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ARS Home » Northeast Area » Washington, D.C. » National Arboretum » Floral and Nursery Plants Research » Research » Research Project #434195

Research Project: Evaluation and Genetic Improvement of Woody Ornamental Landscape Plants

Location: Floral and Nursery Plants Research

Project Number: 8020-21000-071-000-D
Project Type: In-House Appropriated

Start Date: Feb 14, 2018
End Date: Feb 13, 2023

Objective 1: Characterize and evaluate, breed, select, and release improved germplasm for woody landscape plants that have superior ornamental value, are tolerant of biotic and abiotic stress, and are not invasive. [NP301, C1, PS1B; C2, PS2A] Sub-objective 1a: Characterize germplasm and develop hybrids or breeding lines in genera currently under investigation, including Buxus, Cercis, Lagerstroemia, Prunus, and Ulmus. Sub-objective 1b: Propagate and evaluate (in-house and via cooperators) advanced selections of Buxus, Catalpa, Cercis, Nyssa, Lagerstroemia, Prunus, and Tsuga developed in previous cycles. Sub-objective 1c: Name, release, distribute, and promote new cultivars. Objective 2: Incorporate modern breeding tools to accelerate the creation, characterization, identification, selection, or evaluation of priority plant materials. [NP301, C1, PS1B; C2, PS2A] Sub-objective 2a: Test genes for altered plant architecture (developed previously by ARS scientists) in several woody ornamental plant genera. Sub-objective 2b: Use molecular markers to characterize germplasm or hybrids in Buxus and Tsuga, where phenotypic traits are ambiguous. Additional resources in the merged project will strengthen the research in the current Objective 2: Objective 2: Incorporate modern breeding tools to accelerate the creation, characterization, identification, selection, or evaluation of priority plant materials. [NP301, C1, PS1B; C2, PS2A]

Objective 1: For classical breeding work, parental germplasm will be collected from native habitats, botanical repositories, and commercial sources, and will be evaluated in the polyhouse or field plots. Controlled hybridizations will be carried out in the field or greenhouse by hand or by insects in pollination cages or greenhouses to produce hybrid progeny, to determine compatibility among parents, and to study breeding systems and inheritance of traits of interest. Appropriate reciprocal and test crosses will be conducted for inheritance studies. In addition to traditional evaluations and classical breeding methodologies, several techniques will be used to characterize parental germplasm and develop hybrids. This includes ploidy analysis and manipulation and creating interploid hybrids and wide hybrids in order to develop seedless selections of priority genera. Resultant progeny will be screened for ploidy and evaluated for traits of interest. Promising selections will be propagated and transplanted to the field for further evaluation. Selections developed during previous project cycles that have performed well will also be propagated. These include elite clones of Buxus, Catalpa, Cercis, Nyssa, Lagerstroemia, Prunus, and Tsuga. Nursery cooperators, botanical gardens, or other cooperators will be chosen based on hardiness zone and production system, and at least three plants of each selection will be sent to each cooperator for evaluation. In consultation with ARS’s Office of Technology Transfer, plants selected for release will undergo stock increase by volunteer cooperators and will be released following the standard ARS administrative approval procedures. Promotional materials will be prepared and distributed. Propagation material will be sent to nurseries upon request until the cultivar is routinely available in the trade. Objective 2: For the first few years of this five-year plan, we will focus on establishing in vitro cultures of diverse woody taxa that would have the most impact from altered plant architecture (for example maples, crapemyrtles, beech, oaks, elms, flowering cherries). We will attempt to establish many diverse taxa in culture, recognizing that some taxa won’t be successful, and then focus on those few that perform well in terms of multiplication and regeneration using updates of protocols established already in our lab. Explants will consist of shoot tips, dormant buds, or seeds. Different protocols for regeneration, including organogenesis and embryogenesis, will be tested with ARS collaborators. Appropriate molecular markers will be used in conjunction with classical taxonomy and, when appropriate, ploidy analysis to determine genetic relationships among taxa and verify parentage of hybrids. Efforts will focus on markers in hemlock and boxwood for the first few years.