苹果柱型性状的SRAP分析

为了更深入研究苹果柱型基因,为苹果树型性状改良奠定基础,以舞姿与富士杂交的F1代群体为材料,利用SRAP分子标记技术与BSA法相结合的方法分析了苹果柱型性状。筛选出了1对SRAP引物组合M10E4,其在柱型池与普通型池间表现出分离,分离片段约为310bp。选用柱型与普通型的极端类型进行验证,柱型群体中多数单株都出现此片段,有2株出现交换,普通型群体中有3株出现交换,交换率为7.14%,用Mapmaker/Exp3.0软件对标记与目标性状进行连锁分析,测算遗传距离为7.7cM,并将此标记命名为M10E4-310。研究结果表明,利用SRAP技术初步找到了与柱型基因连锁较紧密的标记位点。     

苹果叶片再生体系建立研究

以乔纳金苹果试管苗叶片为外植体诱导不定芽再生，在培养基中添加不同浓度TDZ与NAA或IAA配合，使用琼脂或Polygel作为固化剂。结果表明，较适宜的叶片再生不定芽的培养基为TDZ 2．0mg／L和NAA 1．0mg／L，或TDZ 2．0mg／L与IAA 4．0mg／L。较适宜的组培固化剂为5．0g／L的Polygel。在不同的组培固化剂中，卡那霉素均能抑制不定芽的发生数量，但琼脂和Polygel效果不同。     

Sources of N for leaf growth in a high-density apple (Malus domestica) orchard irrigated with ammonium nitrate solution

Elstar apple trees (Malus domestica Borkh.) on M.9 rootstock received either 5 or 35 g N tree(-1) year(-1) during the first two growing seasons after planting, applied as Ca(NO(3))(2) on a daily basis for nine weeks through a drip irrigation system. During the third growing season (1994), all trees were treated with 20 g N tree(-1) year(-1) as (15)NH(4) (15)NO(3) with applications starting on April 22 and continuing for 10 weeks. Soil solution nitrate-N and ammonium-N were monitored weekly with suction lysimeters located 30 cm beneath the drip emitters. Spur and shoot leaves were sampled intensively from full bloom to the end of rapid shoot growth. During the period of nitrogen application, soil solution nitrate-N and ammonium-N were relatively constant, at about 24 and 1.0 mg l(-1) respectively. Growth of the spur leaves was completed by one week after full bloom (May 12), whereas biomass of the shoot leaves increased until mid-June. Nitrogen for growth of the spur leaves was supplied mainly from remobilization, which was dependent on previous N supply. Accumulation of fertilizer N in spur leaves was independent of previous N treatments and continued until the end of the monitoring period (June 24), but contributed only 13% to total spur leaf N. Nitrogen for shoot leaf growth was independent of previous N treatments and was initially supplied primarily by remobilization, but by the end of extension growth, fertilizer N contributed 48% to total shoot leaf N. Linear increases in leaf N uptake throughout the period of rapid shoot growth and the large contribution of fertilizer N to total shoot leaf N were attributed to the constant supply of N available in the root zone through daily N fertilization.     

Nitrogen absorption,translocation and distribution from urea applied in autumn to leaves of young potted apple (Malus domestica) trees

We studied the absorption, assimilation, translocation and distribution of nitrogen (N) from urea applied in autumn to leaves of 1-year-old potted Fuji/M26 apple (Malus domestica Borkh) trees. In early October, all leaves of each tree were painted with either 3% urea (enriched to 10 atom % with 15N) or water (control trees). Four trees were harvested before the treatment and N and amino acid contents were determined. Four trees from each treatment were harvested at 2, 4, 7, 10, 15 and 20 days after urea or water application. Total N, amino acids and 15N in leaves, bark, xylem, shank and roots were analyzed to determine uptake and mobilization of N from urea. Most uptake of 15N by leaves occurred during the first 2 days following application of urea. The mean rate of absorption during these 2 days was 0.29 g m-2 day-1. Amino acids in leaves, bark and roots increased significantly after urea application compared with control values. The highest concentrations of amino acids in leaves and bark occurred 4 days after application, whereas the highest concentrations of amino acids in roots occurred 10 days after application. Total 15N content in leaves peaked 2 days after urea application and then decreased, whereas 15N content in roots and bark increased throughout the experiment. Total 15N content in xylem and shank was low. Leaves absorbed 35% of the 15N applied as urea, and 63.6% of absorbed 15N was translocated out of leaves within 20 days after urea application. We conclude that N from urea was converted to amino acids in leaves after foliar application in autumn, and roots and bark were the main sinks of N from urea applied to leaves.     

Remobilization and uptake of N by newly planted apple (Malus domestica) trees in response to irrigation method and timing of N application

Environmentally sound management of N in apple orchards requires that N supply meets demand. In 1997, newly planted apple trees (Malus domestica Borkh. var. Golden Delicious on M.9 rootstock) received daily applications of N for six weeks as Ca(15NO3)(2) through a drip irrigation system at a concentration of 112 mg l(-1) at 2-8, 5-11 or 8-14 weeks after planting. Irrigation water was applied either to meet estimated evaporative demand or at a fixed rate. In 1997, trees were harvested at 5, 8, 11 and 14 weeks after planting; and in 1998 at 3 weeks after full bloom. The amount of fertilizer N recovered was similar in trees in both irrigation treatments, but efficiency of fertilizer use was greater for trees receiving demand-controlled irrigation than fixed-rate irrigation. This was attributed to lower N inputs, greater retention time in the root zone and less N leaching in the demand-controlled irrigation treatments compared with fixed-rate irrigation treatments. Less fertilizer N was recovered by trees receiving an early application of N than a later application of N and this was related to the timing of N supply with respect to tree demand. Demand for root-supplied N was low until 11 weeks after planting, because early shoot and root growth was supported by N remobilized from woody tissue, which involved 55% of the total tree N content at planting. Rapid development of roots > 1 mm in diameter occurred between 11 and 14 weeks after planting, after remobilization ended, and was greater for trees receiving an early application of N than for trees receiving a later application of N. Late-season tree N demand was supplied by native soil N, and uptake and background soil solution N concentrations were higher for trees receiving demand-supplied irrigation compared with fixed-rate irrigation. Total annual N uptake by roots was unaffected by treatments and averaged 6-8 g tree(-1). Nitrogen applications in 1997 affected growth and N partitioning in 1998. Trees receiving early applications of N had more flowers, spur leaves and bourse shoots than trees receiving later applications of N. Consequently, more N was remobilized into fruits in trees receiving early applications of N compared with fruits in trees receiving later applications of N. Demand for N in the young apple trees was low. Early season demand was met by remobilization from woody tissues and the timing of demand for root-supplied N probably depends on whether flowering occurs. Method of N delivery affected the efficiency of N use. We conclude that N demand can be met at soil solution N concentrations of around 20 mg l(-1).     

Root-zone temperatures affect phenology of bud break, flower cluster development, shoot extension growth and gas exchange of 'Braeburn' (Malus domestica) apple trees

We investigated the effects of root-zone temperature on bud break, flowering, shoot growth and gas exchange of potted mature apple (Malus domestica (Borkh.)) trees with undisturbed roots. Soil respiration was also determined. Potted 'Braeburn' apple trees on M.9 rootstock were grown for 70 days in a constant day/night temperature regime (25/18 degrees C) and one of three constant root-zone temperatures (7, 15 and 25 degrees C). Both the proportion and timing of bud break were significantly enhanced as root-zone temperature increased. Rate of floral cluster opening was also markedly increased with increasing root-zone temperature. Shoot length increased but shoot girth growth declined as root-zone temperatures increased. Soil respiration and leaf photosynthesis generally increased as root-zone temperatures increased. Results indicate that apple trees growing in regions where root zone temperatures are < or = 15 degrees C have delayed bud break and up to 20% fewer clusters than apple trees exposed to root zone temperatures of > or = 15 degrees C. The effect of root-zone temperature on shoot performance may be mediated through the mobilization of root reserves, although the role of phytohormones cannot be discounted. Variation in leaf photosynthesis across the temperature treatments was inadequately explained by stomatal conductance. Given that root growth increases with increasing temperature, changes in sink activity induced by the root-zone temperature treatments provide a possible explanation for the non-stomatal effect on photosynthesis. Irrespective of underlying mechanisms, root-zone temperatures influence bud break and flowering in apple trees.     

Chlorophyll fluorescence and CO(2) assimilation of black spruce seedlings following frost in different temperature and light conditions

Effects of artificial frosts on light-saturated photosynthesis (A(max)) and ground, maximal and variable fluorescence variables (F(o), F(m), and F(v) and F(v)/F(m)) were monitored on 1-year-old foliage of black spruce seedlings (Picea mariana (Mill.) BSP) grown at high (25 degrees C), moderate (15 degrees C) and low (5 degrees C) temperatures and moderate (240 &mgr;mol m(-2) s(-1)) and low (80 &mgr;mol m(-2) s(-1)) irradiances. Photoinhibition of 1-year-old foliage was greater in seedlings grown in moderate light than in seedlings grown in low light. Photoinhibition increased with decreasing growth chamber temperature at both irradiances. Most changes in F(v)/F(m) were caused by changes in F(v). Exposure to -4 degrees C decreased both F(v)/F(m) and A(max) compared with control values. The effect of the -4 degrees C frost treatment was greater in seedlings grown in low light than in seedlings grown in moderate light, probably because seedlings grown in moderate light were already partially photoinhibited before the frost treatment. Following -4 degrees C treatment, neither F(v)/F(m) nor A(max) recovered in seedlings grown in low light. Light-saturated photosynthesis decreased with decreasing growth chamber temperature. Light-saturated photosynthesis was more sensitive to the -3 and -4 degrees C frost treatments in seedlings grown at 25 degrees C than in seedlings grown at 15 and 5 degrees C. The A(max) of seedlings grown at 15 degrees C was sensitive only to the -4 degrees C frost treatment, whereas A(max) of seedlings grown at 5 degrees C was not sensitive to any of the frost treatments. Recovery of A(max) following frost took longer in seedlings grown at high temperatures than in seedlings grown at low temperatures. For seedlings grown at the same temperature but under different irradiances, both A(max) and F(v)/F(m) reflected damage to the photosynthetic system following a moderate frost. However, for seedlings grown at the same irradiance but different temperatures, A(max) provided a more sensitive indicator of frost damage to the photosynthetic system than F(v)/F(m) ratio.     

Method for measuring viscoelastic properties of wood under high temperature and high pressure steam conditions

A method for measuring the viscoelastic properties of wood under high temperature and high pressure steam was developed using a testing machine with a built-in autoclave. A newly developed load cell capable of resisting a steam pressure of 16kgf/cm² and a temperature of 200°C was installed in the autoclave. This load cell could be used to determine precisely the loads while steaming at temperatures from 100°C to 200°C. In addition to load-detection problems, it was necessary to avoid the nonuniform thermal degradation of wood during the measurement process under steaming at high temperatures. This nonuniform degradation could be minimized by shortening the time required for the wood to attain thermal equilibrium using specimens conditioned to the fiber saturation point. According to this method, a stress relaxation curve for sugi (Cryptomeria japonica D. Don) wood being compressed while steaming at 180°C was obtained. The stress was seen to decrease rapidly with time, reaching almost zero at 3000s.     

初春气象条件对苹果开花期的影响分析

通过分析苹果开花期年际变化特征及气象条件对苹果花期的影响,证明初春温度是影响苹果开花期早晚的主要气象因子。3月至4月上旬≥0℃积温每增加或减少10℃,开花期提早或推迟1 d;3月下旬至4月上旬平均最高气温每偏高或偏低0.5℃,开花期提早或推迟1 d;根据初春气象条件,准确预报苹果开花期,为做好果园田间管理,有效防御霜冻灾害提供科学依据。     

Heating and temperature distribution under cyclic deflection in the non-linear region for wood

Summary Temperature distribution during a fatigue process was examined under cyclic deflection in the non-linear region. The cyclic deflection caused a remarkable and local rise in temperature by the heating due to viscosity of air-dried wood. The appearance of the peak in temperature versus the logarithmic cyclic number was explained on the basis of viscosity change due to moisture movement and vaporization by heating during the fatigue process. The change of the temperature distribution was related to the heat transfer and the heat capacity of wood.     

Changes of crystallinity in wood cellulose by heat treatment under dried and moist conditions

The different effects of heat treatment on wood, especially on the cellulose crystallites of wood under ovendried and highly moist conditions, were investigated by X-ray diffractometer. Heat was found to increase significantly the crystallinity of wood cellulose; moreover, almost twice as much crystallization was observed after heat treatment of spruce and buna under a highly moist condition than under the oven-dried condition. In pure cellulose almost the same crystallization was observed under both the conditions, whereas more crystallization occurred in wood cellulose than in pure cellulose. Absolute crystallization was observed for the wood species and pure cellulose under both conditions, considering the thermal decomposition of the amorphous region in addition to crystallization. Our results suggested that other components accomparying wood cellulose were involved in the increase of crystallinity by heat treatment, and that wood cellulose contained more quasicrystalline regions than pure cellulose. Moreover, calculated apparent activation energies revealed that crystallization and decrystallization in pure and wood cellulose under heat treatment of highly moist condition were some-what easier than those under the oven-dried condition. The behavior of the piezoelectric modulusd ₂₅ almost paralleled that of crystallinity.     

Winter frost resistance of Pinus cembra measured in situ at the alpine timberline as affected by temperature conditions

Winter frost resistance (WFR), midwinter frost hardening and frost dehardening potential of Pinus cembra L. were determined in situ by means of a novel low-temperature freezing system at the alpine timberline ecotone (1950 m a.s.l., Mt Patscherkofel, Innsbruck, Austria). In situ liquid nitrogen (LN?)-quenching experiments should check whether maximum WFR of P. cembra belonging to the frost hardiest conifer group, being classified in US Department of Agriculture climatic zone 1, suffices to survive dipping into LN? (-196 °C). Viability was assessed in a field re-growth test. Maximum in situ WFR (LT??) of leaves was <-?75 °C and that of buds was less (-70.3 °C), matching the lowest water contents. In midwinter, in situ freezing exotherms of leaves, buds and the xylem were often not detectable. Ice formed in the xylem at a mean of -2.8 °C and in leaves at -3.3 °C. In situ WFR of P. cembra was higher than that obtained on detached twigs, as reported earlier. In situ LN?-quenching experiments were lethal in all cases even when twigs of P. cembra were exposed to an in situ frost hardening treatment (12 days at -20 °C followed by 3 days at -50 °C) to induce maximum WFR. Temperature treatments applied in the field significantly affected the actual WFR. In January a frost hardening treatment (21 days at -20 °C) led to a significant increase of WFR (buds: -62 °C to <-?70 °C; leaves: -59.6 °C to -65.2 °C), showing that P. cembra was not at its specific maximum WFR. In contrast, simulated warm spells in late winter led to premature frost dehardening (buds: -32.6 °C to -10.2 °C; leaves: -32.7 to -16.4 °C) followed by significantly earlier bud swelling and burst in late winter. Strikingly, both temperature treatments, either increased air temperature (+10.1 °C) or increased soil temperature (+6.5 °C), were similarly effective. This high readiness to frost harden and deharden in winter in the field must be considered to be of great significance for future winter survival of P. cembra. Determination of WFR in field re-growth tests appears to be a valuable tool for critically judging estimates of WFR obtained on detached twigs in an ecological context.     

Nitrogen uptake of maize (Zea mays. L) from isotope-labeled biomass of Paraserianthes falcataria grown under controlled conditions

Roots can be an important though poorly quantified source of nitrogen (N) in agroforestry systems. Nitrogen uptake of maize using P. falcataria below- and aboveground biomass separately, and their combination, as source of N, was assessed in a controlled experiment using ¹⁵N isotope labeling techniques. The ¹⁵N-direct and the ¹⁵N-indirect labeling techniques were compared for discrepancies in measuring N cycling from P. falcataria tree residues. N contribution to maize production was as follows; 40–57% from below ground biomass and 10–18% from above ground biomass (P < 0.05). Residue N use efficiency (%rNE) by maize was between 99 and 106% for belowground biomass, 4–4.5% for aboveground biomass. This implies that though nutrient release characteristics of aboveground biomass are commonly used as a basis for selection of agroforestry trees, those of belowground biomass would be of fundamental importance as well. Combining P. falcataria below and aboveground biomass did not result in significant (P < 0.05) effects on N recovered by maize, suggesting the absence of decomposition interactions between the two bio-chemically contrasting residues. There were no significant methodological differences reflected in measured N cycled by maize from leaves (Ndfr); 15% and 18% as estimated by ¹⁵N direct and indirect method, respectively. The two methods compared very well (P < 0.05) as tools of estimating N cycling from surface applied leaves. However, the ability of the direct method to measure N without disturbing either the tree or the soil, would make it a more attractive and valuable tool in N cycling studies in agroforestry systems.This revised version was published online in November 2005 with corrections to the Cover Date.     

新疆野苹果与部分栽培品种花粉形态的比较

为了从孢粉学角度探讨新疆野苹果与部分栽培品种的亲缘关系,以新疆伊犁地区的新源县、巩留县、伊宁县、霍城县和塔城地区的托里县共5个居群中的野苹果及18份不同栽培苹果品种的花粉为试材,采用扫描电镜技术对其形态、大小、萌发孔和纹饰进行了观察,并以电子显微镜对其进行了定量测定。结果表明:与新疆栽培品种相比,除了纹饰有细微不同之外,新疆野苹果的其它形态特征相近,差异不明显,这说明新疆野苹果是新疆栽培苹果品种的重要种源之一。     

Diameter growth of Scots pine (Pinus sylvestris) trees grown at elevated temperature and carbon dioxide concentration under boreal conditions

We investigated the impacts of elevated temperature and carbon dioxide concentration ([CO2]) on diameter growth of Scots pine (Pinus sylvestris L.), aged about 20 years, grown with a low nitrogen supply in closed chambers at (i) ambient temperature and [CO2] (AT+AC), (ii) ambient temperature and elevated [CO2] (AT+EC), (iii) elevated temperature and ambient [CO2] (ET+AC), and (iv). elevated temperature and [CO2] (ET+EC). Each treatment was replicated four times. Diameter growth was monitored with a band dendrograph at 15-min intervals throughout the growing seasons of 1997, 1998 and 1999. Over the monitoring period, diameter growth began 2-3 weeks earlier in trees in the ET+EC and ET+AC chambers than in trees in the AT+AC and AT+EC chambers. However, the cessation of growth occurred about a week later in trees in the ET+EC, ET+AC and AT+EC chambers compared with the AT+AC chambers. The duration of the growing season was 115 and 108 days in the ET+EC and ET+AC chambers, respectively, and 95 and 84 days in the AT+EC and AT+AC chambers, respectively. The ET+AC and ET+EC treatments enhanced diameter growth most early in the growing season, whereas in trees in the AT+AC and AT+EC treatments diameter growth rate was highest in the middle of the growing season. Diameter growth rate leveled off more slowly in trees in the ET+EC and AT+EC treatments than in the other treatments. The growth response to elevated T, elevated [CO2] or both decreased with time and it was less than the maximum observed in other studies for small seedlings and under optimal growth conditions. Nevertheless, cumulative diameter growth for the 3-year period was 67% greater in trees in the ET+EC treatment, and 57 and 26% greater in trees in the AT+EC and ET+AC treatments, respectively, compared with trees in the AT+AC treatment. Over the 3 years, [CO2] had a statistically significant (P < 0.10) effect on both absolute and relative diameter growth, but the interaction between [CO2] and temperature was not significant.     

Dynamics and potentials of carbon sequestration in managed stands and wood products in Finland under changing climatic conditions

Carbon (C) sequestration was studied in managed boreal forest stands and in wood products under current and changing climate in Finland. The C flows were simulated with a gap-type forest model interfaced with a wood product model. Sites in the simulations represented medium fertile southern and northern Finland sites, and stands were pure Scots pine and Norway spruce stands or mixtures of silver and pubescent birch.

Changing climate increased C sequestration clearly in northern Finland, but in southern Finland sequestration even decreased. Temperature is currently the major factor limiting tree growth in northern Finland. In southern Finland, the total average C balance over the 150 year period increased slightly in Scots pine stands and wood products, from 0.78 Mg C ha⁻¹ per year to 0.84 Mg C ha⁻¹ per year, while in birch stands and wood products the increase was larger, from 0.64 Mg C ha⁻¹ per year to 0.92 Mg C ha⁻¹ per year. In Norway spruce stands and wood products, the total average balance decreased substantially, from 0.96 Mg C ha⁻¹ per year to 0.32 Mg C ha⁻¹ per year. In northern Finland, the total average C balance of the 150 year period increased under changing climate, regardless of tree species: in Scots pine stands and wood products from 1.10 Mg C ha⁻¹ per year to 1.42 Mg C ha⁻¹ per year, in Norway spruce stands and wood products from 0.69 Mg C ha⁻¹ per year to 0.99 Mg C ha⁻¹ per year, and in birch stands and wood products from 0.43 Mg C ha⁻¹ per year to 0.60 Mg C ha⁻¹ per year.

C sequestration in unmanaged stands was larger than in managed systems, regardless of climate. However, wood products should be included in C sequestration assessments since 12–55% of the total 45–214 Mg C ha⁻¹ after 150 years' simulation was in products, depending on tree species, climate and location. The largest C flow from managed system back into the atmosphere was from litter, 36–47% of the total flow, from vegetation 22–32%, from soil organic matter 25–30%. Emissions from the production process and burning of discarded products were 1–6% of the total flow, and emissions from landfills less than 1%.