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Lampetra fluviatilis (Linnaeus, 1758)

River lamprey
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Lampetra fluviatilis   AquaMaps   Data sources: GBIF OBIS
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Image of Lampetra fluviatilis (River lamprey)
Lampetra fluviatilis
Picture by Zauke, G.P.


Croatia country information

Common names: [No common name]
Occurrence: questionable
Salinity: freshwater
Abundance: | Ref:
Importance: | Ref:
Aquaculture: | Ref:
Regulations: | Ref:
Uses: no uses
Comments: Occurrence not supported by Ref. 59043. Material used by both Ref. 3161 and Ref. 59043 should be checked.
National Checklist:
Country Information: https://www.cia.gov/library/publications/resources/the-world-factbook/geos/hr.html
National Fisheries Authority:
Occurrences: Occurrences Point map
Main Ref: Vladykov, V.D., 1984
National Database:

Common names from other countries

Classification / Names ชื่อสามัญ | ชื่อพ้อง | Catalog of Fishes(สกุล, ชนิด) | ITIS | CoL | WoRMS | Cloffa

> Petromyzontiformes (Lampreys) > Petromyzontidae (Northern lampreys) > Lampetrinae
Etymology: Lampetra: lambo (L.), to lick; petra (Gr.), rock or stone, referring to their suctorial behavior (adults attach to rocks during nest building and mating). (See ETYFish);  fluviatilis: Latin for “of a river,” referring to its upstream river spawning migration. (See ETYFish).
  More on author: Linnaeus.

Issue
Berg (1931) suggested that this species consists of two races; a normal form (forma typica) and a smaller praecox form. The praecox form has been reported from the Neva River and Lake Ladoga in the Russian Federation and the Severn River in England (UK) (Ref. 89241).

Environment: milieu / climate zone / depth range / distribution range นิเวศวิทยา

เกี่ยวกับทะเล,น้ำเค็ม; น้ำจืด; กร่อย สัตว์น้ำหน้าดิน; ปลาที่อพยพจากแหล่งน้ำเค็มไปวางไข่ในแหล่งน้ำจืด (Ref. 59043); ระดับความลึก 10 - ? m.   Temperate; 5°C - 18°C (Ref. 12468); 69°N - 38°N, 11°W - 29°E (Ref. 59043)

การแพร่กระจาย ประเทศต่างๆ | พื้นที่จำแนกตาม FAO | ระบบนิเวศหลายระบบ | การปรากฏขึ้น,การเกิดขึ้น,พบ | Point map | การแนะนำ | Faunafri

Europe: southern Norway to France, including Ireland and the British Isles. Also in the Baltic Sea and along the French and western Italian coasts of the Mediterranean Sea (Ref. 59043). Absent from Black, Caspian and Polar seas (Ref. 3161). Landlocked populations from Lake Mjosa in Norway (Ref. 12269), Lakes Ladoga and Onega, upper Volga in Russia, Loch Lomond in Scotland, some Finnish lakes and possibly in Lough Neagh in Ireland (Ref. 59043).

Length at first maturity / ขนาด / น้ำหนัก / Age

Maturity: Lm 34.8, range 32 - 34 cm
Max length : 50.0 cm TL เพศผู้/กระเทย; (Ref. 30578); common length : 35.0 cm TL เพศผู้/กระเทย; (Ref. 30578); common length :32 cm TL (female); น้ำหนักสูงสุดที่มีการรายงาน: 150.00 g (Ref. 40476); อายุสูงสุดที่ได้รายงาน: 10 ปี (Ref. 30578)

Short description เครื่องมือที่ใช้ในการแยกชนิดสัตว์,สิ่งมีชีวิตออกจากกัน | สัณฐานวิทยา | ความยาวต่างๆ

เงี่ยงครีบหลัง (รวม) : 0; เงี่ยงครีบก้น: 0; ก้านครีบอ่อนที่ก้น: 0. It is jawless with a round sucker-like mouth and has an outer circle of small teeth and an inner circle of large teeth (Ref. 88171). It has a typical eel-like shape with 2 dorsal fins and 7 gill openings behind the eye. It lacks paired fins. Young adults are uniformly greyish in colour. As it ages, the river lamprey becomes greenish-brown dorsally, golden yellow along the sides and white ventrally (Ref. 58137). In coastal waters of Germany, it can be confused with the sea lamprey (Petromyzon marinus), which is distinguished by having its teeth arranged in many consecutive circular rows (Ref. 88171). Other diagnostic features: Adults 8.6-49.2 cm TL. Body wet weight in individuals 18.0-49.2 cm TL, 30-150 g. Body proportions, as percentage of TL (based on 48 specimens measuring 10.8-38.6 cm TL): prebranchial length, 10.0-12.9; branchial length, 7.9-11.3; trunk length, 46.2-54.3; tail length, 24.1-30.3; eye length, 1.4-3.1; disc length, 4.6-7.0. Urogenital papilla length, as a percentage of branchial length, in 19 spawning males measuring 19.7-28.3 cm TL, 15.9-37.5. Trunk myomeres, 58-66. Dentition: marginals, 70-95; supraoral lamina, 2 unicuspid teeth; infraoral lamina, 5-9 either all unicuspid teeth or, more frequently, the lateralmost are bicuspid and the internal ones unicuspid; 3 endolaterals on each side; endolateral formula, typically 2-3-2, rarely 1-3-2 or 2-3-1; 1-2 rows of anterials; first row of anterials, 4-7 unicuspid teeth; exolaterals absent; posterials absent; transverse lingual lamina, 8-18, usually 12-14, unicuspid laminae straight or parentheses-shaped and each with 9-13 unicuspid teeth. Marginal membrane present. Velar tentacles, 4-10, with tubercles; no velar wings. Body coloration in recently metamorphosed individuals silvery; in preserved upstream migrants, bluish brown or lead gray on the dorsal aspect tending towards silvery on the lateral aspects and whitish or yellowish on ventral aspect. Early upstream spawning migrants returning from the sea have a bronze sheen. Dorsal fins of maturing individuals may have a purplish tint. Iris is golden yellow. Body coloration in the landlocked population in Lake Ladoga is completely black. Lateral line neuromasts unpigmented or darkly pigmented. Extent of caudal fin pigmentation, absent or trace in young adults and 75% or more in spawning individuals. Caudal fin shape, spade-like. Oral fimbriae, 84-112. Oral papillae, 11-20 (Ref. 89241).

ชีววิทยา     ภาคผนวก (เช่น epibenthic)

In fresh waters, in rivers, brooks, and lakes. Anadromous, but some populations are permanent freshwater residents (e.g. Lough Neagh, Northern Ireland (UK); Loch Lomond, Scotland (UK); lakes Ladoga and Onega, Russian Federation) (Ref. 89241). Amphihaline species (Ref. 51442). Metamorphosis takes place at a length of about 13 cm and they migrate to the sea (Ref. 51442). Most river lampreys live 4-7 years and reach 30-35 cm length (Ref. 88187). Females grow larger than males (Ref. 58137). Adults spend 1-2 years at sea, often along the coast or in estuaries (Ref. 59043). They live on hard bottoms or attached to larger fish like cod and herring (Ref. 88174). Adults are parasitic, feeding on fishes by sucking their blood and afterwards consuming the flesh (Ref. 1998). Adults predatory on marine fishes from the end of July to October. Trematodes and cestodes have been found in the intestine of prespawning adults at sea. (Ref. 89241). In autumn, adults commonly undergo reproductive migration from the sea to shallow middle or upper reaches of rivers and streams with strong currents (1.0-2.0 m/s in British rivers) and gravel bottoms (Ref. 51442, 59043, 88171). Spawning migration upriver (Vistula and Neman rivers) begins near the end of September in the Baltic Sea Basin. In tributaries to the Gulf of Finland (Narva, Neva, and Luga rivers), upstream spawning migrations occur twice yearly; once in summer-fall and once in spring. In the upper Rhine River, the spawning season is February to April; in England (UK) from April to May; and in the lower Neva River, Russian Federation, from early June to early July (Ref. 89241). During reproductive migration and reproduction, adults do not feed but instead utilize their lipid reserves (Ref. 30578) and are known to undergo a considerable shortening of up to 27 per cent (Ref. 83507). Fecundity is highly variable and ranges from 650 to 42,500 eggs/female; 10,000-16,000 eggs/female in Lake Ladoga. Communal spawning in the same redd by L. fluviatilis and L. planeri has been reported in the River Tywi Basin, Wales (UK), in April, at a water temperature of 11 °C. Both species participated in constructing a redd about 23 cm in diameter and 5-8 cm deep, consisting of pebbles, gravel and coarse sand (Ref. 89241). Spawning takes place in pre-excavated pits in river beds, its depth between 50-100 cm; after spawning the adults die (Ref. 51442). The blind ammocoetes are filter feeders of detritus and microorganisms; they live mostly buried in sand, silt or clay sediments for up to 4.5 years, often at the edges of rivers and streams where currents are slow (Ref. 51442, 59043, 88184, 88185). Sometimes they are found in substrates with submerged vegetation and plant debris (Ref. 12285). Ammocoetes may tolerate low oxygen levels but when burrows reach near anoxic levels, the larvae need to emerge from the substrate in order to survive (Ref. 88184). Fisheries exist in England (UK), Finland, France, and the Russian Federation. In the 19th century, up to 450,000 adults yearly were used by the English fishing fleet as bait in the fisheries for Gadus morhua and Psetta maxima. In Finland, the catch in 1983 was 2.3-2.4 million individuals (about 100 t) for a value of $800,000 US. There are reports of intoxication through eating this species (Halstead 1967). The mucus and serum are poisonous and the flesh must be thoroughly washed and all the blood removed before consumption (Ref. 5504). Cooking method involves de-sliming, removal of heads and branchial regions, the rest of the body covered in sunflower flour, and cooked in sunflower oil (Ref.89241). Utilized fresh and smoked; eaten fried (Ref. 9988).

Life cycle and mating behavior Maturities | การสืบพันธุ์ | Spawnings | Egg(s) | Fecundities | ตัวอ่อน

Adults migrate from the sea to the rivers to spawn (Ref. 51442), ascending rivers at night, anytime between autumn and spring but this movement ceases when water temperature drops (Ref. 59043). During the early stages of its spawning migration, the river lamprey has been shown to be attracted to chemical odours given off by ammocoetes (Ref. 88188). Males reach the spawning grounds first and build nests at depths between 50-100 cm, which have a diameter of 20-40 cm and a height of 10 cm (Ref. 12285, 51442, 59043, 88186). The river lamprey forms spawning aggregations, often during sunny days, when water temperature rises above 9 °C (Ref. 59043). Females may spawn with up to 6 males on separate occasions. One nest is usually utilized by a single mating pair (Ref. 59043). Adults spawn only once in their lifetime and usually die within 2 weeks after spawning (Ref. 12285, 51442). Eggs hatch in 15-30 days (Ref. 88184). The ammocoetes live in the calm zones of the river until metamorphosis at about 13 cm length before migrating to the sea (Ref. 51442).

Main reference Upload your references | อ้างอิง | ผู้ประสานงาน | ผู้ร่วมมือ

Vladykov, V.D., 1984. Petromyzonidae. p. 64-67. In P.J.P. Whitehead, M.-L. Bauchot, J.-C. Hureau, J. Nielsen, and E. Tortonese (eds.) Fishes of the north-eastern Atlantic and Mediterranean. UNESCO, Paris. vol. 1. (Ref. 3161)

IUCN Red List Status (Ref. 130435)

  Least Concern (LC) ; Date assessed: 05 March 2010

CITES (Ref. 128078)

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

Threat to humans

  Poisonous to eat (Ref. 5504)




Human uses

การประมง: มีการค้าเพียงเล็กน้อย; เหยื่อ: usually
FAO(การประมง: การผลิต; publication : search) | FishSource |

ข้อมูลเพิ่มเติม

Trophic ecology
รายการอาหาร
Diet compositions
Food consumptions
Food rations
ผู้ล่า
Ecology
นิเวศวิทยา
Home ranges
Population dynamics
Growths
Max. ages / sizes
Length-weight rel.
Length-length rel.
Length-frequencies
Mass conversions
Recruitments
Abundances
Anatomy
Gill areas
สมอง
Otoliths
Physiology
Body compositions
Nutrients
Oxygen consumptions
รูปแบบการว่ายน้ำ
Swimming speeds
Visual pigment(s)
เสียงของปลา
Diseases / Parasites
Toxicities (LC50s)
Genetics
พันธุศาสตร์
Electrophoreses
Heritabilities
Human related
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เครื่องมือ

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Estimates based on models

Preferred temperature (Ref. 115969): 5.2 - 12.2, mean 9.8 (based on 394 cells).
Phylogenetic diversity index (Ref. 82804):  PD50 = 0.5002   [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.00126 (0.00075 - 0.00212), b=3.06 (2.91 - 3.21), in cm Total Length, based on LWR estimates for this species & (Sub)family-body (Ref. 93245).
ระดับชั้นอาหาร (Ref. 69278):  4.5   ±0.80 se; based on food items.
ความสามารถในการกลับคืนสู่ปกติ (Ref. 120179):  ต่ำ, เวลาต่ำสุดที่จะทำให้ประชากรเพิ่มขึ้นเป็น 2 เท่าใช้เวลา 4.5 - 14 ปี (Semelparous species, assuming tm (= tmax) > 4).
Fishing Vulnerability (Ref. 59153):  Moderate vulnerability (40 of 100).
Price category (Ref. 80766):   Unknown.