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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


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]
   |    |--L. hisingeri
   |    `--L. irregularis
   |    |--*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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(continued) "The key to curing more prostate cancer is to give higher does of radiation," observed Horwitz. "And over the last few years, more and more men have been getting higher dose radiation, because the radiation oncology community knows that dose matters and that low dose radiation is just not effective compared to high dose. And this study shows that we have the ability to give these high doses in different ways, and in all these ways, men do very well." Are you depressed? Fig. 2: Cellular perspective of the erection pathway. The signal (nitric oxide) is released from nerve endings or from endothelial cells and activates a cascade reaction, which ultimately leads to an increased cellular concentration of cGMP (cyclic guanosine monophosphate). This second messenger molecule induces a series of events that lead to smooth-muscle relaxation through a reduction in the intracellular calcium ion concentration. The enzyme PDE-5 (phosphodiesterase type 5) reverses this effect by metabolizing the cGMP to GMP rapidly. The clinically important inhibitors of this enzyme (sildenafil, vardenafil and tadalafil) all act to promote smooth-muscle relaxation by their ability to allow cGMP to accumulate when nitric oxide is released, as is the case when sexual stimulation is present. Photo: Christine Kenney Vasoactive injection: During this test, an erection is produced by injecting special solutions that cause the blood vessels to dilate (enlarge), allowing blood to enter the penis. These medications work when there is sexual stimulation. Depending on the treatment, it will need to be taken 20 minutes to 1 hour before sex and the period of time over which it works can vary between 3 hours and up to 36 hours. Medical and sexual histories help define the degree and nature of ED. A medical history can disclose diseases that lead to ED, while a simple recounting of sexual activity might distinguish among problems with sexual desire, erection, ejaculation, or orgasm. High cholesterol or blood pressure Talk to a sex counselor: If ED is straining your relationship, consider seeking care from a professional therapist. *Monoamine oxidase inhibitors The following health professionals can evaluate symptoms of erection problems: buy sildenafil citrate online All of these conditions or lifestyle factors contribute to erectile difficulties in three major ways: By reducing blood flow, causing nerve damage, or changing the hormonal environment. The workers had levels of exposure to BPA that were 50 times what an average U.S. man faces. But the findings raise questions about whether exposure at lesser levels can affect sexual function, Li said. "This was a highly exposed group, and we see the effect," he said. "Now, we have to worry about lower-level exposure." 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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