White smokers emitting liquid rich in barium, calcium, silicon and carbon dioxide at the Champagne vent, Northwest Eifuku volcano, Marianas Trench Marine National Monument
A hydrothermal vent is a fissure on the seafloor from which geothermally heated water issues. Hydrothermal vents are commonly found near volcanically active places, areas where tectonic plates are moving apart at spreading centers, ocean basins, and hotspots. Hydrothermal deposits are rocks and mineral ore deposits formed by the action of hydrothermal vents.
Hydrothermal vents exist because the earth is both geologically active and has large amounts of water on its surface and within its crust. Under the sea, hydrothermal vents may form features called black smokers or white smokers. Relative to the majority of the deep sea, the areas around submarine hydrothermal vents are biologically more productive, often hosting complex communities fueled by the chemicals dissolved in the vent fluids. Chemosynthetic bacteria and archaea form the base of the food chain, supporting diverse organisms, including giant tube worms, clams, limpets and shrimp. Active hydrothermal vents are thought to exist on Jupiter's moon Europa, and Saturn's moon Enceladus, and it is speculated that ancient hydrothermal vents once existed on Mars.
- 1 Physical properties
- 2 Black smokers and white smokers
- 3 Biological communities
- 4 Animal-bacterial symbiosis
- 5 Biological theories
- 6 Discovery and exploration
- 7 Distribution
- 8 Exploitation
- 9 Conservation
- 10 See also
- 11 References
- 12 Further reading
- 13 External links
Hydrothermal vents in the deep ocean typically form along the mid-ocean ridges, such as the East Pacific Rise and the Mid-Atlantic Ridge. These are locations where two tectonic plates are diverging and new crust is being formed.
The water that issues from seafloor hydrothermal vents consists mostly of sea water drawn into the hydrothermal system close to the volcanic edifice through faults and porous sediments or volcanic strata, plus some magmatic water released by the upwelling magma. In terrestrial hydrothermal systems, the majority of water circulated within the fumarole and geyser systems is meteoric water plus ground water that has percolated down into the thermal system from the surface, but it also commonly contains some portion of metamorphic water, magmatic water, and sedimentary formational brine that is released by the magma. The proportion of each varies from location to location.
In contrast to the approximately 2 °C (36 °F) ambient water temperature at these depths, water emerges from these vents at temperatures ranging from 60 °C (140 °F) up to as high as 464 °C (867 °F). Due to the high hydrostatic pressure at these depths, water may exist in either its liquid form or as a supercritical fluid at such temperatures. The critical point of (pure) water is 375 °C (707 °F) at a pressure of 218 atmospheres.
However, introducing salinity into the fluid raises the critical point to higher temperatures and pressures. The critical point of seawater (3.2 wt. % NaCl) is 407 °C (765 °F) and 298.5 bars, corresponding to a depth of ~2,960 m (9,710 ft) below sea level. Accordingly, if a hydrothermal fluid with a salinity of 3.2 wt. % NaCl vents above 407 °C (765 °F) and 298.5 bars, it is supercritical. Furthermore, the salinity of vent fluids have been shown to vary widely due to phase separation in the crust. The critical point for lower salinity fluids is at lower temperature and pressure conditions than that for seawater, but higher than that for pure water. For example, a vent fluid with a 2.24 wt. % NaCl salinity has the critical point at 400 °C (752 °F) and 280.5 bars. Thus, water emerging from the hottest parts of some hydrothermal vents can be a supercritical fluid, possessing physical properties between those of a gas and those of a liquid.
Examples of supercritical venting are found at several sites. Sister Peak (Comfortless Cove Hydrothermal Field, phase-separated, vapor-type fluids. Sustained venting was not found to be supercritical but a brief injection of 464 °C (867 °F) was well above supercritical conditions. A nearby site, Turtle Pits, was found to vent low salinity fluid at 407 °C (765 °F), which is above the critical point of the fluid at that salinity. A vent site in the Cayman Trough named Beebe, which is the world's deepest known hydrothermal site at ~5,000 m (16,000 ft) below sea level, has shown sustained supercritical venting at 401 °C (754 °F) and 2.3 wt% NaCl., depth 2,996 m or 9,829 ft) vents low salinity
Although supercritical conditions have been observed at several sites, it is not yet known what significance, if any, supercritical venting has in terms of hydrothermal circulation, mineral deposit formation, geochemical fluxes or biological activity.
The initial stages of a vent chimney begin with the deposition of the mineral anhydrite. Sulfides of copper, iron, and zinc then precipitate in the chimney gaps, making it less porous over the course of time. Vent growths on the order of 30 cm (1 ft) per day have been recorded. An April 2007 exploration of the deep-sea vents off the coast of Fiji found those vents to be a significant source of dissolved iron (see iron cycle).
Black smokers and white smokers
Some hydrothermal vents form roughly cylindrical chimney structures. These form from minerals that are dissolved in the vent fluid. When the superheated water contacts the near-freezing sea water, the minerals precipitate out to form particles which add to the height of the stacks. Some of these chimney structures can reach heights of 60 m. An example of such a towering vent was "Godzilla", a structure on the Pacific Ocean deep seafloor near Oregon that rose to 40 m before it fell over in 1996.
A black smoker or deep sea vent is a type of hydrothermal vent found on the seabed, typically in the bathyal zone (with largest frequency in depths from 2500 m to 3000 m), but also in lesser depths as well as deeper in abyssal zone. They appear as black, chimney-like structures that emit a cloud of black material. Black smokers typically emit particles with high levels of sulfur-bearing minerals, or sulfides. Black smokers are formed in fields hundreds of meters wide when superheated water from below Earth's crust comes through the ocean floor (water may attain temperatures above 400 °C). This water is rich in dissolved minerals from the crust, most notably sulfides. When it comes in contact with cold ocean water, many minerals precipitate, forming a black, chimney-like structure around each vent. The deposited metal sulfides can become massive sulfide ore deposits in time. Some black smokers on the Azores portion of the Mid Atlantic Ridge are extremely rich in metal content, such as Rainbow with 24,000 μM concentrations of iron.
Black smokers were first discovered in 1979 on the East Pacific Rise by scientists from Scripps Institution of Oceanography during the RISE Project. They were observed using the deep submergence vehicle ALVIN from the Woods Hole Oceanographic Institution. Now, black smokers are known to exist in the Atlantic and Pacific Oceans, at an average depth of 2100 metres. The most northerly black smokers are a cluster of five named Loki's Castle, discovered in 2008 by scientists from the University of Bergen at 73°N, on the Mid-Atlantic Ridge between Greenland and Norway. These black smokers are of interest as they are in a more stable area of the Earth's crust, where tectonic forces are less and consequently fields of hydrothermal vents are less common. The world's deepest known black smokers are located in the Cayman Trough, 5,000 m (3.1 miles) below the ocean's surface.
White smoker vents emit lighter-hued minerals, such as those containing barium, calcium and silicon. These vents also tend to have lower-temperature plumes probably because they are generally distant from their heat source.
Black and white smokers may coexist in the same hydrothermal field, but they generally represent proximal and distal vents to the main upflow zone, respectively. However, white smokers correspond mostly to waning stages of such hydrothermal fields, as magmatic heat sources become progressively more distant from the source (due to magma crystallization) and hydrothermal fluids become dominated by seawater instead of magmatic water. Mineralizing fluids from this type of vents are rich in calcium and they form dominantly sulfate-rich (i.e., barite and anhydrite) and carbonate deposits.
Life has traditionally been seen as driven by energy from the sun, but deep-sea organisms have no access to sunlight, so they must depend on nutrients found in the dusty chemical deposits and hydrothermal fluids in which they live. Previously, benthic oceanographers assumed that vent organisms were dependent on marine snow, as deep-sea organisms are. This would leave them dependent on plant life and thus the sun. Some hydrothermal vent organisms do consume this "rain", but with only such a system, life forms would be sparse. Compared to the surrounding sea floor, however, hydrothermal vent zones have a density of organisms 10,000 to 100,000 times greater.
Hydrothermal vent communities are able to sustain such vast amounts of life because vent organisms depend on chemosynthetic bacteria for food. The water from the hydrothermal vent is rich in dissolved minerals and supports a large population of chemoautotrophic bacteria. These bacteria use sulfur compounds, particularly hydrogen sulfide, a chemical highly toxic to most known organisms, to produce organic material through the process of chemosynthesis.
The ecosystem so formed is reliant upon the continued existence of the hydrothermal vent field as the primary source of energy, which differs from most surface life on Earth, which is based on solar energy. However, although it is often said that these communities exist independently of the sun, some of the organisms are actually dependent upon oxygen produced by photosynthetic organisms, while others are anaerobic.
The chemosynthetic bacteria grow into a thick mat which attracts other organisms, such as amphipods and copepods, which graze upon the bacteria directly. Larger organisms, such as snails, shrimp, crabs, tube worms, fish (especially eelpout, cutthroat eel, ophidiiforms and Symphurus thermophilus), and octopuses (notably Vulcanoctopus hydrothermalis), form a food chain of predator and prey relationships above the primary consumers. The main families of organisms found around seafloor vents are annelids, pogonophorans, gastropods, and crustaceans, with large bivalves, vestimentiferan worms, and "eyeless" shrimp making up the bulk of nonmicrobial organisms.
Siboglinid tube worms, which may grow to over 2 m (6.6 ft) tall in the largest species, often form an important part of the community around a hydrothermal vent. They have no mouth or digestive tract, and like parasitic worms, absorb nutrients produced by the bacteria in their tissues. About 285 billion bacteria are found per ounce of tubeworm tissue. Tubeworms have red plumes which contain hemoglobin. Hemoglobin combines with hydrogen sulfide and transfers it to the bacteria living inside the worm. In return, the bacteria nourish the worm with carbon compounds. Two of the species that inhabit a hydrothermal vent are Tevnia jerichonana, and Riftia pachyptila. One discovered community, dubbed "Eel City", consists predominantly of the eel Dysommina rugosa. Though eels are not uncommon, invertebrates typically dominate hydrothermal vents. Eel City is located near Nafanua volcanic cone, American Samoa.
In 1993, already more than 100 gastropod species were known to occur in hydrothermal vents. Over 300 new species have been discovered at hydrothermal vents, many of them "sister species" to others found in geographically separated vent areas. It has been proposed that before the North American plate overrode the mid-ocean ridge, there was a single biogeographic vent region found in the eastern Pacific. The subsequent barrier to travel began the evolutionary divergence of species in different locations. The examples of convergent evolution seen between distinct hydrothermal vents is seen as major support for the theory of natural selection and of evolution as a whole.
Although life is very sparse at these depths, black smokers are the centers of entire ecosystems. Sunlight is nonexistent, so many organisms – such as archaea and extremophiles – convert the heat, methane, and sulfur compounds provided by black smokers into energy through a process called chemosynthesis. More complex life forms, such as clams and tubeworms, feed on these organisms. The organisms at the base of the food chain also deposit minerals into the base of the black smoker, therefore completing the life cycle.
A species of phototrophic bacterium has been found living near a black smoker off the coast of Mexico at a depth of 2,500 m (8,200 ft). No sunlight penetrates that far into the waters. Instead, the bacteria, part of the Chlorobiaceae family, use the faint glow from the black smoker for photosynthesis. This is the first organism discovered in nature to exclusively use a light other than sunlight for photosynthesis.
New and unusual species are constantly being discovered in the neighborhood of black smokers. The Pompeii worm Alvinella pompejana, which is capable of withstanding temperatures up to 80 °C (176 °F), was found in the 1980s, and a scaly-foot gastropod Chrysomallon squamiferum in 2001 during an expedition to the Indian Ocean's Kairei hydrothermal vent field. The latter uses iron sulfides (pyrite and greigite) for the structure of its dermal sclerites (hardened body parts), instead of calcium carbonate. The extreme pressure of 2500 m of water (approximately 25 megapascals or 250 atmospheres) is thought to play a role in stabilizing iron sulfide for biological purposes. This armor plating probably serves as a defense against the venomous radula (teeth) of predatory snails in that community.
In March 2017, researchers reported evidence of possibly the oldest forms of life on Earth. Putative fossilized microorganisms were discovered in hydrothermal vent precipitates in the Nuvvuagittuq Belt of Quebec, Canada, that may have lived as early as 4.280 billion years ago, not long after the oceans formed 4.4 billion years ago, and not long after the formation of the Earth 4.54 billion years ago.
Hydrothermal vent ecosystems have enormous biomass and productivity; but this rests on the symbiotic relationships that have evolved at vents. Deep-sea hydrothermal vent ecosystems differ from their shallow-water and terrestrial hydrothermal counterparts due to the symbiosis that occurs between macro invertebrate hosts and chemoautotrophic microbial symbionts in the former. Since sunlight does not reach deep-sea hydrothermal vents, organisms in deep-sea hydrothermal vents cannot obtain energy from the sun to perform photosynthesis. Instead, the microbial life found at hydrothermal vents are chemosynthetic; they fix carbon by using energy from chemicals such as sulfide, as opposed to light energy from the sun. In other words, the symbiont converts inorganic molecules (H2S, CO2, O) to organic molecules that the host then uses as nutrition. However, sulfide is an extremely toxic substance to most life on Earth. For this reason, scientists were astounded when they first found hydrothermal vents teeming with life in 1977. What was discovered was the ubiquitous symbiosis of chemoautotrophs living in (endosymbiosis) the vent animals’ gills; the reason why multicellular life is capable to survive the toxicity of vent systems. Scientists are therefore now studying how the microbial symbionts aid in sulfide detoxification (therefore allowing the host to survive the otherwise toxic conditions). Work on microbiome function shows that host-associated microbiomes are also important in host development, nutrition, defense against predators, and detoxification. In return, the host provides the symbiont with chemicals required for chemosynthesis, such as carbon, sulfide, and oxygen.
In the early stages of studying life at hydrothermal vents, there were differing theories regarding the mechanisms by which multicellular organisms were able to acquire nutrients from these environments, and how they were able to survive in such extreme conditions. In 1977, it was hypothesized that the chemoautotrophic bacteria at hydrothermal vents might be responsible for contributing to the diet of suspension feeding bivalves.
Finally, in 1981, it was understood that giant tubeworm nutrition acquisition occurred as a result of chemoautotrophic bacterial endosymbionts. As scientists continued to study life at hydrothermal vents, it was understood that symbiotic relationships between chemoautotrophs and macrofauna invertebrate species was ubiquitous. For instance, in 1983, clam gill tissue was confirmed to contain bacterial endosymbionts; in 1984 vent bathymodiolid mussels and vesicomyid clams were also found to carry endosymbionts.
However, the mechanisms by which organisms acquire their symbionts differ, as do the metabolic relationships. For instance, tubeworms have no mouth and no gut, but they do have a "trophosome", which is where they deal with nutrition and where their endosymbionts are found. They also have a bright red plume, which they use to uptake compounds such as O, H2S, and CO2, which feed the endosymbionts in their trophosome. Remarkably, the tubeworms hemoglobin (which incidentally is the reason for the bright red color of the plume) is capable of carrying oxygen without interference or inhibition from sulfide, despite the fact that oxygen and sulfide are typically very reactive. In 2005, it was discovered that this is possible due to zinc ions that bind the hydrogen sulfide in the tubeworms hemoglobin, therefore preventing the sulfide from reacting with the oxygen. It also reduces the tubeworms tissue from exposure to the sulfide and provides the bacteria with the sulfide to perform chemoautotrophy. It has also been discovered that tubeworms can metabolize CO2 in two different ways, and can alternate between the two as needed as environmental conditions change.
In 1988, research confirmed thiotrophic (sulfide-oxidizing) bacteria in Alvinochonca hessleri, a large vent mollusk. In order to circumvent the toxicity of sulfide, mussels first convert it to thiosulfate before carrying it over to the symbionts. In the case of motile organisms such as alvinocarid shrimp, they must track oxic (oxygen-rich) / anoxic (oxygen-poor) environments as they fluctuate in the environment.
Organisms living at the edge of hydrothermal vent fields, such as pectinid scallops, also carry endosymbionts in their gills, and as a result their bacterial density is low relative to organisms living nearer to the vent. However, the scallop's dependence on the microbial endosymbiont for obtaining their nutrition is therefore also lessened.
Furthermore, not all host animals have endosymbionts; some have episymbionts—symbionts living on the animal as opposed to inside the animal. Shrimp found at vents in the Mid-Atlantic Ridge were once thought of as an exception to the necessity of symbiosis for macroinvertebrate survival at vents. That changed in 1988 when they were discovered to carry episymbionts. Since then, other organisms at vents have been found to carry episymbionts as well, such as Lepetodrilis fucensis.
Furthermore, while some symbionts reduce sulfur compounds, others are known as "methanotrophs" and reduce carbon compounds, namely methane. Bathmodiolid mussels are an example of a host that contains methanotrophic endosymbionts; however, the latter mostly occur in cold seeps as opposed to hydrothermal vents.
While chemosynthesis occurring at the deep ocean allows organisms to live without sunlight in the immediate sense, they technically still rely on the sun for survival, since oxygen in the ocean is a byproduct of photosynthesis. However, if the sun were to suddenly disappear and photosynthesis ceased to occur on our planet, life at the deep-sea hydrothermal vents could continue for millennia (until the oxygen was depleted).
The Deep Hot Biosphere
At the beginning of his 1992 paper The Deep Hot Biosphere, Thomas Gold referred to ocean vents in support of his theory that the lower levels of the earth are rich in living biological material that finds its way to the surface. He further expanded his ideas in the book The Deep Hot Biosphere.
An article on abiogenic hydrocarbon production in the February 2008 issue of Science journal used data from experiments at the Lost City hydrothermal field to report how the abiotic synthesis of low molecular mass hydrocarbons from mantle derived carbon dioxide may occur in the presence of ultramafic rocks, water, and moderate amounts of heat.
Hydrothermal origin of life
The chemical and thermal dynamics in hydrothermal vents makes such environments highly suitable thermodynamically for chemical evolution processes to take place. Therefore, thermal energy flux is a permanent agent and contributed to the evolution of the planet, including prebiotic chemistry.
Günter Wächtershäuser proposed the iron-sulfur world theory and suggested that life might have originated at hydrothermal vents. Wächtershäuser proposed that an early form of metabolism predated genetics. By metabolism he meant a cycle of chemical reactions that release energy in a form that can be harnessed by other processes.
It has been proposed that amino acid synthesis could have occurred deep in the Earth's crust and that these amino acids were subsequently shot up along with hydrothermal fluids into cooler waters, where lower temperatures and the presence of clay minerals would have fostered the formation of peptides and protocells. This is an attractive hypothesis because of the abundance of CH4 (methane) and NH3 (ammonia) present in hydrothermal vent regions, a condition that was not provided by the Earth's primitive atmosphere. A major limitation to this hypothesis is the lack of stability of organic molecules at high temperatures, but some have suggested that life would have originated outside of the zones of highest temperature. There are numerous species of extremophiles and other organisms currently living immediately around deep-sea vents, suggesting that this is indeed a possible scenario.
Experimental research and computing modeling indicate that the surfaces of mineral particles inside hydrothermal vents have similar catalytic properties to enzymes and are able to create simple organic molecules, such as methanol (CH3OH) and formic acid (HCO2H), out of the dissolved CO2 in the water.
Discovery and exploration
In 1949, a deep water survey reported anomalously hot brines in the central portion of the Red Sea. Later work in the 1960s confirmed the presence of hot, 60 °C (140 °F), saline brines and associated metalliferous muds. The hot solutions were emanating from an active subseafloor rift. The highly saline character of the waters was not hospitable to living organisms. The brines and associated muds are currently under investigation as a source of mineable precious and base metals.
In June 1976, scientists from the Scripps Institution of Oceanography obtained the first evidence for submarine hydrothermal vents along the Galápagos Rift, a spur of the East Pacific Rise, on the Pleiades II expedition, using the Deep-Tow seafloor imaging system. In 1977, the first scientific papers on hydrothermal vents were published by scientists from the Scripps Institution of Oceanography; research scientist Peter Lonsdale published photographs taken from deep-towed cameras, and PhD student Kathleen Crane published maps and temperature anomaly data. Transponders were deployed at the site, which was nicknamed "Clam-bake", to enable an expedition to return the following year for direct observations with the DSV ALVIN.
Chemosynthetic ecosystems surrounding the Galápagos Rift submarine hydrothermal vents were first directly observed in 1977, when a group of marine geologists funded by the National Science Foundation returned to the Clambake sites. The principal investigator for the submersible study was Jack Corliss of Oregon State University. Corliss and Tjeerd van Andel from Stanford University observed and sampled the vents and their ecosystem on February 17, 1977, while diving in the DSV ALVIN, a research submersible operated by the Woods Hole Oceanographic Institution (WHOI). Other scientists on the research cruise included Richard (Dick) Von Herzen and Robert Ballard of WHOI, Jack Dymond and Louis Gordon of Oregon State University, John Edmond and Tanya Atwater of the Massachusetts Institute of Technology, Dave Williams of the U.S. Geological Survey, and Kathleen Crane of Scripps Institution of Oceanography. This team published their observations of the vents, organisms, and the composition of the vent fluids in the journal Science. In 1979, a team of biologists led by J. Frederick Grassle, at the time at WHOI, returned to the same location to investigate the biological communities discovered two year earlier.
High temperature hydrothermal vents, the "black smokers", were discovered in spring 1979 by a team from the Scripps Institution of Oceanography using the submersible ALVIN. The RISE expedition explored the East Pacific Rise at 21° N with the goals of testing geophysical mapping of the sea floor with the ALVIN and finding another hydrothermal field beyond the Galápagos Rift vents. The expedition was led by Fred Spiess and Ken Macdonald and included participants from the U.S., Mexico and France. The dive region was selected based on the discovery of sea floor mounds of sulfide minerals by the French CYAMEX expedition in 1978. Prior to dive operations, expedition member Robert Ballard located near-bottom water temperature anomalies using a deeply towed instrument package. The first dive was targeted at one of those anomalies. On Easter Sunday April 15, 1979 during a dive of ALVIN to 2600 meters, Roger Larson and Bruce Luyendyk found a hydrothermal vent field with a biological community similar to the Galápagos vents. On a subsequent dive on April 21, William Normark and Thierry Juteau discovered the high temperature vents emitting black mineral particle jets from chimneys; the black smokers.(WHOI website) Following this Macdonald and Jim Aiken rigged a temperature probe to ALVIN to measure the water temperature at the black smoker vents. This observed the highest temperatures then recorded at deep sea hydrothermal vents (380±30 °C). Analysis of black smoker material and the chimneys that fed them revealed that iron sulfide precipitates are the common minerals in the "smoke" and walls of the chimneys.
In 2005, Neptune Resources NL, a mineral exploration company, applied for and was granted 35,000 km² of exploration rights over the Kermadec Arc in New Zealand's Exclusive Economic Zone to explore for seafloor massive sulfide deposits, a potential new source of lead-zinc-copper sulfides formed from modern hydrothermal vent fields. The discovery of a vent in the Pacific Ocean offshore of Costa Rica, named the Medusa hydrothermal vent field (after the serpent-haired Medusa of Greek mythology), was announced in April 2007. The Ashadze hydrothermal field (13°N on the Mid-Atlantic Ridge, elevation -4200 m) was the deepest known high-temperature hydrothermal field until 2010, when a hydrothermal plume emanating from the Beebe site ( , elevation -5000 m) was detected by a group of scientists from NASA Jet Propulsion Laboratory and Woods Hole Oceanographic Institution. This site is located on the 110 km long, ultraslow spreading Mid-Cayman Rise within the Cayman Trough. In early 2013, the deepest known hydrothermal vents were discovered in the Caribbean at a depth of almost 5,000 metres (16,000 ft).
Hydrothermal vents and other geothermal manifestations are currently being explored in the Bahía de Concepción, Baja California Sur, Mexico.
Hydrothermal vents tend to be distributed along the Earth's plate boundaries, although they may also be found at intra-plate locations such as hotspot volcanoes. As of 2009 there were approximately 500 known active submarine hydrothermal vent fields, with about half visually observed at the seafloor and the other half suspected from water column indicators and/or seafloor deposits. The InterRidge program office hosts a global database for the locations of known active submarine hydrothermal vent fields.
- Mid-Atlantic Ridge province,
- East Scotia Ridge province,
- northern East Pacific Rise province,
- central East Pacific Rise province,
- southern East Pacific Rise province,
- south of the Easter Microplate,
- Indian Ocean province,
- four provinces in the western Pacific.
Hydrothermal vents, in some instances, have led to the formation of exploitable mineral resources via deposition of seafloor massive sulfide deposits. The Mount Isa orebody located in Queensland, Australia, is an excellent example. Many hydrothermal vents are rich in cobalt, gold, copper, and rare earth metals essential for electronic components. Hydrothermal venting on the Archean seafloor is considered to have formed Algoma-type banded iron formations which have been a source of iron ore.
Recently, mineral exploration companies, driven by the elevated price activity in the base metals sector during the mid-2000s, have turned their attention to extraction of mineral resources from hydrothermal fields on the seafloor. Significant cost reductions are, in theory, possible.
In countries such as Japan where mineral resources are primarily derived from international imports, there is a particular push for the extraction of seafloor mineral resources. The world's first "large-scale" mining of hydrothermal vent mineral deposits was carried out by Japan Oil, Gas and Metals National Corporation (JOGMEC) in August - September, 2017. JOGMEC carried out this operation using the Research Vessel Hakurei. This mining was carried out at the 'Izena hole/cauldron' vent field within the hydrothermally active back-arc basin known as the Okinawa Trough which contains 15 confirmed vent fields according to the InterRidge Vents Database.
Two companies are currently engaged in the late stages of commencing to mine seafloor massive sulfides. Nautilus Minerals is in the advanced stages of commencing extraction from its Solwarra deposit, in the Bismarck Archipelago, and Neptune Minerals is at an earlier stage with its Rumble II West deposit, located on the Kermadec Arc, near the Kermadec Islands. Both companies are proposing using modified existing technology. Nautilus Minerals, in partnership with Placer Dome (now part of Barrick Gold), succeeded in 2006 in returning over 10 metric tons of mined SMS to the surface using modified drum cutters mounted on an ROV, a world first. Neptune Minerals in 2007 succeeded in recovering SMS sediment samples using a modified oil industry suction pump mounted on an ROV, also a world first.
Potential seafloor mining has environmental impacts including dust plumes from mining machinery affecting filter-feeding organisms, collapsing or reopening vents, methane clathrate release, or even sub-oceanic land slides. A large amount of work is currently being engaged in by both the above-mentioned companies to ensure that potential environmental impacts of seafloor mining are well understood and control measures are implemented, before exploitation commences. However, this process has been arguably hindered by the disproportionate distribution of research effort among vent ecosystems: the best studied and understood hydrothermal vent ecosystems are not representative of those targeted for mining.
Attempts have been made in the past to exploit minerals from the seafloor. The 1960s and 70s saw a great deal of activity (and expenditure) in the recovery of manganese nodules from the abyssal plains, with varying degrees of success. This does demonstrate however that recovery of minerals from the seafloor is possible, and has been possible for some time. Mining of manganese nodules served as a cover story for the elaborate attempt in 1974 by the CIA to raise the sunken Soviet submarine K-129, using the Glomar Explorer, a ship purpose built for the task by Howard Hughes. The operation was known as Project Azorian, and the cover story of seafloor mining of manganese nodules may have served as the impetus to propel other companies to make the attempt.
The conservation of hydrothermal vents has been the subject of sometimes heated discussion in the oceanographic community for the last 20 years. It has been pointed out that it may be that those causing the most damage to these fairly rare habitats are scientists. There have been attempts to forge agreements over the behaviour of scientists investigating vent sites but although there is an agreed code of practice there is as yet no formal international and legally binding agreement.
- Brine pool
- Endeavour Hydrothermal Vents
- Magic Mountain (hydrothermal field)
- 9° North
- Origin of life
- Pito Seamount
- Submarine volcano
- VMS deposit
- Colín-García, María (2016). "Hydrothermal vents and prebiotic chemistry: a review". Boletín de la Sociedad Geológica Mexicana. 68 (3): 599–620. doi:10.18268/BSGM2016v68n3a13.
- Chang, Kenneth (13 April 2017). "Conditions for Life Detected on Saturn Moon Enceladus". New York Times. Retrieved 14 April 2017.
- "Spacecraft Data Suggest Saturn Moon's Ocean May Harbor Hydrothermal Activity". NASA. 11 March 2015. Retrieved 12 March 2015.
- Paine, M. (15 May 2001). "Mars Explorers to Benefit from Australian Research". Space.com. Archived from the original on 21 February 2006.
- Garcia, Elena Guijarro; Ragnarsson, Stefán Akí; Steingrimsson, Sigmar Arnar; Nævestad, Dag; Haraldsson, Haukur; Fosså, Jan Helge; Tendal, Ole Secher; Eiríksson, Hrafnkell (2007). Bottom trawling and scallop dredging in the Arctic: Impacts of fishing on non-target species, vulnerable habitats and cultural heritage. Nordic Council of Ministers. p. 278. ISBN 978-92-893-1332-2.
- Haase, K. M.; et al. (2007). "Young volcanism and related hydrothermal activity at 5°S on the slow-spreading southern Mid-Atlantic Ridge". Geochemistry Geophysics Geosystems. 8 (11): Q11002. Bibcode:2007GGG.....811002H. doi:10.1029/2006GC001509.
- Haase, K. M.; et al. (2009). "Fluid compositions and mineralogy of precipitates from Mid Atlantic Ridge hydrothermal vents at 4°48'S". Pangaea. doi:10.1594/PANGAEA.727454.
- Bischoff, James L; Rosenbauer, Robert J (1988). "Liquid-vapor relations in the critical region of the system NaCl-H2O from 380 to 415°C: A refined determination of the critical point and two-phase boundary of seawater". Geochimica et Cosmochimica Acta (Submitted manuscript). 52 (8): 2121–2126. Bibcode:1988GeCoA..52.2121B. doi:10.1016/0016-7037(88)90192-5.
- Von Damm, K L (1990). "Seafloor Hydrothermal Activity: Black Smoker Chemistry and Chimneys". Annual Review of Earth and Planetary Sciences (Submitted manuscript). 18 (1): 173–204. Bibcode:1990AREPS..18..173V. doi:10.1146/annurev.ea.18.050190.001133.
- Webber, A.P.; Murton, B.; Roberts, S.; Hodgkinson, M. "Supercritical Venting and VMS Formation at the Beebe Hydrothermal Field, Cayman Spreading Centre". Goldschmidt Conference Abstracts 2014. Geochemical Society. Retrieved 29 July 2014.
- Tivey, M. K. (1 December 1998). "How to Build a Black Smoker Chimney: The Formation of Mineral Deposits At Mid-Ocean Ridges". Woods Hole Oceanographic Institution. Retrieved 2006-07-07.
- Petkewich, Rachel (September 2008). "Tracking ocean iron". Chemical & Engineering News. 86 (35): 62–63. doi:10.1021/cen-v086n035.p062.
- Perkins, S. (2001). "New type of hydrothermal vent looms large". Science News. 160 (2): 21. doi:10.2307/4012715. JSTOR 4012715.
- Kelley, Deborah S. "Black Smokers: Incubators on the Seafloor" (PDF). p. 2.
- Douville, E; Charlou, J.L; Oelkers, E.H; Bienvenu, P; Jove Colon, C.F; Donval, J.P; Fouquet, Y; Prieur, D; Appriou, P (March 2002). "The rainbow vent fluids (36°14′N, MAR): the influence of ultramafic rocks and phase separation on trace metal content in Mid-Atlantic Ridge hydrothermal fluids". Chemical Geology. 184 (1–2): 37–48. Bibcode:2002ChGeo.184...37D. doi:10.1016/S0009-2541(01)00351-5.
- Spiess, F. N.; Macdonald, K. C.; Atwater, T.; Ballard, R.; Carranza, A.; Cordoba, D.; Cox, C.; Garcia, V. M. D.; Francheteau, J.; Guerrero, J.; Hawkins, J.; Haymon, R.; Hessler, R.; Juteau, T.; Kastner, M.; Larson, R.; Luyendyk, B.; Macdougall, J. D.; Miller, S.; Normark, W.; Orcutt, J.; Rangin, C. (28 March 1980). "East Pacific Rise: Hot Springs and Geophysical Experiments". Science. 207 (4438): 1421–1433. Bibcode:1980Sci...207.1421S. doi:10.1126/science.207.4438.1421. PMID 17779602.
- "Boiling Hot Water Found in Frigid Arctic Sea". LiveScience. 24 July 2008. Retrieved 2008-07-25.
- "Scientists Break Record By Finding Northernmost Hydrothermal Vent Field". Science Daily. 24 July 2008. Retrieved 2008-07-25.
- Cross, A. (12 April 2010). "World's deepest undersea vents discovered in Caribbean". BBC News. Retrieved 2010-04-13.
- "Extremes of Eel City". Astrobiology Magazine. 28 May 2008. Retrieved 2007-08-30.
- Sysoev, A. V.; Kantor, Yu. I. (1995). "Two new species of Phymorhynchus (Gastropoda, Conoidea, Conidae) from the hydrothermal vents" (PDF). Ruthenica. 5: 17–26.
- Botos, S. "Life on a hydrothermal vent". Hydrothermal Vent Communities.
- Van Dover, C. L. "Hot Topics: Biogeography of deep-sea hydrothermal vent faunas". Woods Hole Oceanographic Institution.
- Beatty, J.T.; et al. (2005). "An obligately photosynthetic bacterial anaerobe from a deep-sea hydrothermal vent". Proceedings of the National Academy of Sciences. 102 (26): 9306–10. Bibcode:2005PNAS..102.9306B. doi:10.1073/pnas.0503674102. PMC 1166624. PMID 15967984.
- Dodd, Matthew S.; Papineau, Dominic; Grenne, Tor; Slack, John F.; Rittner, Martin; Pirajno, Franco; O’Neil, Jonathan; Little, Crispin T. S. (2 March 2017). "Evidence for early life in Earth's oldest hydrothermal vent precipitates" (PDF). Nature. 543 (7643): 60–64. Bibcode:2017Natur.543...60D. doi:10.1038/nature21377. PMID 28252057.
- Zimmer, Carl (1 March 2017). "Scientists Say Canadian Bacteria Fossils May Be Earth's Oldest". New York Times. Retrieved 2 March 2017.
- Ghosh, Pallab (1 March 2017). "Earliest evidence of life on Earth 'found'". BBC News. Retrieved 2 March 2017.
- Van Dover 2000[full citation needed]
- Lonsdale, Peter (1977). "Clustering of suspension-feeding macrobenthos near abyssal hydrothermal vents at oceanic spreading centers". Deep Sea Research. 24 (9): 857–863. Bibcode:1977DSR....24..857L. doi:10.1016/0146-6291(77)90478-7.
- Cavanaug eta al 1981[full citation needed]
- Felback 1981[full citation needed]
- Rau 1981[full citation needed]
- Cavanaugh 1983[full citation needed]
- Fiala-Médioni, A. (1984). "Ultrastructural evidence of abundance of intracellular symbiotic bacteria in the gill of bivalve molluscs of deep hydrothermal vents". Comptes rendus de l'Académie des Sciences. 298 (17): 487–492.
- Le Pennec, M.; Hily, A. (1984). "Anatomie, structure et ultrastructure de la branchie d'un Mytilidae des sites hydrothermaux du Pacifique oriental" [Anatomy, structure and ultrastructure of the gill of a Mytilidae of the hydrothermal sites of the eastern Pacific]. Oceanologica Acta (in French). 7 (4): 517–523.
- Flores, J. F.; Fisher, C. R.; Carney, S. L.; Green, B. N.; Freytag, J. K.; Schaeffer, S. W.; Royer, W. E. (2005). "Sulfide binding is mediated by zinc ions discovered in the crystal structure of a hydrothermal vent tubeworm hemoglobin". Proceedings of the National Academy of Sciences. 102 (8): 2713–2718. Bibcode:2005PNAS..102.2713F. doi:10.1073/pnas.0407455102. PMC 549462. PMID 15710902.
- Thiel, Vera; Hügler, Michael; Blümel, Martina; Baumann, Heike I.; Gärtner, Andrea; Schmaljohann, Rolf; Strauss, Harald; Garbe-Schönberg, Dieter; Petersen, Sven; Cowart, Dominique A.; Fisher, Charles R.; Imhoff, Johannes F. (2012). "Widespread Occurrence of Two Carbon Fixation Pathways in Tubeworm Endosymbionts: Lessons from Hydrothermal Vent Associated Tubeworms from the Mediterranean Sea". Frontiers in Microbiology. 3: 423. doi:10.3389/fmicb.2012.00423. PMC 3522073. PMID 23248622.
- Stein et al 1988[full citation needed]
- Biology of the Deep Sea, Peter Herring[full citation needed]
- Van Dover et al 1988[full citation needed]
- Desbruyeres et al 1985[full citation needed]
- de Burgh, M. E.; Singla, C. L. (December 1984). "Bacterial colonization and endocytosis on the gill of a new limpet species from a hydrothermal vent". Marine Biology. 84 (1): 1–6. doi:10.1007/BF00394520.
- Gold, T. (1992). "The Deep Hot Biosphere". Proceedings of the National Academy of Sciences. 89 (13): 6045–9. Bibcode:1992PNAS...89.6045G. doi:10.1073/pnas.89.13.6045. PMC 49434. PMID 1631089.
- Gold, T. (1999). The Deep Hot Biosphere. Springer. ISBN 978-0-387-95253-6.
- Proskurowski, G.; Lilley, M. D.; Seewald, J. S.; Fru h-Green, G. L.; Olson, E. J.; Lupton, J. E.; Sylva, S. P.; Kelley, D. S. (1 February 2008). "Abiogenic Hydrocarbon Production at Lost City Hydrothermal Field". Science. 319 (5863): 604–607. doi:10.1126/science.1151194. PMID 18239121.
- Wachtershauser, G. (1 January 1990). "Evolution of the first metabolic cycles". Proceedings of the National Academy of Sciences. 87 (1): 200–204. Bibcode:1990PNAS...87..200W. doi:10.1073/pnas.87.1.200. PMC 53229. PMID 2296579.
- Tunnicliffe, V. (1991). "The Biology of Hydrothermal Vents: Ecology and Evolution". Oceanography and Marine Biology: An Annual Review. 29: 319–408.
- Chandru, Kuhan; Imai, EiIchi; Kaneko, Takeo; Obayashi, Yumiko; Kobayashi, Kensei (2013). "Survivability and Abiotic Reactions of Selected Amino Acids in Different Hydrothermal System Simulators". Origins of Life and Biosphere. 43 (2): 99–108. Bibcode:2013OLEB...43...99C. doi:10.1007/s11084-013-9330-9. PMID 23625039.
- Chemistry of seabed’s hot vents could explain emergence of life. Astrobiology Magazine 27 April 2015.
- Roldan, A.; Hollingsworth, N.; Roffey, A.; Islam, H.-U.; Goodall, J. B. M.; Catlow, C. R. A.; Darr, J. A.; Bras, W.; Sankar, G.; Holt, K. B.; Hogartha, G.; de Leeuw, N. H. (24 March 2015). "Bio-inspired CO2 conversion by iron sulfide catalysts under sustainable conditions" (PDF). Chemical Communications. 51 (35): 7501–7504. doi:10.1039/C5CC02078F. PMID 25835242.
- Aubrey, A. D.; Cleaves, H.J; Bada, J.L (2008). "The Role of Submarine Hydrothermal Systems in the Synthesis of Amino Acids". Origins of Life and Biosphere. 39 (2): 91–108. Bibcode:2009OLEB...39...91A. doi:10.1007/s11084-008-9153-2. PMID 19034685.
- Joseph F. Sutherland: on The Origin Of Tha Bacteria And The Archaea, auf B.C vom 16. August 2014
- Nick Lane: The Vital Question - Energy, Evolution, and the Origins of Complex Life, Ww Norton, 2015-07-20, ISBN 978-0-393-08881-6, PDF
- Hannington, M.D. (2014). "Volcanogenic Massive Sulfide Deposits". Treatise on Geochemistry. pp. 463–488. doi:10.1016/B978-0-08-095975-7.01120-7. ISBN 978-0-08-098300-4.
- Degens, E. T. (1969). Hot Brines and Recent Heavy Metal Deposits in the Red Sea. Springer-Verlag.[page needed]
- Kathleen., Crane (2003). Sea legs : tales of a woman oceanographer. Boulder, Colo.: Westview Press. ISBN 9780813342856. OCLC 51553643.[page needed]
- "What is a hydrothermal vent?". National Ocean Service. National Oceanic and Atmospheric Administration. Retrieved 10 April 2018.
- Lonsdale, P. (1977). "Clustering of suspension-feeding macrobenthos near abyssal hydrothermal vents at oceanic spreading centers". Deep-Sea Research. 24 (9): 857–863. Bibcode:1977DSR....24..857L. doi:10.1016/0146-6291(77)90478-7.
- Crane, Kathleen; Normark, William R. (10 November 1977). "Hydrothermal activity and crestal structure of the East Pacific Rise at 21°N". Journal of Geophysical Research. 82 (33): 5336–5348. Bibcode:1977JGR....82.5336C. doi:10.1029/jb082i033p05336.
- "Dive and Discover: Expeditions to the Seafloor". www.divediscover.whoi.edu. Retrieved 2016-01-04.
- Davis, Rebecca; Joyce, Christopher (December 5, 2011). "The Deep-Sea Find That Changed Biology". NPR.org. Retrieved 2018-04-09.
- Corliss, John B.; Dymond, Jack; Gordon, Louis I.; Edmond, John M.; von Herzen, Richard P.; Ballard, Robert D.; Green, Kenneth; Williams, David; Bainbridge, Arnold; Crane, Kathy; van Andel, Tjeerd H. (16 March 1979). "Submarine Thermal Springs on the Galápagos Rift". Science. 203 (4385): 1073–1083. Bibcode:1979Sci...203.1073C. doi:10.1126/science.203.4385.1073. PMID 17776033.
- Francheteau, J (1979). "Massive deep-sea sulphide ore deposits discovered on the East Pacific Rise" (PDF). Nature. 277 (5697): 523. Bibcode:1979Natur.277..523F. doi:10.1038/277523a0.
- Macdonald, K. C.; Becker, Keir; Spiess, F. N.; Ballard, R. D. (1980). "Hydrothermal heat flux of the "black smoker" vents on the East Pacific Rise". Earth and Planetary Science Letters. 48 (1): 1–7. Bibcode:1980E&PSL..48....1M. doi:10.1016/0012-821X(80)90163-6.
- Haymon, Rachel M.; Kastner, Miriam (1981). "Hot spring deposits on the East Pacific Rise at 21°N: preliminary description of mineralogy and genesis". Earth and Planetary Science Letters. 53 (3): 363–381. Bibcode:1981E&PSL..53..363H. doi:10.1016/0012-821X(81)90041-8.
- "New undersea vent suggests snake-headed mythology" (Press release). EurekAlert!. 18 April 2007. Retrieved 2007-04-18.
- "Beebe". Interridge Vents Database.
- German, C. R.; et al. (2010). "Diverse styles of submarine venting on the ultraslow spreading Mid-Cayman Rise" (PDF). Proceedings of the National Academy of Sciences. 107 (32): 14020–5. Bibcode:2010PNAS..10714020G. doi:10.1073/pnas.1009205107. PMC 2922602. PMID 20660317. Retrieved 2010-12-31. Lay summary – SciGuru (11 October 2010).
- Shukman, David (21 February 2013). "Deepest undersea vents discovered by UK team". BBC News. Retrieved 21 February 2013.
- Broad, William J. (2016-01-12). "The 40,000-Mile Volcano". The New York Times. ISSN 0362-4331. Retrieved 2016-01-17.
- Leal-Acosta, María Luisa; Prol-Ledesma, Rosa María (2016). "Caracterización geoquímica de las manifestaciones termales intermareales de Bahía Concepción en la Península de Baja California" [Geochemical characterization of the intertidal thermal manifestations of Concepción Bay in the Baja California Peninsula]. Boletín de la Sociedad Geológica Mexicana (in Spanish). 68 (3): 395–407. doi:10.18268/bsgm2016v68n3a2. JSTOR 24921551.
- Beaulieu, Stace E.; Baker, Edward T.; German, Christopher R.; Maffei, Andrew (November 2013). "An authoritative global database for active submarine hydrothermal vent fields". Geochemistry, Geophysics, Geosystems. 14 (11): 4892–4905. Bibcode:2013GGG....14.4892B. doi:10.1002/2013GC004998.
- Rogers, Alex D.; Tyler, Paul A.; Connelly, Douglas P.; Copley, Jon T.; James, Rachael; Larter, Robert D.; Linse, Katrin; Mills, Rachel A.; Garabato, Alfredo Naveira; Pancost, Richard D.; Pearce, David A.; Polunin, Nicholas V. C.; German, Christopher R.; Shank, Timothy; Boersch-Supan, Philipp H.; Alker, Belinda J.; Aquilina, Alfred; Bennett, Sarah A.; Clarke, Andrew; Dinley, Robert J. J.; Graham, Alastair G. C.; Green, Darryl R. H.; Hawkes, Jeffrey A.; Hepburn, Laura; Hilario, Ana; Huvenne, Veerle A. I.; Marsh, Leigh; Ramirez-Llodra, Eva; Reid, William D. K.; Roterman, Christopher N.; Sweeting, Christopher J.; Thatje, Sven; Zwirglmaier, Katrin; Eisen, Jonathan A. (3 January 2012). "The Discovery of New Deep-Sea Hydrothermal Vent Communities in the Southern Ocean and Implications for Biogeography". PLoS Biology. 10 (1): e1001234. doi:10.1371/journal.pbio.1001234. PMC 3250512. PMID 22235194.
- Perkins, W. G. (1 July 1984). "Mount Isa silica dolomite and copper orebodies; the result of a syntectonic hydrothermal alteration system". Economic Geology. 79 (4): 601–637. doi:10.2113/gsecongeo.79.4.601.
- We Are About to Start Mining Hydrothermal Vents on the Ocean Floor. Nautilus; Brandon Keim. 12 September 2015.
- Ginley, S.; Diekrup, D.; Hannington, M. (2014). "Categorizing mineralogy and geochemistry of Algoma type banded iron formation, Temagami, ON" (PDF). Retrieved 2017-11-14.
- "The dawn of deep ocean mining". The All I Need. 2006.
- Government of Canada, Global Affairs Canada (2017-01-23). "Mining Sector Market Overview 2016 – Japan". www.tradecommissioner.gc.ca. Retrieved 2019-03-11.
- "Liberating Japan's resources". The Japan Times. 25 June 2012.
- "Nautilus Outlines High Grade Au - Cu Seabed Sulphide Zone" (Press release). Nautilus Minerals. 25 May 2006. Archived from the original on 29 January 2009.
- "Neptune Minerals". Retrieved August 2, 2012.
- Birney, K.; et al. "Potential Deep-Sea Mining of Seafloor Massive Sulfides: A case study in Papua New Guinea" (PDF). University of California, Santa Barbara, B.
- "Treasures from the deep". Chemistry World. January 2007.
- Amon, Diva; Thaler, Andrew D. (2019-08-06). "262 Voyages Beneath the Sea: a global assessment of macro- and megafaunal biodiversity and research effort at deep-sea hydrothermal vents". PeerJ. 7: e7397. doi:10.7717/peerj.7397. ISSN 2167-8359.
- The secret on the ocean floor. David Shukman, BBC News. 19 February 2018.
- Devey, C.W.; Fisher, C.R.; Scott, S. (2007). "Responsible Science at Hydrothermal Vents" (PDF). Oceanography. 20 (1): 162–72. doi:10.5670/oceanog.2007.90. Archived from the original (PDF) on 2011-07-23.
- Johnson, M. (2005). "Oceans need protection from scientists too". Nature. 433 (7022): 105. Bibcode:2005Natur.433..105J. doi:10.1038/433105a. PMID 15650716.
- Johnson, M. (2005). "Deepsea vents should be world heritage sites". MPA News. 6: 10.
- Tyler, P.; German, C.; Tunnicliff, V. (2005). "Biologists do not pose a threat to deep-sea vents". Nature. 434 (7029): 18. Bibcode:2005Natur.434...18T. doi:10.1038/434018b. PMID 15744272.
- Haymon, R.M. (2014). "Hydrothermal Vents at Mid-Ocean Ridges". Reference Module in Earth Systems and Environmental Sciences. doi:10.1016/b978-0-12-409548-9.09050-3. ISBN 978-0-12-409548-9.
- Van Dover, C. L.; Humphris, SE; Fornari, D; Cavanaugh, CM; Collier, R; Goffredi, SK; Hashimoto, J; Lilley, MD; Reysenbach, AL; Shank, TM; Von Damm, KL; Banta, A; Gallant, RM; Gotz, D; Green, D; Hall, J; Harmer, TL; Hurtado, LA; Johnson, P; McKiness, ZP; Meredith, C; Olson, E; Pan, IL; Turnipseed, M; Won, Y; Young CR, 3rd; Vrijenhoek, RC (13 September 2001). "Biogeography and Ecological Setting of Indian Ocean Hydrothermal Vents". Science. 294 (5543): 818–823. Bibcode:2001Sci...294..818V. doi:10.1126/science.1064574. PMID 11557843.
- Van Dover; Cindy Lee (2000). The Ecology of Deep-Sea Hydrothermal Vents. Princeton University Press. ISBN 978-0-691-04929-8.
- Beatty, J. T.; Overmann, J.; Lince, M. T.; Manske, A. K.; Lang, A. S.; Blankenship, R. E.; Van Dover, C. L.; Martinson, T. A.; Plumley, F. G. (20 June 2005). "An obligately photosynthetic bacterial anaerobe from a deep-sea hydrothermal vent". Proceedings of the National Academy of Sciences. 102 (26): 9306–9310. Bibcode:2005PNAS..102.9306B. doi:10.1073/pnas.0503674102. PMC 1166624. PMID 15967984.
- Glyn Ford and Jonathan Simnett, Silver from the Sea, September/October 1982, Volume 33, Number 5, Saudi Aramco World Accessed 17 October 2005
- Ballard, Robert D., 2000, The Eternal Darkness, Princeton University Press.
- Csotonyi, J. T.; Stackebrandt, E.; Yurkov, V. (4 July 2006). "Anaerobic Respiration on Tellurate and Other Metalloids in Bacteria from Hydrothermal Vent Fields in the Eastern Pacific Ocean". Applied and Environmental Microbiology. 72 (7): 4950–4956. doi:10.1128/AEM.00223-06. PMC 1489322. PMID 16820492.
- Koschinsky, Andrea; Garbe-Schönberg, Dieter; Sander, Sylvia; Schmidt, Katja; Gennerich, Hans-Hermann; Strauss, Harald (2008). "Hydrothermal venting at pressure-temperature conditions above the critical point of seawater, 5°S on the Mid-Atlantic Ridge". Geology. 36 (8): 615. Bibcode:2008Geo....36..615K. doi:10.1130/G24726A.1.
- Catherine Brahic (4 August 2008). "Found: The hottest water on Earth". New Scientist. Retrieved 18 June 2010.
- Josh Hill (5 August 2008). "'Extreme Water' Found at Atlantic Ocean Abyss". The Daily Galaxy. Retrieved 18 June 2010.
|Wikimedia Commons has media related to Hydrothermal vents.|
|Scholia has a topic profile for Hydrothermal vent.|
- Ocean Explorer (www.oceanexplorer.noaa.gov) – Public outreach site for explorations sponsored by the Office of Ocean Exploration.
- What are hydrothermal vents & why are they important? From Woods Hole Oceanographic Institution
- Hydrothermal Vents - Interactive Module from Dive and Discover
- Hydrothermal vents video – The Smithsonian Institution's ocean portal
- Vent geochemistry
- A good overview of hydrothermal vent biology, published in 2006 (PDF)
- Images of hydrothermal vents in Indian Ocean – released by the National Science Foundation
- How to build a hydrothermal vent chimney
- NOAA, Ocean Explorer YouTube channel