Related Experiment Video
Updated: Feb 6, 2026

08:57
Focussed Ion Beam Milling and Scanning Electron Microscopy of Brain Tissue
Published on: July 6, 2011
28.8K
A crustacean statocyst with only three hairs: Light and scanning electron microscopy
1Department of Biology, Emory University, Atlanta, Georgia 30322.
Journal of Morphology
|August 17, 2018
Summary
The isopod Cyathara polita uses six hairs within paired statocysts in its telson for equilibrium. These unique organs connect to the external environment, controlling balance in this crustacean species.
Area of Science:
- * Crustacean biology
- * Comparative anatomy
- * Sensory organ morphology
Background:
- * The telson of the isopod Cyathara polita houses paired statocyst organs.
- * Statocysts are crucial for maintaining equilibrium in many invertebrates.
- * Previous research has not detailed the specific structure of these organs in C. polita.
Purpose of the Study:
- * To investigate the detailed structure of the statocyst organs in Cyathara polita.
- * To understand the functional morphology of these organs in relation to equilibrium maintenance.
- * To identify all sensory structures involved in balance for this species.
Main Methods:
- * Standard histological techniques were employed.
- * Scanning Electron Microscopy (SEM) was utilized for detailed examination.
- * Anatomical structures of the telson statocysts were analyzed.
Main Results:
- * Each statocyst is an invagination of the dorsal cuticle, narrowing to a stalk with a connecting canal.
- * Three pits on the luminal floor correlate with nodules, each bearing a bifurcating hair.
- * A single concretion resides within the statocyst lumen, contacted by the hairs.
- * No other balance organs were identified in C. polita.
Conclusions:
- * Equilibrium in Cyathara polita is primarily controlled by six hairs within the two statocysts.
- * The statocysts possess a unique structure with a direct external connection via a canal.
- * The findings highlight a specialized and potentially minimal system for balance in this isopod.
Related Concept Videos
Scanning Electron Microscopy
5.5K
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...
5.5K
Hair Cells
45.1K
Hair cells are the sensory receptors of the auditory system—they transduce mechanical sound waves into electrical energy that the nervous system can understand. Hair cells are located in the organ of Corti within the cochlea of the inner ear, between the basilar and tectorial membranes. The actual sensory receptors are called inner hair cells. The outer hair cells serve other functions, such as sound amplification in the cochlea, and are not discussed in detail here.
45.1K
Overview of Electron Microscopy
14.9K
The wavelengths of visible light ultimately limit the maximum theoretical resolution of images created by light microscopes. Most light microscopes can only magnify 1000X, and a few can magnify up to 1500X. Electrons, like electromagnetic radiation, can behave like waves, but with wavelengths of 0.005 nm, they produce significantly greater resolution up to 0.05 nm as compared to 500 nm for visible light. An electron microscope (EM) can create a sharp image that is magnified up to 2,000,000X.
14.9K
Transmission Electron Microscopy
7.3K
In 1931, physicist Ernst Ruska—building on the idea that magnetic fields can direct an electron beam just as lenses can direct a beam of light in an optical microscope—developed the first prototype of the electron microscope. This development led to the development of the field of electron microscopy. In the transmission electron microscope (TEM), electrons are produced by a hot tungsten element and accelerated by a potential difference in an electron gun, which gives them up to 400...
7.3K
Immunogold Electron Microscopy
5.5K
Immunoelectron microscopy utilizes immunogold labeling of endogenous proteins with specific antibodies to detect and localize these proteins in cells and tissues. The procedure provides insights into the distribution and quantification of protein under different stimulation conditions offering clues about their functions. Conjugating highly electron-dense gold particles with primary or secondary antibodies allow antigen detection on and within cells, with high resolution and specificity.
5.5K
Cryo-electron Microscopy
4.4K
Conventional electron microscopy (EM) involves dehydration, fixation, and staining of biological samples, which distorts the native state of biological molecules and results in several artifacts. Also, the high-energy electron beam damages the sample and makes it difficult to obtain high-resolution images. These issues can be addressed using cryo-EM, which uses frozen samples and gentler electron beams. The technique was developed by Jacques Dubochet, Joachim Frank, and Richard Henderson, for...
4.4K

