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Note: that under this latest enactment, the date letter is no longer a compulsory part of the hallmark. It is likely that an 'offshore' assay mark will have to be added to signify that the item was not assayed in the UK.
As it now stands, the compulsory part of the UK hallmark consists of the sponsor or maker's mark, the assay office mark, and the standard of fineness in this case silver, parts in These are shown in the top of the two example hallmarks.
The bottom example shows the extra marks that can also be struck, the lion passant, indicating Sterling silver, the date mark lowercase a for '' , and in this example, the 'Millennium mark', which was only available for the years and The bottom example bears the Yorkshire rose mark for the Sheffield Assay Office.
The Hallmarking Act was amended in July to include palladium from January Although hallmarking in the Swiss territories dates back to Geneva in the fifteenth century, there was no uniform system of hallmarking in Switzerland until Before that time, hallmarking was undertaken at the local level by the Swiss cantons.
With the introduction of Federal hallmarking laws starting in , increased uniformity was established. Under the current law, on all gold, silver, platinum or palladium watches cases made in Switzerland or imported into Switzerland, there shall be affixed,  near the Maker's Responsibility Mark and his indication of purity, the official Hallmark, the head of a Saint Bernard dog.
Only precious metal watch cases must be hallmarked. Swiss hallmarking for other articles such as jewelry and cutlery is optional. In addition to the Swiss hallmark, all precious metal goods may be stamped with the Common Control Mark of the Vienna Convention.
The Netherlands, who are members of the International hallmarking Convention, have been striking hallmarks since at least Like many other nations, the Netherlands require the registration and use of Responsibility Marks, however, perhaps somewhat unusual, there is a book published entitled "Netherlands' Responsibility Marks since " in three volumes and in the English language illustrating all the responsibility marks registered there since that time.
This is significant since producers that exported precious metal goods to the Netherlands would have been required to register their marks. The Netherlands' hallmarks are also recognized in Belgium, Denmark, Finland and Sweden, which have voluntary hallmarking systems.
One of the two Dutch assay offices, WaarborgHolland b. The other one is located in Joure, called Edelmetaal Waarborg Nederland b.
The Netherlands recognises platinum, gold, silver and palladium as precious metals. Traditionally, the hallmarks are "struck" using steel punches.
Punches are made in different sizes, suitable for tiny pieces of jewelry to large silver platters. Punches are made in straight shank or ring shank, the latter used to mark rings.
The problem with traditional punching is that the process of punching displaces metal, causing some distortion of the article being marked.
This means that re-finishing of the article is required after hallmarking. For this reason, and that off-cuts from sprues are often used for assay, many articles are sent unfinished to the assay office for assay and hallmarking.
A new method of marking using lasers is now available, which is especially valuable for delicate items and hollowware , which would be damaged or distorted by the punching process.
Laser marking also means that finished articles do not need to be re-finished. Laser marking works by using high-power lasers to evaporate material from the metal surface.
Two methods exist: 2D and 3D laser marking. Precious metal items of art or jewelry are frequently hallmarked depending upon the requirements of the laws of either the place of manufacture or the place of import.
Where required to be hallmarked, semi-finished precious metal items of art or jewelry pass through the official testing channels where they are analyzed or assayed for precious metal content.
While different nations permit a variety of legally acceptable finenesses, the assayer is actually testing to determine that the fineness of the product conforms with the statement or claim of fineness that the maker has claimed usually by stamping a number such as for 18k gold on the item.
In the past the assay was conducted by using the touchstone method but currently most often it is done using X-ray Fluorescence XRF. XRF is used because this method is more exacting than the touchstone test.
The most exact method of assay is known as fire assay or cupellation. This method is better suited for the assay of bullion and gold stocks rather than works or art or jewelry because it is a completely destructive method.
The age-old touchstone method is particularly suited to the testing of very valuable pieces, for which sampling by destructive means, such as scraping, cutting or drilling is unacceptable.
A rubbing of the item is made on a special stone, treated with acids and the resulting color compared to references. Differences in precious metal content as small as 10 to 20 parts per thousand can often be established with confidence by the test.
It is not indicated for use with white gold, for example, since the color variation among white gold alloys is almost imperceptible.
The modern X-ray fluorescence is also a non-destructive technique that is suitable for normal assaying requirements. It typically has an accuracy of 2—5 parts per thousand and is well-suited to the relatively flat and large surfaces.
It is a quick technique taking about three minutes, and the results can be automatically printed out by the computer.
It also measures the content of the other alloying metals present. It is not indicated, however, for articles with chemical surface treatment or electroplated metals.
The most elaborate, but totally destructive, assay method is the fire assay , or cupellation. As applied to gold bearing metallics, as in hallmark assaying, it is also known as cupellation and can have an accuracy of 1 part in 10, In this process the article is melted, the alloys separated and constituents weighed.
Since this method is totally destructive, when this method is employed for the assay of jewelry, it is done under the guise of random or selective sampling.
For example, if a single manufacturer deposits a lot of rings or watch cases, while most are assayed using the non-destructive methods a few pieces from the lot are randomly selected for fire assay.
There are methods of assay noted above which are more properly suited for finished goods while other methods are suitable for use on raw materials before artistic workmanship has begun.
Raw precious metals bullion or metal stock are assayed by the following methods: silver is assayed by titration , gold is assayed by cupellation and platinum is assayed by ICP OES spectrometry.
From Wikipedia, the free encyclopedia. Redirected from Hallmarks. For other uses, see Hallmark disambiguation. For the meanings of gold standard hallmarks, see Carat purity.
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December Learn how and when to remove this template message. The assay office marks — from left to right, the leopard 's head of London , the anchor of Birmingham , the Yorkshire rose of Sheffield , and the castle of Edinburgh.
The assay office marks are no longer an indicator that an item was assayed in the city, or in the UK. Examples of British hallmarks for silver.
Nelson-Atkins Museum of Art. Cites: Dodd, Erica Cruikshank Byzantine Silver Stamps. Dumbarton Oaks Studies.
Kent excursus on the comes sacrarum largitionum. Compare : Dubler, Anne-Marie 27 November They include sustaining proliferative signaling, evading growth suppressors, resisting cell death, enabling replicative immortality, inducing angiogenesis, and activating invasion and metastasis.
Underlying these hallmarks are genome instability, which generates the genetic diversity that expedites their acquisition, and inflammation, which fosters multiple hallmark functions.
Conceptual progress in the last decade has added two emerging hallmarks of potential generality to this list—reprogramming of energy metabolism and evading immune destruction.
By November , the paper had been referenced over 15, times by other research papers, and was downloaded 20, times a year between and In an update published in "Hallmarks of cancer: the next generation" , Weinberg and Hanahan proposed two new hallmarks: 1 abnormal metabolic pathways and 2 evading the immune system, and two enabling characteristics: 1 genome instability, and 2 inflammation.
Cancer cells have defects in the control mechanisms that govern how often they divide, and in the feedback systems that regulate these control mechanisms i.
Normal cells grow and divide, but have many controls on that growth. They only grow when stimulated by growth factors. If they are damaged, a molecular brake stops them from dividing until they are repaired.
If they can't be repaired, they commit programmed cell death apoptosis. They can only divide a limited number of times. They are part of a tissue structure, and remain where they belong.
They need a blood supply to grow. All these mechanisms must be overcome in order for a cell to develop into a cancer. Each mechanism is controlled by several proteins.
A critical protein must malfunction in each of those mechanisms. These proteins become non-functional or malfunctioning when the DNA sequence of their genes is damaged through acquired or somatic mutations mutations that are not inherited but occur after conception.
This occurs in a series of steps, which Hanahan and Weinberg refer to as hallmarks. Typically, cells of the body require hormones and other molecules that act as signals for them to grow and divide.
Cancer cells, however, have the ability to grow without these external signals. There are multiple ways in which cancer cells can do this: by producing these signals themselves, known as autocrine signalling ; by permanently activating the signalling pathways that respond to these signals; or by destroying 'off switches' that prevents excessive growth from these signals negative feedback.
In addition, cell division in normal, non-cancerous cells is tightly controlled. In cancer cells, these processes are deregulated because the proteins that control them are altered, leading to increased growth and cell division within the tumor.
To tightly control cell division, cells have processes within them that prevent cell growth and division.
These processes are orchestrated by proteins known as tumor suppressor genes. These genes take information from the cell to ensure that it is ready to divide, and will halt division if not when the DNA is damaged , for example.
In cancer, these tumour suppressor proteins are altered so that they don't effectively prevent cell division, even when the cell has severe abnormalities.
Another way cells prevent over-division is that normal cells will also stop dividing when the cells fill up the space they are in and touch other cells; known as contact inhibition.
Cancer cells do not have contact inhibition, and so will continue to grow and divide, regardless of their surroundings. Cells have the ability to 'self-destruct'; a process known as apoptosis.
This is required for organisms to grow and develop properly, for maintaining tissues of the body, and is also initiated when a cell is damaged or infected.
Cancer cells, however, lose this ability; even though cells may become grossly abnormal, they do not undergo apoptosis.
The cancer cells may do this by altering the mechanisms that detect the damage or abnormalities. This means that proper signaling cannot occur, thus apoptosis cannot activate.
They may also have defects in the downstream signaling itself, or the proteins involved in apoptosis, each of which will also prevent proper apoptosis.
Cells of the body don't normally have the ability to divide indefinitely. They have a limited number of divisions before the cells become unable to divide senescence , or die crisis.
The cause of these barriers is primarily due to the DNA at the end of chromosomes, known as telomeres.
Telomeric DNA shortens with every cell division, until it becomes so short it activates senescence, so the cell stops dividing.
Cancer cells bypass this barrier by manipulating enzymes telomerase to increase the length of telomeres. Thus, they can divide indefinitely, without initiating senescence.
Mammalian cells have an intrinsic program, the Hayflick limit , that limits their multiplication to about 60—70 doublings, at which point they reach a stage of senescence.
Most tumor cells are immortalized. The counting device for cell doublings is the telomere, which decreases in size loses nucleotides at the ends of chromosomes during each cell cycle.
Normal tissues of the body have blood vessels running through them that deliver oxygen from the lungs.
Cells must be close to the blood vessels to get enough oxygen for them to survive. New blood vessels are formed during the development of embryos, during wound repair and during the female reproductive cycle.
An expanding tumour requires new blood vessels to deliver adequate oxygen to the cancer cells, and thus exploits these normal physiological processes for its benefit.
To do this, the cancer cells acquire the ability to orchestrate production of new vasculature by activating the 'angiogenic switch'. In doing so, they control non-cancerous cells that are present in the tumor that can form blood vessels by reducing the production of factors that inhibit blood vessel production, and increasing the production of factors that promote blood vessel formation.
One of the most well known properties of cancer cells is their ability to invade neighboring tissues. It is what dictates whether the tumor is benign or malignant, and is the property which enables their dissemination around the body.