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Jump to: ,
Parent taxa:
(check the following menu and phylogeny - the taxon in bold refers to the topic on this page)


Taxonomy Phylogeny

:
:
:: Pteriomorpha
:

  • : Pectinina
    • Superfamily Pectinoidea
    • Superfamily Anomioidea
  • Suborder
    • Superfamily Dimyoidea
    • Superfamily
    • Superfamily Plicatuloidea
`-- 
   |--
   |  |-- 
   |  |  |- 
   |  |  |-- canada viagra 
   |  |  `-- 
   |  |--Dimyidae
   |  `--Plicatulidae
   `--o Pectinina
      |--o Pectinoidea
      |  |-- Pectinidae [+Entoliidae]
      |  |-- Spondylidae
      |  |-- Syncyclonemidae
      |  `-- Propeamussiidae [+Amusiidae]
      `--o Anomiodea
         |-- Anomiidae
         `-- Placunidae


Ostreidae


True Oysters

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The members of the Ostreidae are the true oysters, and include all the that are commonly eaten under the title "". They do not include the Pearl Oysters; these species are only distantly related to the true oysters, since although they are also , they are members of the family , in the order .

the following two paragraphs are from :

Like scallops (family ), true oysters have a central , which means that the shell has a characteristic central scar, marking its point of attachment. Oysters have a larger adductor muscle than scallops. Their shell shape tends to be irregular as a result of attaching to other objects.

Both (egg bearing) and (larvae bearing) species are known within the Ostreidae. Both types are . However, the larviparous species (which include the Edible Oyster Ostrea edulis) show a pattern of alternating sex within each individual, whereas the oviparous species (such as the Eastern Oyster Crassostrea virginica) are simultaneous hermaphrodites producing either female or male according to circumstances.

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| | and many more genera


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Left (cemented) very convex. Shell with variable , edge folded and lamellar (Lindner 1977 p.105)

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  • Lindner, Gert, 1977, Seashells of the World, translated and edited by Gwynne Vevers, Sydney: Australia and New Zealand Book Co.,

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Environment: Shallow water or intertidal

Geographic distribution:

Stratigraphic range: to

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  • Family canada viagra Rafinesque 1815 (true oysters)
    • Subfamily Crassostreinae
      • Genera , , Striostrea
    • Subfamily Malchus, 1990
      • Genera Liostrea, Praeexogyra
    • Subfamily Lophinae Vyalov, 1936
      • Genera Alectryonella, Anomiostrea, Dendostrea, Lopha
    • Subfamily Ostreinae Rafinesque 1815
      • Genera Booneostrea, Nanostrea, , Planostrea, Pretostrea, Pustulostrea

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Ostreinae [Ostreidae, Ostreina]
   |--Liostrea
   |    |--L. hisingeri
   |    `--L. irregularis
   |--Praeexogyra
   |    |--*P. acuminata
   |    `--P. hebridica [=Ostrea hebridica]
   |-- Sacco 1897
   |    |--C. angulata
   |    |--C. cusseta
   |    |--C. gigas (Thunberg 1793)
   |    |--C. glomerata
   |    |--C. kawauchidensis
   |    |--C. ryosekiensis
   |    |--C. sikamea
   |    |--C. soleniscus
   |    |--C. tetoriensis Komatsu, Chinzei et al. 2002
   |    |--C. virginica
   |    `--C. yoshimoensis
   `--Ostrea Linnaeus 1758
        |--O. angasi
        |--O. arenicola
        |--O. boucheroni
        |--O. cerata Sowerby 1871
        |--O. clotbeyi
        |--O. cloti
        |--O. corrugata
        |--O. cristagalli (Linnaeus 1758) [=Mytilus cristagalli]
        |--O. cucullata Born 1778
        |--O. curvirostris
        |--O. dichotoma
        |--O. edulis Linnaeus 1758
        |--O. edwilsoni Stoyanov 1949
        |--O. elegans
        |--O. fraasi
        |--O. glomerata
        |--O. imbricata Lamarck 1819
        |--O. incurva Nilsson 1827
        |--O. lutaria
        |--O. mackayi
        |--O. manubriata
        |--O. mordax
        |--O. nigromarginata Sowerby 1871
        |--O. reili
        |--O. reniformis
        |--O. tatei
        |--O. tuberculata Lamarck 1804
        |--O. virginica
        |--O. wegmanniana
        `--O. wollastoni Finlay 1927 [=O. incurva Hutton 1873 non Nilsson 1827]

* Type species of generic name indicated

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Allan, R. S. 1927. The geology and palaeontology of the Lower Waihao Basin, south Canterbury, New Zealand. Transactions and Proceedings of the New Zealand Institute 57: 265-309.

Barash, A., & Z. Danin. 1986. Further additions to the knowledge of Indo-Pacific Mollusca in the Mediterranean Sea (Lessepsian migrants). Spixiana 9 (2): 117-141.

Carlton, J. T., J. B. Geller, M. L. Reaka-Kudla & E. A. Norse. 1999. Historical extinctions in the sea. Annual Review of Ecology and Systematics 30: 315-338.

Castro, P., & M. E. Huber. 1997. Marine Biology, 2nd ed. WCB McGraw-Hill: Boston.

Finlay, H. J. 1927a. A further commentary on New Zealand molluscan systematics. Transactions and Proceedings of the New Zealand Institute 57: 320-485.

Finlay, H. J. 1927b. New specific names for austral Mollusca. Transactions and Proceedings of the New Zealand Institute 57: 488-533.

Gingerich, P. D. 1992. Marine mammals (Cetacea and Sirenia) from the Eocene of Gebel Mokattam and Fayum, Egypt: Stratigraphy, age, and paleoenvironments. University of Michigan Papers on Paleontology 30: i-ix, 1-84.

Hayward, B. W., A. B. Stephenson, M. S. Morley, W. M. Blom, H. R. Grenfell, F. J. Brook, J. L. Riley, F. Thompson & J. J. Hayward. 2001. Marine biota of Parengarenga Harbour, Northland, New Zealand. Records of the Auckland Museum 37: 45-80.

Hedley, C. 1909. The Marine Fauna of Queensland: Address by the President of Section D. Australasian Association for the Advancement of Science: Brisbane.

Hodges, P. 2000. The Early Jurassic Bivalvia from the Hettangian and Lower Sinemurian of south-west Britain. Part. 1. Monograph of the Paleontographical Society 614: 1-64.

Komatsu, T., K. Chinzei, M. S. Zakhera & H. Matsuoka. 2002. Jurassic soft-bottom oyster Crassostrea from Japan. Palaeontology 45 (6): 1037-1048.

Leloup, E. 1970. Recherches sur l'ostreiculture dans le bassin de chasse d'Ostende. Bulletin de l’Institut Royal des Sciences Naturelles de Belgique 46 (6): 1-24.

Prescott, L. M., J. P. Harley & D. A. Klein. 1996. Microbiology (3rd ed.) Wm. C. Brown Publishers: Dubuque (Iowa).

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Phylogeny 11:51, 30 June 2009 (UTC); Introduction, Description, etc MAK061205

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Gr-1+ cells are known to facilitate tumor outgrowth. As such, it is conceivable that strategies seeking to eliminate this population may have a measurable antitumor effect. In certain tumor models, the Gr-1 depleting antibody inhibited tumor outgrowth even in the absence of T cells, although the antitumor effect was more pronounced in immune competent mice (32, 33). In light of these results and to verify that MDSCs are the target of sildenafil-mediated antitumor activity, we examined the effect of antibody-mediated MDSC depletion in combination with PDE5 inhibition in vivo. BALB/c mice were challenged on day 0 with C26GM tumor and were (a) left untreated; (b) injected with 100 µg of anti–Gr-1 antibody i.p. on days 0, 3, and 6; (c) treated with sildenafil; or (d) treated with a combination of the two treatments. As shown in Fig. 6 E, Gr-1 depletion delayed tumor outgrowth similarly to PDE5 inhibition, whereas no synergistic effect was seen with the combination. 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