Related Experiment Video
Updated: Jul 3, 2026

10:09
Sample Preparation Method of Scanning and Transmission Electron Microscope for the Appendages of Woodboring Beetle
Published on: February 3, 2020
Insect cuticular growth layers seen under the scanning electron microscope: A new display method.
1University of Bristol Department of Zoology, Woodland Road, Bristol, BS8 1UG UK.
Tissue & Cell
|January 1, 1987
Summary
Scanning electron microscopy (SEM) reveals insect cuticle growth layers. Chitin fibrils in the endocuticle are staggered, and surface relief explains daily growth layer imaging in grasshoppers.
Area of Science:
- Entomology
- Materials Science
- Microscopy
Background:
- Insect cuticle structure is crucial for understanding growth and biomechanics.
- Previous studies have not fully elucidated the microstructural organization of daily growth layers.
Purpose of the Study:
- To demonstrate the utility of Scanning Electron Microscopy (SEM) for analyzing insect cuticular growth.
- To investigate the microstructural composition of endocuticle helicoids and their relation to growth layers.
Main Methods:
- Utilized Scanning Electron Microscopy (SEM) for high-resolution imaging of insect cuticle.
- Focused on the short-horned grasshopper, *Romalea microptera*, for detailed analysis.
- Examined the orientation and arrangement of chitin fibrils within the endocuticle.
Main Results:
- SEM effectively visualized discrete chitin fibrils comprising the endocuticle helicoids.
- Chitin fibrils are arranged in a staggered orientation, contributing to cuticle properties.
- Surface relief features observed under SEM correlate with daily growth layer patterns.
Conclusions:
- SEM is a valuable tool for studying insect cuticular growth layer microstructures.
- The staggered arrangement of chitin fibrils is a key feature of the endocuticle.
- Surface topography provides insights into the daily deposition of cuticular material.
Related Concept Videos
Scanning Electron Microscopy
A scanning electron microscope (SEM) is used to study the surface features of a sample by using an electron beam that scans the sample surface in a two-dimensional manner. Typically, areas between ~1 centimeter to 5 micrometers in width can be imaged. SEM can be used to image bacteria, viruses, tissues as well as larger samples like insects. Conventional SEM gives a magnification ranging from 20X to 30,000X and spatial resolution of 50 to 100 nanometers.
Fundamental Principles
Accelerated...
Fundamental Principles
Accelerated...
Preparation of Samples for Electron Microscopy
To be visualized by an electron microscope, either transmission or scanning, biological samples need to be fixed (stabilized) so the electron beam does not destroy them and dried thoroughly (desiccated/dehydrated) so the vacuum does not affect them. Fixation needs to be done as quickly as possible because the sample properties will start changing as soon as it is removed from its natural environment. For example, in a tissue sample, the oxygen levels begin decreasing, causing an altered...

