Little is known about environmental and physiological factors affecting centipedegrass [Eremochloa ophiruoides (Munro) Hackell winter survival. Stolons of common and ‘Oklawn’ centipedegrass were sampled from field‐ or growth chamber‐grown turf in three separate experiments to (i) determine freezing tolerance of acclimated and nonacclimated turf; (ii) identify and quantify nonstructural carbohydrates (NSC) in acclimated and nonacclimated turf, and (iii) relate levels to freezing tolerance. Lethal temperatures for common and Oklawn were similar throughout all studies. Freezing tolerance estimated by electrolyte leakage for turf sampled from the field in winter 1988–1989, indicated that lethal temperatures ranged from about −7 to −8 °C in February and March, to −9 °C in December and January. In a 1990–1991 field and growth chamber studies, injury was estimated by stolon recovery growth in the greenhouse after freezing at −2, −4, −6, −8, and −10 °C for 1 h. Lethal temperatures in mid‐winter were −2 °C lower than in fall or spring during active growth. In stolons, starch and sucrose were the primary NSC ranging from ≈2 to 13 mg (100 rag)−1 dry weight. Sucrose was higher in acclimated than pre‐ or post‐acclimated turf. In a growth chamber study, 47% more sucrose was present in acclimated vs. preacclimated turf. Sixty‐nine percent more acclimated stolons survived −4 °C than preacclimated stolons, and a positive correlation (r = 0.78) was observed between sucrose level and number of surviving stolons. Higher sucrose concentrations in low‐temperature‐acclimated vs. nonacclimated common centipedegrass stolons may be a component of improved freezing tolerance.

Xylem vessel anatomy was examined in tissues surrounding the graft union of sweet cherry (Prunus avium L.) scion (stem) and nondwarfing, semi-dwarfing, or dwarfing rootstock (root) combinations, to characterize potential changes in anatomical features during the initial stages of graft union formation. Vessel element length, frequency, diameter, lumen area (LAV), and mean vessel hydraulic diameter (VDh) were examined in `Rainier' (P. avium) scion wood grafted onto nondwarfing `Colt' (P. pseudocerasus L. × P. avium) or `F 12/1' (P. avium) rootstock and semi-dwarfing `Gisela 6' [`Gi 6' (P. cerasus L. × P. canescens L.)], or dwarfing `Gisela 5' [`Gi 5' (P. cerasus × P. canescens)] rootstock systems in: heterograft combinations (commercial scion-rootstock combinations); homografts (scion and rootstock are the same genetic material); and reciprocal heterografts (rootstock tissue grafted onto scion tissue). Vessel element length was not affected by rootstock, but vessel frequency and lumen area in graft union tissues were smaller in `Rainier'/`Gi 5' (dwarfing combination) than in `Rainier'/`Colt' (nondwarfing combination). The heterograft combination of `Rainier'/`Gi 5' had smaller scion LAV, lower VDh and narrower vessels than homograft or reciprocal heterograft combinations. As callus differentiated into vascular elements, xylem rays in `Rainer'/`Gi 5' tended to develop at an acute angle to the longitudinal axis of the tree and there was an increase in nonfunctional phloem in `Rainer'/`Gi 5' compared to `Rainer'/`F 12/1'. Collectively, the data provides further evidence that a combination of smaller and fewer vessels in the scion and graft union, as well as irregular vessel orientations in the vascular tissue within dwarfing combinations could contribute to hydraulic resistance in the graft union resulting in reduced scion growth (dwarfing).

No abstract

Leaf blackening on cut flower Protea nerii[olia R. Br. stems was dramatically reduced under a 12-hour photosynthetic light period (120 μmol·m-2·s-1) at 25C for 15 days compared with stems kept in the dark. In the light, addition of 0.5% exogenous sugar to the vase solution resulted in a maximum of 2.5% leaf blackening, while stems with no exogenous sugar had a maximum of 16.5%. Continuous darkness resulted in 94% leaf blackening by day 7, irrespective of sugar treatment. Starch and sucrose concentrations were markedly lower in leaves on dark-held stems than in leaves on stems held in the light; thus, carbohydrate depletion could be the primary stress that initiates leaf blackening. In the light, rates of carbon exchange and assimilate export were similar, indicating that the amount of carbon fixed maybe regulated by sink demand. The pattern of carbon partitioning changed in light-held leaves of the 0% sugar treatment during rapid floral expansion and senescence. Inflorescence expansion appears to influence partitioning of photoassimilates and storage reserves into transport carbohydrates; under decreased sink demand, the assimilate export rate decreases and photoassimilates are partitioned into starch. The data suggest that sink strength of inflorescences held in darkness may be responsible for the depletion of leaf carbohydrates and. consequently, blackening.

Little is known about intraspecific variability in St. Augustinegrass [Stenotaphrum secundatum (Walt.) Kuntze] freezing tolerance and the physiological factors that may influence survival. Stolons of field-grown `Raleigh', `Floratam', and FX-332 St. Augustinegrass were sampled between October and March in 1990 to 1991 and 1991 to 1992 to measure freezing tolerance, nonstructural carbohydrates, and water content. Stolons were exposed to temperatures between 1 and -8C in a freezer, and regrowth was evaluated in the greenhouse. Generally, freezing tolerance of `Raleigh' > `Floratam' = FX-332. `Raleigh' exhibited >60% survival in December and January, while survival of `Floratam' and FX-332 was <20%. `Raleigh' was the only cultivar that acclimated, as indicated by a 75% increase in survival between October and December 1990. Starch and sucrose were the primary storage carbohydrates extracted from stolons, but neither was correlated with freezing tolerance. A negative (r = -0.80) correlation was observed between `Raleigh' survival and stolon water content between January and March 1991. Reduced water content in `Raleigh' stolons during winter months may contribute to acclimation.