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Friday, December 18, 2020

Coral reef

From Wikipedia, the free encyclopedia

Coral reefs are diverse underwater ecosystems held together by calcium carbonate structures secreted by corals. Coral reefs are built by colonies of tiny animals found in marine water that contain few nutrients. Most coral reefs are built from stony corals, which in turn consist of polyps that cluster in groups. The polyps belong to a group of animals known as Cnidaria, which also includes sea anemones and jellyfish. Unlike sea anemones, corals secrete hard carbonate exoskeletons which support and protect the coral polyps. Most reefs grow best in warm, shallow, clear, sunny and agitated water.

Often called "rainforests of the sea", shallow coral reefs form some of the most diverse ecosystems on Earth. They occupy less than 0.1% of the world's ocean surface, about half the area of France, yet they provide a home for at least 25% of all marine species, including fish, mollusks, worms, crustaceans, echinoderms, sponges, tunicates and other cnidarians. Paradoxically, coral reefs flourish even though they are surrounded by ocean waters that provide few nutrients. They are most commonly found at shallow depths in tropical waters, but deep water and cold water corals also exist on smaller scales in other areas.

Coral reefs deliver ecosystem services to tourism, fisheries and shoreline protection. The annual global economic value of coral reefs is estimated between US$30–375 billion. However, coral reefs are fragile ecosystems, partly because they are very sensitive to water temperature. They are under threat from climate change, oceanic acidification, blast fishing, cyanide fishing for aquarium fish, sunscreen use, overuse of reef resources, and harmful land-use practices, including urban and agricultural runoff and water pollution, which can harm reefs by encouraging excess algal growth.

Formation

Most of the coral reefs we can see today were formed after the last glacial period when melting ice caused the sea level to rise and flood the continental shelves. This means that most modern coral reefs are less than 10,000 years old. As communities established themselves on the shelves, the reefs grew upwards, pacing rising sea levels. Reefs that rose too slowly could become drowned reefs. They are covered by so much water that there was insufficient light. Coral reefs are found in the deep sea away from continental shelves, around oceanic islands and as atolls. The vast majority of these islands are volcanic in origin. The few exceptions have tectonic origins where plate movements have lifted the deep ocean floor on the surface. 


In 1842 in his first monograph, The Structure and Distribution of Coral Reefs, Charles Darwin set out his theory of the formation of atoll reefs, an idea he conceived during the voyage of the Beagle. He theorized uplift and subsidence of the Earth's crust under the oceans formed the atolls. Darwin’s theory sets out a sequence of three stages in atoll formation. It starts with a fringing reef forming around an extinct volcanic island as the island and ocean floor subsides. As the subsidence continues, the fringing reef becomes a barrier reef, and ultimately an atoll reef.

Darwin predicted that underneath each lagoon would be a bed rock base, the remains of the original volcano. Subsequent drilling proved this correct. Darwin's theory followed from his understanding that coral polyps thrive in the clean seas of the tropics where the water is agitated, but can only live within a limited depth range, starting just below low tide. Where the level of the underlying earth allows, the corals grow around the coast to form what he called fringing reefs, and can eventually grow out from the shore to become a barrier reef.
A fringing reef can take ten thousand years to form, and an atoll can take up to 30 million years.

Where the bottom is rising, fringing reefs can grow around the coast, but coral raised above sea level dies and becomes white limestone. If the land subsides slowly, the fringing reefs keep pace by growing upwards on a base of older, dead coral, forming a barrier reef enclosing a lagoon between the reef and the land. A barrier reef can encircle an island, and once the island sinks below sea level a roughly circular atoll of growing coral continues to keep up with the sea level, forming a central lagoon. Barrier reefs and atolls do not usually form complete circles, but are broken in places by storms. Like sea level rise, a rapidly subsiding bottom can overwhelm coral growth, killing the coral polyps and the reef, due to what is called coral drowning. Corals that rely on zooxanthellae can drown when the water becomes too deep for their symbionts to adequately photosynthesize, due to decreased light exposure.

The two main variables determining the geomorphology, or shape, of coral reefs are the nature of the underlying substrate on which they rest, and the history of the change in sea level relative to that substrate.

The approximately 20,000-year-old Great Barrier Reef offers an example of how coral reefs formed on continental shelves. Sea level was then 120 m (390 ft) lower than in the 21st century. As sea level rose, the water and the corals encroached on what had been hills of the Australian coastal plain. By 13,000 years ago, sea level had risen to 60 m (200 ft) lower than at present, and many hills of the coastal plains had become continental islands. As the sea level rise continued, water topped most of the continental islands. The corals could then overgrow the hills, forming the present cays and reefs. Sea level on the Great Barrier Reef has not changed significantly in the last 6,000 years, and the age of the modern living reef structure is estimated to be between 6,000 and 8,000 years. Although the Great Barrier Reef formed along a continental shelf, and not around a volcanic island, Darwin's principles apply. Development stopped at the barrier reef stage, since Australia is not about to submerge. It formed the world's largest barrier reef, 300–1,000 m (980–3,280 ft) from shore, stretching for 2,000 km (1,200 mi).

Healthy tropical coral reefs grow horizontally from 1 to 3 cm (0.39 to 1.18 in) per year, and grow vertically anywhere from 1 to 25 cm (0.39 to 9.84 in) per year; however, they grow only at depths shallower than 150 m (490 ft) because of their need for sunlight, and cannot grow above sea level.

Materials

As the name implies, the bulk of coral reefs is made up of coral skeletons from mostly intact coral colonies. As other chemical elements present in corals become incorporated into the calcium carbonate deposits, aragonite is formed. However, shell fragments and the remains of calcareous algae such as the green-segmented genus Halimeda can add to the reef's ability to withstand damage from storms and other threats. Such mixtures are visible in structures such as Eniwetok Atoll.

Types

The three principal reef types are:
  • Fringing reef – directly attached to a shore, or borders it with an intervening shallow channel or lagoon
  • Barrier reef – reef separated from a mainland or island shore by a deep channel or lagoon
  • Atoll reef – more or less circular or continuous barrier reef extends all the way around a lagoon without a central island
A small atoll in the Maldives
 
Inhabited cay in the Maldives
Other reef types or variants are:
  • Patch reef – common, isolated, comparatively small reef outcrop, usually within a lagoon or embayment, often circular and surrounded by sand or seagrass
  • Apron reef – short reef resembling a fringing reef, but more sloped; extending out and downward from a point or peninsular shore
  • Bank reef – linear or semicircular shaped-outline, larger than a patch reef
  • Ribbon reef – long, narrow, possibly winding reef, usually associated with an atoll lagoon
  • Table reef – isolated reef, approaching an atoll type, but without a lagoon
  • Habili – reef specific to the Red Sea; does not reach the surface near enough to cause visible surf; may be a hazard to ships (from the Arabic for "unborn")
  • Microatoll – community of species of corals; vertical growth limited by average tidal height; growth morphologies offer a low-resolution record of patterns of sea level change; fossilized remains can be dated using radioactive carbon dating and have been used to reconstruct Holocene sea levels
  • Cays – small, low-elevation, sandy islands formed on the surface of coral reefs from eroded material that piles up, forming an area above sea level; can be stabilized by plants to become habitable; occur in tropical environments throughout the Pacific, Atlantic and Indian Oceans (including the Caribbean and on the Great Barrier Reef and Belize Barrier Reef), where they provide habitable and agricultural land
  • Seamount or guyot – formed when a coral reef on a volcanic island subsides; tops of seamounts are rounded and guyots are flat; flat tops of guyots, or tablemounts, are due to erosion by waves, winds, and atmospheric processes

Zones

The three major zones of a coral reef: the fore reef, reef crest, and the back reef

Coral reef ecosystems contain distinct zones that represent different kinds of habitats. Usually, three major zones are recognized: the fore reef, reef crest, and the back reef (frequently referred to as the reef lagoon).

All three zones are physically and ecologically interconnected. Reef life and oceanic processes create opportunities for exchange of seawater, sediments, nutrients, and marine life among one another.

Thus, they are integrated components of the coral reef ecosystem, each playing a role in the support of the reefs' abundant and diverse fish assemblages.

Most coral reefs exist in shallow waters less than 50 m deep. Some inhabit tropical continental shelves where cool, nutrient rich upwelling does not occur, such as Great Barrier Reef. Others are found in the deep ocean surrounding islands or as atolls, such as in the Maldives. The reefs surrounding islands form when islands subside into the ocean, and atolls form when an island subsides below the surface of the sea.

Alternatively, Moyle and Cech distinguish six zones, though most reefs possess only some of the zones.
Water in the reef surface zone is often agitated. This diagram represents a reef on a continental shelf. The water waves at the left travel over the off-reef floor until they encounter the reef slope or fore reef. Then the waves pass over the shallow reef crest. When a wave enters shallow water it shoals, that is, it slows down and the wave height increases.

The reef surface is the shallowest part of the reef. It is subject to the surge and the rise and fall of tides. When waves pass over shallow areas, they shoal, as shown in the diagram at the right. This means the water is often agitated. These are the precise condition under which corals flourish. Shallowness means there is plenty of light for photosynthesis by the symbiotic zooxanthellae, and agitated water promotes the ability of coral to feed on plankton. However, other organisms must be able to withstand the robust conditions to flourish in this zone.

The off-reef floor is the shallow sea floor surrounding a reef. This zone occurs by reefs on continental shelves. Reefs around tropical islands and atolls drop abruptly to great depths, and do not have a floor. Usually sandy, the floor often supports seagrass meadows which are important foraging areas for reef fish.

The reef drop-off is, for its first 50 m, habitat for many reef fish who find shelter on the cliff face and plankton in the water nearby. The drop-off zone applies mainly to the reefs surrounding oceanic islands and atolls.

The reef face is the zone above the reef floor or the reef drop-off. This zone is often the most diverse area of the reef. Coral and calcareous algae growths provide complex habitats and areas which offer protection, such as cracks and crevices. Invertebrates and epiphytic algae provide much of the food for other organisms. A common feature on this forereef zone is spur and groove formations which serve to transport sediment downslope.

The reef flat is the sandy-bottomed flat, which can be behind the main reef, containing chunks of coral. This zone may border a lagoon and serve as a protective area, or it may lie between the reef and the shore, and in this case is a flat, rocky area. Fishes tend to prefer living in that flat, rocky area, compared to any other zone, when it is present.

The reef lagoon is an entirely enclosed region, which creates an area less affected by wave action that often contains small reef patches.

However, the "topography of coral reefs is constantly changing. Each reef is made up of irregular patches of algae, sessile invertebrates, and bare rock and sand. The size, shape and relative abundance of these patches changes from year to year in response to the various factors that favor one type of patch over another. Growing coral, for example, produces constant change in the fine structure of reefs. On a larger scale, tropical storms may knock out large sections of reef and cause boulders on sandy areas to move."

Locations

Locations of coral reefs
 
Boundary for 20 °C isotherms. Most corals live within this boundary. Note the cooler waters caused by upwelling on the southwest coast of Africa and off the coast of Peru.
 
This map shows areas of upwelling in red. Coral reefs are not found in coastal areas where colder and nutrient-rich upwellings occur.
 
Marine biodiversity of Raja Ampat Islands, Indonesia. It is estimated that about 75% of world coral reef population are in the Raja Ampat Islands

Coral reefs are estimated to cover 284,300 km2 (109,800 sq mi), just under 0.1% of the oceans' surface area. The Indo-Pacific region (including the Red Sea, Indian Ocean, Southeast Asia and the Pacific) account for 91.9% of this total. Southeast Asia accounts for 32.3% of that figure, while the Pacific including Australia accounts for 40.8%. Atlantic and Caribbean coral reefs account for 7.6%.

Although corals exist both in temperate and tropical waters, shallow-water reefs form only in a zone extending from approximately 30° N to 30° S of the equator. Tropical corals do not grow at depths of over 50 meters (160 ft). The optimum temperature for most coral reefs is 26–27 °C (79–81 °F), and few reefs exist in waters below 18 °C (64 °F). However, reefs in the Persian Gulf have adapted to temperatures of 13 °C (55 °F) in winter and 38 °C (100 °F) in summer. There are 37 species of scleractinian corals identified in such harsh environment around Larak Island.

Deep-water coral can exist at greater depths and colder temperatures at much higher latitudes, as far north as Norway. Although deep water corals can form reefs, very little is known about them.

Coral reefs are rare along the west coasts of the Americas and Africa, due primarily to upwelling and strong cold coastal currents that reduce water temperatures in these areas (respectively the Peru, Benguela and Canary streams). Corals are seldom found along the coastline of South Asia—from the eastern tip of India (Chennai) to the Bangladesh and Myanmar borders—as well as along the coasts of northeastern South America and Bangladesh, due to the freshwater release from the Amazon and Ganges Rivers respectively.
  • The Great Barrier Reef—largest, comprising over 2,900 individual reefs and 900 islands stretching for over 2,600 kilometers (1,600 mi) off Queensland, Australia
  • The Mesoamerican Barrier Reef System—second largest, stretching 1,000 kilometers (620 mi) from Isla Contoy at the tip of the Yucatán Peninsula down to the Bay Islands of Honduras
  • The New Caledonia Barrier Reef—second longest double barrier reef, covering 1,500 kilometers (930 mi)
  • The Andros, Bahamas Barrier Reef—third largest, following the east coast of Andros Island, Bahamas, between Andros and Nassau
  • The Red Sea—includes 6000-year-old fringing reefs located around a 2,000 km (1,240 mi) coastline
  • The Florida Reef Tract—largest continental US reef and the third largest coral barrier reef system in the world, extends from Soldier Key, located in Biscayne Bay, to the Dry Tortugas in the Gulf of Mexico
  • Pulley Ridge—deepest photosynthetic coral reef, Florida
  • Numerous reefs scattered over the Maldives
  • The Philippines coral reef area, the second largest in Southeast Asia, is estimated at 26,000 square kilometers and holds an extraordinary diversity of species. Scientists have identified 915 reef fish species and more than 400 scleractinian coral species, 12 of which are endemic.
  • The Raja Ampat Islands in Indonesia's West Papua province offer the highest known marine diversity.
  • Bermuda is known for its northernmost coral reef system, located at 32.4° N and 64.8° W. The presence of coral reefs at this high latitude is due to the proximity of the Gulf Stream. Bermuda has a fairly consistent diversity of coral species, representing a subset of those found in the greater Caribbean.
  • The world's northernmost individual coral reef so far discovered is located within a bay of Japan's Tsushima Island in the Korea Strait.
  • The world's southernmost coral reef is at Lord Howe Island, in the Pacific Ocean off the east coast of Australia.

Biology

Anatomy of a coral polyp


Alive corals are colonies of small animals embedded in calcium carbonate shells. It is a mistake to think of coral as plants or rocks. Coral heads consist of accumulations of individual animals called polyps, arranged in diverse shapes. Polyps are usually tiny, but they can range in size from a pinhead to 12 inches (30 cm) across.

Reef-building or hermatypic corals live only in the photic zone (above 50 m), the depth to which sufficient sunlight penetrates the water, allowing photosynthesis to occur. Coral polyps do not photosynthesize, but have a symbiotic relationship with microscopic algae of the genus Symbiodinium, commonly referred to as zooxanthellae. These organisms live within the tissues of polyps and provide organic nutrients that nourish the polyp. Because of this relationship, coral reefs grow much faster in clear water, which admits more sunlight. Without their symbionts, coral growth would be too slow to form significant reef structures. Corals get up to 90% of their nutrients from their symbionts.

Reefs grow as polyps and other organisms deposit calcium carbonate, the basis of coral, as a skeletal structure beneath and around themselves, pushing the coral head's top upwards and outwards. Waves, grazing fish (such as parrotfish), sea urchins, sponges, and other forces and organisms act as bioeroders, breaking down coral skeletons into fragments that settle into spaces in the reef structure or form sandy bottoms in associated reef lagoons. Many other organisms living in the reef community contribute skeletal calcium carbonate in the same manner. Coralline algae are important contributors to reef structure in those parts of the reef subjected to the greatest forces by waves (such as the reef front facing the open ocean). These algae strengthen the reef structure by depositing limestone in sheets over the reef surface.

Typical shapes for coral species are wrinkled brains, cabbages, table tops, antlers, wire strands and pillars. These shapes can depend on the life history of the coral, like light exposure and wave action, and events such as breakages.

Close up of polyps are arrayed on a coral, waving their tentacles. There can be thousands of polyps on a single coral branch.

Corals reproduce both sexually and asexually. An individual polyp uses both reproductive modes within its lifetime. Corals reproduce sexually by either internal or external fertilization. The reproductive cells are found on the mesenteries, membranes that radiate inward from the layer of tissue that lines the stomach cavity. Some mature adult corals are hermaphroditic; others are exclusively male or female. A few species change sex as they grow.

Internally fertilized eggs develop in the polyp for a period ranging from days to weeks. Subsequent development produces a tiny larva, known as a planula. Externally fertilized eggs develop during synchronized spawning. Polyps release eggs and sperm into the water en masse, simultaneously. Eggs disperse over a large area. The timing of spawning depends on time of year, water temperature, and tidal and lunar cycles. Spawning is most successful when there is little variation between high and low tide. The less water movement, the better the chance for fertilization. Ideal timing occurs in the spring. Release of eggs or planula usually occurs at night, and is sometimes in phase with the lunar cycle (three to six days after a full moon). The period from release to settlement lasts only a few days, but some planulae can survive afloat for several weeks. They are vulnerable to predation and environmental conditions. The lucky few planulae which successfully attach to substrate next confront competition for food and space.

There are eight clades of Symbiodinium phylotypes. Most research has been completed on the Symbiodinium clades A–D. Each one of the eight contributes their own benefits as well as less compatible attributes to the survival of their coral hosts. Each photosynthetic organism has a specific level of sensitivity to photodamage of compounds needed for survival, such as proteins. Rates of regeneration and replication determine the organism's ability to survive. Phylotype A is found more in the shallow regions of marine waters. It is able to produce mycosporine-like amino acids that are UV resistant, using a derivative of glycerin to absorb the UV radiation and allowing them to become more receptive to warmer water temperatures. In the event of UV or thermal damage, if and when repair occurs, it will increase the likelihood of survival of the host and symbiont. This leads to the idea that, evolutionarily, clade A is more UV resistant and thermally resistant than the other clades.

Clades B and C are found more frequently in the deeper water regions, which may explain the higher susceptibility to increased temperatures. Terrestrial plants that receive less sunlight because they are found in the undergrowth can be analogized to clades B, C, and D. Since clades B through D are found at deeper depths, they require an elevated light absorption rate to be able to synthesize as much energy. With elevated absorption rates at UV wavelengths, the deeper occurring phylotypes are more prone to coral bleaching versus the more shallow clades. Clade D has been observed to be high temperature-tolerant, and as a result it has a higher rate of survival than clades B and C.

Darwin's paradox

In The Structure and Distribution of Coral Reefs, published in 1842, Darwin described how coral reefs were found in some areas of the tropical seas but not others, with no obvious cause. The largest and strongest corals grew in parts of the reef exposed to the most violent surf and corals were weakened or absent where loose sediment accumulated.

Tropical waters contain few nutrients yet a coral reef can flourish like an "oasis in the desert". This has given rise to the ecosystem conundrum, sometimes called "Darwin's paradox": "How can such high production flourish in such nutrient poor conditions?"

 
Coral reefs cover less than 0.1% of the surface of the world’s ocean, about half the land area of France, yet they support over one-quarter of all marine species. This diversity results in complex food webs, with large predator fish eating smaller forage fish that eat yet smaller zooplankton and so on. However, all food webs eventually depend on plants, which are the primary producers. Coral reefs' primary productivity is very high, typically producing 5–10 grams of carbon per square meter per day (gC·m−2·day−1) biomass.

One reason for the unusual clarity of tropical waters is they are deficient in nutrients and drifting plankton. Further, the sun shines year-round in the tropics, warming the surface layer, making it less dense than subsurface layers. The warmer water is separated from deeper, cooler water by a stable thermocline, where the temperature makes a rapid change. This keeps the warm surface waters floating above the cooler deeper waters. In most parts of the ocean, there is little exchange between these layers. Organisms that die in aquatic environments generally sink to the bottom, where they decompose, which releases nutrients in the form of nitrogen (N), phosphorus (P) and potassium (K). These nutrients are necessary for plant growth, but in the tropics, they do not directly return to the surface.

 
Plants form the base of the food chain, and need sunlight and nutrients to grow. In the ocean, these plants are mainly microscopic phytoplankton which drift in the water column. They need sunlight for photosynthesis, which powers carbon fixation, so they are found only relatively near the surface. But they also need nutrients. Phytoplankton rapidly use nutrients in the surface waters, and in the tropics, these nutrients are not usually replaced because of the thermocline.

Coral polyps

Explanations

Around coral reefs, lagoons fill in with material eroded from the reef and the island. They become havens for marine life, providing protection from waves and storms.

Most importantly, reefs recycle nutrients, which happens much less in the open ocean. In coral reefs and lagoons, producers include phytoplankton, as well as seaweed and coralline algae, especially small types called turf algae, which pass nutrients to corals. The phytoplankton are eaten by fish and crustaceans, who also pass nutrients along the food web. Recycling ensures fewer nutrients are needed overall to support the community.

Coral reefs support many symbiotic relationships. In particular, zooxanthellae provide energy to coral in the form of glucose, glycerol, and amino acids. Zooxanthellae can provide up to 90% of a coral’s energy requirements. In return, as an example of mutualism, the corals shelter the zooxanthellae, averaging one million for every cubic centimeter of coral, and provide a constant supply of the carbon dioxide they need for photosynthesis.

The color of corals depends on the combination of brown shades provided by their zooxanthellae and pigmented proteins (reds, blues, greens, etc.) produced by the corals themselves.

Corals also absorb nutrients, including inorganic nitrogen and phosphorus, directly from water. Many corals extend their tentacles at night to catch zooplankton that brush them when the water is agitated. Zooplankton provide the polyp with nitrogen, and the polyp shares some of the nitrogen with the zooxanthellae, which also require this element. The varying pigments in different species of zooxanthellae give them an overall brown or golden-brown appearance, and give brown corals their colors. Other pigments such as reds, blues, greens, etc. come from colored proteins made by the coral animals. Coral which loses a large fraction of its zooxanthellae becomes white (or sometimes pastel shades in corals that are richly pigmented with their own colorful proteins) and is said to be bleached, a condition which, unless corrected, can kill the coral.

Sponges are another key: they live in crevices in the coral reefs. They are efficient filter feeders, and in the Red Sea they consume about 60% of the phytoplankton that drifts by. The sponges eventually excrete nutrients in a form the corals can use.

Most coral polyps are nocturnal feeders. Here, in the dark, polyps have extended their tentacles to feed on zooplankton.

The roughness of coral surfaces is the key to coral survival in agitated waters. Normally, a boundary layer of still water surrounds a submerged object, which acts as a barrier. Waves breaking on the extremely rough edges of corals disrupt the boundary layer, allowing the corals access to passing nutrients. Turbulent water thereby promotes reef growth and branching. Without the nutritional gains brought by rough coral surfaces, even the most effective recycling would leave corals wanting in nutrients.

Studies have shown that deep nutrient-rich water entering coral reefs through isolated events may have significant effects on temperature and nutrient systems. This water movement disrupts the relatively stable thermocline that usually exists between warm shallow water to deeper colder water. Leichter et al. (2006) found that temperature regimes on coral reefs in the Bahamas and Florida were highly variable with temporal scales of minutes to seasons and spatial scales across depths.

Water can be moved through coral reefs in various ways, including current rings, surface waves, internal waves and tidal changes. Movement is generally created by tides and wind. As tides interact with varying bathymetry and wind mixes with surface water, internal waves are created. An internal wave is a gravity wave that moves along density stratification within the ocean. When a water parcel encounters a different density it will oscillate and create internal waves. While internal waves generally have a lower frequency than surface waves, they often form as a single wave that breaks into multiple waves as it hits a slope and moves upward. This vertical break up of internal waves causes significant diapycnal mixing and turbulence. Internal waves can act as nutrient pumps, bringing plankton and cool nutrient-rich water up to the surface.

The irregular structure characteristic of coral reef bathymetry may enhance mixing and produce pockets of cooler water and variable nutrient content. Arrival of cool, nutrient-rich water from depths due to internal waves and tidal bores has been linked to growth rates of suspension feeders and benthic algae as well as plankton and larval organisms. Leichter et al. proposed that the seaweed Codium isthmocladum reacts to deep water nutrient sources due to their tissues having different concentrations of nutrients dependent upon depth. Wolanski and Hamner noted aggregations of eggs, larval organisms and plankton on reefs in response to deep water intrusions. Similarly, as internal waves and bores move vertically, surface-dwelling larval organisms are carried toward the shore. This has significant biological importance to cascading effects of food chains in coral reef ecosystems and may provide yet another key to unlocking "Darwin's Paradox".

Cyanobacteria provide soluble nitrates for the reef via nitrogen fixation.

Coral reefs also often depend on surrounding habitats, such as seagrass meadows and mangrove forests, for nutrients. Seagrass and mangroves supply dead plants and animals which are rich in nitrogen and also serve to feed fish and animals from the reef by supplying wood and vegetation. Reefs, in turn, protect mangroves and seagrass from waves and produce sediment in which the mangroves and seagrass can root.

Biodiversity

Tube sponges attracting cardinal fishes, glassfishes and wrasses
 
Over 4,000 species of fish inhabit coral reefs.
 
Organisms can cover every square inch of a coral reef.

Coral reefs form some of the world's most productive ecosystems, providing complex and varied marine habitats that support a wide range of other organisms. Fringing reefs just below low tide level have a mutually beneficial relationship with mangrove forests at high tide level and sea grass meadows in between: the reefs protect the mangroves and seagrass from strong currents and waves that would damage them or erode the sediments in which they are rooted, while the mangroves and sea grass protect the coral from large influxes of silt, fresh water and pollutants. This level of variety in the environment benefits many coral reef animals, which, for example, may feed in the sea grass and use the reefs for protection or breeding.

Reefs are home to a large variety of animals, including fish, seabirds, sponges, cnidarians (which includes some types of corals and jellyfish), worms, crustaceans (including shrimp, cleaner shrimp, spiny lobsters and crabs), mollusks (including cephalopods), echinoderms (including starfish, sea urchins and sea cucumbers), sea squirts, sea turtles and sea snakes. Aside from humans, mammals are rare on coral reefs, with visiting cetaceans such as dolphins being the main exception. A few of these varied species feed directly on corals, while others graze on algae on the reef. Reef biomass is positively related to species diversity.

The same hideouts in a reef may be regularly inhabited by different species at different times of day. Nighttime predators such as cardinalfish and squirrelfish hide during the day, while damselfish, surgeonfish, triggerfish, wrasses and parrotfish hide from eels and sharks.

Algae

Reefs are chronically at risk of algal encroachment. Overfishing and excess nutrient supply from onshore can enable algae to outcompete and kill the coral. Increased nutrient levels can be a result of sewage or chemical fertilizer runoff from nearby coastal developments. Runoff can carry nitrogen and phosphorus which promote excess algae growth. Algae can sometimes out-compete the coral for space. The algae can then smother the coral by decreasing the oxygen supply available to the reef. Decreased oxygen levels can slow down coral's calcification rates weakening the coral and leaving it more susceptible to disease and degradation. In surveys done around largely uninhabited US Pacific islands, algae inhabit a large percentage of surveyed coral locations. The algal population consists of turf algae, coralline algae, and macro algae.

Sponges

Sponges are essential for the functioning of the coral reef's ecosystem. Algae and corals in coral reefs produce organic material. This is filtered through sponges which convert this organic material into small particles which in turn are absorbed by algae and corals.

Fish

Over 4,000 species of fish inhabit coral reefs. The reasons for this diversity remain unclear. Hypotheses include the "lottery", in which the first (lucky winner) recruit to a territory is typically able to defend it against latecomers, "competition", in which adults compete for territory, and less-competitive species must be able to survive in poorer habitat, and "predation", in which population size is a function of postsettlement piscivore mortality. Healthy reefs can produce up to 35 tons of fish per square kilometer each year, but damaged reefs produce much less.

Invertebrates

Sea urchins, Dotidae and sea slugs eat seaweed. Some species of sea urchins, such as Diadema antillarum, can play a pivotal part in preventing algae from overrunning reefs. Nudibranchia and sea anemones eat sponges.

A number of invertebrates, collectively called "cryptofauna," inhabit the coral skeletal substrate itself, either boring into the skeletons (through the process of bioerosion) or living in pre-existing voids and crevices. Those animals boring into the rock include sponges, bivalve mollusks, and sipunculans. Those settling on the reef include many other species, particularly crustaceans and polychaete worms.

Seabirds

Coral reef systems provide important habitats for seabird species, some endangered. For example, Midway Atoll in Hawaii supports nearly three million seabirds, including two-thirds (1.5 million) of the global population of Laysan albatross, and one-third of the global population of black-footed albatross. Each seabird species has specific sites on the atoll where they nest. Altogether, 17 species of seabirds live on Midway. The short-tailed albatross is the rarest, with fewer than 2,200 surviving after excessive feather hunting in the late 19th century.

Other

Sea snakes feed exclusively on fish and their eggs. Marine birds, such as herons, gannets, pelicans and boobies, feed on reef fish. Some land-based reptiles intermittently associate with reefs, such as monitor lizards, the marine crocodile and semiaquatic snakes, such as Laticauda colubrina. Sea turtles, particularly hawksbill sea turtles, feed on sponges.

Importance

Coral reefs deliver ecosystem services to tourism, fisheries and coastline protection. The global economic value of coral reefs has been estimated to be between US $29.8 billion and $375 billion per year. Coral reefs protect shorelines by absorbing wave energy, and many small islands would not exist without their reefs to protect them. According to the environmental group World Wide Fund for Nature, the economic cost over a 25-year period of destroying one kilometer of coral reef is somewhere between $137,000 and $1,200,000. About six million tons of fish are taken each year from coral reefs. Well-managed coral reefs have an annual yield of 15 tons of seafood on average per square kilometer. Southeast Asia's coral reef fisheries alone yield about $2.4 billion annually from seafood.

To improve the management of coastal coral reefs, another environmental group, the World Resources Institute (WRI) developed and published tools for calculating the value of coral reef-related tourism, shoreline protection and fisheries, partnering with five Caribbean countries. As of April 2011, published working papers covered St. Lucia, Tobago, Belize, and the Dominican Republic, with a paper for Jamaica in preparation. The WRI was also "making sure that the study results support improved coastal policies and management planning". The Belize study estimated the value of reef and mangrove services at $395–559 million annually.

Bermuda's coral reefs provide economic benefits to the Island worth on average $722 million per year, based on six key ecosystem services, according to Sarkis et al (2010).

Threats

Island with fringing reef off Yap, Micronesia


Coral reefs are dying around the world. In particular, coral mining, agricultural and urban runoff, pollution (organic and inorganic), overfishing, blast fishing, disease, and the digging of canals and access into islands and bays are localized threats to coral ecosystems. Broader threats are sea temperature rise, sea level rise and pH changes from ocean acidification, all associated with greenhouse gas emissions. A 2014 study lists factors such as population explosion along the coast lines, overfishing, the pollution of coastal areas, global warming and invasive species among the main reasons that have put reefs in danger of extinction.

A study released in April 2013 has shown that air pollution can also stunt the growth of coral reefs; researchers from Australia, Panama and the UK used coral records (between 1880 and 2000) from the western Caribbean to show the threat of factors such as coal-burning coal and volcanic eruptions. Pollutants, such as Tributyltin, a biocide released into water from in anti-fouling paint can be toxic to corals.

In 2011, researchers suggested that "extant marine invertebrates face the same synergistic effects of multiple stressors" that occurred during the end-Permian extinction, and that genera "with poorly buffered respiratory physiology and calcareous shells", such as corals, were particularly vulnerable.

Rock coral on seamounts across the ocean are under fire from bottom trawling. Reportedly up to 50% of the catch is rock coral, and the practice transforms coral structures to rubble. With it taking years to regrow, these coral communities are disappearing faster than they can sustain themselves.

Another cause for the death of coral reefs is bioerosion. Various fishes graze corals, dead or alive and change the morphology of coral reefs making them more susceptible to other physical and chemical threats. It has been generally observed that only the algae growing on dead corals is eaten and the live ones are not. However, this act still destroys the top layer of coral substrate and makes it harder for the reefs to sustain.

In El Niño-year 2010, preliminary reports show global coral bleaching reached its worst level since another El Niño year, 1998, when 16% of the world's reefs died as a result of increased water temperature. In Indonesia's Aceh province, surveys showed some 80% of bleached corals died. Scientists do not yet understand the long-term impacts of coral bleaching, but they do know that bleaching leaves corals vulnerable to disease, stunts their growth, and affects their reproduction, while severe bleaching kills them. In July, Malaysia closed several dive sites where virtually all the corals were damaged by bleaching.

To find answers for these problems, researchers study the various factors that impact reefs. The list includes the ocean's role as a carbon dioxide sink, atmospheric changes, ultraviolet light, ocean acidification, viruses, impacts of dust storms carrying agents to far-flung reefs, pollutants, algal blooms and others. Reefs are threatened well beyond coastal areas. Coral reefs with one type of zooxanthellae are more prone to bleaching than are reefs with another, more hardy, species.

General estimates show approximately 10% of the world's coral reefs are dead. About 60% of the world's reefs are at risk due to destructive, human-related activities. The threat to the health of reefs is particularly high in Southeast Asia, where 95% of reefs are at risk from local threats. By the 2030s, 90% of reefs are expected to be at risk from both human activities and climate change; by 2050, all coral reefs will be in danger.

Current research is showing that ecotourism in the Great Barrier Reef is contributing to coral disease, and that chemicals in sunscreens may contribute to the impact of viruses on zooxanthellae.

Some scientists, including those associated with the National Oceanic and Atmospheric Administration, posit that US coral reefs are likely to disappear within a few decades as a result of global warming.

Protection

A diversity of corals

Marine protected areas (MPAs) have become increasingly prominent for reef management. MPAs promote responsible fishery management and habitat protection. Much like national parks and wildlife refuges, and to varying degrees, MPAs restrict potentially damaging activities. MPAs encompass both social and biological objectives, including reef restoration, aesthetics, biodiversity, and economic benefits. However, there are very few MPAs that have actually made a substantial difference. Research in Indonesia, Philippines and Papua New Guinea shows that there is no significant difference between an MPA site and an unprotected site. Conflicts surrounding MPAs involve lack of participation, clashing views of the government and fisheries, effectiveness of the area, and funding. In some situations, as in the Phoenix Islands Protected Area, MPAs can also provide revenue, potentially equal to the income they would have generated without controls, as Kiribati did for its Phoenix Islands.

According to the Caribbean Coral Reefs - Status Report 1970-2012 made by the IUCN. States that; stopping overfishing especially key fishes to coral reef like parrotfish, coastal zone management which reduce human pressure on reef, (for example restricting the coastal settlement, development and tourism in coastal reef) and controlling pollution specially sewage wastage, may not only reduce coral declining but also reverse it and may let to coral reef more adaptable to changes relates to climate and acidification. The report shows that healthier reef in the Caribbean are those with large population of parrotfish in countries which protect these key fishes and sea urchins, banning fish trap and Spearfishing creating "resilient reefs".

To help combat ocean acidification, some laws are in place to reduce greenhouse gases such as carbon dioxide. The Clean Water Act puts pressure on state government agencies to monitor and limit runoff of pollutants that can cause ocean acidification. Stormwater surge preventions are also in place, as well as coastal buffers between agricultural land and the coastline. This act also ensures that delicate watershed ecosystems are intact, such as wetlands. The Clean Water Act is funded by the federal government, and is monitored by various watershed groups. Many land use laws aim to reduce CO2 emissions by limiting deforestation. Deforestation causes erosion, which releases a large amount of carbon stored in the soil, which then flows into the ocean, contributing to ocean acidification. Incentives are used to reduce miles traveled by vehicles, which reduces the carbon emissions into the atmosphere, thereby reducing the amount of dissolved CO2 in the ocean. State and federal governments also control coastal erosion, which releases stored carbon in the soil into the ocean, increasing ocean acidification. High-end satellite technology is increasingly being employed to monitor coral reef conditions.

Biosphere reserve, marine park, national monument and world heritage status can protect reefs. For example, Belize's barrier reef, Sian Ka'an, the Galapagos islands, Great Barrier Reef, Henderson Island, Palau and Papahānaumokuākea Marine National Monument are world heritage sites.

In Australia, the Great Barrier Reef is protected by the Great Barrier Reef Marine Park Authority, and is the subject of much legislation, including a biodiversity action plan. They have compiled a Coral Reef Resilience Action Plan. This detailed action plan consists of numerous adaptive management strategies, including reducing our carbon footprint, which would ultimately reduce the amount of ocean acidification in the oceans surrounding the Great Barrier Reef. An extensive public awareness plan is also in place to provide education on the “rainforests of the sea” and how people can reduce carbon emissions, thereby reducing ocean acidification.

Inhabitants of Ahus Island, Manus Province, Papua New Guinea, have followed a generations-old practice of restricting fishing in six areas of their reef lagoon. Their cultural traditions allow line fishing, but no net or spear fishing. The result is both the biomass and individual fish sizes are significantly larger than in places where fishing is unrestricted.

Restoration

Coral fragments growing on nontoxic concrete

Coral aquaculture, also known as coral farming or coral gardening, is showing promise as a potentially effective tool for restoring coral reefs, which have been declining around the world. The process bypasses the early growth stages of corals when they are most at risk of dying. Coral seeds are grown in nurseries, then replanted on the reef. Coral is farmed by coral farmers who live locally to the reefs and farm for reef conservation or for income.

Efforts to expand the size and number of coral reefs generally involve supplying substrate to allow more corals to find a home. Substrate materials include discarded vehicle tires, scuttled ships, subway cars, and formed concrete, such as reef balls. Reefs also grow unaided on marine structures such as oil rigs. In large restoration projects, propagated hermatypic coral on substrate can be secured with metal pins, superglue or milliput. Needle and thread can also attach A-hermatype coral to substrate.

A substrate for growing corals referred to as Biorock is produced by running low voltage electrical currents through seawater to crystallize dissolved minerals onto steel structures. The resultant white carbonate (aragonite) is the same mineral that makes up natural coral reefs. Corals rapidly colonize and grow at accelerated rates on these coated structures. The electrical currents also accelerate formation and growth of both chemical limestone rock and the skeletons of corals and other shell-bearing organisms. The vicinity of the anode and cathode provides a high-pH environment which inhibits the growth of competitive filamentous and fleshy algae. The increased growth rates fully depend on the accretion activity.

During accretion, the settled corals display an increased growth rate, size and density, but after the process is complete, growth rate and density return to levels comparable to natural growth, and are about the same size or slightly smaller.

One case study with coral reef restoration was conducted on the island of Oahu in Hawaii. The University of Hawaii has come up with a Coral Reef Assessment and Monitoring Program to help relocate and restore coral reefs in Hawaii. A boat channel on the island of Oahu to the Hawaii Institute of Marine Biology was overcrowded with coral reefs. Also, many areas of coral reef patches in the channel had been damaged from past dredging in the channel. Dredging covers the existing corals with sand, and their larvae cannot build and thrive on sand; they can only build on to existing reefs. Because of this, the University of Hawaii decided to relocate some of the coral reef to a different transplant site. They transplanted them with the help of the United States Army divers, to a relocation site relatively close to the channel. They observed very little, if any, damage occurred to any of the colonies while they were being transported, and no mortality of coral reefs has been observed on the new transplant site, but they will be continuing to monitor the new transplant site to see how potential environmental impacts (i.e. ocean acidification) will harm the overall reef mortality rate. While trying to attach the coral to the new transplant site, they found the coral placed on hard rock is growing considerably well, and coral was even growing on the wires that attached the transplant corals to the transplant site. This gives new hope to future research on coral reef transplant sites. As a result of this coral restoration project, no environmental effects were seen from the transplantation process, no recreational activities were decreased, and no scenic areas were affected by the project. This is a great example that coral transplantation and restoration can work and thrive under the right conditions, which means there may be hope for other damaged coral reefs.

Another possibility for coral restoration is gene therapy. Through infecting coral with genetically modified bacteria, it may be possible to grow corals that are more resistant to climate change and other threats.

Reefs in the past

Ancient coral reefs

Throughout Earth history, from a few thousand years after hard skeletons were developed by marine organisms, there were almost always reefs. The times of maximum development were in the Middle Cambrian (513–501 Ma), Devonian (416–359 Ma) and Carboniferous (359–299 Ma), owing to order Rugosa extinct corals, and Late Cretaceous (100–66 Ma) and all Neogene (23 Ma–present), owing to order Scleractinia corals.

Not all reefs in the past were formed by corals: those in the Early Cambrian (542–513 Ma) resulted from calcareous algae and archaeocyathids (small animals with conical shape, probably related to sponges) and in the Late Cretaceous (100–66 Ma), when there also existed reefs formed by a group of bivalves called rudists; one of the valves formed the main conical structure and the other, much smaller valve acted as a cap.

Measurements of the oxygen isotopic composition of the aragonitic skeleton of coral reefs, such as Porites, can indicate changes in the sea surface temperature and sea surface salinity conditions of the ocean during the growth of the coral. This technique is often used by climate scientists to infer the paleoclimate of a region.

Friday, December 11, 2020

Molecular paleontology

From Wikipedia, the free encyclopedia

Molecular paleontology refers to the recovery and analysis of DNA, proteins, carbohydrates, or lipids, and their diagenetic products from ancient human, animal, and plant remains. The field of molecular paleontology has yielded important insights into evolutionary events, species' diasporas, the discovery and characterization of extinct species. By applying molecular analytical techniques to DNA in fossils, one can quantify the level of relatedness between any two organisms for which DNA has been recovered.

Advancements in the field of molecular paleontology have allowed scientists to pursue evolutionary questions on a genetic level rather than relying on phenotypic variation alone. Using various biotechnological techniques such as DNA isolation, amplification, and sequencing scientists have been able to gain expanded new insights into the divergence and evolutionary history of countless organisms.

History

The study of molecular paleontology is said to have begun with the discovery by Abelson of 360 million year old amino acids preserved in fossil shells. However, Svante Pääbo is often the one considered to be the founder of the field of molecular paleontology.

The field of molecular paleontology has had several major advances since the 1950s and is a continuously growing field. Below is a timeline showing notable contributions that have been made.

A visual graphic of the events listed in the timeline section.
A timeline demonstrating important dates in molecular paleontology. All of these dates are listed and specifically sourced in the History section under Timeline.

mid-1950s: Abelson found preserved amino acids in fossil shells that were about 360 million years old. Produced idea of comparing fossil amino acid sequences with existing organism so that molecular evolution could be studied.

1970s: Fossil peptides are studied by amino acid analysis. Start to use whole peptides and immunological methods.

Late 1970s: Palaeobotanists (can also be spelled as Paleobotanists) studied molecules from well-preserved fossil plants.

1984: The first successful DNA sequencing of an extinct species, the quagga, a zebra-like species.

1991: Published article on the successful extraction of proteins from the fossil bone of a dinosaur, specifically the seismosaurus.

2005: Scientists resurrect extinct 1918 influenza virus.

2006: Neanderthals nuclear DNA sequence segments begin to be analyzed and published.

2007: Scientists synthesize entire extinct human endogenous retrovirus (HERV-K) from scratch.

2010: A new species of early hominid, the Denisovans, discovered from mitochondrial and nuclear genomes recovered from bone found in a cave in Siberia. Analysis showed that the Denisovan specimen lived approximately 41,000 years ago, and shared a common ancestor with both modern humans and Neanderthals approximately 1 million years ago in Africa.

2013: The first entire Neanderthal genome is successfully sequenced. More information can be found at the Neanderthal genome project.

2013: A 400,000-year-old specimen with remnant mitochondrial DNA sequenced and is found to be a common ancestor to Neanderthals and Denisovans, later named Homo heidelbergensis.

2015: A 110,000-year-old fossil tooth containing DNA from Denisovans was reported.

The quagga

The first successful DNA sequencing of an extinct species was in 1984, from a 150-year-old museum specimen of the quagga, a zebra-like species. Mitochondrial DNA (also known as mtDNA) was sequenced from desiccated muscle of the quagga, and was found to differ by 12 base substitutions from the mitochondrial DNA of a mountain zebra. It was concluded that these two species had a common ancestor 3-4 million years ago, which is consistent with known fossil evidence of the species.

Denisovans

The Denisovans of Eurasia, a hominid species related to Neanderthals and humans, was discovered as a direct result of DNA sequencing of a 41,000-year-old specimen recovered in 2008. Analysis of the mitochondrial DNA from a retrieved finger bone showed the specimen to be genetically distinct from both humans and Neanderthals. Two teeth and a toe bone were later found to belong to different individuals with the same population. Analysis suggests that both the Neanderthals and Denisovans were already present throughout Eurasia when modern humans arrived. In November 2015, scientists reported finding a fossil tooth containing DNA from Denisovans, and estimated its age at 110,000-years-old.

Mitochondrial DNA analysis

A photo of Neanderthal DNA extraction in process
Neanderthal DNA extraction. Working in a clean room, researchers at the Max Planck Institute for Evolutionary Anthropology in Leipzig, Germany, took extensive precautions to avoid contaminating Neanderthal DNA samples - extracted from bones like this one - with DNA from any other source, including modern humans. NHGRI researchers are part of the international team that sequenced the genome of the Neanderthal, Homo neanderthalensis.

The mtDNA from the Denisovan finger bone differs from that of modern humans by 385 bases (nucleotides) in the mtDNA strand out of approximately 16,500, whereas the difference between modern humans and Neanderthals is around 202 bases. In contrast, the difference between chimpanzees and modern humans is approximately 1,462 mtDNA base pairs. This suggested a divergence time around one million years ago. The mtDNA from a tooth bore a high similarity to that of the finger bone, indicating they belonged to the same population. From a second tooth, an mtDNA sequence was recovered that showed an unexpectedly large number of genetic differences compared to that found in the other tooth and the finger, suggesting a high degree of mtDNA diversity. These two individuals from the same cave showed more diversity than seen among sampled Neanderthals from all of Eurasia, and were as different as modern-day humans from different continents.

Nuclear genome analysis

Isolation and sequencing of nuclear DNA has also been accomplished from the Denisova finger bone. This specimen showed an unusual degree of DNA preservation and low level of contamination. They were able to achieve near-complete genomic sequencing, allowing a detailed comparison with Neanderthal and modern humans. From this analysis, they concluded, in spite of the apparent divergence of their mitochondrial sequence, the Denisova population along with Neanderthal shared a common branch from the lineage leading to modern African humans. The estimated average time of divergence between Denisovan and Neanderthal sequences is 640,000 years ago, and the time between both of these and the sequences of modern Africans is 804,000 years ago. They suggest the divergence of the Denisova mtDNA results either from the persistence of a lineage purged from the other branches of humanity through genetic drift or else an introgression from an older hominin lineage.

Homo heidelbergensis

A photo of the Denisovan cranium found at Sima de los Huesos
"Homo heidelbergensis Cranium 5 is one of the most important discoveries in the Sima de los Huesos, Atapuerca (Spain). The mandible of this cranium appeared, nearly intact, some years after its find, close to the same location.

Homo heidelbergensis was first discovered in 1907 near Heidelberg, Germany and later also found elsewhere in Europe, Africa, and Asia. However it was not until 2013 that a specimen with retrievable DNA was found, in a ~400,000 year old femur found in the Sima de los Huesos Cave in Spain. The femur was found to contain both mtDNA and nuclear DNA. Improvements in DNA extraction and library preparation techniques allowed for mtDNA to be successfully isolated and sequenced, however the nuclear DNA was found to be too degraded in the observed specimen, and was also contaminated with DNA from an ancient cave bear (Ursus deningeri) present in the cave. The mtDNA analysis found a surprising link between the specimen and the Denisovans, and this finding raised many questions. Several scenarios were proposed in a January 2014 paper titled "A mitochondrial genome sequence of a hominin from Sima de los Huesos", elucidating the lack of convergence in the scientific community on how Homo heidelbergensis is related to other known hominin groups. One plausible scenario that the authors proposed was that the H. heidelbergensis was an ancestor to both Denisovans and Neanderthals. Completely sequenced nuclear genomes from both Denisovans and Neanderthals suggest a common ancestor approximately 700,000 years ago, and one leading researcher in the field, Svante Paabo, suggests that perhaps this new hominin group is that early ancestor.

Applications

Discovery and characterization of new species

Molecular paleontology techniques applied to fossils have contributed to the discovery and characterization of several new species, including the Denisovans and Homo heidelbergensis. We have been able to better understand the path that humans took as they populated the earth, and what species were present during this diaspora.

De-extinction

An artist's color drawing of the Pyrenean ibex
The Pyrenean ibex was temporarily brought back from extinction in 1984.

It is now possible to revive extinct species using molecular paleontology techniques. This was first accomplished via cloning in 2003 with the Pyrenean ibex, a type of wild goat that became extinct in 2000. Nuclei from the Pyrenean ibex's cells were injected into goat eggs emptied of their own DNA, and implanted into surrogate goat mothers. The offspring lived only seven minutes after birth, due to defects in its lungs. Other cloned animals have been observed to have similar lung defects.

There are many species that have gone extinct as a direct result of human activity. Some examples include the dodo, the great auk, the Tasmanian tiger, the Chinese river dolphin, and the passenger pigeon. An extinct species can be revived by using allelic replacement of a closely related species that is still living. By only having to replace a few genes within an organism, instead of having to build the extinct species' genome from scratch, it could be possible to bring back several species in this way, even Neanderthals.

The ethics surrounding the re-introduction of extinct species are very controversial. Critics of bringing extinct species back to life contend that it would divert limited money and resources from protecting the world's current biodiversity problems. With current extinction rates approximated to be 100 to 1,000 times the background extinction rate, it is feared that a de-extinction program might lessen public concerns over the current mass extinction crisis, if it is believed that these species can simply be brought back to life. As the editors of a Scientific American article on de-extinction pose: Should we bring back the woolly mammoth only to let elephants become extinct in the meantime? The main driving factor for the extinction of most species in this era (post 10,000 BC) is the loss of habitat, and temporarily bringing back an extinct species will not recreate the environment they once inhabited.

Proponents of de-extinction, such as George Church, speak of many potential benefits. Reintroducing an extinct keystone species, such as the woolly mammoth, could help re-balance the ecosystems that once depended on them. Some extinct species could create broad benefits for the environments they once inhabited, if returned. For example, woolly mammoths may be able to slow the melting of the Russian and Arctic tundra in several ways such as eating dead grass so that new grass can grow and take root, and periodically breaking up the snow, subjecting the ground below to the arctic air. These techniques could also be used to reintroduce genetic diversity in a threatened species, or even introduce new genes and traits to allow the animals to compete better in a changing environment.

Research and technology

When a new potential specimen is found, scientists normally first analyze for cell and tissue preservation using histological techniques, and test the conditions for the survivability of DNA. They will then attempt to isolate a DNA sample using the technique described below, and conduct a PCR amplification of the DNA to increase the amount of DNA available for testing. This amplified DNA is then sequenced. Care is taken to verify that the sequence matches the phylogenetic traits of the organism. When an organism dies, a technique called amino acid dating can be used to age the organism. It inspects the degree of racemization of aspartic acid, leucine, and alanine within the tissue. As time passes, the D/L ratio (where "D" and "L" are mirror images of each other) increase from 0 to 1. In samples where the D/L ratio of aspartic acid is greater than 0.08, ancient DNA sequences can not be retrieved (as of 1996).

Mitochondrial DNA vs. nuclear DNA

An infographic contrasting inheritance of mitochondrial and nuclear DNA
Unlike nuclear DNA (left), mitochondrial DNA is only inherited from the maternal lineage (right).

Mitochondrial DNA (mtDNA) is separate from one's nuclear DNA. It is present in organelles called mitochondria in each cell. Unlike nuclear DNA, which is inherited from both parents and rearranged every generation, an exact copy of mitochondrial DNA gets passed down from mother to her sons and daughters. The benefits of performing DNA analysis with Mitochondrial DNA is that it has a far smaller mutation rate than nuclear DNA, making tracking lineages on the scale of tens of thousands of years much easier. Knowing the base mutation rate for mtDNA, (in humans this rate is also known as the Human mitochondrial molecular clock) one can determine the amount of time any two lineages have been separated. Another advantage of mtDNA is that thousands of copies of it exist in every cell, whereas only two copies of nuclear DNA exist in each cell. All eukaryotes, a group which includes all plants, animals, and fungi, have mtDNA. A disadvantage of mtDNA is that only the maternal line is represented. For example, a child will inherit 1/8 of its DNA from each of its eight great-grandparents, however it will inherit an exact clone of its maternal great-grandmother's mtDNA. This is analogous to a child inheriting only his paternal great-grandfather's last name, and not a mix of all of the eight surnames.

Isolation

There are many things to consider when isolating a substance. First, depending upon what it is and where it is located, there are protocols that must be carried out in order to avoid contamination and further degradation of the sample. Then, handling of the materials is usually done in a physically isolated work area and under specific conditions (i.e. specific Temperature, moisture, etc...) also to avoid contamination and further loss of sample.

Once the material has been obtained, depending on what it is, there are different ways to isolate and purify it. DNA extraction from fossils is one of the more popular practices and there are different steps that can be taken to get the desired sample. DNA extracted from amber-entombed fossils can be taken from small samples and mixed with different substances, centrifuged, incubated, and centrifuged again. On the other hand, DNA extraction from insects can be done by grinding the sample, mixing it with buffer, and undergoing purification through glass fiber columns. In the end, regardless of how the sample was isolated for these fossils, the DNA isolated must be able to undergo amplification.

Amplification

An infographic showing the replication process of PCR
Polymerase chain reaction

The field of molecular paleontology benefited greatly from the invention of the polymerase chain reaction(PCR), which allows one to make billions of copies of a DNA fragment from just a single preserved copy of the DNA. One of the biggest challenges up until this point was the extreme scarcity of recovered DNA because of degradation of the DNA over time.

Sequencing

DNA sequencing is done to determine the order of nucleotides and genes. There are many different materials from which DNA can be extracted. In animals, the mitochondrial chromosome can be used for molecular study. Chloroplasts can be studied in plants as a primary source of sequence data.

An evolutionary tree of mammals
An evolutionary tree of mammals

In the end, the sequences generated are used to build evolutionary trees. Methods to match data sets include: maximum probability, minimum evolution (also known as neighbor-joining) which searches for the tree with shortest overall length, and the maximum parsimony method which finds the tree requiring the fewest character-state changes. The groups of species defined within a tree can also be later evaluated by statistical tests, such as the bootstrap method, to see if they are indeed significant.

Limitations and challenges

Ideal environmental conditions for preserving DNA where the organism was desiccated and uncovered are difficult to come by, as well as maintaining their condition until analysis. Nuclear DNA normally degrades rapidly after death by endogenous hydrolytic processes, by UV radiation, and other environmental stressors.

Also, interactions with the organic breakdown products of surrounding soil have been found to help preserve biomolecular materials. However, they have also created the additional challenge of being able to separate the various components in order to be able to conduct the proper analysis on them. Some of these breakdowns have also been found to interfere with the action of some of the enzymes used during PCR.

Finally, one of the largest challenge in extracting ancient DNA, particularly in ancient human DNA, is in contamination during PCR. Small amounts of human DNA can contaminate the reagents used for extraction and PCR of ancient DNA. These problems can be overcome by rigorous care in the handling of all solutions as well as the glassware and other tools used in the process. It can also help if only one person performs the extractions, to minimize different types of DNA present.

Thursday, December 10, 2020

Ancient pathogen genomics

From Wikipedia, the free encyclopedia
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Ancient pathogen genomics is a scientific field related to the study of pathogen genomes recovered from ancient human, plant or animal remains. Ancient pathogens are microorganisms, now extinct, that in the past centuries caused several epidemics and deaths worldwide. Their genome, to which we referred as ancient DNA (aDNA), is isolated from the burial's remains (bones and teeth) of victims of the pandemics caused by these pathogens.

The analysis of the genomic features of ancient pathogen genomes allows researchers to understand the evolution of modern microbial strains that can hypothetically generate new pandemics or outbreaks. The analysis of aDNA is carried out by bioinformatic tools and molecular biology techniques to compare ancient pathogens with the modern descendants. The comparison also provides phylogenetic information of these strains.

Reconstructing ancient pathogen genomes through NGS technologies

Pathogen DNA detection in ancient remains can be achieved with laboratory or computational methods. In both cases, the procedure starts with the extraction of DNA from ancient specimens. The laboratory methods are based on the construction of NGS libraries and the subsequent capture-based screening. Computational tools are used to map the reads obtained by NGS against a single- or multi-genome reference (targeted approach); alternatively, metagenomic profiling or taxonomic assignment of shotgun NGS reads methods can be applied (broad approach).

Isolating ancient DNA

The limited preservation and thus low abundance, the highly fragmented and damaged state and the presence of modern DNA contamination and environmental DNA background makes the retrieval of ancient DNA (aDNA) a challenging procedure.

In order to efficiently recover aDNA, DNA is generally isolated from tissues that contain a high quantity of aDNA, like bone and teeth, which are abundant in archaeological record. The preservation of pathogens across different anatomical elements is very variable according to the type of pathogen and its tissue tropism, its route of entry into the body and the resulting disease. Pathogens that cause chronic infections in their hosts typically produce diagnostic bone changes as opposed to acute blood-borne infections. Therefore, for that infections that have caused the death of the host in the acute phase, the preferred sampling material is the inner chamber of the teeth since this is a tissue that is highly vascularized during life.

aDNA is characterised by damages that are accumulated over the course of time: the evaluation of DNA 'damage pattern' through computational tools is useful to authenticate ancient pathogen DNA since the same pattern is not found in modern contaminants.

The most represented chemical damage that affects the DNA post-mortem is the hydrolytic deamination of cytosines, converting them in uracils, which are then read as thymines. Due to this reaction, ancient DNA contains an unexpected proportion of cytosine to thymine transitions, in particular at the ends of the molecules. Other common DNA modifications, besides the deamination of cytosine into thymine (this occurs when cytosines were methylated), is the presence of abasic sites and single-strand breaks.

aDNA is extensively fragmented (most of the fragments are less than 100 base pairs long): this tendency can be used as a quantitative measure of authenticity, as modern contaminant molecules are expected to be longer. To exploit this characteristic feature of ancient DNA, improved silica-based extraction protocols with modified volume and composition of the DNA-binding buffer were introduced.

Construction of DNA libraries

In order to be sequenced with second generation sequencing methods, template molecules have to be modified through ligation of adaptors. Both the steps of library construction and the PCR amplification that follows are subject to errors. In particular, adaptor binding biases can occur and the relative efficacy of PCR enzymes in amplifying the construct can be variable.

There are three most common types of aDNA libraries. The double-stranded DNA library uses double-stranded DNA templates and firstly requires a step for the repair of the ends of aDNA fragments. Then, fragments are ligated to double-stranded adaptors and the resultant nicks are filled in. This method has some limitations, like the presence of a fraction of constructs that do not contain both the different adaptors and the possible formation of adaptor dimers.

To overcome this latter problem, a method for the construction of an A-tailed library was developed. In this method, aDNA is end-repaired and then an adenine residue is added to the 3' ends of the strands, which can facilitate the ligation of the template with adaptors that contain a tailor of thymine. Furthermore, the use of these T-tailed adaptors prevents the formation of adaptor dimers. The type of adaptor that is typically used is double-stranded and has a Y shape, which means that it has a region located at the T-tailed end where it is complementary and a region at the other end where it is non-complementary. The use of this type of adaptors allows to generate a template of aDNA flanked by different non-complementary adaptor sequences at each end that are useful for the unidirectional sequencing.

Another strategy is based on the use of single-stranded DNA libraries. In this method, DNA is first denatured to generate a single strand through heat and then ligated to a single-stranded biotinylated adaptor. The DNA strand is then used as a template by a DNA-polymerase which produces the complementary strand. Subsequently, a second adaptor is ligated at the 3' end of the complementary strand and the full construct is amplified through PCR and then sequenced. The purification step is performed using streptavidin-coated paramagnetic beads which allow minimising the DNA loss during this phase of the procedure.

Enriching libraries for aDNA

Different methods (called enrichment methods) have been developed to improve accessibility to endogenous DNA in ancient remains. These approaches can mainly be divided into three types: those used during library construction, by preferentially incorporating aDNA fragments characterised by the high level of damage, those applied after library construction, by separating exogenous and endogenous fractions through annealing to pre-defined sets of probes (in solution or on microarrays), or those based on targeted digestion of environmental microbial DNA using restriction enzymes and primer extension capture (PEC).

Selective uracil enrichment

During the construction of the library, the ssDNA fragments are bound through a biotinylated adaptor to streptavidin-coated beads. In the polymerase extension step, the DNA strand complementary to the original template is generated. In this kind of enrichment, the constructs undergo phosphorylation at the 5' end, to enable the ligation of a non-phosphorylated adaptor (ligation between the 3' end of the adaptor and the 5' end of the newly synthesized strand). DNA is then treated with uracil DNA glycosylase (UDG) and endonuclease VIII (USER mix): UDG generates abasic sites at cytosine that were deaminated into uracils post-mortem, endo VIII cuts at the resulting abasic site. This cleavage generates new 3' termini, which are then dephosphorylated, resulting in 3'OH ends that can be used as starting points for a new step of extension. This results in the elongation of the damaged strand, from the damaged region towards the bounded bead: while the new DNA molecule is synthesised, the original fragment is displaced. As a result, the dsDNA molecules newly formed no longer contain the adaptor bound to the beads, leaving in the supernatant a dsDNA library of the strands that originally harboured deaminated cytosines, available for further amplification and sequencing. The undamaged DNA template fraction remains attached to the paramagnetic beads.

Extension-free target enrichment in solution

This approach is based on in solution target-probe hybridization to screen for only a single microorganism, after the construction of the library. It is a species-specific assay that requires heat denaturation of DNA libraries and the construction of a probe DNA library using long-range PCR if fresh DNA material from closely related species is available, or through custom design and synthesis of oligonucleotides. This method is useful when the microorganism to target is known, for example, when the hypothesis exists for the causative agent of an epidemic or in presence of skeletal lesions in the studied individuals.

Solid-phase target enrichment

Another enriching strategy applied after constructing the library is the direct application of microarrays. They are applied for a wide laboratory-based pathogen screening that searches simultaneously for various pathogenic microorganisms. This kind of approach is favourable for those pathogens that leave no physical skeletal evidence and whose presence cannot be easily hypothesized a priori. The probes are designed to represent conserved or unique regions from a range of pathogenic viruses, parasites or bacteria.

Since microarrays contain sequences derived from modern strains of ancient pathogens, the limits of this method are the poor detection of the most divergent genomic regions and the omission of regions with important genomic rearrangements or unknown additional plasmids.

Whole-genome enrichment

The whole-genome in-solution capture (WISC) allows the characterization of the entire genome sequence of ancient individuals. This technique is based on the use of a genome-wide biotinylated RNA probe library generated through in vitro transcription of fresh modern DNA extracts from species closely related to the target aDNA sample. The heat-denatured aDNA library is then annealed to the RNA probes. To improve stringency and reduce enrichment for highly repetitive regions, low-complexity DNA and adaptor-blocking RNA oligonucleotides are added. The library fraction of interest in then recovered through elution from streptavidin-coated paramagnetic beads (to which the RNA probes are bound).

Computational analysis

The analysis of sequence data obtained by NGS relies on the same computational approaches used for modern DNA, with some peculiarities. A widely used tool to align reads from aDNA against reference genomes is the PALEOMIX package, which can quantify DNA damage levels through mapDamage2 and perform phylogenomic and metagenomic analyses. It is important to consider that the alignment will always exhibit substantial fractions of nucleotides mismatched that do not result from sequencing errors or polymorphisms but from the presence of damaged bases. For this reason, the acceptance threshold for read-to-reference edit distance should be chosen according to the phylogenetic distance to the reference genome. Probabilistic aligners that take into account the damage pattern of aDNA have been developed to improve alignments.

MALT

Studies of the ancient DNA of pathogens is restricted to skeletal collections that change their appearance as a result of infections. A pathogen linked to a known epidemiological context is identified through screening without prior knowledge of its presence. Methods include broad-spectrum molecular approaches focused on pathogen detection via fluorescence hybridization-based microarray technology, identification via DNA enrichment of certain microbial regions or computational screening of non-enriched sequence data against human microbiome data sets. These approaches offer improvements but remain biased in the bacterial taxa used for species-level assignments.

MEGAN alignment tool (MALT) is a new program for the fast alignment and taxonomic assignment method to the identification of ancient DNA. MALT is similar to BLAST as it computes local alignments between highly conserved sequences and references. MALT can also calculate semi-global alignments where reads are aligned end-to-end. All references, complete bacterial genomes, are contained in a database called National Center for Biotechnology Information (NCBI) RefSeq. MALT consists of two programs: malt-build and malt-run. Malt-build is used to construct an index for the given database of reference sequences. Instead, malt-run is used to align a set of query sequences against the reference database. The program then computes the bit-score and the expected value (E-value) of the alignment and decides whether to keep or discard the alignment depending on user-specified thresholds for the bit-score, the E-value or the per cent identity. The bit-score is the requires size of a sequence database in which the current match could be found just by chance. The higher the bit-score, the better the sequence similarity. E-value is the number of expected hits of similar quality (score) that could be found just by chance. The smaller is the E-value, the better is the match.

MALT allows the screening of non-enriched sequence data in the search for unknown candidate bacterial pathogens that are involved in past disease outbreaks and for the exclusion of the environmental bacterial background. MALT is very important because it offers the advantage of genome-level screening without selection of a particular target organism, avoiding errors that are common to other screening approaches. To authenticate the candidate taxonomic assignments complete alignments are needed, but the target DNA is often present in a low amount so a small number of a marked region may not be sufficient for identification. This approach can detect only bacterial DNA and viral DNA, so it is not possible to identify other infectious agents that may be present in a population. This method is useful for studies dealing with the identification of pathogens responsible for ancient and modern disease, especially in cases for which candidate organisms are not known a priori.

Applications

Ancient pathogen genomics as a tool against future epidemics

One interesting application of the different sequencing techniques available nowadays is the investigation of historical disease outbreaks to provide an answer to important and long-standing questions in epidemiology, pathogen evolution and also human history.

So, much effort is spent to find more and more information about the aetiology of infectious diseases of historical importance, such as plague and the cocoliztli epidemic, to describe the geographic spread of viruses and to try defining the pathogenic mechanism of these infectious agents that are actually active elements of the evolutionary process. Today Y.pestis and S. enterica seem to be so far from us and no more dangerous at all, but scientists are still interested in the long-term tracing of genetic adaptation of these bacteria and accurate quantification of rates of their evolutionary change. This is because they can extract from this knowledge of the past the right ideas to develop a strategy against future epidemics.

Being perfectly aware of the fact that bacteria and viruses are one of most variable elements in nature, prone to unlimited mutational events, and taking for granted that it is impossible to manage all the external factors that can influence the development of a pathogenic virus, nobody is talking about defeating a new possible outbreak of plague or any other infective agent of the past: here the aim is to define a strategy, a "guideline", to be more prepared when a new dangerous pathogen will come. The contribution of the environment in infections is to be defined and factors such as human migration, climate change, overcrowding in cities or animal domestication are some of the major causes that contribute to the emergence and spread of disease. Of course, these factors are unpredictable and this is a reason why researchers are trying to bring relevant information from the past, that can be useful, today and tomorrow. While they continue to develop strategies to defeat emerging threats using diagnostic, molecular and advanced tools, they are still looking back at how ancient pathogens have evolved and adapted through historical events. The more it's known about the genomic basis of virulence in historical diseases, the more it can be understood about the emergence and re-emergence of infectious diseases today and in the future.

Ancient infections and human evolution

The analyses of phylogenic relationships between the human host and viral pathogens suggest that many diseases have been coevolving with humans for millennia, since the very start of human history in Africa.

In particular, the long-term interaction with pathogens is considered a selection that can be very strong since not all the individuals could survive in touch with all infectious agents that they had met over the years: the natural selection by pathogens is implicated in the evolution of species. This interaction has been already used to track human population movements and to reconstruct human migration flows within and out of Africa.

A pretty new application and interpretation of this feature is using aDNA to better understand human evolution. Many tropical infections probably played a significant role in the human evolutionary process. The correlation between humans and viruses can be understood if it is seen as a "fight" that continues for millennia and that is not still won by anyone: when viruses have changed their features in order to be infective for the other "fighters", humans had to find a strategy to increase their fitness and survived among changes.

In this continuous challenge through the years, next to infective diseases and other illnesses afflicting modern human society, cancer recently represents one of the most enigmatical ailments. Scientists are investigating if neoplastic diseases are restricted to postindustrial human society or if their origins can be found further back in time, maybe into prehistory. The difficulty is that cancer, lethal and fast, leaves very few indications in skeletons in those cases that succumb to death shortly, and even no signs of existence at all, in the case of extraskeletal tumours. Anyway, the knowledge about the aetiology of cancer is incomplete and microorganisms are taking their part with the role of their infection: migration movements in the past could have brought with them viruses, so possible reservoir of tropical disease as well as predisposition to cancer. For this reason, molecular analytical techniques are applied to archaeological remains to study hominin evolution, but also to improve the research in understanding the epidemiology and aetiology of tumours. Information derived from the aDNA can be used to anchor pathogen mutations and reconstruct back from the presence of microorganisms the evolutionary process, it can be useful to develop new vaccines or to discover possible future pathogenic threats.

Past pandemics are much more than just ancient history

What happened in the past is not all history, there is something hidden that can still drive human genetic diversity and natural selection, something that went in contact with humankind hundreds of years ago but that can still have an impact on global human health. Since epidemics are one of the most frequent phenomena that have affected and potentially devastated human populations, it is important to detect, prevent and control potential infective agents. After all, archaeologists, geneticists, and medical scientists are concerned in exploring the influences of pathogens that can contribute, threatening or improving, human health and longevity.

Evolution and phylogenesis of Yersinia pestis

Yersinia pestis is a gram-negative bacterium and belongs to the family of Enterobatteriaceae. Its closest relatives are Yersinia pseudotuberculosis and Yersinia enterocolitica, which are environmental species.

Y. pestis bacillus.

They all possess the plasmid pCD1, which encodes for a type III secretory system. Among chromosomal protein-coding genes, their nucleotide genomic identity rates 97%. They are different in terms of their virulence potential and transmission mechanisms.

Y. pestis is not a human-adapted bacteria. Its main reservoirs are rodents (like marmots, mice, great gerbils, voles and prairie dogs) and it is transmitted to humans by the flea. One of the most studied vectors of this pathogen is Xenopsylla cheopis.

After the bite of an infected flea, the bacteria enter into the host organism and travel to the closest lymph node, where bacteria replicate causing the large swellings called buboes. Bacteria can also disseminate into the bloodstream (causing septicaemia) and to the lung (causing pneumonia). The pulmonary disease has a direct human-to-human transmission.

It has been determined that Y. pestis became so dangerous because of the acquisition of ymt (yersina murine toxin). This gene is present on the pMT1 plasmid and allowed the survival of the bacterium in the flea vector and facilitated colonization of the midgut in arthropod, giving rise to the past millennium large-scale pandemics.

Early evolution and divergence from Yersinia pseudotuberculosis

Y. pestis is distinguishable from the other two species because of its pathogenicity and transmission mechanism. These differences are given by two plasmids: pPCP1, that confer to the bacterium its invasive properties in humans and pMT1, which is involved in flea colonisation (along with some loss of function on bacterial chromosomal genes).

Samples dated on the Late Neolithic and Bronze Age allowed identifying a first genetic divergence between Y. pseudotuberculosis and Y. pestis ancestors. The characteristics that confer to Y. pestis its virulence were absent in these strains: they lack of ymt, a gene necessary to the colonization of the vector; also, they presented an active form of genes required for biofilm formation (inactive in the pathogen Y. pestis) and an active flagellin gene, that is an inducer of immune response (is a pseudogene in Y. pestis).

The comparison of a draft of the genome and the two plasmids (pCD1 and pMT1) with samples of Black Death victims (1348-1349) in the East Smithfield burial ground underlined a very high genetic conservation of the sequence: only 97 single-nucleotide differences over 660 years.

Y. pestis microevolution

The London 6330 individual strain owns mutations absent in other isolates of the same period (1348-1350): the reason may be either the presence of multiple strains circulating in Europe at the same time or the microevolution of one single strain during the pandemic.

Three major outbreaks of plague

There are three pandemic outbreaks of Y. Pestis:

  1. The first is known as the Plague of Justinian, it first occurred in Egypt in 541-543 and then spread to Constantinople and neighbouring regions. It had outbreaks in Europe until 750 CE. Phylogenetic analysis showed that both genomes belong to a lineage that is extinct today and is closely related to stains from modern-day China, which suggest the possibility of an East Asian origin of the first pandemic.
  2. The second pandemic is known as the Black Death or as Great Pestilence. It occurred in 1346-1352 in Europe and had a lot of resurgences of plague, it continued until the 18th century. It could be possible that in this pandemic there were two different strains of Y. pestis that entered the continent through different pulses.
  3. The third pandemic started in China in 1860. It has a fast spread to other countries, due to the use of railways and steamships.

The strains associated with the Justinian Plague appear on a novel branch, which is phylogenetically distinct from the second and the third plague pandemics. The first strain of Y. pestis found during the second outbreak survives and give rise to modern branch 1 strains associated with the third pandemic outbreak.

The first plague bacteria and the second and third plague strain have a common ancestor.

Linkage between 2nd and 3rd pandemics

In a recent study, genomes of Y. pestis from three samples resumed in Barcelona (deceased between 1300-1420), Ellwangen (between 1486-1627) and Bolgar city (between 1298-1388). The date of death of the individuals analysed was determined thanks to radiocarbon dates; the last one was confirmed by the presence of a coin produced only after the year 1362. Of 223 samples from 178 individuals, only one for each site had a suitable amount of DNA and was finally selected for the whole genome sequencing of the bacillus (through a genome-capture assay, using as a draft Y. pseudotuberculosis genome and pMT1 and pCD1 from Y. pestis).

The alignment with a Y. pestis phylogeny tree created with previously know ancient genomes revealed an increase genetic diversity outside of China in comparison to what was previously thought; all the three new genomes mapped in Branch 1 and possess two SNPs associated to the Black Death (all the genomes of Y. pestis dated to the Black Death map in Branch 1). The Barcelona strain has no differences with the London strain; the two individuals from which the genome was obtained died of plague with a distance of some months (spring and autumn 1348) underlining the presence in Europe of a single wave of plague with low genetic diversity. The Ellwangen strain maps in a sub-branch of Branch 1 and is ancestral to a previously sequenced strain (L'Observance). it descends from the one circulating in London and Barcelona during the Black Death but also have additional mutations. Is therefore considered a lineage diverged from Branch 1 before the 16th century (Ellwangen outbreak) and with no known modern descendants.

In comparison with isolates from the Black Death, the Bolgar city strain presents:

  • p3 and p4, shared by the "London individual 6330";
  • p6, shared with all modern Branch 1 strains;
  • p7, unique of this strain;

The Bolgar City strain possesses SNPs associated to the Black Death and can be an evidence of a movement of plague towards east; These findings give credit to one of the models that try to explain the linkage between 2nd and 3rd pandemic: in this scenario, there was a single exit of plague to Europe (causing the Black Death) that after a radiation event, travelled eastward to establish in former soviet union and Asia, from which it spread in the 18th century to give raise to the 3rd pandemic.

Another hypothesis is that the 3rd pandemic's lineage may have been generated by a pre-existing genetic variability in Y. pestis strains in China: this hypothesis is actually supported by the correlation between following waves of the pandemic in Europe and climatic fluctuations that would have allowed its spread in the continent. This model can't explain the genetic diversity of the Black Death (four different lineages at least, that would have required the introduction from Asia of four different strains).

Again, there are two models that try to explain the multiple plague outbreaks in Europe following the black death:

  • Repeated introduction of plague from Asia. This scenario is compatible with the 2nd theory discussed before that sees a genetic variability of Y. pestis in China;
  • Presence in Europe of a reservoir (now extinct) that caused continue outbreaks until the 18th century;

Both models can be valid and nowadays we're not able to demonstrate one over the other. However, the Ellwangen strain genome sequenced in this study may be considered a proof of the second hypothesis due to the geographical position of the city that tends to exclude the possibility of an introduction of plague from eastward.

Modern Y. pestis strains

Sequencing of Y. pestis genomes allowed to discover a variation event preceding Black Death that gave rise to many strains that circulate today.

Salmonella enterica genomes analysis

During the 16th an epidemic occurred in Mexico and it caused high mortality in Indigenous populations of the Americas. This high mortality has been the consequence of the influence of the demographic collapse of many indigenous populations. This epidemic has been called "cocoliztli" by the native Aztec because of the symptoms, in particular, high fever and bleeding.

This pestilence is considered one of the worst epidemics in the history of Mexico and the cause of this outbreaks is remained a mystery for over 500 years.

A group of scientists from Harvard and Max-Planck Institute published a study in the journal of Nature ecology and Evolution, and they suggest Salmonella enterica as a good candidate for the strong epidemic in Mexico during the 16th century. Many studies suggest that this bacterium has been introduced in the Indigenous populations by Europeans.

The group of scientists analyzed the aDNA extracted from the teeth of 24 skeletons buried in a cemetery in the city of Teposcolula-Yucundaa and they found in 10 of the 24 skeletons aDNA traces of Salmonella enterica. Also, to demonstrate that the bacterium was introduced in Mexico by the Europeans, they analyzed five individuals that were buried before the influx of Europeans. The results revealed that there was no evidence of Salmonella enterica in the pre-contact era.

Analysis of Salmonella enterica genomes

The scientists performed the extraction of the aDNA from the teeth of 24 indigenous individuals' remains from the contact era epidemic cemetery and of 5 individuals buried in the pre-contact era cemetery. The extraction was performed according to the protocol for aDNA extraction. The group of researchers examined, in parallel, also a soil sample of the cemeteries to get an overview of the environment microorganisms that could have penetrated the samples.

After the extraction, the genomes were sequenced using Illumina genome analyzer. Then, using a bioinformatic tool, called MALT, the researchers performed an analysis of metagenomic sequences data. This program lets the researchers align the extracted sequences with a reference without specifying a precise target. The researchers performed MALT run two times: one using the complete bacterial genomes that were available through NCBI (National Center for Biotechnology Information) RefSeq as a reference, and the second run was carried out using the full NCBI Nucleotide database to screen for viral DNA.

The result of the screening process was positive for the presence of Salmonella enterica DNA in 10 sequences up to 24 collected from the samples and three tooth sample had a high amount of reads assigned to S. enterica. In particular, the major S. enterica strain present in the samples is the S. Paratyphi C. This strain causes enteric fever in human individuals. In the pre-contact era samples, they did not find any evidence of S. enterica, supporting the hypothesis that S. enterica was not a local bacteria.

A further analysis was carried out to identify the classical pattern of damage of aDNA in the three positive tooth samples and this was conducted by mapping the data sets to the S. Paratyphy C genome reference. The results were positive and supported the thesis of S.enterica as the cause of cocolitzli.

To go in-depth with the analyses and confirm the thesis, the researchers conducted further experiments and computational analysis. They performed a whole-genome target array and in-solution hybridization capture using probes that include the modern S. enterica genome differences and using S. Paratyphi C as reference. The hybridization was successful for the ten positive samples, while the other samples resulted negative for the ancient DNA.

 

Ancient DNA

From Wikipedia, the free encyclopedia
 
Cross-linked DNA extracted from the 4,000-year-old liver of the ancient Egyptian priest Nekht-Ankh.

Ancient DNA (aDNA) is DNA isolated from ancient specimens. Due to degradation processes (including cross-linking, deamination and fragmentation) ancient DNA is more degraded in comparison with contemporary genetic material. Even under the best preservation conditions, there is an upper boundary of 0.4–1.5 million years for a sample to contain sufficient DNA for sequencing technologies. 

Genetic material has been recovered from paleo/archaeological and historical skeletal material, mummified tissues, archival collections of non-frozen medical specimens, preserved plant remains, ice and from permafrost cores, marine and lake sediments and excavation dirt.

History of ancient DNA studies

1980s

The first study of what would come to be called aDNA was conducted in 1984, when Russ Higuchi and colleagues at the University of California, Berkeley reported that traces of DNA from a museum specimen of the Quagga not only remained in the specimen over 150 years after the death of the individual, but could be extracted and sequenced. Over the next two years, through investigations into natural and artificially mummified specimens, Svante Pääbo confirmed that this phenomenon was not limited to relatively recent museum specimens but could apparently be replicated in a range of mummified human samples that dated as far back as several thousand years.

The laborious processes that were required at that time to sequence such DNA (through bacterial cloning) were an effective brake on the development of the field of ancient DNA (aDNA). However, with the development of the Polymerase Chain Reaction (PCR) in the late 1980s, the field began to progress rapidly. Double primer PCR amplification of aDNA (jumping-PCR) can produce highly skewed and non-authentic sequence artifacts. Multiple primer, nested PCR strategy was used to overcome those shortcomings.

1990s

The post-PCR era heralded a wave of publications as numerous research groups claimed success in isolating aDNA. Soon a series of incredible findings had been published, claiming authentic DNA could be extracted from specimens that were millions of years old, into the realms of what Lindahl (1993b) has labelled Antediluvian DNA. The majority of such claims were based on the retrieval of DNA from organisms preserved in amber. Insects such as stingless bees, termites, and wood gnats, as well as plant and bacterial sequences were said to have been extracted from Dominican amber dating to the Oligocene epoch. Still older sources of Lebanese amber-encased weevils, dating to within the Cretaceous epoch, reportedly also yielded authentic DNA. Claims of DNA retrieval were not limited to amber.

Reports of several sediment-preserved plant remains dating to the Miocene were published. Then in 1994, Woodward et al. reported what at the time was called the most exciting results to date— mitochondrial cytochrome b sequences that had apparently been extracted from dinosaur bones dating to more than 80 million years ago. When in 1995 two further studies reported dinosaur DNA sequences extracted from a Cretaceous egg, it seemed that the field would revolutionize knowledge of the Earth's evolutionary past. Even these extraordinary ages were topped by the claimed retrieval of 250-million-year-old halobacterial sequences from halite.

As the field developed a better understanding of the kinetics of DNA preservation, the risks of sample contamination and other complicating factors, along with the failure of attempts to replicate many of the findings, all of the decade's claims of multi-million year old aDNA would come to be dismissed as inauthentic results.

2000s

Single primer extension amplification was introduced in 2007 to address postmortem DNA modification damage. Since 2009 the field of aDNA studies has been revolutionized with the introduction of much cheaper research-techniques, leading to new insights in human migrations. The use of high-throughput Next Generation Sequencing (NGS) techniques in the field of ancient DNA research has been essential for reconstructing the genomes of ancient or extinct organisms. A single-stranded DNA (ssDNA) library preparation method has sparked great interest among ancient DNA (aDNA) researchers.

In addition to these technical innovations, the start of the decade saw the field begin to develop better standards and criteria for evaluating DNA results, as well as a better understanding of the potential pitfalls.

Problems and errors

Degradation processes

Due to degradation processes (including cross-linking, deamination and fragmentation) ancient DNA is of lower quality in comparison with modern genetic material. The damage characteristics and ability of aDNA to survive through time restricts possible analyses and places an upper limit on the age of successful samples.  There is a theoretical correlation between time and DNA degradation, although differences in environmental conditions complicates things. Samples subjected to different conditions are unlikely to predictably align to a uniform age-degradation relationship. The environmental effects may even matter after excavation, as DNA decay rates may increase, particularly under fluctuating storage conditions. Even under the best preservation conditions, there is an upper boundary of 0.4–1.5 million years for a sample to contain sufficient DNA for contemporary sequencing technologies.

Research into the decay of mitochondrial and nuclear DNA in Moa bones has modelled mitochondrial DNA degradation to an average length of 1 base pair after 6,830,000 years at −5 °C. The decay kinetics have been measured by accelerated aging experiments further displaying the strong influence of storage temperature and humidity on DNA decay. Nuclear DNA degrades at least twice as fast as mtDNA. As such, early studies that reported recovery of much older DNA, for example from Cretaceous dinosaur remains, may have stemmed from contamination of the sample.

Age limit

A critical review of ancient DNA literature through the development of the field highlights that few studies after about 2002 have succeeded in amplifying DNA from remains older than several hundred thousand years. A greater appreciation for the risks of environmental contamination and studies on the chemical stability of DNA have resulted in concerns being raised over previously reported results. The alleged dinosaur DNA was later revealed to be human Y-chromosome, while the DNA reported from encapsulated halobacteria has been criticized based on its similarity to modern bacteria, which hints at contamination. A 2007 study also suggests that these bacterial DNA samples may not have survived from ancient times, but may instead be the product of long-term, low-level metabolic activity.

aDNA may contain a large number of postmortem mutations, increasing with time. Some regions of polynucleotite are more susceptible to this degradation, so sequence data can bypass statistical filters used to check the validity of data. Due to sequencing errors, great caution should be applied to interpretation of population size. Substitutions resulting from deamination cytosine residues are vastly over-represented in the ancient DNA sequences. Miscoding of C to T and G to A accounts for the majority of errors.

Contamination

Another problem with ancient DNA samples is contamination by modern human DNA and by microbial DNA (most of which is also ancient). New methods have emerged in recent years to prevent possible contamination of aDNA samples, including conducting extractions under extreme sterile conditions, using special adapters to identify endogenous molecules of the sample (over ones that may have been introduced during analysis), and applying bioinformatics to resulting sequences based on known reads in order approximate rates of contamination.

Non-human aDNA

Despite the problems associated with 'antediluvian' DNA, a wide and ever-increasing range of aDNA sequences have now been published from a range of animal and plant taxa. Tissues examined include artificially or naturally mummified animal remains, bone, paleofaeces, alcohol preserved specimens, rodent middens, dried plant remains, and recently, extractions of animal and plant DNA directly from soil samples.

In June 2013, a group of researchers including Eske Willerslev, Marcus Thomas Pius Gilbert and Orlando Ludovic of the Centre for Geogenetics, Natural History Museum of Denmark at the University of Copenhagen, announced that they had sequenced the DNA of a 560–780 thousand year old horse, using material extracted from a leg bone found buried in permafrost in Canada's Yukon territory.

In 2013, a German team reconstructed the mitochondrial genome of an Ursus deningeri more than 300,000 years old, proving that authentic ancient DNA can be preserved for hundreds of thousand years outside of permafrost.

Researchers in 2016 measured chloroplast DNA in marine sediment cores, and found diatom DNA dating back to 1.4 million years. This DNA had a half-life significantly longer than previous research, of up to 15,000 years. Kirkpatrick's team also found that DNA only decayed along a half-life rate until about 100 thousand years, at which point it followed a slower, power-law decay rate.

Human aDNA

Due to the considerable anthropological, archaeological, and public interest directed toward human remains, they have received considerable attention from the DNA community. There are also more profound contamination issues, since the specimens belong to the same species as the researchers collecting and evaluating the samples.

Sources

Due to the morphological preservation in mummies, many studies from the 1990s and 2000s used mummified tissue as a source of ancient human DNA. Examples include both naturally preserved specimens, for example, those preserved in ice, such as the Ötzi the Iceman, or through rapid desiccation, such as high-altitude mummies from the Andes, as well as various sources of artificially preserved tissue (such as the chemically treated mummies of ancient Egypt). However, mummified remains are a limited resource. The majority of human aDNA studies have focused on extracting DNA from two sources that are much more common in the archaeological recordbone and teeth. The bone that is most often used for DNA extraction is the petrous bone, since its dense structure provides good conditions for DNA preservation. Several other sources have also yielded DNA, including paleofaeces, and hair. Contamination remains a major problem when working on ancient human material.

Ancient pathogen DNA has been successfully retrieved from samples dating to more than 5,000 years old in humans and as long as 17,000 years ago in other species. In addition to the usual sources of mummified tissue, bones and teeth, such studies have also examined a range of other tissue samples, including calcified pleura, tissue embedded in paraffin, and formalin-fixed tissue. Efficient computational tools have been developed for pathogen and microorganism aDNA analyses in a small (QIIME) and large scale (FALCON).

Results

Taking preventative measures in their procedure against such contamination though, a 2012 study analyzed bone samples of a Neanderthal group in the El Sidrón cave, finding new insights on potential kinship and genetic diversity from the aDNA. In November 2015, scientists reported finding a 110,000-year-old tooth containing DNA from the Denisovan hominin, an extinct species of human in the genus Homo.

The research has added new complexity to the peopling of Eurasia. It has also revealed new information about links between the ancestors of Central Asians and the indigenous peoples of the Americas. In Africa, older DNA degrades quickly due to the warmer tropical climate, although, in September 2017, ancient DNA samples, as old as 8,100 years old, have been reported.

Moreover, ancient DNA has helped researchers to estimate modern human divergence. By sequencing African genomes from three Stone Age hunter gatherers (2000 years old) and four Iron Age farmers (300 to 500 years old), Schlebusch and colleagues were able to push back the date of the earliest divergence between human populations to 350,000 to 260,000 years ago.

Human brain

From Wikipedia, the free encyclopedia https://en.wikipedia.org/wiki/Human_brain Human brain The human br...