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"dark field microscope"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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¿µ¹® visual field test ÇÑ±Û ½Ã¾ß°Ë»ç
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  ´«À» ÇѰ÷¿¡ °íÁ¤½ÃŲ Ã¤, °üÂûÇÒ ¼ö Àִ ÁÖº¯°ø°£À» ½Ã¾ß¶ó ÇÑ´Ù. ½Ã¾ß¸¦ °Ë»çÇϴ °¡Àå °£´ÜÇÑ ¹æ¹ýÀº ´ë¸é°Ë»ç(confronting test)ÀÌ´Ù. À̰ÍÀº Çǰ˻çÀÚÀÇ ´«À» °Ë»çÀÚÀÇ ´«¿¡ ¸ÂÃ߾¸µµ·Ï ÇÏ¿© ´«À» °íÁ¤½ÃŲä, °Ë»çÀÚ°¡ ¼Õ°¡¶ô³¡À» À§ÂÊ, ¾Æ·¡ÂÊ, ¿ÞÂÊ, ¿À¸¥ÂÊ, ±×¸®°í ºñ½ºµëÈ÷ °æ»çÁø °÷ µîÀ¸·Î ¿Å°Üº¸¾Æ Çǰ˻çÀÚ°¡ °üÂûÇÒ ¼ö ÀÖ´ÂÁö ¿©ºÎ¸¦ Á¤Çϴ °Ë»ç¹ýÀÌ´Ù. À̺¸´Ù Á¤È®ÇÑ °Ë»ç¹ýÀº ÀÚµ¿½Ä ÄÄÇ»Åͽþ߰˻ç¹ýÀÌ ÀÖ´Ù. ´ë°³, ´«ÀÚüÀÇ ÀÌ»óÀÌ À־ ½Ã¾ß°Ë»ç¿¡¼­ ÀÌ»óÀÌ ³ª¿ÀÁö¸¸, À̿ܠ³úÀÇ ÀÌ»óÀ¸·Î ½Ã°¢ÀÇ Çü¼º°æ·Î¿¡ ÀÌ»óÀÌ À־ ¿ª½Ã ÀÌ»ó¼Ò°ßÀ» º¸ÀδÙ.
¿µ¹® electron microscope ÇÑ±Û ÀüÀÚÇö¹Ì°æ
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  Àü±â ¸¶´ç ¶Ç´Â Àڱ⠸¶´çÀ» ÀÌ¿ëÇÏ¿© ÀüÀÚ·ù¸¦ ÀüÀÚ ·»Áî¿¡ Áý¼Ó½ÃÄÑ, ±× Åë·Î¿¡ ³õÀΠǥº»ÀÇ »óÀ» È®´ëÇϴ ÀåÄ¡. ±¤ÇРÇö¹Ì°æº¸´Ù ÈξÀ ¶Ù¾î³­ ºÐÇØ ´É·ÂÀ» °¡Áø´Ù. 
¿µ¹® microscope ÇÑ±Û Çö¹Ì°æ
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  ¹°Ã¼ÀÇ ¹Ì¼¼ÇÑ ºÎºÐÀ» È®´ëÇÏ¿© °üÂûÇϴ ÀåÄ¡. ´ë°³ÀÇ °æ¿ì´Â ´ë¹°·»Áî¿Í Á¢¾È·»Á °®Ãß°í Àִ Çö¹Ì°æÀ» ¸»Çϳª, ³ÐÀº ¶æÀ¸·Î´Â ÀüÀÚ¼±À» ÀÌ¿ëÇϴ ÀüÀÚÇö¹Ì°æÀ» Æ÷ÇÔÇϸç, È®´ë°æµµ ´ÜÀÏ ·»Áî°è¸¦ °®´Â ´ÜÇö¹Ì°æÀ̶ó ÇÒ ¼ö ÀÖ´Ù. Á¾·ù¿Í ÇüÀº »ç¿ë¸ñÀû-Á¦ÀÛ¿¬´ë-Á¦À۠ȸ»çÀÇ Â÷ÀÌ¿¡ µû¶ó ¿©·¯ °¡Áö°¡ ÀÖÀ¸³ª ±¸Á¶ÀûÀ¸·Î ºÐ·ùÇϸé, °¡Àå ÀϹÝÀûÀΠÅõ°úÇö¹Ì°æ À̿ܿ¡ ±Ý¼ÓÇö¹Ì°æ-Æí±¤Çö¹Ì°æ-Çü±¤Çö¹Ì°æ-À§»óÂ÷Çö¹Ì°æ-Àڿܼ±Çö¹Ì°æ µîÀǠƯ¼öÇÑ °ÍµéÀÌ ÀÖ´Ù. Çö¹Ì°æÀÌ ¹°Ã¼ÀÇ »óÀ» È®´ëÇϴ ¿ø¸®´Â ÃÊÁ¡°Å¸®°¡ ÂªÀº ´ë¹°·»Áî¿¡ ÀÇÇÏ¿© ¾ò¾îÁö´Â È®´ëµÈ µµ¸³½Ç»óÀ» Á¢¾È·»Áî·Î ´Ù½Ã È®´ëÇϴ °ÍÀÌ´Ù. ÀÌ °á»ó°ü°è´Â ´ë´ÜÈ÷ ¿¹¹ÎÇÏ¿© ¹°Ã¼¿Í ´ë¹°·»Áî »çÀÌÀÇ °Å¸®°¡ Á¶±Ý¸¸ º¯ÇÏ¿©µµ ¹Ù¸¥ »óÀ» ¸ÎÁö ¸øÇÑ´Ù.
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  • ¿µ¹®
    ÇѱÛ
  • dark field microscope
    ¾Ï½Ã¾ßÇö¹Ì°æ
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  • ¿µ¹®
    ÇѱÛ
  • dark field microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ°Ë»ç(¹ý)
  • dark-field illumination
    ¾Ï½Ã¾ßÁ¶¸í
  • dark adaptation
    ¾Ï¼øÀÀ, ¾îµÒÀûÀÀ
  • dark cell
    ¾îµÒ¼¼Æ÷
  • dark current
    ¾ÏÀü·ù
  • dark repair
    ¾Ï¹ÝÀÀº¹±¸
  • binocular microscope
    µÎ´«Çö¹Ì°æ, ¾ç¾ÈÇö¹Ì°æ
  • biological microscope
    »ý¹°Çö¹Ì°æ
  • compound lens microscope
    º¹ÇÕ·»ÁîÇö¹Ì°æ
  • confocal microscope
    µ¿ÀÏÃÊÁ¡Çö¹Ì°æ
  • dissecting microscope
    ÇØºÎÇö¹Ì°æ
  • electron microscope
    ÀüÀÚÇö¹Ì°æ
  • fluorescence microscope
    Çü±¤Çö¹Ì°æ
  • inverted microscope
    µµ¸³Çö¹Ì°æ
  • interference microscope
    °£¼·Çö¹Ì°æ
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dark adaptation
    ¾Ï¼øÀÀ
  • microscope
    Çö¹Ì°æ
  • electron microscope
    ÀüÀÚÇö¹Ì°æ
  • inverted microscope
    µµ¸³Çö¹Ì°æ
  • optical microscope
    ±¤ÇÐÇö¹Ì°æ
  • phase-contrast microscope
    À§»óÂ÷Çö¹Ì°æ
  • polarizing microscope
    Æí±¤Çö¹Ì°æ
  • transmission electron microscope
    Åõ°úÀüÀÚÇö¹Ì°æ
  • visual field defect
    ½Ã¾ß°á¼Õ
  • field
    1. ºÐ¾ß, ¿µ¿ª, ¹üÀ§, 2. ºÎÀ§, 3. ½Ã¾ß, 4. Àü±âÀå
  • boost field
    Á¶»ç¿µ¿ª, Á¶»ç¸é
  • electropmagnetic field
    ÀüÀÚ±âÀå
  • irradiation field
    Á¶»ç¿µ¿ª
  • radiation field
    ¹æ»ç¼±Á¶»ç¿µ¿ª
  • sound field
    À½¿ª
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dark field microscope
    ¾Ï½Ã¾ßÇö¹Ì°æ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dark field microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ°Ë»ç
  • dark-field illumination
    ¾Ï½Ã¾ßÁ¶¸í
  • dark adaptation
    ¾Ï¼øÀÀ
  • dark cell
    ¾îµÒ¼¼Æ÷
  • dark current
    ¾ÏÀü·ù
  • dark repair
    ¾Ï¹ÝÀÀº¹±¸
  • dark room test
    ¾Ï½Ç°Ë»ç
  • binocular microscope
    µÎ´«Çö¹Ì°æ
  • biological microscope
    »ý¹°Çö¹Ì°æ
  • compound lens microscope
    º¹ÇÕ·»ÁîÇö¹Ì°æ
  • dissecting microscope
    ÇØºÎÇö¹Ì°æ
  • electron microscope
    ÀüÀÚÇö¹Ì°æ
  • fluorescence microscope
    Çü±¤Çö¹Ì°æ
  • interference microscope
    °£¼·Çö¹Ì°æ
  • inverted microscope
    µµ¸³Çö¹Ì°æ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • illumination, dark-field
    ¾Ï½Ã¾ßÁ¶¸í
  • polarizing microscope
    Æí±¤Çö¹Ì°æ(ø¶Îà úéÚ°Ìð).
  • polarizing microscope
    Æí±¤Çö¹Ì°æ(ø¶ÎÃúéÚ°Ìð)
  • B1 field gradient
    ȸÀü ÀÚÀå Àڱ⠰æ»ç
  • FFE, fast field echo
    ±Þ¼Ó ÀÚÀå ¿¡ÄÚ
  • FOV(field of view)
    ¿µ»ó ¿µ¿ª, ¿µ»ó ¹üÀ§
  • Goldman constant-field equation
    °ñµå¸¸ Á¤Àü·ù(ïÒï³×µ) ½Ä
  • abutted field
    ÀÎÁ¢Á¶»ç¸é, -¿µ¿ª, Á¢ÃËÁ¶»ç¸é
  • altitudinal visual field defect
    ¼öÆò½Ã¾ß°á¼Õ
  • fringe field
    ÁÖº¯ ¾ß
  • fringe magnetic field strength
    ÁÖº¯ ÀÚÀå ¼¼±â
  • frontal adversive field
    ÀüµÎ¿±´ëÃø¾ß(¡­Óßö´å¯), Àü¿îµ¿¿ª(îñê¡ÔÑæ´).
  • geometric field distortion artifact
    ±âÇÏÇÐÀû ÀÚÀå ¿Ö°î Àΰø¹°
  • geometric field separtion
    ±âÇÏÇÐÀûÁ¶»ç¿µ¿ªºÐ¸®
  • geometrical field
    ±âÇÏÇÐÀûÁ¶»ç¿µ¿ª
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dark field microscope
    ¾Ï½Ã¾ßÇö¹Ì°æ
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dark field microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ
  • dark-field illumination
    ¾Ï½Ã¾ßÁ¶¸í
  • illumination, dark-field
    ¾Ï½Ã¾ßÁ¶¸í
  • field within a field technique
    Áߺ¹Á¶»ç¿µ¿ª¹ý
  • dark adaptation
    ¾Ï¼øÀÀ(äÞâ÷ëë)
  • dark adaptation
    ¾Ï¼øÀÀ
  • dark cell
    ¾îµÎ¿î¼¼Æ÷
  • dark cell norepinephrine cell
    ¾îµÎ¿î¼¼Æ÷ ³ë¸£¿¡Çdz×ÇÁ¸°¼¼Æ÷
  • dark current
    ¾ÏÀü·ù<<ºÐ±¤±¤µµÃøÁ¤¿¡¼­>>
  • dark repair
    ¾Ï¹ÝÀÀº¹±¸
  • dark room test
    ¾Ï½Ç°Ë»ç
  • interstitial cell dark cell
    »çÀÌÁú¼¼Æ÷
  • macular dark spot
    Ȳ¹Ý¾ÏÈæºÎ
  • binocular microscope
    ½Ö¾ÈÇö¹Ì°æ(äªäÑúéÚ°Ìð).
  • binocular microscope
    ½Ö¾ÈÇö¹Ì°æ, ¾ç¾ÈÇö¹Ì°æ
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 6 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • Nail field
    ¹ßÅ鱸¿ª
    [¿¾ ¿ë¾î] Á¶¾ß
  • Nail field
    ¼ÕÅ鱸¿ª
    [¿¾ ¿ë¾î] Á¶¾ß
  • Interstitial cell [Dark cell]
    »çÀÌÁú¼¼Æ÷
    [¿¾ ¿ë¾î] °£Áú¼¼Æ÷
  • Dark cell
    ¾îµÎ¿î¼¼Æ÷
    [¿¾ ¿ë¾î] ¾Ï¼¼Æ÷
  • Dark cell
    ¾îµÎ¿î¼¼Æ÷
    [¿¾ ¿ë¾î] ¾ÏÁÖ¼¼Æ÷
  • Dark cell [Norepinephrine cell]
    ¾îµÎ¿î¼¼Æ÷ [³ë¸£¿¡Çdz×ÇÁ¸°¼¼Æ÷]
    [¿¾ ¿ë¾î] ¾Ï¼¼Æ÷(³ë¸£¿¡Çdz×ÇÁ¸°ºÐºñ¼¼Æ÷)
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • field ion microscope
    Àå(íÞ) À̿ Çö¹Ì°æ(úéÚ°Ìð)
  • dark reaction
    ¾Ï¹ÝÀÀ(äÞÚãëë)
  • dark reactivation
    ¾Ï ÀçȰ¼ºÈ­(äÞî¢üÀàõûù)
  • dark recovery
    ¾Ï ȸº¹(äÞüÞÜÖ) (ÔÒ) dark reactivation
  • dark repair
    "¾Ï¼öº¹(äÞáóÜÖ), (ÔÒ) dark reactivation"
  • compound microscope
    º¹ÇÕÇö¹Ì°æ(ÜÜùêúéÚ°Ìð)
  • electron microscope
    ÀüÀÚÇö¹Ì°æ(ï³í­úéÚ°Ìð)
  • electron microscope radioautography
    ÀüÀÚÇö¹Ì°æ ÀÚ°¡¹æ»ç±â·Ï¹ý(ï³í­úéÚ°Ìðí»Ê«Û¯ÞÒÑÀÖâÛö)
  • fluorescence microscope
    Çü±¤ Çö¹Ì°æ(û«ÎÃúéÚ°Ìð)
  • light microscope
    ±¤ÇÐÇö¹Ì°æ(ÎÃùÊúéÚ°Ìð)
  • phase contrast microscope
    À§»óÂ÷(êÈßÓó¬) Çö¹Ì°æ(ßÓÓßðÎúéÚ°Ìð)
  • poloarizatin microscope
    Æí±Ø Çö¹Ì°æ(ø¶Ð¿úéÚ°Ìð)
  • scanning electron microscope
    ÁÖ»ç ÀüÀÚ Çö¹Ì°æ(ñËÞÛï³í­úéÚ°Ìð)
  • scanning tunneling microscope
    ÁÖ»ç(ñËÞÛ)Çö¹Ì°æ(úéÚ°Ìð)
  • transmission electron microscope
    Åõ°ú ÀüÀÚ Çö¹Ì°æ(÷âΦï³í­úéÚ°Ìð)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dark room
    ¾Ï½Ç
  • electron microscope
    ÀüÀÚÇö¹Ì°æ
  • microscope
    Çö¹Ì°æ
  • B1 field gradient
    ȸÀüÀÚÀå°æ»ç
  • constant field gradient spin echo method
    °íÁ¤°æ»çÀ彺ÇÉ¿¡ÄÚ¹ý
  • demagnetizing field
    ¹ÝÀÚÀå
  • electromagnetic field
    ÀüÀÚ(±â)Àå
  • far field
    ¿ø°Å¸®±¸¿ª
  • fast field echo [=FFE]
    ±Þ¼ÓÀÚÀå¿¡ÄÚ
  • FFE [=fast field echo]
    ±Þ¼ÓÀÚÀå¿¡ÄÚ
  • field
    ¾ß, ¿µ¿ª, Çʵå, Ç׸ñ
  • field echo
    ÀÚÀå¿¡ÄÚ
  • field gradient
    ÀÚÀå°æ»ç
  • field inhomogeneity
    ÀÚÀåºÒ±ÕÀÏ(¼º)
  • field of view [=FOV]
    ¿µ»ó¿µ¿ª, ¿µ»ó¹üÀ§
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
DA dark adaptation; dark agouti [rat]; daunomycin; degenerative arthritis; delayed action; Dental Assis...
FADF fluorescent antibody dark field
HPF heparin-precipitable fraction; hepatic plasma flow; high-pass filter; high-power field [microscope];...
A [band] the dark-staining zone of a striated muscle
DK dark; decay; diabetic ketoacidosis; diet kitchen; diseased kidney; dog kidney [cells]
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
DFM Dark field microscopy
E-field Electric field
D Dark
DA Dark Agouti
DR Dark-reared
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • dark-field microscope
    ¾Ï½Ã¾ß Çö¹Ì°æ
    ¾Ï½Ã¾ß Á¶¸í¹ý¿¡ ÀÇÇØ º¸ÅëÀÇ Çö¹Ì°æÀ¸·Î´Â º¸ÀÌÁö ¾Ê´Â ¹Ì¼¼ÇÑ ÀÔÀÚ¸¦ º¼ ¼ö ÀÖ´Â Çö¹Ì°æ. ÇÑ¿Ü Çö¹Ì°æÀ» ¸»Çϴµ¥, ¾Ï½Ã¾ß Á¶¸í°ú ±× Áý±¤ ·»Á »ç¿ëÇϹǷΠÀÌ¿Í °°ÀÌ ºÒ¸®±âµµ ÇÑ´Ù.
  • dark feld microscope
    ¾Ï½Ã¾ß Çö¹Ì°æ
  • order dark field
    ±ÔÄ¢ÀûÀ¸·Î ¾îµÎ¿î ºÎÀ§
  • biological microscope
    »ý¹° Çö¹Ì°æ
  • inverted microscope
    µµ¸³ Çö¹Ì°æ
  • leukocyte electron microscope
    ¹éÇ÷±¸ ÀüÀÚÇö¹Ì°æ
  • light microscope
    ±¤ÇÐÇö¹Ì°æ
    Ç¥º»À» ºûÀÇ ¹Ý»ç, ±¼Àý µîÀÇ ¼ºÁúÀ» ÀÌ¿ëÇØ¼­ °üÂûÇÏ´Â Çö¹Ì°æ.
  • optical microscope
    ±¤ÇÐ Çö¹Ì°æ
    Ç¥º»À¸·ÎºÎÅÍÀÇ ºûÀ» »ç¿ëÇÏ¿© ´ë¹° ·»Áî¿¡ ÀÇÇØ Ç¥º»ÀÌ È®´ëµÈ ½Ç»óÀ» ¸Î°í, À̰ÍÀ» Á¢¾È ·»Áî¿¡ ÀÇÇØ¼­ ÀçÈ®´ëÇÏ´Â ÀåÄ¡. ÀϹÝÀûÀ¸·Î Çö¹Ì°æÀ̶ó°í ÇÒ ¶§´Â À̰ÍÀ» °¡¸®Å²´Ù. Á¾·ù¿¡´Â º¸Åë Çö¹Ì°æ, Àڿܼ± Çö¹Ì°æ, Àû¿Ü¼± Çö¹Ì°æ, Çü±¤ Çö¹Ì°æ, ¾Ï½Ã¾ß Çö¹Ì°æ, À§»óÂ÷ Çö¹Ì°æ, Æí±¤ Çö¹Ì°æ, °£¼· Çö¹Ì°æ µîÀÌ ÀÖ´Ù.
  • dark
    ¾îµÎ¿î
  • dark blood
    £Àº »öÀÇ Ç÷¾×
  • dark blue pinhead
    ¾Ïû»öÀÇ ÇÉ ¸Ó¸®
  • dark blue-red
    ¾ÏûÀû»ö
  • dark brown
    ¾Ï°¥»ö
  • dark pigmentation
    £Àº Âø»ö
  • dark room
    ¾Ï½Ç
    »çÁø °¨±¤ Àç·áÀÇ Ãë±Þ, Çʸ§ÀÇ Çö»ó, È®´ë µîÀÇ Ã³¸®¸¦ ÇÏ´Â Â÷±¤ ¼³ºñ¸¦ ÇÑ ÀÛ¾÷½Ç.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
dark-field microscope <instrument> A microscope that has a special condenser and objective with a diaphragm or stop that scatters light from the object observed, with the result that the object appears bright on a dark background.
(05 Mar 2000)
cardioid dark field condenser <microscopy> A condenser designed with two reflecting surfaces, the first, a spherical surface which reflects the rays to a second, cardioid (heart-shaped) surface. The virtue in such an arrangement is that, if the cardioid surface is of true figure, the lens is both achromatic and aplanatic. It has a limiting numerical aperture of about 1.0. Thus objectives of a greater numerical aperture cannot be used successfully with it. A true cardioid figure is the trace of a point on the circumference of a circle rolling around an equal, fixed circle.
(05 Aug 1998)
paraboloid dark field condenser <microscopy> A lens of parabolic shape. The vertex end is ground back so that its focus can be brought into coincidence with the specimen on the slide. A central stop is provided to block the central rays. It is used chiefly for medium- power work.
(05 Aug 1998)
condenser, dark field <microscopy> A condenser forming a hollow cone of light with its apex (or focal point) in the plane of the specimen. When used with an objective having a numerical aperture lower than the minimum numerical aperture of the hollow cone, only light deviated by the specimen enters the objective. Objects are seen as bright images against a dark background.
The ordinary bright field condenser of low power, used with a central stop, makes a good dark field condenser. They all form a dark field while illuminating the specimen with a hollow cone of light. The lower limiting aperture of the condenser must be greater than the numerical aperture of the objective with which it is to be used. Thus, no direct light enters the objective, the specimen is seen by reflected or scattered light on a dark background.
See: condensers
See: special dark field condensers: paraboloid, cardioid and Cassegrainian.
(05 Aug 1998)
dark-field condenser An apparatus for throwing reflected light through the microscope field, so that only the object to be examined is illuminated, the field itself being dark.
(05 Mar 2000)
dark field illumination <microscopy> Any method of illumination which illuminates the specimen but does not admit light directly to the objective. It may be by substage (dark field) condensers, by stagespot lighting, by special condensers fitted around special objectives for reflected illumination or by the slit ultramicroscope.
(05 Aug 1998)
dark field imaging <microscopy> Using a single diffracted beam to form the image in a transmission electron microscope. This causes all regions of the specimen not of the same crystal structure and orientation as the region which produced the diffracted beam to be represented as very dark in the final image, allowing phase differentiation visually in the transmission electron microscope.
(05 Aug 1998)
dark field microscopy <procedure> A system of microscopy in which particles are illuminated at a very low angle from the side so that the background appears dark and the objects are seen by diffracted and reflected patches of light against a dark background.
(18 Nov 1997)
dark field objective <microscopy> Certain objectives for high-power, dark fieldwork equipped with iris diaphragms or funnel stops so that their apertures may be reduced to correspond to the dark field con-denser with which they are used.
(05 Aug 1998)
dark field slides <microscopy> Owing to the exacting demands of dark field illumination, not only must the microscope slide be especially clean, but also the glass of which the slide is composed must be optically clear under dark field conditions. The glass should not fluoresce.
(05 Aug 1998)
dark field stop <microscopy> A central stop for obtaining a dark field effect for low-power objectives. It is customarily used with a high numerical aperture, bright field condenser.
(05 Aug 1998)
microscope, field emission <microscopy> An image-forming device in which a strong electrostatic field causes cold emission of electrons from a sharply rounded point or from a specimen that has been placed on that point. The electrons are accelerated to a phosphorescent screen, or photographic film, giving a visible picture of the variation of emission over the specimen surface.
(05 Aug 1998)
field-emission microscope <instrument, microscopy> Either one of two kinds of point-projection microscopes, both invented by E. W. Muller: (1) The older device (1936) is a specialised cathode-ray tube, employing field-emission of electrons from a negatively charged tip of a very sharp needle in a vacuum, by point-projection of the image onto a positively charged, fluorescent screen. (2) A later device (field-ion-mission microscope, 1950) emits absorbed helium ions from an anode.
(05 Aug 1998)
field ion microscope <instrument> Type of microscopy in which the specimen is illuminated with ions, often gallium ions, that are focussed electrostatically. The ions remove components of the specimen, lower atomic masses first. These are imaged and provide information on elemental distribution with a resolution of perhaps 30 nm.
(18 Nov 1997)
dark adaptation The adjustment of the eye occurring under reduced illumination in which the sensitivity to light is greatly increased or the light threshold is greatly reduced.
Dark adaptation is slower than light adaptation. During dark adaptation rhodopsin is built up in the retinal rods.
(12 Dec 1998)
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