Mnemiopsis

Warty comb jelly
M. leidyi at the New England Aquarium
Scientific classification
Kingdom:	Animalia
Phylum:	Ctenophora
Class:	Tentaculata
Order:	Lobata
Family:	Bolinopsidae
Genus:	Mnemiopsis Agassiz, 1860
Species:	M. leidyi
Binomial name
Mnemiopsis leidyi A. Agassiz, 1865
Synonyms
M. gardeni Agassiz, 1860 M. mccradyi Mayer, 1900

The warty comb jelly or sea walnut (Mnemiopsis leidyi) is a species of tentaculate ctenophore (comb jelly), originally native to the western Atlantic coastal waters. Three species have been named in the genus Mnemiopsis, but they are now believed to be different ecological forms of a single species M. leidyi by most zoologists.^[1]

Description and ecology

Mnemiopsis have a lobed body that is oval-shaped and transparent, with four rows of ciliated combs that run along the body vertically and glow blue-green when disturbed. They have several feeding tentacles. Unlike cnidarians, Mnemiopsis doesn't sting. Their body contains 97% water. They are small animals, having a maximum body length of roughly 7–12 centimetres (3–5 in) and a diameter of 2.5 centimetres (1 in).

It is euryoecious, tolerating a wide range of salinity (2 to 38 psu), temperature (2–32 °C or 36–90 °F), and water quality.

Mnemiopsis is a carnivore that consumes zooplankton including crustaceans,^[2] other comb jellies, and eggs and larvae of fish; it is sometimes known to eat smaller individuals of its own kind. It also has several other predators. Many are vertebrates, including species of birds and fish. Some predators include other members of gelatinous zooplankton such as Beroe ctenophores and various Scyphozoa (jellyfish).

This comb jelly has the capacity for self fertilization, as they are hermaphroditic. They have gonads that contain the ovary and spermatophore bunches in their gastrodermis. This animal carries 150 eggs along each meridional canal. Eggs and sperm are released into the water column where external fertilization takes place. The spawning commences at late evening or at 1:00 or 2:00 a.m. The spawning eggs develop a thick outer layer within 1 minute after touching the seawater. As many as 10,000 eggs can be produced from large specimens in areas with good prey abundance. Egg production can start when the animals reach about 15 mm in length. Egg production increases with ctenophore size, and it is unclear when senescence occurs.

As an invasive species

1980s – Black Sea

Mnemiopsis leidyi was introduced in the Black Sea in the 1980s, where only one species of comb jelly, the small sea gooseberry Pleurobrachia pileus occurred until then. The most likely cause of its introduction is accidentally by merchant ships' ballast water. The first Black Sea record was in 1982.^[3]

By 1989, the Black Sea population had reached the highest level, with some 400 specimens per m³ of water (>10 animals/cubic foot) in optimal conditions.^[4] Afterwards, due to depletion of foodstocks resulting in lower carrying capacity, the population dropped somewhat.

In the Black Sea, M. leidyi eats eggs and larvae of pelagic fish. It caused a dramatic drop in fish populations, notably the commercially important anchovy Engraulis encrasicholus (known locally as hamsi, hamsiya, hamsa, etc), by competing for the same food sources and eating the young and eggs.^[4] Biological control was tried with Beroe ovata, another comb jelly, with some degree of success; it appears as if a fairly stable predator-prey dynamic has been reached.^[5]

1999 – Caspian Sea

In 1999 the species was introduced in the Caspian Sea. The result was that 75% of the zooplankton was depleted, thereby affecting the entire food chain of the lake.

2006 – North and Baltic Seas

Since then, the species has apparently spread throughout the Mediterranean basin and the northwestern Atlantic. In 2006, it was first recorded in the North Sea,^[6] and since October 17, 2006^[7] in the western Baltic Sea, namely the Kiel Fjord and The Belts. Up to 100 animals/m³ (c. 3/cubic ft) were counted in the Baltic, whereas the population density in the North Sea was at a much lower 4 animals/m³ (about 1 animal/9 cubic ft) at most.^[4]

M. leidyi at the Monterey Bay Aquarium

One year later, the Baltic population of M. leidyi was found to have spread east to the Gotland Basin and the Bay of Puck.^[8] The impact of the species on the already heavily stressed Baltic ecosystem is unknown. The species overwinters in the deep waters where temperature does not drop below 4 °C (39 °F); the fact that the Baltic is heavily stratified, with the waters above and below the halocline mixing little, is believed to aid its survival.^[4]

Apart from the widespread P. pileus, 3 comb jelly species are occasionally drifted into the Baltic from the North Sea but do not seem to be present as a stable population of significant size: Bolinopsis infundibulum, Beroe cucumis and Beroe gracilis. The second species might potentially be used for biological control.^[9]

The route of dispersal of M. leidyi to the North Sea/Baltic region is unknown. It might have occurred naturally by drifting individuals, or with ballast water of ships, either from its natural range or from the Black Sea, via the Mediterranean and eastern Atlantic.^[10] At least technically possible given the species' euryhaline habits is an alternate route of dispersal through continental Europe, being carried with ballast water in ships travelling from the Black Sea to the Rhine Estuary via the Rhine-Main-Danube Canal. The latter route is known to be the point of entry into continental Europe for numerous invasive freshwater neozoons from the Ponto-Caspian region, such as the zebra mussel, the quagga mussel, the amphipods Dikerogammarus villosus and Chelicorophium curvispinum, and the polychaete Hypania invalida.

Genomics

The ~155 megabase genome of Mnemiopsis leidyi has been sequenced.^[11]

Its mitochondrion shows several interesting features.^[12] It is 10 kilobases in length making it the smallest animal mitochondrial DNA sequence known to date. It has lost at least 25 genes, including atp6 and all the tRNA genes. The atp6 gene has been relocated to the nuclear genome and has acquired introns and a mitochondrial targeting presequence. All tRNA genes have been genuinely lost along with nuclear-encoded mitochondrial aminoacyl tRNA synthetases. The mitochondrial rRNA molecules possess little similarity with their homologs in other organisms and have highly reduced secondary structures.

See also

• S. Faris (November 2, 2009). "A Gelatinous Invasion". Time: 49–50. http://www.time.com/time/magazine/article/0,9171,1931659,00.html. 

Footnotes

1. ^ Hansson (2006)
2. ^ E.g. the calanoid copepod Acartia tonsa (Kube et al. 2007)
3. ^ Zaika & Sergeyeva (1990)
4. ^ ^{a b c d} Kube et al. (2007)
5. ^ Kideys (2002)
6. ^ Faasse & Bayha (2006)
7. ^ Javidpour et al. (2006)
8. ^ "Invasion der Rippenquallen [Invasion of the Comb Jellies]" (in German). Scinexx. http://www.scinexx.de/dossier-465-1.html. Retrieved January 15, 2011. 
9. ^ Hansson (2006), Kube et al. (2007)
10. ^ Oliveira (2007)
11. ^ Ryan et al. (2010)
12. ^ Pett W, Ryan JF, Pang K, Mullikin JC, Martindale MQ, Baxevanis AD, Lavrov DV (2011) Extreme mitochondrial evolution in the ctenophore Mnemiopsis leidyi: Insight from mtDNA and the nuclear genome. Mitochondrial DNA

References

• Goodwin, G.; Bogert, C. M.; Gilliard, E. & Coates, C. W. (1961): The Illustrated Encyclopedia of Animal Life 13: 1671. Odham Books.
• Hansson, Hans G. (2006): Ctenophores of the Baltic and adjacent Seas - the invader Mnemiopsis is here! Aquatic Invasions 1 (4): 295–298. PDF fulltext
• Javidpour, Jamileh; Sommer, Ulrich & Shiganova, Tamara A. (2006): First record of Mnemiopsis leidyi A. Agassiz 1865 in the Baltic Sea. Aquatic Invasions 1 (4): 299–302. PDF fulltext
• Faasse, Marco A. & Bayha, Keith M. (2006): The ctenophore Mnemiopsis leidyi A. Agassiz 1865 in coastal waters of the Netherlands: an unrecognized invasion?. Aquatic Invasions 1 (4): 270–277. PDF fulltext
• Kideys, Ahmet E. (2002): Fall and Rise of the Black Sea Ecosystem. Science 297 (5586): 1482–1484. doi:10.1126/science.1073002 (HTML abstract)
• Kube, Sandra; Postel, Lutz; Honnef, Christopher & Augustin, Christina B. (2007): Mnemiopsis leidyi in the Baltic Sea - distribution and overwintering between autumn 2006 and spring 2007. Aquatic Invasions 2 (2): 137–145. PDF fulltext
• Oliveira, Otto M. P. (2007): The presence of the ctenophore Mnemiopsis leidyi in the Oslofjorden and considerations on the initial invasion pathways to the North and Baltic Seas. Aquatic Invasions 2 (3): 185–189. PDF fulltext
• Purcell, Jennifer E.; Shiganova, Tamara A.; Decker, Mary Beth & Houde, Edward D. (2001): The ctenophore Mnemiopsis in native and exotic habitats: US estuaries versus the Black Sea basin. Hydrobiologia 451: 145–176.doi:10.1023/A:1011826618539 PDF fulltext
• Ryan, Joseph F.; Pang, K.; NISC Comparative Sequencing Program, Nisc; Mullikin, J. C.; Martindale, M. Q.; Baxevanis, A. D. (October 2010). "The homeodomain complement of the ctenophore Mnemiopsis leidyi suggests that Ctenophora and Porifera diverged prior to the ParaHoxozoa". EvoDevo 1 (1): 9. doi:10.1186/2041-9139-1-9. PMC 2959044. PMID 20920347. http://www.evodevojournal.com/content/1/1/9. 
• Zaika, V. Ye. & Sergeyeva, N. G. (1990): Morphology and Development of Mnemiopsis mccradyi (Ctenophora, Lobata) in the Black Sea. Zoologicheskiy Zhurnal 69 (2): 5–11 [Russian version]; Hydrobiological Journal 26: 1–6 [English version]. HTML abstract

External links

• Research group Limnology at Ghent University, Belgium
• Ctenophores from the São Sebastião Channel