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      "title": "显微镜",
      "body": "光学显微镜的结构\n为了研究小生物和细胞，我们使用显微镜。最常见的显微镜是光学显微镜或复合显微镜。\n光学显微镜有两组玻璃镜片：物镜和目镜。大多数显微镜都有两个或三个物镜连接到一个旋转的鼻梁上。这些镜头通常是 5x、10x、20x、40x 和 100x。 （10x 镜头放大物镜的图像。它的放大倍率范围从 5x 到 15x。http://www.fluomedia.org/science/\n![Screenshot_2022-04-22-16-09-14-1.jpg](https://cdn.steemitimages.com/DQmNPTE4dR6aGLNz7goMrRW4hiCTKWZbkS3z9WypKCRUJ47/Screenshot_2022-04-22-16-09-14-1.jpg)\n\n显微镜的放大倍率是物镜和目镜放大倍数的乘积：如果目镜放大15x和物镜40x，总放大倍数是15x 40=600x。显微镜的分辨率\n显微镜不仅可以放大图像，还可以分离微小的细节。显微镜将两个非常接近的物体区分开来的能力是它的分辨率或分辨能力。因此，如果我们通过低分辨率显微镜观察两个靠得很近的物体，我们会将它们视为一个物体。然而，通过高分辨率显微镜，我们可以区分这两个物体。分辨率约为光波长的一半（约 250 NM）。因此，光学显微镜的分辨率是有限的。最多可以分辨两点相距250nm（0.25um），放大1500倍左右。由于大多数细胞器小于 200nm，因此无法通过光学显微镜看到。\n注意显微镜物体以微米为单位测量。一个微米是 1/1000 毫米。微米的符号是希腊字母 u (mu)，即 1/1000000mm。如何使用显微镜\n第 1 步：将载玻片夹在显微镜载物台上。确保样品位于载物台上的孔上方。\n第 2 步：旋转鼻架，使低倍物镜刚好位于样品上方。\n第三步：在显微镜前放一盏灯，倾斜显微镜镜，使光线向上通过目镜。\n第四步：通过目镜观察，调整光圈的光阑，直到光线明亮但不刺眼。\n第五步：从显微镜侧面看，转动粗调旋钮，降低物镜，直到靠近载玻片。\n第六步：通过目镜观察，慢慢转动粗调旋钮，抬起一键，使试样清晰对焦。\n 要在高倍镜下观察样品，请旋转鼻子，直到高倍物镜在样品上方。然后，通过目镜观察并使用微调旋钮仔细聚焦样品。必要时调整照明制作样品的湿镶嵌\n通过显微镜观察的标本通常准备成薄片或切片。根尖等软组织被压扁，而血液等液体组织则被涂抹。标本的透明部分用适当的染料染色以使其可见。然后将准备好的样品安装在玻璃显微镜载玻片上，如下所示：\n第 1 步：将一滴封固液（通常是水或甘油）滴入干净干燥的显微镜载玻片中央，然后将标本放入该液中\n步骤2：将盖玻片以45°角立在侧面。沿着幻灯片拉它，直到它接触到液滴。使用安装针，非常小心，降低盖玻片，直到它平放在液滴的顶部。如果有的话，用一张滤纸吸掉盖玻片周围多余的封固液。电子显微镜\n细胞中的许多细胞器太小而无法通过光学显微镜观察。电子显微镜用于研究这些物体。它使用了一束波长比光短得多的电子束。光束由强大的电磁铁聚焦。产生的图像无法直接查看。在荧光屏上，拍摄称为光电子显微照片的黑白照片。\n电子显微镜的分辨率约为 1nm，可将物体放大 500 000 倍以上。因此，它可以提供比最强大的光学显微镜更详细的细胞结构图片。\n\n第一台原子力显微镜\n\n^ 聚合物的表征和分析。新泽西州霍博肯：Wiley-Interscience。 2008.ISBN 978-0-470-23300-9。^ Bardell, David（2004 年 5 月）。 “显微镜的发明”。 BIOS。 75 (2): 78–84。 doi:10.1893/0005-3155(2004)75<78:tiotm>2.0.co;2. JSTOR 4608700.^ 望远镜的历史，Henry C. King，Harold Spencer Jones Publisher Courier Dover Publications，2003 年，第 25-27 页 ISBN 0-486-43265-3, 978-0-486-43265-6^ Atti Della Fondazione Giorgio Ronchi E Con​​tributi Dell'Istituto Nazionale Di Ottica，第 30 卷，La Fondazione-1975，p。 554^ a b 墨菲，道格拉斯 B.；戴维森，迈克尔 W. (2011)。光学显微镜和电子成像的基础知识（第 2 版）。牛津：威利-布莱克威尔。 ISBN 978-0-471-69214-0。^ Norman Lockyer 爵士 (1876)。自然卷 14。^ 阿尔伯特·范·海尔登；斯文·杜普雷；罗布·范根特 (2010)。望远镜的起源。阿姆斯特丹大学出版社。 pp. 32–36, 43. ISBN 978-90-6984-615-6.^“谁发明了显微镜？”。 2017 年 3 月 31 日检索。^ Eric Jorink (2010-10-25)。在 1575-1715 年的荷兰黄金时代阅读自然之书。 ISBN 978-90-04-18671-2。^威廉·罗森塔尔，眼镜和其他视力辅助工具：收藏的历史和指南，诺曼出版社，1996 年，第 391-92 页^ 雷蒙德·J·西格，物理学家：伽利略·伽利略，他的生活和他的作品，Elsevier – 2016，p。 24 ^ J. William Rosenthal，眼镜和其他助视器：收藏的历史和指南，诺曼出版社，1996 年，第 391 页^ uoregon.edu，伽利略 伽利略·伽利莱（摘自大英百科全书）^ 古尔德，斯蒂芬·杰伊（2000 年）。 “第 2 章：眼尖的猞猁，被大自然打败”。马拉喀什的谎言：自然历史中的倒数第二个反思。纽约：和谐。 ISBN 978-0-224-05044-9。^ a b Wootton, David (2006)。坏药：自希波克拉底以来，医生在做伤害。牛津 [Oxfordshire]：牛津大学出版社。页。 110.ISBN 978-0-19-280355-9。[需要页面]^ Liz Logan（2016 年 4 月 27 日）。 “早期的显微镜揭示了微小生物的新世界”。史密森尼网站。 2016 年 6 月 3 日检索。^ Knoll, Max (1935)。 “Aufladepotentiel und Sekundäremission elektronenbestrahlter Körper”。 Zeitschrift für Technische Physik。 16: 467–475.^ Goldsmith, Cynthia S.;米勒，萨拉 E. (2009-10-01)。 “电子显微镜在病毒检测中的现代应用”。临床微生物学评论。 22 (4): 552–563。 doi:10.1128/cmr.00027-09。 ISSN 0893-8512。 PMC 2772359。PMID 19822888。^ Morita, Seizo (2007)。扫描探针显微镜的路线图。柏林，海德堡：Springer-Verlag Berlin Heidelberg。 ISBN 978-3-540-34315-8。^ a b c d e f g h i j Lodish，Harvey；伯克，阿诺德； Zipursky，S.劳伦斯；松平，保罗；巴尔的摩，大卫；达内尔，詹姆斯 (2000)。 “显微镜和细胞结构”。分子细胞生物学。第 4 版。^ a b c d e f g Alberts，布鲁斯；约翰逊，亚历山大；刘易斯，朱利安；拉夫，马丁；罗伯茨，基思；沃尔特，彼得（2002 年）。 “在显微镜下观察细胞的结构”。细胞的分子生物学。第 4 版。^“2014 年诺贝尔化学奖 – 科学背景”(PDF)。 www.nobelprize.org。检索 2018 年 3 月 20 日。^“2014 年诺贝尔化学奖”。 www.nobelprize.org。 检索 2018 年 3 月 20 日。^ a b Erko, A. (2008)。 X 射线和中子光学的现代发展。柏林：施普林格。 ISBN 978-3-540-74561-7。^ Pennycook, S.J.；瓦雷拉，M。赫瑟灵顿，C.J.D.；柯克兰，人工智能（2011）。 “材料通过像差校正电子显微镜取得进展”（PDF）。夫人公报。 31：36-43。 doi:10.1557/mrs2006.4.^ Aspden, Reuben S.;格梅尔，内森 R.；莫里斯，彼得 A.；塔斯卡，丹尼尔 S.；梅尔滕斯，莉娜；坦纳，迈克尔 G。柯克伍德，罗伯特 A.；鲁杰里，亚历山德罗；托西，阿尔贝托；博伊德，罗伯特 W.；布勒，杰拉德 S.；哈德菲尔德，罗伯特 H。帕吉特，迈尔斯 J.（2015 年）。 “光子稀疏显微镜：使用红外照明的可见光成像”（PDF）。光学。 2 (12): 1049.\"Account of a newly discovered variety of green fluor spar, of very uncommon beauty, and with remarkable properties of colour and phosphorescence\" Bibcode:2015Optical...2.1049A。 doi:10.1364/OPTICA.2.001049。 ISSN 2334-2536。^ a b Bhushan，Bharat，编辑。 （2010）。 Springer 纳米技术手册（第 3 版和扩展版）。柏林：施普林格。页。 620.ISBN 978-3-642-02525-9。^ Sakurai, T.;渡边，Y.，编辑。 （2000 年）。扫描探针显微镜的进展。柏林：施普林格。 ISBN 978-3-642-56949-4.^“活体生物学量子显微镜”。科学日报。 2013 年 2 月 4 日。2013 年 2 月 5 日检索。",
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      "title": "ADAPTATIONS",
      "body": "ADAPTATIONS\n\n![Screenshot_2022-04-21-23-14-51-1.jpg](https://cdn.steemitimages.com/DQmWsYNJNWGzN5EvTVcoUFs7AwYcrGk8KqG5PvDjACLUU4J/Screenshot_2022-04-21-23-14-51-1.jpg)\nLiving organisms are found in many types of  ecosystem The environment in these ecosystem very considerably.Generally, organisms show features that enable them to live successfully and reproduce in a particular environment. These features may be structural,functional or behavioural.such features are known as adaptations.Adaptations to a particular environment are evolved over a long period of time.\n\nAquatic and Terrestrial Adaptations\nThe two most contrasting environment are The aquatic and Terrestrial environment. Organ ism living in each of these environment show adaptations that are suited to their particular environment.\n\nNature of medium\nWater is denser medium than air .it is difficult to move rapidly through it .As a result, active aquatic animals like fish have streamlined bodies. Water, however, helps to support the body mass of large aquatic animals. This is not the case with large aquatic animals. This is not the case with large land plants and animals as air is a much lighter medium than water. Hence, large terrestrial plants and animals have better developed supporting (vascular xylem and skeleton) than aquatic ones.these adaptations are mainly structural.\n\nOsmoregulation and water loss\nMost marine organisms have body fluids that are nearly the same concentration as the sea water, in which they live. So the body fluids of freshwater organisms are at a much higher concentration than the surrounding water. So more water enters the body cell than leaves them. Successful freshwater organisms have osmoregulatory structures that get rid of the excess water that enters the body cells. The contractile vacuole in Amoeba is such a structure. The adaptation here is mainly functional.\nBony fishes are the most successful aquatic organisms. The body fluid of the marine bony fish is less concentrated than its surrounding water, while the body fluid of the freshwater bony fish is more concentrated. Shows how each has adapted successfully to its environment. The adaptation are mainly functional.\nUnlike most aquatic organisms, Terrestrial organisms are faced with a great problem of water loss from their bodies. Plants overcome this by having waterproof cuticles covering their external surfaces.they also have well developed roots for the Terrestrial animals have developed\nExoskeletons (invertebrates) which envelop the whole body, and covering such as scales, features and hair (vertebrates) and trachear systems (insect) so that water loss is greatly reduced; and\nGaseous exchange surfaces enclosed within the body such as lungs (vertebrates) and trachear systems (insect) so that water loss is greatly reduced; and\nExcretory structures like the Malpighian tubules and kidneys which are efficient at reabsorbing water and saits.\nThus, to conserve water, Terrestrial organisms had to adapt both structurally and functionally \nNOTE In aquatic organisms where there is no need to conserve water, gaseous exchange occurs through the whole body surface or through special structures Callen gills.\n\nMovement\nAquatic organisms that move actively use appendages like fins which are modified for swimming. Many plankton which drift In the water have devices go for keeping them afloat such as oil droplets and ciliated bands. Animals are the actively moving Terrestrial organisms. They have\nJointed limbs (arthropods),and \nPentadactyl limbs(verthropods)\nThat are specially adapted for running, jumping , crawling, climbing and digging.in birds, the pentadactyl upper limbs have been structurally adapted into wings for flying.\n\nPlant Adaptations to water Availability\nRainfall is the main factor that is responsible for the major bioms of the world. This is be cause plants (the organisms that characterise biomes) are greatly affected by the availableility of water in their environment. They shows various adaptations that are related to the amount of water in their environment.\n\nHydrophytes\nHydrophytes are plants, such as water hyacinth and water lily, that live in freshwater. All or part of their body is in water. In these plants, the cuticle of the immersed body parts is thin and allows water to enter freely over the whole body surfast . As a result , special water absorbing and water conducting structures are not important. In addition , since there are surrounded by water, they do not need much mechanical support like land plants. Hence , in hydrophytes,\nThe roots (water absorbing), and \nVascular xylem or wood (water conducting and mechanical ) is poorly developed.\nShows the differences in the internal\nStricture of the stems of water and land plants. Water contains less oxgen than air. Most aquatic plants , therefore, not only provide a supply of oxgen to the underwater parts of the plant but also make the plant buoyant and so help it to float.\nNOTE The floating parts of hydrophytes that are exposed to air are covered with a thick cuticle to prevent water loss.\n\nMesophytes\nMesophytes are land plants , such as the Hibiscus and cassava , that are found in an environment with an adequate water supply. A waxy cuticle covers the body surface to minimise water loss. Stomata are present on leaves for gaseous exchange to occur.\n\nXerophytes\nXerophytes are plants that can survive in an environment, such as the desert, where water supply is scarce. They show the following adaptations:\nThe roots are well developed. They grow down to great depths if necessary, and branch extensively in order to absorb water from as large an area as possible.\nSome xerophytes have swolled stems or leaves containing water storage cells. These are known as succulents and can withstand long periods of drought. Example include cacti, Euphorbia and Aloe.\nXerophytes have various ways of reducing water loss from leaves by transpiration. For example, in many cacti, the leaves are reduced to spines . the stems become fleshy and green and take over the function of photosynthesis . in Acacia , the leaf blade is absent and the leaf stalk becomes flattened to carry out photo synthesis. The leaves of some xerophytes are covered with thick waxy cuticles or hairls, while in some , the number of stomata are greatly reduced or sunken  into pits.\nThe protoplasm in the cells of xerophytes can tolerate a high degree of water loss without being damaged. This is an extremely important adaptation that enable xerophytes to withstand prolonged droughts.\n\nReference\n\n Leroi, Armand Marie (2015). The Lagoon: How Aristotle Invented Science. Bloomsbury. pp. 91–92, 273, 288. ISBN 978-1408836224.^ Desmond 1989, pp. 31–32, fn 18^ Voltaire (1759). Candide. Cramer et al.^ Sober 1993, chpt. 2^ Darwin 1872, p. 397: \"Rudimentary, Atrophied, and Aborted Organs\"^ Bowler, Peter J. (1989) [1983]. Evolution The History of an Idea (Revised ed.). University of California Press. p. 86. ISBN 978-0-520-06386-0.^ See, for example, the discussion in Bowler 2003, pp. 86–95: \"Whatever the true nature of Lamarck's theory, it was his mechanism of adaptation that caught the attention of later naturalists.\" (p. 90)^ Provine 1986^ Ford 1975^ a b Orr, H. Allen (February 2005). \"The genetic theory of adaptation: a brief history\". Nature Reviews Genetics. 6 (2): 119–127. doi:10.1038/nrg1523. PMID 15716908. S2CID 17772950.^ Huxley 1942, p. 449^ Mayr 1982, p. 483: \"Adaptation... could no longer be considered a static condition, a product of a creative past, and became instead a continuing dynamic process.\"^ Price 1980^ Daintith, John; Martin, Elizabeth A., eds. (2010) [First published 1984 as Concise Science Dictionary]. \"adaptation\". A Dictionary of Science. Oxford Paperback Reference (6th ed.). Oxford University Press. p. 13. ISBN 978-0-19-956146-9. LCCN 2010287468. OCLC 444383696. Any change in the structure or functioning of successive generations of a population that makes it better suited to its environment.\n\n\n![Screenshot_2022-04-21-23-15-23-1.jpg](https://cdn.steemitimages.com/DQmRYCvUFs3zZ6bYnmm5hJHni6V65ZeGBEPVYoueVCWTSSL/Scree(https://cdn.steemitimages.com/DQmWsYNJNWGzN5EvTVcoUFs7AwYcrGk8KqG5PvDjACLUU4J/Screenshot_2022-04-21-23-14-51-1.jpg)",
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      "body": "부럽다.. 졌다. 출처 : pixabay\n\n휴식이 필요하다.\n최근 주말에 쉬지 않고 강행군을 했더니\n몸이 삐걱삐걱~~\n\n사실 난 인간에 몸은 한계가 없다고 생각한다.\n단련하면 맨손으로 차돌멩이도 깰 수 있다.\n\n현재 내 몸음 다리부터 어께까지 여기저기\n조금씩 삐걱거린다. 강철몸??이 되는 과정이라\n생각해서 크게 신경은 안쓴다.\n그런대 졸립긴 하다. ㅎㅎㅎ\n\n우선 며칠 가볍게 운동하고 관리를 해야 겠다.\n비꺽거리는게 그냥 가벼운 근육통과 관절통정도\n\n요즘 식욕이 왕성해져서\n엄청 먹었더니 배가 나오기 시작했다.\n이것만 쏙 집어넣어 초코렛복근을 만들면\n완전 굿인데.. 쩝!!\n\n암튼 이번주는 살살모드로 갈 생각이다.\n모두 건강조심하기고\n튼튼몸매 만드시길~~~~",
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      "body": "MICROSCOPE\n\n\n\n\n![images (2).jpeg](https://cdn.steemitimages.com/DQmVMPtRy8V8sfn8jq9HerL4ceGcN3Kp1b1bUjxW5jwZw56/images%20(2).jpeg)\n![images (2).jpeg](https://cdn.steemitimages.com/DQmVMPtRy8V8sfn8jq9HerL4ceGcN3Kp1b1bUjxW5jwZw56/images%20(2).jpeg)\n![images (3).jpeg](https://cdn.steemitimages.com/DQmPQXZdd155HZtZvGULFVsv3uBJEvWiZdAsmLUriYpAqFW/images%20(3).jpeg)\n\nStricture of a light microscope\nTo study small organisms and cells we use a microscope. The most common microscope is the light or compound microscope.\nA light microscope has two set of glass lenses: the objective lenses and the eyepiece lenses. Most microscope have two or three objective attached to a rotating nose piece. These lenses usually are 5x,10x, 20x, 40x, and 100x. (A 10x lens magnifies the image of the objective lens. Its magnification ranges from 5x to 15x.\nThe magnifying power of microscope is the product of the magnifications of the objective and the eyepiece: if the eyepiece magnifies 15x and the objective 40x, the total magnification is 15x 40=600x.\n\nResolution of a microscope\nA microscope not only magnifies the image but also separates minute details. the ability of a microscope to distinguish two very close objects as being separated from each other is its resolution or resolving power. Thus, if we look at two objects which are close together through a low resolution microscope, we see them as a single object. However, through a high resolution microscope we can distinguish the two objects. The resolution power is about half the wavelength of light (approximately 250 NM).Therefore, the resolving power of a light microscope is limited. At the most, it can distinguish two point which are 250nm (0.25 um) apart and magnife about 1 500 times. Since most cell organelles are smaller than 200nm, they cannot be seen through a light microscope.\nNote microscope objects are measured in micros. A micros is 1/1000mm. The symbol for micron is the Greek letter u (mu) which is 1/1000000mm.\n\nHow to use the microscope\nStep 1: Clip the specimen slide on the stage of the microscope. Make sure the specimen is over the hole in the stage.\nStep 2: Rotate the nose piece to bring the low power objective lens just above the specimen.\nStep 3: place a lamp in front of the microscope and tilt the microscope mirror so that the light is directed up through the eyepiece.\nStep 4: look through the eyepiece and adjust the diaphragm of the iris until the light is bright, but not dazzling.\nStep 5: look from the side of the microscope, and turn the coarse adjustment knob and lower the objective lens until it is close to the slide.\nStep 6: look through the eyepiece and slowly turn the coarse adjustment knob and raise the one Ken to focus the specimen sharply.\n To look at the specimen under high power, Rotate the nose until the high power objective lens is over the specimen. Then, look through the eyepiece and carefully focus the specimen, using the fine adjustments knob. Adjust the illumination if necessary\n\nMaking a wet mount of a specimen\nSpecimen for viewing through a microscope are usually prepared as thin slices or secrions. Soft tissue like root tips are squashed, while liquid tissue like blood is smeared. Transparent part of a specimen are offer stained with appropriate dyes to make them visibe. The prepared specimen is then mounted on a glass microscope slide as follows:\nStep 1: place a drop of the mounting liquid (usually water or glycerine) in the central of a clean dry microscope slide and put the specimen in this liquid\nStep 2: stand a cover slip on the side at an angle of 45°. Pull it along the slide until it touches the drop of liquid. Using a mounting needle, very carefully, lower the cover slip until it is flat on the top of the liquid drop. With a piece of filter paper, draw off, if any , excess mounting liquid around the cover slip.\n\nElectron microscope\nMany organelles in cells are too small to be  viewed through a light microscope. An electron microscope is used to study such objects. It used a beam of electron whose wavelength is very much shorter than that of light. the beam is focused by powerful electromagnets.the image produced cannot be viewed directly. Onto a fluorescent screen, from which black and white photographs of the image called photoelectron micrographs are taken.\nAn electron microscope has a resolving power of around 1nm and magnifies objects over 500 000 times. Thus, it can give a far more detailed picture of the structures in a cell than the most powerful light microscope.\n\nFirst atomic force microscope\n\n^ Characterization and Analysis of Polymers. Hoboken, NJ: Wiley-Interscience. 2008. ISBN 978-0-470-23300-9.^ Bardell, David (May 2004). \"The Invention of the Microscope\". BIOS. 75 (2): 78–84. doi:10.1893/0005-3155(2004)75<78:tiotm>2.0.co;2. JSTOR 4608700.^ The history of the telescope by Henry C. King, Harold Spencer Jones Publisher Courier Dover Publications, 2003, pp. 25–27 ISBN 0-486-43265-3, 978-0-486-43265-6^ Atti Della Fondazione Giorgio Ronchi E Contributi Dell'Istituto Nazionale Di Ottica, Volume 30, La Fondazione-1975, p. 554^ a b Murphy, Douglas B.; Davidson, Michael W. (2011). Fundamentals of light microscopy and electronic imaging (2nd ed.). Oxford: Wiley-Blackwell. ISBN 978-0-471-69214-0.^ Sir Norman Lockyer (1876). Nature Volume 14.^ Albert Van Helden; Sven Dupré; Rob van Gent (2010). The Origins of the Telescope. Amsterdam University Press. pp. 32–36, 43. ISBN 978-90-6984-615-6.^ \"Who Invented the Microscope?\". Retrieved 31 March 2017.^ Eric Jorink (2010-10-25). Reading the Book of Nature in the Dutch Golden Age, 1575-1715. ISBN 978-90-04-18671-2.^ William Rosenthal, Spectacles and Other Vision Aids: A History and Guide to Collecting, Norman Publishing, 1996, pp. 391–92^ Raymond J. Seeger, Men of Physics: Galileo Galilei, His Life and His Works, Elsevier – 2016, p. 24^ J. William Rosenthal, Spectacles and Other Vision Aids: A History and Guide to Collecting, Norman Publishing, 1996, page 391^ uoregon.edu, Galileo Galilei (Excerpt from the Encyclopedia Britannica)^ Gould, Stephen Jay (2000). \"Chapter 2: The Sharp-Eyed Lynx, Outfoxed by Nature\". The Lying Stones of Marrakech: Penultimate Reflections in Natural History. New York: Harmony. ISBN 978-0-224-05044-9.^ a b Wootton, David (2006). Bad medicine: doctors doing harm since Hippocrates. Oxford [Oxfordshire]: Oxford University Press. p. 110. ISBN 978-0-19-280355-9.[page needed]^ Liz Logan (27 April 2016). \"Early Microscopes Revealed a New World of Tiny Living Things\". Smithsonian.com. Retrieved 3 June 2016.^ Knoll, Max (1935). \"Aufladepotentiel und Sekundäremission elektronenbestrahlter Körper\". Zeitschrift für Technische Physik. 16: 467–475.^ Goldsmith, Cynthia S.; Miller, Sara E. (2009-10-01). \"Modern Uses of Electron Microscopy for Detection of Viruses\". Clinical Microbiology Reviews. 22 (4): 552–563. doi:10.1128/cmr.00027-09. ISSN 0893-8512. PMC 2772359. PMID 19822888.^ Morita, Seizo (2007). Roadmap of Scanning Probe Microscopy. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg. ISBN 978-3-540-34315-8.^ a b c d e f g h i j Lodish, Harvey; Berk, Arnold; Zipursky, S. Lawrence; Matsudaira, Paul; Baltimore, David; Darnell, James (2000). \"Microscopy and Cell Architecture\". Molecular Cell Biology. 4th Edition.^ a b c d e f g Alberts, Bruce; Johnson, Alexander; Lewis, Julian; Raff, Martin; Roberts, Keith; Walter, Peter (2002). \"Looking at the Structure of Cells in the Microscope\". Molecular Biology of the Cell. 4th Edition.^ \"The Nobel Prize in Chemistry 2014 – Scientific Background\" (PDF). www.nobelprize.org. Retrieved 2018-03-20.^ \"The Nobel Prize in Chemistry 2014\". www.nobelprize.org. Retrieved 2018-03-20.^ a b Erko, A. (2008). Modern developments in X-ray and neutron optics. Berlin: Springer. ISBN 978-3-540-74561-7.^ Pennycook, S.J.; Varela, M.; Hetherington, C.J.D.; Kirkland, A.I. (2011). \"Materials Advances through Aberration-Corrected Electron Microscopy\" (PDF). MRS Bulletin. 31: 36–43. doi:10.1557/mrs2006.4.^ Aspden, Reuben S.; Gemmell, Nathan R.; Morris, Peter A.; Tasca, Daniel S.; Mertens, Lena; Tanner, Michael G.; Kirkwood, Robert A.; Ruggeri, Alessandro; Tosi, Alberto; Boyd, Robert W.; Buller, Gerald S.; Hadfield, Robert H.; Padgett, Miles J. (2015). \"Photon-sparse microscopy: visible light imaging using infrared illumination\" (PDF). Optica. 2 (12): 1049. Bibcode:2015Optic...2.1049A. doi:10.1364/OPTICA.2.001049. ISSN 2334-2536.^ a b Bhushan, Bharat, ed. (2010). Springer handbook of nanotechnology (3rd rev. & extended ed.). Berlin: Springer. p. 620. ISBN 978-3-642-02525-9.^ Sakurai, T.; Watanabe, Y., eds. (2000). Advances in scanning probe microscopy. Berlin: Springer. ISBN 978-3-642-56949-4.^ \"Quantum Microscope for Living Biology\". Science Daily. 4 February 2013. Retrieved 5 February 2013.\n\n\n\n\n\n\n![images (2).jpeg](https://cdn.steemitimages.com/DQmVMPtRy8V8sfn8jq9HerL4ceGcN3Kp1b1bUjxW5jwZw56/images%20(2).jpeg)",
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