Lymnaea stagnalis

Summary

Lymnaea stagnalis, better known as the great pond snail, is a species of large air-breathing freshwater snail, an aquatic pulmonate gastropod mollusk in the family Lymnaeidae. The great pond snail is a model organism to study parasitology, neurology, embryonal development and genetic regulation.[3]

Great Pond Snail
Lymnaea stagnalis
Water snail Rex 2.jpg
Scientific classification edit
Kingdom: Animalia
Phylum: Mollusca
Class: Gastropoda
Subclass: Heterobranchia
Superorder: Hygrophila
Family: Lymnaeidae
Genus: Lymnaea
Species:
L. stagnalis
Binomial name
Lymnaea stagnalis
(Linnaeus, 1758)[2]

Limnaea stagnalis var. baltica Lindström, 1868: synonym of Lymnaea stagnalis (Linnaeus, 1758)

DistributionEdit

The distribution of this species is holarctic, mainly the temperate zones of Northern America, Europe and Asia. The snail can be found in many ponds, lakes and very slow-moving rivers with a rich underwater vegetation. The northernmost populations exist in northern Norway, and in Central Europe, it inhabits even montane ecosystems at 1700 meters above sea level. In the Saprobiensystem used in Germany to judge the quality of freshwater biotopes, the species has a value of 1.9 and indicates a biotope with a water quality class II, the second-highest.[4]

ShellEdit

For the terms used in this section, see gastropod shell. The shells vary from light brown to dark brown, and the height of an adult shell ranges from 45 to 60 millimeters. Rarely, snails with a 70 mm shell can be found. The width of an adult shell ranges from 20 to 30 mm.

The shell has 4.5 to 6 weakly convex whorls. The upper whorls are pointed, while the last whorl is suddenly inflated. Young great pond snails can be confused with those of the genus Physa, and rarely, in cases of irregularly grown shells, great pond snails can be mixed up with Radix peregra — though adults of the latter species are a lot smaller, with shell heights of only 12 to 20 millimeters.

Nervous systemEdit

 
The dissected central ring ganglia of Lymnaea stagnalis. Scale bar is 1 mm.
LBuG and RBuG: left and right buccal ganglia
LCeG and RCeG: left and right cerebral ganglia
LPeG and RPeG: left and right pedal ganglia
LPIG and RPIG: left and right pleural ganglia
LPaG and RPaG: left and right parietal ganglia
VG: visceral ganglion.

Lymnaea stagnalis is widely used for the study of learning, memory and neurobiology.[5]

Lymnaea stagnalis has a relatively simple central nervous system (CNS) consisting of a total of ~20,000 neurons, many of them individually identifiable, organized in a ring of interconnected ganglia. Most neurons of the Lymnaea stagnalis central nervous system are large in size (diameter: up to ~100 μm), thus allowing electrophysiological dissection of neuronal networks that has yielded profound insights in the working mechanisms of neuronal networks controlling relatively simple behaviors such as feeding, respiration, locomotion, and reproduction. Studies using the central nervous system of Lymnaea stagnalis as a model organism have also identified novel cellular and molecular mechanisms in neuronal regeneration, synapse formation, synaptic plasticity, learning and memory formation, the neurobiology of development and aging, the modulatory role of neuropeptides, and adaptive responses to hypoxic stress.[5]

 
Lymnaea stagnalis in typical mating position of this species. The top snail is performing the male role (sperm donor), its white preputium (penis-carrying organ, Pp) can be seen inserted under the shell of the sperm recipient, where the female opening is located. During insemination, sperm (from the seminal vesicles) and seminal fluids (from the prostate gland) are transferred. Since these are simultaneous hermaphrodites, sexual roles can be swapped immediately afterwards.[6]

Life cycleEdit

 
Eggs of Lymnaea stagnalis

Lymnaea stagnalis is a simultaneously hermaphroditic species and can mate in the male and female role, but within one copulation only one sexual role is performed at a time.[7] Lymnaea stagnalis perform more inseminations in larger groups and prefer to inseminate novel over familiar partners. Such higher motivation to copulate when a new partner is encountered is known as the Coolidge effect and has been demonstrated in hermaphrodites firstly in 2007.[7]

ParasitesEdit

Lymnaea stagnalis is an intermediate host for:

  • Moliniella anceps (Molin, 1859) Hubner, 1939[8]

Other parasites of Lymnaea stagnalis include:

Lymnaea stagnalis has been experimentally infected with Elaphostrongylus rangiferi.[11]

As aquarium petsEdit

Lymnaea stagnalis snails can be easily be kept in a freshwater aquarium at room temperature, and fed with various sorts of vegetables, salad, cabbage and dandelion leaves. Fish food will also be eaten, as well as aquarium pests like algae, the Hydra viridissima polyp, and the eggs of other water snails.

Due to the development of toxic nitrates, leftover food must be removed in time, and the water exchanged often. Using a water conditioner is also recommended. Depending on water hardness, a piece of cuttlebone must be offered to cover the snails' calcium needs.

ReferencesEdit

This article incorporates CC-BY-2.0 text from references[5][7] and CC-BY-2.5 text from the reference[6]

  1. ^ Seddon, M.B.; Van Damme, D.; Cordeiro, J. (2017). "Lymnaea stagnalis". IUCN Red List of Threatened Species. 2017: e.T155475A42428297. doi:10.2305/IUCN.UK.2017-3.RLTS.T155475A42428297.en. Retrieved 12 November 2021.
  2. ^ Linnaeus C. (1758) Systema Naturae per regna tria naturae, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. 10th edition. Vermes. Testacea: 700–781. Holmiae. (Salvius).
  3. ^ Kuroda, Reiko; Abe, Masanori (2020). "The pond snail Lymnaea stagnalis". EvoDevo. doi:10.1186/s13227-020-00169-4.
  4. ^ Strictly speaking, the Saprobiensystem looks at the ability of a biotope to self-regulate its organic matter content under aerobic conditions.
  5. ^ a b c Feng Z-P., Zhang Z., Kesteren R. E. van, Straub V. A., Nierop P. van, Jin K., Nejatbakhsh N., Goldberg J. I., Spencer G. E., Yeoman M. S., Wildering W., Coorssen J. R., Croll R. P., Buck L. T., Syed N. I. & Smit A. B. (23 September 2009) "Transcriptome analysis of the central nervous system of the mollusc Lymnaea stagnalis". BMC Genomics 10: 451. doi:10.1186/1471-2164-10-451
  6. ^ a b Koene J. M., Sloot W., Montagne-Wajer K., Cummins S. F., Degnan B. M., Smith J. S., Nagle G. T. & Maat A. ter (2010). "Male Accessory Gland Protein Reduces Egg Laying in a Simultaneous Hermaphrodite". PLoS ONE 5(4): e10117. doi:10.1371/journal.pone.0010117.
  7. ^ a b c Koene J. M. & Maat A. T. (6 November 2007) "Coolidge effect in pond snails: male motivation in a simultaneous hermaphrodite". BMC Evolutionary Biology 7: 212. doi:10.1186/1471-2148-7-212
  8. ^ Kudlai O. S. (2009). "The discovery of the intermediate host for the trematode Moliniella anceps (Trematoda, Echinostomatidae) in Ukraine". Vestnik zoologii 43(4): e-11–e-13. doi:10.2478/v10058-009-0014-x.
  9. ^ Leicht K. & Seppälä O. (2014). "Infection success of Echinoparyphium aconiatum (Trematoda) in its snail host under high temperature: role of host resistance". Parasites & Vectors 7:192. doi:10.1186/1756-3305-7-192.
  10. ^ a b c d e f Soldanova M., Selbach C., Sures B., Kostadinova A. & Perez-del-Olmo A. (2010). "Larval trematode communities in Radix auricularia and Lymnaea stagnalis in a reservoir system of the Ruhr River". Parasites & Vectors 2010, 3: 56. doi:10.1186/1756-3305-3-56.
  11. ^ Skorping A. (1985). "Lymnea stagnalis as experimental intermediate host for Elaphostrongylus rangiferi". Zeitschrift für Parasitenkunde 71: 265–270.

External linksEdit

  • Lymnaea stagnalis at Animalbase taxonomy,short description, distribution, biology,status (threats), images
  • Hoffer J. N. A., Ellers J. & Koene J. M. (2010). "Costs of receipt and donation of ejaculates in a simultaneous hermaphrodite". BMC Evolutionary Biology 10: 393. doi:10.1186/1471-2148-10-393.
  • Lymnaea – Scholarpedia article
  • https://web.archive.org/web/20090925182719/http://www.lymnaea.org/ – Lymnaea stagnalis Sequencing Consortium
  • Arnaud Giusti, Pierre Leprince, Gabriel Mazzucchelli, Jean-Pierre Thomé, Laurent Lagadic, Virginie Ducrot, Célia Joaquim-Justo : Proteomic Analysis of the Reproductive Organs of the Hermaphroditic Gastropod Lymnaea stagnalis Exposed to Different Endocrine Disrupting Chemicals; PLOS|ONE 19 November 2013