Frost hardiness gradients in shoots and roots of picea mariana seedlings

Frost hardiness of tissues along the length of the stem and the root was investigated in first‐year black spruce (Picea mariana (Mill.) B.S.P.) seedlings. Frost hardiness of 1 cm long stem and root segments was evaluated based on Index of Injury, calculated from post‐freezing electrolyte leakage. Frost hardiness was tested approximately weekly beginning seven weeks after seedlings were transferred from an 18 to a 10 h photoperiod, both at day/night temperatures of 26°C/16°C. Trees were transferred to temperatures of 10°C day and 5°C night at a 10 h photoperiod after a further 18 days. Frost hardiness was greater at the terminal bud and least at the root tips. Although shoots were generally more frost hardy than roots, differences in hardiness along the stem and root axes were gradual, rather than abruptly differing at the shoot‐root interface. All tissues, including root tips, increased in frost hardiness after conditioning for 18 days under short photoperiods (10 h) and warm temperatures (26?C/16°C, day/night). Under cold temperatures (10°C/5°C, day/night) all tissues, excepting the root tips, tolerated — 16°C with little subsequent electrolyte leakage.     

Timing of cold temperature exposure affects root and shoot frost hardiness of Picea Mariana container seedlings

Seventeen‐week‐old black spruce seedlings were hardened under short daylengths and one of three short day length environments, which were either warm (24/16°C, day/night) throughout a 10 week hardening period (WW), cool (10/5°C) throughout hardening (CC), or warm for three weeks followed by seven weeks of cool temperatures (WC). Greatest root and shoot frost hardiness resulted from the exposure of seedlings to three weeks of warm followed by seven weeks of cool temperatures. Seedlings receiving warm temperatures throughout hardening increased in root and shoot frost hardiness, but to a lesser extent than seedlings exposed to cool temperatures. The frost hardiness of woody roots was generally greater than that of fine roots, but the extent of the difference in frost hardiness depended on the time since bud initiation and on the hardening treatment.     

Plantlets regeneration from root explants ofRobinia pseudoacacia L. by suspension culture

A rapid and efficient method for the regeneration of plantlets from root explants ofRobinia pseudoacacia L. by suspension culture was established. The roots taken from aseptically grown 15-day-old seedlings were used as explants. It was determined that photoperiodicity was necessary for root proliferation, and that the promotive effect of IAA (3-indoleacetic acid) on root proliferation was better than that of IBA (3-indolebutyric acid). The roots cultured in 1/2 MS liquid medium containing 3 μM IAA and 1% sucrose at 25°C under 16-hour photoperiod with 50 μmol m⁻²s⁻¹ PPFD (photosynthetic photon flux density) shaking at 100 times/min reciprocally showed high efficiency for root proliferation. BAP (6-benzylaminopurine) was found to be essential to induce adventitious shoots from the roots, and the roots cultured in the medium supplied with 3 μM BAP combined with 1–6 μM IAA for 3 weeks under the same conditions as in the root proliferation period were most suitable for adventitious shoot inducement.     

Effects of nutritional factors on frost hardening in Larix leptolepis (Sieb & Zucc.) Gord.

A method for estimating frost hardiness in seedlings of Larix leptolepis in their first stage of acclimation is demonstrated. Cuttings of the shoot tip were frozen linearly from +2°C to ‐36°C. The viability was determined by TTC‐assay. Data were fitted to a logistic regression model, and hardiness was calculated from the fitting parameters. It was shown that hardiness is influenced by the duration of the fertilizer application period. No effect of the nutrient status of N, P or K in the shoots was found.     

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.     

Growth responses of seedlings of six Betula pubescens Ehrh. Provenances to six ozone exposure regimes

Seedlings of six provenances of Betula pubescens Ehrh. from different latitudes (59–70°N) were grown under six ozone exposure regimes by combining different concentrations and daily exposure periods. The different treatments at increasing O₃ exposure over 40 nmol mol^?1 (AOT40 given in parentheses) were: 19 nmol mol^?1/24 h day^?1 (0.1 μmol mol^?1‐h), 42 nmol mol^?1/12 h day^?1 (2.5 μmol mol^?1‐h), 44 nmol mol^?1/24 h day^?1 (7.1 μmol mol^?1‐h), 76 nmol mol^?1/6 h day^?1 (9.4 μmol mol^?1‐h), 75 nmol mol^?1/12 h day^?1 (17.8 μmol mol^?1) and 116 nmol mol^?1/6 h day^?1 (19.8 μmol mol^?1) for 40 days at a 24 h day^?1 photoperiod in growth chambers placed in a greenhouse. The effect of increasing the O₃ exposure from 19 nmol mol^?1/24 h (0.1 μmol mol^?1‐h AOT40) to 42 nmol mol^?1/12 h (2.5 μmol mol^?1‐h AOT40) was a decrease in root but not shoot dry weight. A further increase in the exposure to 44 nmol mol^?1/24 h (7.1 μmol mol^?1‐h AOT40) also decreased the shoot dry weight. An increase in the O₃ concentration to 75 (9.4–17.8 μmol mol^?1‐h AOT40) and 116 nmol mol^?1 (19.8 μmol mol^?1‐h AOT40) further decreased shoot and root dry weights. A moderate O₃ exposure (42 nmol mol^?1/12 h = 2.5 μmol mol^?1‐h AOT40) increased the plant height and leaf size, while a further increase in O₃ concentration and exposure time decreased both of these variables. The birch provenances generally had a similar response to the O₃ treatments. The accumulated O₃ exposure over the 0, 10, 20, 30, 40 and 50 nmol mol^?1 concentrations (AOT0, AOT10, AOT20, AOT30, AOT40 and AOT50, respectively) was calculated for all O₃ treatments. The shoot and root dry weights were correlated best with AOT40 and AOT30, and were estimated to decrease by 10% at an AOT40 of 7.0 and 5.5 μmol mol^?1‐h, respectively. The development of O₃ injury (yellow stipples/chlorosis) was most marked when correlated with AOT40.     

Photosynthetic responses to lightflecks ofFagus crenata seedlings grown in a gap and understory of a deciduous forest

Photosynthetic responses to a series of 1-min lightflecks (1,000μmol m⁻² s⁻¹) superimposed on a background with different duration (1, 5, and 10 min) and intensity (25 and 50μmol m⁻² s⁻¹) of low background photosynthetic photon flux density (PPFD) were measured in the leaves ofFagus crenata grown in a gap and understory of aFagus crenata forest in the Naeba Mountains. The two background PPFD intensities most frequently occurred in understory and gap sites respectively. The maximum net photosynthetic rate (P _Nmax) and maximum stomatal conductance (g _smax) were higher in the gap seedlings than in the understory seedlings. However, when the background PPFD was 25μmol m⁻²s⁻¹, the net photosynthetic rate (P ₂₅) and stomatal conductance (g _s25) were almost the same between the gap and understory. When the background PPFD duration was 1-min, the net photosynthetic rate (P _N ) at the end of each lightfleck increased progressively. When the background PPFD duration was 5- and 10-min, the increase inP _N at the end of each lightfleck was less. This indicates that background PPFD duration is important to photosynthetic responses to lightflecks. The higher ratios ofP ₂₅/P _Nmax andg _s25/g _smax in the understory seedlings indicate that the understory seedlings can maintain relatively lower levels of biochemical and stomatal limitations than the gap seedlings under low light conditions. The ratios ofP _N /P _Nmax at the end of each lightfleck (IS) and light utilization efficiency of single lightflecks (LUE _s) that showed the influence of lightflecks on carbon gain were higher in the understory seedlings than in the gap seedlings when the background PPFD was 25μmol m⁻² s⁻¹. This means that understory seedling are capable of utilizing fluctuating light more efficiently under low light conditions than the gap seedlings although the net carbon gain of single lightflecks (CG _s) in the understory seedlings was not higher than that in the gap seedlings. There were no significant differences inIS andLUE _s between understory seedlings at a background PPFD of 25μmol m⁻² s⁻¹ and gap seedlings at a background PPFD of 50μmol m⁻² s⁻¹. However,CG _s in gap seedlings was higher than in understory seedlings. These results provide more evidence thatF. crenata acclimate to a natural light environment in respect to relative induction state at low background PPFD and can capture the fluctuating light at the same efficiency in both the gap and understory seedlings under natural light environments. This study was funded by the research project, Evaluation of Total CO₂ Budget in Forest Ecosystems, coordinated by the Ministry of Agriculture, Forestry and Fisheries of Japan.     

An integrated model for predicting maximum net photosynthetic rate of cocksfoot (Dactylis glomerata) leaves in silvopastoral systems

Net light-saturated photosynthetic rate (A_max) of field grown cocksfoot (Dactylis glomerata L.) leaves in a radiata pine (Pinus radiata D. Don) silvopastoral system (Canterbury, New Zealand) was measured at different times under severe shade (85–95 μmol m^–2 s^–1 photosynthetic photon flux density, PPFD) and in full sunlight (1900 μmol m^–2 s^–1 PPFD). The aim was to integrate individual functions for A_max against air temperature (2 to 37 oC), water status, expressed as pre-dawn leaf water potential (ψ_lp) (-0.01 to −1.6 MPa), herbage nitrogen (N) (1.5 to 5.9%), regrowth duration (20 to 60 days) and time under shade (1 to 180 min) into a multiplicative model. The highest A_max value obtained was 27.4 μmol CO₂ m^–2 s^–1 in non-limiting conditions with full sunlight. This value was defined as standardised dimensionless A_maxs = 1 for comparison of factor effects. The canopy temperature of the cocksfoot sward was up to 7.4 oC cooler than air temperature for plants under shade. Therefore, canopy temperature was used to predict A_max. The only interaction was between time under severe shade (5% of the open PPFD) and water stress (ψ_lp = −0.4 to −1.3 MPa) and this was included in the model. Validation of this model indicated 78% of the variation in A_max could be accounted for using these five factors by the addition of the interaction function. This model could be used to assist the prediction of pasture growth in silvopastoral systems through incorporation into a canopy photosynthesis model. This revised version was published online in June 2006 with corrections to the Cover Date.     

Effects of CO2 enrichment at varying photon flux density on the growth of picea abies (L) karst. seedlings

Seedlings of Norway spruce (Picea abies (L.)) were grown at 335 and 1000 μl CO₂ 1^?1 for 118 days in growth rooms at different irradiance levels. Photon flux density ranging from 8.6 to 34.6 mol m^?2 day^?t (PAR) was given either as constant light or as alternating levels in intervals of two or six hours. CO₂ enrichment increased the plant dry weight from 36% to 105% by increasing photon flux density from 8.6 to 25.9 mol m^?2 day^?1. At constant light the dry weight apparently reached its maximum at a photon flux density of 25.9 mol m^?2 day^?t. At the lower radiation levels alternating in CO₂ enriched air gave slightly higher dry weights compared to constant light levels. At the highest radiations the effect on dry weight was the opposite. High CO₂ concentration and 300 μmol m^?2 s^?1 constant light (25.9 mol m^?2 day^?1) gave the best growth and quality of plants. Top, root, stem and foliage weight were proportionally affected. Shoot length was enhanced by CO₂ enrichment. Shoot weight per cm was substantially increased both by CO₂ enrichment and increasing photon flux density.     

Influence of photosynthetic photon flux density on growth and transpiration in seedlings of Fagus sylvatica

Beech seedlings (Fagus sylvatica L.) were grown in various combinations of three photosynthetic photon flux densities (PPFD, 0.7, 7.3 or 14.5 mol m(-2) day(-1)) for two years in a controlled environmental chamber. Dry mass of leaves, stem and roots, leaf area and number of leaves, and unit leaf rate were affected by both previous-year and current-year PPFD. Number of shoots and length of the main shoot were affected by previous-year PPFD but not by current-year PPFD. Number of leaves per shoot did not change with PPFD, whereas leaf dry mass/leaf area ratio was mainly affected by current-year PPFD. During the first 10 days that newly emerged seedlings were grown at a PPFD of 0.7 or 14.5 mol m(-2) day(-1), transpiration rate per unit leaf area declined. Thereafter, transpiration increased to a constant new rate. Transpiration rate per seedling was closely related to leaf area but the relationship changed with time. In two-year-old seedlings grown at various PPFD combinations of 0.7, 7.3 and 14.5 mol m(-2) day(-1) during Years 1 and 2, leaf area and transpiration rate per seedling were closely correlated at Weeks 7 and 11 after bud burst. Weak correlations were found between root dry mass and transpiration rate per seedling. During Year 2, transpiration rate per leaf area was higher at a particular PPFD in seedlings grown at a previous-year PPFD of 0.7 mol m(-2) day(-1) than in seedlings grown at a previous-year PPFD of 14.5 mol m(-2) day(-1). After transfer of two-year-old seedlings at the end of the experiment to a new PPFD (7.3 or 14.5 mol m(-2) day(-1)) for one day, transpiration rates per leaf area, measured at the new PPFD, were correlated with leaf area and root dry mass, irrespective of former PPFD treatment.     

Frost resistance and frost damage in pinus sylvestris seedlings during shoot elongation

No differences were found in the frost resistance of the different‐aged (2–7 weeks) germlings of Scots pine. The critical temperature was ‐6°C to —3°C. A temperature of ‐4°C killed half of the germlings and produced damage in one fifth of the surviving seedlings; the needles turned brown and growth ceased. The frost resistance of the previous year's shoots of two‐year‐old seedlings, measured by the impedance method, decreased during the shoot elongation period from — 10°C to — 4°C. Damage to the current shoots during shoot elongation appeared as deformation and discolouration of the needles and abnormal development or death of the apical bud. The results indicate that frost is not the cause of growth disturbances observed in Finnish nurseries.     

Field measurements of gas exchange in Avicennia marina and Bruguiera gymnorrhiza

Diurnal gas exchange characteristics were measured simultaneously in two mangrove species, Avicennia marina and Bruguiera gymnorrhiza, over 7 d in summer (February–March), to compare their productivity. The study was undertaken in the Beachwood Mangroves Nature Reserve, Durban, South Africa, using fully expanded leaves of young and mature trees at the top of the canopy. Gas exchange was strongly influenced by photosynthetic photon flux density (PPFD), leaf temperature and the accompanying leaf to air vapour pressure deficit ( w). Carbon dioxide exchange was saturated at a PPFD of about 600 mol m^-2s^-1 in B. gymnorrhiza compared to 800 mol m^-2s^-1 in A. marina. Maximal CO₂ exchange occurred between 12h00 and 14h00 and was consistently greater in A. marina (8.8 mol m^-2s^-1) than in B. gymnorrhiza (5.3 mu;mol m^-2s^-1). Mean internal CO₂ concentrations ( c_i) were 260 l l^-1 in A. marina and 252 l l^-1 in B. gymnorrhiza. Photorespiratory activity was 32% in A. marina and 30% in B. gymnorrhiza. Mean water use efficiency (WUE) was 8.0 mol mmol^-1 in A. marina and 10.6 mol mmol^-1 in B. gymnorrhiza. Diurnal leaf water potentials ranged from –0.8 to –3.5 MPa and were generally lower in A. marina.     

Effects of warming basal ends of Carolina poplar (Populus × canadensis Moench.) softwood cuttings at controlled low-air-temperature on their root growth and leaf damage after planting

We investigated the effects of warming the basal ends of Carolina poplar (Populus × canadensis Moench.) softwood cuttings at controlled low-air-temperature on their root growth and leaf damage after planting. The warming treatment was applied to the cuttings by soaking 10 mm beyond the cut end in warmed water maintained at 30 °C in a cold chamber maintained at an air temperature of 10 °C and a photosynthetic photon flux density (PPFD) of 10 μmol m^?2 s^?1 (near the light compensation point at 10 °C) until rooting was observed. The warmed cuttings were then grown in a growth chamber at an air temperature of 30 °C, relative humidity 85–90 %, and a PPFD of 100 μmol m^?2 s^?1. Control cuttings were grown in the growth chamber throughout the experiment. Rooting occurred simultaneously for both warmed and control cuttings, irrespective of air temperature. Root development was greater and leaf damage, evaluated on the basis of extent of necrosis, was less for warmed cuttings than for control cuttings. The reduction of leaf damage for warmed cuttings probably resulted from reduced post-planting water stress and leaf senescence, because of improved root development as a result of the pre-planting warming treatment. This technique could improve the propagation of cuttings of woody plants, because it would ensure that the cuttings are ready to develop roots with minimum loss of carbohydrates, irrespective of weather conditions.     

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.     

Effects of nitrogen fertilization and temperature on frost hardiness of Aleppo pine (Pinus halepensis Mill.) seedlings assessed by chlorophyll fluorescence

In a 14-week study, 1-year-old Aleppo pine seedlings were grownin two growth chambers. Seedlings were artificially hardenedby decreasing photoperiod and temperature. In each chamber halfof the seedlings were fertilized with nitrogen (8.4 mg seedling^–1).In order to determine the relative importance of the hardeningenvironment versus fertilization, each chamber was programmedto decrease night temperatures down to a low of 8 or 4°C.Chlorophyll fluorescence and frost hardiness was measured fivetimes during the experiment. A sample of seedlings from eachtreatment was exposed to an artificial frost at –5°Cand the freezing effects were assessed by measurements of chlorophyllfluorescence and visual evaluation of needle damage. Seedlingsincreased their frost hardiness during the experiment in allthe treatments but the ratio of variable to maximal chlorophyllfluorescence (F_v/F_m) measured before freezing did not vary duringthe experiment. This indicates that Aleppo pine maintains itsphotosynthetic ability during hardening in contrast to otherconiferous species from colder climates. The effect of nitrogenfertilization on frost hardiness was small in comparison withchamber effect. Nitrogen fertilization slightly delayed theacquisition of hardening in the coldest chamber. Seedlings inthe warmest chamber did not become fully resistant to –5°C,but in the coldest chamber, where night temperature reached4°C, all the seedlings were resistant to the frost. Severedamage caused by frost could be related to a rapid rise of minimalfluorescence (F₀) but the best index of damage was the dropof F_v/F_m after freezing.     

Temperature step response of dehardening in Pinus sylvestris seedlings

The time constant of the dehardening of one‐year‐old Scots pine (Pinus sylvestris L.) seedlings was studied in three experiments started at different times of the year. The seedlings were transferred from outside to the different controlled conditions in January (Exp. 1), March (Exp. 2) and April (Exp. 3). Changes in the frost resistance of the seedlings were followed on the basis of the temperature response of the specific impedance difference in the shoot. The time constant for dehardening at a temperature of 7.5°C was found to be about 12 days in Exp. 1, about 8 days in Exp. 2, and about 5 days in Exp. 3. the terminal bud burst when the frost resistance of the shoot had risen to about ‐10°C.     

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.     

The Influence of Desiccation, Rough Handling and Cold Storage on the Quality and Establishment of Sitka Spruce Planting Stock

In January 3-year-old Sitka spruce were lifted and treated eithercarefully or roughly. Plants in each treatment were either transferredto the laboratory for testing, or transferred to cold storageat –1°C. In the laboratory, half of the plants ineach treatment were desiccated to shoot water potentials ofless than –2.0 MPa. Plants were then tested for root growthpotential (RGP), bud dormancy, frost hardiness and carbohydratecontent before transplanting at a field site, Additional plantswere removed from the nursery and cold store at approximatelymonthly intervals until late April, and then treated as above.In April, plants in each treatment were transferred to on-sitefield storage (sheughs), for 2 or 4 weeks prior to testing asabove. Carefully handled plants maintained large RGP which was positivelycorrelated with plant water potential, root water content, shootrelative growth rate and field survival. Overall RGP was reduced: 59 per cent by desiccation; 85 percent by rough handling; and 98 per cent by desiccation and roughhandling in combination. On site storage for 4 weeks in April/May reduced RGP. Whereplants produced more than 30 new roots > 1 cm long in RGPtests, field survival exceeded 90 per cent. Cold storage at–1°C maintained RGP, (of carefully handled plants),bud dormancy and shoot frost hardiness at approximately pre-storagevalues. In contrast, total nonstructural carbohydrate contentdeclined in cold store but increased in March/April for plantsin the nursery.     

Validation of a canopy photosynthesis model for cocksfoot pastures grown under different light regimes

Daily net canopy photosynthesis (P _n) was predicted for cocksfoot (Dactylis glomerata L.) canopies grown under different light regimes by integration of a leaf photosynthesis model developed for the light-saturated photosynthetic rate (P _max), photosynthetic efficiency (α) and the degree of curvature (θ) of the leaf light–response curve. When shade was the only limiting factor, the maximum P _n (P _nmax) was predicted to decrease approximately linearly from 33.4 g CO₂ m⁻² d⁻¹ to zero as photosynthetic photon flux density (PPFD) fell from full sunlight (1800 μmol m⁻² s⁻¹ PPFD) to 10% of this in a fluctuating light regime. It was also predicted that at 50% transmissivity P _nmax was higher for a continuous light regime (10.4 g CO₂ m⁻² d⁻¹) than for a fluctuating light regime with the same intensity (8.4 g CO₂ m⁻² d⁻¹). The canopy photosynthesis model was then used to predict dry matter (DM) production for cocksfoot field grown pastures under a diverse range of temperature, herbage nitrogen content and water status conditions in fluctuating light regimes. This prediction required inclusion of leaf area index and leaf canopy angle from field measurements. The model explained about 85% of the variation in observed cocksfoot DM production for a range from 6 to 118 kg DM ha⁻¹ d⁻¹. The proposed model improves understanding of pasture growth prediction through integration of relationships between shade limitations in fluctuating light regimes and other environmental factors that affect the canopy photosynthetic rate of cocksfoot pastures in silvopastoral systems.     

No difference in frost hardiness between high and low altitude Pinus sylvestris (L.) offspring

Seedlings representing offspring from 46 Swedish natural stands of Pinus sylvestris (L.) from latitude 63° to 68° and altitude 75 to 675 m were artifically frost hardened and tested for autumn frost hardiness using artifical freeze testing in a programmable freezing chamber. A clinal variation in frost hardiness was observed over latitude. Altitude had no effect on the frost hardiness. The results are discussed in relation to the reproduction‐ and migration biology of P. sylvestris.