ライフサイエンスコーパス: squid

1 superconducting quantum interference device (SQUID).

2 oral sequences [7, 8] earlier than uninjured squid.

3 s and snails but none in oyster, octopus and squid.

4 nents and their roles in colonization of the squid.

5 arly phases of bacterial colonization of the squid.

6 ure to HHP for lowering the allergenicity of squid.

7 mbda(max)) at 528 nm in bovine and 554 nm in squid.

8 fect on competitive colonization of the host squid.

9 e, motility, and competitive colonization of squid.

10 alopods, such as the octopus, cuttlefish and squid.

11 fresh squid fit for consumption and spoiled squid.

12 and survival of injured, but not uninjured, squid.

13 cilitate foraging opportunities for Humboldt squid.

14 t mainly feed on crustaceans; large fish and squid; a mixture of crustaceans, small fish and squid; o

15 Large squid abandoned seasonal coastal-shelf habitats in 2010

16 Squid-adaptive binK alleles promoted colonization and im

17 Site-directed mutagenesis of squid ADAR2a showed that its increased affinity and edit

18 efects in their ability to colonize juvenile squid, although the impact of the loss of SypB or SypI w

19 this sensitization during encounters between squid and a natural fish predator.

20 o-PSB11 and 5,6-dihydro-PSB11 analogues into squid and bovine rhodopsin environments.

21 hic species, its purpose in pelagic species (squid and certain fish and crustaceans) is poorly unders

22 The robust sucker ring teeth (SRT) from squid and cuttlefish are one notable exception of thermo

23 Coleoid cephalopods (octopus, squid and cuttlefish) are active, resourceful predators

24 utation does cause poly(ADP-ribosyl)ation of Squid and hrp38 protein, as well as their dissociation f

25 demonstrated that poly(ADP-ribosyl)ation of Squid and hrp38 proteins inhibits splicing of the intron

26 en rise to descendants as different as giant squid and microscopic pea clams.

27 Juvenile squid and octopods hatch from the egg already swimming i

28 simulate the microgravity environment, host squid and symbiosis-competent bacteria were incubated to

29 cally stimulating the optic lobe of the oval squids and observing their body pattern changes, surpris

30 observed in superconducting devices such as SQUIDs and qubits is still a major unsolved puzzle.

31 insically influences the phase difference in SQUIDs and qubits.

32 lected from specialized cells in the skin of squids and related cephalopods.

33 uperconducting quantum interference devices (SQUIDs) and qubits are feasible.

34 EPR-silent (smif)(2)Ni (3) has S = 1 (SQUID), and calculations show that the unpaired spins re

35 ctroelectrochemistry, magnetic measurements (SQUID), and structural and morphological investigations

36 f the visual system of cephalopods (octopus, squid, and cuttlefish) that have a single unfiltered pho

37 disrupt fast axonal transport in Drosophila, squid, and mice.

38 excised single neurons from marine worm and squid, and then exterior to intact, optically opaque mar

39 um) and in numerous representatives (fishes, squids, and crustaceans) of their lower trophic level pr

40 ariables, our analyses suggest that Humboldt squid are indirectly affected by OMZ shoaling through ef

41 one hour later further ingested raw tuna and squid as an evening meal at a bar.

42 ng squid oriented toward and pursued injured squid at greater distances than uninjured squid, regardl

43 gly, mutant FUS-induced impairment of FAT in squid axoplasm and of axonal outgrowth in mammalian prim

44 Vesicle motility assays in isolated squid axoplasm further demonstrated that both mutant mer

45 Experiments presented here using isolated squid axoplasm reveal inhibition of FAT as a common toxi

46 In squid axoplasm, the M1 peptide dramatically inhibits fas

47 Using isolated squid axoplasm, we show that MPP+ produces significant a

48 s impaired anterograde and retrograde FAT in squid axoplasm, whereas FUS WT had no effect.

49 nhibited anterograde transport when added to squid axoplasm.

50 exposure of PAD inhibited anterograde FAT in squid axoplasm.

51 ch may provide a means to reduce the size of SQUID-based superconducting electronics.

52 is a feasible technological alternative for squid-based surimi production improving its yield and ge

53 Structure of the squid bathorhodopsin is characterized by formation of a

54 d were found to be very similar to those for squid bathorhodopsin.

55 Similar to the squid beak, we have developed nanocomposites where the d

56 nhanced mechanical gradient character of the squid beak, we herein report a nanocomposite that mimics

57 eptidyl-dopa, to be sclerotization agents of squid beak.

58 Once targeted, injured squid began defensive behavioral sequences [7, 8] earlie

59 Hydro-acoustic data, reveal that squid biomass in this study area nearly doubled between

60 al models of Huntington's disease (mouse and squid), but the molecular basis of this effect remains u

61 efficient colonization of Euprymna scolopes squid by bioluminescent Vibrio fischeri from the North P

62 As in mammals, injury in squid can cause persistent SA in peripheral afferents.

63 Cephalopods, such as octopus and squid, can change their coloration in an instant, and ev

64 interactions between sqADAR2 and RNA because squid cells have a approximately 3-fold higher ionic str

65 A Deltahmp mutant of V. fischeri initiates squid colonization less effectively than wild type, but

66 ts that were reproducibly depleted following squid colonization represented 380 genes, including 37 t

67 ocalization, and role in the early stages of squid colonization.

68 approximately 16 kcal/mol energy is lost in squid compared to only approximately 8 kcal/mol in bovin

69 Magnetic susceptibility measurements (SQUID) confirm the paramagnetic scaffold with repeating

70 ice, fish, insects, and the Hawaiian bobtail squid, continue to provide critical insight into how hos

71 Cephalopods (squid, cuttlefish and octopuses) have a unique set of bi

72 (smif)(2)Co (2) has S = 1/2 according to SQUID data at 10 K.

73 ementing previous X-ray crystallographic and SQUID data for solid material, the electronic structure

74 bacterial surface molecules known to induce squid development are up-regulated by symbiont light pro

75 measured low-frequency flux noise spectra in SQUID devices if one takes as a source of fluctuations t

76 aggressive predators, Dosidicus gigas (jumbo squids) do not use minerals in their powerful mouthparts

77 h with extensive validation to show that the squid Doryteuthis pealeii recodes proteins by RNA editin

78 tion of behavioral and neuronal responses in squid, Doryteuthis pealei [5, 6].

79 The beak of the Humboldt squid Dosidicus gigas represents one of the hardest and

80 Humboldt (jumbo) squid (Dosidicus gigas) are highly migratory predators a

81 ates were evaluated and compared to those of squid (Dosidicus gigas) muscle proteins (SM).

82 structural modifications in beta-chitin from squid (Dosidicus gigas, d'Orbigny, 1835) pens and their

83 (31%) and activity levels (45%) in the jumbo squid, Dosidicus gigas, a top predator in the Eastern Pa

84 ys in Monterey Bay reveals that the Humboldt squid, Dosidicus gigas, has substantially expanded its p

85 superconducting quantum interference device (SQUID) down to temperatures of 2 K and in fields up to 7

86 Squid dynamically tune the intensity and colors of iride

87 Previously, we isolated a squid editing enzyme (sqADAR2) that shows a unique struc

88 Structural and magnetic characterization (SQUID, EPR) of the bis-pyridine adducts of (dpm)Mn(II)(p

89 microgravity on the interactions between the squid Euprymna scolopes and its beneficial symbiont Vibr

90 Here, we used the symbiosis between the host squid Euprymna scolopes and its luminescent bacterium Vi

91 namic stability of the mutualism between the squid Euprymna scolopes and its specific, bioluminescent

92 the initiation of the symbiosis between the squid Euprymna scolopes and the bioluminescent bacterium

93 thm that occurs in the symbiosis between the squid Euprymna scolopes and the luminous bacterium Vibri

94 The light-organ symbiosis between the squid Euprymna scolopes and the luminous bacterium Vibri

95 , is required for normal colonization of the squid Euprymna scolopes and, in culture, is necessary fo

96 Colonization of the Hawaiian squid Euprymna scolopes by the marine bacterium Vibrio f

97 The Hawaiian squid Euprymna scolopes forms a natural symbiosis with V

98 dence that a galaxin protein, EsGal1, of the squid Euprymna scolopes participates in both: (i) select

99 re we show that bioluminescent organs of the squid Euprymna scolopes possess the molecular, biochemic

100 strain MJ1 and in ES114, an isolate from the squid Euprymna scolopes that is not visibly luminescent

101 te a symbiotic partnership with the Hawaiian squid Euprymna scolopes, likely due to its role in contr

102 normal light-organ morphogenesis in the host squid Euprymna scolopes, resulting in regression of cili

103 etween the bacterium Vibrio fischeri and the squid Euprymna scolopes, which proceeds via a biofilm-li

104 ote colonization of its eukaryotic host, the squid Euprymna scolopes.

105 eri to form a symbiotic association with the squid Euprymna scolopes.

106 model V. fischeri host, the Hawaiian bobtail squid Euprymna scolopes.

107 t organ in the mantle cavity of the sepiolid squid Euprymna scolopes.

108 tive accessory nidamental gland (ANG) of the squid Euprymna scolopes.

109 on and growth within the light organs of the squid Euprymna scolopes.

110 hat enters into a symbiosis with the bobtail squid Euprymna scolopes.

111 initiation of symbiotic colonization of the squid Euprymna scolopes.

112 rsistent symbiosis in the light organ of the squid Euprymna scolopes.

113 rio fischeri during colonization of its host squid Euprymna scolopes.

114 onospecific symbiont of the Hawaiian bobtail squid, Euprymna scolopes, and the establishment of this

115 Female Hawaiian bobtail squid, Euprymna scolopes, have an accessory nidamental g

116 iotic relationship with the Hawaiian bobtail squid, Euprymna scolopes, where the squid provides a hom

117 iotic relationship with the Hawaiian bobtail squid, Euprymna scolopes, whose light organ it colonizes

118 iosis within the light organ of the Hawaiian squid, Euprymna scolopes.

119 h the light organs of adult Hawaiian bobtail squid, Euprymna scolopes.

120 gest the enormous eyes of giant and colossal squid evolved to see the bioluminescence induced by the

121 Thus, while squid exhibit peripheral alterations in afferent neurons

122 Second, RNA-Seq analysis of squid exposed to modeled microgravity conditions exhibit

123 array was able to discriminate between fresh squid fit for consumption and spoiled squid.

124 rn provide camouflage that helps protect the squid from night-time predators.

125 superconducting quantum interfering device (SQUID), FT Raman, and X-ray crystallographic analysis, a

126 superconducting quantum interference device (SQUID), FT Raman, X-ray crystallographic etc.) and densi

127 The temperature difference between the squid giant axon (6.3 degrees C) and RGCs (37 degrees C)

128 lity assays performed with axoplasm from the squid giant axon showed a requirement for a Rab GTPase i

129 regeneratively during the action potential (squid giant axon); a wasteful 85% enter during the falli

130 In addition, working with the squid giant axon, Cole and Moore noted that strong hyper

131 he falling phase of action potentials in the squid giant axon, the diversity of voltage-gated potassi

132 nd Huxley model and for eliciting a spike in squid giant axons, the preparation for which the model w

133 By applying rapid voltage steps to squid giant axons, we previously identified three compon

134 nd, more recently, in axoplasm isolated from squid giant axons.

135 n of this pathway in axoplasms isolated from squid giant axons.

136 Photolysis of this caged peptide in the squid giant presynaptic terminal caused an abrupt (0.2 s

137 of MPP+ into the presynaptic terminal of the squid giant synapse blocks synaptic transmission without

138 utely inhibited synaptic transmission at the squid giant synapse.

139 nsport to the presynaptic active zone in the squid giant synapse.

140 lyzed before and after colonization of 1,500 squid hatchlings.

141 d their possible role in colonization of the squid have not previously been determined.

142 Squids have used their tunable iridescence for camouflag

143 The protein structure analysis of squid Hc showed that while HHP treatment decreased the a

144 t decrease in the allergenicity (P< 0.05) of squid Hc.

145 dary, tertiary, and quaternary structures of squid hemocyanin (Hc) were characterised, and the relati

146 d more efficient in initially colonizing the squid host than the wild type; similarly, in mixed inocu

147 etween the bacterium Vibrio fischeri and its squid host, which can be observed directly and in real t

148 th in culture and during colonization of the squid host.

149 The Japanese firefly squid Hotaru-ika (Watasenia scintillans) produces intens

150 pADPr) interacts with two Drosophila hnRNPs, Squid/hrp40 and Hrb98DE/hrp38, and that this function is

151 culate that it can cooperate with endogenous squid Hsp(c)70 to mediate binding and/or disaggregation

152 onic system for the shelf-life assessment of squid in cold storage.

153 ze the light-organ transcriptome of juvenile squid in response to the initiation of symbiosis.

154 r of the ongoing range expansion of Humboldt squid in the northeastern Pacific Ocean.

155 companied by a collapse of this fishery, and squid in the region showed major changes in the distribu

156 uperconducting quantum interference devices (SQUIDs) incorporating topological insulator weak links.

157 eutral, while NMR and magnetic measurements (SQUID) indicate an S =1 paramagnetic ground state.

158 EPR spectroscopy and magnetic studies (SQUID) indicate that the diradical in the dichloromethan

159 has a competitive defect when colonizing the squid, indicating the importance of proper control of ac

160 Loss of a larger amount of energy in squid is attributed to the presence of a flexible bindin

161 n which the light organ of Euprymna scolopes squid is colonized exclusively by Vibrio fischeri bacter

162 The squid is the only organism known to produce light using

163 sm of high Q10 - which is not present in the squid - is active in RGCs.

164 Dosidicus gigas (jumbo or Humboldt squid) is a semelparous, major predator of the eastern P

165 Superconducting Quantum Interference Device (SQUID), is developed for preparation of the first m-phen

166 es in a manner comparable to that of natural squid isolates.

167 RNA by 30- or 100-fold in vertebrate-like or squid-like conditions, respectively.

168 We found that squid-like salt conditions severely impair the binding a

169 Properties of gelatin films from splendid squid (Loligo formosana) skin bleached with hydrogen per

170 SQUID magnetic measurements on the isomeric iron imides,

171 Through an extensive set of SQUID magnetic measurements, X-ray absorption spectrosco

172 transition above 80 K as inferred by the dc SQUID magnetic susceptibility measurement.

173 IR, UV-vis, and EPR spectroscopy as well as SQUID magnetization and single-crystal X-ray crystallogr

174 The ac SQUID magnetization data, at zero field and between freq

175 y UV/vis/NIR and EPR spectroscopy as well as SQUID magnetization studies.

176 ystalline sample of 4-6 is held at 10 K in a SQUID magnetometer and irradiated with white light (lamb

177 th for a dinuclear complex (DeltaT = 22 K by SQUID magnetometer in "settle" mode) and show a remarkab

178 O2 laser heating approach and direct-current SQUID magnetometer measurements to obtain palaeodirectio

179 imaging with EDX analysis, XPS analysis, and SQUID magnetometry analysis of catalytic solutions.

180 th CASSCF-SO calculations and confirmed with SQUID magnetometry and EPR spectroscopy, showing easy-ax

181 Squid magnetometry and EPR studies yield data that are c

182 exchange coupling, Aex, is determined using SQUID magnetometry and ferromagnetic resonance (FMR), di

183 Variable-temperature SQUID magnetometry and IR, NIR, and EPR spectroscopies o

184 ition properties have been characterized via SQUID magnetometry and Raman spectroscopy.

185 Using SQUID magnetometry and X-ray absorption spectroscopy, we

186 Furthermore, SQUID magnetometry from 5 to 300 K of solid [(+)-NDI-Del

187 SQUID magnetometry indicates hysteresis below 6 K, while

188 SQUID magnetometry measurements indicate that 5 is a mac

189 (V) but single-crystal X-ray diffraction and SQUID magnetometry suggest a Np(III) -U(VI) assignment.

190 SQUID magnetometry suggests that the iron containing sam

191 scopy, photoelectron spectroscopy (XPS), and SQUID magnetometry to gain information on its morphologi

192 EPR spectroscopy, SQUID magnetometry, and DFT calculations thoroughly char

193 haracterized by X-ray crystallography, while SQUID magnetometry, EPR spectroscopy, and UV-vis-NIR spe

194 -ray diffraction analysis, (57)Fe Mossbauer, SQUID magnetometry, mass spectrometry, and combustion an

195 ies, as investigated by variable-temperature SQUID magnetometry, reveal weak intramolecular antiferro

196 onic properties of 1-4 have been assessed by SQUID magnetometry, while a DFT analysis of complexes 1

197 ic circular dichroism (MCD) spectroscopy and SQUID magnetometry.

198 netic properties of 1-3 were investigated by SQUID magnetometry.

199 ion, infrared spectroscopy (DRIFT), XPS, and SQUID magnetometry.

200 re also investigated by NIR spectroscopy and SQUID magnetometry.

201 been confirmed by X-ray crystallography and SQUID magnetometry.

202 ffording an S = 2 spin state as confirmed by SQUID magnetometry.

203 e of macroscopic ferromagnetism was found in SQUID magnetometry.

204 Superconducting quantum interference device (SQUID) magnetometry confirmed and quantitatively charact

205 superconducting quantum interference device (SQUID) magnetometry, double-coil mutual inductance, and

206 The magnetic susceptibility was studied by SQUID measurements for TTT-NN and TPT-NN.

207 superconducting quantum interference device (SQUID) microscopy and secondary ion mass spectrometry (S

208 free exception (e.g., marine polychaetes and squids), minerals are thought to be indispensable for to

209 This was confirmed by SQUID monitoring during H2 release from solid 2[K(DB18C6

210 is particularly common in coding regions of squid mRNAs.

211 Results demonstrate that washing squid muscle under the proposed acidic conditions is a f

212 The samples were mussel tissue, squid muscle, crab claw meat, whale meat, cod muscle, Gr

213 urface, we found that, unlike both human and squid Na(+)-driven Cl-HCO(3) exchangers, human NCBE does

214 resistance to the high Cl(-) levels found in squid neurons.

215 A study in squid now suggests that nociceptive sensitization enhanc

216 five morphological cell types described for squid OE, paraformaldehyde-fixed olfactory organs were c

217 In squid olfactory receptor neurons (ORNs), physiological s

218 uperconducting quantum interference devices (SQUIDs) on a transmission line.

219 d A292T) in bovine and at site 111 (Y111) in squid opsins.

220 the CNS from rat cerebellar mossy fiber and squid optic lobe.

221 id; a mixture of crustaceans, small fish and squid; or carrion.

222 ack sea bass given access to freely swimming squid oriented toward and pursued injured squid at great

223 pate in olfactory transduction in non-type 2 squid ORNs.

224 in single-junction diffraction patterns and SQUID oscillations are lifted and independent of chemica

225 The node-lifting of the SQUID oscillations is consistent with low-energy Andreev

226 At high temperatures, the SQUID oscillations revert to conventional behaviour, rul

227 Serial squid passaging of bacteria produced eight distinct muta

228 We show that in squid, patchy colloidal physics resulted from an evoluti

229 ing powder (CCP), shrimp shell powder (SSP), squid pen powder (SPP), alpha-chitin, and beta-chitin, T

230 f adding the cells of four lactobacilli to a squid pen powder (SPP)-containing medium on prodigiosin

231 Squid pen protein recovered from chitosan processing was

232 Squid pens were subjected to alkali hydrolysis to extrac

233 form a complex that crystallises inside the squid photophores, and that in the crystal one or more o

234 We demonstrate that squid possess nociceptors that selectively encode noxiou

235 sult suggests that the repetitions in native squid proteins could have a genetic advantage for increa

236 bobtail squid, Euprymna scolopes, where the squid provides a home for the bacteria, and the bacteria

237 nal injection of a specific antibody against squid Rab27 (anti-sqRab27 antibody) combined with confoc

238 ed squid at greater distances than uninjured squid, regardless of previous anesthetic treatment.

239 udied despite the high biomass of fishes and squids residing at depths beyond the euphotic zone.

240 y model is based on the crystal structure of squid rhodopsin (lambda(max) = 490 nm) and shows a maxim

241 performed a molecular dynamics simulation of squid rhodopsin embedded in a hydrated bilayer of polyun

242 tein interaction reveals the binding site of squid rhodopsin to be malleable and ductile, while that

243 performed molecular dynamics simulations of squid rhodopsin with 11-cis and all-trans retinal, and w

244 tures of five prototypical GPCRs, bovine and squid rhodopsin, engineered A(2A)-adenosine, beta(1)- an

245 ally lacks the rscS gene and cannot colonize squid, RscS permits colonization, thereby extending the

246 rigger morphological changes in the juvenile squid's light organ that occur upon colonization.

247 neural basis of body patterning in the oval squid, Sepioteuthis lessoniana Most areas in the optic l

248 entrations of H(2)O(2) used for bleaching of squid skin prior to gelatin extraction directly affected

249 ystal structure of the visual rhodopsin from squid solved recently suggests that a chain of water mol

250 s (bacterial photophores) from two divergent squid species.

251 Squid spoilage was monitored simultaneously by the color

252 Squid (Sqd) is an RNA-binding protein that is required f

253 ulation involves the translational repressor Squid (Sqd).

254 Here we describe thermoplastic processing of squid SRT via hot extrusion of fibres, demonstrating the

255 lymers), which is inspired by animals (e.g., squid, starfish, worms) that do not have hard internal s

256 superconducting quantum interference device (SQUID), steady-state and transient absorption spectrosco

257 ng the magnetic Compton scattering data with SQUID studies that measure the total magnetic moment sug

258 re based on a structural protein produced in squid suction cups that has a segmented copolymer struct

259 , robust changes far from sites of injury in squid suggest that persistently enhanced afferent activi

260 e lyophilized liposomes were incorporated in squid surimi gels at 10.5% concentration.

261 uid-surimi control (C), glucomannan-enriched squid-surimi (G) and glucomannan-spirulina enriched squi

262 urimi (G) and glucomannan-spirulina enriched squid-surimi (GS).

263 s of eight rats each received for 7weeks the squid-surimi control (C), glucomannan-enriched squid-sur

264 The effect of high-fat squid-surimi diets enriched in glucomannan or glucomanna

265 In the squid symbiont V. fischeri ES114, RscS controls light-or

266 The squid symbiont Vibrio fischeri uses an elaborate TCS pho

267 ison revealed that rscS, although present in squid symbionts, is absent from the fish symbiont V. fis

268 ding of the role that NO plays in the Vibrio-squid symbiosis, and provides the first indication of a

269 ortant role for rscS in the evolution of the squid symbiosis.

270 ft genome sequence of Vibrio fischeri SR5, a squid symbiotic isolate from Sepiola robusta in the Medi

271 oscopy demonstrated that Rab27 is present on squid synaptic vesicles.

272 ocomotion and other spontaneous behaviors of squid that received distal injury to a single arm (with

273 , primarily due to a large increase in small squid that were not susceptible to the fishery.

274 Juvenile squid thus appeared to respond to El Nino with an altern

275 uggesting increased levels of RNA editing in squids thus raise the question of the nature and effects

276 which it generates light that might help the squid to hide its silhouette from animals beneath it.

277 gella prompts its host, the Hawaiian bobtail squid, to prepare for its arrival.

278 MCD), electron paramagnetic resonance (EPR), SQUID, UV-vis absorption, and X-ray absorption spectrosc

279 d, more specifically, how one symbiosis, the squid-vibrio association, provides insight into the pers

280 Using the squid-vibrio model system, we provide a characterization

281 ed symbioses through the study of the binary squid-vibrio model.

282 Thus, the persistent maintenance of the squid-vibrio symbiosis is tied to a dynamic diel rhythm

283 (2013) reveal that first contact within the squid-vibrio symbiosis triggers profound molecular and c

284 our understanding of the early stages of the squid-vibrio symbiosis, and more generally inform the tr

285 During the early stages of the squid-vibrio symbiosis, the bacterial symbiont Vibrio fi

286 mventing, host immune responses in the model squid-vibrio symbiosis.

287 /w) from the molecular distillation of crude squid visceral oil.

288 ed for vertebrate (bovine) and invertebrate (squid) visual photoreceptors shows that such a mechanism

289 ertebrate (bovine, monkey) and invertebrate (squid) visual pigments was carried out using a hybrid qu

290 etween vertebrate (bovine) and invertebrate (squid) visual pigments, the mechanism of molecular rearr

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

292 n the Guaymas Basin from 2010 to 2012, small squid were abundant and matured at an unusually small ma

293 rangements observed for 7-cis-rhodopsin from squid were found to be very similar to those for squid b

294 wild type did; however, the mutant-infected squid were more prone to later superinfection by a secon

295 Although large squid were not found in the Guaymas Basin from 2010 to 2

296 Both small and large mature squid, were present in the Salsipuedes Basin during 2011

297 als, documented especially in cuttlefish and squid, where they are used both in camouflage and a rang

298 -like protein), possibly infested in the raw squid which he had ingested just before manifestation of

299 Moreover, as the OML shoals, squids will have to retreat to these shallower, less hos

300 ificantly delayed in its ability to colonize squid within the first 12 h, but eventually it establish