Fossil

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Fossils (from Latin fossus, literally "having been dug up") are the mineralized or otherwise preserved remains or traces (such as footprints) of animals, plants, and other organisms. The totality of fossils, both discovered and undiscovered, and their placement in fossiliferous (fossil-containing) rock formations and sedimentary layers (strata) is known as the fossil record. The study of fossils across geological time, how they were formed, and the evolutionary relationships between taxa (phylogeny) are some of the most important functions of the science of paleontology.

Using radiometric dating techniques, geologists have determined most fossils to be several thousands to several billions of years old. Yet there is no minimum age for a fossil. Fossils vary in size from microscopic, such as single cells, to gigantic, such as dinosaurs. A fossil normally preserves only a portion of the deceased organism, usually that portion that was partially mineralized during life, such as the bones and teeth of vertebrates, or the chitinous exoskeletons of invertebrates. Preservation of soft tissues is exquisitely rare in the fossil record. Fossils may also consist of the marks left behind by the organism while it was alive, such as the footprint or feces of a reptile. These types of fossil are called trace fossils (or ichnofossils) as opposed to body fossils. Finally, past life leaves some markers that cannot be seen but can be detected in the form of biochemical signals; these are known as chemical fossils or biomarkers.

Contents 1 Places of exceptional fossilization 2 Earliest fossiliferous sites 3 Developments in interpretation of the fossil record 4 Rarity of fossils 5 Permineralization 6 Replacement and compression fossils 7 Trace fossils 8 Microfossils 9 Resin fossils 10 Pseudofossils 11 Living fossils 12 See also 13 References 14 External links

Places of exceptional fossilization

Fossil sites with exceptional preservation -- sometimes including preserved soft tissues -- are known as Lagerstätten. These formations may have resulted from carcass burial in an anoxic environment with minimal bacteria, thus delaying decomposition. Lagerstätten span geological time from the Cambrian period to the present. Worldwide, some of the best examples of near-perfect fossilization are the Cambrian Maotianshan shales and Burgess Shale, the Devonian Hunsrück Slates, the Jurassic Solnhofen limestone, and the Carboniferous Mazon Creek localities.

Paleobiologists have studied the frozen flesh of prehistoric mammoths, and the preserved muscle tissue of archosaurs.

Earliest fossiliferous sites

Earth’s oldest fossils are the stromatolites consisting of rock built from layer upon layer of sediment and precipitants.^[1] Based on studies of now-rare (but living) stromatolites (specifically, certain blue-green bacteria), the growth of fossil stromatolitic structures was biogenetically mediated by mats of microorganisms through their entrapment of sediments. However, abiotic mechanisms for stromatolitic growth are also known, leading to a decades-long and sometimes-contentious scientific debate regarding biogenesis of certain formations, especially those from the lower to middle Archaean eon.

It is more widely accepted that stromatolites from the late Archaean and through the middle Proterozoic eon were mostly formed by massive colonies of cyanobacteria (formerly known as blue-green "algae"), and that the oxygen byproduct of their photosynthetic metabolism first resulted in earth’s massive banded iron formations and subsequently oxygenated earth’s atmosphere.

Though rare, microstructures resembling cells are sometimes found within stromatolites; but these are also the source of scientific contention. The Gunflint Chert contains abundant microfossils widely accepted as a diverse consortium of 2.0 bya microbes.^[2]

In contrast, putative fossil cyanobacteria cells from the 3.4 bya Warrawoona Group in Western Australia are in dispute since abiotic processes cannot be ruled out.^[3] Confirmation of the Warrawoona microstructures as cyanobacteria would profoundly impact our understanding of when and how early life diversified, pushing important evolutionary milestones further back in time (reference). The continued study of these oldest fossils is paramount to calibrate complementary molecular phylogenetics models.

Developments in interpretation of the fossil record

See also: History of paleontology

Ever since recorded history began, and probably before, people have found fossils, pieces of rock and minerals which have replaced the remains of biologic organisms or preserved their external form. These fossils, and the totality of their occurrence within the sequence of Earth's rock strata is referred to as the fossil record.

The fossil record was one of the early sources of data relevant to the study of evolution and continues to be relevant to the history of life on Earth. Paleontologists examine the fossil record in order to understand the process of evolution and the way particular species have evolved. Various explanations have been put forth throughout history to explain what fossils are and how they came to be where they were found. Many of these explanations relied on folktales or mythologies. In China the fossil bones of ancient mammals including Homo erectus were often mistaken for “dragon bones” and used as medicine and aphrodisiacs. In the West the presence of fossilized sea creatures high up on mountainsides was seen as proof of the biblical deluge. More scientific views of fossils began to emerge during the Renaissance. For example, Leonardo Da Vinci noticed discrepancies with the use of the biblical flood narrative as an explanation for fossil origins:

"If the Deluge had carried the shells for distances of three and four hundred miles from the sea it would have carried them mixed with various other natural objects all heaped up together; but even at such distances from the sea we see the oysters all together and also the shellfish and the cuttlefish and all the other shells which congregate together, found all together dead; and the solitary shells are found apart from one another as we see them every day on the sea-shores.

And we find oysters together in very large families, among which some may be seen with their shells still joined together, indicating that they were left there by the sea and that they were still living when the strait of Gibraltar was cut through. In the mountains of Parma and Piacenza multitudes of shells and corals with holes may be seen still sticking to the rocks..."

William Smith (1769-1839), an English canal engineer, observed that rocks of different ages (based on the law of superposition) preserved different assemblages of fossils, and that these assemblages succeeded one another in a regular and determinable order. He observed that rocks from distant locations could be correlated based on the fossils they contained. He termed this the principle of faunal succession.

Smith, who preceded Charles Darwin, was unaware of biological evolution and did not know why faunal succession occurred. Biological evolution explains why faunal succession exists: as different organisms evolve, change and go extinct, they leave behind fossils. Faunal succession was one of the chief pieces of evidence cited by Darwin that biological evolution had occurred.

Early naturalists well understood the similarities and differences of living species leading Linnaeus to develop a hierarchical classification system still in use today. It was Darwin and his contemporaries who first linked the hierarchical structure of the great tree of life in living organisms with the then very sparse fossil record. Darwin eloquently described a process of descent with modification, or evolution, whereby organisms either adapt to natural and changing environmental pressures, or they perish.

When Charles Darwin wrote On the Origin of Species, the oldest animal fossils were those from the Cambrian Period, now known to be about 540 million years old. The absence of older fossils worried Darwin about the implications for the validity of his theories, but he expressed hope that such fossils would be found, noting that: "only a small portion of the world is known with accuracy." Darwin also pondered the sudden appearance of many groups (i.e. phyla) in the oldest known Cambrian fossiliferous strata^[4].

Since Darwin's time, the fossil record has been pushed back to 3.5 billion years before the present^[5]. Most of these Precambrian fossils are microscopic bacteria or microfossils. However, macroscopic fossils are now known from the late Proterozoic. The Ediacaran biota (also called Vendian biota) dating from 575 million years ago collectively constitutes a richly diverse assembly of early multicellular eukaryotes.

The fossil record and faunal succession form the basis of the science of biostratigraphy or determining the age of rocks based on the fossils they contain. For the first 150 years of geology, biostratigraphy and superposition were the only means for determining the relative age of rocks. The geologic time scale was developed based on the relative ages of rock strata as determined by the early paleontologists and stratigraphers.

Since the early years of the twentieth century, absolute dating methods, such as radiometric dating (including potassium/argon, argon/argon, uranium series, and carbon-14 dating) have been used to verify the relative ages obtained by fossils and to provide absolute ages for many fossils. Radiometric dating has shown that the earliest known fossils are over 3.5 billion years old. Various dating methods have been used and are used today depending on local geology and context, and while there is some variance in the results from these dating methods, nearly all of them provide evidence for a very old Earth, approximately 4.6 billion years.

“The fossil record is life’s evolutionary epic that unfolded over four billion years as environmental conditions and genetic potential interacted in accordance with natural selection.”^[6] The earth’s climate, tectonics, atmosphere, oceans, and periodic disasters invoked the primary selective pressures on all organisms, which they either adapted to, or they perished with or without leaving descendants. Modern paleontology has joined with evolutionary biology to share the interdisciplinary task of unfolding the tree of life, which inevitably leads backwards in time to the microscopic life of the Precambrian when cell structure and functions evolved. Earth’s deep time in the Proterozoic and deeper still in the Archaean is only “recounted by microscopic fossils and subtle chemical signals”^[7]. Molecular biologists, using phylogenetics, can compare protein amino acid or nucleotide sequence homology (i.e., similarity) to infer taxonomy and evolutionary distances among organisms, but with limited statistical confidence. The study of fossils, on the other hand, can more specifically pin point when and in what organism branching occurred in the tree of life. Modern phylogenetics and paleontology work together in the clarification of science’s still dim view of the appearance life and its evolution during deep time on earth^[8].

Niles Eldredge’s study of the Phacops trilobite genus supported the hypothesis that modifications to the arrangement of the trilobite’s eye lenses proceeded by fits and starts over millions of years during the Devonian^[9]. Eldredge's interpretation of the Phacops fossil record was that the aftermaths of the lens changes, but not the rapidly occurring evolutionary process, were fossilised. This and other data led Stephen Jay Gould and Niles Eldredge to publish the seminal paper on punctuated equilibrium in 1971.

An example of modern paleontological progress is the application of synchrotron X-ray tomographic techniques to early Cambrian bilaterian embryonic microfossils that has recently yielded new insights of metazoan evolution at its earliest stages. The tomography technique provides previously unattainable three-dimensional resolution at the limits of fossilization. Fossils of two enigmatic bilaterians, the worm-like Markuelia and a putative, primitive protostome, Pseudooides, provide a peek at germ layer embryonic development. These 543 Ma old embryos support the emergence of some aspects of arthropod development earlier than previously thought in the late Proterozoic. The preserved embryos from China and Siberia underwent rapid diagenetic phosphatization resulting in exquisite preservation, including cell structures. This research is a notable example of how knowledge encoded by the fossil record continues to contribute otherwise unattainable information on the emergence and development of life on Earth. For example, the research suggests Markuelia has closest affinity to priapulid worms, and is adjacent to the evolutionary branching of Priapulida, Nematoda and Arthropoda^[10].

Even with the wealth of information now known about fossils, some groups maintain non-scientific beliefs based on the earlier views of the fossil record.

Rarity of fossils

Fossilization is actually a rare occurrence because most components of formerly-living things tend to decompose relatively quickly following death. In order for an organism to be fossilized, the remains normally need to be covered by sediment as soon as possible. However there are exceptions to this, such as if an organism becomes frozen, desiccated, or comes to rest in an anoxic (oxygen-free) environment such as at the bottom of a lake. There are several different types of fossils and fossilization processes.

Due to the combined effect of taphonomic processes and simple mathematical chance, fossilization tends to favor organisms with hard body parts, those that were widespread, and those that lived for a long time. On the other hand, it is very unusual to find fossils of small, soft bodied, geographically restricted and geologically ephemeral organisms, because of their relative rarity and low likelihood of preservation.

Larger specimens (macrofossils) are more often observed, dug up and displayed, although microscopic remains (microfossils) are actually far more common in the fossil record.

Some casual observers have been perplexed by the rarity of transitional species within the fossil record. The conventional explanation for this rarity was given by Darwin, who stated that "the extreme imperfection of the geological record," combined with the short duration and narrow geographical range of transitional species, made it unlikely that many such fossils would be found. Simply put, the conditions under which fossilization takes place are quite rare; and it is highly unlikely that any given organism will leave behind a fossil. Eldredge and Gould developed their theory of punctuated equilibrium in part to explain the pattern of stasis and sudden appearance in the fossil record.

Permineralization

Permineralization occurs after burial, as the empty spaces within an organism (spaces filled with liquid or gas during life) become filled with mineral-rich groundwater and the minerals precipitate from the groundwater, thus occupying the empty spaces. This process can occur in very small spaces, such as within the cell wall of a plant cell. Small scale permineralization can produce very detailed fossils. For permineralization to occur, the organism must become covered by sediment soon after death or soon after the initial decaying process. The degree to which the remains are decayed when covered determines the later details of the fossil. Some fossils consist only of skeletal remains or teeth; other fossils contain traces of skin, feathers or even soft tissues. This is a form of diagenesis.

Replacement and compression fossils

In some cases the original remains of the organism have been completely dissolved or otherwise destroyed. When all that is left is an organism-shaped hole in the rock, it is called a mould fossil or typolite. If this hole is later filled with other minerals, it is called a cast fossil and is considered a replacement fossil since the original materials have been completely replaced by new, unrelated ones. In some cases replacement occurs so gradually and at such fine scales that no "hole" in the rock can ever be discerned and microstructural features are preserved despite the total loss of original material.

Compression fossils such as those of fossil ferns are the result of chemical reduction of the complex organic molecules composing the organism's tissues. In this case the fossil consists of original material, albeit in a geochemically altered state. This chemical change is an expression of diagenesis.

To sum up, fossilization processes proceed differently for different kinds of tissues and under different kinds of conditions.

Trace fossils

Main article: Trace fossil

Trace fossils are the remains of trackways, burrows, footprints, eggs and eggshells, nests, droppings and other types of impressions. Fossilized droppings, called coprolites, can give insight into the feeding behavior of animals and can therefore be of great importance.

Microfossils

Main article: Micropaleontology

'Microfossil' is a descriptive term applied to fossilized plants and animals whose size is just at or below the level at which the fossil can be analyzed by the naked eye. A commonly applied cut-off point between "micro" and "macro" fossils is 1 mm, although this is only an approximate guide. Microfossils may either be complete (or near-complete) organisms in themselves (such as the marine plankters foraminifera and coccolithophores) or component parts (such as small teeth or spores) of larger animals or plants. Microfossils are of critical importance as a reservoir of paleoclimate information, and are also commonly used by biostratigraphers to assist in the correlation of rock units.

Resin fossils

Fossil resin (colloquially called amber) is a natural polymer found in many types of strata throughout the world, even the Arctic. The oldest fossil resin dates to the Triassic, though most dates to the Tertiary. The excretion of the resin by certain plants is thought to be an evolutionary adaptation for protection from insects and to seal wounds caused by damage elements. Fossil resin often contains other fossils called inclusions that were captured by the sticky resin. These include bacteria, fungi, other plants, and animals. Animal inclusions are usually small invertebrates, predominantly arthropods such as insects and spiders, and only extremely rarely a vertebrate such as a small lizard. Preservation of inclusions can be exquisite, including small fragments of DNA.

Pseudofossils

Pseudofossils are visual patterns in rocks that are produced by naturally occurring geologic processes rather than biologic processes. They can easily be mistaken for real fossils. Some pseudofossils, such as dendrites, are formed by naturally occurring fissures in the rock that get filled up by percolating minerals. Other types of pseudofossils are kidney ore (round shapes in iron ore) and moss agates, which look like moss or plant leaves. Concretions, round or oval-shaped nodules found in some sedimentary strata, were once thought to be dinosaur eggs, and are often mistaken for fossils as well.

Living fossils

Main article: Living fossil

Living fossil is a term used for any living species which closely resembles a species known from fossils, i.e., as if the fossil had "come to life". This can be a species known only from fossils until living representatives were discovered, such as the coelacanth and the ginkgo tree, or a single living species with no close relatives, or a small group of closely related species with no other close relatives, such as the horseshoe crabs or the nautilus, that are the sole survivors of a once large and widespread group in the fossil record.

See also

• Fossils and the geological timescale
• Fossil collecting
• Fossil Hunters
• List of transitional fossils
• List of notable fossils
• List of fossil sites (with link directory)
• Fossil fuels
• Prehistoric life
• Lazarus taxon
• Elvis taxon
• Paleobiology
• History of paleontology

References

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