Abstract

The Extended Low Temperature Method (ELTM) for the in-situ preparation of plant samples in an environmental scanning electron microscope enables carrying out repetitive topographical and material analysis at a higher resolution in the vacuum conditions of a scanning electron microscope or in the low gas pressure conditions of an environmental scanning electron microscope. The method does not require any chemical intervention and is thus suitable for imaging delicate structures rarely observable with common treatment methods. The method enables both sample stabilization as close to their native state as possible, as well as the transfer of the same sample from a low vacuum to an atmospheric condition for sample storage or later study. It is impossible for wet samples in the environmental scanning electron microscope. Our studies illustrate the high applicability of the ELTM for different types of plant tissue, from imaging of plant waxes at higher resolution, the morphological study of highly susceptible early somatic embryos to the elemental microanalysis of root cells. The method established here provides a very fast, universal and inexpensive solution for plant sample treatment usable in a commercial environmental scanning electron microscope equipped with a cooling Peltier stage.

Highlights

  • The scanning electron microscope (SEM) has become a routine technique for the morphological study of a wide range of samples with a resolution up to nanometres; most plant samples require at least dehydration prior to observation

  • This paper proves the applicability of this method for observation of the identical sample in their hydrated state in environmental scanning electron microscope (ESEM) and completely dried in SEM with a well-preserved surface morphology

  • The application possibilities of the Extended Low Temperature Method (ELTM) method presented in this paper to prepare plant samples for observation in various ESEM modes are presented in the following paragraphs

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Summary

Introduction

The scanning electron microscope (SEM) has become a routine technique for the morphological study of a wide range of samples with a resolution up to nanometres; most plant samples require at least dehydration prior to observation. Samples can be studied after removing or changing the liquids from the samples using various techniques[2], after application of special chemical treatment[3], in their frozen hydrated state (CryoSEM, Low Temperature SEM)[4], or in their fresh and fully hydrated state in the environmental scanning electron microscope (ESEM)[5,6]. A very popular technique for electron microscopy of biological samples is a Low Temperature SEM (LTSEM) or a CryoSEM, which allows the preservation and recording of biological samples in a fully hydrated and chemically unmodified state. These techniques involve the study of samples at temperatures between −100 °C to −175 °C. Susceptible biological samples which need to be fully hydrated tend to be damaged due to the influence of free radicals, local heating and drying[13]

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