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There are two main types of fossils; body and trace. The absence of heat or compression which might destroy the fossil Fossils are most often preserved within sediments that were deposited in water, such as wetlands, river basins, or the ocean.Body fossils include the remains of organisms that were once living (bones, shells, teeth, eggs, etc), while trace fossils are the signs that organisms were once present (footprints, tracks, burrow, coprolites). Permineralization or Petrification - After an organism is buried, minerals carried by water such as silica, calcite or pyrite replace the organic material in the fossil.The atoms in some chemical elements have different forms, called isotopes.These isotopes break down at a very consistent rate over time through radioactive decay.Fossilization of an organism requires a unique set of circumstances so that it doesn’t just decay without a trace. Carbonization - Carbonization is a process in which the more volatile substances of the organism (hydrogen, oxygen, nitrogen, etc) are removed, leaving behind the carbon.These fossils typically appear as a thin, dark film on the rock.Potassium-40 on the other hand breaks down much slower and is common in rocks and minerals.

The convention is that a fossil must predate recorded human history.

Very rare, and typically found in very recent fossils.

Some examples include freezing (woolly mammoths in the permafrost), mummification, fossilization in amber.

There are two main types of dating: Relative Dating The majority of the time fossils are dated using relative dating techniques.

Using relative dating the fossil is compared to something for which the age is already known.

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By measuring the ratio of the amount of the original isotope to the amount of the isotopes that it breaks down into an age can be determined.

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  1. You will be amazed by their understanding of the differences between the two sexes, they clearly understand that such a harmonious relationship and what is the place in which a man and a woman.

  2. The luminescence of each sample is measured using industry-standard Luminescence Readers (manufactured by Risoe National Laboratories, Denmark) which incorporate 90Sr beta-sources, and 470nm LED optical stimulation.