Proterozoic

, which are colored by hematite, indicate an increase in atmospheric oxygen 2 Ga. Such massive iron oxide formations are not found in older rocks. The oxygen buildup was probably due to two factors: Exhaustion of the chemical sinks, and an increase in carbon sequestration, which sequestered that would have otherwise been oxidized by the atmosphere.

The first surge in atmospheric oxygen at the beginning of the Proterozoic is called the Great Oxygenation Event, or alternately the Oxygen Catastrophe – to reflect the mass extinction of almost all life on Earth, which at the time was virtually all obligate anaerobic. A second, later surge in oxygen concentrations is called the Neoproterozoic Oxygenation Event, occurred during the Middle and Late Neoproterozoic and drove the rapid evolution of multicellular life towards the end of the era.

The late Archean Eon to Early Proterozoic Eon corresponds to a period of increasing crustal recycling, suggesting subduction. Evidence for this increased subduction activity comes from the abundance of old granites originating mostly after 2.6 Ga.

The occurrence of eclogite (a type of metamorphic rock created by high pressure, > 1 GPa), is explained using a model that incorporates subduction. The lack of eclogites that date to the Archean Eon suggests that conditions at that time did not favor the formation of high grade metamorphism and therefore did not achieve the same levels of subduction as was occurring in the Proterozoic Eon.

As a result of remelting of oceanic crust due to subduction, the cores of the first continents grew large enough to withstand the crustal recycling processes.

The long-term tectonic stability of those is why we find continental crust ranging up to a few billion years in age. It is believed that 43% of modern continental crust was formed in the Proterozoic, 39% formed in the Archean, and only 18% in the Phanerozoic. Studies by Condie (2000) and Rino et al. (2004) suggest that crust production happened episodically. By isotopically calculating the ages of Proterozoic granitoids it was determined that there were several episodes of rapid increase in continental crust production. The reason for these pulses is unknown, but they seemed to have decreased in magnitude after every period.

Evidence of collision and rifting between continents raises the question as to what exactly were the movements of the Archean cratons composing Proterozoic continents. Paleomagnetism and geochronological dating mechanisms have allowed the deciphering of Precambrian Supereon tectonics. It is known that tectonic processes of the Proterozoic Eon resemble greatly the evidence of tectonic activity, such as or ophiolite complexes, we see today. Hence, most geologists would conclude that the Earth was active at that time. It is also commonly accepted that during the Precambrian, the Earth went through several supercontinent breakup and rebuilding cycles (Wilson cycle).

In the late Proterozoic (most recent), the dominant supercontinent was Rodinia (~1000–750 Ma). It consisted of a series of continents attached to a central craton that forms the core of the North American Continent called Laurentia. An example of an orogeny (mountain building processes) associated with the construction of Rodinia is the Grenville orogeny located in Eastern North America. Rodinia formed after the breakup of the supercontinent Columbia and prior to the assemblage of the supercontinent Gondwana (~500 Ma). The defining orogenic event associated with the formation of Gondwana was the collision of Africa, South America, Antarctica and Australia forming the Pan-African orogeny.

Columbia was dominant in the early-mid Proterozoic and not much is known about continental assemblages before then. There are a few plausible models that explain tectonics of the early Earth prior to the formation of Columbia, but the current most plausible hypothesis is that prior to Columbia, there were only a few independent cratons scattered around the Earth (not necessarily a supercontinent, like Rodinia or Columbia).

The emergence of advanced single-celled eukaryotes began after the Oxygen Catastrophe. This may have been due to an increase in the oxidized that eukaryotes use, as opposed to cyanobacteria. It was also during the Proterozoic that the first symbiosis relationships between mitochondria (found in nearly all eukaryotes) and (found in and some only) and their hosts evolved.

By the late Palaeoproterozoic, eukaryotic organisms had become moderately biodiverse. The blossoming of eukaryotes such as did not preclude the expansion of cyanobacteria – in fact, stromatolites reached their greatest abundance and diversity during the Proterozoic, peaking roughly 1.2 Ga.

The earliest possessing features typical of Fungus date to the Paleoproterozoic Era, some 2.4 Ga; these multicellular benthic organisms had filamentous structures capable of anastomosis.

The Viridiplantae evolved sometime in the Palaeoproterozoic or Mesoproterozoic, according to molecular data.

Eukaryote fossils from before the Cryogenian are sparse, and there seems to be low and relatively constant rates of species appearance, change, and extinction. This contrasts with the Ediacaran and early Cambrian periods, in which the quantity and variety of speciations, changes, and extinctions exploded.

Classically, the boundary between the Proterozoic and the Phanerozoic eons was set at the base of the Cambrian Period when the first fossils of animals, including and archaeocyatha, as well as the animal-like Caveasphaera, appeared. In the second half of the 20th century, a number of fossil forms have been found in Proterozoic rocks, particularly in ones from the Ediacaran, proving that multicellular life had already become widespread tens of millions of years before the Cambrian Explosion in what is known as the Avalon explosion. Nonetheless, the upper boundary of the Proterozoic has remained fixed at the base of the Cambrian, which is currently placed at 538.8 Ma.

• Boring Billion
• Timeline of natural history
• Volyn biota