ライフサイエンスコーパス: gastropod

1 al cyanobacteria and from marine sponges and gastropods.

2 roduction of beads from the shells of marine gastropods.

3 ive function in Aplysia, as it does in other gastropods.

4 multaneous hermaphroditism in the Euthyneura gastropods.

5 encoded within the genomes of photosynthetic gastropods.

6 ly Solariellidae, a group of small, deep-sea gastropods.

7 igochaetes to bivalves, aquatic insects, and gastropods.

8 d, which is the principle digestive organ of gastropods.

9 and the validation of this method for TTX in gastropods.

10 content decreased with latitude in buccinid gastropods.

11 marker development were implemented in three gastropods.

12 lasticity in aquatic (marine and freshwater) gastropods, a common system for studying plasticity.

13 d, the egg coat of the non-vertebrate marine gastropod abalone (Haliotis spp.) is also known to conta

14 ean acidification did not drive increases in gastropod abundance directly, but indirectly as a functi

15 verse assemblage of ammonites, bivalves, and gastropods, abundant benthic foraminifera, and rare plan

16 tant and Pleistocene populations of a marine gastropod (Acanthinucella spirata) in conjunction with m

17 Gastropods also differed significantly in the type of TE

18 ,000 years, explains the faunal turnover for gastropods, amphibians and reptiles, whereas most mammal

19 milation of (65)Cu by two benthic grazers, a gastropod and a larval mayfly.

20 rile-containing marine natural products from gastropod and bivalve molluscs.

21 hic species were ranked the most vulnerable (gastropod and bivalve species).

22 In the present work, data from within the gastropods and a broad survey of metazoan mtDNA suggest

23 responders (mean 22%, range 7-44%), such as gastropods and pteropods, while threshold responders sho

24 Intermediate hosts (gastropods) and an accidental host, a symptomatic horse,

25 , Eurasian perch, Anolis lizards, intertidal gastropods, and a community of neotropical frogs.

26 Here, we demonstrate that deep-sea isopods, gastropods, and bivalves in the North Atlantic do exhibi

27 for detecting edible mollusks (cephalopods, gastropods, and bivalves) has not been reported.

28 ve life history characteristics of bivalves, gastropods, and bryozoans.

29 of herbivores (including amphipods, isopods, gastropods, and sea urchins) that graze on giant kelp (M

30 .), stalked barnacles, limpets, peltospiroid gastropods, anemones, and a predatory sea star.

31 euronal genes between this relatively simple gastropod Aplysia (20,000 neurons) and Octopus (500 mill

32 ns that have been examined are in one marine gastropod (Aplysia, a sea hare), in jellyfish and in the

33 Shells of hydrothermal vent gastropods are often covered by inorganic coatings whose

34 formation of male characteristics in female gastropods, because of the activation of retinoid X rece

35 role of these neurons in the organization of gastropod behavior.

36 thin the calcitic opercula of the freshwater gastropod Bithynia, to provide the most comprehensive da

37 nto two sister clades, Conchifera (including gastropods, bivalves and cephalopods) and Aculifera(9),

38 Familiar molluscan groups-gastropods, bivalves, and cephalopods-each represent a d

39 " an assemblage of higher taxa that includes gastropods, bivalves, and echinoids, has been a key comp

40 nto the continental slope, including corals, gastropods, bivalves, shocked quartz grains, an andesiti

41 le suffer from a range of diseases caused by gastropod-borne helminths, predominantly flatworms and r

42 presence of HA in the chemosensory organs of gastropods but is different than the sensory systems in

43 xatilis gene order and that of the pulmonate gastropod Cepaea nemoralis.

44 Cone snails are predatory marine gastropods characterized by a sophisticated venom appara

45 er stage in the evolution and adaptations of gastropod chemosensory biology, whereas among the opisth

46 sing distance from vents is dominated by the gastropods Chrysomallon squamiferum and Gigantopelta aeg

47 found pyrite only in coatings of the modern gastropods collected near high-temperature vent sites, i

48 been compared with nemerteans, polychaetes, gastropods, conodonts, and the stem arthropod Opabinia.

49 Previously, the gastropod Conus was the only known invertebrate with a d

50 The littorinimorph gastropod Crepidula fornicata shows a spiralian cleavage

51 eruption, most notably the appearance of the gastropod Ctenopelta porifera, an immigrant from possibl

52 n acidification effects on the reef-building gastropod Dendropoma petraeum.

53 The Recent gastropod distribution is mainly a geologically young pa

54 Based on Miocene to Recent gastropod distributions, we show that the existence and

55 n 20,000 species and account for most of the gastropod diversity.

56 of THli neurons indicates that, as in other gastropods, dopamine functions as a sensory neurotransmi

57 stinct taxa (a crustacean, an annelid, and a gastropod) during pulse exposures to four chemicals in t

58 for fatty acid and metal content resulted in gastropods (e.g. Bursa ventricosa) as being the least be

59 ing bivalve (Corbicula fluminea) and grazing gastropod (Elimia proxima), collected downstream from a

60 ungus Rhizophagus irregularis and the marine gastropod Elysia marginata, suggesting that widespread h

61 Here we show that the specialist gastropod Elysia tuca hunts its seaweed prey, Halimeda i

62 hickness decreased with latitude in buccinid gastropods (excepting the Australian temperate buccinid)

63 fferent feeding strategies, the bivalves and gastropods exhibited similar BFR water and sediment accu

64 systematic revision of the largest deep-sea gastropod family (Turridae) has provided a unique databa

65 Gastropod fossils from ancient vent sites are preserved

66 ertebrate fossils represented by bivalve and gastropod fossils with predictions from an ecophysiologi

67 ification rates of North American freshwater gastropods from the Late Triassic to the Pleistocene and

68 deformities and repair marks on bivalves and gastropods from the Triassic Hindeodus parvus Conodont Z

69 is of amino acid variation for all available gastropod genomes including the new turbinid mtgenome pr

70 r sequence data for 70 species of the marine gastropod genus Conus and used it to map the evolution o

71 Predatory snails in the marine gastropod genus Conus stun prey by injecting a complex m

72 cloned, and sequenced from 18 members of the gastropod genus Littorina.

73 nal-scale niche partitioning among symbiotic gastropods (genus Alviniconcha) in the Lau Basin.

74 dividuals m(-2)), followed by a peltospiroid gastropod (>1,500 individuals m(-2)), eolepadid barnacle

75 orum, a cephalopod Nautilus pompilius, and a gastropod Haliotis asinina We demonstrate that the fabri

76 ross two seasons using embryos of the marine gastropod Haminoea vesicula.

77 The fossil record of marine gastropods has been used as evidence to support the oper

78 In the gastropod Ilyanassa obsoleta, early development is media

79 In the embryos of the gastropod Ilyanassa obsoleta, the development of several

80 In embryos of the gastropod Ilyanassa obsoleta, the first-quartet micromer

81 paraensei, providing a direct link between a gastropod immune molecule and resistance to trematodes.

82 ecessary for successful preservation of vent gastropods in the fossil record.

83 Gastropods in the subfamily Physinae have been especiall

84 is known of the fundamental biology of their gastropod intermediate hosts, or of the interactions occ

85 ew strategies for disease control focused on gastropod intermediate hosts.

86 assessment of freshwater mollusk (bivalves & gastropods) isotope data from 25 river basins that have

87 Similarly, up to 87% of gastropod larvae metamorphosed in response to burnt oil

88 vel substrates for 5alpha-reductase exist in gastropods, lending support to the contention that mollu

89 individual behavioural responses in a marine gastropod, Littoraria irrorata.

90 e that the sensitivity of populations of the gastropod Littorina littorea to future OA is shaped by r

91 rom the mitochondrial DNA of the prosobranch gastropod Littorina saxatilis has been sequenced and sho

92 anges of 3,916 species of marine prosobranch gastropods living on the shelves of the western Atlantic

93 In the basal gastropod Lottia, the apical region of the oocyte is nor

94 enous control of hemocyte development in any gastropod model.

95 e of a mitochondrial genome of the pulmonate gastropod mollusc Cepaea nemoralis has been determined.

96 e first and second cleavage divisions in the gastropod mollusc Crepidula fornicata.

97 ysomallon squamiferum, a recently discovered gastropod mollusc from the Kairei Indian hydrothermal ve

98 Eggs and egg masses of the freshwater gastropod mollusc Lymnaea provide a microenvironment for

99 Laternula elliptica, Aequiyoldia eightsii, a gastropod mollusc Marseniopsis mollis and an echinoderm

100 rization of an endogenous growth factor of a gastropod mollusc, and provides direct evidence of gain

101 by the abalone, Haliotis rufescens, a marine gastropod mollusc.

102 Limpet, Patella vulgata is an underutilized gastropod mollusc.

103 lothuria forskali Chiaje (sea cucumber), the gastropod molluscs Aplysia fasciata Poiret and Aplysia p

104 example of endocrine disruption occurred in gastropod molluscs which led to the banning of tributylt

105 vertebrate nervous systems, such as those of gastropod molluscs, allows behaviors to be dissected at

106 composition were investigated in bivalve and gastropod molluscs, brachiopods, and echinoids.

107 rsal abilities: coastal fishes, echinoderms, gastropod molluscs, brachyuran decapod crustaceans, poly

108 otransmitter in the nervous systems of adult gastropod molluses.

109 sicles obtained from the atrial gland of the gastropod mollusk Aplysia californica were chemically an

110 The gastropod mollusk Aplysia is an important model for cell

111 ne mechanisms that control egg laying in the gastropod mollusk Aplysia, relatively little is known ab

112 l cells in the central nervous system of the gastropod mollusk Lymnaea stagnalis produces a soluble p

113 ng nucleotide diversities in three genera of gastropod mollusks (Littorina, Crepidula, and Hydrobia),

114 serotonergic cerebral giant cells (CGCs) of gastropod mollusks have important extrinsic modulatory a

115 Cone snails are gastropod mollusks of the genus Conus that live in tropi

116 e center of origin for numerous taxa such as gastropod mollusks.

117 tory FMRFa-gated sodium channel (FaNaC) from gastropod mollusks.

118 due of amorphous material surrounding mature gastropod nacre tablets, and have only once been observe

119 lagos in two amphidromous species of Neritid gastropod (Neritina canalis and Neripteron dilatatus).

120 ic plasticity versus evolutionary changes in gastropod nervous systems.

121 tibility to predation of an important marine gastropod (Nucella lapillus).

122 Abalone, Haliotis spp., are marine gastropods of high economic value extracted worldwide fo

123 osition of marine bivalves, brachiopods, and gastropods over one-million-year time steps during the E

124 that of Ischnochiton rissoi, as well as the gastropod, Patella vulgata.

125 eries of AMS radiocarbon dates on the marine gastropod Phorcus turbinatus associated with modern huma

126 marine invertebrates, the Lusitanian trochid gastropods Phorcus lineatus and Gibbula umbilicalis, bas

127 ride elicited the same phenotype in a second gastropod, Physella acuta.

128 es (28 groups including barnacles, decapods, gastropods, polychaetes, etc.) were more universally pre

129 had strong, negative relationships with two gastropod predators-the Caribbean spiny lobster (Panulir

130 For instance, freshwater annelids and gastropods responded markedly to imidacloprid, while mar

131 acidification increases energetic demands on gastropods resulting in altered energy allocation, i.e.

132 of 5HTli neurons suggests that, as in other gastropods, serotonin regulates the locomotion, reproduc

133 Here, I report that the gastropod shell has another function and has been co-opt

134 Gastropod shell morphologies are famously diverse but ge

135 The gastropod shell shows a vast array of different sizes, s

136 edge epithelium contribute to shell shape in gastropod shells and identify cellular mechanisms that m

137 en isotope values with strong seasonality in gastropod shells and mammal teeth from Myanmar, and by a

138 Perforated marine gastropod shells at the western Asian site of Skhul and

139 , obtained from the growth front of nacre in gastropod shells from red abalone (Haliotis rufescens),

140 algal biomass was significantly reduced and gastropod shells were dissolving due to periods of carbo

141 rrestrial organisms (for example, spiralling gastropod shells).

142 ion feed on prey trapped inside large marine gastropod shells.

143 However, the nature of MYP in the freshwater gastropod snail Biomphalaria glabrata remains elusive.

144 Embryos of the gastropod snail Crepidula fornicata exhibit a typical sp

145 wn in the most obviously chiral animals, the gastropod snails.

146 ness gradient of eastern Pacific rocky shore gastropods (spanning c.

147 data of Melanoides tuberculata, a freshwater gastropod species found in the same geoarchaeological se

148 ch possess two-domain (bidominial) MTs, some gastropod species have evolved Cd(2+)-selective multidom

149 The average size of rocky intertidal gastropod species in MSA and later coastal middens allow

150 c DNA from B. glabrata, and from two related gastropod species, Biomphalaria pfeifferi and Helisoma t

151 onstitutive defenses have evolved in several gastropod species.

152 Within marine gastropods, species with planktonic development had simi

153 nvestigated the mineral coatings of six vent gastropod specimens (one each of the species Lepetodrilu

154 f-recruitment in a broadcast-spawning marine gastropod that exists as a single meta-population throug

155 The gastropods that form these reefs brood encapsulated larv

156 Cone snails are venomous marine gastropods that hydraulically propel a hollow, chitinous

157 lished studies on fossil marine bivalves and gastropods that span 458 million years to uncover how gl

158 te in gammarids, daphnids, drosophilids, and gastropods that the assay validated in Vg-sequenced spec

159 keyhole limpet and a more distantly related gastropod, the Chilean abalone.

160 ocomotion in an unsegmented, ciliolocomoting gastropod, the sea slug Pleurobranchaea californica, whi

161 genetic structure in the native area of the gastropod Tritia neritea, using Bayesian skyline plots (

162 and its specialist predator, the nudibranch gastropod Tritonia striata, from potential predators.

163 lower activity in the ganglia of the related gastropod Tritonia.

164 A gastropod, Trochus erithreus, and a muscle tissue of fis

165 ctions in bivalve size and simplification of gastropod trophic structure further implicate increasing

166 the CNS of Sepia is a similarity shared with gastropods, vertebrates, and arthropods.

167 elta47 of aragonite shells of the freshwater gastropod Viviparus lentus from the Solent Group, Hampsh

168 macrophyte Vallisneria spiralis (L.) or the gastropod Viviparus viviparus (Linnaeus, 1758)) treatmen

169 The increased abundance of some alien gastropods was positively related to taxonomic diversity

170 from the coast as the lower Midwest, marine gastropods were imported in raw form and converted into

171 In gastropods, where a twist is intrinsic to the body, the

172 between parasitic nematodes and terrestrial gastropods which have co-evolved for 90-130 MY.

173 In a gastropod with a different coiling geometry, Planorbella

174 n Lottia is much later than it is in derived gastropods with a precocious specification of the D quad

175 ean acidification on a calcifying herbivore (gastropod) within the natural complexity of an ecologica

176 othalonil increased mortality of amphibians, gastropods, zooplankton, algae and a macrophyte (reducin

177 nvestigates the potential of the terrestrial gastropod Zootecus insularis collected from geoarchaeolo