Beroe ovata naturally inhabits the Atlantic Ocean and coastal waters near both the United States and Canada as well as in the Gulf of Mexico and European waters. Beroe ovata has also been found in the East China Sea as well as the Indo-West Pacific Ocean. These ctenophores were introduced to the Alborán Sea, the Black Sea, and the Caspian Sea in the Mediterranean to control populations of their prey Mnemiopsis leidyi. They were temporarily considered an invasive species; however, populations have since declined. ("Ecosystems where Beroe ovata occurs", 2010; Mills, 1996)
Beroe ovata is a pelagic marine organism that swims freely in the water column. Beroe ovata has been found at depths ranging from just below the surface at 0.5 meters to 1719 meters below the surface, meaning B. ovata is capable of surviving in the epipelagic zone, mesopelagic zone, and the upper range of the bathypelagic zone. In addition to oceanic habitats, B. ovata inhabits coastal waters as well as estuaries including the York River, the Mississippi River and the Chesapeake Bay. This species survives in varying levels of salinity ranging from 1.2% in the Caspian Sea to 3.3-3.7% at the surface of the Atlantic Ocean. Besides its ability to survive in varying levels of salinity, B. ovata can inhabit areas of varying temperatures including polar, temperate, and tropical regions. ("Beroe ovata Bruguière, 1789", 2011; "Ecosystems where Beroe ovata occurs", 2010)
Beroe ovata has a pinkish color and an oval shaped body. The young organisms have wider bodies at both the oral and aboral ends. After development, the oral end of the adult organism is wider and the body tapers down toward the aboral end. Though it tapers down, the body does not end at a point. The length is 10 and 120 millimeters with an average mass of 0.85 milligrams. This organism also uses cilia for movement and feeding. In the Black Sea, smaller specimens of Beroe ovata are by the coast. Offshore, moderate to large organisms are found. Larvae are beroid, meaning they lack tentacles for feeding. A distinguishing characteristic for this species is their meridian canals have anostomoes (connecting canals) between them. (Finenko, et al., 2003; Shiganova, et al., 2001)
There is little known specifically about B. ovata development, but the life cycles of ctenophores are very simple. The ctenophores are hermaphroditic, meaning that they include both male and female gonads. They release both egg and sperm cells. The eggs remain free-floating until larvae hatch. Ctenophores do not change their general body types, only increase their body size. (Mills, 2001)
While there is very little information specifically about the species Beroe ovata, ctenophores in general are hermaphroditic, a single organism having both male and female gonads. Each organism releases eggs and sperm into the water. It is not known what cues trigger these ctenophores to mate, but they will continually release eggs and sperm under favorable temperatures and feeding conditions. (Finenko, et al., 2003; Mills, 2001)
While there is very little information specifically about the species Beroe ovata, ctenophores in general are hermaphroditic, a single organism having both male and female gonads. Each organism releases eggs and sperm into the water. The externally fertilized eggs stay free-floating until the larvae hatch. Ctenophores are able to reproduce at very early ages while small in size allowing for rapid generation times. As long as adequate food sources are present, the ctenophores will undergo production of egg and sperm and release them for several weeks. (Finenko, et al., 2003; Mills, 2001)
Beroe ovata release sperm and eggs simultaneously into the water. The eggs are fertilized at random so there is no parental involvement in the fertilization or development of the larvae and young Beroe ovata. (Finenko, et al., 2003; Mills, 2001)
While there is no information known specifically on the species Beroe ovata, other ctenophores have a seasonal lifespan. One species of ctenophore lives less than a month in the summer, while lasting three months in the winter. Study on the Beroe ovata could find seasonally dependent numbers also due to different factors. (Kasuya, et al., 2002)
Beroe ovata will bend and stretch while swimming rapidly if an escape response is initiated. When repeatedly exposed to similar stimuli in this way, Beroe ovata can turn itself inside out. While foraging, Beroe ovata swims in a spiral pattern and is also bioluminescent. While swimming and hunting, Beroe ovata employs reversible epithelial adhesion in order to keep the mouth closed, promoting a streamlined shape. This is accomplished without the assistance of a muscular or nervous system and instead with opposing paired strips of adhesive epithelial cells. (Matsumoto and Harbison, 1991; Tamm and Tamm, 1991)
Like most ctenophores, Beroe ovata is a pelagic organism, meaning that it swims freely throughout the water column. As it is found in many regions of the world’s oceans, its territory is large and likely transient due to ocean currents. ("Ecosystems where Beroe ovata occurs", 2010)
In the phylum Ctenophora, B. ovata has a net-like nervous system, spread out consistently throughout the entire epidermis. This species has no centralization of the nervous system or senses as seen in other phyla. Although bioluminescent, this is not likely used for communication. (Haddock and Case, 1999; Hay-Schmidt, 2000)
Beroe ovata primarily feeds on other ctenophores, including Bolinopsis infundibulum, Cestum veneris, Mnemiopsis leidyi, and various species of Ocyropsis. Beroe ovata is a non-visual predator. While foraging, B. ovata swims in a spiral pattern. The presence of prey causes chemokinetic responses in B. ovata which cause adjustments in swimming behavior. Beroe ovata also senses its prey by coming into contact with them while swimming. Macrocilia are employed to efficiently cut tissue from prey into a manageable size. Food is ingested due to the negative pressure generated when the ctenophore opens its mouth. (Matsumoto and Harbison, 1991; Swanberg, 1974)
Little information is available on the predators of Beroe ovata specifically; however it is likely that it would share predators with other members of its phylum. Ctenophores typically fall prey to a wide variety of organisms, including sharks, sea turtles, many species of boned fish, sea birds, as well as other ctenophores.
In the Black Sea, the invasive Beroe ovata helped to save the ecosystem from a harmful invasive species of Mnemiopsis leidyi. By feeding on the fellow invasive ctenophore, Beroe ovata has helped create a balance between the organisms living in the Black Sea. While most studies discuss the importance of this species in the Black Sea, it is likely it plays the same important roles in the bodies of water where it is a native species. (Finenko, et al., 2003; Mutlu, 2009)
In places where Beroe ovata occurs naturally, it is of little economic importance for humans. However, when introduced to the Black Sea in the late 1980s as a method of population control for the invasive species Mnemiopsis leidyi, B. ovata indirectly effected economic resources. By consuming up to 10% of the M. leidyi population daily, populations of zooplankton, ichthyplankton, and pelagic fish eaten by M. leidyi increased. One of the pelagic fish that increased with the control of M. leidyi was the anchovy species, Engraulis encrasicolus, which is economically important in the Black Sea region. (Kube, et al., 2007; Shiganova, et al., 2001)
Beroe ovata does not pose any threat of physical harm to humans as it does not have stinging tentacles commonly associated with ctenophores. However, the introduction into the Black Sea showed the ability of this species to completely and rapidly dominate an ecosystem. Unmanaged introductions could potentially effect pelagic fish and other valuable populations. (Kube, et al., 2007; Shiganova, et al., 2001)
Collette Dougherty (author), Radford University, Sarah Rimmer (author), Radford University, Gregory Zagursky (editor), Radford University, Renee Mulcrone (editor), Special Projects.
the body of water between Africa, Europe, the southern ocean (above 60 degrees south latitude), and the western hemisphere. It is the second largest ocean in the world after the Pacific Ocean.
body of water between the southern ocean (above 60 degrees south latitude), Australia, Asia, and the western hemisphere. This is the world's largest ocean, covering about 28% of the world's surface.
an animal that mainly eats meat
uses smells or other chemicals to communicate
the nearshore aquatic habitats near a coast, or shoreline.
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
an area where a freshwater river meets the ocean and tidal influences result in fluctuations in salinity.
fertilization takes place outside the female's body
union of egg and spermatozoan
a method of feeding where small food particles are filtered from the surrounding water by various mechanisms. Used mainly by aquatic invertebrates, especially plankton, but also by baleen whales.
having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.
Animals with indeterminate growth continue to grow throughout their lives.
the area of shoreline influenced mainly by the tides, between the highest and lowest reaches of the tide. An aquatic habitat.
referring to animal species that have been transported to and established populations in regions outside of their natural range, usually through human action.
having the capacity to move from one place to another.
specialized for swimming
the area in which the animal is naturally found, the region in which it is endemic.
generally wanders from place to place, usually within a well-defined range.
An aquatic biome consisting of the open ocean, far from land, does not include sea bottom (benthic zone).
the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.
a form of body symmetry in which the parts of an animal are arranged concentrically around a central oral/aboral axis and more than one imaginary plane through this axis results in halves that are mirror-images of each other. Examples are cnidarians (Phylum Cnidaria, jellyfish, anemones, and corals).
mainly lives in oceans, seas, or other bodies of salt water.
uses touch to communicate
breeding takes place throughout the year
animal constituent of plankton; mainly small crustaceans and fish larvae. (Compare to phytoplankton.)
2011. "Beroe ovata Bruguière, 1789" (On-line). Encyclopedia of Life. Accessed June 22, 2011 at http://www.eol.org/pages/509867?text_id=9024923.
2010. "Ecosystems where Beroe ovata occurs" (On-line). SeaLifeBase. Accessed June 22, 2011 at http://www.sealifebase.org/trophiceco/EcosysList.php?ID=87891&GenusName=Beroe&SpeciesName=ovata.
Arashkevich, E. 2001. Reproduction strategy of Beroe ovata (Ctenophora, Atentaculata, Beroida): a new invader in the Black Sea. Okeanologiya, 41: 116.
Bayha, K. 2006. The molecular systematics and population genetics of four coastal ctenophores and scyphozoan jellyfish of the United States Atlantic and Gulf of Mexico. Dissertation Abstracts International Part B: Science and Engineering, 66: 3590.
Carré, D., C. Sardet. 1984. Fertilization and early development in Beroe ovata. Developmental Biology, 105 (1): 188-195. Accessed June 22, 2011 at http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WDG-4DKTPG1-3V&_user=768496&_coverDate=09%2F30%2F1984&_rdoc=1&_fmt=high&_orig=search&_origin=search&_sort=d&_docanchor=&view=c&_acct=C000042521&_version=1&_urlVersion=0&_userid=768496&md5=bdaea1e0f1ebab05ebf730343642c2a6&searchtype=a.
Finenko, G., Z. Romanova, G. Abolmasova, B. Anninsky, L. Svetlichny, E. Hubavera, L. Bat, A. Kidneys. 2003. Population dynamics, ingestion, growth and reproduction rates of the invader Beroe ovata and its impact on plankton community in Sevastopol Bay, the Black Sea. Journal of Plankton Research, 25 (5): 539-549. Accessed June 22, 2011 at http://plankt.oxfordjournals.org/content/25/5/539.full.
Haddock, S., J. Case. 1999. Bioluminescence spectra of shallow and deep-sea gelatinous zooplankton: ctenophores, medusae and siphonophores. Marine Biology, 133: 571-582.
Hay-Schmidt, A. 2000. The evolution of the serotonergic nervous system. Proceedings of the Royal Society B: Biological Sciences, 267: 1071-1079.
Kasuya, T., T. Ishimaru, M. Murano. 2002. Laboratory study of growth of the lobate ctenophore Bolinopsis mikado (Moser). Plankton Biol Ecol, 49: 81-87.
Kideys, A., G. Finenko, B. Anninsky, T. Shiganova, A. Roohi. 2004. Physiological characteristics of the ctenophore Beroe ovata in Caspian Sea water. Marine Ecology, 226: 111.
Kube, S., L. Postel, C. Honnef, C. Augustin. 2007. Mnemiopsis leidyi in the Baltic Sea – distribution and overwintering between autumn 2006 and spring 2007. Aquatic Invasions, 2 (2): 137-145.
Matsumoto, G., G. Harbison. 1991. In situ observations of foraging, feeding, and escape behavior in three orders of oceanic ctenophores: Lobata, Cestida, and Beroida. Marine Biology, 117 (2): 279-287. Accessed June 22, 2011 at http://www.springerlink.com/content/q9245n0282972844/.
Miller, R., R. Williams. 1978. Energy requirements and food supplies of ctenophores and jellyfish in the Patuxent River estuary. Chesapeake Science, 13 (4): 328-331. Accessed June 22, 2011 at http://www.springerlink.com/content/50571138j5341m76/.
Mills, C. 1996. Medusae, siphonophores and ctenophores of the Alborán Sea, south western Mediterranean. Scientia Marina, 60: 145-163.
Mills, C. 2001. "Ctenophores" (On-line). Accessed June 22, 2011 at http://faculty.washington.edu/cemills/Ctenophores.html.
Mutlu, E. 2009. Recent distribution and size structure of gelatinous organisms in the southern Black Sea and their interactions with fish catches. Marine Biology, 156 (5): 935-957. Accessed June 22, 2011 at http://www.springerlink.com/content/l2n6uw5652u2701w/.
Nelson, T. 1925. On the occurrence and food habits of ctenophores in New Jersey inland coastal waters. The Biological Bulletin, 48 (2): 92-111. Accessed June 22, 2011 at http://www.jstor.org/stable/1536706.
Purcell, J., W. Graham, H. Dumont. 2001. Jellyfish blooms: ecological and societal importance. Hydrobiologia, 451: 333.
Shiganova, T., Y. Bulgakova, S. Volovik, Z. Mirzoyan, S. Dudkin. 2001. The new invader Beroe ovata Mayer 1912 and its effect on the ecosystem in the northeastern Black Sea. Hydrobiologia, 451 (1-3): 187-197. Accessed June 22, 2011 at http://www.springerlink.com/content/u417x62p70646858/.
Swanberg, N. 1974. The feeding behavior of Beroe ovata. Marine Biology, 24 (1): 69-76. Accessed June 22, 2011 at http://www.springerlink.com/content/x348516010343p0t/.
Tamm, S., S. Tamm. 1991. Reversible epithelial adhesion closes the mouth of Beroe, a carnivorous marine jelly. Biological Bulletin, 181: 463-473.
Tamm, S., S. Tamm. 1993. Diversity of macrociliary size, tooth patterns, and distribution in Beroe (Ctenophora). Zoomorphology, 113 (2): 78-89. Accessed June 22, 2011 at http://www.springerlink.com/content/n4221u9437088041/.
Vostokov, S., E. Arashkevich, A. Dritz, Y. Lukashev. 2001. Ecological and physiological characteristics of the ctenophore Beroe ovata in the coastal waters of the Black Sea: abundance, biomass, size distribution, behavior, feeding and metabolism. Russian Academy of Sciences, 41: 105.