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Sea Lamprey

Petromyzon marinus Linnaeus 1758

Associations

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Sea lampreys do not have many known predators, and their most common predator are humans. While sea lampreys in the Great Lakes region are often killed in preservation efforts of native fish, sea lampreys are also trapped in Europe, Asia, and India to be consumed and are even considered a delicacy. Many European countries capture sea lampreys and use them in a variety of dishes.

Known Predators:

  • humans Homo sapiens
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Cherry, S. 2011. "Petromyzon marinus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Petromyzon_marinus.html
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Selisha Cherry, Radford University
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Karen Francl, Radford University
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Gail McCormick, Special Projects
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Morphology

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Sea lampreys, Petromyzon marinus, belong to a group of fish called Agnathans, which lack a jaw. Although classified in the subphylum Vertebrata, this species lacks vertebrae, and their entire skeleton is cartilaginous. Commonly known for their smooth, scaleless physique and long cylindrical bodies, they are often misidentified as eels. Sea lampreys also lack swim bladders and a lateral line system. Members of this species have a visible eye spot located on each side of their head behind a single nostril and above a set of seven gill openings. Their mouth takes on an oval shape while attached to their host, but once opened it becomes larger than the head and pharynx together. Inside the oval-shaped mouth are numerous rows of large teeth pointing inward. Sea lampreys have two dorsal fins but lack any paired fins. When spawning occurs, males develop a distinct ridge along their back and females develop a pronounced fold of skin behind their vent.

Sea lampreys are the largest and most aggressive species of lamprey, ranging from 15.2 to 30 cm in length as juveniles and 30 to 100 cm in length as adults. Adults can weigh up to 2.5 kg. Besides length, there are several key differences between adult and young sea lampreys. Color is often a good indicator of age; larvae generally are dark, greenish brown with a light grey underbelly, while adults are brownish grey and tend to lighten in color when about to spawn. Another key difference involves the dorsal fins; while separate in young lampreys, the dorsal fins migrate closer together as sea lampreys reach adulthood.

Range mass: 1 to 2.5 kg.

Range length: 15.2 to 30 cm.

Other Physical Features: bilateral symmetry ; polymorphic

Sexual Dimorphism: sexes shaped differently

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Cherry, S. 2011. "Petromyzon marinus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Petromyzon_marinus.html
author
Selisha Cherry, Radford University
editor
Karen Francl, Radford University
editor
Gail McCormick, Special Projects
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Life Expectancy

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Sea lampreys die soon after spawning. They can survive up to 5 years in the wild waiting for the opportune time to reproduce. Most lampreys, however, live 1.5 to 5 years in the wild.

Range lifespan
Status: wild:
1.5 to 5 years.

Typical lifespan
Status: wild:
1.5 to 5 years.

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bibliographic citation
Cherry, S. 2011. "Petromyzon marinus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Petromyzon_marinus.html
author
Selisha Cherry, Radford University
editor
Karen Francl, Radford University
editor
Gail McCormick, Special Projects
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Habitat

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Sea lampreys are anadromous, and migration is triggered by changes in water temperature. In general, they prefer shallow coastal areas, though they are found at depths between 0.91 and 4.57 m. Young lampreys are hatched in gravel or rock beds in small, freshwater streams and rivers. After the larval stage, they migrate into saltwater ocean habitats. They return to freshwater to lay their eggs. Sea lampreys thrive in systems where the following are present: 1) waterways lacking obstructions (like dams or waterfalls) with clean sand and gravel areas for spawning; 2) sand beds free of pollutants with a large supply of organic matter for their developing young; and 3) large waterways with a plentiful supply of fish to serve as hosts for their fully developed offspring.

Range depth: 0.91 to 4.57 m.

Habitat Regions: saltwater or marine ; freshwater

Aquatic Biomes: lakes and ponds; rivers and streams; coastal

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Cherry, S. 2011. "Petromyzon marinus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Petromyzon_marinus.html
author
Selisha Cherry, Radford University
editor
Karen Francl, Radford University
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Gail McCormick, Special Projects
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Distribution

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Sea lampreys are native to the Atlantic Ocean. Between the months of March and October, they can be found along the coast of the United States as far north as Massachusetts and as far south as South Carolina. In October, North American lampreys migrate south along the Atlantic coast to warmer climates, some travelling as far south as Florida. Sea lampreys can also be found along the Atlantic coast of Europe as far north as Norway and ranging as far south as the Mediterranean. In October, they can travel as far south as Africa and to parts of the Indian coast. Sea lampreys have also been introduced to the Great Lakes region of the United States many times over within the past 200 years. Reports of this species in Lake Ontario date back to the early 1800s. Great Lake sea lampreys must first travel through the Gulf of St. Lawrence in order to gain access to the Atlantic coastal region.

Biogeographic Regions: nearctic (Introduced , Native ); palearctic (Native ); oriental (Native ); atlantic ocean (Introduced , Native ); mediterranean sea (Introduced , Native )

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Cherry, S. 2011. "Petromyzon marinus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Petromyzon_marinus.html
author
Selisha Cherry, Radford University
editor
Karen Francl, Radford University
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Gail McCormick, Special Projects
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Trophic Strategy

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Newly hatched larval sea lampreys are freshwater filter-feeders that consume detritus, algae, and other organic material found at river bottoms. Once in a saline environment (or in the Great Lakes), sea lampreys develop parasitic abilities, attach themselves to a fish and ingest their blood and skin. Sea lampreys ultimately breaks down the fish while the fish is still alive. This species is capable of attaching itself to a variety of species of fish and does not seem to have a preference of host species. Once sea lampreys reach sexual maturity, they no longer feed.

Animal Foods: fish; blood; body fluids; carrion

Plant Foods: algae

Other Foods: detritus

Foraging Behavior: filter-feeding

Primary Diet: carnivore (Piscivore , Sanguivore , Eats body fluids); herbivore (Algivore); omnivore ; detritivore

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bibliographic citation
Cherry, S. 2011. "Petromyzon marinus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Petromyzon_marinus.html
author
Selisha Cherry, Radford University
editor
Karen Francl, Radford University
editor
Gail McCormick, Special Projects
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Behavior

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Communication patterns of sea lampreys are not well known. It is thought male sea lampreys emit a pheromone composed of bile acids that alerts ovulating females to their presence. This signal may also be related to mating preferences and may be sent over large distances.

Other Communication Modes: pheromones

Perception Channels: visual ; chemical

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Cherry, S. 2011. "Petromyzon marinus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Petromyzon_marinus.html
author
Selisha Cherry, Radford University
editor
Karen Francl, Radford University
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Gail McCormick, Special Projects
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Conservation Status

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Sea lampreys are not protected. Indeed, as invasive species, efforts are in place to eradicate them from the Great Lakes region. Both federal and state governments have created programs to manage populations of and educate the community about this invasive, harmful species. Barriers and traps are set in the waterways to capture adult sea lampreys before they reproduce. Lampricides are also added to prime habitat of sea lampreys. These treatments specifically target lampreys and are designed not to harm other species. Each program has been tested for several years and has proven an effective control of sea lampreys.

US Federal List: no special status

CITES: no special status

State of Michigan List: no special status

IUCN Red List of Threatened Species: least concern

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bibliographic citation
Cherry, S. 2011. "Petromyzon marinus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Petromyzon_marinus.html
author
Selisha Cherry, Radford University
editor
Karen Francl, Radford University
editor
Gail McCormick, Special Projects
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Life Cycle

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There are four stages in the life cycle of sea lampreys, which usually spans 18 months but can last as long as 5 years. The first of these stages is the spawning phase, which occurs during spring and early summer. From April to June, sea lampreys search freshwater rivers and streams, seeking an ideal location in which to construct a nest and lay their eggs. Once the area is selected, male sea lampreys construct a nest, often moving rocks to create a large indenture or depression in the river or lake bed. A female then lays 30,000 to 100,000 eggs, which the male externally fertilizes. Both male and female adult sea lampreys float away and die soon after spawning. Unique to this phase is the disintegration of the digestive system; adult sea lampreys cannot feed while spawning. During the second phase, fertilized eggs settle into the sand or gravel and begin to grow. Within a few weeks, the eggs hatch and the larvae burrow further into the sand or gravel. Larvae filter-feed on algae and other aquatic organic matter. This larval phase can last for more than three years. In the third phase, known as transformation, larvae metamorphose into adult sea lampreys. During this phase sea lampreys develop a mouth, teeth and eyes. They also migrate to larger bodies of water, such as oceans or freshwater systems like the Great Lakes. Sea lampreys remain in this habitat for 12 to 18 months as a mature adult and begin to feed, attaching themselves to fish. This is known as the parasitic phase, during which sexual reproductive organs develop.

Development - Life Cycle: metamorphosis ; indeterminate growth

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bibliographic citation
Cherry, S. 2011. "Petromyzon marinus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Petromyzon_marinus.html
author
Selisha Cherry, Radford University
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Karen Francl, Radford University
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Gail McCormick, Special Projects
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Benefits

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Because of their over-aggressive behavior and generalist diet, sea lampreys parasitize many species of fish, contributing to the severe decline of commercial fishing industries, including those on the Atlantic coast of North America and in the Great Lakes region. Each sea lamprey kills more than 18.2 kg of fish each year. This species has parasitized many species of native fish in the Great Lakes region since the early 1800s, leading to the collapse of the Great Lakes commercial fishing industry and costing it millions of dollars. Population declines of native fish in the region have also negatively impacted sport fishing and tourism. In one case, a sea lamprey bit a human, though this is thought to have been accidental.

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bibliographic citation
Cherry, S. 2011. "Petromyzon marinus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Petromyzon_marinus.html
author
Selisha Cherry, Radford University
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Karen Francl, Radford University
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Gail McCormick, Special Projects
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Benefits

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Sea lampreys are considered a delicacy in many foreign countries like Asia and India and are harvested for food.

Positive Impacts: food

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bibliographic citation
Cherry, S. 2011. "Petromyzon marinus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Petromyzon_marinus.html
author
Selisha Cherry, Radford University
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Karen Francl, Radford University
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Gail McCormick, Special Projects
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Associations

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Parasitic sea lampreys have a detrimental effect on fish within their ecosystem. Specifically, sea lampreys feed on salmon, lake trout, rainbow trout, whitefish, chubs, burbot, walleye, and some catfish. Fish populations as as well as those industries that depend on fish are declining. Sea lampreys have no known predators except humans. In the Great Lakes region, a small percentage of sea lampreys carried cestode parasites or roundworms during some portion of its life. Of these parasites, only roundworms caused severe damage to their lamprey hosts.

Ecosystem Impact: parasite

Species Used as Host:

  • salmon Salmo salar
  • lake trout Salvelinus namaycush
  • rainbow trout Oncorhynchus mykiss
  • whitefish Coregonus clupeaformis
  • chubs Gila ditaenia
  • burbot Lota iota
  • walleye Sander vitreus
  • catfish Siluriformes

Commensal/Parasitic Species:

  • flatworms Cestoda
  • roundworms Nematoda
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Cherry, S. 2011. "Petromyzon marinus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Petromyzon_marinus.html
author
Selisha Cherry, Radford University
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Karen Francl, Radford University
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Gail McCormick, Special Projects
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Reproduction

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Little is known about the mating systems of sea lampreys. It is thought that male sea lampreys emit a pheromone composed of bile acids that alerts ovulating females to their presence. This signal may also be related to mating preferences and may be sent over large distances. Male sea lampreys selectively dig holes into river or stream bottoms and fertilize eggs once the female has laid them. This external fertilization allows multiple males to fertilize eggs.

Mating System: polygynous

From April to June, female sea lampreys lay between 30,000 and 100,000 eggs. These eggs are fertilized externally by males. Fertilized eggs hatch in 3 to 8 weeks. Larvae spend 1 to 3 years filter-feeding and do not associate with other sea lampreys. By 3 to 5 years of age, sea lampreys reach sexual maturity.

Breeding interval: Sea lampreys breed once at the end of their lifetime.

Breeding season: Sea lampreys breed between April and June.

Range number of offspring: 30,000 to 100,000.

Range gestation period: 3 to 8 weeks.

Range age at sexual or reproductive maturity (female): 3 to 5 years.

Range age at sexual or reproductive maturity (male): 3 to 5 years.

Key Reproductive Features: seasonal breeding ; sexual ; fertilization (External ); oviparous

Male sea lampreys selectively locate a nesting area. Sea lampreys do not allocate energy toward parental investment after laying and fertilizing eggs, as both male and female sea lampreys die shortly after spawning.

Parental Investment: no parental involvement; pre-fertilization (Provisioning, Protecting: Male, Female); pre-hatching/birth

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bibliographic citation
Cherry, S. 2011. "Petromyzon marinus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Petromyzon_marinus.html
author
Selisha Cherry, Radford University
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Karen Francl, Radford University
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Gail McCormick, Special Projects
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Biology

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Adults of this anadromous species migrate up rivers in March and April, but spawning actually takes place the following year between May and July (4). Mating occurs in pairs, unlike the other lampreys in which a female is mated by a succession of males (4). The female lays up to 300,000 eggs into a depression in the river bed created by the male. After hatching, the larvae, known as ammocoetes burrow into the sediment where they live for three to five years, feeding by filtering organic particles from the water (4). During metamorphosis, the eyes and the sucker-like mouth develop and the adults then migrate to the sea where they adopt a parasitic lifestyle, feeding by attaching to the bodies of large fish with the mouth and rasping away at the flesh. They remain in the sea for a few years and then return to freshwater in order to spawn. They do not feed during this return trip because the digestive organs degenerate, and shortly after spawning they die (4). Roman, Viking and Medieval Britons regarded river and sea lampreys as delicacies (2).
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Conservation

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A number of UK sites that support sea lampreys have been designated as candidate Special Areas of Conservation (SACs). Although this will be a good foundation for conserving the species, further action will be required. To this end, a draft Action Plan has been produced to guide future conservation efforts (7). Furthermore the Life in UK Rivers Project is helping to conserve this species (8).
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Description

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Lampreys are some of the most primitive vertebrates alive today, they are known as cyclostomes, which means 'round mouths' and refers to the fact that they are jawless, having instead a round sucker-like mouth. A further primitive characteristic is that the skeleton consists of cartilage and not bone (2). Lampreys are similar in shape to eels, and have a series of uncovered round gill openings (known as gill pores) on the sides of the head and a single nostril on the upper surface of the head (2). The sea lamprey is the largest cyclostome in Europe. It can be distinguished from the other lampreys by its larger size, the marbling of the greyish-green back, and the two dorsal fins, which are widely separated (4). An alternative common name is 'stone sucker' (5), which may have arisen from the habit of males during spawning, when they create a depression in the river bed by wriggling and removing stones with the mouth (4).
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Habitat

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Breeds in high quality, deep, fast flowing rivers with clean gravel in which to spawn and a sandy substrate for the larvae to burrow into (6). The adults migrate out to sea (4).
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Range

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The sea lamprey is fairly widespread in UK rivers, but it has declined to extinction in some areas. It is absent north of the Great Glen, Scotland, possibly as it prefers warm water (6). Current strongholds are the rivers Wye and Severn (2). Outside of the UK it is known from most of the Atlantic coastal areas of western and northern Europe between Norway and the Mediterranean. It is also found in eastern parts of North America (6).
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Status

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Classified as Least Concern (LC) on the IUCN Red List (1). Listed in Appendix III of the Bern Convention and Annex II of the EC Habitats Directive (3).
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Threats

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Pollution and changes in land use have affected this species (2), and river construction works have prevented migration along many traditionally used rivers (4).
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Brief Summary

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Just like other lampreys, sea lampreys have a monstrous suction mouth with rows of small grating teeth. Using these teeth, they clamp onto large fish to suck their blood. This is necessary for survival. They attach themselves so tightly that the victims are not usually able to shake them off, despite the suffering they incur from these parasitic fish. The wounds made by the lampreys can cause death in the victims. Sea lampreys are born in fresh water. They live in the mud as larva for several years. Only after maturing do they move to the sea, only returning to the river to lay eggs.
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Migration

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Anadromous. Fish that ascend rivers to spawn, as salmon and hilsa do. Sub-division of diadromous. Migrations should be cyclical and predictable and cover more than 100 km.
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Recorder
Rainer Froese
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Trophic Strategy

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Amphihaline species making important migrations. Spends its adult life in the sea for about 20 to 30 months. Adults enter freshwater/estuaries for spawning in spring; after spawning they normally die (Ref. 51442). The larvae are reported to spend 6-8 years in the substrate followed by metamorphosis and movement to sea. They remain in the estuarine/marine environment for a juvenile feeding period lasting 23-28 months, during which they grow from ca. 4 to 900 g; at the end of this period, they move into rivers as adults and reproduce (Ref. 58185). Larvae live in rivers where they feed on microorganisms and detritus (Ref. 30578, Ref. 51442). During juvenile feeding phase, they may not only feed on dead or netted fish, but also attach themselves to healthy fish (e.g. wide variety of bony fishes, sharks and marine mammals) by scraping a hole in their skin and sucking out the blood, body fluids and flesh. Adults are hematophageous predators of fishes (Ref. 51442). The ammocoetes-larvae is microphageous feeding mostly on diatoms (Ref. 51442).
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Recorder
Pascualita Sa-a
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Morphology

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Vertebrae: 0
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Recorder
Susan M. Luna
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Life Cycle

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Mature adults ascend rivers during spring and early summer (Ref. 35387, 88186) when water temperature ranges from 10-18°C (Ref. 88184) and gather in small groups (Ref. 5504). Behavioural experiments suggest that mature sea lampreys can smell the presence of ammocoetes and use this as a guide to functional spawning grounds (Ref. 88714). Spawning occurs in fast-flowing highly oxygenated areas with gravel, pebbles and sand bottoms (Ref. 12324). Females release small eggs (< 1 mm diameter) in nests exclusively built by males, which have been observed to reach the spawning grounds first (Ref. 5504, 12324, 51442). Spawning takes place mostly during sunny days, when water temperature is at least 15°C (Ref. 88171). Ammocoetes hatch after 7-14 days (41851, 88186). Successful hatching requires water temperatures of 15-25°C (Ref. 88715). Ammocoetes develop in freshwater and migrate to the sea after metamorphosis (Ref. 5504). Also Ref. 30578, 51442.
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Rainer Froese
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Diagnostic Description

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Anguilliform body (Ref. 51442). Jawless with a round sucker-like mouth and sharp teeth arranged in many consecutive circular rows (Ref. 88171). Presence of 7 branchial openings behind the eye (Ref. 51442, 88171). Lacks paired fins (Ref. 88171). Number of myomeres: 67-74 (Ref. 6258, 89241). Olive or brown-yellow on the dorsal and lateral part of the body, with black marblings; becomes lighter ventrally (Ref. 35388, 51442, 58137). Back, side and fins with prominent black mottling; oral disc as wide or wider than head (Ref. 86798). Adults: 11.4-120.0 cm TL. Body wet weight of the 120 cm TL individual was 2.3 kg. Maximum size attained by landlocked populations in the Laurentian Great Lakes, 60 cm TL. Body proportions, as percentage of TL (based on a variable number of specimens and sizes as indicated after the ranges): prebranchial length, 9.2-16.0 (in 46 specimens 19.2-82.75 cm TL); branchial length, 8.1-16.0 (in 46 specimens 19.2-82.75 cm TL); trunk length, 45.6-58.5 (in 42 specimens 25.6-82.75 cm TL); tail length, 22.0-42.2 (in 46 specimens 19.2-82.75 cm TL); eye length, 0.8-3.6 (in 49 specimens 13.5-82.75 cm TL); disc length, 4.5-9.3 (in 58 specimens 13.5-83.5 cm TL); snout length, 6.5-10.9 (in 41 specimens 25.6-82.75 cm TL). Urogenital papilla length, as a percentage of branchial length, in seven spawning males measuring 38.5-49.2 cm TL, 9.5-13.0. Spawning males develop a rope-like dorsal ridge ahead of the first dorsal fin and extending to the level of the posterior part of the branchial region, and hence, are sometimes called corded males. Dentition: supraoral lamina, 1 bicuspid tooth; infraoral lamina, 6-10 unicuspid teeth, the lateralmost sometimes bicuspid; 4 endolaterals on each side; endolateral formula, typically 2-2-2-2; 3 rows of anterials; first row of anterials, 1 unicuspid tooth; 5-7 rows of exolaterals on each side; 3 rows of posterials; first row of posterials, 10 unicuspid teeth; transverse lingual lamina strongly w-shaped, with 12-14 cusps, the median one not enlarged; longitudinal lingual laminae j-shaped, each with 12-14 cusps. Moderately well-developed marginal membrane. Velar tentacles, 2-3, smooth. Body coloration (preserved), newly-transformed individuals 13.5-17.5 cm TL have their colour grading from gray-bluish dorsally to silvery white ventrally while in individuals 45 cm TL or more the dorsal and lateral aspects become mottled and the ventral aspect remains uniformly pale. The iris is golden yellow. Lateral line neuromasts unpigmented or darkly pigmented. Extent of caudal fin pigmentation, 75% or more. Caudal fin shape, spade-like. Oral fimbriae, 114-150. Oral papillae, 24-33 (Ref. 89241).
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Susan M. Luna
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Biology

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Some populations are permanent freshwater residents [Laurentian Great Lakes, Finger Lakes (Lake Cayuga), Lake Champlain], while others are anadromous. Occupies a wide range of streams and habitats. Larvae are found in streams with summer flows 0.03-4,400 m3/s and summer water temperatures 10-26.1 °C. Relatively abundant in cool, pool-riffle streams with sand-gravel substrate, high water quality and stable flows, but is also tolerant of fluctuating flows. In Michigan, ammocoetes have been reported in lentic habitats up to 450 m from the presumed originating stream, at water depths 1-16 m, where substrates vary from sand-silt, with or without detritus, to gravel-rubble-sand. Feeding adults of permanent freshwater populations can be found in small to large lakes and large rivers and, in the case of anadromous populations, in small to large rivers and in the ocean. In the ocean, it occurs both pelagically and benthically, possibly to a depth of 4,099 m. Spawning adults can be found in creeks or lake inlets (Ref. 89241). Amphihaline species making important migrations. Spends its adult life in the sea for about 20-36 months, moving further offshore as it grows (Ref. 59043). Adults are parasitic, using their sharp teeth to attach themselves to cetaceans and large fish and feed off their host’s blood, body fluids and flesh for several days, usually without killing the host (Ref. 59043). An anticoagulant substance prevents the blood of the prey from clotting. Mature adults enter rivers and streams to spawn in spring (Ref. 12324, 35387, 88186). Movements from the sea to spawning sites may cover distances from 20-850 km inland (Ref. 12324). After spawning adults normally die (Ref. 51442). Ammocoetes drift downstream and bury in detritus-rich mud, silt or sand-silt bottoms (Ref. 59043, 88712) for 5.5-8 years, often at the edges of rivers and streams where currents are slow (Ref. 58185, 59043, 88184). Duration of larval life is usually a minimum of 5 yrs, but has been reported as short as 2 years and as long as 19 or more years (Ref. 89241). Ammocoetes are filter feeders of diatoms and detritus (Ref. 30578, 51442, 59043). Upon metamorphosis, individuals move downstream towards the sea. Juveniles remain in the estuaries and shallow coastal areas for a feeding period lasting 23-28 months, during which they grow from ca. 4 to 900 g (Ref. 58185, 88171). Most individuals attain 60-75 cm length (Ref. 88187). Duration of adult life in anadromous populations approximately two years. Metamorphosis occurs in July-October, but has been reported as early as April, in Michigan. Adults are parasitic on marine and freshwater fishes, and marine mammals. Multiple attachments can occur (e.g., 3 on Cetorhinus maximus, 2-3 on Urophycis chuss). Adults are preyed upon by Porbeagle Sharks in northwestern Atlantic waters. Feeding migrations in landlocked parasitic adults in the Laurentian Great Lakes can reach 628 km (Ref. 89241). They may not only feed on dead or netted fish, but also attach themselves to healthy fish. The landlocked form is very destructive to freshwater fishes and occasionally annoys bathers by clinging to them (Ref. 51442). In Michigan, the spawning period is from 27 May to 2 September, at water temperatures between 11.1-26.1 °C, with peak spawning activity in late May to mid-June. In Ontario, nest building occurs from 4 to 21 June at water temperatures 18-23 °C. In Québec and New York streams spawning also occurs in June, but in New York lakes spawning is from the end of May to the beginning of July. Nests are built in streams having 1.5-43 m width, 15-90 cm depth, and 0.01-54 m3/s flow. Up to ten spawning lampreys have been found in a nest. Fecundity, 43,997-101,932 [up to 108,000 according to Gage (1928)] eggs/female in landlocked populations and 151,836-304,832 eggs/female in anadromous populations. There are reported occurrences in Michigan of communal spawning of Sea Lamprey with Chestnut Lamprey (Pine, Platte, and Muskegon rivers), of Sea Lamprey with Northern Brook Lamprey (Devils River), of Sea Lamprey with Silver Lamprey (Carp Lake, Devils, East Au Gres, and Rifle rivers), of Sea Lamprey with American Brook Lamprey (Carp Lake, Pine and Pentwater rivers), of Sea Lamprey with American Brook Lamprey and Chestnut Lamprey (Betsie River), and of Sea Lamprey with American Brook Lamprey and Silver Lamprey (Carp Lake). Invaded the upper Laurentian Great Lakes (Huron-Michigan-Superior) in the late 1930s, where it contributed to some extent to the collapse of the Lake Trout and various cisco (Coregonus johannae, C. nigripinnis, and C. zenithicus) fisheries. The fishes that did not die directly from the lamprey attacks or indirectly from secondary fungal infection had reduced market value because of the unsightly wounds. Splake, a fast-growing hybrid between Brook Trout and Lake Trout was developed specifically in response to the effect of Sea Lamprey on Lake Trout. Overfishing was also a major consideration in the demise of Lake Trout populations and Gilbertson (1992) has suggested that another contributing factor would be the extreme sensitivity of eggs and sac fry of this species to a persistent dioxin-like PCB isomer that was probably present in the Great Lakes by the 1930s and resulted in its reduced reproductive success. Sea Lamprey has been targeted by control measures in the Laurentian Great Lakes’ Basin that include lampricide treatments (3-trifluoromethyl-4-nitrophenol, abbreviated as TFM, with or without the synergist 2’,5-dichloro-4’-nitrosalicylanilide, abbreviated as Bayer 73) aimed at ammocoetes, beginning in 1957, electromechanical barriers that intercept upstream migrants, beginning before 1957, and later low-head barriers, adjustable-crest barriers, also known as inflatable barriers, traps, and chemosterilization of males. Approximately 258,000 adult Sea Lamprey, were taken between 1953 and 1960 at electrical barriers operated in Lake Superior Basin alone. Between 1958 and 1980, 54.5 million Canadian dollars where spent for Sea Lamprey control and research. Despite some attempts at developing a fishery oriented towards ethnic communities in large cities around the Great Lakes such as Toronto, a fishery for landlocked Sea Lamprey has not become established. Additionally, high levels of mercury in adults preclude their use for human consumption. Historical fisheries for the anadromous form existed in the 1800s on the Merrimack and Connecticut rivers, Massachusetts, when it was abundant, before dams and pollution. Such fisheries have existed for centuries in Europe [England (UK), France, Portugal]. Recipes include Lamproie à la bordelaise, which involves cooking in red wine. There are reports of intoxication through eating this species (Halstead, 1967) (Ref. 89241).
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Sea lamprey

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The sea lamprey (Petromyzon marinus) is a parasitic lamprey native to the Northern Hemisphere. It is sometimes referred to as the "vampire fish".

Description

The sea lamprey has an eel-like body without paired fins. Its mouth is jawless, round and sucker-like, and as wide or wider than the head; sharp teeth are arranged in many concentric circular rows. There are seven branchial or gill-like openings behind the eye. Sea lampreys are olive or brown-yellow on the dorsal and lateral part of the body, with some black marblings, with lighter coloration on the belly. Adults can reach a length of up to 120 cm (47 in) and a body weight up to 2.3 kg (5.1 lb).[4]

Etymology

The etymology of the genus name Petromyzon is from petro- "stone" and myzon "sucking"; marinus is Latin for "of the sea".

Distribution and habitat

The species is found in the northern and western Atlantic Ocean along the shores of Europe and North America, in the western Mediterranean Sea, the Black Sea, and as an invasive species in the shores of the Great Lakes.[1] They have been found at depths up to 4000 meters and can tolerate temperatures of 1–20 °C (34–68 °F).[4]

In North America, they are native to the Connecticut River basin in the United States.[5] The largest European populations of sea lampreys are located throughout the southwestern areas of Europe (north-central Portugal, north-northwest of Spain, and west–southwest of France).[6] These countries also support the main fisheries of the species.[7]

Ecology

Sea lampreys are anadromous; from their lake or sea habitats, they migrate up rivers to spawn. Females deposit a large number of eggs in nests made by males in the substrate of streams with moderately strong current. Spawning is followed by the death of the adults. Larvae burrow in the sand and silt bottom in quiet water downstream from spawning areas and filter-feed on plankton and detritus.[1]

After several years in freshwater habitats, the larvae undergo a metamorphosis that allows young, post-metamorphic lampreys to migrate to the sea or lakes, and start the adult hematophagous method of feeding.[8] Some individuals start hematophagous feeding in the river before migrating to the sea,[9] where sea lampreys prey on a wide variety of fish.[10]

The lamprey uses its suction cup-like mouth to attach itself to the skin of a fish and rasps away tissue with its sharp, probing tongue and keratinized teeth. A fluid produced in the lamprey's mouth, called lamphredin,[11] prevents the victim's blood from clotting. Victims typically die from excessive blood loss or infection. After one year of hematophagous feeding, lampreys return to the river to spawn and die, a year and a half after the completion of metamorphosis.[12]

Lampreys are considered a delicacy in some parts of Europe, and are seasonally available in France, Spain, and Portugal. They are served pickled in Finland.[13]

Physiology

Two sea lamprey preying on a brown trout.

Due to its lifecycle that switches between fresh and salt water, the sea lamprey is adapted to tolerate a wide range of salinities. Cell membranes on the surface of the gills are major contributors to ionoregulation. Changes in membrane composition influence the movement of different ions across the membrane, changing amounts of components to change the membranes' environment.

As the larvae (called ammocoetes) move towards the oceans, the ratio between saturated fatty acids (SFA) and polyunsaturated fatty acids (PUFA) in the gills shifts towards higher amounts of SFA, as they affect the fluidity of the membrane, and higher levels of SFA lead to a decrease in permeability compared to PUFA.[14] Lamprey ammocoetes have a relatively narrow range of salinity tolerance, but become better able to withstand wider ranges of salinity concentrations as they reach later stages of life. Tight regulation of Na/K-ATPase and an overall decrease in expression of H-ATPase assists in regulating the lamprey's internal fluid and ion balance as it moves to areas of higher salinity.[15]

Lampreys also maintain acid-base homeostasis. When introduced to higher levels of acids, they are able to excrete excess acids at higher rates than most other saltwater fishes, and in much shorter times, with the majority of the transfer of ions occurring at the gill surface.[16]

Sea lampreys parasitize other fishes for their diet, including elasmobranchs such as sharks and rays, which have naturally high levels of urea in their blood. Urea is toxic to most fishes in high concentrations, and is usually excreted immediately. Lampreys are able to tolerate much higher concentrations than most other fish and excrete it at extremely high rates, obtained from ingested blood. Trimethylamine oxides present in ingested elasmobranch blood aid in counteracting the detrimental effects of high urea concentration in the lamprey's bloodstream as it feeds.[17]

Immunology

Two presumptive apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like (APOBEC)s expressed in lymphocytesCDA1 and CDA2—have been discovered in P. marinus.[18]

Genetics

The genome of Petromyzon marinus was sequenced in 2013.[19] This sequencing effort revealed that the lamprey has unusual guanine-cytosine content and amino acid usage patterns compared to other vertebrates. The full sequence and annotation of the lamprey genome is available on the Ensembl genome browser.

The lamprey genome may serve as a model for developmental biology and evolution studies involving transposition of repetitive sequences. The lamprey genome undergoes drastic rearrangements during early embryogenesis in which about 20% of the germline DNA from somatic tissues is shed. The genome is highly repetitive. About 35% of the current genome assembly is composed of repetitive elements with high sequence identity.[19] Northern lampreys have the highest number of chromosomes (164–174) among vertebrates.[20]

Two genes important to immune function—CDA1 and CDA2—were first discovered in P. marinus and then found to be conserved across lampreys. See §Immunology above.[18]

Invasive species

Sea lampreys are considered a pest in the Great Lakes region. The species is native to the inland Finger Lakes and Lake Champlain in New York and Vermont. Whether it is native to Lake Ontario, where it was first noticed in the 1830s, or whether it was introduced through the Erie Canal which opened in 1825 is not clear.[21] Improvements to the Welland Canal in 1919 are thought to have allowed its spread from Lake Ontario to Lake Erie, and while it was never abundant in either lake, it soon spread to Lake Michigan, Lake Huron, and Lake Superior, where it decimated indigenous fish populations in the 1930s and 1940s.[22]

In its original habitats, the sea lamprey coevolved with its hosts, and those hosts evolved a measure of resistance to the sea lampreys. However, in the Great Lakes, the sea lamprey attacks native fish such as lake trout, lake whitefish, chub, and lake herring, which historically did not face sea lampreys. Elimination of these predators allowed the alewife, another invasive species, to explode in population, with adverse effects on many native fish species.

The lake trout plays a vital role in the Lake Superior ecosystem. The lake trout has traditionally been considered an apex predator, which means that it has no predators. The sea lamprey is an aggressive predator by nature, which gives it a competitive advantage in a lake system where it has no predators and its prey lacks defenses against it. The sea lamprey played a large role in the destruction of the Lake Superior trout population. Lamprey introduction along with poor, unsustainable fishing practices caused the lake trout populations to decline drastically. The relationship between predators and prey in the Great Lakes ecosystem then became unbalanced.[23] Each individual sea lamprey has the potential of killing 40 pounds of fish through its 12–18 month feeding period.[24]

Efforts at control

Mouth of a sea lamprey, Petromyzon marinus
Video of the breathing of sea lamprey. Gijón Aquarium

Control efforts, including electric current and chemical lampricides[25] have met with varied success. The control programs are carried out under the Great Lakes Fishery Commission, a joint Canada–U.S. body, specifically by the agents of the Fisheries and Oceans Canada and the United States Fish and Wildlife Service.

Genetic researchers have mapped the sea lamprey's genome in the hope of finding out more about evolution; scientists trying to eliminate the Great Lakes problem are coordinating with these genetic scientists, hoping to find out more about its immune system and fitting it into its place in the phylogenetic tree.

Researchers from Michigan State University have teamed up with others from the Universities of Minnesota, Guelph, and Wisconsin, and others in a research effort into newly synthesized pheromones. These are believed to have independent influences on the sea lamprey behavior. One group of pheromones serves a migratory function in that when they are made by larvae, they are thought to lure maturing adults into streams with suitable spawning habitat. Sex pheromones emitted from males are capable of luring females long distances to specific locations. These pheromones are both several different compounds thought to elicit different behaviors that collectively influence the lampreys to exhibit migratory or spawning behaviors. Scientists are trying to characterize the function of each pheromone, and each part of the molecules, to determine if they can be used in a targeted effort at environmentally friendly lamprey control. However, as of 2017, the most effective control measures still involve the application of (3-trifluoromethyl-4-nitrophenol), or TFM, a selective pesticide, into rivers.[26] As of 2018 no lampricide resistance has been detected in the Great Lakes. Further research and combined use of multiple control methods are needed to forestall future development of resistance.[25]

Another technique used in the prevention of lamprey population growth is the use of barriers in major reproduction streams of high value to the lamprey. The purpose of the barriers is to block their upstream migration to reduce reproduction. The issue with these barriers is that other aquatic species are also inhibited by this barrier. Fish that use tributaries are impeded from traveling upstream to spawn. To account for this, barriers have been altered and designed to allow the passage of most fish species, but still impede others.[27][28]

Restoration

The intent of lamprey control programs is a safer habitat and a healthier population growth for vulnerable native fish species such as lake trout. The Connecticut Department of Energy and Environmental Protection (DEEP) has taken a different path to this same goal by introducing sea lampreys to freshwater rivers and lakes of the Connecticut River watershed, and providing easier access around dams and other barriers for the lampreys to reach spawning sites high upstream.[29] After preying on larger fish at sea, the adult lampreys migrate up the rivers to spawn, whereupon they quickly die of natural causes and decompose, thus providing a food source for the native freshwater fish species.

See also

References

  1. ^ a b c NatureServe (2013). "Petromyzon marinus". IUCN Red List of Threatened Species. 2013: e.T16781A18229984. doi:10.2305/IUCN.UK.2013-1.RLTS.T16781A18229984.en. Retrieved 19 November 2021.
  2. ^ Froese, R.; Pauly, D. (2017). "Petromyzontidae". FishBase version (02/2017). Retrieved 18 May 2017.
  3. ^ "Petromyzontidae" (PDF). Deeplyfish – fishes of the world. Retrieved 18 May 2017.
  4. ^ a b "Petromyzon marinus – Sea lamprey". FishBase.
  5. ^ Snyder, Alec (25 June 2020). "A 'vampire fish' is spawning in Vermont's waters. Experts say most of them are nothing to worry about". CNN. Retrieved 2020-06-30.
  6. ^ Silva, S.; Vieira-Lanero, R.; Barca, S.; Cobo, F. (2016). "Densities and biomass of larval Sea Lamprey populations (Petromyzon marinus Linnaeus, 1758) in North West Spain and data comparisons with other European regions". Marine and Freshwater Research. 68: 116. doi:10.1071/MF15065.
  7. ^ Araújo, M.J., Silva, S., Stratoudakis, Y., Gonçalves, M., Lopez, R., Carneiro, M., Martins, R., Cobo, F. and Antunes, C. (2016). "Ch. 20. Sea lamprey fisheries in the Iberian Peninsula". In A. Orlov and R. Beamish (ed.). Jawless Fishes of the World. Vol. 2. Cambridge Scholars Publishing. pp. 115–148. ISBN 978-1-4438-8582-9.{{cite book}}: CS1 maint: multiple names: authors list (link)
  8. ^ Silva, S.; Servia, M. J.; Vieira-Lanero, R.; Cobo, F. (2013a). "Downstream migration and hematophagous feeding of newly metamorphosed sea lampreys (Petromyzon marinus Linnaeus, 1758)". Hydrobiologia. 700: 277–286. doi:10.1007/s10750-012-1237-3. S2CID 16752713.
  9. ^ Silva, S., Servia, M. J., Vieira-Lanero, R., Nachón, D. J. & Cobo, F. (2013). "Hematophagous feeding of newly metamorphosed European sea lampreys Petromyzon marinus on strictly freshwater species". Journal of Fish Biology. 82 (5): 1739–1745. doi:10.1111/jfb.12100. PMID 23639169.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  10. ^ Silva, S.; Araújo, M. J.; Bao, M.; Mucientes, G.; Cobo, F. (2014). "The haematophagous feeding stage of anadromous populations of sea lamprey Petromyzon marinus: low host selectivity and wide range of habitats". Hydrobiologia. 734 (1): 187–199. doi:10.1007/s10750-014-1879-4. hdl:10261/98126. S2CID 17796757.
  11. ^ Fig. 1 Effect of lamphredin from the buccal glands of lampreys in Chi, Shaopeng; Xiao, Rong; Li, Qingwei; Zhou, Liwei; He, Rongqiao; Qi, Zhi (2009). "Suppression of neuronal excitability by the secretion of the lamprey (Lampetra japonica) provides a mechanism for its evolutionary stability". Pflügers Archiv: European Journal of Physiology. 458 (3): 537–545. doi:10.1007/s00424-008-0631-1. PMID 19198874. S2CID 375194.
  12. ^ Silva, S., Servia, M.J., Vieira-Lanero, R., Barca, S. & Cobo, F. (2013). "Life cycle of the sea lamprey Petromyzon marinus: duration of and growth in the marine life stage". Aquatic Biology. 18: 59–62. doi:10.3354/ab00488.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  13. ^ "Lamprey: a prehistoric sea monster sucks blood, then gets cooked in its own". Atlas Obscura. 2018. Retrieved 15 September 2018.
  14. ^ João, Maria; Machado, Maria; Ferreira, Ana; Quintella, Bernardo; Almeida, Pedro (2015). "Structural lipid changes and Na+/K+-ATPase activity of gill cells' basolateral membranes during saltwater acclimation in sea lamprey (Petromyzon marinus, L.) juveniles". Comparative Biochemistry and Physiology. 189: 67–75. doi:10.1016/j.cbpa.2015.07.018. hdl:10174/16601. PMID 26244517.
  15. ^ Reis-Santos, Patrick; McCormick, Stephen; Wilson, Jonathan (2008). "Ionoregulatory changes during metamorphosis and salinity exposure of juvenile sea lamprey (Petromyzon marinus L.)". The Journal of Experimental Biology. 211 (Pt 6): 978–988. doi:10.1242/jeb.014423. PMID 18310123.
  16. ^ Wilkie, Michael; Couturier, Jennifer; Tufts, Bruce (1998). "Mechanisms of acid-base regulation in migrant sea lampreys (Petromyzon marinus) following exhaustive exercise". The Journal of Experimental Biology. 201 (9): 1473–1482. doi:10.1242/jeb.201.9.1473. PMID 9547326.
  17. ^ Wilkie, Michael; Turnbull, Steven; Bird, Jonathan; Wang, Yuxiang; Claude, Jaime; Youson, John (2004). "Lamprey parasitism of sharks and teleosts: High capacity urea excretion in an extant vertebrate relic". Comparative Biochemistry and Physiology. 138 (4): 485–492. doi:10.1016/j.cbpb.2004.06.001. PMID 15369838.
  18. ^ a b Boehm, Thomas; Hirano, Masayuki; Holland, Stephen J.; Das, Sabyasachi; Schorpp, Michael; Cooper, Max D. (2018-04-26). "Evolution of Alternative Adaptive Immune Systems in Vertebrates". Annual Review of Immunology. Annual Reviews. 36 (1): 19–42. doi:10.1146/annurev-immunol-042617-053028. ISSN 0732-0582. PMID 29144837.
  19. ^ a b Smith, Jeramiah J; Kuraku, Shigehiro; Holt, Carson; Sauka-Spengler, Tatjana; Jiang, Ning; Campbell, Michael S; Yandell, Mark D; Manousaki, Tereza; Meyer, Axel; Bloom, Ona E; Morgan, Jennifer R; Buxbaum, Joseph D; Sachidanandam, Ravi; Sims, Carrie; Garruss, Alexander S; Cook, Malcolm; Krumlauf, Robb; Wiedemann, Leanne M; Sower, Stacia A; Decatur, Wayne A; Hall, Jeffrey A; Amemiya, Chris T; Saha, Nil R; Buckley, Katherine M; Rast, Jonathan P; Das, Sabyasachi; Hirano, Masayuki; McCurley, Nathanael; Guo, Peng; Rohner, Nicolas; Tabin, Clifford J; Piccinelli, Paul; Elgar, Greg; Ruffier, Magali; Aken, Bronwen L; Searle, Stephen M J; Muffato, Matthieu; Pignatelli, Miguel; Herrero, Javier; Jones, Matthew; Brown, C Titus; Chung-Davidson, Yu-Wen; Nanlohy, Kaben G; Libants, Scot V; Yeh, Chu-Yin; McCauley, David W; Langeland, James A; Pancer, Zeev; Fritzsch, Bernd; de Jong, Pieter J; Zhu, Baoli; Fulton, Lucinda L; Theising, Brenda; Flicek, Paul; Bronner, Marianne E; Warren, Wesley C; Clifton, Sandra W; Wilson, Richard K; Li, Weiming (2013). "Sequencing of the sea lamprey (Petromyzon marinus) genome provides insights into vertebrate evolution". Nature Genetics. 45 (4): 415–421. doi:10.1038/ng.2568. PMC 3709584. PMID 23435085.
  20. ^ Froese, Rainer, and Daniel Pauly, eds. (2011). "Petromyzontidae" in FishBase. February 2011 version.
  21. ^ Nonindigenous Aquatic Species Factsheet: Petromyzon marinus. U.S. Geological Survey (USGS), Nonindigenous Aquatic Species Program (NAS). Retrieved on 2007-08-04.
  22. ^ Dunbar, Willis (May 3, 1949). "May 3, 1949". Western Michigan at Work. WKZO. Retrieved December 17, 2019.
  23. ^ McClelland, Edward (2008). "Great Lake Invaders". E – the Environmental Magazine. 19 (2): 10–11.
  24. ^ "Great Lakes Fishery Commission – Sea Lamprey". www.glfc.org. Retrieved 2017-10-24.
  25. ^ a b Dunlop, Erin S.; McLaughlin, Rob; Adams, Jean V.; Jones, Michael; Birceanu, Oana; Christie, Mark R.; Criger, Lori A.; Hinderer, Julia L.M.; Hollingworth, Robert M.; Johnson, Nicholas S.; Lantz, Stephen R.; Li, Weiming; Miller, James; Morrison, Bruce J.; Mota-Sanchez, David; Muir, Andrew; Sepúlveda, Maria S.; Steeves, Todd; Walter, Lisa; Westman, Erin; Wirgin, Isaac; Wilkie, Michael P. (2018). "Rapid evolution meets invasive species control: the potential for pesticide resistance in sea lamprey". Canadian Journal of Fisheries and Aquatic Sciences. National Research Council Canada. 75 (1): 152–168. doi:10.1139/cjfas-2017-0015. hdl:1807/78674. ISSN 0706-652X.
  26. ^ "TFM fact sheet" (PDF). glfc.org. Retrieved 8 April 2018.
  27. ^ Pratt, T. C.; O’Connor, L. M.; Hallett, A. G. (2009). "Balancing Aquatic Habitat Fragmentation and Control of Invasive Species: Enhancing Selective Fish Passage at Sea Lamprey Control Barriers". Transactions of the American Fisheries Society. 138 (3): 652–65. doi:10.1577/t08-118.1.
  28. ^ AIS - Aquatic Invasive Species. "Sea lamprey" (PDF). Indiana State Government.
  29. ^ "Recovery: Why Sea Lampreys Need to Be Restored and Killed". nature.org. 11 December 2017. Retrieved 8 April 2018.

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Sea lamprey: Brief Summary

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The sea lamprey (Petromyzon marinus) is a parasitic lamprey native to the Northern Hemisphere. It is sometimes referred to as the "vampire fish".

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Diet

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Algae, as well as live cod, haddock, hake, mackerel, shad, salmon, sturgeon, swordfish and basking sharks

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North-West Atlantic Ocean species (NWARMS)

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Distribution

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Western Atlantic from Labrador to Gulf of Mexico

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North-West Atlantic Ocean species (NWARMS)

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Habitat

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Anadromous species, spends adult life in saltwater except to spawn in freshwater streams.

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North-West Atlantic Ocean species (NWARMS)

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Habitat

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benthic

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North-West Atlantic Ocean species (NWARMS)

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