Related Experiment Video
Updated: Feb 13, 2026

08:11
Collection and Identification of Pollen from Honey Bee Colonies
Published on: January 19, 2021
8.2K
Identification of monocot flora using pollen features through scanning electron microscopy.
Siraj Bahadur1, Mushtaq Ahmad1,2, Sehrosh Mir1
1Department of Plant Sciences, Quaid-I-Azam University, Islamabad, Pakistan.
Microscopy Research and Technique
|March 15, 2018
Summary
Pollen analysis reveals distinct features for plant classification and evolutionary studies. This research details pollen characteristics of 20 monocot species, aiding in accurate species identification and taxonomic understanding.
Area of Science:
- Palynology
- Plant Taxonomy
- Evolutionary Botany
Background:
- Pollen morphology is crucial for understanding plant evolution and classification.
- Specific pollen features like ornamentation and aperture patterns help differentiate plant genera and species.
- Monocotyledonous plants offer diverse pollen structures for systematic studies.
Purpose of the Study:
- To analyze and compare pollen features of 20 monocot species from six families.
- To identify new species occurrences in Pakistan and document their pollen morphology.
- To develop a taxonomic key based on pollen characteristics for species identification.
Main Methods:
- Light microscopy (LM) for initial pollen visualization.
- Scanning electron microscopy (SEM) for detailed examination of non-acetolyzed and acetolyzed pollen.
- Comparative analysis of pollen features across 15 genera and 20 species.
Main Results:
- Detailed descriptions of pollen morphology for the studied monocot species.
- First-time reporting of Zephyranthes citrina and Tulbaghia violacea pollen from Pakistan.
- Identification of variations in pollen ornamentation, aperture, and symmetry.
Conclusions:
- Pollen micromorphology provides valuable data for the systematic classification of monocots.
- The developed taxonomic key aids in the precise identification of species within the studied families.
- SEM and LM are effective tools for palynological research and taxonomic applications.
Related Concept Videos
Scanning Electron Microscopy
5.6K
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...
5.6K
Overview of Electron Microscopy
15.5K
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.
15.5K
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
5.6K
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.
5.6K
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
Preparation of Samples for Electron Microscopy
7.3K
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...
7.3K

