scholarly journals 561 PB 406 THE EFFECTS OF COLD TEMPERATURES ON THE SURVIVABILITY AND POST-STRESS PERFORMANCE OF CONTAINER-GROWN NURSERY STOCK

HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 512a-512
Author(s):  
Jennifer L. Dwyer ◽  
N. Curtis Peterson ◽  
G. Stanley Howell

The nursery industry continues to develop improved methods for successfully overwintering container-grown nursery stock. Experiments were conducted using several different species of woody ornamentals ranging from species known to be cold hardy to cold tender. Eighteen species were subjected to temperatures ranging from 20F to -20F and observed for post-stress performance and viability. Rates and timing of acclimation, mid-winter hardiness, and deacclimation of seven species were determined by examining the shoots for injury after subjecting them to controlled freezer conditions. The roots of the same seven species were exposed to three different overwintering systems: in a polyhouse, pot-to-pot above the ground, and pot-in-pot below the ground. Cold hardiness of root and shoot systems and the effects of warming temperatures on shoots were determined as well as the post-stress performance of each species. Results of this research will be presented.

HortScience ◽  
1996 ◽  
Vol 31 (4) ◽  
pp. 646f-646
Author(s):  
Kathleen M. Kelley ◽  
N. Curtis Peterson ◽  
G Stanley Howell

The loss of container-grown nursery stock during winter months may be due to lack of root hardiness when exposed to cold temperatures. After Euonymus alatus `Compactus', Weigela florida `Java Red', and Hibiscus syriacus `Paeonyflora' reached midwinter hardiness, replicates of each cultivar were subjected to 12 hours of 21°C followed by 12 hours of 0°C each 24-hour period for up to 16 days. Controlled temperature freezing was conducted after each 48-hour period, with temperatures ranging from –6 to –27°C to determine the level of root hardiness. Plants were placed in a greenhouse environment to observe post-stress performance. Weigela was the most cold hardy, followed by Euonymus and Hibiscus. In general, the early accumulation of warming temperatures decreased root hardiness and delayed budbreak, with a noticeable loss of vigor. Results of this research will be presented.


HortScience ◽  
2011 ◽  
Vol 46 (8) ◽  
pp. 1070-1078 ◽  
Author(s):  
Rajeev Arora ◽  
Lisa J. Rowland

Freezing is a major environmental stress during an annual cycle of overwintering, temperate-zone perennials. The timing and extent of seasonal cold acclimation (development of freezing tolerance in the fall) and deacclimation (loss of acquired freezing tolerance in response to warm temperatures) are of critical importance for winter survival, particularly in view of the climate change, i.e., unpredictable extreme weather occurrences. For example, plants may acclimate inadequately if exposed to a milder fall climate and may be damaged by sudden frosts. Alternatively, they may deacclimate prematurely as a result of unseasonable, midwinter warm spells and be injured by the cold that follows. Efficient cold acclimation ability, high deacclimation resistance, and efficient reacclimation capacity are, therefore, important components of winter survival in overwintering perennials. These components should be evaluated separately for a successful breeding program focused on improving winter-hardiness. Another layer of complexity that should be carefully considered is that endodormant status (shallow versus deep) of the reproductive/vegetative apices can significantly impact these components of winter-hardiness. Winter survival, especially by woody evergreens, requires tolerance of light stress, which can result in photo-oxidative damage at cold temperatures when biochemistry of photosynthesis is somewhat compromised but light harvesting is unaffected. Accumulation of Elips (early light-induced proteins) in overwintering evergreens during winter represents a relatively novel strategy to cope with such light stress, and investigations on the precise cellular mechanism and genetic control of this strategy deserve research in the future. Investigations into the mechanisms for cold acclimation use laboratory-based, artificial acclimation protocols that often do not closely approximate conditions that plants are typically exposed to in nature. To draw meaningful conclusions about the biology of cold acclimation and ultimately improve freeze resistance under field conditions, one should also include in cold acclimation regimens parameters such as exposure to subfreezing temperatures and realistic diurnal temperature fluctuations and light levels to simulate natural conditions. One of the main objectives of this article is to highlight two areas of research that we believe are important in the context of plant cold-hardiness but, so far, have not received much attention. These are: 1) to understand the biology of deacclimation resistance and reacclimation capacity, two important components of freeze-stress resistance (winter-hardiness) in woody perennials; and 2) to investigate the cellular basis for various strategies used by broad-leaved evergreens for photoprotection during winter. Our emphasis, in this context, is on a family of proteins, called Elips. The second objective of this article is to draw attention of the cold-hardiness research community to the importance of using realistic cold acclimation protocols in controlled environments that will approximate natural/field conditions to be better able to draw meaningful conclusions about the biology of cold acclimation and ultimately improve freeze resistance. Results from our work with Rhododendron (deciduous azaleas and broad-leaved evergreens), blueberry, and that of other researchers are discussed to support these objectives.


HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 453d-453
Author(s):  
A.M. Shirazi ◽  
E.A. HedBorn ◽  
S.A. Mehaffey ◽  
A.S. Merritt

The winter hardiness of many groundcover cultivars in northern Illinois is not well-known. This study was designed to evaluate the survival of 172 plants used in the groundcover path at The Morton Arboretum. Once a month, from Sept.1997 to Jan. 1998, the plants chosen for this study were visually evaluated and their vitality rated on a scale of 1 to 5 (1 = alive, 5 = dead). All nine cultivars of Euonymus fortunei remained virtually unchanged throughout the study period. Among six cultivars of Hedera helix, only `Gold Heart' showed minor damage in November. Nine Heuchera were evaluated and all exhibited excellent resistance to cold temperatures. While all the Pulmonarias studied showed some cold damage by November, `Bielefeld Pink', `Little Blue', `Roy Davidson', Pulmonaria longifolia var. cevennensis, and Pulmonaria officinalis `Sissinghurst White' fared the best for the longest period of time. Five cultivars of Pachysandra terminalis were included in this study. None had significant damage until November, and then only rated a “2.” Of the eight Ajuga evaluated, Ajuga pyramidalis `Metallica Crispa', and Ajuga reptans `Braunherz', `Catlin's Giant', and `Gaiety', exhibited the best cold resistance. Four Polygonums varied widely in their response to cold temperatures, but all showed signs of severe damage in November. Polygonum `Border Jewel' exhibited the best tolerance, rating a “1” in October, but in November it was given a rating of “4.” Their recovery in spring will be compared.


1979 ◽  
Vol 57 (9) ◽  
pp. 997-999 ◽  
Author(s):  
R. J. Reader

In laboratory freezing trials, cold hardiness of six types of bog ericad flowers differed significantly (i.e., Chamaedaphne calyculata > Andromeda glaucophylla > Kalmia polifolia > Vaccinium myrtilloides > Ledum groenlandicum > Vaccinium macrocarpon) at air temperatures between −4 and −10 °C but not at temperatures above −2 °C. At the Luther Marsh bog in southern Ontario, low temperatures (−3 to −7 °C) would select against May flowering by the least cold hardy ericads. Availability of pollinators, on the other hand, would encourage May flowering by the most cold hardy species. Presumably, competition for insect pollinators has promoted the diversification of bog ericad flowering peaks, while air temperature, in conjunction with flower cold hardiness, determined the order in which flowering peaks were reached.


Diversity ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 207
Author(s):  
Hana Daneck ◽  
Matthias Benjamin Barth ◽  
Martin Geck ◽  
Anna K. Hundsdoerfer

The spurge hawkmoth Hyles euphorbiae L. (Sphingidae) comprises a remarkable species complex with still not fully resolved taxonomy. Its extensive natural distribution range covers diverse climatic zones. This predestinates particular populations to cope with different local seasonally unfavorable environmental conditions. The ability of the pupae to overcome outer frosty conditions is well known. However, the differences between two main ecotypes (‘euphorbiae’ and ‘tithymali’) in terms of the inherent degree of frost tolerance, its corresponding survival strategy, and underlying mechanism have not been studied in detail so far. The main aim of our study was to test the phenotypic exhibition of pupae (as the relevant life cycle stadia to outlast unfavorable conditions) in response to combined effects of exogenous stimuli, such as daylight length and cooling regime. Namely, we tested the turnout of subitan (with fast development, unadapted to unfavorable conditions) or diapause (paused development, adapted to unfavorable external influences and increased resistance) pupae under different conditions, as well as their mortality, and we measured the super cooling point (SCP) of whole pupae (in vivo) and pupal hemolymph (in vitro) as phenotypic indicators of cold acclimation. Our results show higher cold sensitivity in ‘tithymali’ populations, exhibiting rather opportunistic and short-termed cold hardiness, while ‘euphorbiae’ produces a phenotype of seasonal cold-hardy diapause pupae under a combined effect of short daylight length and continuous cold treatment. Further differences include the variability in duration and mortality of diapause pupae. This suggests different pre-adaptations to seasonal environmental conditions in each ecotype and may indicate a state of incipient speciation within the H. euphorbiae complex.


1997 ◽  
Vol 77 (3) ◽  
pp. 399-420 ◽  
Author(s):  
Pauliina Palonen ◽  
Deborah Buszard

This article gives an overview of the current state of cold hardiness research in fruit crops by reviewing the recently published studies on cold hardiness of both tree fruit and berry crops. Topics discussed include cold hardiness of fruit species, cultivars and different plant organs, biophysical and biochemical aspects of hardiness, evaluation of hardiness, as well as endogenous, cultural and environmental factors affecting cold hardiness in these species. Lack of cold hardiness is a major limiting factor for production of fruit crops in many regions of the world and improved cold hardiness one of the major objectives in numerous breeding programs and research projects. Screening cultivars or selections for cold hardiness is commonly done, and different methods applied to the evaluation of hardiness are discussed. The physical limit of deep supercooling may be a restricting factor for expanding the production of some fruit crops, such as Prunus species and pear. As for biochemical aspects, a relationship between carbohydrates and cold hardiness is most commonly found. Studies have also been made on different hardiness modifying cultural factors including rootstock, crop load, raised beds and application of growth regulators. The latter seems promising for some species. Cold hardiness is an extremely complex phenomenon and understanding different mechanisms involved is critical. Since hardiness is, however, primarily affected by genotype, developing cold-hardy fruit cultivars and effective screening methods for hardiness are essential. Finally, cultural practices may be improved to further enhance hardiness. Key words: Berries, cold hardiness, fruits, small fruits, stress, winter hardiness


2020 ◽  
Vol 40 (7) ◽  
pp. 841-855
Author(s):  
Camilo Villouta ◽  
Beth Ann Workmaster ◽  
Jenny Bolivar-Medina ◽  
Smith Sinclair ◽  
Amaya Atucha

Abstract Plants’ mechanisms for surviving freezing stresses are essential adaptations that allow their existence in environments with extreme winter temperatures. Although it is known that Vaccinium macrocarpon Ait. buds can acclimate in fall and survive very cold temperatures during the winter, the mechanism for survival of these buds is not known. The main objective of this study was to determine which of the two major mechanisms of freezing stress survival, namely, deep supercooling or freeze-induced dehydration, are employed by V. macrocarpon terminal buds. In the present study, no low-temperature exotherms (LTEs) were detected by differential thermal analysis. Furthermore, a gradual reduction of relative liquid water content in the inner portions of buds during magnetic resonance imaging (MRI) scans performed between 0 and −20 °C (where no damage was detected in controlled freezing tests (CFT)) indicates these buds may not deep supercool. The higher ice nucleation activity of outer bud scales and the appearance of large voids in this structure in early winter, in conjunction with the MRI observations, are evidence supportive of a freeze-induced dehydration process. In addition, the presence of tissue browning in acclimated buds as a result of freezing stress was only observed in CFT at temperatures below −20 °C, and this damage gradually increased as test temperatures decreased and at different rates depending on the bud structure. Ours is the first study to collect multiple lines of evidence to suggest that V. macrocarpon terminal buds survive long periods of freezing stress by freeze-induced dehydration. Our results provide a framework for future studies of cold hardiness dynamics for V. macrocarpon and other woody perennial species and for the screening of breeding populations for freezing stress tolerance traits.


1964 ◽  
Vol 96 (4) ◽  
pp. 617-625 ◽  
Author(s):  
A. W. MacPhee

AbstractIn Kings County, Nova Scotia, low temperatures in the coldest nights of winter can differ by as much as 10°F. from one area to another. This has an important bearing on winter survival of some arthropods. Overwintering sites of orchard arthropods range from exposed situations which remain at air temperature to well protected ones on the ground where temperatures rarely go below 20°F. The cold-hardiness of each of 24 species of arthropods was measured: seven were sufficiently cold-hardy to survive any winter conditions in Nova Scotia, five were less cold-hardy but overwinter in well protected sites and twelve had marginal cold-hardiness, their mortality varying with the winter and the locality.


1985 ◽  
Vol 65 (3) ◽  
pp. 487-490 ◽  
Author(s):  
A. E. LIMIN ◽  
J. DVORAK ◽  
D. B. FOWLER

The excellent cold hardiness of rye (Secale cereale L.) makes it a potential source of genetic variability for the improvement of this character in related species. However, when rye is combined with common wheat (Triticum aestivum L.) to produce octaploid triticale (X Triticosecale Wittmack, ABDR genomes), the superior rye cold hardiness is not expressed. To determine if the D genome of hexaploid wheat might be responsible for this lack of expression, hexaploid triticales (ABR genomes) were produced and evaluated for cold hardiness. All hexaploid triticales had cold hardiness levels similar to their tetraploid wheat parents. Small gains in cold hardiness of less than 2 °C were found when very non-hardy wheats were used as parents. This similarity in expression of cold hardiness in both octaploid and hexaploid triticales indicates that the D genome of wheat is not solely, if at all, responsible for the suppression of rye cold hardiness genes. There appears to be either a suppressor(s) of the rye cold hardiness genes on the AB genomes of wheat, or the expression of diploid rye genes is reduced to a uniform level by polyploidy in triticale. The suppression, or lack of expression, of rye cold hardiness genes in a wheat background make it imperative that cold-hardy wheats be selected as parents for the production of hardy triticales.Key words: Triticale, Secale, winter wheat, cold hardiness, gene expression


2008 ◽  
Vol 38 (6) ◽  
pp. 1526-1535 ◽  
Author(s):  
Douglass F. Jacobs ◽  
Anthony S. Davis ◽  
Barrett C. Wilson ◽  
R. Kasten Dumroese ◽  
Rosa C. Goodman ◽  
...  

We tested effects of shortened day length during nursery culture on Douglas-fir ( Pseudotsuga menziesii var. menziesii (Mirb.) Franco) seedling development at dormancy release. Seedlings from a 42°N source were grown either under ambient photoperiods (long-day (LD)) or with a 28 day period of 9 h light : 15 h dark photoperiods (short-day (SD)). Seedlings were periodically removed from freezer storage from January to May. Sensitivity of plant tissues to cold temperatures was investigated via electrolyte leakage at nine test temperatures ranging from 2 to –40 °C. New root growth was assessed with rhizosphere temperatures of 10, 15, 20, and 25 °C. From 2 to –13 °C, there was no difference between treatments in cold hardiness. However, at or below –18 °C, LD seedlings exhibited higher indices of damage than SD seedlings. The LT50 (temperature at which 50% cell electrolyte leakage occurred) was consistently lower for SD than LD seedlings. Rhizosphere temperature differentially influenced new root proliferation: LD seedlings had greater new root production than SD seedlings at 20 °C, whereas the opposite response was detected at 10 °C. Our results confirm photoperiod sensitivity of Douglas-fir sources from relatively low (i.e., <45°N) latitudes. Increased spring cold hardiness and greater rooting at lower rhizosphere temperatures may improve field performance potential of SD-treated seedlings.


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