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Althea (Hibiscus syriacus) is an ornamental shrub prized for its winterhardiness, flower colors, and unique flower forms, including single-flowered and double-flowered types. Although floral traits are most important for breeders of althea, little is known about their segregation patterns. The objective of this study was to determine segregation patterns in flower color, including eyespot, among hybrid seedlings of elite taxa. Over 4 years, more than 3100 flowering seedlings were produced for observation of F₁, F₂, and backcross families. For each plant, data were collected including presence of eyespot and petal body color (CIEL*a*b*) using a colorimeter. Recessive testcrosses and χ² analyses were performed among three taxa (‘Buddha Belly’, ‘Diana’, and White Chiffon^®), and between this recessive group and a suite of colorful taxa. Self-pollination and intercrosses within homozygous dominant and homozygous recessive groups further confirmed their genotypes. Based on these results, we propose that eyespot is controlled by a single gene called spotless, named for the recessive allele that results in a complete elimination of color in flowers. Crosses that resulted in seedlings that all produced eyespots were observed to segregate for color in the petal body. Of these, one group produced white to blush pink petals, which was recessive to full color. Recessive testcrosses and χ² analyses were performed among nine taxa exhibiting eyespots with white to blush petal bodies, and between taxa with full-color petal bodies. These testcrosses resulted in a putative homozygous dominant group composed mostly of blue and dark pink taxa, whereas the heterozygous group was composed mostly of pink taxa. Spotless taxa were also added to these two groups, suggesting an epistatic interaction with the spotless allele. Based on these results, we propose that petal body color is controlled by a single gene called geisha, named for the recessive allele that produces white to blush-pink petal bodies and dark red eyespot. This trait exhibits incomplete dominance and is under epistatic control by spotless. Geisha-type flowers lack pigment in the petal body, or exhibit a blush pink, likely produced by low levels of cyanidin, peonidin, and pelargonidin. The interaction and segregation of these two genes was confirmed in F₁, F₂, and backcross families from two crosses: Lil’ Kim™ × Blue Chiffon™ and Fiji™ × White Chiffon^®. This study on segregation of flower color in H. syriacus contributes substantial and useful information on inheritance of color and will facilitate targeted breeding to improve this vibrant ornamental shrub.

Acer is a large and important genus of woody plants most commonly encountered as small to large trees in urban landscapes. Considerable investigation has been devoted to addressing the taxonomy of maples, but little is known about genome sizes across the genus. Relatively more work has been conducted to determine chromosome numbers and ploidy of more species, but much could be gained by expanding knowledge of genome sizes in combination with traditional cytology. Furthermore, base pair (bp) composition may have implications for a species’ adaptability and also impacts nucleic acid stability at high temperatures. Our objectives were to determine the genome size of 195 accessions of maples, assign ploidy to each using inference as well as cytology, and determine base composition of a subset of 48 accessions. Most species had small genome sizes (1.4–3.5 pg) with the exception of section Rubra, which contains many polyploids. Holoploid genome sizes ranged from 1.39 to 6.10 pg, with the latter being interpreted as 9x. The mean monoploid genome sizes (1Cx) ranged from 0.43 pg in A. carpinifolium (section Indivisa) to 1.66 pg in A. caudatifolium (section Macrantha); mean monoploid genome sizes were significantly different among sections. Forty-four of the 48 accessions measured using both fluorochromes had greater estimates with 4′,6-diamidino-2-phenylindole (DAPI) than propidium iodide (PI). The proportion of the genome composed of guanosine and cytosine (GC%) among the taxa evaluated in this study ranged from just 38.61% to 43.96% and did not appear to be related to ecological adaptability or urban tolerance among these taxa.

Lilacs (Syringa sp.) are a group of ornamental trees and shrubs in the Oleaceae composed of 22–30 species from two centers of diversity: the highlands of East Asia and the Balkan-Carpathian region of Europe. There are six series within the genus Syringa: Pubescentes, Villosae, Ligustrae, Ligustrina, Pinnatifoliae, and Syringa. Intraspecific and interspecific hybridization are proven methods for cultivar development. However, reports of interseries hybridization are rare and limited to crosses among taxa in series Syringa and Pinnatifoliae. Although hundreds of lilac cultivars have been introduced, fertility and cross-compatibility have yet to be formally investigated. Over 3 years, a cross-compatibility study was performed using cultivars and species of shrub-form lilacs in series Syringa, Pubescentes, and Villosae. A total of 114 combinations were performed at an average of 243 ± 27 flowers pollinated per combination. For each combination, we recorded the number of inflorescences and flowers pollinated as well as number of capsules, seed, seedlings germinated, and albino seedlings. Fruit and seed were produced from interseries crosses, but no seedlings were recovered. A total of 2177 viable seedlings were recovered from interspecific and intraspecific combinations in series Syringa, Pubescentes, and Villosae. Albino progeny were produced only from crosses with Syringa pubescens ssp. patula ‘Miss Kim’. In vitro germination was attempted on 161 seed from interseries crosses, resulting in three germinations from S. pubescens Bloomerang^® x Syringa vulgaris ‘Ludwig Spaeth’. None survived, yet cotyledons produced callus for future efforts to induce embryogenic shoots. This study is a comprehensive investigation of lilac hybridization, and the knowledge gained will aid future efforts in lilac cultivar development.

Genome size variation can be used to investigate biodiversity, genome evolution, and taxonomic relationships among related taxa. Plant breeders use genome size variation to identify parents useful for breeding sterile or improved ornamentals. Lilacs (Syringa) are deciduous trees and shrubs valued for their fragrant spring and summer flowers. The genus is divided into six series: Syringa (Vulgares), Pinnatifoliae, Ligustrae, Ligustrina, Pubescentes, and Villosae. Reports conflict on genome evolution, base chromosome number, and polyploidy in lilac. The purpose of this study was to investigate genome size and ploidy variation across a diverse collection. Flow cytometry was used to estimate monoploid (1Cx) and holoploid (2C) genome sizes in series, species, cultivars, and seedlings from parents with three ploidy combinations: 2x x 2x, 2x x 3x, and 3x x 2x. Pollen diameter was measured to investigate the frequency of unreduced gametes in diploid and triploid Syringa vulgaris cultivars. Three triploids of S. vulgaris were observed: ‘Aucubaefolia’, ‘Agincourt Beauty’, and ‘President Grévy’. Across taxa, significant variations in 1Cx genome size were discovered. The smallest and largest values were found in the interspecific hybrids S. ×laciniata (1.32 ± 0.04 pg) and S. ×hyacinthiflora ‘Old Glory’ (1.78 ± 0.05), both of which are in series Syringa. Series Syringa (1.68 ± 0.02 pg) had a significantly larger 1Cx genome size than the other series. No significant differences were found within series Pubescentes (1.47 ± 0.01 pg), Villosae (1.55 ± 0.02 pg), Ligustrina (1.49 ± 0.05 pg), and Pinnatifoliae (1.52 ± 0.02 pg). For S. vulgaris crosses, no significant variation in 2C genome size was discovered in 2x x 2x crosses. Interploid crosses between ‘Blue Skies’ (2x) and ‘President Grévy’ (3x) produced an aneuploid population with variable 2C genome sizes ranging from 3.41 ± 0.03 to 4.35 ± 0.03 pg. Only one viable seedling was recovered from a cross combination between ‘President Grévy’ (3x) and ‘Sensation’ (2x). This seedling had a larger 2C genome size (5.65 ± 0.02 pg) than either parent and the largest 2C genome size currently reported in lilac. ‘Sensation’ produced 8.5% unreduced pollen, which we inferred was responsible for the increased genome size. No unreduced pollen was discovered in the other diploids examined. Increased ploidy may provide a mechanism for recovering progeny from incompatible taxa in lilac breeding.

Lilacs (Syringa sp.) have been used as ornamental plants since the mid-16th century and remain important in modern gardens due to their attractive and fragrant flowers. However, a short flowering season is a critical drawback for their ornamental value. Breeders have identified remontancy (reblooming) in dwarf lilac (Syringa pubescens), and have tried to introgress this trait into related species by interspecific hybridization. Molecular tools for lilac breeding are limited because of the shortage of genome sequence knowledge and currently no molecular markers are available to use in breeding for remontancy. In this study, an F₁ population from crossing Syringa meyeri ‘Palibin’ × S. pubescens ‘Penda’ Bloomerang^® Purple was created and subjected to genotyping-by-sequencing (GBS) analysis and phenotyped for remontancy. Plants were categorized as remontant, semi-remontant, and nonremontant based on the relative quantity of inflorescences during the second flush of flowers. A total of 20,730 single-nucleotide polymorphism (SNP) markers from GBS were used in marker-trait association to find remontant-specific marker(s) without marker position information. Two SNP markers, TP70580 (A locus) and TP82604 (B locus), were correlated with remontancy. The two loci showed a partial epistasis and additive interaction effects on the level of remontancy. Accumulation of recessive alleles at the two loci was positively correlated with increased reblooming. For example, 87% of aabb plants were remontant, and only 9% were nonremontant. In contrast, 100% of AaBB plants were nonremontant. These two SNP markers associated with remontancy will be useful in developing markers for future breeding and demonstrate the feasibility of developing markers for breeding woody ornamental taxa that lack a reference genome or extensive DNA sequence information.

Hibiscus syriacus is a woody shrub in the Malvaceae family that is common in landscapes due to its broad adaptability and variable ornamental characteristics. Interspecific hybridization has been used to improve Hibiscus by building novel floral traits, hybrid vigor, and hybrid infertility. A few interspecific hybrid Hibiscus cultivars (H. syriacus × H. paramutabilis), such as Lohengrin and Resi, are notable because of their vigorous vegetative growth, female infertility, and large flowers. However, little is known about the male fertility and breeding potential of these hybrid cultivars, which could increase flower size by backcrossing to H. syriacus. In this study, we estimated male fertility of the two hybrid cultivars by acetocarmine staining and in vivo pollination and assessed selection methods for floral traits, specifically flower size and petal number. A BC₁F₁ population of 294 individuals was developed by crossing hybrid cultivars Lohengrin or Resi with a variety of double-flowered H. syriacus cultivars. A negative correlation between petal number and petal area was detected by quantile regression, which is a method that circumvents the problem of simple linear regression, which violates statistical assumptions. Quantile regression was used to build simultaneous selection thresholds for different levels of required stringency. As expected, the female fertility of hybrid cultivars was extremely low or zero; however, the male fertility of hybrid cultivars was not reduced compared with H. syriacus cultivars. A negative linear correlation between the petal number and petal area of the BC₁F₁ individuals was observed. In addition, quantile regression was recommended to set a single selection threshold to be applied to the selection of two negatively correlated traits, which was more effective than independent selection of petal numbers and petal areas among progeny.

Althea (Hibiscus syriacus) is a shrub prized for its winterhardiness and colorful summer flowers. Altheas are tetraploids (2n = 4x = 80); however, breeders have developed hexaploids and octoploids. Previous studies report anatomical variation among polyploids, including stomata size. The purpose of this study was 4-fold. First, identify genome size and ploidy variation in cultivars via flow cytometry and chromosome counts. Second, create a ploidy series consisting of 4x, 5x, 6x, and 8x cytotypes. Third, investigate the ploidy series for variation in stomatal guard cell lengths, stomatal density, and copy number of fluorescent ribosomal DNA (rDNA) signals. Fourth, investigate segregation patterns of rDNA signals in a subset of pentaploid seedlings. Flow cytometry revealed most cultivars to be tetraploid with holoploid 2C genome sizes from 4.55 ± 0.02 to 4.78 ± 0.06 pg. Five taxa (‘Aphrodite’, ‘Pink Giant’, ‘Minerva’, Azurri Satin^®, and Raspberry Smoothie™) were hexaploids (6.68 ± 0.13 to 7.05 ± 0.18 pg). Peppermint Smoothie™ was a cytochimera with tetraploid cells (4.61 ± 0.06 pg) and octoploid cells (8.98 ± 0.13 pg). To create pentaploids, reciprocal combinations were made between hexaploid ‘Pink Giant’ and tetraploid cultivars. To create octoploids, seedlings were treated with agar solutions containing 0.2% colchicine or 125 μM oryzalin. Guard cell lengths were significantly different among the four cytotypes: 4x (27.36 ± 0.04 μm), 5x (30.35 ± 1.28 μm), 6x (35.59 ± 0.63 μm), and 8x (40.48 ± 1.05 μm). Measurements of stomatal density revealed a precipitous decline in average density from the 4x cytotype (398.22 ± 15.43 stomata/mm²) to 5x cytotype (194.06 ± 38.69 stomata/mm²) but no significant difference among 5x, 6x, and 8x cytotypes. Fluorescent in situ hybridization (FISH) revealed an increase in 5S and 45S rDNA signals that scaled with ploidy: 4x (two 5S + four 45S), 6x (three 5S + six 45S), and 8x (four 5S + eight 45S). However, pentaploid (5x) seedlings exhibited random segregation of rDNA signals between the 4x and 6x cytotypes, including all six possible combinations (two 5S, three 5S) × (four 45S, five 45S, six 45S).

The genus Cotoneaster (Rosaceae, Maloideae) is highly diverse, containing ≈400 species. Like other maloids, there is a high frequency of naturally occurring polyploids within the genus, with most species being tetraploid or triploid. Apomixis is also prevalent and is associated with polyploidy. The objective of this study was to estimate genome sizes and infer ploidy levels for species that had not previously been investigated as well as compare estimates using two fluorochromes and determine base pair (bp) composition. Chromosome counts of seven species confirmed ploidy levels estimated from flow cytometric analysis of nuclei stained with 4′,6-diamidino-2-phenylindole (DAPI). Monoploid (1Cx) genome sizes ranged from 0.71 to 0.96 pg. Differences in monoploid genome size were not related to current taxonomic treatment, indicating that while chromosome sizes may vary among species, there are no clear differences related to subgeneric groups. A comparison of DAPI and propidium iodide (PI) showed a difference in DNA staining in Cotoneaster comparable to other rosaceous species. Base pair composition (AT%) in Cotoneaster ranged from 58.4% to 60.8%, which led to overestimation of genome size estimates in many cases—assuming the estimates of the DNA intercalator are accurate. Our findings will inform breeders with regard to the reproductive behavior of potential parents and may be used to confirm hybrids from interploid crosses.