ライフサイエンスコーパス: sulphur

1 a cysteine analogue with selenium replacing sulphur.

2 as substrates, including three that contain sulphur.

3 ine microorganisms to assimilate the reduced sulphur.

4 ltenes are identified as the major source of sulphur.

5 no recommended daily intake guide lines for sulphur.

6 e ingress of air is permitted and additional sulphur (30 parts) is introduced before a second calcina

7 sotopic profiles of oxygen ((18)O/(16)O) and sulphur ((33)S/(32)S, (34)S/(32)S) in seawater sulphate

8 r any 'sticky' carbon source) (12 parts) and sulphur (60 parts) at 750 degrees C for ca. 4 hours.

9 ranscriptional regulators for the control of sulphur amino acid metabolism.

10 iculture Organisation standards, but Lys and sulphur amino acids were at limiting concentrations in a

11 his is the first study of the acquisition of sulphur, an essential element, by this pathogen.

12 produced around 3.1 x 10(9) moles of reduced sulphur and 10(10) moles of CO2, promoting the formation

13 e Phosphorus, Zinc, Iron, Manganese, Copper, Sulphur and Boron concentrations under salinity were als

14 nthesized from simple and inexpensive carbon-sulphur and carbon-nitrogen precursors.

15 Outgassed sulphur and erupted fine-grained pyroclastics from these

16 , the surface rocks are richer in nickel and sulphur and have lower manganese/iron ratios than the me

17 surface area, spatial control of solid-state sulphur and lithium sulphide species deposition as a cri

18 that the electrochemical conversion between sulphur and magnesium sulfide can be successfully perfor

19 o increase whereas atmospheric deposition of sulphur and nitrogen has declined in Europe and the USA

20 rom human activity, such as acid deposition (sulphur and nitrogen) and heavy metal pollution.

21 ithium metal, silicon and tin as anodes, and sulphur and oxygen as cathodes.

22 oordinating heteroatoms, including nitrogen, sulphur and phosphorus.

23 alline structure with opposite modulation of sulphur and selenium distributions across the heterostru

24 The mixtures of iron, oxygen, sulphur and silicon are taken from earlier work and fit

25 ortant to elucidate the geochemical cycle of sulphur and the evolution of ocean chemistry.

26 Here we use sulphur and triple oxygen isotope measurements of atmosp

27 rous, potassium, silicon, sodium, strontium, sulphur and zinc.

28 t these two locations showed that classes of sulphur- and nitrogen-containing membrane lipids, which

29 gen, carbon, nitrogen, oxygen, magnesium and sulphur as well as compound-specific nitrogen and oxygen

30 Several genes of the sulphur assimilation pathway are regulated by microRNA-3

31 by SLIM1, a key transcription factor in the sulphur assimilation pathway.

32 Yet how the sulphur atom is incorporated into many sulphur-containin

33 xed onto the sensor gold surface through the sulphur atom of cysteine.

34 identified, containing from one up to three sulphur atoms and with and without allyl moieties.

35 g thickness, and the role of the interfacial Sulphur atoms is clarified.

36 ed C-H activation reactions, any nitrogen or sulphur atoms present in heterocyclic substrates will co

37 , avoiding interference from any nitrogen or sulphur atoms present in the heterocyclic substrates.

38 regulates the geometry of the participating sulphur atoms with sub-angstrom precision to achieve eff

39 modified by carbon monoxide, hydrocarbons or sulphur atoms.

40 from organic compounds that contain reduced sulphur atoms.

41 -Olson (FMO) complex of photosynthetic green sulphur bacteria, however to date little work has focuss

42 roma active in all three rice types, but the sulphur-based, cooked rice character impact volatile, 2-

43 Lithium-sulphur batteries are attractive owing to their high the

44 Lithium-sulphur batteries have high theoretical energy density a

45 the best performance for long-cycle lithium-sulphur batteries so far.

46 Lithium-sulphur batteries with a high theoretical energy density

47 vance progress in the development of lithium-sulphur batteries.

48 ycle life hinder the practicality of lithium-sulphur batteries.

49 ly feasible means of fabricating the lithium-sulphur batteries.

50 simple adjustment to the traditional lithium-sulphur battery configuration to achieve high capacity w

51 tremendous improvement with various lithium-sulphur battery systems.

52 Here we report a new design of lithium-sulphur battery using electrically connected graphite an

53 contaminated through mining and oxidation of sulphur-bearing Zn minerals or engineered nanomaterials

54 ncoding the enzyme that catalyses the carbon-sulphur bond formation reaction and that encoding the co

55 bon, B-C, nitrogen, B-N, phosphorus, B-P and sulphur bonds, B-S, are indicated.

56 t fractionation suggests the assimilation of sulphur both during passage of magmas through the crust

57 mefaciens and was utilized as sole source of sulphur by A. tumefaciens.

58 routes for acquisition of reduced carbon and sulphur by surface ocean heterotrophs.

59 ffects of different sulphuring methods, i.e. sulphuring by "burning the elemental sulphites (BES)," "

60 he persulphide and thiocarboxylate groups on sulphur-carrier (donor) proteins.

61 However, no gene encoding a sulphur-carrier protein could be located in the BE-7585A

62 ation reaction and that encoding the cognate sulphur-carrier protein exist in the same gene cluster.

63 ctivating enzyme can adenylate each of these sulphur-carrier proteins and probably also catalyses the

64 e ability of BexX to selectively distinguish sulphur-carrier proteins is given a structural basis usi

65 me sequencing uncovered a few genes encoding sulphur-carrier proteins that are probably involved in t

66 intercalation cathodes, high-energy-density sulphur cathodes are still in the stage of research beca

67 report an applicable way to recharge lithium-sulphur cells by a simple charge operation control that

68 Lithium-sulphur cells incorporating this hybrid anodes deliver c

69 f an S-S bonding interaction between the two sulphur centres inside the cluster shell.

70 A three-dimensional atmospheric sulphur chemistry and transport model study reveals that

71 fundamental differences between the dominant sulphur chemistry in the atmosphere of Mars and that in

72 lic basalt, chemically identical (except for sulphur, chlorine and zinc) to soils from Gusev crater.

73 nding activity and can provide iron for iron-sulphur cluster assembly in proteins in vitro.

74 Among the iron-sulphur cluster assembly proteins encoded by gene cluste

75 Here we report that among the iron-sulphur cluster assembly proteins, IscA also has a stron

76 an alternative to the housekeeping Isc iron-sulphur cluster assembly system.

77 pendent reports have linked frataxin to iron-sulphur cluster assembly through interactions with the t

78 esting that IscA has a crucial role for iron-sulphur cluster biogenesis.

79 genes involved in lipoate synthesis and iron-sulphur cluster biogenesis.

80 ember of a family of DNA helicases with iron-sulphur cluster domains.

81 s at the deep end of this chamber, near iron-sulphur cluster N2.

82 t NO detoxification (Hmp, NorVW, NrfA), iron-sulphur cluster repair (YtfE), and the expression of the

83 and Yap5 that respond to mitochondrial iron-sulphur cluster status are modulated by copper-BPQ causi

84 of proteins involved in formation of a metal-sulphur cluster that provides a nitrogenase active site.

85 aeon Pyrococcus horikoshii uses a novel iron-sulphur-cluster enzyme, Dph2.

86 malian core subunits that contain eight iron-sulphur clusters and 60 transmembrane helices, identify

87 ant for the repair of oxidatively damaged Fe-sulphur clusters of aconitase and, in contrast to Bfr an

88 es can harm/destroy cysteinyl residues, iron-sulphur clusters, DNA and polyunsaturated lipids, leadin

89 er-BPQ mediated damage to mitochondrial iron-sulphur clusters.

90 total of 64 transmembrane helices and 9 iron-sulphur clusters.

91 , specifically those containing damaged iron-sulphur clusters.

92 The nitrogen/sulphur codoped graphene sponge electrode provides enoug

93 cyclic life using three-dimensional nitrogen/sulphur codoped graphene sponge electrodes.

94 fatty acids (9), aliphatic hydrocarbons (8), sulphur compounds (5) and nitrogen compounds (2) were po

95 inflammation react with endogenous, luminal sulphur compounds (thiosulphate) to form a new respirato

96 tty acid derivatives, Strecker aldehydes and sulphur compounds as volatiles clearly changing during s

97 lets, ketones in tetra hop and aldehydes and sulphur compounds in barley were the predominant chemica

98 These pathways can reduce various oxidized sulphur compounds including sulphate, sulphite and thios

99 and M6 strains were the highest producers of sulphur compounds where dimethyl disulphide and dimethyl

100 present, after cooking, had higher levels of sulphur compounds, 2-nonanone, ethyl octanoate and lower

101 Sulphur compounds, 3-sulfanylhexyl acetate and methional

102 Recycling of organic sulphur compounds, e.g. via the SAM cycle, is an importa

103 major and minor volatile compounds, volatile sulphur compounds, mercaptans, metals, anions and cation

104 lcohols, fatty acids, aldehydes, ketones and sulphur compounds.

105 n of sulphur in foods was developed, and the sulphur concentrations of various fresh and dried food s

106 esults were in good agreement with certified sulphur concentrations of various vegetal CRM samples ap

107 Sulphur containing compounds rise at later time-points a

108 lucosinolate (Gl) biosynthesis, glycosylated sulphur-containing aldoximes containing chemically diffe

109 The sulphur-containing amino acid methionine is a metabolic

110 tein family that is enriched in aromatic and sulphur-containing amino acids, are used by certain ceph

111 ce for bulky hydrophobic amino acids and for sulphur-containing amino acids.

112 ion decreased the antioxidant properties and sulphur-containing compounds, but increased Se-methyl-se

113 odifications in sulphur partitioning between sulphur-containing metabolites.

114 f primary metabolism for the biosynthesis of sulphur-containing natural products is probably a genera

115 w the sulphur atom is incorporated into many sulphur-containing secondary metabolites is poorly under

116 redox stability with tolerance to coking and sulphur contamination from hydrocarbon fuels is demonstr

117 lso complement evidence for recycling of the sulphur content of ancient sedimentary materials to the

118 The sulphur content of foods ranged from less than the LOD t

119 Like their sulphur counterparts, Li2S cathodes require effective en

120 The results suggest that the SAMs restrict sulphur coverage to enhance selectivity without signific

121 evidence for synchronization to a beat in a sulphur-crested cockatoo (Cacatua galerita eleonora).

122 DMS) is important in climate regulation, the sulphur cycle and signalling to higher organisms.

123 Plants play an important role in the global sulphur cycle because they assimilate sulphur from the e

124 The degree to which the cryptic sulphur cycle can fuel a loss of fixed nitrogen in the m

125 l pressure and the evolution of the Cenozoic sulphur cycle, and could be accounted for by geologicall

126 ctionation implies disproportionation in the sulphur cycle, probably involving sulphide-oxidizing bac

127 fficiently coupling the carbon, nitrogen and sulphur cycles.

128 ses, such as the marine carbon, nitrogen and sulphur cycles.

129 Recently, 'cryptic' sulphur cycling was proposed as a partial solution to th

130 r dissolved oxygen concentrations, including sulphur-cycling Chromatiales, for which 16S rRNA was amp

131 In E. cuniculi, the iron (frataxin) and sulphur (cysteine desulphurase, Nfs1) donors and the sca

132 ity of isopropylmalate isomerase, a key iron-sulphur dehydratase.

133 Our results also show that co-opting the sulphur-delivery machinery of primary metabolism for the

134 he receptor promiscuity of the A. orientalis sulphur-delivery system.

135 A proper combination of these sulphur-delivery systems is effective for BexX-catalysed

136 cells throughout filaments after nitrogen or sulphur depletion.

137 We also found that the reduction of sulphur deposition in Europe and the USA lead to higher

138 ion growth and suggest that, so far unknown, sulphur deposition plays a significant role in the carbo

139 ure arbuscule degeneration does not occur in sulphur-deprived mtpt4 plants.

140 % per 1 part per million; 95% CI 2.52-4.54), sulphur dioxide (2.36% per 10 parts per billion; 1.35-3.

141 Volcanic eruptions release a large amount of sulphur dioxide (SO(2)) into the atmosphere.

142 e, white and red wines were produced without sulphur dioxide (SO2) and, at the end of the alcoholic f

143 Sulphur dioxide (SO2) is essential for the preservation

144 Sulphur dioxide (SO2) proved to increase absorbance at 2

145 results also demonstrate the extent to which sulphur dioxide addition can lower the free aldehyde con

146 f this study was to assess the efficiency of sulphur dioxide alone and in combination with either glu

147 ide provided improved inhibition compared to sulphur dioxide alone, in conditions of limited oxygen c

148 f maceration, type of yeast and the level of sulphur dioxide applied on stilbene content and antioxid

149 sor elements and ultra fast determination of sulphur dioxide by cyclic voltammetry makes this techniq

150 sed for biosensor polyphenol index (IBP) and sulphur dioxide concentration (SO2).

151 suppressed and the oxidation peak height for sulphur dioxide corresponds linearly to the concentratio

152 d for simple and selective determinations of sulphur dioxide in wine, especially during winemaking.

153 future scenario that injects 5 Tg yr(-1) of sulphur dioxide into the stratosphere and cross-comparin

154 During winemaking sulphur dioxide is added to prevent undesirable reaction

155 in winemaking for substitution of the use of sulphur dioxide is still at a very early stage of develo

156 e with two electron reduction of quinones by sulphur dioxide or ascorbic acid, and both routes serve

157 ldehyde, erythorbic acid or glutathione with sulphur dioxide provided improved inhibition compared to

158 otometric method to determine free and total sulphur dioxide recommended for beers was applied direct

159 or 45 degrees C) or extent of oxygen supply, sulphur dioxide was equally or more efficient in impedin

160 ing that the biocidic activity is exerted by sulphur dioxide while, in other applications, it is empl

161 ous pollutants (ozone, nitrogen dioxide, and sulphur dioxide), and mixed traffic-related air pollutio

162 t autolysate) were tested in comparison with sulphur dioxide, concerning radical scavenging activity

163 Protection by wine preservatives (sulphur dioxide, glutathione, ascorbic acid and model ta

164 certainties in natural emissions of volcanic sulphur dioxide, marine dimethylsulphide, biogenic volat

165 daily increases in gaseous (carbon monoxide, sulphur dioxide, nitrogen dioxide, ozone) and particulat

166 he simultaneous detection of polyphenols and sulphur dioxide, using cyclic voltammetry at inert elect

167 th compositional changes during storage, and sulphur dioxide-aldehyde apparent equilibrium constants.

168 (HHP) treatments on volatile composition of sulphur dioxide-free wines during bottle storage was stu

169 ilver showed the highest sensitivity towards sulphur dioxide.

170 e three principal axes in the asymmetric-top sulphur dioxide.

171 minis, mitochondrial Hsp70 and the essential sulphur donor (Nfs1) are still in the mitosome, but surp

172 synthesis of bright, multicolor fluorescent sulphur doped carbon dots (CNDs) has been developed by u

173 olarimetry to determine the resistivity of a sulphur-doped plastic target heated to Brown Dwarf condi

174 als were fabricated by bottom-up assembly of sulphur-doped pnictogen chalcogenide nanoplates sculpted

175 ce time, we find that previous estimates for sulphur-driven remineralization and loss of fixed nitrog

176 usly known about how A. tumefaciens acquires sulphur during colonization.

177 on dealing with the volumetric expansion of sulphur during lithiation, which will lead to cracking a

178 y photoelectron spectroscopy analysis of the sulphur electrode confirmed that the electrochemical con

179 mechanism of disulphide reduction by an iron-sulphur enzyme and describe previously unknown interacti

180 at dihydroxyacid dehydratase (IlvD), an iron-sulphur enzyme essential for the BCAA biosynthesis, is c

181 iosynthesis pathway is catalysed by the iron-sulphur enzyme IspH, producing the universal precursors

182 lphur system is appealing in this regard, as sulphur exhibits an order of magnitude higher capacity t

183 several components of the mitochondrial iron-sulphur (Fe-S) cluster assembly machinery.

184 ntal evidence of any RNAP possessing an iron-sulphur (Fe-S) cluster, which may play a structural role

185 ubunit protein complex containing eight iron-sulphur (Fe-S) clusters.

186 59) and has a role in the maturation of iron-sulphur (Fe-S) proteins.

187 Proteins of the cytosolic pathway for iron-sulphur (FeS) cluster assembly are conserved, except tha

188 was realized by incorporating intramolecular sulphur-fluorine interactions and bulky side chains link

189 erature hydrothermal fluids to calculate the sulphur flux of 100 Gmol/y at MOR.

190 tios of high-temperature volcanic gases show sulphur flux of 720 Gmol/y at arc volcanoes (ARC) with a

191 se assimilatory sulphate reduction to supply sulphur for biosynthesis, although many can assimilate s

192 r biosynthesis, although many can assimilate sulphur from organic compounds that contain reduced sulp

193 global sulphur cycle because they assimilate sulphur from the environment and build it into methionin

194 Our findings reveal that for high sulphur heavy oils, the generation of hydrogen sulphide

195 effectiveness of the oxygen-loaded MBs with sulphur hexafluoride (SF6)-loaded MBs and reveal a signi

196 It was showed that distribution of sulphur in CRM and grinded food samples were homogeneous

197 S-cells contain up to 40% of the total sulphur in flower stalk tissues.

198 The new approach for the determination of sulphur in foods was developed, and the sulphur concentr

199 results of the substitution of selenium for sulphur in GLS glass are described.

200 For bond formation between carbon and sulphur in primary metabolites, the major ionic sulphur

201 s in the burial of organic carbon and pyrite sulphur in sediments deposited under large-scale anoxic

202 The effect of varying the proportion of sulphur in the starting material on the colour of the fi

203 Therefore, the discovery of MIF sulphur in these young plume lavas suggests that sulphur

204 g growth rate upon limitation of nitrogen or sulphur influx.

205 Sulphur intake estimations were highly correlated with t

206 Sulphur intake from alliaceous and cruciferous vegetable

207 We estimated sulphur intake from food diaries, and validated the resu

208 us vegetables contributed up to 42% of total sulphur intake.

209 provide strong evidence that assimilation of sulphur into Martian magmas was a common occurrence thro

210 Two groups of sequences related to anaerobic sulphur/iron reducers and sulphate reducers dominated li

211 Sulphur is a universally required cell nutrient found in

212 Sulphur is an attractive cathode material with a high sp

213 Sulphur is an essential element for life and is ubiquito

214 Sulphur is an essential element in the metabolism.

215 Sulphur is another essential macronutrient delivered to

216 cost cathode materials such as electrophilic sulphur is only possible with a non-nucleophilic electro

217 temporally continuous generation of new NMD sulphur isotope anomalies in the atmosphere was likely t

218 Non-mass-dependent (NMD) sulphur isotope anomalies in the rock record are the cen

219 Sulphur isotope data for iron sulphides precipitated soo

220 Numerical box modelling of the paired carbon sulphur isotope data indicates that these isotope shifts

221 We find a positive sulphur isotope excursion in phase with the Steptoean Po

222 The observation of non-mass-dependent sulphur isotope ratios in sedimentary rocks more than ap

223 The carbon, nitrogen and sulphur isotope ratios of feed and fillet were highly po

224 Detailed examination of the sulphur isotope record before 2.45 Gyr ago also reveals

225 Here we present sulphur isotope records from six globally distributed st

226 Terrestrial MIF sulphur isotope signatures (in which the amount of fract

227 Here we report anomalous sulphur isotope signatures indicating mass-independent f

228 igneous sulphides in Martian meteorites with sulphur isotope signatures indicative of mass-independen

229 Sulphur isotope systematics offer insight into some aspe

230 ts of molybdenum and vanadium and low pyrite sulphur isotope values (Delta(34)S values >/=65 per mil)

231 Sulphur isotope values of sulphides are interpreted here

232 f carbonate that preserves marine carbon and sulphur isotopic excursions of about -5 and +15 parts pe

233 for the global postglacial marine carbon and sulphur isotopic excursions, abrupt unidirectional warmi

234 er, the low active material utilization, low sulphur loading and poor cycling stability restrict thei

235 e electrode provides enough space for a high sulphur loading, facilitates fast charge transfer and be

236 centrations of nickel and other chalcophile (sulphur-loving) elements.

237 s and in flower stalks were visualised using sulphur mapping by cryo-SEM/energy-dispersive X-ray anal

238 There were significant effects of variety, sulphuring method and especially storage at 30 degrees C

239 Sulphuring methods and variety did not show significant

240 The effects of different sulphuring methods, i.e. sulphuring by "burning the elem

241 in the infalling rotating envelope, whereas sulphur monoxide (SO) is enhanced in the transition zone

242 Commercial sodium-sulphur or sodium-metal halide batteries typically need

243 This growing chemisorbed sulphur- or nitrogen-atom-initiated poly(CO2) chain furt

244 It is generally assumed that most dietary sulphur originates from intake of methionine and cystein

245 e fossils have been variously interpreted as sulphur-oxidizing bacteria, unicellular protists, mesomy

246 ammox) bacteria and the nitrate-sequestering sulphur-oxidizing Thioploca species--in anoxic sediments

247 Despite much efforts in encapsulating sulphur particles with conducting materials to limit pol

248 d sulphate assimilation and modifications in sulphur partitioning between sulphur-containing metaboli

249 open-ocean tracer release of trifluoromethyl sulphur pentafluoride.

250 nificantly reduced cuticle concentrations of sulphur, phosphorus and calcium under decreasing pH; fur

251 he biomass carbon and other elements source (sulphur, phosphorus, boron and iron), and porous g-C3N4

252 Purple non-sulphur phototrophic bacteria (PNSB) are excellent model

253 ion with other ligands, such as chlorine and sulphur, present in the original containers.

254 hur in these young plume lavas suggests that sulphur--probably derived from hydrothermally altered oc

255 Ester and sulphur production was strongly dependent on the strain

256 In the procedures used to date, a sulphur promoter precursor is added to significantly enh

257 t methyl transfer, namely the corrinoid iron-sulphur protein and its methyltransferase from the model

258 for yeast viability and is involved in iron-sulphur protein biogenesis.

259 rtant role in repairing the NO-modified iron-sulphur proteins in aerobically growing E. coli cells.

260 ar deficiency to repair the NO-modified iron-sulphur proteins may directly contribute to the NO-induc

261 Synechocystis contains three Rieske iron-sulphur proteins, all of which contain typical twin-argi

262 modern ocean requires the quantification of sulphur recycling in OMZ settings.

263 during discharge in the cathode of a lithium-sulphur redox cell are important, but their dissolution

264 des the primary S(0)-reducing enzyme NAD(P)H sulphur reductase.

265 ogy can sustain their initial reactivity and sulphur removal capacity over multiple regeneration cycl

266 space to accommodate the volume expansion of sulphur, resulting in an intact TiO(2) shell to minimize

267 The predicted protein was sulphur rich suggesting the possibility of a contributio

268 e oxygen fugacity during melting of the same sulphur-rich mantle.

269 haracterization of SurR, Pyrococcus furiosus sulphur (S(0)) response regulator.

270 of monolayer 2H-MoS2 for HER by introducing sulphur (S) vacancies and strain.

271 395 (miR395) that is itself induced by a low-sulphur (-S) environment.

272 The H2S-forming sulphur salt Na2S as well as the slow-releasing H2S-libe

273 n states (i.e. nitrogen, manganese, iron and sulphur) serve as both nutrients and sources of chemical

274 n and heteroatoms (such as nitrogen, oxygen, sulphur, silicon and boron) via complexes of transition

275 tructure of Ra-KLP at 1.6 A resolution using sulphur single-wavelength anomalous dispersion reveals t

276 which cadmium replaced the iron at the iron-sulphur site.

277 The hetero-doped nitrogen/sulphur sites are demonstrated to show strong binding en

278 phur in primary metabolites, the major ionic sulphur sources are the persulphide and thiocarboxylate

279 the surface active substances (SAS), reduced sulphur species (RS) and catalytically active compounds

280 Although sulphur species are generally considered to be indiscrim

281 NO(3) reactions with VOCs and organic sulphur species are important, or in some cases even dom

282 tified using retention values from authentic sulphur standards and GC-MS characteristic masses.

283 SAR11 requires exogenous sources of reduced sulphur, such as methionine or 3-dimethylsulphoniopropio

284 of the valance and conduction bands owing to sulphur-sulphur interactions as the interlayer spacing r

285 The lithium-sulphur system is appealing in this regard, as sulphur e

286 ry of hydrogen, carbon, nitrogen, oxygen and sulphur, the identity of molecular species in gaseous vo

287 Here, we demonstrate the design of a sulphur-TiO(2) yolk-shell nanoarchitecture with internal

288 ectory analysis and atmospheric nitrogen and sulphur tracers link these frequent nucleation events to

289 itin-like modifiers evolved from prokaryotic sulphur transfer proteins it is less clear how complex e

290 which increases the availability of organic sulphur used by sulphite-reducing microorganisms like B.

291 order and scattering include defects such as sulphur vacancies in the MoS2 itself as well as extrinsi

292 he dominant category of defects changes from sulphur vacancy in mechanical exfoliation and chemical v

293 Four sulphur volatiles exhibited aroma activity, including tw

294 nts from the principal component analysis of sulphur volatiles explained 60% of the variance.

295 Principal component analysis of sulphur volatiles indicated that there were appreciable

296 Five additional sulphur volatiles were found to have aroma activity: dim

297 Ten sulphur volatiles were observed in two Florida tomato cu

298 uding two of the newly-reported fresh tomato sulphur volatiles, 2-s-butylthiazole and dimethyl sulphi

299 Sulphur was determined in various vegetables via molecul

300 limit of Li2S8 capacity ~\n1,470 mAh g(-1) (sulphur weight) under the loading of hybrid electrode on