A microfossil is a fossil that is generally between one micrometre and one millimetre in size, the visual study of which requires the use of light or electron microscopy. A fossil which can be studied with the naked eye or low-powered magnification, such as a hand lens, is referred to as a macrofossil.
Microfossils are a common feature of the geological record, from the Precambrian to the Holocene. They are most common in deposits of marine environments, but also occur in brackish water, fresh water and terrestrial sedimentary deposits. While every kingdom of life is represented in the microfossil record, the most abundant forms are protist skeletons or microbial cysts from the Chrysophyta, Pyrrhophyta, Sarcodina, acritarchs and chitinozoans, together with pollen and spores from the vascular plants.
Overview
A 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 cutoff point between "micro" and "macro" fossils is 1 mm. 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.
Microfossils are found in rocks and sediments as the microscopic remains of what were once life forms such as plants, animals, fungus, protists, bacteria and archaea. Terrestrial microfossils include pollen and spores. Marine microfossils found in marine sediments are the most common microfossils. Everywhere in the oceans, microscopic protist organisms multiply prolifically, and many grow tiny skeletons which readily fossilise. These include foraminifera, dinoflagellates and radiolarians. Palaeontologists (geologists who study fossils) are interested in these microfossils because they can use them to determine how environments and climates have changed in the past, and where oil and gas can be found today.Campbell, Hamish (12 Jun 2006) "Fossils - Microfossils", Te Ara - the Encyclopedia of New Zealand. Accessed 11 May 2021.
Some microfossils are formed by colonial organisms such as Bryozoa (especially the Cheilostomata), which have relatively large colonies but are classified by fine skeletal details of the small individuals of the colony. As another example, many fossil genera of Foraminifera, which are protists are known from shells (called tests) that were as big as coins, such as the genus Nummulites.
In 2017, fossilized microorganisms, or microfossils, were discovered in hydrothermal vent precipitates in the Nuvvuagittuq Belt of Quebec, Canada that may be as old as 4.28 billion years old, the oldest record of life on Earth, suggesting "an almost instantaneous emergence of life" (in a geological time-scale), after ocean formation 4.41 billion years ago, and not long after the formation of the Earth 4.54 billion years ago. Nonetheless, life may have started even earlier, at nearly 4.5 billion years ago, as claimed by some researchers.
Index fossils
Index fossils, also known as guide fossils, indicator fossils or dating fossils, are the fossilized remains or traces of particular plants or animals that are characteristic of a particular span of geologic time or environment, and can be used to identify and date the containing rocks. To be practical, index fossils must have a limited vertical time range, wide geographic distribution, and rapid evolutionary trends. Rock formations separated by great distances but containing the same index fossil species are thereby known to have both formed during the limited time that the species lived.
Index fossils were originally used to define and identify geologic units, then became a basis for defining geologic periods, and then for faunal stages and zones.
Species of microfossils such as acritarchs, chitinozoans, conodonts, dinoflagellate cysts, ostracods, pollen, spores and foraminiferans are amongst the many species have been identified as index fossils that are widely used in biostratigraphy. Different fossils work well for sediments of different ages. To work well, the fossils used must be widespread geographically, so that they can be found in many different places. They must also be short lived as a species, so that the period of time during which they could be incorporated in the sediment is relatively narrow. The longer lived the species, the poorer the stratigraphic precision, so fossils that evolve rapidly.
Often biostratigraphic correlations are based on a faunal assemblage, rather than an individual species — this allows greater precision as the time span in which all of the species in the assemblage existed together is narrower than the time spans of any of the members. Further, if only one species is present in a sample, it can mean either that (1) the strata were formed in the known fossil range of that organism; or (2) that the fossil range of the organism was incompletely known, and the strata extend the known fossil range. If the fossil is easy to preserve and easy to identify, more precise time estimating of the stratigraphic layers is possible.
Composition
Microfossils can be classified by their composition as: (a) siliceous, as in diatoms and radiolaria, (b) calcareous, as in coccoliths and foraminifera, (c) phosphatic, as in the study of some vertebrates, or (d) organic, as in the pollen and spores studied in palynology. This division focuses on differences in the mineralogical and chemical composition of microfossil remains rather than on taxonomic or ecological distinctions.
Siliceous microfossils: Siliceous microfossils include diatoms, radiolarians, silicoflagellates, ebridians, phytoliths, some scolecodonts (worm jaws), and sponge spicules. Calcareous microfossils: Calcareous (CaCO3) microfossils include coccoliths, foraminifera, calcareous dinoflagellate cysts, and ostracods (seed shrimp). Phosphatic microfossils: Phosphatic microfossils include conodonts (tiny oral structures of an extinct chordate group), some scolecodonts (worm jaws), shark spines and teeth and other fish remains (collectively called ichthyoliths). Organic microfossils: The study of organic microfossils is called palynology. Organic microfossils include pollen, spores, chitinozoans (thought to be the egg cases of marine invertebrates), scolecodonts (worm jaws), acritarchs, dinoflagellate cysts, and fungal remains.
Organic-walled
Palynomorphs
Pollen grain
Pollen has an outer sheath, called a sporopollenin, which affords it some resistance to the rigours of the fossilisation process that destroy weaker objects. It is produced in huge quantities. There is an extensive fossil record of pollen grains, often disassociated from their parent plant. The discipline of palynology is devoted to the study of pollen, which can be used both for biostratigraphy and to gain information about the abundance and variety of plants alive — which can itself yield important information about paleoclimates. Also, pollen analysis has been widely used for reconstructing past changes in vegetation and their associated drivers. Pollen is first found in the fossil record in the late Devonian period, but at that time it is indistinguishable from spores. It increases in abundance until the present day.
Plant spores
A spore is a unit of sexual or asexual reproduction that may be adapted for dispersal and for survival, often for extended periods of time, in unfavourable conditions. Spores form part of the life cycles of many plants, algae, fungi and protozoa. Bacterial spores are not part of a sexual cycle but are resistant structures used for survival under unfavourable conditions.
Fungal spores
Chitinozoa
Chitinozoa are a taxon of flask-shaped, organic walled marine microfossils produced by an as-yet-unknown organism.
Common from the Ordovician to Devonian periods (i.e. the mid-Paleozoic), the millimetre-scale organisms are abundant in almost all types of marine sediment across the globe. This wide distribution, and their rapid pace of evolution, makes them valuable biostratigraphic markers.
Their bizarre form has made classification and ecological reconstruction difficult. Since their discovery in 1931, suggestions of protist, plant, and fungal affinities have all been entertained. The organisms have been better understood as improvements in microscopy facilitated the study of their fine structure, and it has been suggested that they represent either the eggs or juvenile stage of a marine animal. However, recent research has suggested that they represent the test of a group of protists with uncertain affinities.
The ecology of chitinozoa is also open to speculation; some may have floated in the water column, where others may have attached themselves to other organisms. Most species were particular about their living conditions, and tend to be most common in specific paleoenvironments. Their abundance also varied with the seasons.
Acritarchs
Acritarchs, Greek for confused origins,definition of acritarch at dictionary.com are organic-walled microfossils, known from about to the present. Acritarchs are not a specific biological taxon, but rather a group with uncertain or unknown affinities. Most commonly they are composed of thermally altered acid insoluble carbon compounds (kerogen). While the classification of acritarchs into form genera is entirely artificial, it is not without merit, as the form taxa show traits similar to those of genuine taxa — for example the 'explosion' in the Cambrian and the mass extinction at the end of the Permian.
Acritarch diversity reflects major ecological events such as the appearance of predation and the Cambrian explosion. Precambrian marine diversity was dominated by acritarchs. They underwent a boom around , increasing in abundance, diversity, size, complexity of shape, and especially size and number of spines. Their increasingly spiny forms in the last 1 billion years may indicate an increased need for defence against predation.
Acritarchs may include the remains of a wide range of quite different kinds of organisms—ranging from the egg cases of small metazoans to resting cysts of many kinds of chlorophyta (green algae). It is likely that most acritarch species from the Paleozoic represent various stages of the life cycle of algae that were ancestral to the dinoflagellates. The nature of the organisms associated with older acritarchs is generally not well understood, though many are probably related to unicellular marine algae. In theory, when the biological source (taxon) of an acritarch does become known, that particular microfossil is removed from the acritarchs and classified with its proper group.
Acritarchs were most likely eukaryotes. While archaea, bacteria and cyanobacteria (prokaryotes) usually produce simple fossils of a very small size, eukaryotic unicellular fossils are usually larger and more complex, with external morphological projections and ornamentation such as spines and hairs that only eukaryotes can produce; as most acritarchs have external projections (e.g., hair, spines, thick cell membranes, etc.), they are predominantly eukaryotes, although simple eukaryote acritarchs also exist.