Figure 7 shows a 35mm lens using 470nm illumination. Figure 7a is set to f/2.8 and Figure 7b is set to f/5.6. Both graphs go out to 150$ \small{\tfrac{\text{lp}}{\text{mm}}} $—the Nyquist limit of a sensor with 3.45µm pixels. It is easy to see that the performance of Figure 7a is far better than Figure 7b, using this lens at a setting of f/2.8 provides the highest level of imaging quality in a given object plane. However, as discussed in the previous section, sensor tilt will negatively impact the image quality produced, and the higher the number of pixels, the more pronounced the effect.

Figure 8 analyzes the depth of focus for the two cases in Figure 7. In both cases, the far right vertical line is at the best focus for the full image. Each semi-vertical line to the left of best focus represents a position 12.5µm closer to the back of the lens. These simulate the positions of the pixels, assuming a tip/tilt of 12.5µm and 25µm respectively from the center to the corner of the sensor. The blue ray bundle shows the image center and the yellow and red ray bundles show the corners of the image. The yellow and red bundles represent one line pair cycle on the sensor assuming 3.45µm pixels. Notice in Figure 8a, that for f/2.8 there is already bleed-over between the yellow and red ray bundles at the shift to the 12.5µm tilt position. Moving out to 25µm, the red bundle now covers two full pixels and about half the yellow bundle as well. This causes significant blurring. In Figure 8b, for f/5.6, the yellow and red ray bundles stay within one pixel over the full 25µm tilt range. Note that the blue pixel’s position does not change, as the tip/ tilt is centered on this pixel.

Whatdoesthe objectivelens doon a microscope

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Depth of focus is the image-space complement of DOF and is related to how the quality of focus changes on the sensor side of the lens as the sensor is moved, while the object remains in the same position. Depth of focus characterizes how much tip and tilt is tolerated between the lens image plane and the sensor plane itself. As f/# decreases, the depth of focus does as well, which increases the impact that tilt has on achieving best focus across the sensor. Without active alignment, there will always be some degree of variation in the orthogonality between the sensor and the lens that is used; Figure 6 shows how this issue arises. It is generally assumed that problems involving depth of focus only occur with large sensors.

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Do you need an individual objective for your application? Then contact our Leica OEM Optic Center so that we can offer you a customized solution.

“Does this lens have good DOF?” It is difficult to quantify without specifying an object detail size or image space frequency. The smaller the detail, the higher the spatial frequency needed, and the smaller the DOF the lens can produce. A DOF curve can be used to see how a lens performs over a given depth at a specific detail’s size (Lens Performance Curves). These graphs not only consider theoretical limitations associated with the f/# setting, but also the aberrational effects of the lens design.

What is thepurpose ofthe objectivelens inalightmicroscope

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Whatdoestheeyepiece lens doon a microscope

In Figure 1, contrast values (y-axis) are seen over a WD range (x-axis) at a fixed frequency of 20$ \small{\tfrac{\text{lp}}{\text{mm}}} $ (image detail). Note the difference in DOF between Figure 1a, which is set at f/2.8, and Figure 1b, which is set at f/4. Also note that there is more usable DOF beyond the best focus than between the best focus and the lens, due to magnification decreasing. The graphs themselves contain different colored lines denoting different sensor positions. These types of asymmetric DOF curves are common in fixed focal length lenses.

Figure 9 shows the change in MTF performance at the corner of the image for this 35mm lens assuming 25µm of tilt, seen in Figure 8. Figure 9a shows the new performance of the lens at f/2.8; note the decrease in performance from Figure 9a. Figure 9b shows the performance shift at f/5.6, which is minor compared to 9a. Most importantly, the lens at f/5.6 will now outperform the one at f/2.8. The drawback to running systems at f/5.6 is three times less light relative to f/2.8 and this can be problematic in high speed or line scan applications. Finally, if the sensor is tilted about the its center, performance decrease occurs at both the top and bottom of the sensor (and the corresponding points in the FOV), since the ray bundles expand after the best focus. No two camera and lens combinations are identical. When building multiple systems, this fact can manifest at different degrees of magnitude.

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Gauss' lens formula (1/(-a)+1/b=1/f) expresses the depth of field using the distance to a subject from the principal point. The subject distance used in Gauss' ...

Figure 5 shows the same concept as Figure 4, but the cones represent multiple points in the FOV. Each detail and subsequent space represent one line pair. The overlap in the bundles in Figure 5a shows how the information blends together faster than that of Figure 4b and shows how two different object details can blur together due to a lower f/#. In Figure 5b, this does not occur due to the higher f/# of the lens.

Figure 2 features the same lens as Figure 1a but at a different WD. Note an increase in DOF occurs at longer WDs. Eventually, as the lens focuses on objects infinitely far away, the hyperfocal condition occurs. This condition is reached at the distance in which everything appears in equal focus.

To make it easier for you to find which Leica objectives work best for your microscope and application, you can take advantage of the Objective Finder

In general, when lenses are focused at short WDs, the large cone angles cause the cones to diverge very quickly on either side of best focus, leading to limited DOF. For objects in focus at longer WDs, the transition rate of the bundles decreases and DOF will increase.

Opticalmicroscope

Leica apochromats are objectives for applications with highest specifications in the visual range and beyond, offering field flatness up to 25 mm. The absolute values of the focus differences for the red wavelength and the blue wavelength to green wavelength (3 colors) are ≤ 1.0 x depth of field of the objective.

Due to similarity in name and nature, depth of field (DOF) and depth of focus are commonly confused concepts. To simplify the definitions, DOF concerns the image quality of a stationary lens as an object is repositioned, whereas depth of focus concerns a stationary object and a sensor’s ability to maintain focus for different sensor positions, including tilt.

Leica semi-apochromats are objectives for applications in the visual spectral range with higher specifications, offering field flatness up to 25 mm. The absolute values of the focus differences for the red wavelength and the blue wavelength to green wavelength (3 colors) are ≤ 2.5x depth of field of the objective.

Whatdoesthestage doon a microscope

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The objective lens of a microscope forms a magnified, real, intermediate image of the sample or specimen which is then magnified further by the eyepieces or oculars and observed by the user as a virtual image. When a camera is used to observe the sample, then a phototube lens is installed after the objective in addition to, or even in place of, the eyepieces. The phototube lens forms a real image of the sample onto the camera sensor. The objective’s numerical aperture (NA), its ability to gather light, largely determines the microscope’s resolution or resolving power to distinguish fine details of the sample. Also, the working distance, the distance between the sample and objective, and the depth of field, the depth of the space in the field of view within which the sample can be moved without noticeable loss of image sharpness, both greatly depend on the properties of the objective lens. For more information, refer to: Collecting Light: The Importance of Numerical Aperture in Microscopy, How Sharp Images Are Formed, & Optical Microscopes – Some Basics & Labeling of Objectives

All Leica objectives are marked with codes and labels. These identify the objective, its most important optical performance properties, and the main applications it can be used for. For more information, refer to: Labeling of Objectives

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As details get smaller (represented by a smaller red cone), the bundles in Figure 3a and 3b move closer together. Eventually, increasing the f/# too much causes smaller details to blur due to reaching the lens diffraction limit, since the limiting resolution of the lens is inversely proportional to f/#. This limitation means that while increasing the f/# will always increase the DOF, the minimum resolvable feature size (even at best focus) increases. For more information on the diffraction limit and its relationship to f/#, see The Airy Disk and Diffraction Limit. Using short wavelengths helps to salvage some of this resolution. Learn more about how wavelength affects system performance in MTF Curves and Lens Performance. Note that this diffraction effect is not viewable in Figure 3, but that it is mentioned here as something to mind.

So a 10x objective plus a 10x eyepiece = 100x magnification. And a 100x objective lens with 20x eyepieces = 2,000x magnification - right? False! False ...

Changing the f/# of a lens changes DOF, shown in Figure 3. For each configuration shown in Figure 3 there are two bundles of rays. The bundle represented by dotted black lines shows how well the lens is focused. As an object moves away from the best focus position (where the dotted lines cross), object details move into a wider area of the cone. The wider the spread of the cone, the more the image blurs into the surroundings. The f/# of the lens controls how quickly the cone expands and how much information or detail is blurred together at a given distance. Figure 3a shows a lens with a shallow DOF, where Figure 3b shows a lens with a large DOF.

What is thestageon a microscope

Usually, this type of aberration happens when the light is not fully orthogonal to the lens, as is the case when looking at a distant star that is not in the ...

What is objectivelens inmicroscope

The red cone in Figure 3 is an angular representation of the system resolution. Where the lines of the red cone and dotted black cone intersect defines the total range of the DOF. The lower the f/#, the faster the black dotted lines expand, and the lower the DOF.

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For standard applications, Leica Microsystems offers an extensive range of top-class microscope objectives. There are also Leica objectives which have been optimized for special applications. The highest-performance Leica objectives feature maximum correction and optical efficiency and have won several awards. All over the world, scientists are relying on Leica microscope objectives to gain insights into their area of research.

Objectivelens and eyepiece lens magnification

Leica achromats are powerful objectives for standard applications in the visual spectral range, offering field flatness (OFN) up to 25 mm. The absolute value of the focus differences between red wavelength and blue wavelength (2 colors) is ≤ 2x depth of field of the objective.

To overcome these issues, cameras and lenses with tighter tolerances must be used. For sensors, some lenses have tip/tilt control mechanisms to overcome this factor. Note that some line scan sensors can have swale, meaning they are not fully flat; this cannot be mitigated or removed via tip/tilt control.

The DOF of a lens is its ability to maintain a desired amount of image quality (spatial frequency at a specified contrast), without refocusing, if the object position is moved closer and farther from the plane of best focus. DOF also applies to objects with complex geometries or features of different height. As an object is placed closer to or farther than the set focus distance of a lens, the object blurs and both resolution and contrast suffer. As such, DOF only makes sense if it is defined with an associated resolution and contrast. Several targets can be used to directly measure and benchmark an imaging system’s DOF; these targets are detailed in Test Target Overview.

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Leica microscope objective lenses are designed and made by our optics specialists to have the highest performance with a minimum of aberrations. The objectives help to deliver superior microscope image quality for many applications, such as life science and materials research, industrial quality control and failure analysis, and medical and surgical imaging.

However, this issue is independent of sensor size. As the derivation in Equation 3 shows, depth of focus, $\delta $, is heavily dependent on the number of pixels or pixel count, $ p $, and has little to do with array or pixel size, $ s $. As sensors increase in pixel count, this issue is more evident. Particularly in many line scan applications, the large arrays and low f/#s emphasize the need for careful alignment between the object, lens, and sensor.

The optics of the most basic microscope includes an objective lens and ocular or eyepiece. The objective lens is closest to the sample, specimen, or object being observed with the microscope (see the schematic diagram below). For more information, refer to the article: Optical Microscopes – Some Basics Show schematic diagram

Figure 4a illustrates the ray bundle at the center of an object under inspection at f/2.8 (a) and f/8 (b). The vertical lines represent 2mm increments away from best focus. On each vertical line, a square represents the discrete feature size of single pixel of detail. Figure 4a shows that as the width of the ray bundle spreads out, more rays miss the detail. In Figure 4b, the bundle expands more slowly and the rays all strike the detail which is larger than the bundle diameter for all depths shown.

4Lasers standard Brewster-type thin-film polarizers are designed to be used for applications, which include polarization separation.