Mordacia lapicida

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Mordacia lapicida
Mordacia lapicida (Lamprea Chilena).JPG
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Animalia
Phylum: Chordata
Infraphylum: Agnatha
Superclass: Cyclostomi
Class: Petromyzontida
Order: Petromyzontiformes
Family: Mordaciidae
Genus: Mordacia
Species:
M. lapicida
Binomial name
Mordacia lapicida
(J. E. Gray, 1851)
Synonyms [2]
  • Caragola lapicidaJ. E. Gray, 1851
  • Petromyzon anwandteriPhilippi 1863
  • Petromyzon acutidensPhilippi 1865

Identification

Chilean lamprey (Mordacia lapicida), also known as lamprea de agua dulce, is a species of southern top-eyed lamprey endemic to southern Chile that can be found in riverine and marine habitats. Lampreys have eel-like (anguilliform) bodies with a rhomboid caudal fin, no bones or scales, and no lateral line. They have seven gill pores that run along the side of their bodies, a single nostril on the top of their heads, and two dorsal fins located toward the tail-end of their bodies. Southern top-eyed lamprey can reach a length of 54 centimeters (21 in) Standard Length (SL; measure from the snout to the end of the caudal peduncle) as adults, and 154 millimeters Total Length (TL; measure from the snout to the tip of the fully extended tail fin) as ammocoetes. [3] [4]

Contents

Ammocoetes and adults of this species are found in rivers, and occur in fine sand along river banks. [5] The life cycle of a Mordacia lapicida is divided into four life stages: freshwater rearing, an ocean parasite, an adult spawning stage, and a senescent stage. [6] Once in the adult stage, individuals migrate into marine waters where they attack and attach themselves to marine fishes. [7]

Life-History

Species in the Mordacia genus have a life cycle that consists of four main stages: larva (ammocoetes), juvenile, adult, and senescent. In general, lamprey ammocoetes burrow into the sediment of their freshwater habitat and filter feed for several years before undergoing a radical metamorphosis. [3] [8] It is suggested that as larvae, Chilean lamprey feed on unicellular algae. They are found in rivers with fine substrate and abundant organic material near the banks. It is believed that their occurrence near river mouths is influenced by salinity and their preference to lower levels of dissolved oxygen. The duration of the larval stage of Chilean lamprey specifically is unknown, but they begin to metamorphose into juveniles in fall and winter, between August and March. [7] [4] The metamorphosis stage of lamprey involves the development of functional eyes, a suctorial oral disc with a protrusible tongue-like piston, and the enlargement of their dorsal fins. [8] They then enter marine waters between June and August, in austral winter. [4]

Oral disc of Mordacia lapicida. Oral disc of Mordacia lapicida.png
Oral disc of Mordacia lapicida.

M.lapicida are an anadromous species so they migrate out to sea as juveniles to feed, but information about their upstream migration and reproduction remains largely understudied. However, it is known that Chilean lamprey are parasitic blood-feeders due to their large oral discs that allow for a suction seal around the attachment site of their host. This seal prevents a loss in the blood consumed, creates a discreet wound on the host, and allows for the production of lamphredin, an anticoagulant, that promotes tissue breakdown and prevents the host’s blood from clotting as they feed. The exact host species of the Chilean lamprey is not known, though blood-feeding lampreys typically feed on larger hosts than flesh-eating lampreys. Additionally, their bites don’t always end in the death of their host, unlike with flesh-eating lampreys. [6]

Although studies on Southern Hemisphere lampreys are minimal, a study on the lamprey species G. macrostoma, inferred that they prey on Baleen whales and detach from them at the Antarctic Convergence zone. [9] This may give some insight on M. lapicida hosts. Ultimately, spawning behavior and nesting locations are unknown for Chilean lamprey, though it is estimated that they have a slower growth rate compared to Northern Hemisphere lamprey. [7]

All lamprey species are semelparous, with a few exceptions. This means that they die soon after spawning just once in their entire lifetime. After their at-sea juvenile stage, adult lamprey return to freshwater streams to spawn. Spawning results in severe atrophy of the intestine, degeneration of the eyes and liver, depletion of lipids, and the inability to osmoregulate in saltwater for anadromous species, like the Chilean lamprey. Thus, lamprey die within a few days of spawning, with different species having varying survival times. [10]

Taxonomy

The Chilean lamprey belongs to the infraphylum/superclass Agnatha, the jawless fishes. This superclass is only made up of the classes Myxini (hagfish) and Petromyzontida (lampreys). They belong to the order Petromyzontiformes, which includes three families: Geotriidae and Mordaciidae in the Southern Hemisphere, and Petromyzontidae in the Northern Hemisphere. [11]

Summarized phylogeny of Southern Hemisphere lampreys. Lamprey phylogenetic tree.png
Summarized phylogeny of Southern Hemisphere lampreys.

Southern Hemisphere lampreys are divided into two families, Mordaciidae and Geotriidae, both with only a single genus– Mordacia and Geotria respectively. The species within these genera can be distinguished by the position of their eyes, color of their dorsal surface, and caudal fins. The species within the family Mordaciidae are called the Southern top-eyed lampreys because their eyes are positioned dorsolaterally, or closer to the top of their heads. They are also a brownish-grey color as juveniles, and their dorsal fins are contiguous as pre-metamorphosed juveniles. In comparison, Geotria have blue-green stripes and their dorsal fins are not contiguous. Within the genus Mordacia, there are 3 species: M. lapicida, M. praecox, and M. mordax., which are primarily distinguished by their location and dentition. M. preacox and M. mordax are found in Australia, while M. lapicida is found in South America (Chile). Additionally, M. mordax has fewer teeth on its radial plates than M. lapicida. [7]

Distribution

Since Chilean lamprey have not been extensively studied, it is estimated based on sightings that they inhabit coastal zones within the locations highlighted in the map shown below, with the points representing recorded collections. It is suggested that this species stays close to the coast and only inhabits marine waters for short periods in their lifetime. [7] Chilean lamprey have a relatively small distribution area with reports that they occur along the coast of Chile from 33° S to 41° S. [6] [12]

Mordacia distributions Mordacia distributions.png
Mordacia distributions

Conservation Status

Drought and the overuse of water resources in Chile has resulted in water-channel narrowing and may be affecting lamprey populations. As seen with a species in the Geotriidae family (G. australis), the introduction of other fish in these freshwater habitats could be harmful to Chilean lamprey larvae due to predation. Currently, M. lapicida is listed as “endangered” by the Chilean government and there was a 15-year extraction ban issued for them in 2011 by the Chilean Under-secretariat of Fisheries.

Generally, all the life stages of lampreys play an important role for the environments they inhabit. The burrowing and filter-feeding behaviors of larvae increase substrate oxygen levels and convert phytoplankton into stored biomass. In the senescent stage of anadromous lampreys, they transport and leave behind marine-derived nutrients and materials in freshwater streams when they die. [7] Mordacia lapicida, in particular, requires further research to examine the extent of its effects on its environment, how it interacts with conspecifics and prey, and what its role might mean in a human context.

References

  1. Colin, N. (2023). "Mordacia lapicida". IUCN Red List of Threatened Species . 2023 e.T13852A176561424. doi: 10.2305/IUCN.UK.2023-1.RLTS.T13852A176561424.en . Retrieved 9 January 2025.
  2. Froese, Rainer; Pauly, Daniel (eds.). "Family Mordaciidae". FishBase . May 2017 version. 680.
  3. 1 2 "FAMILY Details for Mordaciidae - Southern topeyed lampreys". fishbase.se. Retrieved 2025-11-14.
  4. 1 2 3 Lampreys of the world. An annotated and illustrated catalogue of lamprey species known to date.
  5. Froese, Rainer; Pauly, Daniel (eds.). "Mordacia lapicida". FishBase . April 2013 version.
  6. 1 2 3 Quintella, B.R (2021). "At-sea feeding ecology of parasitic lampreys". Journal of Great Lakes Research. 47: S72 –S89. Bibcode:2021JGLR...47S..72Q. doi: 10.1016/j.jglr.2021.07.008 . hdl: 10174/31175 . S2CID   238706584.
  7. 1 2 3 4 5 6 Miller, Allison (March 2021). "The Southern Hemisphere Lampreys (Geotriidae and Mordaciidae)". Reviews in Fish Biology and Fisheries. 31 (2): 201–232. Bibcode:2021RFBF...31..201M. doi:10.1007/s11160-021-09639-x. S2CID   233676907.
  8. 1 2 Potter, I. C., Gill, H. S., Renaud, C. B., Haoucher, D. (2015). "Lampreys: Biology, Conservation and Control". In Docker, M. F. (ed.). The Taxonomy, Phylogeny, and Distribution of Lampreys. Springer Netherlands. pp. 35–73. doi:10.1007/978-94-017-9306-3_2. ISBN   978-94-017-9305-6.
  9. Phillips, R. A., Waluda, C. M., Miller, A. K. (December 2023). "Distribution, hosts and long-term decline in abundance of the Patagonian lamprey inferred from diet assessment of albatrosses". Reviews in Fish Biology and Fisheries. 33 (4): 1443–1464. doi:10.1007/s11160-023-09786-3. ISSN   1573-5184 0960-3166, 1573-5184.{{cite journal}}: Check |issn= value (help)
  10. Johnson, N. S., Buchinger, T. J., Li, W. (2015). "Lampreys: Biology, Conservation and Control". In Docker, M. F. (ed.). Reproductive Ecology of Lampreys. Springer Netherlands. pp. 265–303. doi:10.1007/978-94-017-9306-3_6. ISBN   978-94-017-9305-6.
  11. Green, S. A., Bronner, M. E. (January 2014). "The lamprey: A jawless vertebrate model system for examining origin of the neural crest and other vertebrate traits". Differentiation. 87 (1–2): 44–51. doi:10.1016/j.diff.2014.02.001. ISSN   0301-4681.
  12. Nardi, C. F., Sánchez, J., Fernández, D. A., Casalinuovo, M. Á., Rojo, J. H., Chalde, T. (April 2020). "Detection of lamprey in Southernmost South America by environmental DNA (eDNA) and molecular evidence for a new species". Polar Biology. 43 (4): 369–383. doi:10.1007/s00300-020-02640-3. ISSN   1432-2056 0722-4060, 1432-2056.{{cite journal}}: Check |issn= value (help)