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Australian Lamprey

Mordacia mordax (Richardson 1846)

Diagnostic Description

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Adults: 11.3-43.2 cm TL; body proportions of pre-spawning specimens, as percentage of TL (based on 125 prespawning specimens measuring 11.3-42.1 cm TL): 8.5-11.3 prebranchial length, 7.1-9.8 branchial length, 60.4-68.3 trunk length, 14.4-20.1 tail length, 1.1-1.7 eye length and 4.9-6.6 disc length. Body proportions of spawning male specimens, as percentage of TL (based on 8 spawning males measuring 27.7-37.6 cm TL): 11.4-16.6 prebranchial length, 8.8-10.1 branchial length, 60.1-65.3 trunk length, 13.3-15.7 tail length, 8.1-11.2 disc length. Mature males with some loose skin in gular region. Urogenital papilla not prominent in mature adults; trunk myomeres, 84-96. Adult dentition: 2 triangular supraoral laminae each with 3 unicuspid teeth, 1 per apex; infraoral lamina, 7-9 unicuspid teeth of various size (these teeth become greatly enlarged with sexual maturation); 5-7 endolateral plates on either side each bearing 2-3 unicuspid teeth, usually 3; endolateral formula, typically 2-3-3-3-3-3 in immature individuals and 5-7 individual cusps on either side in mature individuals; 1 row of anterials; first row of anterials, 2 unicuspid teeth plus 1-2 bicuspid teeth or 3 unicuspid teeth flanked on either side by 1 bicuspid tooth; 1 row of exolaterals on each side; 1 row of posterials; first row of posterials, 12-14 posterial plates, the 2-4 lateralmost tricuspid and the internal ones bicuspid in immature individuals and 12-14 unicuspid teeth in mature individuals; transverse lingual lamina w-shaped, with 29 unicuspid teeth, the median one and the 2 subterminal ones slightly enlarged; longitudinal lingual laminae interrupted j-shaped, each with an undetermined number of unicuspid teeth. Velar tentacles in adults, 3-4, smooth. Body coloration (live) of immature adults brownish gray on dorsal surface and silvery on ventral surface; lateral line neuromasts darkly pigmented; caudal fin pigmentation, 25% to
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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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Trophic Strategy

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Adults inhabit the sea for an undetermined period and are parasitic on fishes; enter freshwater to breed. Majority of adulthood is spent in estuaries or at sea. Upstream spawning migrants occur in fast-flowing sections of rivers with a mud, sand or silt substrate, sometimes seen congregated below barriers to upstream movement such as weirs. Ammocoetes live in slow-flowing streams, burrowed in mud or silt (Ref. 44894).
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Biology

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Adults inhabit the sea for an undetermined period and are parasitic on fishes; enter freshwater to breed. Majority of adulthood is spent in estuaries or at sea. Upstream spawning migrants occur in fast-flowing sections of rivers with a mud, sand or silt substrate, sometimes seen congregated below barriers to upstream movement such as weirs. Ammocoetes live in slow-flowing streams, burrowed in mud or silt. Common length is 35-40 cm (Ref. 44894). Larval life is 3.5 yrs. During the spawning migration, adults burrow in the substrate of rivers during the day and migrate upstream during the night. Fecundity, 3,789-13,372 eggs/female. De Castelnau (1872) states that the adults from the lower Yarra River, Victoria, are considered good food (Ref. 89241).
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Mordacia mordax

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Mordacia mordax, known as the short-headed lamprey, Australian lamprey or Murray lamprey, is a species of Mordacia that lives in south-eastern Australia and Tasmania. Mordaciidae is made up of three species: M. praedox, M. mordax, and M. lapicida.[1] M. mordax is a relatively rare, parasitic vertebrate and, along with the hagfishes, is part of the only surviving group of jawless organisms throughout vertebrate evolution.[2] It has a thin eel-like body up to 50 cm (20 in) long, with two low dorsal fins on the back half. The skin is blue-gray or brown. Its eyes are small, and located on the top of its head.

Evolution

Members of Agnatha have been found in the fossil record for approximately five hundred million years and it has been identified as an important group in tracking vertebrate evolution.[1] Despite being spatially close to the other southern hemisphere family Geotriidae, M. mordax has been shown to have key proteins with vastly different amino acid compositions.[3][2] One such study of insulin extracted from organisms of both species indicated that 18 amino acids are different between G. australis and M. mordax when with northern hemisphere lampreys (P. marinus and L. fluviatilis) there is only a four amino acid difference. This data indicates that the southern hemisphere lampreys likely diverged evolutionarily a long time before.[2] It has also been determined that Geotriidae and Petromyzontidae (the family of northern lampreys) likely share a more recent common ancestor than either does with any Mordacia species.[3]

Behavior and ecology

Adult M. mordax are parasites on other fish. They are anadromous (breeding in fresh water), migrating up streams in southeastern Australia from Shoalhaven River, New South Wales to Gulf St Vincent, South Australia. The ammocoetes (lamprey larvae) remain in fresh water until undergoing extreme physiological changes that allow them to move from eating plankton to larger fish.[1] This leads to them migrating to the South Pacific and Southern Oceans around three to four years after hatching.[2] Adults have been found to travel hundreds of miles to spawn.[4] Feeding occurs in the open ocean until full sexual maturation occurs when M. mordax returns to freshwater rivers, spawns, and dies.[5]

Physiology

Larval M. mordax are between 20 and 150 mm (0.79 and 5.91 in) in length depending on their stage of development and when fully developed typically measure 300 to 420 mm (12 to 17 in).[5] As it develops, M. mordax undergoes a number of extreme dental changes. It starts with a series of radial plates, and as it grows they separate and break into separate teeth.[4] These teeth are pointed, unlike the other southern hemisphere lamprey Geotria australis which has spatulate (broad and rounded) teeth.[4]

The eyes of Mordacia are dorsolaterally located, which is unlike the other known lamprey species, and they contain a photoreceptor that has both rod and cone characteristics.[1] This photoreceptor is also unique to M. mordax and enhances vision in darkness by optimizing photon reception. It is not unlike deep sea fish eye anatomy, in that sense as M. mordax only comes out of the sediment of rivers at night to travel.[5]

The posterior and anterior dorsal fins of Mordacia are continuous to the caudal fin, unlike G. australis. When M. mordax is fully developed those anterior and posterior dorsal fins are well separated, which distinguishes them from northern hemisphere lampreys.[4]

Lampreys have been established as worthy models in understanding the development of higher vertebrate anatomy and physiology, with one such experiment determining that major classes of lipoproteins are similar in Mordacia to those found in humans.[6] M. mordax and the lamprey group have also been shown to be the lowest vertebrate to have clear roles for neurohormones in the hypothalamic-pituitary-gonadal axis.[7]

References

  1. ^ a b c d Collin, S; Hart, N; Wallace, K; Shand, J; Potter, I (2004). "Vision in the southern hemisphere lamprey Mordacia mordax: Spatial distribution, spectral absorption characteristics, and optical sensitivity of a single class of retinal photoreceptor" (PDF). Visual Neuroscience. 21 (5): 765–773. doi:10.1017/S0952523804215103. PMID 15683562. S2CID 11947584.
  2. ^ a b c d Conlon; Wang; Potter (2001). "The structure of Mordacia mordax insulin supports the monophyly of the Petromyzontiformes and an ancient divergence of Mordaciidae and Geotriidae". Comparative Biochemistry and Physiology, Part B. 129 (1): 65–71. doi:10.1016/S1096-4959(00)00365-1. PMID 11337250.
  3. ^ a b Baldwin, Mortimer (1988). "Evolutionary relationships among lamprey families: Amino acid composition analysis of lactate dehydrogenase". Biochemical Systematics and Ecology. 16 (3): 351–353. doi:10.1016/0305-1978(88)90022-1.
  4. ^ a b c d Potter, I; Strahan, F (1968). "The taxonomy of the lampreys Geotria and Mordacia and their distribution in Australia". Proceedings of the Linnean Society of London. 179 (2): 229–240. doi:10.1111/j.1095-8312.1968.tb00980.x.
  5. ^ a b c Potter, I; Hilliard, R; Neira, F (1986). "The Biology of Australian Lampreys". {{cite journal}}: Cite journal requires |journal= (help)
  6. ^ Fellows, Florence; Mclean, Robyn (1982). "A study of the plasma lipoproteins and the tissue lipids of the migrating lamprey, Mordacia mordax". Lipids. 17 (10): 741–747. doi:10.1007/BF02534661. PMID 7176831. S2CID 4024259.
  7. ^ Sower; Mcgregor; Materne; Chase; Potter; Joss (2000). "Evidence for Lamprey GnRH-I and -III-like Molecules in the Brains of the Southern Hemisphere Lampreys Geotria australis and Mordacia mordax". General and Comparative Endocrinology. 120 (2): 168–75. doi:10.1006/gcen.2000.7550. PMID 11078628.
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Mordacia mordax: Brief Summary

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Mordacia mordax, known as the short-headed lamprey, Australian lamprey or Murray lamprey, is a species of Mordacia that lives in south-eastern Australia and Tasmania. Mordaciidae is made up of three species: M. praedox, M. mordax, and M. lapicida. M. mordax is a relatively rare, parasitic vertebrate and, along with the hagfishes, is part of the only surviving group of jawless organisms throughout vertebrate evolution. It has a thin eel-like body up to 50 cm (20 in) long, with two low dorsal fins on the back half. The skin is blue-gray or brown. Its eyes are small, and located on the top of its head.

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