This document discusses colour vision and colour blindness. It begins by explaining that colour vision is mediated by three types of cone cells in the eye that are sensitive to different wavelengths of light corresponding to red, green and blue. It describes theories of colour vision including trichromatic theory. It outlines the pathway of colour vision from the retina to the visual cortex. It discusses concepts such as hue, brightness and saturation. Finally, it describes different types of colour blindness including dichromacy and anomalous trichromacy.
Color vision physiology, defects and different testing ProceduresRaju Kaiti
Color vision Physiology, Different types of Color vision defects, different testing procedures, trichromatic theory, color opponent theory, inheritance of color vision defect, management of color vision defect
Corneal metabolism
1. o Cornea requires energy for normal metabolic activities as well as for maintaining transparency and dehydration o Energy is generated by the breakdown of glucose in the form of ATP o Most actively metabolizing layer are epithelium and endothelium o Sources of nutrients : o Oxygen : mainly from atmosphere through tear film , with minor amount supplied by the aqueous and limbal vasculature o Glucose , amino acid, vitamins and other nutrients supplied to cornea by aqueous humor o Glucose also derived from glycogen stores in corneal epithelium o Epithelium consumes O2 10 times faster then stroma
2. o Three process or pathways – o Pentose shunt (Hexose monophosphate shunt) –occurs both in hypoxic and normoxic condition o Glycolysis (Embden meyerhof pathway) –anaerobic process , glucose / glycogen converted to pyruvate yeilding 2 ATPs o TCA or krebs or citric acid cycle- aerobic condition pyruvate is oxidized to yield 36 ATP, water, CO2.
3. o In normal conditions all the glucose consumed by the cornea o Glucose mostly come from aqueous humor o The rate of glucose consumption by the whole cornea is approx. 100 microgram/hr/cm2. o 1 mol. of glucose will be converted to the pyruvic acid and produced 2 molecules lactic acid and 2 mol. of ATP o In the krebs cycle, 1 mol. of glucose will utilize the pyruvic acid and O2 to produced 36 mol. ATP o Epithelium and endothelium will consume the oxygen
4. o The pentose phosphate pathway is used to metabolize five carbon sugars; one ATP and 2 NADH molecules are produced from oxidation of one glucose molecule o Produced intermediates for nucleic acid synthesis and some amino acids o This process will happen in hypoxic or normoxic condition o The purpose of glucose metabolism through the pentose shunt is the production of NADPH
Color vision physiology, defects and different testing ProceduresRaju Kaiti
Color vision Physiology, Different types of Color vision defects, different testing procedures, trichromatic theory, color opponent theory, inheritance of color vision defect, management of color vision defect
Corneal metabolism
1. o Cornea requires energy for normal metabolic activities as well as for maintaining transparency and dehydration o Energy is generated by the breakdown of glucose in the form of ATP o Most actively metabolizing layer are epithelium and endothelium o Sources of nutrients : o Oxygen : mainly from atmosphere through tear film , with minor amount supplied by the aqueous and limbal vasculature o Glucose , amino acid, vitamins and other nutrients supplied to cornea by aqueous humor o Glucose also derived from glycogen stores in corneal epithelium o Epithelium consumes O2 10 times faster then stroma
2. o Three process or pathways – o Pentose shunt (Hexose monophosphate shunt) –occurs both in hypoxic and normoxic condition o Glycolysis (Embden meyerhof pathway) –anaerobic process , glucose / glycogen converted to pyruvate yeilding 2 ATPs o TCA or krebs or citric acid cycle- aerobic condition pyruvate is oxidized to yield 36 ATP, water, CO2.
3. o In normal conditions all the glucose consumed by the cornea o Glucose mostly come from aqueous humor o The rate of glucose consumption by the whole cornea is approx. 100 microgram/hr/cm2. o 1 mol. of glucose will be converted to the pyruvic acid and produced 2 molecules lactic acid and 2 mol. of ATP o In the krebs cycle, 1 mol. of glucose will utilize the pyruvic acid and O2 to produced 36 mol. ATP o Epithelium and endothelium will consume the oxygen
4. o The pentose phosphate pathway is used to metabolize five carbon sugars; one ATP and 2 NADH molecules are produced from oxidation of one glucose molecule o Produced intermediates for nucleic acid synthesis and some amino acids o This process will happen in hypoxic or normoxic condition o The purpose of glucose metabolism through the pentose shunt is the production of NADPH
Accommodation/ Accommodation of Eye, Measurement of Accommodation of Eye (hea...Bikash Sapkota
CLICK HERE TO DOWNLOAD FULL PPT ❤❤ https://healthkura.com/measurement-of-accommodation-of-eye/ ❤❤
Dear viewers Check Out my other piece of works at ❤❤❤ https://healthkura.com ❤❤❤
Measurement of Accommodation of eye:
Amplitude, Facility,
Relative Accommodation, Fatigue, Lag,
Dynamic Retinoscopy
Presentation Layout:
-Introduction to accommodation of eye
-Mechanism
-Components
-Measurement of accommodation of eye
- Amplitude
- Facility
- Relative accommodation
- Lag
-Dynamic Retinoscopy
Accommodation
-dioptric adjustment of the crystalline lens of the eye
- to obtain clear vision for a given target of regard
-process by which the refractive power of eye is altered
- to ensure a clear retinal image
For further reading
-Clinical Procedures in Optometry by J.D. Bartlett, J.B. Eskridge, J.F. Amos
-Primary Care Optometry by Theodere Grosvenor
-Borish’s Clinical Refraction by W.J. Benjamin
-Clinical Procedures for Ocular examination by Carlson et al
-American Academy of Ophthalmology
-Optometric Clinical Practice Guideline by American Optometric Association
-Internet
Follow me to get in touch with optometric and ophthalmic updates
In this ppt included:-
Color definition
Visual spectrum of light
MUNSELL SYSTEM
CIE SYSTEM
Neuropsychology of color
Genetics
Color vision defects and management
Accommodation/ Accommodation of Eye, Measurement of Accommodation of Eye (hea...Bikash Sapkota
CLICK HERE TO DOWNLOAD FULL PPT ❤❤ https://healthkura.com/measurement-of-accommodation-of-eye/ ❤❤
Dear viewers Check Out my other piece of works at ❤❤❤ https://healthkura.com ❤❤❤
Measurement of Accommodation of eye:
Amplitude, Facility,
Relative Accommodation, Fatigue, Lag,
Dynamic Retinoscopy
Presentation Layout:
-Introduction to accommodation of eye
-Mechanism
-Components
-Measurement of accommodation of eye
- Amplitude
- Facility
- Relative accommodation
- Lag
-Dynamic Retinoscopy
Accommodation
-dioptric adjustment of the crystalline lens of the eye
- to obtain clear vision for a given target of regard
-process by which the refractive power of eye is altered
- to ensure a clear retinal image
For further reading
-Clinical Procedures in Optometry by J.D. Bartlett, J.B. Eskridge, J.F. Amos
-Primary Care Optometry by Theodere Grosvenor
-Borish’s Clinical Refraction by W.J. Benjamin
-Clinical Procedures for Ocular examination by Carlson et al
-American Academy of Ophthalmology
-Optometric Clinical Practice Guideline by American Optometric Association
-Internet
Follow me to get in touch with optometric and ophthalmic updates
In this ppt included:-
Color definition
Visual spectrum of light
MUNSELL SYSTEM
CIE SYSTEM
Neuropsychology of color
Genetics
Color vision defects and management
An overview of color vision with its Theories , mechanism and important concepts. Brief explanation on color vision disorders and tests use for screening and diagnosis. by DR.GAGAN and DR. NEENET
Presented by our respected teacher
Mohammad Siddique (Optometrist)
thank u sir
Final Year Student Of Optometry at ISRA School Of Optometry
All Rights Reserved
Consult Mod- 15-11- 14- Name the visual pigment found in rods- 15- Wha.docxCharlesXMLAllano
Consult Mod. 15.11. 14. Name the visual pigment found in rods. 15. What makes the three kinds of cones different from each other? 16. Which receptor cells use the pigmenit retinal: rods, cones, or both? 17. What vitamin (organic nutrient) is necessary for the formation of retinal? Module 15.11 Photoreception occurs in the outer segment of rod and cone cells The rods and cones of the retina are called phintoreceptors because they detect photoniss, the basic units of visible liglit. Lightil energy is a form of radiant energy that trazels in waves with a characteristie wavelength (distance between wave peaks). Our eves are sensitive to wavelengths of 400 -700 nm, the spectrum of visible light. A nanometer (nm) is one billionth of a meter. 1- This illustrateon shows the ruaor structural features of rods and coties and tha adakeat pugmented epththum and bipelar cells. The pigmented epitholium torms the pigmented layer of the retina (see Module 15.101 . 5. All rods contain the same type of opsin It is most sensitive to blue green wavelengths of light. There are three types of cones: blue cones, green cones, and red cones. Fach type has a different form of opsin that is sensitive to a different range of wavelengths. Their Aimalition in various combinations is the bass for color visicin. In a persen with normal color vision. the cone population consists of 16 percent blue cones, 10 pereent green cones, and 74 pervent red cones. Alitrough their wanelength sensitivities overlap, each type is mase sensitive to is specific portion of the visual spectrum. If all three cone populations are stimulated, we perceive the color as white. We also perceive white if nods (but not cones) are stimulated, which is why everything appears black and whate when we enter dimily le surneundings or walk by starlight.
.
Indian Dental Academy: will be one of the most relevant and exciting training center with best faculty and flexible training programs for dental professionals who wish to advance in their dental practice,Offers certified courses in Dental implants,Orthodontics,Endodontics,Cosmetic Dentistry, Prosthetic Dentistry, Periodontics and General Dentistry.
colour vision &theories
colour vision test( in next)
pptx
including ,defination
detail description of theories
conclusion of theories,absorption of conepigments graph
Reference from{ ak khuranka} book(optometry)
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
ABDOMINAL TRAUMA in pediatrics part one.drhasanrajab
Abdominal trauma in pediatrics refers to injuries or damage to the abdominal organs in children. It can occur due to various causes such as falls, motor vehicle accidents, sports-related injuries, and physical abuse. Children are more vulnerable to abdominal trauma due to their unique anatomical and physiological characteristics. Signs and symptoms include abdominal pain, tenderness, distension, vomiting, and signs of shock. Diagnosis involves physical examination, imaging studies, and laboratory tests. Management depends on the severity and may involve conservative treatment or surgical intervention. Prevention is crucial in reducing the incidence of abdominal trauma in children.
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
DISSERTATION on NEW DRUG DISCOVERY AND DEVELOPMENT STAGES OF DRUG DISCOVERYNEHA GUPTA
The process of drug discovery and development is a complex and multi-step endeavor aimed at bringing new pharmaceutical drugs to market. It begins with identifying and validating a biological target, such as a protein, gene, or RNA, that is associated with a disease. This step involves understanding the target's role in the disease and confirming that modulating it can have therapeutic effects. The next stage, hit identification, employs high-throughput screening (HTS) and other methods to find compounds that interact with the target. Computational techniques may also be used to identify potential hits from large compound libraries.
Following hit identification, the hits are optimized to improve their efficacy, selectivity, and pharmacokinetic properties, resulting in lead compounds. These leads undergo further refinement to enhance their potency, reduce toxicity, and improve drug-like characteristics, creating drug candidates suitable for preclinical testing. In the preclinical development phase, drug candidates are tested in vitro (in cell cultures) and in vivo (in animal models) to evaluate their safety, efficacy, pharmacokinetics, and pharmacodynamics. Toxicology studies are conducted to assess potential risks.
Before clinical trials can begin, an Investigational New Drug (IND) application must be submitted to regulatory authorities. This application includes data from preclinical studies and plans for clinical trials. Clinical development involves human trials in three phases: Phase I tests the drug's safety and dosage in a small group of healthy volunteers, Phase II assesses the drug's efficacy and side effects in a larger group of patients with the target disease, and Phase III confirms the drug's efficacy and monitors adverse reactions in a large population, often compared to existing treatments.
After successful clinical trials, a New Drug Application (NDA) is submitted to regulatory authorities for approval, including all data from preclinical and clinical studies, as well as proposed labeling and manufacturing information. Regulatory authorities then review the NDA to ensure the drug is safe, effective, and of high quality, potentially requiring additional studies. Finally, after a drug is approved and marketed, it undergoes post-marketing surveillance, which includes continuous monitoring for long-term safety and effectiveness, pharmacovigilance, and reporting of any adverse effects.
2. Colour vision is the ability of the eye to
discriminate between colours excited by lights
of different wavelengths.
Colour Vision - Function of cones
Colour - Perceptual phenomenon
- Spectral composition of light from
the object and visual surroundings
also matter.
3. Sensation of colour is a subjective phenomenon i.e Taught
since childhood
All colours are a result of admixture of Primary colours in
different proportions-
Red ( 723-647)
Green ( 575-492)
Blue ( 492-450)
For any colour there is a complementary colour
- when both mixed properly produce a sensation of white
4. 1.Trichromatic Theory
• It postulates the existence of three kinds of cones
- Each containing different photopigment
- Each sensitive maximally to one of three primary
colours ( Red, Green , Blue )
-Any given colour’s sensation is due to relative
frequency of impulse from each of three cone
system
•
5.
6. 1. Red sensitive cone pigment/erythrolabe/LWS
- Absorbs light maximally in yellow position (peak at 564 nm)
- Its spectrum extends to long wavelength to sense
Red
2. Green Sensitive Cone pigment/chlorolabe/MWS
- Absorbs light maximally in green portion ( peak at
534 nm )
3. Blue sensitive cone pigment/cyanolabe/SWS
-Absorbs maximally in Blue-violet portion with a peak at
420nm
7.
8. • Postulated by Ewald Hering
• Some colours are mutually exclusive
• The cone photoreceptors are linked together to form
three opposing colour pairs: blue/yellow, red/green,
and black/white
• Activation of one member of the pair
inhibits activity in the other
• No two members of a pair can be seen at the same
location to be stimulated
• Never "bluish yellow" or "reddish green“colour
experienced
9. • Cone pigment = 11 cis-retinal + opsin part
• 11 cis-retinal part is similar to rhodopsin
• Priciples of photochemistry of rhodopsin can
be applied to cone pigments
• Difference being that three cone pigments
are bleached by light of different wavelength.
10. Opsins of green and red sensitive cone
pigments show 96% homology ( amino
acid sequence )
Both show 43% homology with blue
pigment
All three i.e Red,Green,Blue show 41%
homology with rod pigment rhodopsin.
12. A slow graded potential is recorded in these cells
Increase in amplitude of response with increasing
luminosity is also recorded
These cells show two different response
1. Luminosity response:- Hyperpolarizing response with
a broad spectral function
2. Chromatic response:-Hyperpolarizing for a part of a
spectrum and Depolarizing for the remaining part of
spectrum
This represents first stage in visual system where
chromatic interaction’s evidence is noted.
13. Shows Centre-Surround spatial pattern
Red light striking in centre caused hyperpolarisation and
green light in surroundings caused depolarisation.
Amacrine cells
Automatic colour control
14. There are three distinct groups of ganglion cells:-
1.W
2.X
3.Y
Colour sensation is mediated by ‘X’ type
A single ganglion cell may be stimulated by a number
of cones
When all three types of cones stimulate same
ganglion the resultant signal is White.
15. Two type of colour opponent system is found in
ganglion cells:
1. Opponent colour cell system
Some ganglion cells are excited by one colour type
cone and inhibited by other
Two types of colour opponent ganglion cells:-
1.Red – green opponent colour cells use signals from
red and green cones to detect red/green contrast.
2.Blue – yellow opponent colour cells obtain yellow
signal from summated output of red and green cones
which is contrasted with output from blue cones.
16.
17. This system is concerned in successive colour system
(Phenomenon of coloured after images )
Example:-when one sees at green spot for several
seconds , then looks at grey card , one
sees a red spot on the card
18. 2. Double opponent colour cell system
These ganglion cells have opponent for both colour
and space.
Example:- Response may be ‘on’ to red in centre and
‘off’ to it in surround, while ‘off’ to green in centre
and ‘on’ to it in surround.
19. This system is concerned with ‘Simultaneous colour
contrast’ – Phenomenon of perception of a particular
coloured spot against coloured background ( grey
spot appear greenish in red surround and reddish in
green surround ).
20. Trichromatic vision extends 20 to 30 degrees from point of
fixation.
Peripheral to this red and green become indistinguishable.
In far periphery all colour sense is lost.
Very centre of fovea (1/8 degree) is blue blind.
21. All LGB neurons carry information from more than one cone
cell.
Colour information is transmitted from ganglion cells to
parvocellular portion of LGB.
Two type of LGB neurons:-
1. Nonopponent cells ( 30% of total LGB neurons )
Give same response to any monochromatic light
2. Opponent cells ( 60% of total LGB neurons )
Excited by some wavelengths and inhibited by others
22. 1. +R/-G :- Red and green antagonism
2. +G/-R :- Red and green antagonism
3. +B/-Y :- Blue and yellow antagonism
4. +Y/-B :- Blue and yellow anatgonism
23. Colour Signal from parvocellular portion
Layer 4c of striate cortex ( area 17 )
Blobs in layers 2 and 3
( blobs have centre surround cells)
Visual association area
Lingual and fusiform gyri of
occipital lobe
24. Color coded cells are arranged in a hierarchy.
Opponent color cells are found among ganglion cells of retina
and LGB.
Double opponent cells are found in layer 4 of striate
cortex(area 17)
25. Hue
Identification of colour,dominant spectral colour is determined
by the wavelength of particular colour
Brightness
Intensity of colour,it depends on the luminosity
of the component wavelength.
In photoptic vision-peak luminosity function at approximately
555 nm and in scotopic vision at about 507 nm.
The Wavelength shift of maximum luminosity from photopic to
scotopic viewing is called Purkinje Shift Phenomenon’
26.
27. Saturation
It refers to degree of freedom to dilution with white.
It can be estimated by measuring how much of a
particular wavelength must be added to white before
it is distinguishable from white.
28. It describes what mixtures of wavelength can be substituted
for each other without changing the colour.
29. A colour triangle can be drawn to describe
trichromacy of colour mixture.
Three axis are scaled to represent various amounts of
pigment absorption by each of the three cone
pigments.
A particular colour is represented by a line or a
vector.
Length of line identifies brightness.
Angle or direction of line represents hue.
All colours seen by human eye fall inside the colour
triangle.
30. 1. CIE (Commission Internal de Eclairage)
CIE colour space system is based on amounts of three
primary colours necessary to match a specified colour.
CIE chromaticity diagram is constructed by placing the
three reference wavelengths say 450 at X , 520 at Y and
650 at Z of the triangle.
31. *2.The Munsell colour system
All the colours are represented in a cylinderin terms
of hue and chroma.
Hue dimension i.e dominant spectral colour is
located on circumference of the cylinder.
Value dimension i.e lightness is indicated by moving
up or down the cylinder
47. *Standard source A is a defined tungsten lamp
run at a defined current and voltage.
*Standard source C is a substitue for daylight
and consist of a tungsten lamp with a defined
blue filter in front.
*Point E represents a source radiating equal
amount of energy in equal intervals of
wavelength throughout the spectrum.
48.
49.
50.
51.
52.
53.
54.
55.
56. *Colour blindness is also called “Daltonism”
*Defective perception of colour -anomalous
* Absence of colour perception is anopia
*It may be-
*Congenital
*Acquired
57. 1.Monochromacy /Total colour blindness
When two or all 3 cone pigments are missing.
Types:-
1.Rod monochromacy
2.Cone monochromacy
2.Dichromacy - When one of the 3 colour pigment is
absent
Protanopia - RED retinal photoreceptors absent
Deuteranopia -GREEN retinal photoreceptors absent.
Tritanopia -BLUE retinal photoreceptors absent
58. 3.TRICHROMACY [Anomalous Trichromacy]
Colour vision deficiency rather than loss
Protanomaly - RED colour deficiency [Hereditary,
Sex linked, Male1%, ]
Deuteranomaly - GREEN colour
deficiency[Hereditary, Sex linked, Male 5% ]
Tritanomaly - BLUE colour deficienc [ Rare,Not
hereditary ]
59. *
Gene rhodopsin - chromosome 3.
Gene for blue sensitive cone - chromosome 7
The genes for red and green sensitive cones
are arranged in tandem array on the ‘q’ arm of
x chromosome so defect is inherited as x-
linked recessive
Tritanopia is inherited as an autosomal
dominant defect
60. Congenital colour blindness is two type
Achromatopsia
Dyschromatopsia
More common in male (3-4%)than female(0.4%)
It is x-linked recessive inherited condition.
61. Cone monochromatism:
Presence of only one primary colour
So person is truely colour blind
Rod monochromatism:
Complete or incomplete
Inherited as autosomal recessive trait
Total colour blindness
Day blindness(visual acquity is about 6/60)