HORTSCIENCE 37(7):1139–1141. 2002. diam.), covered by only 3–4 perules; dark brown (RHS 200/b); rounded at the base of the long shoot and in the short shoot. The apical ‘San Zanobi’ and ‘Plinio’ Trees bud of the short shoot is larger than the sub- dominant buds and it is typically oblique and 1 2 2 3 A. Santini , A. Fagnani , F. Ferrini , and L. Mittempergher inward-folded. Corky wings are absent. Istituto per la Protezione delle Piante, C.N.R. Florence P.le Cascine 28 50144 Flowering starts late, only from the fifth year Florence, Italy of age on selfrooted trees. Fruits are ovate- roundish sessile samara measuring 1.5 × 1.8 Additional index words. tree breeding, Ulmus, cm. Flushing occurs at the same time or only slightly later than in Mill.. Elm (Ulmus L.) has been utilized by hu- elm (Heybroek, 1983) [( The name ‘San Zanobi’ comes from the mans since prehistoric times for food, medi- “Exoniensis” x Ulmus wallichiana p39) x (U. reported prodigious flushing of a dead elm, cine, fiber, fodder for cattle, timber for con- minor 1 x U. minor 28)] with U. pumila S.15. acknowledgement of the passage of the relics struction, firewood, and [in the Mediterra- ‘Plinio’ (Patent RM 97 NV 0005) was ob- of the saint bishop St. Zenobius, coming from nean Basin from ancient Roman times (Col- tained by controlled pollination of ‘Plantyn’ outside town to the Florence (Italy) Cathedral umella ≈60 C.E.) to the mid-20th century] as with U. pumila S.2. during the year 429 C.E.; the event is com- a living support for grapevine. In the last Pollen from S.15 and S.2 was collected in memorated by a marble stele flanking the three centuries, elm has also been widely a warm room from cut fruiting twigs, filtered Baptistry. used as an ornamental tree to embellish the and dried to 10% relative humidity (RH) (Mit- ‘Plinio’ grows rapidly, although slightly avenues and gardens of Europe, North tempergher and La Porta, 1991). In January, slower than ‘San Zanobi’, roughly similar to America, and China. However, during the the female flowers of ‘Plantyn’ were covered that of fast-growing benchmark ‘Lobel’ past century, this tree suffered major losses, with terylene bags of adequate size tied to the (Table 1). It adapts readily to Mediterranean with near-total disappearance of adult trees branch to protect the flowers and prevent un- mountainous climates of Northern Italy in some areas of the world as a result of two controlled pollination. Pollination was carried (unpub. data). ‘Plinio’ is used as an ornamen- epidemic outbreaks of Dutch Elm Disease out by forced air injection of pollen into the tal shade tree (Fig. 2). The crown is about (DED), caused by two ascomycetes, bags. The pollination bags were kept in place oval in 5-year-old trees. In isolated trees, the Ophiostoma ulmi (Buisman) Nannf. and until fruit maturity. width of the crown can be up to 70% of its Ophiostoma novo-ulmi Brasier. The Euro- height. The trunk is straight, at times slightly pean elm species, U. glabra Huds., U. laevis Description sinuous, short. Branching begins at a height Pall., U. procera Salisb. and U. minor Mill., of 2–3 m. The bark is grey-green (RHS 198/ are generally susceptible, although rare indi- ‘San Zanobi’ is monocormic and shows a) and is still smooth in 5-year-old trees. viduals of the last species and its hybrid U. exceptionally rapid growth on fertile soils and Leaves are alternating and deciduous, re- ×hollandica Mill. showed enough resistance in temperate climates, suggesting that it could maining green and active on the tree longer to form the main basis of a breeding program be used for production of construction timber than is usual in other . The leaf blade is (Heybroek, 1993). L., an Asian (Table 1). Its habit is cone-shaped with pro- glabrous on both surfaces. Tertiary venation species introduced as an ornamental tree in nounced apical dominance, resulting in limited is rare. The leaf has a biserrate margin; an the Mediterranean areas, proved to be moder- lateral branching on the developing shoots of acute apex, and a noticeably asymmetric base. ately to highly resistant. the current season’s growth (Fig. 1). The crown Color = yellowish green (RHS 147/a). The Another source of genes for resistance to the is therefore narrow and columnar. Apical domi- second leaf of the short shoot is broadly fungus that causes DED has been found in nance is so marked that seedlings rarely need elliptic or oval. The petiole is glabrous and 6– several species growing in central-eastern Asia, pruning or training. The trunk is straight, long, 9 mm long. The branches are rather slender; one of the most important centers of genetic and the bark is grey-green [n° 197/c Royal the glabrous twig is grey-green in color (RHS diversity of Ulmus (Smalley and Guries, 1993). Horticultural Society (RHS), 1966]. 197/a). Vegetative buds are fairly large (2–3 Unfortunately, the Asian species do not always The alternating deciduous leaves remain mm diam.), ovoid, with a non-pointed tip, meet ornamental and production requirements, green in fall and are shed late. Their margins and dark brown in color (RHS 200/a). The or do not adapt easily to different environmen- are often undulate; green-yellowish in color apical bud of the short branch is inward- tal conditions. Consequently, the main breed- (RHS 147/c). The second leaf of the short folded. Corky wings are absent. Flowering ing programs set up in Europe and in North shoot is roughly elliptic or oval, with an acute starts early, from the third year of age and is America to develop DED-resistant trees in- apex and the base is asymmetric. The petiole is abundant. Fruits are ovate-roundish sessile volve cross-breeding of Asian with other indig- glabrous and 6–9 mm long. Rather slender samara with central seed measuring 2 × 2 cm. enous species in order to produce individuals twig is hairless and grey-green in color (RHS Flushing occurs a few days after that of Ulmus that combine the disease resistance of Asian 197/a). Vegetative buds are small (<2 mm minor. elm with the growth characteristics and higher degree of environmental adaptability of Euro- Table 1. Mean annual increments in height (cm) and diameter (cm) of the pean elm. ‘San Zanobi’ and ‘Plinio’ are two selections compared to the Dutch release ‘Lobel’, which was included as recent results of such research. a benchmark for vigor. Data refer to obtained from self-rooted cuttings. Values were obtained from the mean of measurements made during the first 6 years of age in four experimental plots. Origin Cultivar Nz Mean STDx CV%w ‘San Zanobi’ (Patent RM 97 NV 0006) was Height increment (cm) (F = 12.53; P ≤ 0.001) selected among seedlings obtained by con- S. Zanobi 84 122.0 23.73 19.4 c trolled pollination of Heybroek’s ‘Plantyn’ Plinio 45 104.9 47.11 44.9 b Lobel 24 79.4 39.41 49.6 a Diameter increment (cm) (F = 7.48; P ≤ 0.001) Received for publication 31 July 2001. Accepted for S. Zanobi 84 1.75 0.47 26.7 a publication 10 Feb. 2002. The field work of Mr. Plinio 45 1.44 0.49 35.0 b Abdellah Dahmani is gratefully acknowledged. Lobel 24 1.46 0.48 32.8 b 1Researcher: to whom reprint requests should be addressed. E-mail: [email protected] zN = number of samples; xSTD = Standard deviation; wCV% = Percent 2Undergraduate Technician. coefficient of variation. Means not sharing same letters are significantly 3Professor (retired). different for LSD test (P < 0.05).

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The name ‘Plinio’ derives from the Roman growth in the field (4-year-old plants), trees after 4 weeks and at 3 (not reported) and 8 naturalist and historian Pliny the Elder of the were inoculated in the upper third of the main months by three independent assessors. Seed- first century C.E., who wrote about elm in his stem. Inoculation was performed with a single lings presenting less than 10% dieback were “Naturalis Historia”. wound per , by cutting through the bark vegetatively propagated and planted out the ‘San Zanobi’ and ‘Plinio’ are easily propa- to the younger wood using a knife blade following year in a completely randomized gated from hardwood cuttings taken in January carrying two drops of a 0.2 mL of a 1 × 106 mL block design. Twelve rooted cuttings per clone, and February, quickly dipped in EtOH 30% fungal spore mixed suspension of yeast phase divided into three blocks, were used. Inocula- solution containing IBA 3000 ppm, and placed cells, so that the inoculum would be absorbed tions and disease evaluations were performed in warm beds at 18 °C in a mixture of 1 peat : 1 by the tree’s rising sap. The spore suspen- as described above and the symptoms, were perlite : 1 sand (v/v/v). Rooting generally oc- sion, consisting of two tester isolates of the compared with clones having known DED curs within 4 weeks. subsp. novo-ulmi and subsp. americana of O. responses (‘Lobel’, moderately resistant; novo-ulmi (Brasier and Kirk, 2001) found to ‘Urban’ resistant; and CNR 118 highly sus- Disease resistance be very aggressive in previous assays, were ceptible). The resistance levels of the clones Two-year-old seedlings of ‘Plinio’ and prepared by inoculating 50-mL Erlenmeyer described here were significantly higher than ‘S. Zanobi’ grown in the nursery were planted flasks containing 10 mL of modified the resistance levels of ‘Lobel’ and ‘Urban’ in the field in 1983 and 1984, respectively. Tchernoff’s liquid medium (Brasier, 1981), (Table 2). During the third week of May, the time period and incubating for 2 d on a shaker at room Elm Yellows infections have to date never that elm trees are at their highest susceptibil- temperature. Spore concentration was then been reported in these selections (Mit- × 6 ity in this climate, in the second year of adjusted with sterile water to 1 10 mL. tempergher, 2000). Strong winds have not Symptoms of disease (percent of defolia- caused injury in any individual of these selec- tion and percent of dieback) were observed tions.

Fig. 1. The ‘S. Zanobi’ elm. Fig. 2. The ‘Plinio’ elm.

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