[Optical microscopy].

M. Davidson, M. Abramowitz
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引用次数: 125

Abstract

binocular microscopes with image-erecting prisms, and the first stereomicroscope (14). Early in the twentieth century, microscope manufacturers began parfocalizing objectives, allowing the image to remain in focus when the microscopist exchanged objectives on the rotating nosepiece. In 1824, Zeiss introduced a LeChatelier-style metallograph with infinitycorrected optics, but this method of correction would not see widespread application for another 60 years. Shortly before World War II, Zeiss created several prototype phase contrast microscopes based on optical principles advanced by Frits Zernike. Several years later the same microscopes were modified to produce the first time-lapse cinematography of cell division photographed with phase contrast optics (14). This contrast-enhancing technique did not become universally recognized until the 1950s and is still a method of choice for many cell biologists today. Physicist Georges Nomarski introduced improvements in Wollaston prism design for another powerful contrast-generating microscopy theory in 1955 (15). This technique is commonly referred to as Nomarski interference or differential interference contrast (DIC) microscopy and, along with phase contrast, has allowed scientists to explore many new arenas in biology using living cells or unstained tissues. Robert Hoffman (16) introduced another method of increasing contrast in living material by taking advantage of phase gradients near cell membranes. This technique is now termed Hoffman Modulation Contrast, and is available as optional equipment on most modern microscopes. The majority of microscopes manufactured around the world had fixed mechanical tube lengths (ranging from 160 to 210 millimeters) until the late 1980s, when manufacturers largely migrated to infinity-corrected optics. Ray paths through both finite tube length and infinity-corrected microscopes are illustrated in Figure 1. The upper portion of the figure contains the essential optical elements and ray traces defining the optical train Introduction
(光学显微镜)。
具有图像竖立棱镜的双目显微镜和第一立体显微镜(14)。二十世纪初,显微镜制造商开始对物镜进行聚焦,当显微镜师在旋转鼻架上交换物镜时,图像可以保持聚焦。1824年,蔡司推出了一种具有无限校正光学的LeChatelier风格的金相学,但这种校正方法在未来60年内不会得到广泛应用。在第二次世界大战前不久,蔡司根据FritsZernike提出的光学原理制造了几台相差显微镜的原型。几年后,同样的显微镜被修改,产生了第一个用相位对比光学器件拍摄的细胞分裂的延时摄影(14)。这种增强对比度的技术直到20世纪50年代才得到普遍认可,至今仍是许多细胞生物学家的选择方法。1955年,物理学家Georges Nomarski为另一种强大的对比度显微镜理论介绍了沃拉斯顿棱镜设计的改进(15)。这种技术通常被称为Nomarski干涉或微分干涉对比(DIC)显微镜,与相位对比一起,使科学家能够使用活细胞或未染色组织探索生物学中的许多新领域。Robert Hoffman(16)介绍了另一种利用细胞膜附近的相位梯度来增加活性物质对比度的方法。这种技术现在被称为霍夫曼调制对比度,在大多数现代显微镜上都可以作为可选设备使用。直到20世纪80年代末,世界各地制造的大多数显微镜都有固定的机械管长度(从160毫米到210毫米不等),当时制造商主要转向无限校正光学器件。通过有限管长度和无限远校正显微镜的光线路径如图1所示。图的上部包含定义光学序列的基本光学元件和光线轨迹简介
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