Slate Budgerigar Mutation
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Slate Budgerigar Mutation
The Slate budgerigar mutation is one of approximately 30 mutations affecting the colour of budgerigars. It is the underlying mutation of the Slate variety. Appearance The name 'Slate' is derived from the appearance of blue-series Slates, particularly the Skyblue Slate, which is close in colour to a Light Grey but with a more bluish tone. The Light Green Slate is intermediate in shade between a Light Green and a Light Grey-Green. In both blue- and green-series Slates the cheek patch is purplish-grey or deep violet, somewhat like the cheek patches of Mauves. The long tail feathers are a little darker than the corresponding non-Slate. Other features are unaffected by this mutation. The Dark mutation produces a more noticeable effect in combination with Slate than it does with Grey, but these darker Slate shades differ from one another very much less than Skyblue, Cobalt and Mauve differ.Taylor, T G and Warner, C (1986) p 43-44 The Cobalt Slate and Mauve Slate are distinctly da ...
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Slate Color Mutation Budgerigar
Slate is a fine-grained, foliation (geology), foliated, homogeneous metamorphic rock derived from an original shale-type sedimentary rock composed of clay or volcano, volcanic ash (volcanic), ash through low-grade regional metamorphism. It is the finest grained foliated metamorphic rock. Foliation may not correspond to the original sedimentary layering, but instead is in planes perpendicular to the direction of metamorphic compression. The foliation in slate is called "slaty cleavage". It is caused by strong compression causing fine grained clay flakes to regrow in planes perpendicular to the compression. When expertly "cut" by striking parallel to the foliation, with a specialized tool in the quarry, many slates will display a property called fissility (geology), fissility, forming smooth flat sheets of stone which have long been used for roofing, floor tiles, and other purposes. Slate is frequently grey in color, especially when seen, en masse, covering roofs. However, slate o ...
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Gene
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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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 stria ...
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Ino Budgerigar Mutation
The Ino budgerigar mutation is one of approximately 30 mutations affecting the colour of budgerigars. It is the underlying mutation of the Albino and Lutino varieties and, with Cinnamon budgerigar mutation, Cinnamon, a constituent mutation of the Lacewing variety. Appearance In the green series the Ino is known as the Lutino, with pure yellow contour feathers, white or pale yellow flight feathers and tail feathers and silvery-white cheek patches. In some lights the body can show a very pale green sheen.Watmough, W (1951) p48 In the blue series the Ino is known as the Albino, and is pure white throughout. The cheek patches are almost the same colour as the body, but slightly more silvery. In some lights the body can show a very pale blue sheen. The eyes of both the Lutino and Albino are red at all ages with white Iris (anatomy), irides when adult, the beak is orange and the feet and legs are pink. The cere of an adult Ino cock is greyish-purple rather than blue. The Worl ...
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Cinnamon Budgerigar Mutation
The Cinnamon Budgerigar Mutation is one of approximately 30 mutations affecting the colour of budgerigars. It is the underlying mutation of the Cinnamon variety and, with Ino, a constituent mutation of the Lacewing variety. Appearance All the markings which appear black or dark grey in the corresponding Normal appear brown in the Cinnamon, of a shade similar to that of white coffee. The Cinnamon markings on cocks tend to be considerably darker than on hens.Taylor, TG; Warner, C (1986), p 13 The long tail feathers are lighter than Normals. The body colour and cheek patches are much paler, being about half the depth of colour of the Normal. The feathers of Cinnamons appear tighter than Normals, giving a silky appearance.Watmough, W (1951), p45 It is these quiet pastel shades and the sleekness of the plumage that give the variety its appeal. The eyes of the newly hatched Cinnamon are not black like the eyes of Normals, but deep plum-coloured. This colour can be seen thr ...
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Genetic Linkage
Genetic linkage is the tendency of DNA sequences that are close together on a chromosome to be inherited together during the meiosis phase of sexual reproduction. Two genetic markers that are physically near to each other are unlikely to be separated onto different chromatids during chromosomal crossover, and are therefore said to be more ''linked'' than markers that are far apart. In other words, the nearer two genes are on a chromosome, the lower the chance of recombination between them, and the more likely they are to be inherited together. Markers on different chromosomes are perfectly ''unlinked'', although the penetrance of potentially deleterious alleles may be influenced by the presence of other alleles, and these other alleles may be located on other chromosomes than that on which a particular potentially deleterious allele is located. Genetic linkage is the most prominent exception to Gregor Mendel's Law of Independent Assortment. The first experiment to demonstrate li ...
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Heterozygous
Zygosity (the noun, zygote, is from the Greek "yoked," from "yoke") () is the degree to which both copies of a chromosome or gene have the same genetic sequence. In other words, it is the degree of similarity of the alleles in an organism. Most eukaryotes have two matching sets of chromosomes; that is, they are diploid. Diploid organisms have the same loci on each of their two sets of homologous chromosomes except that the sequences at these loci may differ between the two chromosomes in a matching pair and that a few chromosomes may be mismatched as part of a chromosomal sex-determination system. If both alleles of a diploid organism are the same, the organism is homozygous at that locus. If they are different, the organism is heterozygous at that locus. If one allele is missing, it is hemizygous, and, if both alleles are missing, it is nullizygous. The DNA sequence of a gene often varies from one individual to another. These gene variants are called alleles. While some gen ...
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Homozygous
Zygosity (the noun, zygote, is from the Greek "yoked," from "yoke") () is the degree to which both copies of a chromosome or gene have the same genetic sequence. In other words, it is the degree of similarity of the alleles in an organism. Most eukaryotes have two matching sets of chromosomes; that is, they are diploid. Diploid organisms have the same loci on each of their two sets of homologous chromosomes except that the sequences at these loci may differ between the two chromosomes in a matching pair and that a few chromosomes may be mismatched as part of a chromosomal sex-determination system. If both alleles of a diploid organism are the same, the organism is homozygous at that locus. If they are different, the organism is heterozygous at that locus. If one allele is missing, it is hemizygous, and, if both alleles are missing, it is nullizygous. The DNA sequence of a gene often varies from one individual to another. These gene variants are called alleles. While some gen ...
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Phenotype
In genetics, the phenotype () is the set of observable characteristics or traits of an organism. The term covers the organism's morphology or physical form and structure, its developmental processes, its biochemical and physiological properties, its behavior, and the products of behavior. An organism's phenotype results from two basic factors: the expression of an organism's genetic code, or its genotype, and the influence of environmental factors. Both factors may interact, further affecting phenotype. When two or more clearly different phenotypes exist in the same population of a species, the species is called polymorphic. A well-documented example of polymorphism is Labrador Retriever coloring; while the coat color depends on many genes, it is clearly seen in the environment as yellow, black, and brown. Richard Dawkins in 1978 and then again in his 1982 book ''The Extended Phenotype'' suggested that one can regard bird nests and other built structures such as cad ...
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Allele
An allele (, ; ; modern formation from Greek ἄλλος ''állos'', "other") is a variation of the same sequence of nucleotides at the same place on a long DNA molecule, as described in leading textbooks on genetics and evolution. ::"The chromosomal or genomic location of a gene or any other genetic element is called a locus (plural: loci) and alternative DNA sequences at a locus are called alleles." The simplest alleles are single nucleotide polymorphisms (SNP). but they can also be insertions and deletions of up to several thousand base pairs. Popular definitions of 'allele' typically refer only to different alleles within genes. For example, the ABO blood grouping is controlled by the ABO gene, which has six common alleles (variants). In population genetics, nearly every living human's phenotype for the ABO gene is some combination of just these six alleles. Most alleles observed result in little or no change in the function of the gene product it codes for. However, ...
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Wild-type
The wild type (WT) is the phenotype of the typical form of a species as it occurs in nature. Originally, the wild type was conceptualized as a product of the standard "normal" allele at a locus, in contrast to that produced by a non-standard, "mutant" allele. "Mutant" alleles can vary to a great extent, and even become the wild type if a genetic shift occurs within the population. Continued advancements in genetic mapping technologies have created a better understanding of how mutations occur and interact with other genes to alter phenotype. It is now appreciated that most or all gene loci exist in a variety of allelic forms, which vary in frequency throughout the geographic range of a species, and that a uniform wild type does not exist. In general, however, the most prevalent allele – i.e., the one with the highest gene frequency – is the one deemed wild type. The concept of wild type is useful in some experimental organisms such as fruit flies ''Drosophila melanogaster'' ...
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Recessive
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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