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Pleurobrachia bachei A. Agassiz 1860

Evolution ( englanti )

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An interdisciplinary team recently sequenced the Pleurobrachia bachei genome.This group analyzed the genetics and neural physiology of P. bachei in the context of genetic sequence available for other ctenophore species, finding that ctenophores have a very different set of genes and signal molecules involved in their nervous system, immune system and development than do all other animals.Ctenophores have a “highly reduced complement of animal-specific genes,” lacking, for example, HOX genes (as do sponges), neuron-specific genes such as classic neurotransmitters, and immune system-related receptors and mediators (Moroz et al., 2014).

The placement of ctenophores in the tree of life has long been controversial.Moroz et al. (2014) found that phylogenetic analyses of 114 genes from representatives of the Ctenophora, Porifera, Placozoa, Cnidaria and Bilateria recover ctenophores as basal to all other animals, suggesting that neural muscular systems evolved twice independently in the animal lineage: once in ctenophores, and subsequently in the bilateria+cnidaria lineage.This is consistent with the remarkably distinct underlying organizations of neural muscular systems in theses two lineages.

This study also recovered strong resolution of relationships within the ctenophores, which suggest a new understanding of ctenophore evolution, including derivation of larval stages, tentacle apparatuses and benthic ecology and bilaterial nature.

Moroz et al. published their work in Nature under a Creative Commons Attribution NonCommercial ShareAlike 3.0 licence, available at this link: http://www.nature.com/nature/journal/v510/n7503/full/nature13400.html

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Habitat ( englanti )

tarjonnut Invertebrates of the Salish Sea
Pelagic, especially in nearshore water
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Invertebrates of the Salish Sea

Distribution ( englanti )

tarjonnut Invertebrates of the Salish Sea
Geographical Range: Alaska to Acapulco, Mexico
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Comprehensive Description ( englanti )

tarjonnut Invertebrates of the Salish Sea
Ctenophores such as this one look similar to jellyfish but have 8 rows of fused cilia along their sides which beat for propulsion. Pleurobrachia bachei is elliptical in shape with no large lobes. The comb rows are nearly equally spaced and extend nearly the entire length of the body. Two long, branched tentacles trail back from sheaths which angle out from near the gut toward the aboral pole. The tentacle branches are abundant, are only from one side of the tentacle, and are not coiled. The animal is clear, but organs and tentacles may be pink, yellow, white, or orange-brown. There may be purplish blotches near the pharynx. Diameter to 1.5 cm; length slightly longer than diameter.
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Look Alikes ( englanti )

tarjonnut Invertebrates of the Salish Sea
How to Distinguish from Similar Species: Euplokamis dunlapae is similar shape but the body is more ovoid and flattened plus the tentacle branches are sparse and coil into bundles when contacted.
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Comprehensive Description ( englanti )

tarjonnut Invertebrates of the Salish Sea
Biology/Natural History: Ctenophores have no nematocysts so they cannot sting. Instead, they have colloblast cells which produce a sticky substance to snare prey. Pleurobrachia bachei feeds on almost anything small enough for it to engulf, and may consume many copepods, eggs, and larval fish. It is a sit-and-wait predator. It swims horizontally in a semicircle while gradually extending its two tentacles until the tentillae hang down evenly spaced. Then it stops and waits suspended with its mouth upright. When prey contacts the sticky net of tentillae and is snared, Pleurobrachia begins swimming forward while retracting its tentacles until the prey is close to its body. Then it begins rotating its body so the prey is brought around to the mouth and ingested. This species is the most common species of ctenophore likely to be encountered in the Northwest. Large aggregations may be seen in spring and summer. Individuals are hermaphrodites. Eggs and sperm are released through the mouth and fertilized in the water. Not bioluminescent. May harbor a small colored symbiotic amphipod, Hyperoche sp. An extensive review article about cilia, swimming, neural circuitry, and behavior in ctenophores including Pleurobrachia can be found in Tamm
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Pleurobrachia bachei ( englanti )

tarjonnut wikipedia EN

Pleurobrachia bachei is a member of the phylum Ctenophora and is commonly referred to as the Pacific sea gooseberry. These comb jellies are often mistaken for medusoid Cnidaria, but lack stinging cells.

Morphology

An individual sea gooseberry's body length can reach up to 20 mm (0.79 in) with each of the two tentacles stretching 150 mm (5.9 in).[1] Their gelatinous globular bodies are composed of 99% water.[2] They have eight rows of well-developed comb plates consisting of thousands of fused macrocilia controlled by an apical organ. Unlike most other ctenophores, Pleurobrachia lacks a conventional photoprotein and is therefore incapable of producing light.[3] Their bodies are virtually transparent and the many cilia refract the light, producing rainbow-like colors that can give the false appearance of bioluminescence. The branched tentacles can be white, yellow, pink or orange. They have no nematocysts (stinging cells). Instead, the two long extensile branched tentacles are armed with colloblasts: specialized adhesive cells with which to ensnare their prey.[4]

Their mitochondrial genome consist of only 12 genes.[5]

Lifespan

The sea gooseberry is only alive for around 4–6 months.[2]

Reproduction

Pleurobrachia lack any sessile (attached) stages and are wholly planktonic in their life cycle. They are self-fertile hermaphrodites[6] that spawn eggs and sperm freely into the sea, and develop thereafter without any parental protection with indirect development.[2]

Feeding

Foraging behavior

Pleurobrachia bachei is a selective carnivore and its feeding habits are analogous to other ambush "sit and wait" predators, such as the orb-weaving spider. When searching for prey the Pleurobrachia swims with its oral pole forward to set its tentacles. To allow the two main tentacles and numerous lateral tentilla to relax and expand behind it they are often in a curved or helical pathway. Once the tentacles are set, the ctenophore drifts passively. Occasionally, it will retract its tentacles to varying degrees into the sheaths before swimming to another location where it then resets them. This behavior appears to be regulated by its hunger level[4] and can be construed as an attempt to find an area with more prey abundance.

When handling prey both tentacles contract and carry the prey to the mouth. This is achieved by several rapid rotations of the body which swipes the tentacle bearing the food across the oral region. The Pleurobrachia has its oral end opposite of where its tentacles originate.[4]

Trophic strategy

Sea gooseberries are insatiable feeders of copepods and other small plankton, rarely fish eggs and larvae. It has been shown that their prey is more susceptible at an early age (naupliar/larval stages) because of minimal swimming speeds and small size which makes handling more efficient. This generalization is not necessarily true for all Pleurobrachia. In one experiment the ctenophore favored adult Pseudocalanus minutus more than other forms of zooplankton.[7]

Ecology and distribution

Geographic range

P. bachei is found along the West coast of North America from Southeast Alaska to Mexico.[2][8]

Habitat

The sea gooseberry occurs primarily in surface waters of the coastal NW Pacific within 5 km of shore to about 50 m deep, though is usually in the upper 15 m during the day.[6]

Conservation

Conservation status

Pleurobrachia bachei has not been evaluated by the International Union for Conservation of Nature (IUCN), but seems to be prevalent and is not considered threatened.[9]

Economic importance for humans

Negative

Although Pleurobrachia has not been associated with declines in other populations, a closely related species Mnemiopsis leidyi has. This ctenophore had catastrophic effects on fish catches after its introduction into the Black and Azov Seas. It is believed to have been the main cause of decline in these waters after dissection confirmed its stomach contents had large quantities of the local fish eggs and larvae.[10] Because of their diets Pleurobrachia and other ctenophore species can directly or indirectly affect trophic cascades and ultimately regulate yield of commercially important fish stocks.

Positive

As predators, ctenophores have a tremendous capacity to regulate abundance of their prey and therefore help to balance an ecosystem. While they can decimate other populations they can also restrain an overabundance of copepods which, when left to their own devices, could virtually eliminate all phytoplankton from the water column.[4]

References

  1. ^ Hanby, Andy Lamb and Bernard P. Hanby ; seaweed and annelid worm sections in collaboration with Michael W. Hawkes and Sheila C. Byers respectively ; photography by Bernard P. (2005). Marine life of the Pacific Northwest : a photographic encyclopedia of invertebrates, seaweeds and selected fishes. Madeira Park, BC: Harbour Pub. ISBN 978-1550173611.
  2. ^ a b c d "Sea gooseberry". The Blue Planet. BBC. Archived from the original on 2010-10-18.
  3. ^ Haddock, SHD; Case, JF (1995). "Not all ctenophores are bioluminescent: Pleurobrachia". The Biological Bulletin. 189 (3): 356–362. doi:10.2307/1542153. JSTOR 1542153. PMID 29244577.
  4. ^ a b c d Greene, Charles H; Landry, Michael R; Monger, Bruce C (December 1986). "Foraging behavior and prey selection by the ambush entangling predator Pleurobrachia bachei". Ecology. 67 (6): 1493–1501. doi:10.2307/1939080. JSTOR 1939080.
  5. ^ Rapid evolution of the compact and unusual mitochondrial genome in the ctenophore, Pleurobrachia bachei
  6. ^ a b Hirota, J. 1974. Quantitative natural history of Pleurobrachia bachei in La Jolla Bight. Fishery Bulletin 72: 295-335.
  7. ^ Bisjop, John W (September 1968). "A Comparative Study of Feeding Rates of Tentaculate Ctenophores". Ecology. 49 (5): 996–997. doi:10.2307/1936552. JSTOR 1936552.
  8. ^ Wrobel, D. and C. Mills, 1998. Pacific Coast Pelagic Invertebrates: a Guide to the Common Gelatinous Animals. Sea Challengers and the Monterey Bay Aquarium, Monterey, California, iv plus 108 pages.
  9. ^ Bishop, John W. (1968). "Sea Gooseberry (Pleurobrachia bachei)". Encyclopedia of Life. EOL. 49 (5): 996–997. JSTOR 1936552.
  10. ^ Chandy, Shonali T; Greene, Charles H (1995). "Estimating the predatory impact of gelatinous zooplankton" (PDF). Limnology and Oceanography. 40 (5): 947–955. Bibcode:1995LimOc..40..947C. doi:10.4319/lo.1995.40.5.0947. Archived from the original (PDF) on 2012-02-13. Retrieved 2012-04-22.
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Pleurobrachia bachei: Brief Summary ( englanti )

tarjonnut wikipedia EN

Pleurobrachia bachei is a member of the phylum Ctenophora and is commonly referred to as the Pacific sea gooseberry. These comb jellies are often mistaken for medusoid Cnidaria, but lack stinging cells.

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Pleurobrachia bachei ( ranska )

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Pleurobrachia bachei est une espèce de cténophores de la famille des Pleurobrachiidae.

Habitat et répartition

Cette espèce est présente dans le Nord de l'océan Atlantique et au large de l'Irlande.

Références taxinomiques

Notes et références

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Pleurobrachia bachei: Brief Summary ( ranska )

tarjonnut wikipedia FR

Pleurobrachia bachei est une espèce de cténophores de la famille des Pleurobrachiidae.

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Pleurobrachia bachei ( flaami )

tarjonnut wikipedia NL

Pleurobrachia bachei is een ribkwal uit de familie Pleurobrachiidae.

De wetenschappelijke naam van de soort werd in 1860 al genoemd[1] maar pas in 1865 voor het eerst geldig gepubliceerd door Alexander Agassiz.[2]

Bronnen, noten en/of referenties
Geplaatst op:
09-12-2011
Dit artikel is een beginnetje over biologie. U wordt uitgenodigd om op bewerken te klikken om uw kennis aan dit artikel toe te voegen. Beginnetje
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Identification ( englanti )

tarjonnut World Register of Marine Species
Pl. Bachei, discovered by my son on the shores of Washington Territory, is another species with red tentacles, but differs from Pl. rhododactyla in having a longer funnel, a shorter coeliac cavity , and the actinal part of the tentacular sac also shorter.

Viite

Agassiz, L. (1860). Contributions to the Natural History of the United States of America. 3 :1-301.

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World Register of Marine Species