent pour l’optimisation de la production de biocarburant à partir des graines de l’arbre à suif chinois[32].
Les feuilles, l’écorce des rameaux et des racines sont utilisées en médecine traditionnelle chinoise. Les feuilles sont récoltées en générale fraiches, les écorces peuvent être récoltées en toute saison, puis tranchées et séchées.
Pour Li Shizhen, la nature des racines du wujiu est de s’enfoncer et de descendre, c’est le yin du yin, (donc) elle est bonne pour induire l’excrétion d’urine et ouvrir l’intestin. Si une personne souffre de gonflements, elle doit piler cette racine et en prendre un bol en décoction. Ne doit pas être utilisée par les personnes souffrant de déficience du qi[18]. Il signale aussi le danger des feuilles pour le bétail. Pour l’huile, il reprend l’usage de Chen Cangqi, donné ci-dessus (teindre en noir les cheveux blancs, et fournir de l’huile pour les lampes d’éclairage).
Selon l’encyclopédie médicale en ligne A::医学百科[23], présentant le savoir actuel de la médecine chinoise, la matière médicale wujiu est de nature « amère, légèrement chaude ». Elle est légèrement toxique (xiaodu 小毒). Elle entre dans les méridiens des poumons, de la rate, des reins et du gros intestin (tous ces termes appartiennent à la terminologie de la médecine traditionnelle chinoise).
Mise en garde: la matière médicale wujiu 乌桕 est intrinsèquement toxique et ne doit en aucun cas être utilisée. Les informations sont données à titre historique et encyclopédique.
Arbre à suif
Triadica sebifera ou Gluttier, Arbre à suif chinois (ou Arbre à beurre, Croton, Suiffier),, est une espèce d’arbres de la famille des Euphorbiaceae, originaire du sud de la Chine, de Taiwan, du Vietnam et du Japon. L’espèce a été mise en culture dans de nombreuses régions tropicales, subtropicales et tempérées chaudes où elle a pu se naturaliser et parfois devenir envahissante.
En Chine, depuis le VIIe siècle, l’arbre est exploité pour ses graines oléagineuses avec lesquelles on fabrique des savons, des chandelles et des peintures. Actuellement, il est aussi planté comme arbre d’ornement le long des routes et dans les parcs.
Toutes les parties de l’arbre sont toxiques, c’est d’ailleurs pourquoi elles ont été employées dans la pharmacopée chinoise traditionnelle.
Smokrzyn łojodajny (Triadica sebifera), zwany także łojowym drzewem i maścierzą łojodajną – gatunek drzewa z rodziny wilczomleczowatych (Euphorbiaceae). Pochodzi z wschodniej Azji, występuje przede wszystkim we wschodniej części kontynentalnych Chin i na Tajwanie[2]. Występuje również w południowej części Stanów Zjednoczonych jako gatunek inwazyjny, gdzie roślinę sprowadzono w czasach kolonialnych.
Smokrzyn łojodajny (Triadica sebifera), zwany także łojowym drzewem i maścierzą łojodajną – gatunek drzewa z rodziny wilczomleczowatych (Euphorbiaceae). Pochodzi z wschodniej Azji, występuje przede wszystkim we wschodniej części kontynentalnych Chin i na Tajwanie. Występuje również w południowej części Stanów Zjednoczonych jako gatunek inwazyjny, gdzie roślinę sprowadzono w czasach kolonialnych.
Sapium sebiferum (vulgo pau-de-sebo),[1] da família Euphorbiaceae, é uma árvore nativa da China, Formosa e Japão introduzida durante o século XVIII nos Estados Unidos. Nestas regiões, a capa cerosa das sementes é usada para a fabricação de velas, sabão, roupas e combustível e suas folhas, na medicina fitoterápica.[2]
O pau-de-sebo pode ser utilizado para a produção de biodiesel, sendo considerada a terceira planta mais produtiva de óleo do mundo, após o dendezeiro e as algas.[carece de fontes?] A seiva da planta e as folhas são tóxicas para os humanos e animais.[3][4]
A extração da cera das sementes se dá através da imersão destas em água quente, o que faz com que a cera emerja à superfície, podendo assim ser coletada. A cera pode ser utilizada como substituto para o azeite vegetal na cozinha. O néctar é utilizado pelas abelhas para a produção de mel. O mel não é de alta qualidade, porém é produzido e vendido durante a época estéril do ano, quando a maioria das outras plantas não estão florindo. Os demais produtos derivados da planta são tóxicos e não devem ser consumidos.
O pau-de-sebo é uma árvore ornamental, de crescimento rápido, excelente como barreira visual. No outono, suas folhas adquirem uma multiciplicidade de cores que, pela beleza, rivalizam com as demais plantas e contribuem para a sua popularidade.[5]
Folhas durante o outono
Frutos
Árvores durante o outono
Exemplar no arboreto da Universidade da Califórnia em Davis, EUA
Sapium sebiferum (vulgo pau-de-sebo), da família Euphorbiaceae, é uma árvore nativa da China, Formosa e Japão introduzida durante o século XVIII nos Estados Unidos. Nestas regiões, a capa cerosa das sementes é usada para a fabricação de velas, sabão, roupas e combustível e suas folhas, na medicina fitoterápica.
O pau-de-sebo pode ser utilizado para a produção de biodiesel, sendo considerada a terceira planta mais produtiva de óleo do mundo, após o dendezeiro e as algas.[carece de fontes?] A seiva da planta e as folhas são tóxicas para os humanos e animais.
A extração da cera das sementes se dá através da imersão destas em água quente, o que faz com que a cera emerja à superfície, podendo assim ser coletada. A cera pode ser utilizada como substituto para o azeite vegetal na cozinha. O néctar é utilizado pelas abelhas para a produção de mel. O mel não é de alta qualidade, porém é produzido e vendido durante a época estéril do ano, quando a maioria das outras plantas não estão florindo. Os demais produtos derivados da planta são tóxicos e não devem ser consumidos.
O pau-de-sebo é uma árvore ornamental, de crescimento rápido, excelente como barreira visual. No outono, suas folhas adquirem uma multiciplicidade de cores que, pela beleza, rivalizam com as demais plantas e contribuem para a sua popularidade.
Galeria de fotosFolhas durante o outono
Frutos
Árvores durante o outono
Exemplar no arboreto da Universidade da Califórnia em Davis, EUA
Triadica sebifera là một loài thực vật có hoa trong họ Đại kích. Loài này được (L.) Small miêu tả khoa học đầu tiên năm 1913.[1]
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Bài viết về phân họ Đại kích này vẫn còn sơ khai. Bạn có thể giúp Wikipedia bằng cách mở rộng nội dung để bài được hoàn chỉnh hơn. Triadica sebifera là một loài thực vật có hoa trong họ Đại kích. Loài này được (L.) Small miêu tả khoa học đầu tiên năm 1913.
Са́льное де́рево, или Сапиум салоносный (Triadica sebifera, ранее Sapium sebiferum) — растение семейства Молочайные. Используется как декоративное растение, как источник для мёда, производства красок. Благодаря высокой производительности в показателях масел (получаемых из воскоподобного жира, которым окружены семена) на гектар представляет интерес для производства биодизеля.
Это заготовка статьи по ботанике. Вы можете помочь проекту, дополнив её. Са́льное де́рево, или Сапиум салоносный (Triadica sebifera, ранее Sapium sebiferum) — растение семейства Молочайные. Используется как декоративное растение, как источник для мёда, производства красок. Благодаря высокой производительности в показателях масел (получаемых из воскоподобного жира, которым окружены семена) на гектар представляет интерес для производства биодизеля.
烏桕[註 1]（学名：Sapium sebiferum），又名烏槔[註 2]、烏臼、鴉臼。俗稱木蠟樹、樁仔、瓊仔等。
在中国，主要分布於黄河以南地区，北至陕西、甘肃。日本、越南、印度等国亦有分布[1]。18世纪进入美国。[2]
落葉喬木，高可达15米，无毛，具乳状汁，樹皮灰黑色，有縱裂。枝广展。葉互生，呈菱形、菱狀卵形，顶部具尖头，秋季時會轉為紅、橙、紫、褐、深綠或釉綠等色，甚至有可能一葉數色。花单性，雌雄同株，聚集成顶生总状花序，黃綠色細穗狀，在春季時吐出。蒴果綠色，梨状球形，成熟時黑色，並裂開為3瓣。種子則近圓形，外被白蠟質假種皮。[1]
叶
秋天红叶
总状花序
蒴果
成熟果
種子
中國將烏桕視為經濟作物而栽植已有千年歷史，主要因其種子外部含蠟，可為蠟燭。種子本身含油，作肥皂原料。而葉部亦可為中藥，民間有治蛇毒、消腹水的傳說。烏桕也可用作制度生質柴油。
由於秋季葉片能變色，目前常作為觀賞植物，在行道樹尤為常見。另外，烏桕木材密緻，易於加工，為家具及雕刻良品。烏桕種子所能提煉出的植物油可加工製造成生質柴油。
(Ha)
引用错误：页面中存在标签，但没有找到相应的标签
烏桕（学名：Sapium sebiferum），又名烏槔、烏臼、鴉臼。俗稱木蠟樹、樁仔、瓊仔等。
ナンキンハゼ（南京櫨・南京黄櫨、学名: Triadica sebifera）は、トウダイグサ科ナンキンハゼ属の落葉高木である。以前はシラキ属（英語版）に分類され、Sapium sebiferum の学名で呼ばれていた。種小名の sebifera は「脂肪のある」の意[2]。別名、トウハゼ、カンテラギ。中国名烏桕〔木偏に臼〕、烏臼、烏臼木[3]。
和名は、ハゼノキの代わりに蝋をとる材料として使われるようになった、中国原産の木の意味である。
樹高6 m。
花は雌雄同株であり、5-6月開花する。雄花は総状花序で、その葉腋に雌花をつける。
果実は秋、少し三角のかかった球形の蒴果（さくか）を黒熟させ、3個の種子を出す。種皮は黒色であるが、その表面は脂肪に富んだ白色の蝋状物質で覆われる。蒴果が裂開しても、種子は果皮から自然に離脱することはなく、紅葉期から落葉後まで長く樹上に留まり、白い星を散らしたようで非常に目立つ。ムクドリなどの鳥類がこの種子を摂食し、蝋状物質を消化吸収して種子を排泄することで、種子分散が起こる。
紅葉した葉
果実
よく紅葉することから、庭木、街路樹、公園樹の用途で使われている。
根皮、果実は乾燥して、利尿剤、瀉下剤にする。これを烏臼（うきゅう）という。 種子の油脂の烏臼油は、石鹸・蝋燭の原料や、薬用（腫物、皮膚病）とされる。
この項目は、植物に関連した書きかけの項目です。この項目を加筆・訂正などしてくださる協力者を求めています（プロジェクト:植物／Portal:植物）。
