ライフサイエンスコーパス: sulphur

1 ltenes are identified as the major source of sulphur.

2 an impact on transformation of nitrogen and sulphur.

3 as substrates, including three that contain sulphur.

4 ine microorganisms to assimilate the reduced sulphur.

5 no recommended daily intake guide lines for sulphur.

6 a cysteine analogue with selenium replacing sulphur.

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

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

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

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

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

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

13 rpreted and the combination of strontium and sulphur analysis has the potential to estimate origins.

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

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

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

17 Outgassed sulphur and erupted fine-grained pyroclastics from these

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

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

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

21 The isolated quinoa starch is rich in Sulphur and Magnesium.

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

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

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

25 oordinating heteroatoms, including nitrogen, sulphur and phosphorus.

26 OsCADT1 mutation resulted in higher sulphur and selenium accumulation in the shoots and grai

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

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

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

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

31 nd is currently controlled by fungicides and sulphur applications in conventional and organic product

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

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

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

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

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

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

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

39 wn to 0.762) and a persistent plate of green sulphur bacteria that connects these two (0.958-0.956 wa

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

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

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

43 Lithium-sulphur batteries have high theoretical energy density a

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

45 Lithium-sulphur batteries with a high theoretical energy density

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

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

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

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

50 tremendous improvement with various lithium-sulphur battery systems.

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

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

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

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

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

56 reased the rate of organic carbon and pyrite sulphur burial and hence atmospheric pO(2).

57 sential first step in oxidation of elemental sulphur, but an ancillary role for SOR as a 'recycle' en

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

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

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

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

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

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

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

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

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

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

68 tivity and volumetric capacity comparable to sulphur cathodes.

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

70 Lithium-sulphur cells incorporating this hybrid anodes deliver c

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

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

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

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

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

81 e-protein) contains an unusual [4Fe:4S] iron-sulphur cluster that is stable in three oxidation states

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

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

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

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

86 , specifically those containing damaged iron-sulphur clusters.

87 The nitrogen/sulphur codoped graphene sponge electrode provides enoug

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

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

90 Strecker aldehydes, sulphur compounds and furan compounds were identified as

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

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

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

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

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

96 Sulphur compounds, 3-sulfanylhexyl acetate and methional

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

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

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

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

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

102 Sulphur containing compounds rise at later time-points a

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

104 The sulphur-containing amino acid methionine is a metabolic

105 Nevertheless, the lower TID of sulphur-containing amino acids in tofu than in soya milk

106 re with notable levels of branched chain and sulphur-containing amino acids.

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

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

109 odifications in sulphur partitioning between sulphur-containing metabolites.

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

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

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

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

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

115 ident with dramatic increases in atmospheric sulphur, copper, and nickel concentrations.

116 Like their sulphur counterparts, Li2S cathodes require effective en

117 Here we report that a sulphur-crested cockatoo (Cacatua galerita eleonora) res

118 ience to collect observations of wing-tagged sulphur-crested cockatoos in central Sydney and record t

119 ocial systems such as those observed in wild sulphur-crested cockatoos.

120 Here, we report an enrichment of sulphur cycle -associated bacteria inside intertidal ben

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

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

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

124 tly provide the best constraints on the deep sulphur cycle, their restricted age range (<200 Ma) mean

125 The detection of sulphur-cycle related bacterial genes in this study sugg

126 foraminiferal/endobiont contribution to the sulphur-cycle.

127 fficiently coupling the carbon, nitrogen and sulphur cycles.

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

129 nities that might be involved in carbon- and sulphur-cycling between and within the lake's three main

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

131 volved in the anaerobic steps of carbon- and sulphur-cycling); and (iv) that species richness and hab

132 selenate transporter gene OsSULTR1;1 and the sulphur-deficiency-inducible gene OsSDI1.

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 on (delta(13) C), nitrogen (delta(15) N) and sulphur (delta(34) S) stable isotopes from predator whit

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

140 lytical device is developed for detection of sulphur dioxide (SO(2)) concentration.

141 -10 mum diameter), nitrogen dioxide (NO(2)), sulphur dioxide (SO(2)), carbon monoxide (CO), and ozone

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 = 10 mum (PM10), nitrogen dioxide (NO2), and sulphur dioxide (SO2) with all-cause infant, neonatal, a

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

147 a healthier complement and/or alternative to sulphur dioxide against white wine oxidative spoilage.

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

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

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

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

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

153 lour, polyphenols, flavonoids, minerals, and sulphur dioxide content, were measured.

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

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

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

157 During winemaking sulphur dioxide is added to prevent undesirable reaction

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

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

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

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

162 tion had a better effect than adding 50 mg/L sulphur dioxide to the experimental Chardonnay wine on t

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

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

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

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

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

168 terized by a bluish color, higher amounts of sulphur dioxide, higher content of octanoic acid, isobut

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

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

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

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

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

174 ilver showed the highest sensitivity towards sulphur dioxide.

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

176 value, was related to the presence of total sulphur dioxide.

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

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

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

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

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

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

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

184 role in global biogeochemical cycles of the sulphur element between land and the sea.

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

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

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

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

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

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

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

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

193 The lowest solubility inert gases, sulphur hexafluoride (SF(6) ) and ethane were used becau

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

195 nge in canines for O(2) and two inert gases, sulphur hexafluoride and ethane, by measuring these gase

196 this was quantitatively similar for oxygen, sulphur hexafluoride and ethane.

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

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 rough the oxidation of inorganic substrates, sulphur in particular, and acquiring carbon through the

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

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

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

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

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

206 Sulphur intake estimations were highly correlated with t

207 Sulphur intake from alliaceous and cruciferous vegetable

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

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

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

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

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

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

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

218 Sulphur isotope data for iron sulphides precipitated soo

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

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

221 Here, we present a detailed study of sulphur isotope fractionation in a Mesoproterozoic alkal

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

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

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

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

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

227 Sulphur isotope systematics offer insight into some aspe

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

229 Sulphur isotope values of sulphides are interpreted here

230 we report unexpected, large mass-independent sulphur isotopic compositions of pyrite with Delta(33)S

231 The in-gap states in sulphur line vacancies cause 1D electron-rich channels t

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

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

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

235 tains numerous functional genes for iron and sulphur metabolism, nitrogen fixation, secondary metabol

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

237 Sulphuring methods and variety did not show significant

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

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

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

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

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

243 se (TQO) from Sulfolobus tokodaii 'restored' sulphur oxidation capacity in Sulfolobus acidocaldarius

244 The current model for sulphur oxidation in the Sulfolobales is based on the bi

245 Acidianus brierleyi, a chemolithoautotrophic sulphur oxidizer, and S. acidocaldarius DSM639 showed th

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

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

248 roteins from Acidianus ambivalens, including sulphur oxygenase reductase (SOR) that disproportionates

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

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

251 open-ocean tracer release of trifluoromethyl sulphur pentafluoride.

252 (90 or 120 lbs/acre) with or without 15 lbs sulphur per acre).

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

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

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

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

257 Ester and sulphur production was strongly dependent on the strain

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

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

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

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

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

263 Earth's surface and mantle sulphur reservoirs are connected via subduction, crustal

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

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

266 Sulphur-rich alkaline magmas offer the solution because

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

268 effect on forests is modulated by changes in sulphur (S(dep)) and nitrogen (N(dep)) deposition and ho

269 Sulphur (S) isotope values in pyrite extracted from a Pl

270 w analytical method that uses carbon (C) and sulphur (S) natural abundance stable isotope data to ass

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

272 g. carbon (C), nitrogen (N), phosphorus (P), sulphur (S), and heavy metals.

273 strong transcriptional response to elemental sulphur, S. acidocaldarius DSM639 failed to upregulate k

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

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

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

281 Carbon, nitrogen and sulphur stable isotope analysis of the fauna provides pa

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

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

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

285 w that this increase in the total carbon and sulphur throughput of the Earth system increased the rat

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

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

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

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

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

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

292 Sulphur values are more restricted (13.1 per mille-17.1

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