Abstract
Scanning electron microscopy (SEM) is widely used to investigate the surface morphology, and physiological state of plant leaves. Conventionally used methods for sample preparation are invasive, irreversible, require skill and expensive equipment, and are time and labor consuming. This study demonstrates a method to obtain in vivo surface information of plant leaves by imaging replicas with SEM that is rapid and non-invasive. Dental putty was applied to the leaves for 5 minutes and then removed. Replicas were then imaged with SEM and compared to fresh leaves, and leaves that were processed conventionally by chemical fixation, dehydration and critical point drying. The surface structure of leaves was well preserved on the replicas. The outline of epidermal as well as guard cells could be clearly distinguished enabling determination of stomatal density. Comparison of the dimensions of guard cells revealed that replicas did not differ from fresh leaves, while conventional sample preparation induced strong shrinkage (-40% in length and -38% in width) of the cells when compared to guard cells on fresh leaves. Tilting the replicas enabled clear measurement of stomatal aperture dimensions. Summing up, the major advantages of this method are that it is inexpensive, non-toxic, simple to apply, can be performed in the field, and that results on stomatal density and in vivo stomatal dimensions in 3D can be obtained in a few minutes.
Highlights
Scanning electron microscopy (SEM) is widely used to characterize the surface of plant leaves
Shrinkage of epidermal cells was induced by chemical fixation and critical point drying and resulted in a wave-let like artifact on the cuticle, especially around guard cells and the middle of epidermal cells (Fig 2A and 2B)
Replicas are well suited to investigate the surface of leaves by SEM and calculate stomatal density (SD), and to sub-surface 3D morphology like pore width
Summary
Scanning electron microscopy (SEM) is widely used to characterize the surface of plant leaves. It is a valuable tool to investigate the morphology of trichomes, stomatal density (SD), epicuticular waxes, accumulation of nano-particles, and infection with pathogens [1,2,3,4,5,6,7,8,9]. Biological samples for SEM have to be extensively prepared to withstand the vacuum and the high energy of the beam. Sample preparation is usually invasive, irreversible, requires skill and expensive equipment, and is time and labor consuming.
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