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 " fishery, to reduce predation on commercial bivalves.

4 e essential for salinity tolerance in marine bivalves.

5 sulting in higher bioaccumulation of zinc in bivalves.

6 ful bacteria, which can accumulate in marine bivalves.

7 en biogeographic patterns of brachiopods and bivalves.

8 using recurrent massive mortalities in other bivalves.

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

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

11 ermaphrodite) and the introduced (dioecious) bivalves.

12 hat DUI may be a widespread phenomenon among bivalves.

13 f predation by the introduced crab on native bivalves.

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

15 within the ranges reported as favorable for bivalves.

16 ly important marine invertebrates, including bivalves.

17 n further facilitating their displacement by bivalves.

18 en hard-shelled foods like marine snails and bivalves.

19 entified in Tasmanian devils, dogs, and four bivalves.

20 raising the question of its origin in these bivalves.

21 plasticity remains largely unknown in marine bivalves.

22 did not coincide with declines in commercial bivalves.

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

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

25 The bivalve accumulated copper faster than the amphipod, and

26 dianthus in association with the large size bivalves Acesta excavata and Neopycnodonte zibrowii.

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

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

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

30 e extinctions in some fossil groups, such as bivalves, ammonoids, conodonts, radiolarians.

31 in enigmatic for many invertebrates, such as bivalves, an ecologically and economically important tax

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

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

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

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

36 We present quantitative size data of bivalves and brachiopods across the TOAE from oxygenated

37 Marine bivalves and brachiopods have overlapping niches such th

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

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

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

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

42 Changes in bivalves and other invertebrates were subtle.

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

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

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

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

47 esent the first finding of a TRIM element in bivalves, and among the first known in the kingdom Anima

48 Familiar molluscan groups-gastropods, bivalves, and cephalopods-each represent a diverse radia

49 nities and microplastic uptake pathways into bivalves, and discuss whether they represent a human and

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

51 fferent spatial responses of brachiopods and bivalves, and of habitat specialists and generalists, bu

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

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

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

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

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

57 These small bivalves are demonstrating ecophysiological responses to

58 Bivalves are frequently high impact IAS, but have proven

59 Bivalves are hypothesized to be key organisms in the fat

60 Marine bivalves are important components of ecosystems and expl

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

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

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

64 c example was the switch from brachiopods to bivalves as major seabed organisms following the Permian

65 325 amino acids and is 55% identical to the bivalve aspartate racemase, EC 5.1.1.13, and 41% identic

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

67 Using the shell of the marine bivalve Atrina rigida as a model system, and through a c

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

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

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

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

72 The marine bivalved Brachiopoda are abundant throughout the geologi

73 cupancy and assemblage composition of marine bivalves, brachiopods, and gastropods over one-million-y

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

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

76 xtension and net calcification rates, of the bivalve Chamelea gallina between Northern Adriatic Sea a

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

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

79 manifest across three ecologically disparate bivalve clades.

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

81 This CWC-bivalve co-occurrence represents a novel biotope for the

82 A river biota sample (bivalves) collected from the Seine with no detectable TR

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

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

85 e correlation between the mean shell size of bivalve communities and isotope-derived temperature esti

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

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

88 orrelation between E. coli concentration and bivalve density.

89 Here, using bivalve-derived environmental reconstructions, we show t

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

91 ad any detectable influence on brachiopod or bivalve diversification.

92 hiopod diversity declined through time while bivalve diversity increased.

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

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

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

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

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

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

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

100 nally appendage morphology of the Chengjiang bivalved euarthropod Ercaicunia multinodosa [25] from th

101 suggested crustacean affinities for Cambrian bivalved euarthropods [8-11], this view has fallen out o

102 cheirans, panchelicerates, 'great-appendage' bivalved euarthropods and isoxyids.

103 Bivalved euarthropods represent a conspicuous component

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

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

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

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

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

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

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

111 Our findings highlight that the freshwater bivalve fauna of Southeast Asia primarily originated wit

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

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

114 t a global assessment of freshwater mollusk (bivalves & gastropods) isotope data from 25 river basins

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

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

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

118 In bivalves, giant clams (Cardiidae: Tridacninae) gape open

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

120 ion, the number and types of MP found in the bivalve gut will depend upon the physical characteristic

121 of microplastics (MP) by suspension-feeding bivalves has been well-documented.

122 dible mollusks (cephalopods, gastropods, and bivalves) has not been reported.

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

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

125 Bivalves have been used as biomonitors for many pollutan

126 and age, suggesting that smaller and younger bivalves have greater bioaccumulation potential and are

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

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

129 ally and economically relevant edible marine bivalve, highly invasive and resilient to biotic and abi

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

131 Bivalves host archaeal methanogenic symbionts carrying o

132 rich and widely distributed family of marine bivalves hosting autotrophic bacterial endosymbionts.

133 The bivalve, however, appears to regulate the metabolically

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

135 Oysters are unusual among bivalves in that they possess chambers, often filled wit

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

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

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

139 h into microencapsulated diets could support bivalve industry expansion, and contribute towards a ste

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

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

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

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

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

145 Here, we expand the list of shallow-marine bivalves known to be exploited worldwide, with 720 explo

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

147 In marine bivalves, leukaemia-like transmissible cancers, called h

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

149 a and ~20% of family-level diversity, marine bivalves lost only ~5% of their functional diversity, in

150 crophytobenthos (MPB), a key deposit-feeding bivalve, Macomona liliana, and sediment nutrient pools.

151 organisms such as annelids, crustaceans and bivalves, mainly colonizing softgrounds in marine oxygen

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

153 cean-wild fisheries, finfish mariculture and bivalve mariculture-to estimate 'sustainable supply curv

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

155 indings provide a basic understanding of the bivalve molecular response to a mortality-inducing cilia

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

157 and Zn levels and, consequently, the risk of bivalve mollusc consumption in humans.

158 The bivalve mollusc Lucina pectinata harbors sulfide-oxidizi

159 In the bivalve mollusc Mytilus edulis shell thickening occurs f

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

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

162 Four species of bivalve molluscs (Anomalocardia brasiliana, Iphigenia br

163 Bivalve molluscs are descendants of an early-Cambrian li

164 Recently, proposals have been made to adopt bivalve molluscs as bioindicators of MP pollution.

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

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

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

168 Bivalve molluscs quality depends mainly on the water qua

169 Among these, bivalve molluscs such as mussels are filter-feeding and

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

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

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

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

174 cts, to 9 in common spider, and up to 132 in bivalve molluscs.

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

176 d the Manila clam Ruditapes philippinarum, a bivalve mollusk of high commercial interest with worldwi

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

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

179 Bivalve mollusks are consumed worldwide and can provide

180 Brachiopods and bivalve mollusks have also convergently evolved a bivalv

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

182 Bivalve mollusks of the North Atlantic, most prominently

183 in the determination of Cd(II) and Pb(II) in bivalve mollusks samples with excellent results.

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

185 Copper (Cu) isotope compositions in bivalve mollusks used in marine-monitoring networks is a

186 or the determination of Cd(II) and Pb(II) in bivalve mollusks using square wave anodic stripping volt

187 chins and burrowing fauna (polychaete worms, bivalve mollusks) increased from N to S with declining c

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

189 -ray fluorescence (WDXRF) in pressed pellets bivalve mollusks.

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

191 due to increased run-off can make intertidal bivalves more susceptible to summer heat stress.

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

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

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

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

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

197 the mollusk ontogeny, between both shells of bivalves or across the shell length.

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

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

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

201 We show that bivalve oxygen isotope data are recording multidecadal A

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

203 and contributing to global declines of some bivalve populations.

204 Several bivalves possess favourable stress tolerance and phenoty

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

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

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

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

209 ar(-1), and relies upon a supply of juvenile bivalves produced by adult broodstock in hatcheries.

210 Bivalves protect themselves from predators using both me

211 Every tonne bivalve protein produced instead of fish spares 9 ha, 67

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

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

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

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

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

217 Bivalves serve as an ideal ecological indicator; hence,

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

219 Therefore, bivalve shell shape is a critical determinant of how suc

220 st of their kind to isolate the influence of bivalve shell shape on strength and quantitatively demon

221 elieved to be related to shell strength with bivalve shell shapes converging on a select few morpholo

222 n may contribute to explain the diversity of bivalve shell structures and their vulnerability to envi

223 ve mollusks have also convergently evolved a bivalved shell that displays an apparently mundane, yet

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

225 The global bivalve shellfish industry makes up 25% of aquaculture,

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

227 hile their shells serve as mechanical armor, bivalve shells also enable evasive behaviors such as swi

228 Freshwater bivalve shells have the ability to record past environme

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

230 isotopes ((87)Sr/(86)Sr) measured in fossil bivalve shells to reconstruct patterns of fresh water in

231 Biominerals, such as nacreous bivalve shells, are important archives of environmental

232 These worms burrow into bivalve shells, creating unsightly mud blisters that are

233 Biogenic carbonates, including bivalve shells, record past environmental conditions, bu

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

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

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

237 Reductions in bivalve size and simplification of gastropod trophic str

238 o be exploited worldwide, with 720 exploited bivalve species added beyond the 81 in the United Nation

239 However, exploited bivalve species in certain regions such as the tropical

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

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

242 The edible part of 53 fish, shrimp and bivalve species presented significant differences in NO(

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

244 alysis of 204 pesticides in seven commercial bivalve species spiked at three concentrations (0.01, 0.

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

246 but the intrinsic vulnerability of exploited bivalve species to global changes is poorly known.

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

248 re ranked the most vulnerable (gastropod and bivalve species).

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

250 ral isotope profiles were analogous for both bivalve species, and an overall shift toward positive de

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

252 nce similarity to satellite DNA from several bivalve species.

253 We have identified biv-TRIM in several bivalve species: Donax trunculus, Ruditapes decussatus,

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

255 ion on and subsequent collapse of commercial bivalve stocks.

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

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

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

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

260 ng the PTME set the stage for the brachiopod-bivalve switch, with differential responses to high ocea

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

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

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

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

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

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

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

268 explore the specialized sensory function of bivalve tentacles in the common jingle shell, Anomia sim

269 ington, which currently produces more farmed bivalves than any other US state.

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

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

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

273 we investigated Cu isotope variations of two bivalves-the oyster Crassostrea gigas and the mussel Myt

274 e research on hemocytes, the immune cells of bivalves, their characterization remains elusive.

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

276 sing avoidance responses and accumulating in bivalves through their prodigious filter feeding.

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

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

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

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

281 demonstrate the potential of Cu isotopes in bivalves to infer Cu bioavailability changes related to

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

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

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

285 Uptake of compounds was independent of bivalve type.

286 of shells from 3 major molluscan classes: A bivalve Unio pictorum, a cephalopod Nautilus pompilius,

287 In bivalves, vitellogenin levels are usually estimated usin

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

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

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

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

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

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

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

295 rlooked local endemic lineages of freshwater bivalves, which may be on the brink of extinction due to

296 ly sampled fossil history of brachiopods and bivalves, while accounting for inconsistent sampling cov

297 ch is also stronger for brachiopods than for bivalves, while the relationship collapses during severe

298 Thus, bivalves will be poor bioindicators of MP pollution in t

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

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