大气SO2和NO2污染及植物的抗性和净化能力研究进展

SO2和NO2为我国大气污染主要污染物,城市森林对SO2和NO2具有一定的抵抗能力和吸收净化能力,利用城市森林对大气污染进行修复具有良好的应用前景.文章概述了我国SO2和NO2气体污染的状况,总结了污染物进入植物体的过程及其损伤机理,并从植物抗性和吸附净化能力两方面总结了城市景观树种与SO2和NO2气体污染的关系研究,并基于研究结论提出今后研究可能发展方向,如SO2、NO2与悬浮颗粒物等复合污染对城市树种生长的影响、树种抗性和吸附能力综合研究等.     

翠冠梨茎段组织培养的研究

以翠冠梨茎段为外植体进行组织培养研究,筛选出了较为适合该品种离体繁殖的基本培养基为1/2M S,并通过无芽茎段培养获得了愈伤组织,通过有芽茎段培养获得了无菌苗.     

山东省高速公路绿化对空气的净化效果研究

采用测定SO2、NO2和CO2气体含量的方法,研究了山东省主要高速公路路侧绿化带,互通立交区、入口匝道区和服务区绿地对空气的净化效果。测定结果表明,路侧绿化带对SO2有较明显的净化作用,互通立交区、入口匝道区和服务区的绿化对SO2和NO2均有较好的吸收净化作用,而高速路绿化对CO2含量的影响则较小。     

沉水樟体外植株再生体系的建立

以沉水樟幼嫩茎段为材料,对其体外植株高效再生系统进行了研究。在对比激素种类和激素浓度组合对沉水樟茎段芽诱导和根诱导影响的基础上,筛选出了其茎段芽诱导的最适培养基为MS+0 2IBA+5BA,根诱导的最适培养基为1/2MS+0 3IAA。芽诱导率最高可达到86 7%。该研究结果为沉水樟基因工程、细胞工程操作、新品种培育及其工厂化育苗奠定了坚实的基础。     

二氧化氯漂白技术用于提高竹浆粕白度的研究

探讨了竹浆粕生产过程中二氧化氯漂白(D1、D2段)的重要性和必要性,D1段和D2段分别研究了ClO2用量、NaOH用量、温度、时间4个因素及ClO2用量单因素对二氧化氯漂白效果的影响,包括α-纤维素、聚戊糖、白度、卡伯值、黏度、灰分等性能,其中D1段分析了白度提高与浆粕α-纤维素、聚戊糖及灰分的关系。结果表明,D1段最优工艺条件为:ClO2用量1.52%且NaOH用量0.76%(NaOH与ClO2质量比1∶2),温度75℃,时间120 min,浆质量分数10%。经D1段处理后,竹浆白度提高率达到了78.8%,黏度下降率仅为19.55%,漂白选择性高。在D1段漂白工艺的基础上,确定D2段的ClO2用量0.8%,且漂白时间120 min,漂白温度75℃,浆质量分数10%。浆料白度增加的过程中,一定程度上提高了α-纤维素含量同时降低了聚戊糖及灰分等杂质的含量,达到了调整竹浆粕质量指标和提高反应性能的目的。经含有两段二氧化氯漂白的无元素氯漂白流程处理后,竹浆粕最终白度达到了88.2%(ISO)。     

下的降解

对木质素磺酸盐在紫外光/双氧水(UV/H2O2)体系下的降解过程进行了研究,通过对比处理前后木质素磺酸盐溶液的紫外可见光谱、凝胶渗透色谱(GPC)谱图、红外光谱谱图、1H NMR谱图及溶液化学耗氧量(COD)的变化对其降解过程进行了跟踪和讨论。此外,通过对木质素的模型化合物——愈创木酚降解的研究,推测了降解中苯环的开环过程。实验结果表明,木质素磺酸盐在UV/H2O2体系处理下能够发生降解,降解过程中首先生成一些中间产物,随着反应时间的加长,最终能够降解成CO2、H2O等小分子化合物。     

城郊结合型城区 PM 2．5防治措施

指出了新修订的《环境空气质量标准》（GB3095-2012）增加了PM2．5指标，同时，青岛市已于2013年1月1日起执行这一新标准。针对城阳城郊结合型城区的特点，研究了PM2．5监测技术原理和方法，开展了PM 2．5来源分析，提出了PM 2．5污染防治对策。     

八角组织培养试验初报

以八角顶芽为材料,试验了几种基本培养基对茎段组织培养的影响,并研究了八角茎段组织培养技术.结果表明:0.1%HgCl2消毒12 min效果较好;春季外植体比秋季外植体更适离体培养;MS比1/2 MS、White、MS改培养基适于茎段的萌芽培养,萌动率达27.6%.最适的初代培养基为:MS+IBA1.0 mg·L-1+6-BA3.5 mg·L-1,萌芽率达76.7%.     

质量平衡法估测树干呼吸的理论与应用

介绍质量平衡法的理论、估测方法及其应用,并对其进行评价.质量平衡理论认为:一段树干组织产生的CO2,应该是CO2通量的总和,包括通过树皮向外扩散的CO2释放通量、该段树干液流中的CO2运输通量(流入和流出液流的CO2浓度之差)及液流中的CO2储存通量(液流中CO2浓度在时间上的变化量).应用质量平衡法测定树干呼吸的关键是要估测树干内部的CO2通量,即液流中CO2的储存、运输和扩散.对于液流中CO2的估测主要有2种方法:1)用仪器直接测定木质部液流中的CO2浓度;2)通过测定树干液流停止流动或相对很低时(夜间)树干的CO2释放通量与液流流动时(白天)树干CO2释放通量的差值,间接估测木质部液流中CO2浓度.质量平衡方法提供了一个更为精确地估测木本组织呼吸的方法,其结果更为合理.     

南充市大气环境容量核定及影响评价

以南充市的两控区为研究对象，分别对点源、线源、面源运用A—P值法进行了理想大气容量和实际大气容量测定。通过核定得出了南充近年来SO2、PM10均有超标现象，NO2没有超标但实际环境容量较小。就南充市目前的环境现状，提出了相应的削减对策。     

扭叶松实木板材三种动态弹性模量和静态弹性模量比较研究(英文)

采用Pundit、Metriguard、FFT等三种无损检测方法和常规弯曲法对加拿大扭叶松(lodgepole pine)蓝变与非蓝变实木板材的动态及静态弹性模量进行检测和比较研究。结果表明,蓝变材三种动态弹性模量及静态弹性模量均高于非蓝变材;对比分析表明,蓝变材和非蓝变材的动态及静态弹性模量存在差异,其中动态弹性模量差异均达到0.01显著性水平,静态弹性模量差异达到0.05显著性水平,并且心、边材及密度值不同是导致以上差异的主要原因。相关性分析表明,动态与静态弹性模量间相关性达到0.01显著性水平;尽管三种无损检测方法测量结果存在差异,但它们之间仍存在密切相关性,FFT 技术测量的准确性高于Pundit和Metriguard;板材中结子数影响木材动态和静态弹性模量,随着板材结子数增加弹性模量相应地降低。     

Spread of Cryphonectria hypovirus1 into 45 vegetative compatibility types of Cryphonectria parasitica on grafted American chestnut trees

A mixture of hypovirulent strains of Cryphonectria parasitica, including four white (European) strains infected with Cryphonectria hypovirus1 (CHV1), was used in 1982 and 1983 to inoculate natural blight cankers located within a zone ranging from the ground to 183 cm on grafted American chestnut trees. These four white strains belonged to three vegetative compatibility (vc) types. Using pigmented, single‐spore colonies from white isolates, 48 vc types were identified among 110 white isolates recovered in 1996, 1998, and 1999 from cankers located outside the inoculated zone. Twenty‐five of the 48 white vc types consisted of two or more isolates. The 25 major white vc types were vegetatively incompatible with all four of the original white hypovirulent strains, providing evidence for spread of CHV1 but not for spread of the original inoculated strains. Forty‐five vc types represent the minimum number of `new' vc types into which CHV1 had spread. The ratio of white vc types to white isolates tested (S/N) and Shannon diversity index were 0.436 and 3.64, respectively. The spatial pattern of white vc types on the grafts was found to be non‐random (p=0.019). White single‐spore colonies of white isolates were placed into four cultural morphology (CM) groups. The two largest groups contained 37 (CM group 3) and 33 (CM group 1) isolates. Single‐spore colonies from the original, white inoculated strain, Ep 49, were classified into CM groups 3 and 1, and colonies of Ep 51 W were classified into CM group 1.     

A growth model of a single sugi (Cryptomeria japonica) tree based on the dry matter budget of its aboveground parts

Growth of a single sugi (Cryptomeria japonica (L.f.) D. Don.) tree was analyzed on the basis of a dry matter budget. The aboveground net production rate and death rate were defined as the anabolic rate and catabolic rate, respectively. Growth rate of aboveground tree weight, v(w) (kg(dw) year(-1)), was defined as follows: v(w) = v(p) - v(d) (1) where v(p) (kg(dw) year(-1)) is the aboveground net production rate and v(d) (kg(dw) year(-1)) is the aboveground death rate. The value of v(d) is obtained by measuring the monthly clippings of new dead leaves and branches attached to a sample tree. The value of v(w) was calculated as the annual difference in the estimated aboveground tree weight, w(T) (kg(dw)). Finally, the value of v(p) was estimated as the sum of the values of v(d) and v(w). The following allometric relationships were found between v(p) and w(T) and between v(d) and w(T): v(p) = aw(T) (alpha), v(d) = bw(T) (beta) (2). Combining Equations 1 and 2 gives a growth equation, Bertalanffy's equation, of the sample tree. dw(T)/dt = v(w) = aw(T) (alpha) - bw(T) (beta) (3). Because the growth curve of w(T) was derived from Equation 3, the analysis of the growth of w(T) is based on direct measurement of the dry matter budget.     

An analysis of light effects on foliar morphology,physiology, and light interception in temperate deciduous woody species of contrasting shade tolerance

Maximum Rubisco activities (V(cmax)), rates of photosynthetic electron transport (J(max)), and leaf nitrogen and chlorophyll concentrations were studied along a light gradient in the canopies of four temperate deciduous species differing in shade tolerance according to the ranking: Populus tremula L. < Fraxinus excelsior L. < Tilia cordata Mill. = Corylus avellana L. Long-term light environment at the canopy sampling locations was characterized by the fractional penetration of irradiance in the photosynthetically active spectral region (I(sum)). We used a process-based model to distinguish among photosynthesis limitations resulting from variability in fractional nitrogen investments in Rubisco (P(R)), bioenergetics (P(B), N in rate-limiting proteins of photosynthetic electron transport) and light harvesting machinery (P(L), N in chlorophyll and thylakoid chlorophyll-protein complexes). On an area basis, V(cmax) and J(max) (V(a) (cmax) and J(a) (max)) increased with increasing growth irradiance in all species, and the span of variation within species ranged from two (T. cordata) to ten times (C. avellana). Examination of mass-based V(cmax) and J(max) (V(m) (cmax) and J(m) (max)) demonstrated that the positive relationships between area-based quantities and relative irradiance mostly resulted from the scaling of leaf dry mass per area (M(A)) with irradiance. Although V(m) (cmax) and J(m) (max) were positively related to growth irradiance in C. avellana, and J(m) (max) was positively related to irradiance in P. tremula, the variation range was only a factor of two. Moreover, V(m) (cmax) and J(m) (max) were negatively correlated with relative irradiance in T. cordata. Rubisco activity in crude leaf extracts generally paralleled the gas-exchange data, but it was independent of light in T. cordata, suggesting that declining V(m) (cmax) with increasing relative irradiance was related to increasing diffusive resistances from the intercellular air spaces to the sites of carboxylation in this species. Because irradiance had little effect on foliar nitrogen concentration, the relationships of P(B) and P(R) with irradiance were similar to those of V(m) (cmax) and J(m) (max). Shade-intolerant species tended to have greater P(B) and P(R) and also larger V(a) (cmax) and J(a) (max) than more shade-tolerant species. However, for the whole material, P(B) and P(R) varied only about 50%, whereas V(a) (cmax) and J(a) (max) varied more than 15-fold, further emphasizing the importance of leaf anatomical plasticity in determining photosynthetic acclimation to high irradiance. Leaf chlorophyll concentrations and fractional nitrogen investments in light harvesting increased hyperbolically with decreasing irradiance to improve quantum use efficiency for incident irradiance. The effect of irradiance on P(L) was of the same order as its effect in the opposite direction on M(A), leading to either a constant model estimate of leaf absorptance with I(sum) or a slightly positive correlation. We conclude that leaf morphological plasticity is a more relevant determinant of foliage adaptation to high irradiance than foliage biochemical properties, whereas biochemical adaptation to low irradiance is of the same magnitude as the anatomical adjustments. Although shade-tolerant species did not have greater chlorophyll concentrations and P(L) than shade-intolerant species, they possessed lower M(A), and could maintain a more extensive foliar display for light capture with constant biomass investment in leaves.     

Metabolism of deuterium- and tritium-labeled gibberellins in cambial region tissues of Eucalyptus globulus stems

Deuterium- and tritium-labeled gibberellins (GAs) were applied to stems of 3-year-old Eucalyptus globulus Labill. saplings and 9-month-old potted seedlings. Cambial region tissues surrounding the application point were collected 6, 24 or 48 h later. Twenty-four hours after application of 5 &mgr;g of [(2)H(2)]GA(20), 7% of the cambial region GA(20) pool, 7% of the GA(1) pool and 58% of the GA(29) pool were labeled with deuterium based on selected ion monitoring of purified extracts subjected to gas chromatography-mass spectrometry. The relatively low percent dilution of endogenous GAs by [(2)H(2)]GAs suggests that the exogenous application of [(2)H(2)]GA(20) did not result in substrate overloading, indicating that these conversions probably occur naturally within cambial region tissues. Extracts from similar cambial region tissues fed tritium-labeled GAs were sequentially fractionated by SiO(2) partition chromatography, C(18) reversed phase HPLC and N(CH(3))(2) HPLC. The radioactivity profiles indicated metabolism of GA(20) to GA(1) and GA(29), GA(1) conversion to GA(8), GA(4) to GA(34) and GA(9) to GA(51). Gibberellins GA(34), GA(51) and GA(29) are C-2beta-hydroxylated catabolites of low biological activity, whereas GA(1) and GA(4) are probably effectors of growth in the Eucalyptus stem and shoot. Evidence for C-13 hydroxylation of GA(4) to GA(1), GA(9) to GA(4) or GA(9) to GA(20) in the stem was inconclusive. Thus, although GA(4) and GA(9) are native to cambial region tissues, GA(1) is probably not produced from them in significant quantities. We conclude that the early C-13-hydroxylation pathway; i.e., conversion of GA(19) to GA(20) to GA(1), is the major pathway of GA(1) biosynthesis.     

Partititioning concurrent influences of nitrogen and phosphorus supply on photosynthetic model parameters of Pinus radiata

Responses of photosynthesis (A) to intercellular CO(2) concentration (C(i)) were measured in a fast- and a slow-growing clone of Pinus radiata D. Don cultivated in a greenhouse with a factorial combination of nitrogen and phosphorus supply. Stomatal limitations scaled with nitrogen and phosphorus supply as a fixed proportion of the light-saturated photosynthetic rate (18.5%) independent of clone. Photosynthetic rates at ambient CO(2) concentration were mainly in the V(cmax)-limited portion of the CO(2) response curve at low-nitrogen supply and at the transition between V(cmax) and J(max) at high-nitrogen supply. Nutrient limitations to photosynthesis were partitioned based on the ratio of foliage nitrogen to phosphorus expressed on a leaf area basis (N(a)/P(a)), by minimizing the mean square error of segmented linear models relating photosynthetic parameters (V(cmax), J(max), T(p)) to foliar nitrogen and phosphorus concentrations. A value of N(a)/P(a) equal to 23 (mole basis) was identified as the threshold separating nitrogen (N(a)/P(a) < or = 23) from phosphorus (N(a)/P(a) > 23) limitations independent of clones. On an area basis, there were significant positive linear relationships between the parameters, V(cmax), J(max), T(p) and N(a) and P(a), but only the relationships between T(p) and N(a) and P(a) differed significantly between clones. These findings suggest that, in genotypes with contrasting growth, the responses of V(cmax) and J(max) to nutrient limitation are equivalent. The relationships between the parameters V(cmax), J(max), T(p) and foliage nutrient concentration on a mass basis were unaffected by clone, because the slow-growing clone had a significantly greater leaf area to mass ratio than the fast-growing clone. These results may be useful in discriminating nitrogen-limited photosynthesis from phosphorus-limited photosynthesis.     

Responses of foliar gas exchange to long-term elevated CO(2) concentrations in mature loblolly pine trees

Branches of field-grown mature loblolly pine (Pinus taeda L.) trees were exposed for 2 years (1992 and 1993) to ambient or elevated CO(2) concentrations (ambient + 165 micro mol mol(-1) or ambient + 330 micro mol mol(-1) CO(2)). Exposure to elevated CO(2) concentrations enhanced rates of net photosynthesis (P(n)) by 53-111% compared to P(n) of foliage exposed to ambient CO(2). At the same CO(2) measurement concentration, the ratio of intercellular to atmospheric CO(2) concentration (C(i)/C(a)) and stomatal conductance to water vapor did not differ among foliage grown in an ambient or enriched CO(2) concentration. Analysis of the relationship between P(n) and C(i) indicated no significant change in carboxylation efficiency of ribulose-1,5-bisphosphate carboxylase/oxygenase during growth in elevated CO(2) concentrations. Based on estimates derived from P(n)/C(i) curves, there were no apparent treatment differences in dark respiration, CO(2) compensation point or P(n) at the mean C(i). In 1992, foliage in the three CO(2) treatments yielded similar estimates of CO(2)-saturated P(n) (P(max)), whereas in 1993, estimates of P(max) were higher for branches grown in elevated CO(2) than in ambient CO(2). We conclude that field-grown loblolly pine trees do not exhibit downward acclimation of leaf-level photosynthesis in their long-term response to elevated CO(2) concentrations.