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All issues Volume 26 / No 3 (July-September 2013) Aquat. Living Resour., 26 3 (2013) 221-228 References
Issue
Aquat. Living Resour.
Volume 26, Number 3, July-September 2013
Thematic Section: Physiology in Marine Molluscs
Page(s) 221 - 228
DOI https://doi.org/10.1051/alr/2013047
Published online 17 April 2013
  • Adams S.L., Hessian P.A., Mladenov P.V., 2003, Flow cytometric evaluation of mitochondrial function and membrane integrity of marine invertebrate sperm. Invert. Reprod. Dev. 44, 45–51. [CrossRef] [Google Scholar]
  • Akcha F., Spagnol C., Rouxel J., 2012, Genotoxicity of diuron and glyphosate in oyster spermatozoa and embryos. Aquat. Toxicol. 106-107, 104–113. [CrossRef] [PubMed] [Google Scholar]
  • Anderson D.M., Alpermann T.J., Cembella A.D., Collos Y., Masseret Et, Montresor M., 2012, The globally distributed genus Alexandrium: Multifaceted roles in marine ecosystems and impacts on human health. Harmful Algae 14, 10–35. [CrossRef] [PubMed] [Google Scholar]
  • Basti L., Go, J., Higuchi, K., Nagai K., Segawa S., 2011, Effects of the toxic dinoflagellate Heterocapsa circularisquama on larvae of the pearl oyster Pinctada fucata martensii (Dunker, 1873). J. Shellfish Res. 30, 177–186. [CrossRef] [Google Scholar]
  • Basti L., Nagai K., Tanaka Y., Segawa S., 2013, Sensitivity of gametes, fertilization, and embryo development of the Japanese pearl oyster, Pinctada fucuta martensii, to the harmful dinoflagellate, Heterocapsa circularisquama. Mar Biol. 160, 211–219. [CrossRef] [Google Scholar]
  • Bricelj V.M., MacQuarrie S.P., 2007, effects of brown tide (Aureococcus anophagefferens) on hard clam, Mercenaria mercenaria, larvae and implications for benthic recruitment. Mar Ecol. Prog. Ser. 333, 147–159. [CrossRef] [Google Scholar]
  • Collos Y., Gagné C., Laabir M, Vaquer A., Cecchi P., Souchu P., 2004, Nitrogenous nutrition of Alexandrium catenella (Dinophyceae) in cultures and in Thau lagoon, southern France. J. Phycol. 40, 96–103. [CrossRef] [Google Scholar]
  • Cordelli E., Eleuteri P., Leter G., Rescia M., Spanò M., 2005, Flow cytometry applications in the evaluation of sperm quality: semen analysis, sperm function and DNA integrity. Contraception 72, 273–279. [CrossRef] [PubMed] [Google Scholar]
  • Dong Q., Eudeline B., Allen Jr. S.K., Tiersch T.R., 2002, Factors affecting sperm motility of tetraploid Pacific oysters. J. Shellfish Res. 21, 719–723. [Google Scholar]
  • Erard-Le Denn E., Morlaix M., Dao J.C., 1990, Effects of Gyrodinium cf. aureolum on Pecten maximus (post larvae, juveniles and adults). In: Graneli E., Sundstrom B, Edler L., Anderson D.M. (Eds.) Toxic Marine Phytoplankton, Elsevier 132–136. [Google Scholar]
  • Favret P., Lynn J.W., 2010, Flow-cytometric analyses of viability biomarkers in pesticide-exposed sperm of three aquatic invertebrates. Arch. Environ. Contam. Toxicol. 58, 973–84. [CrossRef] [PubMed] [Google Scholar]
  • Flajshans M., Cosson J., Rodina M., Linhart O., 2004, The application of image cytometry to viability assessment in dual fluorescence-stained fish spermatozoa. Cell Biol. Int. 28, 955–959. [CrossRef] [PubMed] [Google Scholar]
  • Franco A., Kellner K., Mathieu M., Lelong C., Goux D., Heude-Brethelin C., 2011, Male germ cells of the Pacific oyster Crassostrea gigas: flow cytometry analysis, cell sorting and molecular expression. Aquat. Living Resour. 24, 237–245. [CrossRef] [EDP Sciences] [Google Scholar]
  • Garner D.L., Johnson L.A., Yue S.T., Roth B.L., Haugland R.P., 1994, Dual DNA staining assessment of bovine sperm viability using SYBR-14 and propidium iodide. J. Androl. 15, 620–629. [PubMed] [Google Scholar]
  • Garner D.L., Johnson L.A., 1995, Viability assessment of mammalian sperm using SYBR-14 and propidium iodide. Biol. Reprod. 53, 276–284 [CrossRef] [PubMed] [Google Scholar]
  • Gillan L., Evans G., Maxwell W.M.C., 2005, Flow cytometric evaluation of sperm parameters in relation to fertility potential. Theriogenology 63, 445–457. [CrossRef] [PubMed] [Google Scholar]
  • Graham J.K., 2001, Assessment of sperm quality: a flow cytometric approach. Anim. Reprod. Sci. 68, 239–24. [CrossRef] [PubMed] [Google Scholar]
  • Granmo A., Havenhand J., Magnusson K, Svane I., 1988, Effects of the planktonic flagellate Chrysochromulina polylepis Manton et Park on fertilization and early development of the ascidian Ciona intestinalis (L.) and the blue mussel Mytilus edulis L. J. Exp. Mar. Biol. Ecol. 124, 65–71. [CrossRef] [Google Scholar]
  • Guillard R.R.L. andHargraves P.E., 1993, Stichochrysis immobilis is a diatom, not a chrysophyte. Phycologia 32, 234–236. [CrossRef] [Google Scholar]
  • Haberkorn H., Lambert C., Le Goïc N., Moan J., Suquet M., Guéguen M., Sunila I., Soudant P., 2010, Effects of Alexandrium minutum exposure on nutrition-related processes and reproductive output in oysters Crassostrea gigas. Harmful Algae 9, 427–439. [CrossRef] [Google Scholar]
  • Haberkorn H., Tran D., Massabuau J-C., Ciret P., Savar V., Soudant P., 2011, Relationship between valve activity, microalgae concentration in the water and toxin accumulation in the digestive gland of the Pacific oyster Crassostrea gigas exposed to Alexandrium minutum. Mar. Pollut. Bull. 62, 1191–1197. [CrossRef] [PubMed] [Google Scholar]
  • Hégaret H., Brokordt K.B., Gaymer C.F., Lohrmann K.B., Garcia C., Varela D., 2012, Effects of the toxic dinoflagellate Alexandrium catenella on histopathogical and escape responses of the Northern scallop Argopecten purpuratus. Harmful Algae 18, 74–83. [CrossRef] [Google Scholar]
  • Kasai T., Ogawa K., Mizuno K., Nagai S., Uchida Y., Ohta S., Fujie M., Suzuki K., Hirata S, Hoshi K., 2002, Relationship between sperm mitochondrial membrane potential, sperm motility, and fertility potential. Japan Asian J. Androl. 4, 97–103. [Google Scholar]
  • Leverone J., Blake N.J., Pierce R.H., Shumway S.E., 2006, Effects of the dinoflagellate Karenia brevis on larval development in three species of bivalve mollusk from Florida. Toxicon 48, 75–84. [CrossRef] [PubMed] [Google Scholar]
  • Lewis C. andGalloway T., 2009, Reproductive consequences of paternal genotoxin exposure in marine invertebrates. Environ. Sci. Technol. 43, 928–933. [CrossRef] [PubMed] [Google Scholar]
  • Lewis C., Ford A.T., 2012, Infertility in male aquatic invertebrates: a review. Aquat. Toxicol. 120-121, 79–89. [CrossRef] [PubMed] [Google Scholar]
  • Lilly E.L., Kulis D.M., Gentien P., Anderson D.M., 2002, Paralytic shellfish poisoning toxins in France linked to human-introduced strain of Alexandrium catenella from the western Pacific: evidence from DNA and toxin analysis. J. Plankton Res. 24, 443–452. [CrossRef] [Google Scholar]
  • Lu X.Y. andWu R.S.S., 2005, UV induces reactive oxygen species, damages sperm, and impairs fertilization in the sea urchin Anthocidaris crassispina. Mar. Biol. 148, 51–57. [Google Scholar]
  • Marchetti C., Jouy N., Leroy-Martin B., Defossez A., Formstecher P., Marchetti P., 2004, Comparison of four fluorochromes for the detection of the inner mitochondrial membrane potential in human spermatozoa and their correlation with sperm motility. Hum. Reprod. 19 2267–2276. [CrossRef] [PubMed] [Google Scholar]
  • Mukai C., Okuno M., 2004, Glycolysis plays a major role for adenosine triphosphate supplementation in mouse sperm flagellar movement. Biol. Reprod. 71, 540–547. [Google Scholar]
  • Navarro, J.M., Contreras A.M., 2010, An integrative response by Mytilus chilensis to the toxic dinoflagellate Alexandrium catenella. Mar. Biol., 157, 1967–1974. [CrossRef] [Google Scholar]
  • Nice H.E., 2005, Sperm motility in the Pacific oyster (Crassostrea gigas) is affected by nonylphenol. Mar. Pollut. Bull. 50, 1668–1674. [CrossRef] [PubMed] [Google Scholar]
  • Ogier de Baulny B., LeVern Y., Kerboeuf D., Maisse G., 1997, Flow cytometric evaluation of mitochondrial activity and membrane integrity in fresh and cryopreserved rainbow trout (Onchorhynchus mykiss) spermatozoa. Cryobiology 34, 141–149. [CrossRef] [Google Scholar]
  • Paniagua-Chavez C.G., Jenkins J., Segovia M., Tiersch T.R., 2006, Assessment of gamete quality for the eastern oyster (Crassostrea virginica) by use of fluorescent dyes. Cryobiology 53, 128–138. [CrossRef] [PubMed] [Google Scholar]
  • Reers M., Smiley S.T., Mottola-Hartshorn C., Chen A., Lin M., Chen L.B., 1995, Mitochondrial membrane potential monitored by JC-1 dye. Methods Enzymol. 260, 406–414. [CrossRef] [PubMed] [Google Scholar]
  • REPHY Ifremer, espèces toxiques et toxines : Zones touchées par une interdiction de vente des coquillages 1992–2001. http://envlit.ifremer.fr/var/envlit/storage/documents/dossiers/toxines10ans/pdf/secteursfermes.pdf. [Google Scholar]
  • Silva P.F.N., Gadella B.M., 2006, Detection of damage in mammalian sperm cells. Theriogenology 65, 958–978. [CrossRef] [PubMed] [Google Scholar]
  • Summerson H.C., Peterson C.H., 1990, Recruitment failure of the Bay Scallop, Argopecten irradians concentricus, during the first red tide, Ptychodiscus brevis, outbreak recorded in North Carolina. Estuaries 13, 322–331. [CrossRef] [Google Scholar]
  • Tang Y.Z., Gobler C.J., 2009, Cochlodinium polykrikoides blooms and clonal isolates from the northwest Atlantic coast cause rapid mortality in larvae of multiple bivalve species. Mar. Biol. 156, 2601–2611. [CrossRef] [Google Scholar]
  • Thomas C.A., Garner D.L., DeJarnette J.M., Marshall C.E., 1998, Effect of cryopreservation of bovine sperm organelle function and viability as determined by flow cytometry. Biol. Reprod. 58.3.786. [Google Scholar]
  • Whedon W.F., Kofoid C.A., 1936, Dinoflagellata of the San Francisco region. I. On the skeletal morphology of two new species, Gonyaulax catanella and G. acatenella. Univ. Calif. Publs. Zool. 41, 25–34. [Google Scholar]

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