Euxinia or euxinic conditions occur when water is both anoxic and sulfidic. This means that there is no oxygen (O2) and a raised level of free hydrogen sulfide (H2S). Euxinic bodies of water are frequently strongly stratified; have an oxic, highly productive, thin surface layer; and have anoxic, sulfidic bottom water. The word "euxinia" is derived from the Greek name for the Black Sea (Εὔξεινος Πόντος (Euxeinos Pontos)) which translates to "hospitable sea". [1] Euxinic deep water is a key component of the Canfield ocean, a model of oceans during part of the Proterozoic eon (a part specifically known as the Boring Billion) proposed by Donald Canfield, an American geologist, in 1998. [2] There is still debate within the scientific community on both the duration and frequency of euxinic conditions in the ancient oceans. [3] Euxinia is relatively rare in modern bodies of water, but does still happen in places like the Black Sea and certain fjords.
Euxinia most frequently occurred in the Earth's ancient oceans, but its distribution and frequency of occurrence are still under debate. [4] The original model was that it was quite constant for approximately a billion years. [2] Some meta-analyses have questioned how persistent euxinic conditions were based on relatively small black shale deposits in a period when the ocean should have theoretically been preserving more organic matter. [1]
Before the Great Oxygenation Event happened approximately 2.3 billion years ago, there was little free oxygen in either the atmosphere or the ocean. [5] It was originally thought that the ocean accumulated oxygen soon after the atmosphere did, but this idea was challenged by Canfield in 1998 when he proposed that instead of the deep ocean becoming oxidizing, it became sulfidic. [2] This hypothesis is partially based on the disappearance of banded iron formations from the geological records 1.8 billion years ago. Canfield argued that although enough oxygen entered the atmosphere to erode sulfides in continental rocks, there was not enough oxygen to mix into the deep ocean. [2] This would result in an anoxic deep ocean with an increased flux of sulfur from the continents. The sulfur would strip iron ions from the sea water, resulting in iron sulfide (pyrite), a portion of which was eventually buried. When sulfide became the major oceanic reductant instead of iron, the deep water became euxinic. [1] This has become what is known as the Canfield ocean, a model backed by the increase in presence of δ34S in sedimentary pyrite [2] and the discovery of evidence of the first sulfate evaporites. [6]
Anoxia and sulfidic conditions often occur together. In anoxic conditions anaerobic, sulfate reducing bacteria convert sulfate into sulfide, creating sulfidic conditions. [4] The emergence of this metabolic pathway was very important in the pre-oxygenated oceans because adaptations to otherwise inhabitable or "toxic" environments like this may have played a role in the diversification of early eukaryotes and protozoa in the pre-Phanerozoic. [4]
Euxinia still occurs occasionally today, mostly in meromictic lakes and silled basins such as the Black Sea and some fjords. [1] It is rare in modern times; less than 0.5% of today's sea floor is euxinic. [4]
The basic requirements for the formation of euxinic conditions are the absence of oxygen (O2), and the presence of sulfate ions (SO42−), organic matter (CH2O), and bacteria capable of reducing sulfate to hydrogen sulfide (H2S). [1] The bacteria utilize the redox potential of sulfate as an oxidant and organic matter as a reductant to generate chemical energy through cellular respiration. The chemical species of interest can be represented via the reaction:
2CH2O + SO42− → H2S + 2HCO3−
In the reaction above, the sulfur has been reduced to form the byproduct hydrogen sulfide, the characteristic compound present in water under euxinic conditions. Although sulfate reduction occurs in waters throughout the world, most modern-day aquatic habitats are oxygenated due to photosynthetic production of oxygen and gas exchange between the atmosphere and surface water. Sulfate reduction in these environments is often limited to occurring in seabed sediments that have a strong redox gradient and become anoxic at some depth below the sediment-water interface. In the ocean the rate of these reactions is not limited Archived 2017-03-15 at the Wayback Machine by sulfate, which has been present in large quantities throughout the oceans for the past 2.1 billion years. [6] The Great Oxygenation Event increased atmospheric oxygen concentrations such that oxidative weathering of sulfides became a major source of sulfate to the ocean. [7] [8] Despite plentiful sulfate ions being present in solution, they are not preferentially used by most bacteria. The reduction of sulfate does not give as much energy to an organism as reduction of oxygen or nitrate, so the concentrations of these other elements must be nearly zero for sulfate-reducing bacteria to out-compete aerobic and denitrifying bacteria. In most modern settings these conditions only occur in a small portion of sediments, resulting in insufficient concentrations of hydrogen sulfide to form euxinic waters. [4]
Conditions required for the formation of persistent euxinia include anoxic waters, high nutrient levels, and a stratified water column. [1] These conditions are not all-inclusive and are based largely on modern observations of euxinia. Conditions leading up to and triggering large-scale euxinic events, such as the Canfield ocean, are likely the result of multiple interlinking factors, many of which have been inferred through studies of the geologic record at relevant locations. [9] [10] [11] [12] The formation of stratified anoxic waters with high nutrient levels is influenced by a variety of global and local-scale phenomena such as the presence of nutrient traps and a warming climate. [1]
In order for euxinic conditions to persist, a positive feedback loop must perpetuate organic matter export to bottom waters and reduction of sulfate under anoxic conditions. Organic matter export is driven by high levels of primary production in the photic zone, supported by a continual supply of nutrients to the oxic surface waters. A natural source of nutrients, such as phosphate (PO3−
4), comes from weathering of rocks and subsequent transport of these dissolved nutrients via rivers. [13] In a nutrient trap, increased input of phosphate from rivers, high rates of recycling of phosphate from sediments, and slow vertical mixing in the water column allow for euxinic conditions to persist. [14]
The arrangement of the continents has changed over time due to plate tectonics, resulting in the bathymetry of ocean basins also changing over time. The shape and size of the basins influences the circulation patterns and concentration of nutrients within them. Numerical models simulating past arrangements of continents have shown that nutrient traps can form in certain scenarios, increasing local concentrations of phosphate and setting up potential euxinic conditions. [1] On a smaller scale, silled basins often act as nutrient traps due to their estuarine circulation. [14] Estuarine circulation occurs where surface water is replenished from river input and precipitation, causing an outflow of surface waters from the basin, while deep water flows into the basin over the sill. This type of circulation allows for anoxic, high nutrient bottom water to develop within the basin. [1]
Stratified waters, in combination with slow vertical mixing, are essential to maintaining euxinic conditions. [1] Stratification occurs when two or more water masses with different densities occupy the same basin. While the less dense surface water can exchange gas with the oxygen-rich atmosphere, the denser bottom waters maintain low oxygen content. In the modern oceans, thermohaline circulation and upwelling prevent the oceans from maintaining anoxic bottom waters. In a silled basin, the stable stratified layers only allow surface water to flow out of the basin while the deep water remains anoxic and relatively unmixed. During an intrusion of dense saltwater however, the nutrient-rich bottom water upwells, causing increased productivity in the surface, further enhancing the nutrient trap due to biological pumping. Rising sea level can exacerbate this process by increasing the amount of deep water entering a silled basin and enhancing estuarine circulation. [15] [16]
A warming climate increases surface temperatures of waters which affects multiple aspects of euxinic water formation. As waters warm, the solubility of oxygen decreases, allowing for deep anoxic waters to form more readily. [17] Additionally, the warmer water causes increased respiration of organic matter leading to further oxygen depletion. Higher temperatures enhance the hydrologic cycle, increasing evaporation from bodies of water, resulting in increased precipitation. This causes higher rates of weathering of rocks and therefore higher nutrient concentrations in river outflows. The nutrients allow for more productivity resulting in more marine snow and subsequently lower oxygen in deep waters due to increased respiration. [1]
Volcanism has also been proposed as a factor in creating euxinic conditions. The carbon dioxide (CO2) released during volcanic outgassing causes global warming which has cascading effects on the formation of euxinic conditions. [1] [16]
Black shales are organic rich, microlaminated sedimentary rocks often associated with bottom water anoxia. [18] This is because anoxia slows the degradation of organic matter, allowing for greater burial in the sediments. Other evidence for anoxic burial of black shale includes the lack of bioturbation, meaning that there were no organisms burrowing into the sediment because there was no oxygen for respiration. [4] There must also be a source of organic matter for burial, generally from production near the oxic surface. Many papers discussing ancient euxinic events use the presence of black shale as a preliminary proxy for anoxic bottom waters, but their presence does not in and of itself indicate euxinia or even strong anoxia. [18] Generally geochemical testing is needed to provide better evidence for conditions. [4] [18]
Some researchers study the occurrence of euxinia in ancient oceans because it was more prevalent then than it is today. Since ancient oceans cannot be directly observed, scientists use geology and chemistry to find evidence in sedimentary rock created under euxinic conditions. Some of these techniques come from studying modern examples of euxinia, while others are derived from geochemistry. [18] Though modern euxinic environments have geochemical properties in common with ancient euxinic oceans, the physical processes causing euxinia most likely vary between the two. [1] [4] [18]
Stable isotope ratios can be used to infer the environmental conditions during the formation of sedimentary rock. Using stoichiometry and knowledge of redox pathways, paleogeologists can use isotopes ratios of elements to determine the chemical composition of the water and sediments when burial occurred. [19]
Sulfur isotopes are frequently used to look for evidence of ancient euxinia. Low δ34S in black shales and sedimentary rocks provides positive evidence for euxinic formation conditions. The pyrite (FeS2) in euxinic basins typically has higher concentrations of light sulfur isotopes than pyrite in the modern ocean. [1] The reduction of sulfate to sulfide favors the lighter sulfur isotopes (32S) and becomes depleted in the heavier isotopes (34S). This lighter sulfide then bonds with Fe2+ to form FeS2 which is then partially preserved in the sediments. In most modern systems, sulfate eventually becomes limiting, and the isotopic weights of sulfur in both sulfate and sulfide (preserved as FeS2) become equal. [1]
Molybdenum (Mo), the most common transition metal ion in modern seawater, is also used to look for evidence for euxinia. [4] Weathering of rocks provides an input of MoO42– into oceans. Under oxic conditions, MoO42– is very unreactive, but in modern euxinic environments such as the Black Sea, molybdenum precipitates out as oxythiomolybdate (MoO4−xSx2– ). [18] [20] [21] The isotope ratio for Molybdenum (δ97/95 Mo) in euxinic sediments appears to be higher than in oxic conditions. [20] Additionally, the concentration of molybdenum is frequently correlated with the concentration of organic matter in euxinic sediments. [4] The use of Mo to indicate euxinia is still under debate. [4]
Under euxinic conditions, some trace elements such as Mo, U, V, Cd, Cu, Tl, Ni, Sb, and Zn, become insoluble. [18] [22] [23] This means that euxinic sediments would contain more of the solid form of these elements than the background seawater. [1] For example, Molybdenum and other trace metals become insoluble in anoxic and sulfidic conditions, so over time the seawater becomes depleted of trace metals under conditions of persistent euxinia, and preserved sediments are relatively enriched with molybdenum and other trace elements. [18] [24]
Bacteria such as green sulfur bacteria and purple sulfur bacteria, which exist where the photic zone overlaps with euxinic water masses, leave pigments behind in sediments. These pigments can be used to identify past euxinic conditions. [1] The pigments used to identify past presence of green sulfur bacteria are chlorobactane and isorenieratene. [25] The pigments used to identify past presence of purple sulfur bacteria is okenane. [26]
Pyrite (FeS2) is a mineral formed by the reaction of hydrogen sulfide (H2S) and bioreactive iron (Fe2+). In oxic bottom waters pyrite can only form in sediments where H2S is present. However, in iron-rich euxinic environments, pyrite formation can occur at higher rates in both the water column and in sediments due to higher concentrations of H2S. [14] [18] Therefore the presence of euxinic conditions can be inferred by the ratio of pyrite-bound iron to the total iron in sediments. High ratios of pyrite-bound iron can be used as an indicator of past euxinic conditions. [9] [27] Similarly, if >45% of the bioreactive iron in sediments is pyrite-bound, then anoxic or euxinic conditions can be inferred. [14] While useful, these methods do not provide definitive proof of euxinia because not all euxinic waters have the same concentrations of bioreactive iron available. [14] These relationships have been found to be present in the modern euxinic Black Sea. [10]
The Proterozoic is the transition era between anoxic and oxygenated oceans. The classic model is that the end of the Banded iron formations (BIFs) was due to the injection of oxygen into the deep ocean, an approximately 0.6 billion year lag behind the Great Oxygenation Event. [28] Canfield, however, argued that anoxia lasted much longer, and the end of the banded iron formations was due to the introduction of sulfide. [2] Supporting Canfield's original hypothesis, 1.84 billion year old sedimentary records have been found in the Animike group in Canada that exhibit close to full pyritization on top of the last of the banded iron formations, showing evidence of a transition to euxinic conditions in that basin. [29] In order for full pyritization to happen, nearly all of the sulfate in the water was reduced to sulfide, which stripped the iron from the water, forming pyrite. Because this basin was open to the ocean, deep euxinia was interpreted as being a widespread phenomena. [29] This euxinia is hypothesized to have lasted until about 0.8 billion years ago, making basin bottom euxinia a potentially widespread feature throughout the Boring Billion. [29]
Further evidence for euxinia was discovered in the McArthur Basin in Australia, where similar iron chemistry was found. The degree of pyritization and the δ34S were both high, supporting the presence of anoxia and sulfide, as well as the depletion of sulfate. [14] A different study found biomarkers for green sulfur bacteria and purple sulfur bacteria in the same area, providing further evidence for the reduction of sulfate to hydrogen sulfide. [30]
Molybdenum isotopes have been used to examine the distribution of euxinia in the Proterozoic eon, and suggest that perhaps euxinia was not as widespread as Canfield initially postulated. Bottom waters may have been more widely suboxic than anoxic, and there could have been negative feedback between euxinia and the high levels of surface primary production needed to sustain euxinic conditions. [31] Further work has suggested that from 700 million years ago (late Proterozoic) and onward, the deep oceans may have actually been anoxic and iron rich with conditions similar to those during the formation of BIFs. [3] [32]
There is evidence for multiple euxinic events during the Phanerozoic. It is most likely that euxinia was periodic during the Paleozoic and Mesozoic, but geologic data is too sparse to draw any large scale conclusions. In this eon, there is some evidence that euxinic events are potentially linked with mass extinction events including the Late Devonian and Permian–Triassic. [1]
The periodic presence of euxinic conditions in the Lower Cambrian has been supported by evidence found on the Yangtze platform in South China. Sulfur isotopes during the transition from Proterozoic to Phanerozoic give evidence for widespread euxinia, perhaps lasting throughout the Cambrian period. [33] Towards the end of the Lower Cambrian, the euxinic chemocline grew deeper until euxinia was present only in the sediments, and once sulfate became limiting, conditions became anoxic instead of euxinic. Some areas eventually became oxic, while others eventually returned to euxinic for some time. [34]
Geological records from the paleozoic in the Selwyn Basin in Northern Canada have also shown evidence for episodic stratification and mixing, where, using δ34S, it was determined that hydrogen sulfide was more prevalent than sulfate. [35] Although this was not originally attributed to euxinia, further studies found that seawater in that time likely had low concentrations of sulfate, meaning that the sulfur in the water was primarily in the form of sulfide. This combined with organic-rich black shale provide strong evidence for euxinia. [36]
There is similar evidence in the black shales in the mid-continent North America from the Devonian and early Mississippian periods. Isorenieratene, a pigment known as a proxy for an anoxic photic zone, has been found in the geological record in Illinois and Michigan. [11] Although present, these events were probably ephemeral and did not last for longer periods of time. [37] Similar periodic evidence of euxinia can also be found in the Sunbury shales of Kentucky. [12]
Evidence for euxinia has also been tied to the Kellwasser events of the Late Devonian Extinction event. Euxinia in basinal waters in what is now central Europe (Germany, Poland, and France) persisted for part of the late Devonian, and may have spread up into shallow waters, contributing to the extinction event. [38]
There was perhaps a period of oxygenation of bottom waters during the Carboniferous, most likely between the Late Devonian Extinction and the Permian-Triassic Extinction, at which point euxinia would be very rare in the paleo oceans. [28]
The Permian–Triassic extinction event may also have some ties to euxinia, with hypercapnia and hydrogen sulfide toxicity killing off many species. [39] Presence of a biomarker for anaerobic photosynthesis by green sulfur bacteria has been found spanning from the Permian to early Triassic in sedimentary rock in both Australia and China, meaning that euxinic conditions extended up quite shallow in the water column, contributing to the extinctions and perhaps even slowed the recovery. [40] It is uncertain, however, just how widespread photic zone euxinia was during this period. Modelers have hypothesized that due to environmental conditions anoxia and sulfide may have been brought up from a deep, vast euxinic reservoir in upwelling areas, but stable, gyre-like areas remained oxic. [41]
The Mesozoic is well known for its distinct Ocean Anoxic Events (OAEs) which resulted in the burial of layers of black shale. Although these OAEs are not stand alone evidence for euxinia, many do contain biomarkers which support euxinic formation. [1] Again, evidence is not universal. OAEs may have spurred the spread of existing euxinia, especially in upwelling regions or semi-restricted basins, but photic zone euxinia did not happen everywhere. [1]
Few episodes of euxinia are evident in the sedimentary record during the Cenozoic. [1] Since the end of the Cretaceous OAEs, it is most likely that the oceanic bottom waters have stayed oxic. [28]
Euxinic conditions have nearly vanished from Earth's open-ocean environments, but a few small scale examples still exist today. Many of these locations share common biogeochemical characteristics. [1] For example, low rates of overturning and vertical mixing of the total water column is common in euxinic bodies of water. [1] Small surface area to depth ratios allow multiple stable layers to form while limiting wind-driven overturning and thermohaline circulation. [1] Furthermore, restricted mixing enhances stratified layers of high nutrient density which are reinforced by biological recycling. [1] Within the chemocline, highly specialized organisms such as green sulfur bacteria take advantage of the strong redox potential gradient and minimal sunlight. [1]
The Black Sea is a commonly used modern model for understanding biogeochemical processes that occur under euxinic conditions. [42] It is thought to represent the conditions of Earth's proto-oceans and thus assists in the interpretation of oceanic proxies. [42] Black Sea sediment contains redox reactions to depths of tens of meters, compared to single centimeters in the open ocean. [43] This unique feature is important for understanding the behavior of the redox cascade under euxinic conditions. [43]
The only connection between the open ocean and the Black Sea is the Bosphorus Strait, through which dense Mediterranean waters are imported. [43] Subsequently, numerous rivers, such as the Danube, Don, Dnieper, and Dniester, drain fresh water into the Black Sea, which floats on top of the more dense Mediterranean water, causing a strong, stratified water column. [42] This stratification is maintained by a strong pycnocline which restricts ventilation of deep waters and results in an intermediate layer called the chemocline, a sharp boundary separating oxic surface waters from anoxic bottom waters usually between 50m and 100m depth, [44] with interannual variation attributed to large scale changes in temperature. [43] Well-mixed, oxic conditions exist above the chemocline and sulfidic conditions are dominant below. [43] Surface oxygen and deep water sulfide do not overlap via vertical mixing, [45] but horizontal entrainment of oxygenated waters and vertical mixing of oxidized manganese into sulfidic waters may occur near the Bosphorus Strait inlet. [43] Manganese and iron oxides likely oxidize hydrogen sulfide near the chemocline, resulting in the decrease in H2S concentrations as one approaches the chemocline from below.
Meromictic lakes are poorly mixed and anoxic bodies of water with strong vertical stratification. [1] While meromictic lakes are frequently categorized as bodies of water with the potential for euxinic conditions, many do not exhibit euxinia. Meromictic lakes are infamous for limnic eruptions. [46] These events usually coincide with nearby tectonic or volcanic activity that disturbs the otherwise stable stratification of meromictic lakes. [47] This can result in the release of immense concentrations of stored toxic gasses from the anoxic bottom waters, such as CO2 [46] and H2S, especially from euxinic meromictic lakes. In high enough concentration, these limnic explosions can be deadly to humans and animals, such as the Lake Nyos disaster in 1986. [48]
Some fjords develop euxinia if the connection to the open ocean is constricted, similar to the case of the Black Sea. This constriction prohibits relatively dense, oxygen-rich oceanic water from mixing with the bottom water of the fjord, which leads to stable stratified layers in the fjord. [1] Low salinity melt water forms a lens of fresh, low density water on top of a more dense mass of bottom water. Ground sources of sulfur are also an important cause for euxinia in fjords. [49]
This fjord was born as a glacial lake that was separated from the open ocean (the North Sea) when it was lifted during glacial rebound. [1] A shallow channel (2m deep) was dug in 1850, providing a marginal connection to the North Sea. [1] A strong pycnocline separates fresh surface water from dense, saline bottom water, and this pycnocline reduces mixing between the layers. Anoxic conditions persist below the chemocline at 20m, and the fjord has the highest levels of hydrogen sulfide in the anoxic marine world. [50] [1] Like the Black Sea, vertical overlap of oxygen and sulfur is limited, but the decline of H2S approaching the chemocline from below is indicative of oxidation of H2S, which has been attributed to manganese and iron oxides, photo-autotrophic bacteria, and entrainment of oxygen horizontally from the boundaries of the fjord. [51] These oxidation processes are similar to those present in the Black Sea.
Two strong seawater intrusion events have occurred through the channel in recent history (1902 and 1942). [1] Seawater intrusions to fjords force dense, salty, oxygen-rich water into the typically anoxic, sulfidic bottom waters of euxinic fjords. [52] These events result in a temporary disturbance to the chemocline, raising the depth at which H2S is detected. The breakdown of the chemocline causes H2S to react with dissolved oxygen in a redox reaction. [52] This decreases the concentration of dissolved oxygen in the biologically active photic zone which can result in basin-scale fish die-offs. [52] The 1942 event, in particular, was strong enough to chemically reduce the vast majority of oxygen and elevate the chemocline to the air-water interface. [52] This caused a temporary state of total anoxia in the fjord, and resulted in dramatic fish mortality. [52]
This fjord is marked by a highly mobile chemocline with a depth that is thought to be related to temperature effects. [4] Local reports of strong rotten egg smell- the smell of sulfur- during numerous summers around the fjord provide evidence that, like the Framvaren fjord, the chemocline has breached the surface of the fjord at least five times in the last century. [4] Sediments export during these events increased the concentrations of dissolved phosphates, inorganic bioavailable nitrogen, and other nutrients, resulting in a harmful algal bloom. [49]
The Cariaco Basin in Venezuela has been used to study the cycle of organic material in euxinic marine environments. [53] An increase in productivity coincident with post glacial nutrient loading probably caused a transition from oxic to anoxic and subsequently euxinic conditions around 14.5 thousand years ago. [54] High productivity at the surface produces a rain of particulate organic matter to the sub surface where anoxic, sulfidic conditions persist. [53] The organic matter in this region is oxidized with sulfate, producing reduced sulfur (H2S) as a waste product. Free sulfur exists deep in the water column and up to 6m in depth in the sediment. [53]
The Late Ordovician mass extinction (LOME), sometimes known as the end-Ordovician mass extinction or the Ordovician-Silurian extinction, is the first of the "big five" major mass extinction events in Earth's history, occurring roughly 445 million years ago (Ma). It is often considered to be the second-largest known extinction event just behind the end-Permian mass extinction, in terms of the percentage of genera that became extinct. Extinction was global during this interval, eliminating 49–60% of marine genera and nearly 85% of marine species. Under most tabulations, only the Permian-Triassic mass extinction exceeds the Late Ordovician mass extinction in biodiversity loss. The extinction event abruptly affected all major taxonomic groups and caused the disappearance of one third of all brachiopod and bryozoan families, as well as numerous groups of conodonts, trilobites, echinoderms, corals, bivalves, and graptolites. Despite its taxonomic severity, the Late Ordovician mass extinction did not produce major changes to ecosystem structures compared to other mass extinctions, nor did it lead to any particular morphological innovations. Diversity gradually recovered to pre-extinction levels over the first 5 million years of the Silurian period.
The purple sulfur bacteria (PSB) are part of a group of Pseudomonadota capable of photosynthesis, collectively referred to as purple bacteria. They are anaerobic or microaerophilic, and are often found in stratified water environments including hot springs, stagnant water bodies, as well as microbial mats in intertidal zones. Unlike plants, algae, and cyanobacteria, purple sulfur bacteria do not use water as their reducing agent, and therefore do not produce oxygen. Instead, they can use sulfur in the form of sulfide, or thiosulfate (as well, some species can use H2, Fe2+, or NO2−) as the electron donor in their photosynthetic pathways. The sulfur is oxidized to produce granules of elemental sulfur. This, in turn, may be oxidized to form sulfuric acid.
Green Lake is the larger of the two lakes in Green Lakes State Park, which lies about 9 miles (14 km) east of downtown Syracuse in Onondaga County, New York. Round Lake is the smaller lake located west of Green Lake. Both lakes are meromictic, which means no seasonal mixing of surface and bottom waters occurs. Meromictic lakes are fairly rare; they have been extensively studied, in part because their sediments can preserve a historical record extending back thousands of years, and because of the euxinic conditions which can form in the deep water.
An anoxic event describes a period wherein large expanses of Earth's oceans were depleted of dissolved oxygen (O2), creating toxic, euxinic (anoxic and sulfidic) waters. Although anoxic events have not happened for millions of years, the geologic record shows that they happened many times in the past. Anoxic events coincided with several mass extinctions and may have contributed to them. These mass extinctions include some that geobiologists use as time markers in biostratigraphic dating. On the other hand, there are widespread, various black-shale beds from the mid-Cretaceous which indicate anoxic events but are not associated with mass extinctions. Many geologists believe oceanic anoxic events are strongly linked to the slowing of ocean circulation, climatic warming, and elevated levels of greenhouse gases. Researchers have proposed enhanced volcanism (the release of CO2) as the "central external trigger for euxinia."
The important sulfur cycle is a biogeochemical cycle in which the sulfur moves between rocks, waterways and living systems. It is important in geology as it affects many minerals and in life because sulfur is an essential element (CHNOPS), being a constituent of many proteins and cofactors, and sulfur compounds can be used as oxidants or reductants in microbial respiration. The global sulfur cycle involves the transformations of sulfur species through different oxidation states, which play an important role in both geological and biological processes. Steps of the sulfur cycle are:
Beggiatoa is a genus of Gammaproteobacteria belonging to the order Thiotrichales, in the Pseudomonadota phylum. These bacteria form colorless filaments composed of cells that can be up to 200 μm in diameter, and are one of the largest prokaryotes on Earth. Beggiatoa are chemolithotrophic sulfur-oxidizers, using reduced sulfur species as an energy source. They live in sulfur-rich environments such as soil, both marine and freshwater, in the deep sea hydrothermal vents, and in polluted marine environments. In association with other sulfur bacteria, e.g. Thiothrix, they can form biofilms that are visible to the naked eye as mats of long white filaments; the white color is due to sulfur globules stored inside the cells.
Anoxic waters are areas of sea water, fresh water, or groundwater that are depleted of dissolved oxygen. The US Geological Survey defines anoxic groundwater as those with dissolved oxygen concentration of less than 0.5 milligrams per litre. Anoxic waters can be contrasted with hypoxic waters, which are low in dissolved oxygen. This condition is generally found in areas that have restricted water exchange.
Donald Eugene Canfield is a geochemist and Professor of Ecology at the University of Southern Denmark known for his work on the evolution of Earth's atmosphere and oceans. The Canfield ocean, a sulfidic partially oxic ocean existing during the middle of the Proterozoic eon, is named after him.
A chemocline is a type of cline, a layer of fluid with different properties, characterized by a strong, vertical chemistry gradient within a body of water. In bodies of water where chemoclines occur, the cline separates the upper and lower layers, resulting in different properties for those layers. The lower layer shows a change in the concentration of dissolved gases and solids compared to the upper layer.
The Boring Billion, otherwise known as the Mid Proterozoic and Earth's Middle Ages, is an informal geological time period between 1.8 and 0.8 billion years ago (Ga) during the middle Proterozoic eon spanning from the Statherian to the Tonian periods, characterized by more or less tectonic stability, climatic stasis and slow biological evolution. Although it is bordered by two different oxygenation events and two global glacial events, the Boring Billion period itself actually had very low oxygen levels and no geological evidence of glaciations.
The Cenomanian-Turonian boundary event, also known as the Cenomanian-Turonian extinction, Cenomanian-Turonian Oceanic Anoxic Event, and referred to also as the Bonarelli Event or Level, was an anoxic extinction event in the Cretaceous period. The Cenomanian-Turonian oceanic anoxic event is considered to be the most recent truly global oceanic anoxic event in Earth's geologic history. There was a large carbon cycle disturbance during this time period, signified by a large positive carbon isotope excursion. However, apart from the carbon cycle disturbance, there were also large disturbances in the ocean's nitrogen, oxygen, phosphorus, sulphur, and iron cycles.
Isorenieratene /ˌaɪsoʊrəˈnɪərətiːn/ is a carotenoid light-harvesting pigment produced exclusively by the genus Chlorobium, which are the brown-colored strains of the family of green sulfur bacteria (Chlorobiaceae). Green sulfur bacteria are anaerobic photoautotrophic organisms, meaning they perform photosynthesis in the absence of oxygen using hydrogen sulfide in the following reaction:
The Canfield Ocean model was proposed by geochemist Donald Canfield to explain the composition of the ocean in the middle to late Proterozoic.
Three Western Interior Seaway anoxic events occurred during the Cretaceous in the shallow inland seaway that divided North America in two island continents, Appalachia and Laramidia. During these anoxic events much of the water column was depleted in dissolved oxygen. While anoxic events impact the world's oceans, Western Interior Seaway anoxic events exhibit a unique paleoenvironment compared to other basins. The notable Cretaceous anoxic events in the Western Interior Seaway mark the boundaries at the Aptian-Albian, Cenomanian-Turonian, and Coniacian-Santonian stages, and are identified as Oceanic Anoxic Events I, II, and III respectively. The episodes of anoxia came about at times when very high sea levels coincided with the nearby Sevier orogeny that affected Laramidia to the west and Caribbean large igneous province to the south, which delivered nutrients and oxygen-adsorbing compounds into the water column.
The δ34S value is a standardized method for reporting measurements of the ratio of two stable isotopes of sulfur, 34S:32S, in a sample against the equivalent ratio in a known reference standard. Presently, the most commonly used standard is Vienna-Canyon Diablo Troilite (VCDT). Results are reported as variations from the standard ratio in parts per thousand, per mil or per mille, using the ‰ symbol. Heavy and light sulfur isotopes fractionate at different rates and the resulting δ34S values, recorded in marine sulfate or sedimentary sulfides, have been studied and interpreted as records of the changing sulfur cycle throughout the earth's history.
Okenane, the diagenetic end product of okenone, is a biomarker for Chromatiaceae, the purple sulfur bacteria. These anoxygenic phototrophs use light for energy and sulfide as their electron donor and sulfur source. Discovery of okenane in marine sediments implies a past euxinic environment, where water columns were anoxic and sulfidic. This is potentially tremendously important for reconstructing past oceanic conditions, but so far okenane has only been identified in one Paleoproterozoic rock sample from Northern Australia.
Carbonate-associated sulfates (CAS) are sulfate species found in association with carbonate minerals, either as inclusions, adsorbed phases, or in distorted sites within the carbonate mineral lattice. It is derived primarily from dissolved sulfate in the solution from which the carbonate precipitates. In the ocean, the source of this sulfate is a combination of riverine and atmospheric inputs, as well as the products of marine hydrothermal reactions and biomass remineralisation. CAS is a common component of most carbonate rocks, having concentrations in the parts per thousand within biogenic carbonates and parts per million within abiogenic carbonates. Through its abundance and sulfur isotope composition, it provides a valuable record of the global sulfur cycle across time and space.
Microbial oxidation of sulfur is the oxidation of sulfur by microorganisms to build their structural components. The oxidation of inorganic compounds is the strategy primarily used by chemolithotrophic microorganisms to obtain energy to survive, grow and reproduce. Some inorganic forms of reduced sulfur, mainly sulfide (H2S/HS−) and elemental sulfur (S0), can be oxidized by chemolithotrophic sulfur-oxidizing prokaryotes, usually coupled to the reduction of oxygen (O2) or nitrate (NO3−). Anaerobic sulfur oxidizers include photolithoautotrophs that obtain their energy from sunlight, hydrogen from sulfide, and carbon from carbon dioxide (CO2).
The chromium cycle is the biogeochemical cycle of chromium through the atmosphere, hydrosphere, biosphere and lithosphere.
The Neoproterozoic Oxygenation Event (NOE), also called the Second Great Oxidation Event, was a geologic time interval between around 850 and 540 million years ago during the Neoproterozoic era, which saw a very significant increase in oxygen levels in Earth's atmosphere and oceans. Taking place after the end to the Boring Billion, an euxinic period of extremely low atmospheric oxygen spanning from the Statherian period of the Paleoproterozoic era to the Tonian period of the Neoproterozoic era, the NOE was the second major increase in atmospheric and oceanic oxygen concentration on Earth, though it was not as prominent as the Great Oxidation Event (GOE) of the Neoarchean-Paleoproterozoic boundary. Unlike the GOE, it is unclear whether the NOE was a synchronous, global event or a series of asynchronous, regional oxygenation intervals with unrelated causes.