Phenologies of sixteen European provenances of sessile oak growing in Scotland

Budburst, budset, leaf yellowing, growth, and frost damage wereassessed on 2- to 4-year-old transplants of 16 provenances ofsessile oak (Quercus petraea) collected in six European countriesand grown in Scotland. There were significant differences indates of budburst between provenances. Provenances from Franceand Austria burst bud earlier than the others (P > 0.05). Budburst date was negatively correlated with altitude of provenanceorigin but positively correlated with latitude, indicating thatsouthern provenances burst bud earlier than northern provenancesand are therefore more prone to spring frost damage. Although there were no significant differences of growth betweenprovenances, French provenances tended to grow later in autumnthan provenances originating in other countries. Consequentlyplants from these French provenances were more badly damagedby autumnal frosts (P > 0.05) than plants from other provenances.Budset and leaf yeljowing in late September were positivelycorrelated.     

Frost Hardiness of Red Alder (Alnus rubra) Provenances in Britain

The phenology and frost hardiness of shoots of 15 provenancesof Alnus rubra growing in Scotland were measured over one autumn,winter and spring. Dates of budset (in September) and the onsetof rapid frost hardening (in October-November) occurred about2 days earlier for each degree latitude of origin northwards,except for an Idaho provenance. However, all provenances dehardenedat about the same time in March and burst their buds between8 and 14 April. Assuming that rapid frost hardening in the autumnwas triggered primarily by shortening daylengths, Alaskan provenancesof A. rubra seemed better adapted to British conditions thansouthern British Columbian provenances, which have been mostcommonly planted. However, even Alaskan provenances are proneto spring frost damage. Scottish A. glutinosa and Alaskan A.sinuata set buds and frost hardened 1–2 weeks before eventhe Alaskan A. rubra, and burst their buds 2–3 weeks laterin April-May. All three species were hardy to below –30°Cfrom December to mid-March.     

Seedling cold hardiness, bud set, and bud break in nine provenances of Pinus greggii Engelm.

Cold hardiness and timing of bud set and bud break are important processes that provide protection of nursery seedlings against low temperatures. Seedlings of 9 provenances of Pinus greggii from two different regions of Mexico were tested to determine cold hardiness, bud set, and bud break timing differences. Needle sections were exposed to freezing temperatures to determine an injury index of each provenance. In addition, bud set and bud break timing were recorded through the fall, winter and spring. There were significant differences in cold hardiness between seedlings from northern and southern provenances. At the maximum cold hardiness, the index of injury (LT₅₀) for northern provenances was LT₅₀ = −18 °C, compared to −12 °C for southern provenances. There was a considerable variation among the provenances in the proportion of seedlings that set terminal buds. Seedlings from northern provenances had greater proportions of seedlings that set a terminal bud than seedlings from southern provenances. There were also significant differences in the bud break timing in the following spring among the 9 provenances. Seedlings from northern provenances broke bud earlier than southern provenances. Cold hardiness, bud set, and bud break timing results may be useful to determine how far a specific seed source can be moved from its natural environment.     

Autumn frost hardiness in Norway spruce plus tree progeny and trees of the local and transferred provenances in central Sweden

Reforestation with provenances from locations remote from the planting site (transferred provenances) or the progeny of trees of local provenances selected for superior form and vigor (plus trees) offer alternative means to increase yield over that obtained by the use of seed from unselected trees of the local provenance. Under Swedish conditions, Norway spruce (Picea abies (L.) Karst.) of certain transferred provenances generally has an advantage in productivity relative to the local provenance comparable to that of progeny of plus trees. The aim of this study was to explore the extent to which productivity gains achieved by provenance transfer or the use of plus tree progeny are associated with reductions in autumn frost hardiness, relative to that of trees of the local provenance. In a field trial with 19-year-old trees in central Sweden, bud hardiness was tested on four occasions during the autumn of 2002. Trees of the local provenance were compared with trees of a south Swedish provenance originating 3 degrees of latitude to the south, a Belarusian provenance and the progeny of plus trees of local origin. The Belarusian provenance was the least hardy and the local provenance the most hardy, with plus tree progeny and the south Swedish provenance being intermediate in hardiness. Both the Belarusian provenance and the plus tree progeny were significantly taller than trees of the other populations. Within provenances, tree height was negatively correlated with autumn frost hardiness. Among the plus tree progeny, however, no such correlation between tree height and autumn frost hardiness was found. It is concluded that although the gain in productivity achieved by provenance transfer from Belarus was comparable to that achieved by using the progeny of plus trees of the local provenance, the use of trees of the Belarus provenance involved an increased risk of autumn frost damage because of later hardening.     

Autumn Frost Damage on Young Picea sitchensis 2. Shoot Frost Hardening, and the Probability of Frost Damage in Scotland

The natural increase in frost hardiness of detached shoots ofPicea sltchensis during August to November was measured usinga programmable freezing chamber. Oregon, Queen Charlotte Islandsand Alaskan provenances were compared, and the effects on hardeningof long days, warm temperatures and frosts were determined.A computer model was constructed to mimic the observed patternsof autumn frost hardening, as functions of air minimum temperatures,daylengths and the occurrence of frosts. The model was used(a) to describe the pattern of autumn frost hardening at differentsites in northern Britain, using past meteorological records,and hence (b) to determine when frosts occurred that might havedamaged young trees. The model accurately predicted known instancesof autumn frost damage at Kirroughtree and Carnwath. The predicted probability of autumn frost damage on young treesof P. sitchensis in upland areas of Scotland was much lowerthan that previously predicted for spring frost damage. Theestimated return time for autumn frost damage to an Oregon provenanceat Eskdalemuir was 8.3 years, and the return time for a Q.C.I.provenance was longer than 10 years. Most damaging frosts occurredin October, but frosts like those on 13–15 October 1971,which followed warm weather and caused wide spread damage inScotland, have been quite rare. Alaskan provenances would rarelybe damaged by autumn frosts, nor would trees of Q.C.I. provenancegrowing in lowland areas of Scotland, or at Masset on the QueenCharlotte Islands.     

Morphological and physiological differences in Scots pine seedlings of six seed origins

One-year-old seedlings of Scots pine (Pinus sylvestris L.) offour native seed origins (Loch Maree Islands, Glengarry/GlenMorriston, Glen Affric and Abernethy), a commercial Britishseedlot, and a seedlot from Hedesunda, in middle Sweden, werecompared at monthly intervals from October 1993 to April 1994.Seedling morphology, root condition, root frost hardiness andbud dry matter were determined at each date. There were clear morphological differences among seed origins.Seedlings raised from the commercial seedlot (A70) were largerbut had a poorer root:shoot ratio than the other seed origins.Of the native pines tested, the Loch Maree Islands origin allocateda larger proportion of its photosynthate to fine roots and needlesand smaller proportion to woody structures. Seedlings raised from the commercial British seedlot tendedto have poorer bud lignification than the other origins andalso, in autumn, higher electrolyte leakage rates from its fineroots. During winter, the Swedish origin had the lowest fineroot electrolyte leakage. Seedlings of all origins showed aprogressive increase in fine root hardiness towards mid-winterwith maximum hardiness (–7°C) in January. Dehardeningoccurred over subsequent months reaching –3°C in April.Differences among origins were evident. The Swedish seedlotdeveloped greater frost resistance than the other origins, hardeningbegan earlier in autumn and dehardening began later in spring.The commercial seedlot hardened later than the other originsbut reached a similar level of frost hardiness by January. Ofthe native pines, seedlings of the Loch Maree Islands originwere slowest to develop root hardiness.     

Within‐population variation in autumn frost hardiness and its relationship to bud‐set and height growth in Picea abies

Artificial freezing tests were performed with two sets of 12 full‐sib families of Picea abies. Each set was selected from a complete diallel cross performed within a natural population. Significant differences in autumn frost hardiness were observed between the two populations, which originate from the same altitude and longitude approximately 60 km apart. Substantial variation in frost hardiness was observed within both populations. Significant pheno‐typic correlations at the individual level were found between freezing injury and the two traits terminal bud‐set and height growth year one. However, no significant relationships were present between freezing injury and bud‐set at the family level, indicating that bud‐set cannot be used to predict autumn frost hardiness for families.     

Performance and Frost Hardiness of Picea sitchensis x Picea glauca Hybrids in Scotland

The growth of seven Picea sitchensis x Picea glauca hybridswas compared with the growth of two P. sitchensis provenancesand Picea glauca var.albertiana at two sites in northern Scotland.The sites were at Aultmore (an exposed, dry site with a mineralsoil) and Shin (a frosty, wet site with deep peat). They wereof the type considered more suited to Pinus contorta than P.sitchensis. At age 10, in 1984, most of the hybrids, at both sites, wereabout 10 and 20 per cent taller than P. sitchensis of Masset(Q.C.I.) and Ketchikan (Alaska) provenance, respectively. P.glauca var. albertiana grew very poorly, especially at Aultmore. At Aultmore, the frost hardiness of three of the tallest hybrids,the two P. sitchensis provenances, and P. glauca var.albertiana,was tested at about 3-weekly intervals throughout 1982 and 1983.Detached shoots were subjected to artificial frosts in a programmablechamber. P. glauca var. albertiana was frost susceptible atbudburst, but at all other times it was relatively very frosthardy (eg. to^–10°C in mid-August). Also, the hybridswere consistently more hardy than P. sitchensis of even Ketchikan(Alaska) provenance from July onwards. However, the hybridswere less frost hardy than P. sitchensis of Masset (Q.C.I.)provenance in early spring (they dehardened a week earlier inMarch-April) and their buds were equally as frost susceptibleat the time of budburst. In 1983, trees of P. glauca var. albertianaburst their buds about a week sooner than P. sitchensis. It was concluded that P. sitchensis x P. glauca hybrids canperform better than P. sitchensis at sites considered ‘marginal’for P. sitchensis, and that their good performance may be partlyattributed to, or associated with, their greater summer andautumn frost hardiness. A programme of inter-specific hybridizationis being pursued.     

Frost hardening and dehardening in Abies procera and other conifers under differing temperature regimes and warm-spell treatments

Frequent bud frost damage in cultivation of Abies procera Rehderand pending climate changes are the background for this studyof cold hardiness under varying acclimation regime (in closed-topchambers) and experimental warm spells during the cold season.LT₅₀ values were established by freezing tests at differenttimes of year. Damage and deaths were assessed on leader buds,subapical lateral buds, needles and cambium. Minor parallelexperiments involved Abies nordmanniana, Picea abies and Piceasitchensis. Lower acclimation temperatures resulted in deeperfrost hardiness during late autumn but less during spring, comparedwith ambient temperature controls. Elevated temperatures resultedin less deep frost resistance. Apical buds generally developeddeeper frost hardiness than lateral buds but less deep thanthe cambium, varying with species, however. Frost damage inbuds ranged from death over partially destroyed bud contentsresulting in distorted shoots to buds seemingly remaining dormant.Responses to warm spells differed with duration, timing andspecies, ranging from dramatic decrease in frost hardiness withor without subsequent recovery to no reaction. Furthermore,the reactions did not show any clear relation to dormancy level.For A. procera, exposure to fluctuating temperatures appearedto be particularly problematic. This explains why this speciesdevelops best in coastal climates, and in sites sheltered fromtemperature extremes either by hedging, a winter snow cover,or topography. The Christmas tree production will suffer severelyon sites with harsh temperatures due to losses of lateral andterminal buds, which destroy the crown symmetry. Clipping ofgreenery is less influenced by frost damages, although the developmentof normal branch whorls is often disturbed.     

Variation in spring and autumn frost tolerance among provenances of Russian larches (Larix Mill.)

Abstract

Spring and autumn frost tolerance was measured using material from a range-wide (50–67° N, 38–158° E) provenance trial of four Russian larch species (Larix sukaczewii Dyl., L. sibirica Ledeb., L. gmelinii Rupr. and L. cajanderi Mayr.) growing in northern Sweden. Shoots were collected in early May and late September and frozen at ?8, ?12, ?16 and ?20°C. Cambial damage was assessed visually after development under ideal conditions for 2 weeks. Differences in frost damage among provenances were highly significant in both spring and autumn. Autumn frost damage was significantly correlated with provenance latitude and longitude and spring frost damage was significantly correlated with provenance longitude but not latitude. Frost damage was not correlated with provenance elevation. North-western provenances showed the least damage and far-eastern provenances the greatest damage in both spring and autumn. A possible explanation for less spring frost damage to north-western provenances is adaptation to maritime conditions in proximity to the Barents Sea, which is often ice free in late winter. This would counteract early loss of frost tolerance and bud flushing if warm spells occurred in late winter. North-eastern Siberian provenances did not show similar adaptation and may exhibit increased spring frost damage if global warming eventually results in the Arctic Ocean north of Siberia becoming ice free in late winter.     

Seasonal Changes in the Frost Hardiness of Provenances of Picea sitchensis in Scotland

Changes in the natural level of frost hardiness of shoots offour provenances of Picea sitchensis were monitored over twogrowing seasons by detaching shoots from 7 to 10-year-old treesgrowing in a nursery in Scotland, and subjecting them to freezingtemperatures under conditions which simulated night frosts. Six seasonal phases of frost hardiness were identified (Fig.3).

1. During each autumn, killing temperatures (the level of hardiness)decreased from –5°C to below –20°C, beginningseveral weeks after shoot elongation ceased. Alaskan provenanceshardened in September, apparently in response to shorteningday lengths alone, whereas an Oregon provenance did not hardenuntil November, after repeated frosts. Queen Charlotte Islandsprovenances were intermediate.
2. From November to March allprovenances were hardy to below –20°C,which is adequateto prevent direct freezing injury at mostplantation sites.
3. In March-April, several weeks before bud-burst, old shootsdehardenedto killing temperatures of about –10°Cin responseto warm temperatures, and southerly provenancesdid so beforenortherly ones.
4. During bud-burst the newly-emergingshoots were hardy to only–3°C to –5°C untilthey were about 3.5 cmlong. All provenances burst bud at thesame time and were equallyfrost susceptible at this time.
5. DuringMay-July the elongating shoots fluctuated in hardinessbetween–5°C and –10°C apparently in responsetofluctuating ambient temperatures.
6. In August 1980 there wasa period of late summer dehardeningto killing temperaturesof about –3°C.

Seasonal changes in hardiness are discussed in relation to changesin shoot growth and environmental factors. The main opportunitiesfor selecting frost hardy genotypes seem to be in the rate ofautumn hardening, the time of pre-bud burst dehardening, andthe time of bud-burst.     

European silver fir (<Emphasis Type="Italic">Abies alba</Emphasis> Mill.) provenances from Calabria,southern Italy: 15-year results from Danish provenance field trials

Height after 15 years, bud burst and mortality varied significantly among 13 southern Italian (Calabrian), a central Italian, a German (Schwarzwald), a Romanian (Carpathian), and a Danish provenance of silver fir (Abies alba Mill.) tested in two field trials in Denmark. The variation in height was especially observed in the field trial that was well protected against late frost in the spring and early frost in the fall by a shelter wood of larch. Provenances from the region of Serra San Bruno (Calabria) and two provenances from the region of Gariglione (Calabria) showed superior height growth at this site compared with the remaining provenances. Height was below average for two provenances from the region of Aspromonte (Calabria). The variation in height correlated significantly with biomasses of the same provenances obtained in early tests. Bud burst was earlier among provenances from the regions of Serra San Bruno and Aspromonte. These were also characterised by poor winter-frost resistance in early tests. The Romanian provenance was not represented in the shelter wood trial. The variation in height between provenances in the other field trial was mainly due to the Romanian and the Danish provenance with superior and poorer growth respectively. Otherwise, differences between the remaining provenances were not significant at this site probably due to the influence of frost. Provenances with poor winter-frost resistance had higher mortality at this site.     

Sitka Spruce and Douglas fir Seedlings in the Nursery and in Cold Storage: Root Growth Potential, Carbohydrate Content, Dormancy, Frost Hardiness and Mitotic Index

Seedlings (transplants) of 2+1 Sitka spruce (Picea sitchensis(Bong.) Carr.) and 1 + 1 Douglas fir (Pseudotsuga menziesii(Mirb.) Franco) were grown in a nursery at the Bush Estate,Scotland. Batches were lifted and cold stored at 0.5°C inNovember, December and January. Changes in growth, shoot apicalmitotic index, root growth potential (RGP), carbohydrate content,bud dormancy and shoot frost hardiness were monitored throughoutthe winter by taking samples at intervals from the nursery andfrom cold storage. Frost hardening occurred during the later stages of bud development(as mitotic indices decreased); autumn hardening was arrestedwhen seedlings were put in cold store, and some dehardeningoccurred in cold storage, especially in spring. Bud dormancystarted, and was greatest, just after bud growth (mitotic activity)virtually ceased; chilling in cold store was almost as effectivein releasing dormancy as natural chilling. The concentrationof total nonstructural carbohydrates stayed more or less constantat 100–150mg g^–1 from September to April in thenursery; in cold storage carbohydrates were depleted at 0.4–0.6mgg^–1 d^–1 (corresponding to respiration at 0.03–0.05mgCO₂ g^–1 h^–1) until there was only 40–50mgg^–1. Root growth potentials in the nursery increased in December,once the buds ceased growth, became dormant and had receivedsome chilling. Sitka spruce was ‘storable’ in November,before RGPs increased, but they then failed to achieve maximalfrost hardiness or ROP. Winter RGPs were high in Sitka spruceand were increased or maintained in cold storage, whereas RGPswere low in Douglas fir and decreased immediately after storage(except when stored in January). By the end of April, the RGPof cold stored Sitka spruce was much higher than that of directlifted plants. ROP changes in the nursery and in cold storagewere not consistently related to changes in seedling carbohydratecontents, shoot frost hardiness or bud dormancy. In practical terms, it was concluded that (1) the optimum dateto start lifting bare- rooted conifer transplants in the autumnis when their shoot apical mitotic indices have decreased tonear zero, and their RGPs have risen sharply; (2) high RGPsmay depend as much on the morphology of the roots (e.g. numberof undamaged root apices) as on the physiology of the shoots(e.g. carbohydrate status, dormancy and frost hardiness); and(3) in spring, transplants kept in cold storage since November,December or January are more frost hardy, slightly more dormant,and (in May) have higher RGPs than transplants lifted from thenursery.     

Winter Frost Hardiness of two Chilean Provenances of Nothofagus procera in Scotland

The frost hardiness of the shoots of individual trees withintwo Chilean provenances of Nothofagus procera (Poepp & Endl.)Oerst. was measured once in each of the months January, February,November and December 1989 and January and February 1990. Therewere significant (P<0.05) differences of frost hardinessbetween provenances but only one tree could be shown to be significantlymore frost hardy than the others within the same provenance.During the winter of 1989/90 both provenances were hardy toabout –14°C (temperature killing 50 per cent of shoots)in December, but the shoots dehardened to about –9°Cin January before hardening again in February. This patternof alternate hardening and dehardening seemed to mirror changesin air temperature and could render N. procera liable to frostdamage where (as happened in 1988/9 in the UK) mild spells occurin winter followed by severe frosts.     

Observations on bud burst phenology in a field trial established with Poplar (Populus spp.)

Bud flushing is very important for the survival and growth of trees, a phenomenon matched each year with the annual course of temperature and the timing of bud flushing in the spring. Essentially it represents a serious ecological and evolutionary tradeoff between survival and growth. The most suitable timing of bud burst permits trees to begin growth sufficiently early to take advantage of favorable spring conditions, but late enough to decrease the risks of tissue damage from late frost. In the present study bud burst spring phenology of poplar (Populus tremula and P. tremuloides) from eight different provenances, originating from Europe and the USA, was observed during March and April, 2009. The experimental plot was located at Solling, Germany (51°44′0″ N, 9°36′0″ E). A six stage subjective scoring system of bud burst phenology was used to identify the phenological stages of the seedlings, where each plant was observed twice a week. The aim of the study was to predict phenotypic variation in poplar, originating from regions between 42° and 60° N latitude, growing in similar environments. Timing of bud flushing of poplar was recorded. It was found that seedlings of provenance 3, which originated from 42.35° N latitude, started and completed flushing significantly earlier than those of other provenances, while seedlings of provenance 5, originating from 54.29° N latitude, started flushing very late and only a few plants reached top scoring at the end of the experimental period. Analysis of variance showed statistically highly significant differences (p < 0.05) in bud flushing among the provenances. The correlation between scoring and flushing periods was very strong within provenances although the flushing pattern differed among provenances (origin of the planted seedlings). Bud flushing showed a negative correlation with the origin of the planted seedlings. Given the field experience gained with this experiment, it is recommended that seedlings from provenances 5 and 8 could be used for future plantations where late frost may be a problem for the young shoots of seedlings.     

Late Autumn Frost Resistance of Twelve North European Provenances of Quercus Species

Twelve north European oak provenances [11 Quercus robur L. and one Quercus petraea (Matt.) Liebl] were tested for late autumn frost hardiness using visual methods and measurements of relative conductivity. Tissue from buds and twigs from 2-yr-old seedlings was used. The test was carried out in November and December. Temperatures between ?20 and ?32°C were necessary to cause serious damage to tissue, even when tissues were tested only a few weeks after leaf fall. Visual methods proved to be fast and could be applied in practical test applications. Estimation of twig viability was found to be a more reliable variable than bud assessment, which appears to be sensitive and not necessarily related to plant mortality. Relative conductivity is a more labour-intensive method and requires some technical equipment, but it provided the most consistent statistical results. Strong correlation between the visual methods and relative conductivity was demonstrated. Provenances originating from locations close to the Atlantic ocean (The Netherlands, the UK, Denmark and Norway) tended to be less frost resistant than more continental provenances (from Norway, Sweden, Finland and Poland). Frost tolerance was correlated with budset, but not with growth of the provenances. The results confirm the existence of specific ecotypes and suggest a high potential for adaptation in Q. robur.     

Phenotypic Differences Between Natural and Selected Populations of Picea Abies. I. Frost Hardiness

The frost hardiness of non-juvenile Norway spruce [Picea abies (L.) Karst.] populations growing in northern Sweden (63°54' N) was monitored during 1996-1997. The investigated progenies originated from 12 natural populations and six seed orchards located between 58° N and 68° N in Sweden. Frost hardiness of needles was assessed by measuring chlorophyll fluorescence and electrolyte leakage after freezing. The loss of frost hardiness in 1-yr-old needles during spring occurred slightly earlier in populations originating north of 63°30' N than in those originating further south. Dehardening was slightly delayed in selected populations compared with natural populations of similar origin. The level of frost hardiness during autumn was higher in populations originating north of 63°30' N than in those originating south of this latitude, but there were no clear differences in frost hardiness between selected and natural populations of similar origin. The results are discussed in relation to climatic factors and inherent growth rhythms.     

Effects of elevated CO(2) and temperature on cold hardiness and spring bud burst and growth in Douglas-fir (Pseudotsuga menziesii)

We examined effects of elevated CO(2) and temperature on cold hardiness and bud burst of Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) seedlings. Two-year-old seedlings were grown for 2.5 years in semi-closed, sunlit chambers at either ambient or elevated (ambient + ~ 4 degrees C) air temperature in the presence of an ambient or elevated (ambient + ~ 200 ppm) CO(2) concentration. The elevated temperature treatment delayed needle cold hardening in the autumn and slowed dehardening in the spring. At maximum hardiness, trees in the elevated temperature treatment were less hardy by about 7 degrees C than trees in the ambient temperature treatment. In general, trees exposed to elevated CO(2) were slightly less hardy during hardening and dehardening than trees exposed to ambient CO(2). For trees in the elevated temperature treatments, date to 30% burst of branch terminal buds was advanced by about 6 and 15 days in the presence of elevated CO(2) and ambient CO(2), respectively. After bud burst started, however, the rate of increase in % bud burst was slower in the elevated temperature treatments than in the ambient temperature treatments. Time of bud burst was more synchronous and bud burst was completed within a shorter period in trees at ambient temperature (with and without elevated CO(2)) than in trees at elevated temperature. Exposure to elevated temperature reduced final % bud burst of both leader and branch terminal buds and reduced growth of the leader shoot. We conclude that climatic warming will influence the physiological processes of dormancy and cold hardiness development in Douglas-fir growing in the relatively mild temperate region of western Oregon, reducing bud burst and shoot growth.     

Two provenances of Quercus ilex ssp. ballota (Desf) Samp. nursery seedlings have different response to frost tolerance and autumn fertilization

Despite evidences that Holm oak has a high plasticity and great adaptability, there is limited or contradictory knowledge of the morphological and physiological variability of this species. Holm oak has been widely used for reforestation projects in Mediterranean areas, but has frequently shown poor field performance. We hypothesized that Holm oak has inter-population differences in physiological responses to abiotic stressors that could affect reforestation success. The influence of nursery culture on the characteristics of Holm oaks from different provenances has not been explored in depth. Thus, we studied the effect of nursery autumn fertilization on morphological traits, frost tolerance, root growth potential, and nutritional status of two Spanish provenances of Holm oak, La Alcarria (a region with inland Mediterranean climate) and Sierra Morena Occidental (a region with a warm coastal Mediterranean climate). There were significant differences between the provenances in frost tolerance, biomass allocation, and leaf nutrient content, suggesting a role of genetic factors. The leaves of seedlings from La Alcarria had less visual damage at ?12°C than seedlings from the warmer provenance (45% vs. 92%). Seedlings from La Alcarria, compared to those from Sierra Morena, had higher leaf P concentration (0.17% vs. 0.15%), greater stem diameter (3.1?mm vs. 2.7?mm), lower shoot-to-root dry mass ratio (0.46 vs. 0.53), and lower slenderness (4.03 vs. 5.31). For both provenances, N autumn fertilization improved growth, root growth potential, cold hardiness, and nutritional status of seedlings. We suggest that forest reforestation programs should consider to a greater extent Holm oak provenances and their tolerances to different abiotic stressors.     

Frost tolerance and bud dormancy of container-grown yellow birch, red oak and sugar maple seedlings

Container-grown seedlings of red oak (Quercus rubra L.), sugar maple (Acer saccharum Marsh.) and yellow birch (Betula alleghaniensis Britton) in their first year of growth were overwintered outdoors. Tolerance of roots and stems to freezing was compared from late summer to the following spring. Mitotic activity in the apical bud was related more closely to air temperature than to bud dormancy as defined by days to bud break. In all species, stem hardening was observed before days to bud break reached a maximum. Dormancy release (days to bud break equal to zero) of yellow birch coincided with loss of stem hardening in the spring. Roots hardened more slowly, had a lower frost tolerance than stems in fall and winter, and dehardened earlier than stems in the spring. There were differences in stem and root hardiness among the species, with yellow birch being the most tolerant, followed by sugar maple and red oak. Primarily because of root sensitivity to frost, winter was a critical period for all three species, but particularly for red oak.