Xanthochroism
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Xanthochroism
Xanthochromism (also called xanthochroism or xanthism) is an unusually yellow pigmentation in an animal. It is often associated with the lack of usual red pigmentation and its replacement with yellow. The cause is usually genetic but may also be related to the animal's diet. A Cornell University survey of unusual-looking birds visiting feeders reported that 4% of such birds were described as xanthochromistic (compared with 76% albinistic). The opposite of xanthochromism, a deficiency in or complete absence of yellow pigment, is known as ''axanthism''. Birds exhibiting genetic xanthochromism, especially deliberately bred mutations of several species of parrot in aviculture, are termed "lutinos". Wild birds in which xanthochromism has been recorded include yellow wagtail, wood warbler, Cape May warbler, rose-breasted grosbeak, evening grosbeak, red-bellied woodpecker, scarlet tanager, northern cardinal, great spotted woodpecker, common tailorbird, crimson-breasted shrike, ...
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Northern Cardinal
The northern cardinal (''Cardinalis cardinalis'') is a bird in the genus ''Cardinalis''; it is also known colloquially as the redbird, common cardinal, red cardinal, or just cardinal (which was its name prior to 1985). It can be found in southeastern Canada, through the eastern United States from Maine to Minnesota to Texas, New Mexico, southern Arizona, southern California, and south through Mexico, Belize, and Guatemala. It is also an introduced species in a few locations such as Bermuda and Hawaii. Its habitat includes woodlands, gardens, shrublands, and wetlands. The northern cardinal is a mid-sized songbird with a body length of . It has a distinctive crest on the head and a mask on the face which is black in the male and gray in the female. The male is a vibrant red, while the female is a reddish olive color. The northern cardinal is mainly granivorous, but also feeds on insects and fruit. The male behaves territorially, marking out his territory with song. During courtshi ...
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Argentine Horned Frog
The Argentine horned frog (''Ceratophrys ornata''), also known as the Argentine wide-mouthed frog, ornate horned frog, ornate horned toad, or the ornate pacman frog, is a species of frog in the family Ceratophryidae. The species is endemic to South America. It is the most common species of horned frog, in the grasslands of Argentina, Uruguay and Brazil. A voracious eater, it will attempt to swallow anything that moves close to its wide mouth, such as insects, rodents, lizards, and other frogs, even if this predator would suffocate in the process. It is also kept as an exotic pet. The nickname "pacman frog" is a reference to the popular 1980's arcade game '' Pac-Man'', where Pac-Man himself eats quite a lot, and has a mouth that takes up most of its body, much like the Argentine horned frog. Description The females of ''C. ornata'' can grow to be 16.5 centimeters (6.5 inches) snout to vent (SV) and the males 11.5 centimeters (4.5 in) SV. The average lifespan is 6 to 7 yea ...
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Genetic Disorders With No OMIM
Genetic may refer to: *Genetics, in biology, the science of genes, heredity, and the variation of organisms **Genetic, used as an adjective, refers to genes ***Genetic disorder, any disorder caused by a genetic mutation, whether inherited or de novo ***Genetic mutation, a change in a gene ****Heredity, genes and their mutations being passed from parents to offspring **Genetic recombination, refers to the recombining of alleles resulting in a new molecule of DNA *Genetic relationship (linguistics), in linguistics, a relationship between two languages with a common ancestor language *Genetic algorithm, in computer science, a kind of search technique modeled on evolutionary biology See also *Genetic memory (other) Genetic memory may refer to: *Genetic memory (psychology) In psychology, genetic memory is a theorized phenomenon in which certain kinds of memories could be inherited, being present at birth in the absence of any associated sensory experience, ...
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Carotenosis
Carotenosis is a benign and reversible medical condition where an excess of dietary carotenoids results in orange discoloration of the outermost skin layer. The discoloration is most easily observed in light-skinned people and may be mistaken for jaundice. Carotenoids are lipid-soluble compounds that include alpha- and beta-carotene, beta- cryptoxanthin, lycopene, lutein, and zeaxanthin. The primary serum carotenoids are beta-carotene, lycopene, and lutein. Serum levels of carotenoids vary between region, ethnicity, and sex in the healthy population. All are absorbed by passive diffusion from the gastrointestinal tract and are then partially metabolized in the intestinal mucosa and liver to vitamin A. From there they are transported in the plasma into the peripheral tissues. Carotenoids are eliminated via sweat, sebum, urine, and gastrointestinal secretions. Carotenoids contribute to normal-appearing human skin color, and are a significant component of physiologic ultraviolet ph ...
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Piebaldism
Piebaldism refers to the absence of mature melanin-forming cells (melanocytes) in certain areas of the skin and hair. It is a rare autosomal dominant disorder of melanocyte development.James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. . Common characteristics include a congenital white forelock, scattered normal pigmented and hypopigmented macules and a triangular shaped depigmented patch on the forehead. There is nevertheless great variation in the degree and pattern of presentation, even within affected families. In some cases, piebaldism occurs together with severe developmental problems, as in Waardenburg syndrome and Hirschsprung's disease. Piebaldism has been documented to occur in all races, and is found in nearly every species of mammal. The condition is very common in mice, rabbits, dogs, sheep, deer, cattle and horses—where selective breeding has increased the incidence of the mutation—b ...
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Melanism
The term melanism refers to black pigment and is derived from the gr, μελανός. Melanism is the increased development of the dark-colored pigment melanin in the skin or hair. Pseudomelanism, also called abundism, is another variant of pigmentation, identifiable by dark spots or enlarged stripes, which cover a large part of the body of the animal, making it appear melanistic. The morbid deposition of black matter, often of a malignant character causing pigmented tumors, is called melanosis. Adaptation Melanism related to the process of adaptation is called adaptive. Most commonly, dark individuals become Fitness (biology), fitter to survive and reproduce in their environment as they are better camouflaged. This makes some species less conspicuous to predators, while others, such as leopards, use it as a foraging advantage during night hunting. Typically, adaptive melanism is Heritability, heritable: A Dominance (genetics), dominant allele, which is entirely or nearly ent ...
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Leucism
Leucism () is a wide variety of conditions that result in the partial loss of pigmentation in an animal—causing white, pale, or patchy coloration of the skin, hair, feathers, scales, or cuticles, but not the eyes. It is occasionally spelled ''leukism''. Some genetic conditions that result in a "leucistic" appearance include piebaldism, Waardenburg syndrome, vitiligo, Chédiak–Higashi syndrome, flavism, isabellinism, xanthochromism, axanthism, amelanism, and Melanophilin mutations. Pale patches of skin, feathers, or fur (often referred to as "depigmentation") can also result from injury. Details ''Leucism'' is often used to describe the phenotype that results from defects in pigment cell differentiation and/or migration from the neural crest to skin, hair, or feathers during development. This results in either the entire surface (if all pigment cells fail to develop) or patches of body surface (if only a subset are defective) having a lack of cells that can make pigment. ...
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Heterochromia Iridum
Heterochromia is a variation in coloration. The term is most often used to describe color differences of the iris, but can also be applied to color variation of hair or skin. Heterochromia is determined by the production, delivery, and concentration of melanin (a pigment). It may be inherited, or caused by genetic mosaicism, chimerism, disease, or injury. It occurs in humans and certain breeds of domesticated animals. Heterochromia of the eye is called heterochromia iridum or heterochromia iridis. It can be complete or sectoral. In complete heterochromia, one iris is a different color from the other. In sectoral heterochromia, part of one iris is a different color from its remainder. In central heterochromia, there is a ring around the pupil or possibly spikes of different colors radiating from the pupil. Though multiple causes have been posited, the scientific consensus is that a lack of genetic diversity is the primary reason behind heterochromia, at least in domestic anima ...
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Erythrism
Erythrism or erythrochroism refers to an unusual reddish pigmentation of an animal's hair, skin, feathers, or eggshells. Causes of erythrism include: * Genetic mutations which cause an absence of a normal pigment and/or excessive production of others * Diet, as in bees feeding on "bright red corn syrup" used in maraschino cherry manufacturing. Erythrism in katydids has been occasionally observed. The coloring might be a camouflage that helps some members of the species survive on red plants. There is also consensus that the erythristic mutation is actually a dominant trait among katydid species, albeit a disadvantageous one, due to the overwhelmingly green coloration of most foliage. Hence, most pink or otherwise vividly colored katydids do not survive to adulthood, and this observation explains their rarity. Erythrism in leopards is rare, but one study reported that two of twenty-eight leopards seen in camera traps in a South African nature reserve were erythristic, and the autho ...
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Dyschromia
Dyschromia refers to an alteration of the color of the skin or nails. "Hyperchromia" can refer to hyperpigmentation, and "hypochromia" can refer to hypopigmentation. "Dyschromatoses" involve both hyperpigmented and hypopigmented macules. __TOC__ See also *Albinism * Albino and white squirrels *Amelanism *Chimera (genetics) *Coloboma *Erythrism *Heterochromia iridum *Leucism *Melanism *Piebaldism *Vitiligo *Xanthochromism Xanthochromism (also called xanthochroism or xanthism) is an unusually yellow pigmentation in an animal. It is often associated with the lack of usual red pigmentation and its replacement with yellow. The cause is usually genetic but may also be ... References Cutaneous congenital anomalies Disturbances of human pigmentation Disturbances of pigmentation {{cutaneous-condition-stub ...
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Amelanism
Amelanism (also known as amelanosis) is a pigmentation abnormality characterized by the lack of pigments called melanins, commonly associated with a genetic loss of tyrosinase function. Amelanism can affect fish, amphibians, reptiles, birds, and mammals including humans. The appearance of an amelanistic animal depends on the remaining non-melanin pigments. The opposite of amelanism is melanism, a higher percentage of melanin. A similar condition, albinism, is a hereditary condition characterised in animals by the absence of pigment in the eyes, skin, hair, scales, feathers or cuticle. This results in an all white animal, usually with pink or red eyes. Melanins and melanin production Melanin is a compound found in plants, animals, and protists, and is derived from the amino acid tyrosine. Melanin is a photoprotectant, absorbing the DNA-damaging ultraviolet radiation of the sun. Vertebrates have melanin in their skin and hair, feathers, or scales. They also have two layers of p ...
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