Search

Differential thermal analysis (DTA) is a technique commonly used to evaluate the cold hardiness of plant organs that supercool as a means for cold survival. The aim of this study was to evaluate the effect of different pretest bud storage conditions, cooling rates, and bud excision techniques on dormant sweet cherry flower bud low temperature exotherms (LTEs) measured using DTA. Furthermore, this study compared cold hardiness estimates made using DTA and controlled freezing tests. We determined that buds stored at warmer temperatures (12.5 °C and room temperature) for 2–6 h prior to DTA or transported to the lab in a moist environment underwent biologically relevant changes in their apparent sensitivity to cold, as indicated by LTEs produced at warmer temperatures. The DTA cooling rate also significantly affected LTEs, with faster cooling resulting in the production of LTEs at warmer temperatures. Overall, LTEs were comparable among buds with varying amounts of plant material remaining attached to the bud base. It is important to note that the region directly subtending the primordia was always left intact on the buds being compared. This study demonstrated that overall, DTA and controlled freezing tests resulted in comparable measures of cold hardiness. The findings presented in this study are pertinent to researchers interested in conducting cold hardiness measurements in sweet cherry and highlight that consistency in DTA pretest conditions and bud preparation are required to achieve reliable LTE results that can be compared among studies. [ABSTRACT FROM AUTHOR]

Global climate change, which is connected to global warming and changes in weather patterns, affects various parts of the environment, including the growth/development of plants. Generally, a number of plant species are capable of acquiring tolerance to frost after exposure to cold (in the cold-acclimation/cold-hardening process). In the last few decades, there have been more and more frequent periods of higher temperatures—warm periods that, e.g., break down the process of cold acclimation. This generates deacclimation, which could stimulate growth and lower frost tolerance in plants. Generally, deacclimation causes the reversal of changes induced by cold acclimation (i.e., in concentration of sugars, accumulation of protective proteins, or hormonal homeostasis). Unlike cold acclimation, the phenomenon of deacclimation has been less studied. The aim of this article was (1) to briefly describe the problem of deacclimation, with more attention being paid to its significance for economically important winter crop species, (2) to review and characterize the physiological-biochemical changes that are induced in plants by deacclimation, and (3) to discuss the possibilities of detecting deacclimation earlier in order to counteract its effects on crops. [ABSTRACT FROM AUTHOR]

Here, two field-grown grape species including Vitis amurensis Rupr. ‘Shuangfeng’ and V. riparia × V. labrusca ‘Beta’ showed different survival capabilities after overwintering. Their shoots’ cold hardiness and associated physiological changes were analyzed during seasonal cold acclimation and deaaclimation to illuminate response mechanisms on low temperature. The fluctuations of cold hardiness were synchronized in the two species, but ‘Shuangfeng’ had a higher tolerance than ‘Beta’ to cold stress, which was consistent with the field performance. Leaves and shoots of ‘Shuangfeng’ reddened, responds quickly to the natural low temperature, while those of ‘Beta’ remained green during the same period. Perhaps owing to variations in the carbohydrate accumulations in different colored leaves, so the freezing tolerance of ‘Shuangfeng’ correlated with total soluble sugars in the phloem, while the starch in the xylem and phloem determined the ‘Beta’s tolerance. The timing and types of the accumulated carbohydrates may be responsible for the difference in the water status, energy accumulation and cold hardiness between the two grape species. [ABSTRACT FROM AUTHOR]

In areas with heavy snowfall in Hokkaido, grapevines overwinter under the snow. Recently, it was suggested that winter buds of several grape cultivars grown in cold areas deacclimate at 0°C. Because the temperature in the snow is maintained at high subzero ranges, deacclimation of grape buds in areas with heavy snowfall might occur earlier than expected. In this study, we investigated the relationship between the temperature in the snow and freezing resistance of grape buds when grape canes were buried in the snow for 1 week. Compared with the outside air temperature, the temperature in the snow was fairly stable. The means were approximately -4°C and -3°C in middle and late February, 2023 in a vineyard in the Tokachi region, respectively. In these temperature conditions, the freezing resistance of winter buds of a cold-hardy interspecific hybrid grape cultivar 'Yamasachi' did not decrease significantly, suggesting deacclimation of the winter buds hardly occurred at lower temperatures than -3°C. It was reported that cold-hardy interspecific hybrid grapes tend to deacclimate earlier than European cultivars. Because European cultivars are mainly grown in areas with heavy snowfall in Hokkaido, significant decrease of freezing resistance of grape buds might not occur under the snow cover in such areas. [ABSTRACT FROM AUTHOR]

The aim of the current work was to characterize disturbances in the hormonal balance and changes in the accumulation of the protective heat shock proteins (HSP) as a result of deacclimation in a few cultivars of oilseed rape. Samples for both analyses were collected from plants that had not been acclimated (before cold acclimation—control), cold acclimated (at 4 °C d/n, three weeks) and then deacclimated at 16/9 °C d/n (one week). The tested hormones included abscisic acid, jasmonic acid, salicylic acid, gibberellins, auxins and cytokinins (including their precursors, intermediates and conjugates). Unambiguous results were obtained for a stress hormone, abscisic acid, whose concentration increased in the leaves of all of the tested cultivars during cold acclimation while it strongly decreased during deacclimation. Deacclimation resulted also in an elevated level of the typical growth hormones. As a result of cold acclimation, the accumulation of protective proteins such as cytoplasmic HSP70 and HSP90 increased in three of the four tested cultivars. The HSP content most often decreased in the deacclimated plants compared to the cold-acclimated plants. The hormonal and protein changes are discussed relative to the frost tolerance changes of the tested cultivar. [ABSTRACT FROM AUTHOR]

Abscisic acid (ABA) plays crucial regulatory roles in cold acclimation and deacclimation of grapevine, making it a potential tool to be utilized in vineyards for the acquisition of preferred phenotypes in winter and spring. To understand the function of ABA, we conducted experiments during cold acclimation and deacclimation and evaluated the impact of exogenous ABA on the grapevine transcriptome. RNA-seq data were collected periodically hours or days after ABA treatment. Transcriptomic data were analyzed using principal component analysis (PCA), hierarchical clustering, unsupervised weighed gene co-expression network analysis (WGCNA), contrast-based differentially expressed genes (DEGs) identification and pre-ranked gene set enrichment analysis (GSEA). Our results suggest that ABA functions differently during cold acclimation and deacclimation by selectively regulating key pathways including auxin/indole acetic acid (IAA) metabolism, galactose metabolism and ribosome biogenesis. We also identified the activation of several apparent negative feedback systems that regulated ABA-induced transcriptomic changes, suggesting the existence of a balancing system in response to excessive ABA. This balancing systems potentially eliminates the long-term negative effect on grapevine growing from using ABA in the field. These findings advance our understanding about the regulation of grapevine physiology during dormancy and supports the potential of applying ABA as a cultural practice to mitigate cold injury in winter and spring.

Chronic hypoxia (CH) during postnatal development attenuates the hypoxic ventilatory response (HVR) in mammals, but there are conflicting reports on whether this plasticity is permanent or reversible. This study tested the hypothesis that CH-induced respiratory plasticity is reversible in neonatal rats and investigated whether the initial plasticity or recovery differs between sexes. Rat pups were exposed to 3 d of normobaric CH (12 % O 2) beginning shortly after birth. Ventilation and metabolic CO 2 production were then measured in normoxia and during an acute hypoxic challenge (12 % O 2) immediately following CH and after 1, 4–5, and 7 d in room air. CH pups hyperventilated when returned to normoxia immediately following CH, but normoxic ventilation was similar to age-matched control rats within 7 d after return to room air. The early phase of the HVR (minute 1) was only blunted immediately following the CH exposure, while the late phase of the HVR (minute 15) remained blunted after 1 and 4–5 d in room air; recovery appeared complete by 7 d. However, when normalized to CO 2 production, the late phase of the hypoxic response recovered within only 1 d. The initial blunting of the HVR and subsequent recovery were similar in female and male rats. Carotid body responses to hypoxia (in vitro) were also normal in CH pups after approximately one week in room air. Collectively, these data indicate that ventilatory and metabolic responses to hypoxia recover rapidly in both female and male neonatal rats once normoxia is restored following CH. • 3 days of chronic hypoxia (CH) elicited respiratory plasticity in neonatal rats. • Normoxic ventilation remained elevated for several days after return to room air. • Hypoxic ventilatory response (HVR) was blunted by CH but recovered within one week. • Recovery of HVR in male rat pups contrasts with studies showing lifelong blunting. • Plasticity after postnatal CH resembled ventilatory acclimatization in adult rats. [ABSTRACT FROM AUTHOR]

The goal of this research was to evaluate resistance of apple rootstocks to late winter deacclimation during a 2-day exposure to warm temperatures in Maine. We measured the cold temperature tolerance of xylem, phloem, and cambium from 0 to −40 °C in 1- and 2-year-old shoot pieces from apple rootstock cultivars and advanced selections ‘M.9 T337’ (M.9), ‘M.7 EMLA’ (M.7), ‘Budagovsky 9’ (B.9), ‘Geneva® 41’ (G.41), ‘Geneva 30’ (G.30), ‘Geneva 935’ (G.935), ‘Geneva 814’ (G.814), G.4013, G.5257, and Vineland 6 (V.6) after a 2-day exposure to warm (22 °C) or cold (2 to 4 °C) temperatures. Injury was measured on a 0 to 10 rating scale based on percentage of discolored cross-sectional xylem and phloem, and cambial length and circumference with brown discoloration, with 0 indicating no browning and 10 indicating browning in the entire tissue. Injury was also measured as intensity of browning on a scale of 0 (no browning) to 5 (dark brown to black). The weighted averages of the two ratings were used to calculate an index of browning. Genotypic variation occurred in the degree of deacclimation, which ranged from none to as much as 15 °C loss in hardiness. Two genotypes, ‘G.41’ and ‘M.9’, showed little change in hardiness in both years they were tested. Two genotypes, G.4013 and ‘G.814’, lost substantial hardiness in both years and may be vulnerable to late winter freeze-thaw events, but were among the hardiest before deacclimation. ‘G.935’ and G.5257 showed a small loss of hardiness, whereas ‘B.9’ lost hardiness in the cambium, but not the xylem, and V.6 lost hardiness after warm exposure, but showed almost no injury at temperatures as cold as −35 °C. The loss of hardiness of these four genotypes that were tested in only one year should be verified with additional testing because of the potential for yearly variation.

Cold acclimation (CA) is a strategy which plants have evolved to increase freezing tolerance. Global climate change could obstruct CA and raise the probability of winter injury, especially for evergreens. Hence, understanding the regulatory mechanism of CA is crucial to improve freezing tolerance in evergreen plants. A comparative study on a pair of closely related evergreen and deciduous iris species in response to cold through CA was conducive to uncovering and complementing the knowledge of CA. We investigated morphological, physiological and biochemical changes, as well as the expression of associated genes in the functional leaves of both iris species from natural CA to deacclimation. Briefly, fast and strong CA in the evergreen iris might cause early expressions of BAM1, NCED3, GPX6, etc., which leads to strong enzyme activity of starch degradation, abscisic acid biosynthesis and reactive oxygen species scavenging. Additionally, genes belonging to the antioxidant system were mainly induced during deacclimation. These results suggest that interspecies differences in the leaf freezing tolerance of irises are associated with the rate and degree of CA, which activates multiple signaling networks with complex interactions and induces the transcription of cold-responsive genes. Moreover, the ICE–CBF–COR signaling cascade may integrate and initiate diverse cold-responsive pathways during CA of the evergreen iris. The findings of this study provide valuable insight to further research on CA mechanisms and implicate genes which could support breeding strategies in herbaceous perennials under climate changes. [ABSTRACT FROM AUTHOR]

The aim of the current work was to characterize disturbances in the hormonal balance and changes in the accumulation of the protective heat shock proteins (HSP) as a result of deacclimation in a few cultivars of oilseed rape. Samples for both analyses were collected from plants that had not been acclimated (before cold acclimation—control), cold acclimated (at 4 °C d/n, three weeks) and then deacclimated at 16/9 °C d/n (one week). The tested hormones included abscisic acid, jasmonic acid, salicylic acid, gibberellins, auxins and cytokinins (including their precursors, intermediates and conjugates). Unambiguous results were obtained for a stress hormone, abscisic acid, whose concentration increased in the leaves of all of the tested cultivars during cold acclimation while it strongly decreased during deacclimation. Deacclimation resulted also in an elevated level of the typical growth hormones. As a result of cold acclimation, the accumulation of protective proteins such as cytoplasmic HSP70 and HSP90 increased in three of the four tested cultivars. The HSP content most often decreased in the deacclimated plants compared to the cold-acclimated plants. The hormonal and protein changes are discussed relative to the frost tolerance changes of the tested cultivar.

Carbohydrate metabolism affects cold hardiness in overwintering deciduous fruit trees. In this study, we compared the changes in starch and soluble sugar contents, related enzyme activity, and gene expression in the shoots of 'Soomee' (SM) and 'Odoroki' (OD) peach (Prunus persica) trees during cold acclimation (CA) and deacclimation (DA). SM was cold-hardier than OD from December to March based on the LT50 value, the temperature at which 50% injury occurred. During this period, starch contents were significantly lower in SM than in OD, along with higher total amylase activity and related gene expression. In contrast, total soluble sugar contents were significantly higher in SM than in OD, exhibiting a close relationship to cold hardiness. Of the detected soluble sugars, sucrose was predominant and its content was most significantly correlated with cold hardiness. Sucrose contents were significantly higher in SM than in OD from December to March. Fructose and glucose contents in SM, but not in OD, increased during CA and then decreased during DA concurrently with increased acid invertase activity and related gene expression. Raffinose and stachyose were detectable only from November to April. Their contents and related synthase gene expression were also significantly correlated with cold hardiness, but were not significantly different between the two cultivars. During CA, the activities of the enzymes involved in the synthesis of sucrose, raffinose, and stachyose increased with the up-regulation of their related gene expression. During DA, in contrast, the activities of the enzymes involved in the degradation of starch, sucrose, raffinose, and stachyose increased with the up-regulation of their related gene expression. Furthermore, the differential cold hardiness in the shoots of different peach cultivars was associated with the difference in enzyme activities and gene expression, especially of acid invertase, regulating soluble sugar content during CA and DA. [ABSTRACT FROM AUTHOR]

In this work, we studied the influence of cold acclimation (first stage – 8 °С/2 °С for 10 days and second stage – subsequence action of -2 °С for 10 days) and deacclimation (10 °С for 2 days) on the content of soluble carbohydrates and the synthesis of dehydrins in leaves of two variety of winter wheat (Triticum aestivum L.) that are differed in frost resistance. It is detected that the winter wheat of Irkutskaya variety and Pamyat variety are differed in the dynamics of accumulation and content of dehydrins in leaves. The most frost resistant Irkutskaya is characterized by a higher content of dehydrins in the leaves during acclimation and deacclimation, compared with the less frost resistant Pamyat.

Climate change has become a topic of increasing significance in viticulture, severely challenged by this issue. Average global temperatures are increasing, but frost events, with a large variability depending on geographical locations, have been predicted to be a potential risk for grapevine cultivation. Grape cold hardiness encompasses both midwinter and spring frost hardiness, whereas the avoidance of spring frost damage due to late budbreak is crucial in cold resilience. Cold hardiness kinetics and budbreak phenology are closely related and affected by bud’s dormancy state. On the other hand, budbreak progress is also affected by temperatures during both winter and spring. Genetic control of bud phenology in grapevine is still largely undiscovered, but several studies have recently aimed at identifying the molecular drivers of cold hardiness loss and the mechanisms that control deacclimation and budbreak. A review of these related traits and their variability in different genotypes is proposed, possibly contributing to develop the sustainability of grapevine production as climate-related challenges rise.

Climate change has become a topic of increasing significance in viticulture, severely challenged by this issue. Average global temperatures are increasing, but frost events, with a large variability depending on geographical locations, have been predicted to be a potential risk for grapevine cultivation. Grape cold hardiness encompasses both midwinter and spring frost hardiness, whereas the avoidance of spring frost damage due to late budbreak is crucial in cold resilience. Cold hardiness kinetics and budbreak phenology are closely related and affected by bud's dormancy state. On the other hand, budbreak progress is also affected by temperatures during both winter and spring. Genetic control of bud phenology in grapevine is still largely undiscovered, but several studies have recently aimed at identifying the molecular drivers of cold hardiness loss and the mechanisms that control deacclimation and budbreak. A review of these related traits and their variability in different genotypes is proposed, possibly contributing to develop the sustainability of grapevine production as climate-related challenges rise. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Agricultural Science & Technology (1008-0864) is the property of Journal of Agricultural Science & Technology and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Grapevine sustainability is impacted by the timing of dormancy initiation and freezing tolerance in fall and winter and chilling fulfillment and bud break in the spring. These traits have genetic and local temperature contributing factors; therefore, this study was undertaken to develop an understanding of these characteristics in four recently developed cold climate cultivars. The cold hardiness and chilling fulfillment profiles were monitored in Brianna, Frontenac gris, La Crescent and Marquette using differential thermal analyses and bud break assays. Bud cold hardiness of all cultivars increased with the declining temperatures from November through February, after which the buds began to lose freezing tolerance. There were significant differences in cold hardiness and chilling fulfillment between cultivars during the endodormant and ecodormant period of winter. Marquette had the greatest freezing tolerance from early November through midwinter suggesting it has potential as a sentinel cultivar for comparisons of new cold climate selections. Brianna was slower to acclimate and deacclimated more rapidly than the other cultivars. Chilling fulfillment under natural field or constant 4 °C conditions showed no main effect differences for chilling accumulation condition; however, there were significant cultivar, condition, and time point interactions, indicating the cultivars differed in chilling fulfillment responses. [ABSTRACT FROM AUTHOR]

Tolerance to deacclimation is an important physiological feature in plants in the face of global warming, which is resulting in incidents of increases in winter temperatures. The aim of the work was to explore how disturbances in the signalling and synthesis of brassinosteroids (BR) influence the deacclimation tolerance of barley. One group of mutants and their reference cultivars (Bowman and Delisa) was cold-acclimated, deacclimated and then tested for frost tolerance at − 12 °C. After cold acclimation, the second group of plants was additionally exposed to frost (− 6 °C) and then, deacclimated and tested for frost tolerance at − 12 °C. The deacclimated brassinosteroid mutants were characterised by an increased tolerance to frost, and consequently, had a higher tolerance to deacclimation than their wild-type cultivars. The mechanism of this phenomenon may be partly explained by analysing the hormonal homeostasis in the crowns. For all of the tested plants, a characteristic feature of the response to the deacclimation phase was an increase in the growth-promoting hormones and abscisic acid compared to the cold acclimation phase. The increase was greater in the BR-deficient (BW084) and BR-insensitive (BW312) mutants compared to the Bowman reference cultivar. Mutant 522DK was characterised by a lower accumulation of total cytokinins and gibberellins as well as an enhanced auxin deactivation compared to the Delisa. In the second group, when the plants were exposed to a temperature of − 6 °C before deacclimation, the hormonal homeostasis was further altered in both the mutants and reference cultivars, but all of the mutants had a higher frost tolerance than the wild types. [ABSTRACT FROM AUTHOR]

Abstract Background During low temperature exposure, temperate plant species increase their freezing tolerance in a process termed cold acclimation. This is accompanied by dampened oscillations of circadian clock genes and disrupted oscillations of output genes and metabolites. During deacclimation in response to warm temperatures, cold acclimated plants lose freezing tolerance and resume growth and development. While considerable effort has been directed toward understanding the molecular and metabolic basis of cold acclimation, much less information is available about the regulation of deacclimation. Results We report metabolic (gas chromatography-mass spectrometry) and transcriptional (microarrays, quantitative RT-PCR) responses underlying deacclimation during the first 24 h after a shift of Arabidopsis thaliana (Columbia-0) plants cold acclimated at 4 °C back to warm temperature (20 °C). The data reveal a faster response of the transcriptome than of the metabolome and provide evidence for tightly regulated temporal responses at both levels. Metabolically, deacclimation is associated with decreasing contents of sugars, amino acids, glycolytic and TCA cycle intermediates, indicating an increased need for carbon sources and respiratory energy production for the activation of growth. The early phase of deacclimation also involves extensive down-regulation of protein synthesis and changes in the metabolism of lipids and cell wall components. Hormonal regulation appears particularly important during deacclimation, with extensive changes in the expression of genes related to auxin, gibberellin, brassinosteroid, jasmonate and ethylene metabolism. Members of several transcription factor families that control fundamental aspects of morphogenesis and development are significantly regulated during deacclimation, emphasizing that loss of freezing tolerance and growth resumption are transcriptionally highly interrelated processes. Expression patterns of some clock oscillator components resembled those under warm conditions, indicating at least partial re-activation of the circadian clock during deacclimation. Conclusions This study provides the first combined metabolomic and transcriptomic analysis of the regulation of deacclimation in cold acclimated plants. The data indicate cascades of rapidly regulated genes and metabolites that underlie the developmental switch resulting in reduced freezing tolerance and the resumption of growth. They constitute a large-scale dataset of genes, metabolites and pathways that are crucial during the initial phase of deacclimation. The data will be an important reference for further analyses of this and other important but under-researched stress deacclimation processes.

Chromatin regulation ensures stable repression of stress-inducible genes under non-stress conditions and transcriptional activation and memory of stress-related genes after stress exposure. However, there is only limited knowledge on how chromatin genes are regulated at the transcriptional and post-transcriptional level upon stress exposure and relief from stress. We reveal that the repressive modification histone H3 lysine 27 trimethylation (H3K27me3) targets genes which are quickly activated upon cold exposure, however, H3K27me3 is not necessarily lost during a longer time in the cold. In addition, we have set-up a quantitative reverse transcription polymerase chain reaction-based platform for high-throughput transcriptional profiling of a large set of chromatin genes. We find that the expression of many of these genes is regulated by cold. In addition, we reveal an induction of several DNA and histone demethylase genes and certain histone variants after plants have been shifted back to ambient temperature (deacclimation), suggesting a role in the memory of cold acclimation. We also re-analyze large scale transcriptomic datasets for transcriptional regulation and alternative splicing (AS) of chromatin genes, uncovering an unexpected level of regulation of these genes, particularly at the splicing level. This includes several vernalization regulating genes whose AS may result in cold-regulated protein diversity. Overall, we provide a profiling platform for the analysis of chromatin regulatory genes and integrative analyses of their regulation, suggesting a dynamic regulation of key chromatin genes in response to low temperature stress.

Chromatin regulation ensures stable repression of stress-inducible genes under non-stress conditions and transcriptional activation and memory of stress-related genes after stress exposure. However, there is only limited knowledge on how chromatin genes are regulated at the transcriptional and post-transcriptional level upon stress exposure and relief from stress. We reveal that the repressive modification histone H3 lysine 27 trimethylation (H3K27me3) targets genes which are quickly activated upon cold exposure, however, H3K27me3 is not necessarily lost during a longer time in the cold. In addition, we have set-up a quantitative reverse transcription polymerase chain reaction-based platform for high-throughput transcriptional profiling of a large set of chromatin genes. We find that the expression of many of these genes is regulated by cold. In addition, we reveal an induction of several DNA and histone demethylase genes and certain histone variants after plants have been shifted back to ambient temperature (deacclimation), suggesting a role in the memory of cold acclimation. We also re-analyze large scale transcriptomic datasets for transcriptional regulation and alternative splicing (AS) of chromatin genes, uncovering an unexpected level of regulation of these genes, particularly at the splicing level. This includes several vernalization regulating genes whose AS may result in cold-regulated protein diversity. Overall, we provide a profiling platform for the analysis of chromatin regulatory genes and integrative analyses of their regulation, suggesting a dynamic regulation of key chromatin genes in response to low temperature stress. [ABSTRACT FROM AUTHOR]

Temperate and boreal plants show natural low temperature acclimation during autumn. This cold acclimation process results in increased freezing tolerance. Global climate change is leading to increasing spring and autumn temperatures that can trigger deacclimation and loss of freezing tolerance, making plants susceptible to both late-autumn and late-spring freezing events. In particular, spring frosts can have devastating effects on whole ecosystems and can significantly reduce the yield of crop plants. Although the timing and speed of deacclimation are clearly of crucial importance for plant winter survival, the molecular basis of this process is still largely unknown. The regulation of deacclimation is, however, not only related to freezing tolerance, but also to the termination of dormancy, and the initiation of growth and development. In this paper, we provide an overview of what is known about deacclimation in both woody and herbaceous plants. We use publicly available transcriptome data to identify a core set of deacclimation-related genes in Arabidopsis thaliana that highlight physiological determinants of deacclimation, and suggest important directions for future research in this area. [ABSTRACT FROM AUTHOR]

Grapevine sustainability is impacted by the timing of dormancy initiation and freezing tolerance in fall and winter and chilling fulfillment and bud break in the spring. These traits have genetic and local temperature contributing factors; therefore, this study was undertaken to develop an understanding of these characteristics in four recently developed cold climate cultivars. The cold hardiness and chilling fulfillment profiles were monitored in Brianna, Frontenac gris, La Crescent and Marquette using differential thermal analyses and bud break assays. Bud cold hardiness of all cultivars increased with the declining temperatures from November through February, after which the buds began to lose freezing tolerance. There were significant differences in cold hardiness and chilling fulfillment between cultivars during the endodormant and ecodormant period of winter. Marquette had the greatest freezing tolerance from early November through midwinter suggesting it has potential as a sentinel cultivar for comparisons of new cold climate selections. Brianna was slower to acclimate and deacclimated more rapidly than the other cultivars. Chilling fulfillment under natural field or constant 4 °C conditions showed no main effect differences for chilling accumulation condition; however, there were significant cultivar, condition, and time point interactions, indicating the cultivars differed in chilling fulfillment responses.

Climate changes, which result in the occurrence of periods with relatively high temperatures during the winter, can lead to the deacclimation of cold-hardened plants and cause problems with their winter survival. The aim of these studies was to investigate the physiological changes (photosynthesis and water relations including aquaporin expression) that accompany deacclimation process in the economically important winter oilseed rape plants. The effect of deacclimation on frost tolerance was also estimated for two tested cultivars: semi-dwarf and plants of a normal height. After cold acclimation at 4 °C (compared to the unacclimated control) the typical changes that accompany cold acclimation such as an increase in the content of water-soluble sugars or a lower water content in the leaves, which lead to an increased frost tolerance, were observed. Deacclimation partially or completely reversed these changes, which resulted in a decreased frost tolerance that was accompanied by a decrease in the content of sugars and an increase of the osmotic potential. The chemical composition of the leaves, which was measured using FT-Raman spectroscopy also clearly confirmed the metabolic differences between the cold-acclimated and deacclimated plants. The plants were significantly different in regard to the content of the various pigments as well as fatty acids and polysaccharides. The phenomenon of a deacclimation-induced decrease in aquaporin PIP1 accumulation, which was accompanied by unchanged PIP1 transcript accumulation, will be discussed in the aspects of the water relations and decreased frost tolerance in deacclimated plants.

Dehydrins are a family of plant proteins that accumulate in response to dehydration stresses, such as low temperature, drought, high salinity, or during seed maturation. We have previously constructed cDNA libraries from Rhododendron catawbiense leaves of naturally non-acclimated (NA; leaf LT50, temperature that results in 50% injury of maximum, approximately −7°C) and cold-acclimated (CA; leaf LT50 approximately −50°C) plants and analyzed expressed sequence tags (ESTs). Five ESTs were identified as dehydrin genes. Their full-length cDNA sequences were obtained and designated as RcDhn 1-5. To explore their functionality vis-à-vis winter hardiness, their seasonal expression kinetics was studied at two levels. Firstly, in leaves of R. catawbiense collected from the NA, CA, and de-acclimated (DA) plants corresponding to summer, winter and spring, respectively. Secondly, in leaves collected monthly from August through February, which progressively increased freezing tolerance from summer through mid-winter. The expression pattern data indicated that RcDhn 1-5 had 6- to 15-fold up-regulation during the cold acclimation process, followed by substantial down-regulation during deacclimation (even back to NA levels for some). Interestingly, our data shows RcDhn 5 contains a histidine-rich motif near N-terminus, a characteristic of metal-binding dehydrins. Equally important, RcDhn 2 contains a consensus 18 amino acid sequence (i.e., ETKDRGLFDFLGKKEEEE) near the N-terminus, with two additional copies upstream, and it is the most acidic (pI of 4.8) among the five RcDhns found. The core of this consensus 18 amino acid sequence is a 11-residue amino acid sequence (DRGLFDFLGKK), recently designated in the literature as the F-segment (based on the pair of hydrophobic F residues it contains). Furthermore, the 208 orthologs of F-segment-containing RcDhn 2 were identified across a broad range of species in GenBank database. This study expands our knowledge about the types of F-segment from the literature-reported single F-segment dehydrins (FSKn) to two or three F-segment dehydrins: Camelina sativa dehydrin ERD14 as F2S2Kn type; and RcDhn 2 as F3SKn type identified here. Our results also indicate some consensus amino acid sequences flanking the core F-segment in dehydrins. Implications for these cold-responsive RcDhn genes in future genetic engineering efforts to improve plant cold hardiness are discussed.

Significant advances have been made in our understanding of the regulation of cold hardiness. The existence of numerous biophysical and biochemical adaptive mechanisms in perennial woody plants and the complexity their regulation has made the development of methods for managing and improving cold hardiness in perennial woody plants has been very difficult. This may be partially attributed to viewing cold hardiness as a single dimensional response, rather than as a complex phenomenon, involving different mechanisms (avoidance and tolerance), different stages (mid-winter vs. late winter), and having an intimate overlap with the genetic regulation of dormancy. In particular separating the molecular regulation of cold hardiness from growth processes has been challenging. ICE and C-repeat binding factor (CBF), transcription factors (Inducer of CBF expression and CRT-binding factor) have been shown to be an important aspect in the regulation of cold-induced gene expression. Evidence has emerged, however, that they are also intimately involved in the regulation of growth, flowering, dormancy, and stomatal development. This evidence includes the presence of CBF binding motifs in genes regulating these processes, or through cross-talk between the pathways that regulate them. Recent changes in climate that have resulted in erratic episodes of unseasonal warming followed by more seasonal patterns of low temperatures has also highlighted the need to better understand the genetic and molecular regulation of deacclimation, a topic of research that is only more recently being addressed. Environmentally-induced epigenetic regulation of stress responses and seasonal processes such as cold acclimation, deacclimation, and dormancy have been documented but are still poorly understood. Advances in the ability to efficiently generate large DNA and RNA datasets and genetic transformation technologies have greatly increased our ability to explore the regulation of gene expression and explore genetic diversity. Greater knowledge of the interplay between epigenetic and genetic regulation of cold hardiness, along with the application of advanced genetic analyses, such as genome-wide-association-studies (GWAS), are needed to develop strategies for addressing the complex processes associated with cold hardiness in woody plants. A cautionary note is also indicated regarding the time-scale needed to examine and interpret plant response to freezing temperatures if progress is to be made in developing effective approaches for manipulating and improving cold hardiness.

Vitis vinifera is mainly cultivated in temperate areas, where seasons are well defined and winter conditions might be severe. To survive under these conditions during the dormant season, grapevines sense environmental parameters to trigger different protective mechanisms that lead to cold hardiness (CH). Crop yield and sustainability will be determined according to the level of CH reached in each organ. Moreover, different cultivars of V. vinifera exhibit different behavior throughout the dormant season, attaining a different status of CH. However, there is scarce information concerning how the same cultivar behaves under contrasting thermal environments. The aim of our research was to unveil how CH varies in trunks of the same cultivar under two contrasting environments and define which are the main thermal and biochemical parameters involved in this process. We submitted 2-year old plants of the same clone of cv. Malbec to two different thermal conditions: natural winter (control) and artificially warm winter (treatment). CH status, thermal and biochemical parameters in trunks were measured periodically over the dormant season, and this experiment was repeated for three years. Our results suggest that grapevine trunks subjected to a different environment reach dissimilar CH status, except at the end of winter. In addition, we determined that daily minimum temperature is the main thermal parameter that drives changes in CH. Also, we found that the total soluble sugars have the greatest relative weight in determining the CH compared with the other compounds evaluated. These results have practical implications in the establishment of vineyards for new growing regions. Moreover, with rising minimum temperature predicted by climate change scenarios, grapevines may be more vulnerable to cold events during the dormant season. [ABSTRACT FROM AUTHOR]

Significant advances have been made in our understanding of the regulation of cold hardiness. The existence of numerous biophysical and biochemical adaptive mechanisms in perennial woody plants and the complexity their regulation has made the development of methods for managing and improving cold hardiness in perennial woody plants has been very difficult. This may be partially attributed to viewing cold hardiness as a single dimensional response, rather than as a complex phenomenon, involving different mechanisms (avoidance and tolerance), different stages (mid-winter vs. late winter), and having an intimate overlap with the genetic regulation of dormancy. In particular separating the molecular regulation of cold hardiness from growth processes has been challenging. ICE and C-repeat binding factor (CBF), transcription factors (Inducer of CBF expression and CRT-binding factor) have been shown to be an important aspect in the regulation of cold-induced gene expression. Evidence has emerged, however, that they are also intimately involved in the regulation of growth, flowering, dormancy, and stomatal development. This evidence includes the presence of CBF binding motifs in genes regulating these processes, or through cross-talk between the pathways that regulate them. Recent changes in climate that have resulted in erratic episodes of unseasonal warming followed by more seasonal patterns of low temperatures has also highlighted the need to better understand the genetic and molecular regulation of deacclimation, a topic of research that is only more recently being addressed. Environmentally-induced epigenetic regulation of stress responses and seasonal processes such as cold acclimation, deacclimation, and dormancy have been documented but are still poorly understood. Advances in the ability to efficiently generate large DNA and RNA datasets and genetic transformation technologies have greatly increased our ability to explore the regulation of gene expression and explore genetic diversity. Greater knowledge of the interplay between epigenetic and genetic regulation of cold hardiness, along with the application of advanced genetic analyses, such as genome-wide-association-studies (GWAS), are needed to develop strategies for addressing the complex processes associated with cold hardiness in woody plants. A cautionary note is also indicated regarding the time-scale needed to examine and interpret plant response to freezing temperatures if progress is to be made in developing effective approaches for manipulating and improving cold hardiness. [ABSTRACT FROM AUTHOR]

Appropriate timing of cold deacclimation is an important component of winter survival of perennial plants, such as trees, in temperate and boreal zones. Recently, concerns about predicted global climate change disturbing deacclimation timing have been increasing. The relationship between ambient temperatures and the manner by which cells' freezing resistance changes is essential for forecasting the timing of deacclimation. In this study, Japanese white birch twigs that underwent deacclimation treatment at a constant temperature of −2, 0, 4, 10, or 20 °C were separated into bark in which cells adapted to subfreezing temperatures by extracellular freezing and xylem in which cells adapted to subfreezing temperatures by deep supercooling, and the freezing resistance of cells in each tissue type was investigated by measuring percentage electrolyte leakage. Birch cells deacclimated in a different manner according to tissue type. Within 7 days under deacclimation treatment, xylem cells decreased their freezing resistance significantly at a high subfreezing temperature (−2 °C). In contrast, bark cells required a temperature of 10 or 20 °C for a detectable decrease in freezing resistance to occur within the same period. At a temperature lower than 0 °C, bark cells did not decrease their freezing resistance, even after 28 days of treatment. The difference in freezing behavior of cells might involve the difference in how deacclimation occurred in bark and xylem cells. [ABSTRACT FROM AUTHOR]

The adaptation of St. Augustinegrass (Stenotaphrum secundatum [Walt.] Kuntze) in the transitional climatic zone of the United States is limited due to a lack of sufficient freeze tolerance. Lab-based freeze testing provides plant breeders with a reliable method for evaluating freeze tolerance. However, in developing protocols for freeze testing it is important to account for the underlying mechanisms that affect freeze tolerance. The objective of this research was to evaluate the effects of cold acclimation and deacclimation on nine St. Augustinegrass genotypes ranging in their levels of freeze tolerance. Results indicated that accounting for all levels of acclimation provided excellent genotype separation across freezing temperatures(- 3 and - 4°C) and supports the hypothesis that the inclusion of acclimation response offers the best overall assessment of freeze tolerance. Genotypes with the highest known field winter survival had also the highest improved freeze tolerance upon cold-acclimation. Other genotypes did not respond to cold-acclimation which resulted in poor survival and recovery rates. Conversely, a significant loss of freeze tolerance was identified when plants were subjected to deacclimation events suggesting that St. Augustinegrass can be negatively affected by rapid temperature changes in the transitional climatic zone leading to increased sensitivity to winterkill. Overall, this study provides preliminary information regarding the complex relationships within and between mechanisms affecting freeze tolerance in St. Augustinegrass. Moreover, results presented here should aid in the development of protocols for selection of freeze tolerant breeding materials under controlled environmental conditions. [ABSTRACT FROM AUTHOR]

Low temperature is a limiting factor that affects vineyard distribution globally. The level of cold hardiness acquired during the dormant season by Vitis sp. is crucial for winter survival. Most research published on this topic has been generated beyond 40° N latitude, where daily mean temperatures may attain injurious levels during the dormant season resulting in significant damage to vines and buds. Symptoms of cold injury have been identified in Mendoza (32-35° S latitude), a Southern Hemisphere wine region characterized by a high thermal amplitude, and warm winds during the dormant season. These symptoms have usually been attributed to drought and/or pathogens, but not to rapid deacclimation followed by injurious low temperatures. Because local information on meteorological events as probable causes is scarce, this research was designed to test and study this assumption by comparing macro-, meso-, and microclimatic data from Mendoza, Argentina, and eastern Washington, USA. The goal was to unveil why freezing damage has occurred in both regions, despite the existence of large climatic differences. Because environmental parameters under field conditions may not correspond to data recorded by conventional weather stations, sensors were installed in vineyards for comparison. Microclimatic conditions on grapevines were also evaluated to assess the most vulnerable portions of field-grown grapevines. In order to better understand if it may be possible to modify cold hardiness status in a short period with high thermal amplitude conditions, deacclimation was induced using a thermal treatment. Hence, despite the fact that Mendoza is warmer, and temperatures are not as extreme as in Washington, high daily thermal amplitude might be partially involved in plant deacclimation, leading to a differential cold hardiness response. [ABSTRACT FROM AUTHOR]

Background: During low temperature exposure, temperate plant species increase their freezing tolerance in a process termed cold acclimation. This is accompanied by dampened oscillations of circadian clock genes and disrupted oscillations of output genes and metabolites. During deacclimation in response to warm temperatures, cold acclimated plants lose freezing tolerance and resume growth and development. While considerable effort has been directed toward understanding the molecular and metabolic basis of cold acclimation, much less information is available about the regulation of deacclimation. Results: We report metabolic (gas chromatography-mass spectrometry) and transcriptional (microarrays, quantitative RT-PCR) responses underlying deacclimation during the first 24 h after a shift of Arabidopsis thaliana (Columbia-0) plants cold acclimated at 4 °C back to warm temperature (20 °C). The data reveal a faster response of the transcriptome than of the metabolome and provide evidence for tightly regulated temporal responses at both levels. Metabolically, deacclimation is associated with decreasing contents of sugars, amino acids, glycolytic and TCA cycle intermediates, indicating an increased need for carbon sources and respiratory energy production for the activation of growth. The early phase of deacclimation also involves extensive down-regulation of protein synthesis and changes in the metabolism of lipids and cell wall components. Hormonal regulation appears particularly important during deacclimation, with extensive changes in the expression of genes related to auxin, gibberellin, brassinosteroid, jasmonate and ethylene metabolism. Members of several transcription factor families that control fundamental aspects of morphogenesis and development are significantly regulated during deacclimation, emphasizing that loss of freezing tolerance and growth resumption are transcriptionally highly interrelated processes. Expression patterns of some clock oscillator components resembled those under warm conditions, indicating at least partial re-activation of the circadian clock during deacclimation. Conclusions: This study provides the first combined metabolomic and transcriptomic analysis of the regulation of deacclimation in cold acclimated plants. The data indicate cascades of rapidly regulated genes and metabolites that underlie the developmental switch resulting in reduced freezing tolerance and the resumption of growth. They constitute a large-scale dataset of genes, metabolites and pathways that are crucial during the initial phase of deacclimation. The data will be an important reference for further analyses of this and other important but under-researched stress deacclimation processes. [ABSTRACT FROM AUTHOR]

• Warm spells reduced frost hardiness in January and March, but not in the late fall. • Buds were more vulnerable to warm spells than needles. • Needles were able to reacclimate from November to January, buds also in March. • Timing of a short-day treatment affected ability of needles to reacclimate in March. • Winter survival of seedlings may be improved by adjusting nursery practices. Warm spells during the late fall and winter are expected to become more frequent in boreal areas due to climate change. The aims of our study were to investigate whether warm spells in the late fall and winter cause deacclimation of Norway spruce (Picea abies (L.) Karst.) seedlings, whether the seedlings are capable of reacclimating in response to a subsequent cold period, and whether a short-day (SD) treatment applied in a nursery affects seedlings' responses to warm and cold spells during the non-growing season (hereafter off-season). During the preceding growing season, the seedlings were treated either with a SD treatment (SD1: June 29 – July 20 or SD2: July 20 – August 10) or were grown in a natural photoperiod. The seedlings were artificially exposed to a 7-day warm spell, followed by a 7-day cold spell on four occasions (late fall: October and November; winter: January and March). The frost hardiness of the needles and the probability of bud damage were determined before and after the warm spell and after the cold spell. The dormancy status of the seedlings was also determined. Warm spells reduced the frost hardiness in needles and increased the probability of bud damage in January and March, but not in October and November. Needles were able to reacclimate from November to January, and buds also in early March. Our results indicate that in boreal areas, warm spells followed by low temperatures may predispose Norway spruce seedlings to freezing damage later in the winter, but not in the late fall. The seedlings that received SD2 treatment retained an ability to reacclimate after a warm spell in March, unlike the seedlings in the other photoperiod treatments, indicating that the responses of seedlings to the fluctuating temperature conditions in winter are affected by the growth conditions during the previous growing season. Therefore, the use and timing of SD treatment may affect survival of fall-planted seedlings and seedlings that overwinter outdoors in nurseries, especially during snowless winters. [ABSTRACT FROM AUTHOR]

Two-year-old seedlings of Norway spruce (Picea abies) during spring deacclimation were subjected to controlled reacclimation by exposure to low temperatures of 4/−3°C (day/night) in a cold room. The highest increase in freezing tolerance (by 7°C) was observed after 12 d of low temperature exposure, when shoot water potential (Ψw shoot) decreased to 0.64 MPa. The process of reacclimation was accompanied by an increase in the phospholipid content of needle cell membranes. This increase applied to total (PL) and individual phospholipids: phosphatidylcholine (PC), phosphatidylglycerol (PG), phosphatidylethanolamine (PE) and phosphatidic acid (PA). After being exposed to the low temperature for 18 d, the seedlings were moved into the open air. This caused deacclimation, with an increase in Ψw shoot to −0.36 MPa and a decrease in the total phospholipid content and freezing tolerance of the needles. Significant correlations were observed between freezing tolerance, the membrane permeability (MP) of the needles and the phospholipid content, Ψw shoot and water content of the needles. The results show that during spring deacclimation, Norway spruce seedlings can be subjected to reacclimation, which is reflected in the phospholipid content, the biophysical changes of the membranes, and the freezing tolerance of the seedlings. During both spring deacclimation and reacclimation, water content in the needles plays a critical role in the cold tolerance of spruce seedlings.

Plants adapted to cold winters go through annual cycles of gain followed by loss of freezing tolerance (cold acclimation and deacclimation). Warm spells during winter and early spring can cause deacclimation, and if temperatures drop, freezing damage may occur. Many plants are vernalized during winter, a process making them competent to flower in the following summer. In winter cereals, a coincidence in the timing of vernalization saturation, deacclimation, downregulation of cold-induced genes, and reduced ability to reacclimate, occurs under long photoperiods and is under control of the main regulator of vernalization requirement in cereals, VRN1, and/or closely linked gene(s). Thus, the probability of freezing damage after a warm spell may depend on both vernalization saturation and photoperiod. We investigated the role of vernalization and the VRN1-region on freezing tolerance of meadow fescue (Festuca pratensis Huds.), a perennial grass species. Two F2 populations, divergently selected for high and low vernalization requirement, were studied. Each genotype was characterized for the copy number of one of the four parental haplotypes of the VRN1-region. Clonal plants were cold acclimated for 2 weeks or vernalized/cold acclimated for a total of 9 weeks, after which the F2 populations reached different levels of vernalization saturation. Vernalized and cold acclimated plants were deacclimated for 1 week and then reacclimated for 2 weeks. All treatments were given at 8 h photoperiod. Flowering response, freezing tolerance and expression of the cold-induced genes VRN1, MADS3, CBF6, COR14B, CR7 (BLT14), LOS2 and IRI1 was measured. We found that some genotypes can lose some freezing tolerance after vernalization and a deacclimation-reacclimation cycle. The relationship between vernalization and freezing tolerance was complex. We found effects of the VRN1-region on freezing tolerance in plants cold acclimated for 2 weeks, timing of heading after 9 weeks of vernalization, expression of COR14B, CBF6 and LOS2 in vernalized and/or deacclimated treatments, and restoration of freezing tolerance during reacclimation. While expression of VRN1, COR14B, CBF6, LOS2 and IRI1 was correlated, CR7 was associated with vernalization requirement by other mechanisms, and appeared to play a role in freezing tolerance in reacclimated plants.

Reductions in snow cover over winter can increase frost exposure in herbaceous plants. Nevertheless, increased exposure to light can potentially increase plant carbon gain during periods of reduced snow cover. We used a combined field and growth chamber experiment to examine how variation in the timing and cumulative duration of light exposure over winter (from one to four 1-week incubation periods at 5 °C) affected subsequent summer growth in the grass Poa pratensis . We also measured net photosynthetic rates, dark respiration and chlorophyll fluorescence both 48 h and 120 h after the start of each winter light exposure period. Summer biomass increased by up to 50% for tillers exposed to light during the final winter incubation period (mid-late February), and the timing of light exposure, not the cumulative duration, was the most influential factor in increasing biomass. In contrast, for tillers incubated in the dark, multiple weeks of incubation at 5 °C resulted in the largest reductions in summer biomass. Leaf-level net photosynthetic rates were highest for the earliest and latest light exposure periods over winter, whereas dark respiration rates were highest in early winter and lowest in late winter. Thus, the gas exchange and biomass results were consistent in revealing that the last period of light exposure promoted the highest carbon gain. Overall, our results reveal that naturally occurring periods of snow melt over winter, or scenarios where snow is removed or melted as an experimental treatment, have the potential to benefit plant growth substantially, as opposed to simply rendering plants vulnerable to frost damage. [ABSTRACT FROM AUTHOR]

This study investigates protocols to evaluate cold tolerance thresholds for overwintering rhizomes of perennial bioenergy grasses. Protocols examined include the temperature at which ice formation occurs, cooling rate, incubation time at the treatment temperature, and the electrolyte leakage ( EL) method to assess mortality thresholds. Using these protocols, we assessed low temperature injury in two genotypes of Miscanthus and two genotypes of lowland switchgrass ( Panicum virgatum). Ice formed near −1 C in the rhizomes cooled at 1 C h−1, but at variable temperatures at cooling rates of 3 and 5 C h−1. Rhizome temperature followed chamber temperature at a cooling rate of 1 C h−1, whereas at faster cooling rates, there was a lag in rhizome temperature that affected treatment exposure time. A 1 C h−1 cooling rate is thus suitable. In rhizomes incubated for <4 h at the treatment temperature, EL values were variable, while there was no change in EL when samples were incubated 4-20 h. A continuous, steady rate of cooling at 1 C h−1 demonstrated the Miscanthus and lowland switchgrass varieties exhibited lethal levels of electrolyte leakage below −6 C. Continuous cooling does not allow for subzero acclimation and reflects thermal tolerances of sampled tissue in situ. To allow for maximum acclimation at subzero temperatures, a prolonged, staged-cooling procedure was adopted. This procedure showed diploid Miscanthus rhizomes could acclimate and adjust their tolerance limit to −12 C, while a triploid Illinois line showed little acclimation and was still killed below −6 C. [ABSTRACT FROM AUTHOR]

Plants adapted to cold winters go through annual cycles of gain followed by loss of freezing tolerance (cold acclimation and deacclimation). Warm spells during winter and early spring can cause deacclimation, and if temperatures drop, freezing damage may occur. Many plants are vernalized during winter, a process making them competent to flower in the following summer. In winter cereals, a coincidence in the timing of vernalization saturation, deacclimation, downregulation of cold-induced genes, and reduced ability to reacclimate, occurs under long photoperiods and is under control of the main regulator of vernalization requirement in cereals, VRN1, and/or closely linked gene(s). Thus, the probability of freezing damage after a warm spell may depend on both vernalization saturation and photoperiod. We investigated the role of vernalization and the VRN1-region on freezing tolerance of meadow fescue (Festuca pratensis Huds.), a perennial grass species. Two F2 populations, divergently selected for high and low vernalization requirement, were studied. Each genotype was characterized for the copy number of one of the four parental haplotypes of the VRN1-region. Clonal plants were cold acclimated for 2 weeks or vernalized/cold acclimated for a total of 9 weeks, after which the F2 populations reached different levels of vernalization saturation. Vernalized and cold acclimated plants were deacclimated for 1 week and then reacclimated for 2 weeks. All treatments were given at 8 h photoperiod. Flowering response, freezing tolerance and expression of the cold-induced genes VRN1, MADS3, CBF6, COR14B, CR7 (BLT14), LOS2, and IRI1 was measured. We found that some genotypes can lose some freezing tolerance after vernalization and a deacclimation-reacclimation cycle. The relationship between vernalization and freezing tolerance was complex. We found effects of the VRN1-region on freezing tolerance in plants cold acclimated for 2 weeks, timing of heading after 9 weeks of vernalization, expression of COR14B, CBF6, and LOS2 in vernalized and/or deacclimated treatments, and restoration of freezing tolerance during reacclimation. While expression of VRN1, COR14B, CBF6, LOS2, and IRI1 was correlated, CR7 was associated with vernalization requirement by other mechanisms, and appeared to play a role in freezing tolerance in reacclimated plants. [ABSTRACT FROM AUTHOR]

Background and Aims Embryonic sporophytes of the moss Aloina ambigua are inducibly desiccation tolerant (DT). Hardening to DT describes a condition of temporary tolerance to a rapid-drying event conferred by a previous slow-drying event. This paper aimed to determine whether sporophytic embryos of a moss can be hardened to DT, to assess how the rate of desiccation influences the post-rehydration dynamics of recovery, hardening and dehardening, and to determine the minimum rate of drying for embryos and shoots. Methods Embryos were exposed to a range of drying rates using wetted filter paper in enclosed Petri dishes, monitoring relative humidity (RH) inside the dish and equilibrating tissues with 50 % RH. Rehydrated embryos and shoots were subjected to a rapid-drying event at intervals, allowing assessments of recovery, hardening and dehardening times. Key Results The minimum rate of slow drying for embryonic survival was ~3.5 h and for shoots ~9h. Hardening to DT was dependent upon the prior rate of drying. When the rate of drying was extended to 22 h, embryonic hardening was strong (>50 % survival) with survival directly proportional to the post-rehydration interval preceding rapid drying. The recovery time (repair/reassembly) was so short as to be undetectable in embryos and shoots desiccated gradually; however, embryos dried in <3.5 h exhibited a lag time in development of ~4d, consistent with recovery. Dehardening resulted in embryos incapable of surviving a rapid-drying event. Conclusions The ability of moss embryos to harden to DT and the influence of prior rate of drying on the dynamics of hardening are shown for the first time. The minimum rate of drying is introduced as a new metric for assessing ecological DT, defined as the minimum duration at sub-turgor during a drying event in which upon rehydration the plant organ of interest survives relatively undamaged from the desiccating event. [ABSTRACT FROM AUTHOR]

Insect performance is limited by the temperature of the environment, and in temperate, polar, and alpine regions, the majority of insects must face the challenge of exposure to low temperatures. The physiological response to cold exposure shapes the ability of insects to survive and thrive in these environments, and can be measured, without great technical difficulty, for both basic and applied research. For example, understanding insect cold tolerance allows us to predict the establishment and spread of insect pests and biological control agents. Additionally, the discipline provides the tools for drawing physiological comparisons among groups in wider studies that may not be focused primarily on the ability of insects to survive the cold. Thus, the study of insect cold tolerance is of a broad interest, and several reviews have addressed the theories and advances in the field. Here, however, we aim to clarify and provide rationale for common practices used to study cold tolerance, as a guide for newcomers to the field, students, and those wishing to incorporate cold tolerance into a broader study. We cover the ‘tried and true’ measures of insect cold tolerance, the equipment necessary for these measurement, and summarize the ecological and biological significance of each. Finally, we suggest a framework and workflow for measuring cold tolerance and low temperature performance in insects. [ABSTRACT FROM AUTHOR]

Copyright of Canadian Journal of Plant Science is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Aim Species ranges are confined by environmental parameters such as minimum temperatures. Beyond correlations of ranges and climatic parameters, however, physiological tolerances (here: cold tolerance) have rarely been linked to the climate of species' ranges. We hypothesize that natural range shifts due to climate warming and proactive-assisted colonization may each be constrained by limits to the tolerance of species to rare frost events. Location Bayreuth, Germany, and the Northern Hemisphere. Methods We quantified cold tolerance ( LT50 obtained by relative electrolyte leakage method) of 27 native and exotic (Northern Hemisphere) tree species in the autumn, mid-winter and spring of 2011-12 at the Ecological Botanical Garden of the University of Bayreuth, Germany, and linked observed cold tolerances as well as changes in cold tolerance between sampling dates to the climate of the native ranges of the species. Results Observed cold tolerance was strongly related to the climate of the native ranges of the species (cross-validated correlations between climate and expressed cold tolerance determined by boosted regression trees were 0.50 in autumn, 0.49 in mid-winter, and 0.65 in spring). Cold tolerance was generally greater for species that experienced colder temperatures and lower levels of precipitation in their native ranges. Changes in cold tolerance between the three sampling dates over the winter, however, were not linked to the climate of the native ranges. Main conclusions Our results demonstrate the evolutionary importance of cold tolerance, which should be acknowledged in assisted colonization trials and projections of range shifts by considering absolute minimum temperature as an important ecological factor. [ABSTRACT FROM AUTHOR]