浅谈人造薄木生产中单板的漂白

详细阐述了木材颜色的成因及漂白机理，重点介绍了人造薄木生产过程中单板漂白工艺。研究表明，经漂白处理的单板，颜色明显变浅，色调也比较均匀，而且还消除了板面污染，对单板的染色十分有利。     

23种广东常见阔叶树材的耐磨性质

本文报导23种广东常见阔叶树材的耐磨性试验结果,并对耐磨性与木材密度、硬度的关系及木材耐磨性各向异性问题作了讨论。     

超临界CO_2流体处理工艺对木材渗透性的影响

以苯—乙醇为夹带剂,研究超临界CO2流体不同处理压力、温度、时间对福建产杉木、马尾松、檫木木材渗透性的影响。结果表明,在35 MPa内,处理压力的增大有利于3种木材渗透性的提高;杉木在处理温度为40℃时,渗透性的变化率达到最大,为493%,马尾松和檫木在处理温度为45℃时,渗透性的变化率达到最大,分别为479%和349%;较佳的处理时间为30 min。     

火炬松短周期工业材不同高度上干缩性能的研究

对湖南同一立地指数（１８）下，５株１７．５年生的火炬松（ＰｉｎａｓｔａｅｄａＬ．）短周期工业材１．３，３．６，５．６，７．６，９．６ｍ５个高度的木材干缩系数、基本密度、生长轮宽度、晚材率和微纤丝角度，按生长轮取样，进行了测量和统计分析．结果表明，弦向、径向、体积干缩系数和干缩比，在树于５个高度之间的差异，均达到了显著水平；各高度干缩系数与生长轮的年龄（离髓心的距离）以及与上述各主要构造因子之间呈显著的线性相关，且相关度度随树干高度的增加而减弱．     

酥梨采后灰霉病生防菌株的鉴定及抑菌作用

以微生物拮抗病原菌是防治病害安全高效的可行手段。通过对果实表面微生物进行筛选鉴定,以期得到一株可以有效抑制灰霉病的生物防治菌株。对拮抗菌株H-1进行形态学特征、生理生化特性分析,结合16S rDNA序列分析和gyrB 基因序列分析构建系统发育树;采用平板对峙法结合果实伤口试验考察拮抗菌H-1在体外及梨果表面的抑菌作用。结果表明：经鉴定H-I菌株为贝莱斯芽孢杆菌（Bacillus velezensis）;B. velezensis H-1在体外条件下可显著抑制灰葡萄孢霉（Botrytis cinerea）、细极链格孢（Alternaria tenuissima）和串珠镰孢菌（Fusarium verticillioides）的菌丝生长,其中对灰葡萄孢霉菌丝的抑制作用最强;果实伤口试验表明,1×1011 CFU/mL的B. velezensis H-1可完全抑制梨果表面灰霉菌生长。由此可见,B. velezensis H-1可以有效抑制梨果采后灰霉病的发生。     

25％啶菌噁唑乳油防治番茄灰霉病药效试验

田间试验表明25%啶菌唑乳油对番茄灰霉病有良好的防治效果,53.3～106.7mL/667m23次药后防效79%以上。     

Further suppression of<Emphasis Type="Italic">Botrytis cinerea</Emphasis> disease in cucumber seedlings by chitosan-copper complex as compared with chitosan alone

Chitosan-copper complex compared with chitosan alone enhanced suppression ofBotrytis cinerea rot development on four-true-leaf cucumber seedlings in controlled growth chambers. This paper constitutes the first report of such enhancement. The optimal concentrations for the most effective suppression ofBotrytis development were 0.2 gl ⁻¹ chitosan and 1.6 mmole copper. After 12 days’ incubation, marked and significantly better disease suppression was obtained with chitosan-copper complex (75% suppression) than with chitosan alone. The chitosan-copper complex could be a very promising decay control agent for use in both conventional and organic agriculture. http://www.phytoparasitica.org posting Dec. 18, 2002.     

Fungi associated with esca disease in grapevine

Cross sections of woody stems of 309 diseased grapevines collected in France showed two kinds of necrosis typical of esca: a) A central light-colored necrosis of soft consistency, consisting of three zones, preceded by a centrally discolored wood, and b) a sectorial light-colored necrosis composed of two zones preceded by a sectorial brown necrosis. Isolations showed that different microflora was associated with each necrosis. Phaeoacremonium aleophilum and Phaeoacremonium chlamydosporum occurred in the discolored wood and the zones bordering the central decayed wood. Eutypa lata was the main fungus isolated from sectorial brown necrosis and the zones adjoining the decay wood. Phellinus punctatus was isolated from the sectorial and central decayed wood. Stereum hirsutum was present in decayed wood of 15 grapevines with esca symptoms not inhabited by P. punctatus. Wood decay tests and pathogenicity tests showed that S. hirsutum and P. punctatus were responsible for the decayed wood. Phaeoacremonium chlamydosporum and S. hirsutum produced a centrally discolored wood similar to that found in esca-affected vines. Phaeoacremonium aleophilum caused a sectorial brown necrosis of soft texture. From these studies, it was found that esca is a complex disease involving several microorganisms whose role in the process leading to wood degradation is discussed.     

木质包装中黄斑星天牛微波处理初探

为了探索微波处理作为木质包装替代处理方法的可能性,对不同规格和含水量的杨树木块进行微波处理试验,结果表明:频率为2450MHz的微波能够穿透厚度为10cm的杨树木材;当微波功率为900W时,规格为10cm×10cm×10cm和10cm×10cm×2.5cm的新木块中黄斑星天牛(Anoplophora nobolis)幼虫完全死亡所需时间分别为5min和2min;而干木块中则仅需3min和30s.对微波处理引起木材温度变化和水分损失以及天牛幼虫的水分损失进行了初步研究.     

Expression of the tobacco β-1,3-glucanase gene, PR-2d, following induction of SAR with Peronospora tabacina

Systemic acquired resistance (SAR) is induced following inoculation of Peronospora tabacina sporangia into the stems of Nicotiana tabacum plants highly susceptible to the pathogen. Previous results have shown that accumulation of acidic β-1,3-glucanases (PR-2's) following induction of SAR by P. tabacina may contribute to resistance to P. tabacina. We showed that up-regulation of the PR-2 gene, PR-2d, following stem inoculation with P. tabacina, is associated with SAR. Studies using plants transformed with GUS constructs containing the full length promoter from PR-2d or promoter deletions, provided evidence that a previously characterized regulatory element that is involved in response to salicylic acid (SA), may be involved in regulation of PR-2d following induction of SAR with P. tabacina. This work provides evidence that regulation of PR-2 genes during P. tabacina-induced SAR may be similar to regulation of these genes during infection of N-gene tobacco by TMV or following exogenous application of SA, and provides further support for the role of SA in regulation of genes during P. tabacina-induced SAR.