Petromyzonti (lampreys) > Petromyzontiformes
(Lampreys) > Petromyzontidae
(Northern lampreys) > Lampetrinae
Etymology: Lethenteron: Greek, letheia = apathetic (lethe = oblivion) + Greek, enteron = intestine (Ref. 45335); referring to the degeneration of the intestine (Ref. 117245); kessleri: In honor of Karl Fëdorovich Kessler, outstanding Russian zoologist and ichthyologist of the 19th century.
Environment: milieu / climate zone / depth range / distribution range
Freshwater; demersal; non-migratory; depth range - m (Ref. ), usually - m (Ref. ). Temperate; 5°C - 25°C (Ref. 12468); 78°N - 53°N, 55°E - 169°W
Asia: Throughout Siberia to the Anadyr and Sakhalin (Ref. 26334). Specimens identified as Lethenteron kessleri from the Arctic basin refer to Lethenteron reissneri (Ref. 59043).
Length at first maturity / Size / Weight / Age
Maturity: Lm ?, range 11 - 13.27 cm
Max length : 26.0 cm TL male/unsexed; (Ref. 12323); max. reported age: 7 years (Ref. 12323)
Morphology | Morphometrics
Adults: 11.2-23.0 cm TL. Body proportions, as percentage of TL (based on 300 specimens measuring 15.3-23.0 cm TL; the values given below represent ranges of means based on samples of 50 specimens): prebranchial length, 11.2-12.0; branchial length, 9.5-9.6 (8.9-11.9 absolute range, Iwata et al. (1985) based on 97 specimens 11.2-18.4 cm TL); trunk length, 48.8 (derived by deduction); tail length, 29.1-30.9; eye length, 2.1-2.2; disc length, 5.6-6.0. The intestinal diameter is less than 1.0 mm. Urogenital papilla length, as a percentage of branchial length, in three spawning males measuring 14.7-16.9 cm TL, 5.9-10.0 [5.8-34.7, Iwata et al. (1985) based on 23 spawning males 12.1-16.0 cm TL]. Succeeding counts/descriptions in parentheses are of resident L. camtschaticum form sensu Kucheryavyi et al. (2007): Trunk myomeres, 65-73 (57-78). Dentition: supraoral lamina, 2 unicuspid teeth, rarely 3; infraoral lamina, 5-10 teeth, usually 6-8, the lateralmost unicuspid or bicuspid (one or both rarely unicuspid) and occasionally some of the internal ones also bicuspid, the rest unicuspid; 3 endolaterals on each side; endolateral formula, typically 2-2-2, variant formulae, 2-2-1 and 2-1-2 (also 2-2-2-2); 2 rows of anterials; first row of anterials, 3-5 unicuspid teeth; total number of anterials, 15-28 (8-30) unicuspid teeth; exolaterals usually absent, but if present, only 1 unicuspid tooth per lateral field; single row of posterials consisting of 16-25 (as low as 12) unicuspid teeth, sometimes completely absent; transverse lingual lamina, numerous unicuspid teeth, the median one enlarged; longitudinal lingual laminae parentheses-shaped, each with numerous unicuspid teeth. Velar tentacles, 7. Body coloration of live specimen, brownish on dorsal and lateral aspects and whitish on the ventral aspect. Second dorsal fin with a dark blotch near the apex; however, specimens from Japan do not have a dark blotch. Extent of caudal fin pigmentation, rarely absent or trace, usually 75% or more. Caudal fin shape, spade-like.
In Europe the upper courses of rivers, in Siberia also in lakes and lowland rivers (Ref. 12323). Freshwater, in rivers, brooks, and lakes. Ammocoetes live in oozy substrate. Metamorphosing ammocoetes are mostly found in areas with abundant aquatic vegetation at the mouth of small streams (Ref. 89241). Ammocoetes feed on detritus, green algae, diatoms, and zooplankton (Ref. 12323. 89241). Larval life lasts 6+ yrs. Onset of metamorphosis is at the end of July beginning of August and is complete at the end of October to the middle of November. The population in the upper Irtysh River Basin is apparently unique among lampreys in that it continues to feed during metamorphosis gradually switching from a detritus and unicellular algae diet to an exclusively unicellular algae diet. This would explain the fact that the maximum total length of the metamorphosing ammocoete exceeds the maximum total length of the ammocoete; mean of 233 mm in the former versus 218 in the latter. Unicellular algae consumed include Cyanophyceae (Oscillatoria), Chlorophyceae (Spirogyra, Chlorella), and Diatomeae (Fragilaria, Pinnularia). This phenomenon is particularly interesting as it implies that the metamorphosing ammocoetes must switch from a filter-feeding mode to a grazing mode of feeding, since, during the process of metamorphosis, the oral cirrhi are lost. The grazing may be achieved possibly with the help of the lingual laminae and the action of the piston cartilage (Ref. 89241). Adults are nonparasitic (Ref. 89241, 12323). Spawning period in Japan in early May. Fecundity, 1,387-2,125 eggs/female in Japan, with long diameter of eggs varying from 1.12 to 1.22 mm and the short diameter from 0.91 to 1.11 mm. Kucheryavyi et al. (2007) reported a fecundity of 468-3,441 eggs/female in non-feeding adult stage resident L. camtschaticum (= L. kessleri?) on Kamchatka (Ref. 89241). Ammocoetes used as lures for bait casting (Ref. 12323).
Holcík, J., 1986. Lethenteron kessleri (Anikin, 1905). p. 220-236. In J. Holcík (ed.) The Freshwater fishes of Europe. Vol.1, Part I, Petromyzontiformes. (Ref. 12323)
IUCN Red List Status (Ref. 124695)
Threat to humans
Fisheries: of no interest; bait: usually
ReferencesAquacultureAquaculture profileStrainsGeneticsAllele frequenciesHeritabilityDiseasesProcessingNutrientsMass conversion
Estimates based on models
Phylogenetic diversity index (Ref. 82805
= 0.5039 [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.00123 (0.00056 - 0.00272), b=3.00 (2.80 - 3.20), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref. 93245
Trophic level (Ref. 69278
): 2.2 ±0.14 se; based on food items.
Resilience (Ref. 120179
): Low, minimum population doubling time 4.5 - 14 years (tmax=tm=7).
Vulnerability (Ref. 59153
): Low to moderate vulnerability (29 of 100) .