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Since 1924, the Univ. of Minnesota herbaceous perennial breeding program has released n = 84 garden chrysanthemums (Dendranthema grandiflora). Recent breeding objectives have focused on development of non-destructive phenotypic markers and laboratory freezing tests for continued selection of cold-tolerant Dendranthema, Gaura, and other herbaceous perennial flowers. Such methods have become critical to flower breeding programs during periods of above-average winter temperatures and minimal snow cover. Two different laboratory freezing tests were evaluated for their effectiveness in determining cold tolerance. Acclimated crowns of n=6 hardy and non-hardy garden chrysanthemum genotypes were used in Omega Block (detached, emergent rhizomes) and chamber (intact crowns with emergent/non-emergent rhizomes) freezing test methods. Comparative winter survival in the field was monitored over locations and years. Cold tolerance was assessed at 0 °C to -12 °C with varying ramp and soak time periods. LT₅₀ temperatures and number of living emergent rhizomes were determined. Rhizome quality at 1 cm, 3 cm, and 5 cm depths was rated on a 0 (dead) to 5 (undamaged) scale. The chamber freezing method was the most powerful to discern LT₅₀ values. Cold tolerant genotypes included `Duluth' and 98-89-7 (LT₅₀ = -12 °C). Three genotypes had intermediate cold tolerance (LT₅₀ = -10 °C) and one genotype was not cold tolerant (LT₅₀ = -6 °C). Cold-tolerant genotypes also had significantly higher regrowth ratings for rhizomes at 1cm and 3cm depths. Future research will use the chamber freezing method to assay the inheritance of winter hardiness in intact crowns of segregating populations.

Global warming has created increased nighttime temperatures both in field and greenhouse production of chrysanthemums during flower bud initiation (FBI) and development, causing heat delay or complete cessation of flowering. Integration of breeding and selection for heat delay insensitivity (HDI) has become imperative for greenhouse (cut, potted types) and must be accomplished on a genotypic basis, similar to winterhardiness. This is a breeding objective in the joint garden chrysanthemum breeding project between the Chungnam Provincial Agricultural Research and Extension Services and the University of Minnesota. The objectives of this research were to test 10 genotypes (cultivars, seedlings) from both breeding programs when grown in low-temperature (LT) and high-temperature (HT) short-day (SD) and long-day (LD) conditions (four environments: LTSD, LTLD, HTSD, and HTLD); determine the extent of heat delay and HDI for visible bud date (VBD), flowering, and other phenotypic traits; evaluate relative injury (RI) and cell membrane thermostability (CMT), and to select future parents with lowered RI values, higher CMT, shorter heat-induced flowering delay, and/or HDI. ‘Magic Ball’ and ‘Minnwhite’ had the shortest plant height in HTLD and HTSD, whereas ‘Geumbangul’ had stability for height in all treatments. Lowest long day leaf numbers (LDLN) occurred under LTSD in seven genotypes. However, both ‘Geumbangul’ and ‘Magic Ball’ had complete stability for LDLN across all environments. Sigmoid curves for RI% and temperature were found for all genotypes and environments with R ² = 0.79–0.89. Only ‘Mellow Moon’ had stability or equal VBDs in HTSD, LTSD, and LTLD conditions. This is the first-ever report of stability for VBD across inductive and noninductive HT/LT treatments. Only ‘Centerpiece’ flowered in all environments and also had 0 day of heat for VBD in LT and 1 day of heat delay in HT, as well as three others (Mn. Sel’n. 01-210-43, ‘Autumn Fire’, and ‘Geumbangul’). Few had linear regressions with positive slopes for heat-induced VBD or flowering delay regressed with RI%; most had no slope (R ² ≈ 0.0) for all treatments (‘Centerpiece’, Mn. Sel’n. 01-210-43), whereas others were negative (‘Mammoth™ Dark Bronze Daisy’, Flw LTLD–LTSD). Surprisingly, one linear regression had a slope of R ² = 1.0 (‘Geumbangul’, Flw LTLD–LTSD). These responses are all novel in chrysanthemums. Selecting the best parents in both breeding programs to maximize stability of all traits across these four environments with minimal crossing and selection across generations could be accomplished by stacking parental traits. A crossing scheme involving just three parents is proposed to incorporate stability for all traits in just a few generations.

Growth response of `Sambok Honey' watermelon grafted onto different rootstocks, including four Citrullus rootstocks and three other cucurbitaceous rootstocks, was evaluated at low and normal temperature regimes. Marked reduction in plant growth rate was observed in plants grown at low temperatures as compared to those grown at normal or optimal temperatures. Relative growth reduction rates were 40% to 48% for vine length, 39% to 51% for total leaf area, 37% to 60% for shoot fresh weight, and 50% to 79% for shoot dry weight, respectively. Watermelon rootstock PI 482322 showed comparable plant growth as the most popular rootstock (Shintozwa pumpkin) even at low temperatures. `Sambok Honey' watermelon grafted onto watermelon hybrids `PI 271969 × PI 296341' and `PI 271769 × Calhoun Gray', showed comparable plant growth as FR Dantos bottle gourd rootstock. Index of growth ability at low temperature (IGALT), which was calculated on the basis of reduced rate of vine length, dry weight, and leaf area, was comparatively high in C. martinezii, Shintozwa, PI 482322, and `PI 271769 × PI 296341' rootstocks (50% or higher) and lowest in own-rooted `Sambok Honey' or in watermelon plants on `Knight' rootstock. Watermelon hybrids `PI 271969 × PI 296341' and `PI 271769 × Calhoun Gray' exhibited better or at least comparable growth at low temperatures as compared to `FR Dantos', thus confirming the feasibility of using watermelon rootstocks even in winter greenhouse conditions.