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A fast method to prepare microslides of wood in advanced stages of decay

机译:一种快速制备腐烂的先进阶段微玻璃纤维的方法

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摘要

Biologically degraded wood in advanced stages of decay has a very soft and brittle structure that causes many problems during sectioning. Embedding wood specimens in different kinds of media ensures preparation of good quality microsections, but the preparation time is very long. The proposed method does not only have a reduced preparation time but also minimizes costs and consumption of chemicals while improving stabilization of the specimen and en hancing the quality of sections. The crux of the method is application of a reinforcing layer of transparent nail polish gel on a dry specimen that has been only stabilized (not embedded) with PEG 1500 medium. The gel is applied on a specimen in two layers just before sectioning. The first layer infiltrates the specimen sufficiently deep to fill the lumens and cell walls and allows preparation of thin sections from decayed wood. The second layer reinforces the section and allows better handling. Subsequently, the reinforcing and embedding layers are removed using pure acetone. This innovative method has so far been successfully tested on specimens that were degraded by the fungus Pleurotus ostreatus (mass loss 55% and 83%) and the fungus Phaeolus schweinitzii (mass loss 45%), taken from Fagus sylvatica and Pinus sylvestris species, a hardwood and softwood respectively with contrasting wide vessels and narrow tracheids.
机译:在衰减的高级阶段中的生物学降解的木材具有非常柔软且脆性的结构,在切割期间引起许多问题。在不同种类的介质中嵌入木材标本可确保制备良好的微观方式,但制备时间很长。所提出的方法不仅具有减少的制备时间,而且还可以最大限度地减少化学品的成本和消费,同时改善样本的稳定和跨越部分的质量。该方法的关键是在干燥的样本上施加透明指甲油凝胶的增强层,该样品仅稳定(未嵌入)PEG 1500培养基。凝胶在切片之前将凝胶施加在两层中的试样。第一层渗透足够深的样品以填充流明和细胞壁,并允许制备来自腐烂的木材的薄片。第二层加强了该部分并允许更好的处理。随后,使用纯丙酮除去增强和包埋层。到目前为止,这种创新方法已经成功地测试了由真菌肺炎(大规模损失55%和83%)降解的标本(质量损失55%)和来自Fagus Sylvatica和Pinus Sylvestris种类的真菌(大众损失45%)的试样硬木和软木分别具有对比的宽血管和狭窄的行李箱。

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