Investigating Fossils. Wilson J. Wall

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natural process of polymerisation takes place over several years, generally at high temperature and pressure. Just like the formation of all fossils, the process of converting resin into amber is one which is fraught with improbabilities. The original resin has to be resistant to mechanical and biological decay for quite long periods of time, which many plant resins are not, so that there is time for the polymerisation to take place. This will render the resin more resistant to decay or destruction, but does not instantly produce the finished product. These conditions are similar to those thought to be needed for creation of coal, so it is hardly surprising that amber can be found in coal seams.

      As one would expect of a product that originates from trees at a time of massive forestation, the distribution of amber is worldwide but heterogeneous in species origin. The majority of amber is generally regarded as being cretaceous or of a more recent in age, which at 142 million years ago, or less, corresponds with the proliferation of flowering plants. Since not all trees produce free resin, it is not so surprising that amber seems to be associated with specific botanical families, of which there are still extant living examples. This is even though the plant families of interest are both ancient and not necessarily flowering. The three family groups that seem to have produced most amber are:

       Araucariaceae, these include the monkey puzzle trees and the kauri trees of New Zealand. They are large evergreen trees which are now almost exclusively found in the wild in the southern hemisphere, but when they were one of the dominant tree species, they were worldwide in distribution. In parts of Turkey, fossilised wood from members of the Araucariaceae is carved and used in jewellery.

       Fabaceae, although most of these legumes are herbs and edible crops, there are some large trees in the family. There is a single tree species in east Africa from which copal is used as incense. They have a widely distributed fossil record, as flowers and pollen as well as leaves.

       Sciadopityaceae, there is only a single species left in this family, the Japanese Umbrella Pine. Although there are no close living relatives, this was a widespread clade with a fossil record extending back more than 200 million years.

      It should be emphasised that these are not the trees which originated amber, they are not ‘living fossils’, they are the current species of the lineage that produced most of the amber we know today. With amber being strictly plant in origin, it should not be a surprise that it is a frequent inclusion in some forms of coal, which were laid down from plant material at more or less the same period as amber was being formed.

      It is not just by the inclusion of animal material in amber that it is possible to preserve organisms in a near life‐like form without the mineralisation normally associated with fossilisation. Along with the inclusion of animal material in amber, there are also conditions in which large‐scale remains can be preserved for quite long periods of time. One of these which has yielded some quite startling finds is effectively pickling, in some cases with associated freezing. Although, as we shall see, this latter process can be good enough on its own to render stunning levels of preservation of details after death.

      The process of pickling involves an organism rapidly finding its way after death into anoxic conditions, as would be expected in a peat bog where the oxygen has been depleted by large‐scale organic decay, usually of plant material. This in itself would cause preservation, although it would depend on long‐term stability of anaerobic conditions to preserve organisms intact. In the composite system of preservation, if the remains move to the next step, which is freezing, then the entire animal may be kept in very good condition for as long as the climate permits it. This can been seen very clearly in mammoths removed from permafrost where very little decay has taken place over the millennia of entombment in deep frozen condition. This process of preservation by partial chemical treatment followed by freezing could take place almost anywhere that long‐term permafrost can be found.

      Completely submerging an organism in what is in effect a preservative is another way in which plant remains or animal corpses can survive for very long periods. One of the ways this can happen is found in tar pits. These are rare sites, but can be quite extensive, for example, Pitch Lake in Trinidad is the largest natural deposit of asphalt in the world, covering about 44 ha. Other such deposits include Binagadi asphalt lake in urban Baka, Azerbaijan, and the second largest lake, Lake Guanoco in Venezuela.

      Probably the most investigated and well known of all the asphalt deposits are the Tar Pits of La Brea in Los Angeles. This is the most well studied of the rare tar pits, and it is also unique in having been an asphalt mine during the nineteenth and early‐twentieth century. The position of the tar pits, in what is now an extensive suburban area of Los Angeles, has added to the development of interest in this particular site. The current pits are mostly man‐made, a leftover from asphalt mining

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