Budgerigar Colour Genetics
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Budgerigar Colour Genetics
The science of budgerigar color genetics deals with the heredity of mutations which cause color variation in the feathers of the species known scientifically as ''Melopsittacus undulatus''. Birds of this species are commonly known by the terms 'budgerigar', or informally just 'budgie'. Background The wildtype (natural-coloured or wild occurring) budgerigar's color is called Lightgreen. The feathers of most parrot species, including budgerigars, contain both a black type of ''melanin'' named ''eumelanin'' along with a basic yellow pigment named psittacofulvin (psittacin for short). Some other parrot species produces a third pigment named advanced-psittacin which enables color & tones ranging from oranges, peaches, pinks to reds. When these feathers are exposed to a white light source, such as sunlight, only the blue part of the spectrum is reflected by the eumelanin granules. This reflected blue light passes through the yellow pigment layer, resulting in the green colouration kno ...
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Melopsittacus Undulatus Revivim 4
The budgerigar ( ; ''Melopsittacus undulatus''), also known as the common parakeet or shell parakeet, is a small, long-tailed, seed-eating parrot usually nicknamed the budgie ( ), or in American English, the parakeet. Budgies are the only species in the genus ''Melopsittacus''. Naturally, the species is green and yellow with black, scalloped markings on the nape, back, and wings. Budgies are bred in captivity with colouring of blues, whites, yellows, greys, and even with small crests. Juveniles and chicks are monomorphic, while adults are told apart by their cere colouring, and their behaviour. The species is the only member of the genus ''Melopsittacus'', which is the only genus in the Melopsittacini tribe. The origin of the budgerigar's name is unclear. First recorded in 1805, budgerigars are popular pets around the world due to their small size, low cost, and ability to mimic human speech. They are likely the third most popular pet in the world, after the domesticated d ...
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Opaline Budgerigar Mutation
The Opaline budgerigar mutation is one of approximately 30 mutations affecting the colour or appearance of budgerigars. It is the underlying mutation of the Opaline variety. When combined with the Yellowface II and Clearwing mutations the Rainbow variety is produced. Appearance The Opaline mutation is characterised by several features which are invariably present, although many show variations in the intensity of their expression. The most obvious effect is on the striations which extend from the top of the head down the neck to between the wings in the non-Opaline. In the Opaline these striations are very much reduced in intensity, being almost absent in many individuals, particularly in small birds of yellow (as opposed to buff) feather. The cap of the Opaline extends further back over the top of the head, gradually merging into an area the same colour as the body which continues down the back of the head to form a 'V' shape between the wings. The intensity of the striat ...
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Yellowface I Budgerigar Mutation
The Yellowface I budgerigar mutation is one of approximately 30 mutations affecting the colour of budgerigars. Appearance The Yellowface I Skyblue variety is the same in appearance as a normal Skyblue except that the forehead and mask, which is white in the normal Skyblue, is replaced by bright yellow, the short tail feathers show yellow instead of the normal white, and the undulations on the wings are often faint yellow. The yellow on the mask tends to leak down onto the breast to a small degree, giving it a green tinge. In juvenile plumage the yellow is considerably fainter and does not appear on the forehead, which is barred in the usual way, nor does it leak onto the breast to as great an extent. The Yellowface I Cobalt and Yellowface I Mauve varieties have similar yellow markings. The appearance of birds with other combinations of the Yellowface I mutation is discussed under Genetics below. Historical notes In the UK, a yellowfaced bird was first produced in 1934–193 ...
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Locus (genetics)
In genetics, a locus (plural loci) is a specific, fixed position on a chromosome where a particular gene or genetic marker is located. Each chromosome carries many genes, with each gene occupying a different position or locus; in humans, the total number of protein-coding genes in a complete haploid set of 23 chromosomes is estimated at 19,000–20,000. Genes may possess multiple variants known as alleles, and an allele may also be said to reside at a particular locus. Diploid and polyploid cells whose chromosomes have the same allele at a given locus are called homozygous with respect to that locus, while those that have different alleles at a given locus are called heterozygous. The ordered list of loci known for a particular genome is called a gene map. Gene mapping is the process of determining the specific locus or loci responsible for producing a particular phenotype or biological trait. Association mapping, also known as "linkage disequilibrium mapping", is a method of ma ...
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Autosomal
An autosome is any chromosome that is not a sex chromosome. The members of an autosome pair in a diploid cell have the same morphology, unlike those in allosome, allosomal (sex chromosome) pairs, which may have different structures. The DNA in autosomes is collectively known as atDNA or auDNA. For example, humans have a diploid human genome, genome that usually contains 22 pairs of autosomes and one allosome pair (46 chromosomes total). The autosome pairs are labeled with numbers (1–22 in humans) roughly in order of their sizes in base pairs, while allosomes are labelled with their letters. By contrast, the allosome pair consists of two X chromosomes in females or one X and one Y chromosome in males. Unusual combinations of XYY syndrome, XYY, Klinefelter syndrome, XXY, Triple X syndrome, XXX, XXXX syndrome, XXXX, XXXXX syndrome, XXXXX or XXYY syndrome, XXYY, among Aneuploidy, other Salome combinations, are known to occur and usually cause developmental abnormalities. Autosomes ...
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Dominance Relationship
In genetics, dominance is the phenomenon of one variant (allele) of a gene on a chromosome masking or overriding the effect of a different variant of the same gene on the other copy of the chromosome. The first variant is termed dominant and the second recessive. This state of having two different variants of the same gene on each chromosome is originally caused by a mutation in one of the genes, either new (''de novo'') or inherited. The terms autosomal dominant or autosomal recessive are used to describe gene variants on non-sex chromosomes ( autosomes) and their associated traits, while those on sex chromosomes (allosomes) are termed X-linked dominant, X-linked recessive or Y-linked; these have an inheritance and presentation pattern that depends on the sex of both the parent and the child (see Sex linkage). Since there is only one copy of the Y chromosome, Y-linked traits cannot be dominant or recessive. Additionally, there are other forms of dominance such as incomplete d ...
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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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Dilution Gene
A dilution gene is any one of a number of genes that act to create a lighter coat color in living creatures. There are many examples of such genes: General Diluted coat colors have melanocytes, but vary from darker colors due to the concentration or type of these pigment-producing cells, not their absence. Pigment dilution, sometimes referred to as hypomelanism, has been called leucism, albinism (perfect, impartial, or dilute), ghosting, paling, and isabellinism. *Albinism describes a condition where pigment cells synthesize little or no pigment *Leucism describes a condition that creates loss of pigment cells Cats *Cat coat genetics discusses many dilution genes in cats Dogs In dogs, a mutation of the MLPH locus known as the dilute gene causes eumelanin to lighten while pheomelanin remains almost unchanged. Dogs of some breeds with the dilute gene often suffer from Colour dilution alopecia (CDA). Appearance Of the colour shades found in the coat of dogs, the light brown cau ...
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Albinism
Albinism is the congenital absence of melanin in an animal or plant resulting in white hair, feathers, scales and skin and pink or blue eyes. Individuals with the condition are referred to as albino. Varied use and interpretation of the terms mean that written reports of albinistic animals can be difficult to verify. Albinism can reduce the survivability of an animal; for example, it has been suggested that albino alligators have an average survival span of only 24 hours due to the lack of protection from UV radiation and their lack of camouflage to avoid predators. It is a common misconception that all albino animals have characteristic pink or red eyes (resulting from the lack of pigment in the iris allowing the blood vessels of the retina to be visible), however this is not the case for some forms of albinism. Familiar albino animals include in-bred strains of laboratory animals (rats, mice and rabbits), but populations of naturally occurring albino animals exist in the wil ...
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White Domesticated Budgerigar
White is the lightest color and is achromatic (having no hue). It is the color of objects such as snow, chalk, and milk, and is the opposite of black. White objects fully reflect and scatter all the visible wavelengths of light. White on television and computer screens is created by a mixture of red, blue, and green light. The color white can be given with white pigments, especially titanium dioxide. In ancient Egypt and ancient Rome, priestesses wore white as a symbol of purity, and Romans wore white togas as symbols of citizenship. In the Middle Ages and Renaissance a white unicorn symbolized chastity, and a white lamb sacrifice and purity. It was the royal color of the kings of France, and of the monarchist movement that opposed the Bolsheviks during the Russian Civil War (1917–1922). Greek and Roman temples were faced with white marble, and beginning in the 18th century, with the advent of neoclassical architecture, white became the most common color of new churches ...
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Genes
In biology, the word gene (from , ; "...Wilhelm Johannsen coined the word gene to describe the Mendelian units of heredity..." meaning ''generation'' or ''birth'' or ''gender'') can have several different meanings. The Mendelian gene is a basic unit of heredity and the molecular gene is a sequence of nucleotides in DNA that is transcribed to produce a functional RNA. There are two types of molecular genes: protein-coding genes and noncoding genes. During gene expression, the DNA is first copied into RNA. The RNA can be directly functional or be the intermediate template for a protein that performs a function. The transmission of genes to an organism's offspring is the basis of the inheritance of phenotypic traits. These genes make up different DNA sequences called genotypes. Genotypes along with environmental and developmental factors determine what the phenotypes will be. Most biological traits are under the influence of polygenes (many different genes) as well as gen ...
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