ライフサイエンスコーパス: crustacean

1 example, a gill) on the leg of an ancestral crustacean.

2 h a host, in this case a species of ostracod crustacean.

3 or milk and egg and 10 mug g(-1) for soy and crustaceans.

4 uch as male sex determination in branchiopod crustaceans.

5 ther mechanosensory functions in insects and crustaceans.

6 lobula plate was also found in malacostracan crustaceans.

7 ross-reactivity testing on a wide variety of crustaceans.

8 is the chitinous exoskeletons of microscopic crustaceans.

9 iological processes pertaining to molting in crustaceans.

10 sIgE titres in response to both molluscs and crustaceans.

11 ra) are the most successful group of decapod crustaceans.

12 hts into defining characteristics of decapod crustaceans.

13 going process in the brains of adult decapod crustaceans.

14 ers) is not a proxy for demasculinization in crustaceans.

15 antis shrimps, which are basal malacostracan crustaceans.

16 r and respiratory organs of both insects and crustaceans.

17 neric avoidance response to large, predatory crustaceans.

18 atopods, a group of highly aggressive marine crustaceans.

19 pendent regulatory mechanisms in insects and crustaceans.

20 the olfactory deutocerebrum of adult decapod crustaceans.

21 il Hanstrom to claim homology in insects and crustaceans.

22 tial hazards to organisms such as planktonic crustaceans.

23 of living bees, dragonflies and many diurnal crustaceans.

24 -inducible paralogs independently from other crustaceans.

25 conductance regulation by neuromodulators in crustaceans.

26 de Pancrustacea, which comprises insects and crustaceans.

27 gut in invertebrates, including insects and crustaceans.

28 ingredient than from those containing other crustaceans.

29 s aspects of reproduction and development in crustaceans.

30 - 10.5 MPs/g in mollusks, 0.1 - 8.6 MPs/g in crustaceans, 0 - 2.9 MPs/g in fish, and 1 MP/g in echino

31 Thirty-one patients with anaphylaxis to crustaceans (14 with mollusc allergy and 17 with mollusc

32 in the ventral neuroectoderm of insects and crustaceans accompanied by changes in the morphogenetic

33 Although early studies suggested crustacean affinities for Cambrian bivalved euarthropods

34 assay was developed for detection of crab, a crustacean allergen, in food products.

35 these findings improve the understanding of crustacean allergens and contribute to the clinical diag

36 sitization patterns of Taiwanese patients to crustacean allergens remain unclear.

37 Several proteins are recognized as crustacean allergens, and tropomyosin is known to be the

38 dy investigated the sensitization pattern of crustacean-allergic patients according to tolerance to m

39 and contribute to the clinical diagnosis of crustacean allergies.

40 protostome invertebrates (mollusk bivalves, crustacean amphipods, branchiopods, copepods and isopods

41 Among patients with crustacean anaphylaxis, patients with mollusc allergy an

42 ction of shellfish-derived tropomyosin in 11 crustacean and 7 mollusc species, and to study the impac

43 e microarray for Daphnia magna, a freshwater crustacean and common indicator species for toxicity, to

44 ontesting views regarding whether centers in crustacean and insect brains that occupy corresponding l

45 uroblast selection have been modified during crustacean and insect evolution and if the segregation o

46 Crustacean and mollusk allergies have different manifest

47 LOX6 were more attractive to a detritivorous crustacean and more sensitive to drought, indicating tha

48 ies analyzed was greater in Egypt, with nine crustacean and two cephalopod species found compared wit

49 ces of five ocean-produced demersal fish and crustaceans and 2.5-fold increase of summer chlorophyll-

50 isms, including salamanders, frogs, insects, crustaceans and arachnids.

51 ts the growing number of studies in insects, crustaceans and chelicerates, and is important for the c

52 Malacostracan crustaceans and dicondylic insects possess large second-

53 ging from bacteria to algae, yeasts, plants, crustaceans and fish such as salmon.

54 +)-K(+)-ATPase in white skeletal muscle from crustaceans and fishes.

55 opoda, particularly among Tetraconata (i.e., crustaceans and hexapods), and indicate that copepods oc

56 d body, provides the ground pattern for both crustaceans and hexapods.

57 Crustaceans and insects share many similarities of brain

58 shared organization of memory centers across crustaceans and insects.

59 lies and more complete retention within some crustaceans and insects.

60 group that branches basally from myriapods, crustaceans and insects.

61 activity, making specific differentiation of crustaceans and molluscs for food labelling very difficu

62 ives: to develop a global database for fish, crustaceans and molluscs with raw, cooked and processed

63 e developed to differentiate tropomyosins in crustaceans and molluscs.

64 waters worldwide is efficiently degraded by crustaceans and molluscs.

65 s) that demonstrate recurring consumption of crustaceans and rotted wood by large Late Cretaceous din

66 ltaneously detect the presence of milk, egg, crustaceans and soy.

67 smaller individuals feeding mainly on small crustaceans and teleost fish, whereas the diet of larger

68 Sunfish fed mainly on crustaceans and teleosts, with cnidarians comprising onl

69 pomyosin is known to be the main allergen in crustaceans and the objective of this study was to inves

70 this, we isolated an identifiable neuron in crustaceans and then either kept this neuron silent or u

71 lopod species found compared with only three crustaceans and three cephalopods in Spain.

72 th functional similarities to certain modern crustaceans and trace these structures through the early

73 ough in several other insect species and one crustacean, and several readthrough candidates in nemato

74 The median annual risk quotients for fish, crustaceans, and algae were 19.6, 5.2, and 4.5, respecti

75 d to monitor the spoilage of raw meat, fish, crustaceans, and preserved meat.

76 hich is used as an energy buffer in insects, crustaceans, and some unicellular organisms.

77 perceived by insects, spiders, cephalopods, crustaceans, and some vertebrates.

78 s (Stomatopoda) possess in common with other crustaceans, and with Hexapoda, specific neuroanatomical

79 igh specificity for crab over other types of crustaceans, and yielded much higher signals from commer

80 tantly related animal lineages from insects, crustaceans, annelid worms, and fishes, we find more spe

81 Stomatopod crustaceans appear to have gone one step further in this

82 within the exocuticle of an impact-resistant crustacean appendage.

83 Here we describe diverse crustacean appendages of Middle and Late Cambrian age fr

84 provides valuable information for enhancing crustacean aquaculture.

85 Viral diseases of crustaceans are increasingly recognised as challenges to

86 Crustaceans are key components of marine ecosystems whic

87 Although adult crustaceans are often resilient to reduced seawater pH,

88 Branchiopod crustaceans are represented by fairy, tadpole, and clam

89 Ostracod crustaceans are the most abundant fossil arthropods and

90 Crustaceans are widely distributed and inhabit very diff

91 nsects and the hemiellipsoid bodies (HBs) of crustaceans] are homologous structures.

92 iverse group of organisms, are nested within crustaceans, arguably the most abundant group of marine

93 ers of feminization should not be applied to crustaceans, as orthologous genes are not induced in fem

94 Its brain is modified from the crustacean brain ground pattern by featuring relatively

95 Descriptions of crustacean brains have focused mainly on three highly de

96 We discuss the diversity of crustacean bunyaviruses and provide an overview of how t

97 ing species (epifaunal echinoderms, infaunal crustaceans) by two to four-fold in areas fished twice a

98 ana, Lucina pectinata, Callinectes sapidus), crustacean (C. sapidus) and fish (Bagre marinus and Diap

99 A small transparent crustacean called Parhyale hawaiensis has become a power

100 e showing hexapods closely related to simple crustaceans called remipedes.

101 f three different neuron types from the same crustacean (Cancer borealis) motor circuit and involved

102 Motor neurons of the crustacean cardiac ganglion generate virtually identical

103 Previous findings suggest that crustacean cardioactive peptide (CCAP) activates the ecd

104 in ecdysis, including Eclosion hormone (EH), Crustacean cardioactive peptide (CCAP) and Bursicon.

105 whereas ecdysis-triggering hormone (ETH) and crustacean cardioactive peptide (CCAP) evolved in the bi

106 Crustacean cardioactive peptide (CCAP) neurons and the p

107 transcript with high sequence similarity to crustacean cardioactive peptide (CCAP) receptors in inse

108 Crustacean cardioactive peptide (CCAP)-expressing neuron

109 We discovered that 2 crustacean cardioactive peptide (CCAP)-expressing neuron

110 se of peptidergic neurons that produce CCAP (crustacean cardioactive peptide), which are key targets

111 short neuropeptides F, extended FMRFamides], crustacean cardioactive peptide, tachykinin-related pept

112 ed by strict morphological criteria although crustacean centers called hemiellipsoid bodies, which se

113 For example, neurons in crustacean central pattern generators generate similar f

114 Life-table response experiments with the crustacean Ceriodaphnia dubia exposed to single and tern

115 l distribution profile within the freshwater crustacean Ceriodaphnia dubia was constructed at a spati

116 Here, we show that a major part of the crustacean class Malacostraca (which includes lobsters,

117 se findings suggest that some "non-analogue" crustacean communities co-existed with the "Mammoth faun

118 These new data on a representative of crustaceans complete the arthropod data set on Notch sig

119 ogenetic proximity of insects and stomatopod crustaceans conflicts with genomic evidence showing hexa

120 Cancer pagurus) is one of the most important crustaceans consumed in Southern European countries, eit

121 We compare physiological responses of the crustacean copepod Calanus pacificus and pelagic pteropo

122 Thick fragments of laminar crustacean cuticle are scattered within the coprolite co

123 pranolol, diazepam, and carbamazepine on the crustacean Daphnia magna at environmentally relevant con

124 Accumulation of storage lipids in the crustacean Daphnia magna can be altered by a number of e

125 FPW toxicity to the model freshwater crustacean Daphnia magna was characterized utilizing acu

126 alpha-cypermethrin, on the mortality of the crustacean Daphnia magna.

127 formulations was assessed on the freshwater crustacean Daphnia magna.

128 zed AgNPs (citrate-AgNPs) against a keystone crustacean Daphnia magna.

129 Here we describe a gut parasite of the crustacean Daphnia that despite having remarkable morpho

130 Additionally, crustaceans (Daphnia, Caligus, and Lepeophtheirus) and s

131 rstand the precise roles of Hox genes during crustacean development.

132 fossils indicate profound secular changes in crustacean ecology in terms of body size and environment

133 in arthropods and analyse segmentation in a crustacean embryo.

134 We demonstrate that the intertidal crustacean Eurydice pulchra (Leach) exhibits robust tida

135 t of hexapods and that equivalent centers in crustaceans evolved independently.

136 e, other arthropods such as chelicerates and crustaceans express two dsx genes, both of which are sho

137 s in the photophore similar to those seen in crustacean eyes, providing further evidence that photoph

138 s (mantis shrimps) are basal eumalacostracan crustaceans famous for their elaborate visual system, th

139 hat the "base set" of data (EC50s for algae, crustaceans, fish) is available.

140 dence was available on four phyla: mollusks, crustaceans, fish, and echinodermata.

141 waters and a wide range of hosts, including crustaceans, fish, mollusks, and humans.

142 er of the Malacostraca clade, which includes crustacean food crop species.

143 Despite the importance of crustaceans for monitoring vulnerable aquatic habitats,

144 is demonstrated on well-preserved fishes and crustaceans from the Late Cretaceous (ca. 95 million yea

145 The present study with the crustacean Gammarus fossarum, a sentinel species in fres

146 We test this hypothesis with the freshwater crustacean Gammarus pulex and four toxicants that act on

147 affecting fitness have also been reported in crustaceans (Gammarus fossarum) [3].

148 cted to revisit the lethal effects of UVB on crustaceans, generate new experimental evidence to fill

149 one paralog lost in mammals, and a number of crustacean genomes (like Caligus rogercresseyi and Lepeo

150 leen whales, which prey on animals (fish and crustaceans), harbor unique gut microbiomes with surpris

151 In contrast to herbivorous insects, most crustaceans have very broad diets, and the increased ric

152 rotein kinase A, specifically label both the crustacean hemiellipsoid bodies and insect mushroom bodi

153 ple correspondences indicate homology of the crustacean hemiellipsoid body and insect mushroom body a

154 the impacts of the invasive freshwater mysid crustacean Hemimysis anomala with a native counterpart M

155 f euarthropods (extant arachnids, myriapods, crustaceans, hexapods) has played a major role in unders

156 ing Crustacean Virus 9' from an unidentified crustacean host.

157 iruses may affect the health and survival of crustacean hosts, including those inhabiting niches outs

158 xopolysaccharide production and virulence to crustacean hosts.

159 rthropod lineage that led to the insects and crustaceans, however, a new allele arose in which RPR is

160 y a major role in reproductive physiology in crustaceans; however their role in reproductive developm

161 Furthermore, the crustacean hyperglycemia hormones (CHHs, 8.5 kDa) were i

162 idence for the recruitment of genes from the Crustacean Hyperglycemic Hormone (CHH) and arthropod Ion

163 to be regulated largely by ecdysteroids and crustacean hyperglycemic hormone (CHH) neuropeptide fami

164 o follow the same sequence as in insects and crustaceans in both species.

165 Flightin was also found in 14 species of crustaceans in orders Anostraca (water flea), Cladocera

166 eages of marine, freshwater, and terrestrial crustaceans (including 64 families and 185 genera) have

167 esses characters uniquely shared with extant crustaceans, including differentiated tritocerebral ante

168 Phylogenomics of crustacean-infecting bunyaviruses place them across mult

169 ed that this virus branches before the other crustacean-infecting nudiviruses and shares low levels o

170 Comparison of gene synteny from known crustacean-infecting nudiviruses reveals conservation be

171 genes (sharing 57 gene homologues with other crustacean-infecting nudiviruses) but appears to lack th

172 We conclude that crustaceans, insects, and other groups of arthropods sha

173 Although poorly understood, crustacean intersexuality is associated with contaminati

174 ion system of arthropods such as insects and crustaceans is based on the compound-eye architecture, c

175 The earliest radiation of crustaceans is largely cryptic in the fossil record, but

176 The early history of crustaceans is obscured by strong biases in fossil prese

177 pelagic species (squid and certain fish and crustaceans) is poorly understood [1].

178 Stomatopods are marine crustaceans known to use colour signals during courtship

179 In crustaceans lacking eyestalks, where the entire brain is

180 , distinguishing species that mainly feed on crustaceans; large fish and squid; a mixture of crustace

181 es in the lateral protocerebrum of a decapod crustacean, Lebbeus groenlandicus, a species belonging t

182 This leads to an alignment of insect and crustacean legs that suggests that two leg segments that

183 Crustaceans, like most mineralized invertebrates, adopte

184 ymenoptera; the recognition of hexapods as a crustacean lineage within Pancrustacea; and the elucidat

185 lution in Hoplocarida and are unique to this crustacean lineage.

186 waterborne cadmium by the freshwater decapod crustacean Macrobrachium australiense.

187 tals from solution by the freshwater decapod crustacean Macrobrachium australiense.

188 the nervous system in insects and in higher crustaceans (malacostracans); in the remaining euarthrop

189 , mosses, leaves, bark, trunk wood, insects, crustaceans, mammal and human tissues; their association

190 te insect-like mushroom bodies in stomatopod crustaceans (mantis shrimps).

191 iptomes for 19 species of terrestrial isopod crustaceans, many of which are infected by Wolbachia bac

192 l size of a copepod, these mesozooplanktonic crustaceans may serve as hotspots of N2 fixation, at 12.

193 layered organization and components of this crustacean medulla and the medullae of insects.

194 lts show that individuals allergic to HDM or crustaceans might be at risk when consuming mealworms, e

195 This study contributes 21 crustacean mitogenomes from several under-represented de

196 ected examples of neuropeptide modulation in crustaceans, mollusks, insects, and nematodes, with a pa

197 Ca(2+) stimulates ecdysteroid production by crustacean molting glands (Y-organs).

198 Crustacean molting is known to be regulated largely by e

199 ast common ancestor of Mandibulata (insects, crustaceans, myriapods).

200 nly one family of mantis shrimp (stomatopod) crustaceans (Nannosquillidae), each crystalline structur

201 nambiguously identified neurons from 2 small crustacean neuronal networks: The stomatogastric and car

202 In the crustacean, Notch controlled mechanisms of neuroblast re

203 The diet of decayed wood and crustaceans offered a substantial supply of plant polysa

204 this protein could be detected in commercial crustacean oils from Antarctic krill (Euphausia superba)

205 Nevertheless, the neural composition of crustacean optic neuropils deeper than the lamina is mos

206 MALDI-MS/MS analyses revealed that IgE from crustaceans or House dust mite (HDM) allergic patients s

207 ugal neuron hitherto not identified in other crustaceans or insects that probably feeds back informat

208 xample, in urodeles, lizards, arthropods and crustaceans) or permanently lost (such as in mammals).

209 Stomatopod crustaceans, or mantis shrimp, are renowned for their co

210 idence that the single representative of the crustacean order Amphionidacea is a decapod shrimp and n

211 nse of six Antarctic marine invertebrates: a crustacean Paraceradocus miersi, a brachiopod Liothyrell

212 nships of arachnid orders and the details of crustacean paraphyly with respect to Hexapoda remain the

213 knockout of five leg patterning genes in the crustacean Parhyale hawaiensis and compare these with th

214 The amphipod crustacean Parhyale hawaiensis is a blossoming model sys

215 egeneration at single-cell resolution in the crustacean Parhyale hawaiensis.

216 ggregations during early gastrulation in the crustacean Parhyale hawaiensis.

217 rovilli of the main rhabdom show the typical crustacean pattern of alternating bands of horizontally

218 erms, gastropod molluscs, brachyuran decapod crustaceans, polychaete annelids, and macroalgae.

219 ding experiments with two herbivorous isopod crustaceans, Porcellio scaber (woodlouse) and Armadillid

220 Crustaceans possess a diverse array of specialized limbs

221 Stomatopod crustaceans possess some of the most complex animal visu

222 ning evidence to support the hypothesis that crustaceans possess structures equivalent to the mushroo

223 No previously described crustacean possesses a mushroom body as defined by stric

224 tive cryoprotectant might be employed during crustacean processing.

225 Two crustaceans producing sharply contrasting bioturbation--

226 including mollusks, nematodes, insects, and crustaceans (referred to here as pigment-dispersing horm

227 e exact position of myriapods or the closest crustacean relatives of hexapods.

228 Preserving quality of crustaceans requires efficient modified atmosphere packa

229 e validation on both lean and fatty fish and crustaceans, results from proficiency tests and routine

230 However, the direct conversion of crustacean shell waste-derived chitin into a wide spectr

231 h and is accessible to humans in the form of crustacean shell waste.

232 abundant polysaccharide in nature, found in crustacean shells, insect exoskeletons and fungal cell w

233 ing toughness by using strategies taken from crustacean shells.

234 ostraca: Peracarida), a lineage of marsupial crustaceans, show an interesting variety of brooding str

235 Among crustaceans, shrimps are the most predominant cause of a

236 staceans; large fish and squid; a mixture of crustaceans, small fish and squid; or carrion.

237 d to denote sensory association neuropils in crustacean species and relates how those terms were depl

238 oss-reactive tropomyosin was detected in all crustacean species, with partial detection in molluscs:

239 generated morphological differences between crustacean species.

240 omenclature for structures in the stomatopod crustacean Squilla mantis that he claimed correspond to

241 ly-conserved physiological properties in the crustacean stomatogastric ganglion (STG) of Cancer borea

242 wed that the Gastric Mill (GM) neuron in the crustacean stomatogastric ganglion (STG) operates like a

243 ions giving rise to rhythmic activity in the crustacean stomatogastric ganglion, and use these result

244 tes activity in the unmyelinated axon of the crustacean stomatogastric pyloric dilator neuron.

245 Like many crustaceans, stomatopods undergo indirect development, p

246 For millimeter-scale aquatic crustaceans such as copepods, ensuring reproductive succ

247 The most landed species are crustaceans such as rose shrimp and Norway lobster, alth

248 ed hemiellipsoid bodies typifying reptantian crustaceans, such as lobsters and crayfish, represent th

249 ill, prawns, lobsters, and other long-tailed crustaceans swim by rhythmically moving limbs called swi

250 Thus, the crustacean swimmeret system serves as a concrete example

251 Given the high metabolic cost of crustacean swimming, our results suggest that natural se

252 of biologically relevant Reynolds numbers in crustacean swimming.

253 today, but additionally by some branchiopod crustacean taxa currently absent or unusual in the regio

254 e, no consensus has been reached as to which crustacean taxon is the closest relative of hexapods.

255 More than any other crustacean taxon, mantis shrimps display sophisticated b

256 g gene network (preWGN) operates both in the crustacean terga and in the proximal leg segments, sugge

257 e chelicerate Limulus polyphemus, all isopod crustaceans tested, and the cave shrimp Troglocaris anop

258 d in the last common ancestor of insects and crustaceans (Tetraconata).

259 inearly polarizing reflector in a stomatopod crustacean that consists of 6-8 layers of hollow, ovoid

260 rse and ecologically crucial group of minute crustaceans that are relatively neglected in terms of st

261 entified in mantis shrimps, basal hoplocarid crustaceans that are sister to Eumalacostraca, the most

262 Calanoid copepods are small crustaceans that constitute a major element of aquatic e

263 e, we show that copepods, abundant migrating crustaceans that graze on phytoplankton, as well as othe

264 perating through the immigration of fish and crustaceans that prey on bivalves, reduce their grazing

265 the dinosaurian defecators consumed sizeable crustaceans that sheltered in rotting logs.

266 first time the role of Notch signalling in a crustacean, the branchiopod Daphnia magna, and show that

267 s study, we show that an abundant intertidal crustacean, the copepod Tigriopus californicus, has lost

268 otopic organization of the lobula plate in a crustacean, the crab Neohelice granulata using a variety

269 ion trends within a diverse group of aquatic crustaceans, the Anomura.

270 Both in insects and malacostracan crustaceans, the bHLH-PAS transcription factor single-mi

271 adult-born neurons in the brains of decapod crustaceans, the deutocerebral proliferative system (DPS

272 Shellfish are classified into mollusks and crustaceans, the latter belonging to the class of arthro

273 Few species of reptant decapod crustaceans thrive in the cold-stenothermal waters of th

274 To increase the relevance of crustaceans to environmental toxicologists, we comprehen

275 standing, will greatly facilitate the use of crustaceans to monitor aquatic habitats.

276 oss evolution, from ancient arthropods, like crustaceans, to humans.

277 ng data from the Vessel Monitoring System of crustacean trawlers along the Portuguese margin, we have

278 possess only one, nematodes two, and decapod crustaceans up to three, but their phylogenetic relation

279 ll (Euphausia superba) are swarming, oceanic crustaceans, up to two inches long, and best known as pr

280 New research shows that some midwater crustaceans use antireflection coatings to enhance their

281 no direct evidence that any of these marine crustaceans use this modality to communicate with conspe

282 In insects and crustaceans, ventral midline cells are present that subd

283 Most show highest identity to the 'Wenling Crustacean Virus 9' from an unidentified crustacean host

284 sed widely as a model to research aspects of crustacean vision and neural pathways.

285 ifferences in delta(15) N of potential prey (crustaceans vs. squid vs. fish and carrion), analysis of

286 resent in the common ancestor of insects and crustaceans were incorporated into the insect body wall,

287 hemiellipsoid bodies are a derived trait of crustaceans, whereas mushroom bodies are a derived trait

288 nisms such as Hyalella azteca, an epibenthic crustacean which forages at the sediment surface, is lik

289 t tiger prawn (Penaeus monodon) is a decapod crustacean widely reared for human consumption.

290 iscuss the possibility that both tissues are crustacean wing homologues, which supports a dual evolut

291 , both of these tissues qualify as potential crustacean wing homologues.

292 prising diversity of endemic animals (mostly crustaceans) within a highly oligotrophic habitat.

293 ting is a critical developmental process for crustaceans, yet the underlying molecular mechanism is u

294 ed data of jellyfish, small pelagic fish and crustacean zooplankton biomass from four major ecosystem

295 a negative association between jellyfish and crustacean zooplankton in the Black Sea, we found no evi

296 recent years suggest that fish predation on crustacean zooplankton is 2-30 times higher than jellyfi

297 anipulated lake, to test the hypothesis that crustacean zooplankton production should subsequently de

298 hese increased DOC concentrations may reduce crustacean zooplankton productivity due to reductions in

299 iomass of small pelagic fish nor to a common crustacean zooplankton resource.

300 his habitat is the chitinous exoskeletons of crustacean zooplankton.