ライフサイエンスコーパス: bivalve

1 to be problematic (e.g., nonmarine, unionoid bivalves).

2 d chitin related proteins were identified in bivalve.

3 raising the question of its origin in these bivalves.

4 ons of the M and F mtDNA genomes in unionoid bivalves.

5 n detected in bacteria, archaea, plants, and bivalves.

6 ermaphrodite) and the introduced (dioecious) bivalves.

7 hat DUI may be a widespread phenomenon among bivalves.

8 f predation by the introduced crab on native bivalves.

9 I) is commonly observed in several genera of bivalves.

10 plasticity remains largely unknown in marine bivalves.

11 did not coincide with declines in commercial bivalves.

12 " fishery, to reduce predation on commercial bivalves.

13 e essential for salinity tolerance in marine bivalves.

14 sulting in higher bioaccumulation of zinc in bivalves.

15 ful bacteria, which can accumulate in marine bivalves.

16 arance rates ranged from 1.2 to 7.4 L hr(-1) bivalve(-1).

17 h spatial changes in species compositions of bivalves, a major component of the benthic marine biota,

18 The bivalve accumulated copper faster than the amphipod, and

19 ions were reduced in the water column due to bivalve activity.

20 ay latitudinal diversity gradients of marine bivalves along the two North American coasts.

21 Bivalve, ammonite and snail shells are described by a sm

22 na deltoidalis alone) and high bioturbation (bivalve and actively burrowing amphipod, Victoriopisa au

23 ion and extinction dynamics of fossil marine bivalve and brachiopod genera from the Ordovician throug

24 phology and composition were investigated in bivalve and gastropod molluscs, brachiopods, and echinoi

25 d by nearly half in sport fish and 74-95% in bivalves and bird eggs.

26 Marine bivalves and brachiopods have overlapping niches such th

27 n the rate of species description for marine bivalves and find a distinct spatial bias in the accumul

28 ion and sampling dynamics of brachiopods and bivalves and five paleoenvironmental proxies.

29 Despite different feeding strategies, the bivalves and gastropods exhibited similar BFR water and

30 alysis of published studies on fossil marine bivalves and gastropods that span 458 million years to u

31 scade resulting from heightened predation on bivalves and suppression of their filtration control on

32 imps, benthic grazers, benthic detritivores, bivalves), and strong indirect effects expected on some

33 SLN specimens were bivalved, and half of each specimen was serially section

34 The SLNs were bivalved, and half of each specimen was submitted for ro

35 e include a diverse assemblage of ammonites, bivalves, and gastropods, abundant benthic foraminifera,

36 assess the possible mercury contamination of bivalves (Anomalocardia brasiliana, Lucina pectinata, Ca

37 abolically available fraction (MAFrate), the bivalve appears more sensitive to copper.

38 ranged from polychaetes and oligochaetes to bivalves, aquatic insects, and gastropods.

39 ios from the shells of the long-lived marine bivalve Arctica islandica (delta(18)O-shell), from the N

40 cceptable Daily Intake and Toxic Equivalent, bivalves are classified as safe for human consumption.

41 These small bivalves are demonstrating ecophysiological responses to

42 Bivalves are hypothesized to be key organisms in the fat

43 While early life-stage marine bivalves are vulnerable to ocean acidification, effects

44 ding economically and ecologically important bivalves, are affected by exposure to seismic signals.

45 eems to be decoupled from extinction risk in bivalves as a whole.

46 325 amino acids and is 55% identical to the bivalve aspartate racemase, EC 5.1.1.13, and 41% identic

47 quency distributions of northeastern Pacific bivalves at the provincial level are surprisingly invari

48 this study indicate the potential utility of bivalve augmentation to improve water quality by removin

49 digestive strategy in the wood-eating marine bivalve Bankia setacea, wherein digestive bacteria are h

50 ophotrochozoans and the origination of their bivalved bauplan preceding the biomineralization of shel

51 nifera changed gradually, and (d) changes in bivalve body size and growth rates parallel changes in t

52 The marine bivalved Brachiopoda are abundant throughout the geologi

53 While both native and invasive bivalves can reduce E. coli levels, the use of native bi

54 backwards-facing marginal serrations of the bivalved carapace may have helped to secure the food ite

55 This molluscan origin implies that all bivalve characters are lost during a radical metamorphos

56 lso present empirical analyses of the marine bivalve clade Pectinidae (scallops) during a major Plio-

57 manifest across three ecologically disparate bivalve clades.

58 thyl acetate-methanol extract of the venerid bivalve clam Paphia malabarica led to isolation of three

59 Chemosynthetic tubeworms and bivalves colonize the sea floor near the asphalt, which

60 These bivalves, commonly known as shipworms, lack a resident m

61 We observed that the filter-feeding bivalve (Corbicula fluminea) and grazing gastropod (Elim

62 in taxa of protostome invertebrates (mollusk bivalves, crustacean amphipods, branchiopods, copepods a

63 orrelation between E. coli concentration and bivalve density.

64 e that K. polythalamia is a chemoautotrophic bivalve descended from wood-feeding (xylotrophic) ancest

65 ad any detectable influence on brachiopod or bivalve diversification.

66 hiopod diversity declined through time while bivalve diversity increased.

67 unts for only 5% of the Cenozoic increase in bivalve diversity, a major component of the marine recor

68 he biodiversity and ecosystem functioning of bivalve-dominated habitats are unknown.

69 and to deleterious effects on coral reef and bivalve ecology.

70 , while also offering an alternative view of bivalve elemental proxy reconstructions.

71 amples in these studies were contaminated by bivalve embryos eaten by Xenoturbella and that Xenoturbe

72 enetic framework, extinction rates of marine bivalves estimated from the fossil record for the last a

73 The bivalved euarthropod Clypecaris serrata sp. nov., recove

74 Bivalved euarthropods represent a conspicuous component

75 ory lifestyle within the context of Cambrian bivalved euarthropods, and contributes towards the bette

76 own at present CO(2) concentrations, whereas bivalves exposed to CO(2) levels expected later this cen

77 erences in Pb and Zn bioaccumulation between bivalves exposed to laboratory and field conditions.

78 Here we show that the symbiotic bivalves extend their feet to form elongated and ramifyi

79 In contrast, elevated bivalve extinction rates causally increased brachiopod o

80 At the clade level, bivalve families shared by the two coasts followed a var

81 the only described member of the wood-boring bivalve family Teredinidae (shipworms) that burrows in m

82 this study show the importance of freshwater bivalves for improving water quality through the removal

83 erite in extinct groups (e.g., fuxianhuiids, bivalved forms, artiopodans [7, 8]) and allows new compa

84 ass extinction show no selectivity of marine bivalve genera by life position (burrowing versus expose

85 over the 500-million-year history of marine bivalves, genus duration and shell composition show few

86 onmental and ecological data recorded in the bivalve geochemistry during shell deposition remain inta

87 Bivalves grown under near preindustrial CO(2) levels dis

88 e methane efflux through bioturbation, while bivalves have a direct effect on methane release.

89 al effects of microplastics on the health of bivalves have been demonstrated elsewhere, but ecologica

90 rachiopod origination rates, suggesting that bivalves have suppressed brachiopod evolution.

91 ganisms and the effects of climate change on bivalve health, or about how this may affect the bivalve

92 es in prevalence of trematodes infesting the bivalve host Abra segmentum through multiple sea-level f

93 Bivalves host archaeal methanogenic symbionts carrying o

94 The bivalve, however, appears to regulate the metabolically

95 red coastal river containing both species of bivalves in an agricultural- and grazing-dominated area

96 trate that deep-sea isopods, gastropods, and bivalves in the North Atlantic do exhibit poleward decre

97 irginica is one of the most common estuarine bivalves in the United States' east coast and is frequen

98 Closely related bivalves (including some thyasirid species) without bact

99 We hypothesized that filtration rates of the bivalves, inorganic nitrogen cycling, primary productivi

100 iated reductions in light may shift seagrass-bivalve interactions from mutualistic to antagonistic, w

101 at posed to larvae of commercially important bivalves is currently unknown.

102 h achieves the greatest length of any extant bivalve, is the only described member of the wood-boring

103 In invertebrates, such as bivalves, it has been used in the last 10 years for the

104 totrophic symbiosis for the giant mud-boring bivalve Kuphus polythalamia This rare and enigmatic spec

105 ly important, small and short lived brooding bivalve Lissarca miliaris from Signy Island, Antarctica.

106 The bivalves maintained a 1-log removal of E. coli for the d

107 Here, we show that bivalves modify the main biomineralization mechanism dur

108 ces in shell damage and shell thickness in a bivalve mollusc (Laternula elliptica) from seven sites a

109 The bivalve mollusc Lucina pectinata harbors sulfide-oxidizi

110 In the bivalve mollusc Mytilus edulis shell thickening occurs f

111 These are the first linkage maps for a bivalve mollusc that use microsatellite DNA markers, whi

112 a, and the chiton, Katharina, but unlike the bivalve mollusc, Mytilus.

113 Bivalve molluscs are descendants of an early-Cambrian li

114 An epidemic of leukemia among bivalve molluscs is spreading along the Atlantic coast o

115 We have studied five species of bivalve molluscs of the family Thyasiridae (that is, thy

116 of the hurricanes on commercial landings of bivalve molluscs or shrimp.

117 Bivalve molluscs quality depends mainly on the water qua

118 to other invertebrate taxa (echinoderms and bivalve molluscs) but not to vertebrates, which signific

119 etic analyses placed Xenoturbella within the bivalve molluscs, and eggs and larvae resembling those o

120 us miersi, a brachiopod Liothyrella uva, two bivalve molluscs, Laternula elliptica, Aequiyoldia eight

121 In bivalve molluscs, related phenomena, marker-associated h

122 lyze changes in the metabolic profile of the bivalve mollusk Mytilus galloprovincialis upon storage a

123 Shipworms are marine wood-boring bivalve mollusks (family Teredinidae) that harbor a comm

124 ied to the analysis of smoked meat and fish, bivalve mollusks and processed cereal-based food for inf

125 r, 906 of 958 living genera and subgenera of bivalve mollusks having a fossil record occur in the Pli

126 Bivalve mollusks of the North Atlantic, most prominently

127 seabed communities are dominated by lucinid bivalve mollusks that live among the seagrass root syste

128 included sharp declines in the abundance of bivalve mollusks, the key phytoplankton consumers in thi

129 s further assumed as a proxy of Vtg in other bivalve mollusks.

130 dated dietary in vivo exposure of the marine bivalve (Mytilus galloprovincialis) to both flame retard

131 tablets, and have only once been observed in bivalve nacre.

132 hydrologic models to determine the number of bivalves needed to maintain removal of E. coli in differ

133 The mud dominant, Mulinia lateralis, is a bivalve often associated with environmental disturbances

134 For marine bivalves, one of the few groups that provide spatially e

135 there is a long-standing debate over whether bivalves outcompeted brachiopods evolutionarily, because

136 l analysis of genera and subgenera of marine bivalves over the past 11 million years supports an "out

137 n of large-scale temporal patterns in marine bivalves owing to preservability is thus apparently weak

138 hly divergent clades, robustly sister to the bivalve parasite Perkinsus.

139 and contributing to global declines of some bivalve populations.

140 tuary, and record high abundances of several bivalve predators: Bay shrimp, English sole, and Dungene

141 that such effects may depend on the dominant bivalve present.

142 produced by shell-drilling muricid snails on bivalve prey reveals that species interactions were subs

143 Octopuses faced with bivalve prey use several techniques to penetrate the she

144 ically investigated in three animal classes: bivalves, ray-finned fishes, and birds.

145 gration of fish and crustaceans that prey on bivalves, reduce their grazing pressure, and allow phyto

146 mpling study showed filtration by freshwater bivalves resulting in 1-1.5 log10 reduction of E. coli o

147 Critical changes to the bivalve's ecology seen today evidence the problem of a s

148 been shown to be a widespread phenomenon in bivalve, S. plana, populations from the southwest coast

149 vel mtDNA-encoded genes can deeply influence bivalve sex determining systems and the evolution of the

150 es of commercially and ecologically valuable bivalve shellfish (Mercenaria mercenaria and Argopecten

151 idification on two species of North Atlantic bivalve shellfish, Mercenaria mercenaria and Argopecten

152 Freshwater bivalve shells have the ability to record past environme

153 es in calcareous skeletal structures such as bivalve shells or fish otoliths.

154 The geologic ages of genera of living marine bivalves show a significant break from a smooth exponent

155 The fossil record of marine bivalves shows, in three successive late Cenozoic time s

156 lities and to develop a relationship between bivalve size and clearance rates.

157 Reductions in bivalve size and simplification of gastropod trophic str

158 pinarum) stands as the second most important bivalve species in fisheries and aquaculture.

159 nd geographic range size--to the duration of bivalve species in the early Cenozoic marine fossil reco

160 oxin-like compounds in two commercial marine bivalve species reared at different sites along the Rio

161 ect and encourage re-establishment of native bivalve species that are in decline.

162 published mitochondrial genomes of unionoid bivalve species with DUI, with an emphasis on characteri

163 ement data from two tree species, two marine bivalve species, and a marine fish species to illustrate

164 boratory batch experiments were used to show bivalve species-specific E. coli removal capabilities an

165 nce similarity to satellite DNA from several bivalve species.

166 All SLNs were bivalved, step-sectioned, and examined with routine hema

167 ion on and subsequent collapse of commercial bivalve stocks.

168 iparental inheritance (DUI), occurs in three bivalve subclasses (Pteriomorpha: Mytiloida, Palaeoheter

169 An analysis of Late Maastrichtian bivalve subgenera from the North American Coastal Plain

170 s not promote survivorship in end-Cretaceous bivalves suggests that the factors influencing survivors

171 ility and toxicity to benthic invertebrates (bivalve survival and amphipod survival and reproduction)

172 ts occurring to the copper-sensitive benthic bivalve, T. deltoidalis.

173 he need to consider the incomplete nature of bivalve taxonomy in quantitative studies of its diversit

174 of sediments disturbance: low bioturbation (bivalve Tellina deltoidalis alone) and high bioturbation

175 osit-feeding organisms (41-day growth in the bivalve Tellina deltoidalis and 11-day reproduction in t

176 the bioavailability of copper to the benthic bivalve Tellina deltoidalis in sediments of varying prop

177 vailability was investigated by exposing the bivalve Tellina deltoidalis to an identical series of me

178 d growth rate of the deposit-feeding benthic bivalve Tellina deltoidalis.

179 e rapid spread and increase of an introduced bivalve that had been rare in the system for nearly 50 y

180 the ribosomal protein (rp) S19 from a marine bivalve, the soft-shell clam (Mya arenaria), and we have

181 5) was studied for two species of freshwater bivalves, the native mussel Anodonta californiensis and

182 can reduce E. coli levels, the use of native bivalves through integration into best management practi

183 aks of fatal leukemia-like cancers of marine bivalves throughout the world have led to massive popula

184 observed distinct contamination profiles in bivalve tissues reared at each sampling site, which may

185 s study support the use of native freshwater bivalves to achieve the co-benefits of rehabilitating a

186 that this proxy should not be used in these bivalves to detect the temperature anomaly, while Ba/Ca

187 cation has been proposed, but application of bivalves to reduce bacterial levels has not been extensi

188 n of two macrofaunal groups, polychaetes and bivalves, to methane and nitrous oxide fluxes from coast

189 lve health, or about how this may affect the bivalve toxin-pathogen load.

190 Uptake of compounds was independent of bivalve type.

191 In bivalves, vitellogenin levels are usually estimated usin

192 he ecological transition from brachiopods to bivalves was more protracted and complex than their simp

193 (iii) gradual extinction of most inoceramid bivalves well before the K-T boundary, and (iv) backgrou

194 Decreases in growth of the bivalve were largely attributable to dietary exposure to

195 These estuarine bivalves were an important food resource during the earl

196 For 10 days bivalves were exposed to 3 sediment samples with differe

197 scs, and eggs and larvae resembling those of bivalves were found within specimens of Xenoturbella.

198 The burrows are formed by the foot of each bivalve, which can extend up to 30 times the length of t

199 the scallop Chlamys farreri, a semi-sessile bivalve with well-developed adductor muscle, sophisticat

200 SLNs were bivalved, with half of each specimen evaluated by histol