Start Date: Jun 01, 2008
End Date: May 31, 2013
Experimental design for this study will be a randomized complete block design with three replications. We will use the expected mean squares from the analysis of variance to calculate broad sense heritabilities, which will distinguish proportions of genetic and environmental variance for each trait. Each replication will consist of one individual per taxa. Plant material will be acquired from Chicago Botanic Garden, the official NAPCC Spiraea collections repository. Cuttings of accessions will be taken in the fall of 2007 and rooted in greenhouses using the protocol of Dirr and Heuser (2006). Plants will be transferred to in-ground beds in the spring of 2008 at two locations: Athens, GA (USDA Zone 7b) and Savannah, GA (USDA Zone 8b). Planting beds will be arranged in linear-rows with individuals planted on 5’ staggered centers. Drip-irrigation will be applied as needed the first growing season while plants are becoming established and subsequently removed for the remainder of the study unless severe drought warrants irrigation. Measurement of the aforementioned USDA-ARS woody landscape plant descriptor traits and mortality will begin April 1, 2009, and conclude on November 15, 2010. Disease and insect measurements will include pathogen/pest ID and percent of plant affected. Attractiveness, floral impact, persistence of foliage, plant vigor, and summer drought/heat tolerance will be measured on a 1-10 scale with one being the least and 10 being the highest. Color measurements will all be performed using the Royal Horticultural Society Colour Chart. All size measurements will be taken in centimeters. Number of fruit produced per umbel will be taken from an average of five randomly selected umbels per individual. All date measurements will be reported on a 1-365 scale beginning with January 1 and ending with December 31. Invasive potential will be measured by calculating the percentage of viable seed and germination percentage of 100 seed per individual using two techniques: 1) Tetrazolium tesing in 0.1% solution of 2,3,5-triphenyltetrazolium chloride (Miller, 2004). 2) Germination test on moist filter paper. Additionally, we will qualitatively measure seed production of each genotype by assessing the mean number of seed produced per umbel using five umbels per plant. We will also calculate the mean number of umbels for each genotype. By multiplying the mean number of seed produced per umbel with the mean number of umbels per genotype, we will ascertain a overall value for seed production of each genotype in the study.