Search Results

You are looking at 1 - 10 of 90 items for :

  • Cercis canadensis x
Clear All

redbud ( Cercis canadensis var. mexicana ) irrigated with water at EC of 1.6, 3.0, or 6.0 dS·m −1 (control, EC 3, or EC 6). Vertical bars represent se s (n = 8). Flushing: all containers were flushed with tap water to leach out salts. Plant

Free access

Cercis canadensis , a leguminous tree, is native to North America and cultivated widely as an ornamental. Flowers emerge directly from the stem or trunk before the leaves early in the spring. Petal colors range from purple to pink to red or white. A

Free access

used to communicate to the consuming public the positive economic and environmental value of trees in the landscape. Materials and Methods The nursery production system modeled in this study was a field-grown, 5-cm (2-in) caliper Cercis canadensis

Free access

Cercis canadensis, Eastern Redbud, is very Cercis canadensis, Eastern Redbud, is very susceptible to infection by Verticillium Wilt caused bysusceotible to infection by Verticillium Wilt caused by the common soil-borne fungi Verticillium albo-atrum and Verticillium dahliae. Little is known about the inoculum levels, the time required for natural infection to occur and how fast the pathogen travels inside the host species. One-year-old Cercis canadensis seedlings were planted in 7.6 liter (2-gallon) containers with a 1:1:2 soil/sand/perlite mix inoculated with five levels (0, 10, 100, 500, and 1000 microsclerotia/g soil) of V. dahliae prior to planting. At the end of the first growing season, half of the plants were removed from the containers, surface sterilized, dissected and root sections plated out on a Verticillium selective media. The remaining plants were grown for a second season. Infection first occurred in plants which received 100, 500 or 1000 ms/g at the end of the first season. The infection had spread at least 5 cm during the first growing season.

Free access

Seed dormancy in Eastern redbud (Cercis canadensis var. canadensis L.) can be overcome by seedcoat scarification to allow water imbibition, followed by chilling stratification to permit germination. During chilling stratification, there was an increase in the growth potential of the embryo as indicated by the ability of the isolated embryo to germinate in osmotic solutions. Penetration resistance of the testa also decreased after chilling stratification. The combination of seedcoat alteration and the increase in embryonic growth potential was associated with overcoming dormancy in redbud seed. GA3 or ethephon (50 μm) stimulated germination (28% and 60%, respectively) and increased the growth potential of treated embryos. Chemical names used: gibberellic acid (GA3), (2-chloroethyl) phosphoric acid (ethephon).

Free access

Abstract

An examination of dormancy in seeds of Eastern Redbud, Cercis canadensis L., showed that dormancy is controlled by permeability of the testa. Scarification by H2SO4 or mechanical abrasion permitted rapid and complete germination of dormant seed. Stratification was necessary only if seed were not scarified. Nonscarified seeds showed almost no water uptake during 55 days at 5°C, while scarified seeds had a steep imbibitional gradient. Germination was not stimulated by adding oxygen. No growth inhibitors were detected in dormant seed, and no promoters were found in chilled seeds.

Open Access

Eastern redbud ( Cercis canadensis L.) is a popular small landscape tree. In the two most recent U.S. Department of Agriculture (USDA) Censuses of Horticultural Specialties, redbud was the fifth most valuable deciduous flowering tree in the

Open Access

Several studies with annual crops have shown that large seeds improve percent germination, seedling growth, and uniformity, yield, seedling vigor, and stress tolerance. Little information is available on the influence of seed size on the resulting seedlings of woody plant species. Cercis canadensis L. seeds were divided into large and small seed size fractions and the seeds scarified, stratified, and planted. A larger percentage of large seeds germinated than did small seeds. Seedlings from large seeds had a greater peak and germination value than small seeds, indicating greater vigor and a more rapid germination rate thus more uniform seedlings. Seedlings from large seeds, as indicated by fresh and dry weights, were larger and contained a greater leaf area than those produced by small seed.

Free access

The seedcoat anatomy in the hilar region was examined in dry, imbibed and germinating seeds of Eastern redbud (Cercis canadensis L.). A discontinuous area was observed between macrosclereid cells in the palisade layer of the seedcoat which formed a hilar slit. A cap was formed during germination as the seedcoat separated along the hilar slit and was hinged by the macrosclereids in the area of the seedcoat opposite to the hilar slit. The discontinuity observed in the palisade layer was the remnant of the area traversed by the vascular trace between the funiculus and the seedcoat of the developing ovule. There were no apparent anatomical differences in the hilar region of the seedcoat between dormant and nondormant imbibed seeds. However, the thickened mesophyll of the seedcoat in this region and the capacity of the endosperm to stretch along with the elongating radicle may contribute to maintaining dormancy in redbud seeds.

Free access

Selected cultivars of redbud (Cercis canadensis L.) and related Cercis species are usually propagated by grafting, but the success rate is low and other problems can be associated with the rootstock. Micropropagation would solve many of these problems. Shoots from a 25 year-old redbud were collected during July 1989 and established in vitro on modified MS medium. Shoots proliferated poorly with lower concentrations of Benzyladenine (BA) and high concentrations of BA caused shoot tip abortion. Similar problems with red-silver hybrid maples were solved by the use of Thidiazuron (TZ) in the medium. Established 2 cm redbud shoots were treated with TZ (0, 0.05, and 0.1 uM) and BA (0, 1 and 5 uM) in a factorial arrangement to test for shoot proliferation. After 4 weeks of the treatment with 0.1 uM TZ and 5 uM BA, mean shoot number was 4.6 compared to 1.1 shoots with no BA or TZ in the medium. Further experiments with rooting treatments will be presented.

Free access