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The sieved or unsieved preparations may be examined using strew mounts on microscope slides that may be examined using a transmitted light biological microscope or ultraviolet (UV) fluorescence microscope. The abundance, composition and preservation of the various components, together with the thermal alteration of the organic matter is considered.
A pollen count is a measurement of the number of pollen grains in a given volume of air. Pollen counts, and forecasts of pollen conditions, are routinely produced and reported to the public because high aerial pollen concentration is associated with increased rates of allergic reaction for those with conditions such as hay fever and asthma.
Polarizing microscope operating principle Depiction of internal organs of a midge larva via birefringence and polarized light microscopy. Polarized light microscopy can mean any of a number of optical microscopy techniques involving polarized light. Simple techniques include illumination of the sample with polarized light.
Pollen itself is not the male gamete. [4] It is a gametophyte, something that could be considered an entire organism, which then produces the male gamete.Each pollen grain contains vegetative (non-reproductive) cells (only a single cell in most flowering plants but several in other seed plants) and a generative (reproductive) cell.
The principle setup of a light sheet fluorescence microscope. Light sheet fluorescence microscopy (LSFM) is a fluorescence microscopy technique with an intermediate-to-high [1] optical resolution, but good optical sectioning capabilities and high speed.
Photographic and light microscopic images: Zoomed-out view of an Aglais io. Closeup of the scales of the same specimen. High magnification of the coloured scales (probably a different species). Electron microscopic images: A patch of wing: Scales close up: A single scale: Microstructure of a scale: Magnification: Approx. ×50 Approx. ×200 × ...
Pollen DNA barcoding is the process of identifying pollen donor plant species through the amplification and sequencing of specific, conserved regions of plant DNA. Being able to accurately identify pollen has a wide range of applications though it has been difficult in the past due to the limitations of microscopic identification of pollen. [1]
The light path of a bright-field microscope is extremely simple; no additional components are required beyond the normal light-microscope setup. The light path begins at the illuminator or the light source on the base of the microscope. Often a halogen lamp is used. The light travels through the objective lens into the ocular lens, through ...