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51. Distribution of Quahog Larvae Along a North-South Transect in Narragansett Bay

53. De novo assembly transcriptome analysis reveals the preliminary molecular mechanism of pigmentation in juveniles of the hard clam Mercenaria mercenaria

55. The invasive red seaweed, Dasysiphonia japonica, forms harmful algal blooms: Mortality in early life stage fish and bivalves and identification of putative toxins.

56. Buffering muds with bivalve shell significantly increases the settlement, growth, survival, and burrowing of the early life stages of the Northern quahog, Mercenaria mercenaria, and other calcifying invertebrates

57. Life span bias explains live–dead discordance in abundance of two common bivalves

58. Cellular responses to in vitro exposures to β-blocking pharmaceuticals in hard clams and Eastern oysters

59. A Reviewof QPX Disease In Thenorthernquahog(= Hard Clam)Mercenaria mercenaria

60. Differential Mortality of North Atlantic Bivalve Molluscs During Harmful Algal Blooms Caused by the Dinoflagellate, Cochlodinium (a.k.a. Margalefidinium) polykrikoides

61. Linking paternally inherited mtDNA variants and sperm performance

62. Cryopreservation of trochophore larvae from the hard clamMercenaria mercenaria: Evaluation of the cryoprotectant toxicity, cooling rate and thawing temperature

63. The effects of red tide (Karenia brevis) on reflex impairment and mortality of sublegal Florida stone crabs, Menippe mercenaria

64. Identification of clam plasma proteins that bind its pathogen Quahog Parasite Unknown

65. Thermal and viscous effects of temperature on Mercenaria mercenaria suspension feeding

66. Stimpson's hard clam Mercenaria stimpsoni; A multi-decadal climate recorder for the northwest Pacific coast

67. Predicting discard mortality in Florida stone crab, Menippe mercenaria, using reflexes

71. Interactive effects of elevated temperature and CO2 levels on energy metabolism and biomineralization of marine bivalves Crassostrea virginica and Mercenaria mercenaria.

72. Characterization of brevetoxin metabolism in Karenia brevis bloom-exposed clams (Mercenaria sp.) by LC-MS/MS

73. Differential immune response in the hard clam (mercenaria mercenaria) against bacteria and the protistan pathogen QPX (quahog parasite unknown)

74. Scale and the guild functional response: Density-dependent predation varies with plot size

75. Biosorption of thorium on the external shell surface of bivalve mollusks: The role of shell surface microtopography

76. Effects of Elevated Temperature and Carbon Dioxide on the Growth and Survival of Larvae and Juveniles of Three Species of Northwest Atlantic Bivalves.

77. Suspension feeding by the Atlantic slipper limpet (Crepidula fornicata) and the northern quahog (Mercenaria mercenaria) in the presence of cultured and wild populations of the harmful brown tide alga, Aureococcus anophagefferens

78. Size-dependent pH effect on calcification in post-larval hard clam Mercenaria spp.

79. A marked gradient in δ13 values of clams Mercenaria mercenaria across a marine embayment may reflect variations in ecosystem metabolism.

80. Mercenaria mercenaria shell: Coagulation-flocculation studies on colour removal by response surface methodology and nephlometric kinetics of an industrial effluent

81. Single-molecule long-read (SMRT) transcriptome sequencing of Mercenaria mercenaria reveals a powerful anti-apoptotic system critical for air exposure endurance

82. A first genomic portrait of the Florida stone crab Menippe mercenaria: Genome size, mitochondrial chromosome, and repetitive elements

83. Molecular identification of glutathione S-transferase gene and cDNAs of two isotypes from northern quahog (Mercenaria mercenaria)

84. Comparative growth of triploid and diploid juvenile hard clams Mercenaria mercenaria notata under controlled laboratory conditions

85. Modulatory effects of hard clam (Mercenaria mercenaria) tissue extracts on the in vitro growth of its pathogen QPX

86. DEAD ZONES ENHANCE KEY FISHERIES SPECIES BY PROVIDING PREDATION REFUGE.

87. A Half Century Assessment of Hard Clam, Mercenaria mercenaria, Growth in Narragansett Bay, Rhode Island.

88. Laboratory transmission studies of QPX disease in the hard clam: Interactions between different host strains and pathogen isolates

89. SHORT-TERM DISPERSAL OF AN INTENTIONALLY- RELEASED PATCH OF LARVAL MERCENARIA SPP. IN THE INDIAN RIVER LAGOON, FLORIDA, USA.

90. Use of the juvenile clam, Mercenaria mercenaria, as a sensitive indicator of aqueous and sediment toxicity

91. Toxicity of fipronil and its enantiomers to marine and freshwater non-targets.

92. Chromosomal mapping of major ribosomal rRNA genes in the hard clam ( Mercenaria mercenaria) using fluorescence in situ hybridization.

93. Community structure of the macroinfauna inhabiting tidal flats characterized by the presence of different species of burrowing bivalves in Southern Chile.

94. Effects of elevated CO2 levels on subcellular distribution of trace metals (Cd and Cu) in marine bivalves

95. Status and Trends of Hard Clam, Mercenaria mercenaria, Populations in a Coastal Lagoon Ecosystem, Barnegat Bay–Little Egg Harbor, New Jersey

96. Triploid hard clams Mercenaria mercenaria produced by inhibiting polar body I or polar body <scp>II</scp>

97. Transgenerational exposure of North Atlantic bivalves to ocean acidification renders offspring more vulnerable to low pH and additional stressors

98. Brown tide alga, Aureococcus anophagefferens, can affect growth but not survivorship of Mercenaria mercenaria larvae

99. Feeding behavior of eastern oysters Crassostrea virginica and hard clams Mercenaria mercenaria in shallow estuaries

100. Nitrogen extraction potential of wild and cultured bivalves harvested from nearshore waters of Cape Cod, USA

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