| 词条 | Pleurobrachia bachei |
| 释义 |
| image = Pleurobrachia_bachei.jpg | image_caption = Pleurobrachia bachei with its oral end down. | taxon = Pleurobrachia bachei | authority = A. Agassiz, 1860 }} Pleurobrachia bachei is a member of the phylum Ctenophora and is commonly referred to as a sea gooseberry. These comb jellies are often mistaken for medusoid Cnidaria, but lack stinging cells. HistoryTraditionally, Ctenophora has been thought to represent an ancient metazoan phylum. Recent genetic data suggests that all extant Ctenophora taxa may have evolved from a relatively recent common ancestor and that this ancestral ctenophore was tentaculate and cydippid-like. Because of the virtual absence of ctenophores in the fossil record, their evolutionary history holds many more questions than answers.[1] MorphologyAn individual sea gooseberry's body length can reach up to {{convert|20|mm|in|abbr=on}} with each of the two tentacles stretching {{convert|150|mm|in|abbr=on}}.[2] Their gelatinous globular bodies are composed of 99% water.[3] 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.[5] Their mitochondrial genome consist of only 12 genes.[4] LifespanThe sea gooseberry is only alive for around 4–6 months.[3] ReproductionPleurobrachia lack any sessile (attached) stages and are wholly planktonic in their life cycle. They are self-fertile hermaphrodites[5] that spawn eggs and sperm freely into the sea, and develop thereafter without any parental protection with direct development.[3]FeedingForaging behaviorPleurobrachia 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[6] 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.[6] Trophic strategySea 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 distributionGeographic rangeP. bachei is found along the West coast of North America from Southeast Alaska to Mexico.[8][9]HabitatThe 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.[5] ConservationConservation statusPleurobrachia bachei has not been evaluated by the International Union for Conservation of Nature (IUCN), but seems to be prevalent and is not considered threatened.[10]Economic importance for humansNegativeAlthough 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.[11] 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. PositiveAs 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.[6] References1. ^{{cite journal|last=Podar|first=M |author2=Haddock, SH |author3=Sogin, ML |author4=Harbison, GR|title=A molecular phylogenetic framework for the phylum Ctenophora using 18S rRNA genes.|journal=Molecular Phylogenetics & Evolution|date=November 2001|volume=21|issue=2|pages=218–30|pmid=11697917|doi=10.1006/mpev.2001.1036|citeseerx=10.1.1.384.6705 }} {{Commons category|Pleurobrachia bachei}}{{Taxonbar|from=Q3015502}}2. ^{{cite book|last=Hanby|first=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.|title=Marine life of the Pacific Northwest : a photographic encyclopedia of invertebrates, seaweeds and selected fishes|year=2005|publisher=Harbour Pub.|location=Madeira Park, BC|isbn=978-1550173611}} 3. ^{{cite journal|last=Haddock|first=SHD|author2=Case, JF |title=Not all ctenophores are bioluminescent: Pleurobrachia|journal=The Biological Bulletin|year=1995|volume=189|issue=3|pages=356–362|url=http://www.biolbull.org/content/189/3/356.short|doi=10.2307/1542153|pmid=29244577|jstor=1542153}} 4. ^[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4024468/ Rapid evolution of the compact and unusual mitochondrial genome in the ctenophore, Pleurobrachia bachei] 5. ^1 Hirota, J. 1974. Quantitative natural history of Pleurobrachia bachei in La Jolla Bight. Fishery Bulletin 72: 295-335. 6. ^1 2 3 {{cite journal|last=Greene|first=Charles H|author2=Landry, Michael R |author3=Monger, Bruce C |title=Foraging behavior and prey selection by the ambush entangling predator Pleurobrachia bachei|journal=Ecology|date=December 1986|volume=67|issue=6|pages=1493–1501|jstor=10.2307/1939080|doi=10.2307/1939080}} 7. ^{{cite journal|last=Bisjop|first=John W|title=A Comparative Study of Feeding Rates of Tentaculate Ctenophores|journal=Ecology|date=September 1968|volume=49|issue=5|pages=996–997|jstor=1936552|doi=10.2307/1936552 }} 8. ^1 2 3 {{cite web|title=Sea gooseberry|url=http://www.bbc.co.uk/nature/blueplanet/factfiles/jellies/gooseberry_bg.shtml|work=The Blue Planet|publisher=BBC|deadurl=yes|archiveurl=https://web.archive.org/web/20101018225213/http://www.bbc.co.uk/nature/blueplanet/factfiles/jellies/gooseberry_bg.shtml|archivedate=2010-10-18|df=}} 9. ^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. 10. ^{{cite journal|title=Sea Gooseberry (Pleurobrachia bachei)|jstor=1936552|journal=Encyclopedia of Life|volume=49|issue=5|pages=996–997|publisher=EOL|last1=Bishop|first1=John W.|year=1968}} 11. ^{{cite journal|last=Chandy|first=Shonali T|author2=Greene, Charles H |title=Estimating the predatory impact of gelatinous zooplankton.|journal=Limnology and Oceanography|year=1995|volume=40|issue=5|pages=947–955|url=http://www.aslo.org/lo/toc/vol_40/issue_5/0947.pdf|doi=10.4319/lo.1995.40.5.0947}} 2 : Tentaculata|Animals described in 1850 |
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