ライフサイエンスコーパス: phosphorus

1 7% (n=10) for a sample containing 2.2% (w/v) phosphorus.

2 crystals through insertion and extraction of phosphorus.

3 ted ocean, microbes can become co-limited by phosphorus.

4 ke transition metal dichalcogenides or black phosphorus.

5 th atomically thin dichalcogenides and black phosphorus.

6 teps of the transformation from white to red phosphorus.

7 oblast growth factor 23 and reduced level of phosphorus.

8 ion of 20 times more soil and 4.3 times more phosphorus.

9 ith differences in total nitrogen than total phosphorus.

10 hene, molybdenum disulphide (MoS2) and black phosphorus.

11 n of limiting nutrients such as nitrogen and phosphorus.

12 n limited by carbon, but not when limited by phosphorus.

13 sites for processing of subsequent incoming phosphorus.

14 the electronic structure of few-layer black phosphorus.

15 icrobes catabolize methylphosphonate for its phosphorus.

16 bioavailable form of the essential nutrient phosphorus.

17 to tree canopy over streets, especially for phosphorus.

18 ide, possessing a cyclohexyl fragment at the phosphorus.

19 nd electronic relatives alpha-GeSe and black phosphorus.

20 element followed by sodium (170mg/100g) and phosphorus (130mg/100g).

21 ity analyses, the addition of serum calcium, phosphorus, 25-hydroxyvitamin D, intact parathyroid horm

22 Phosphorus-31 magnetic resonance spectroscopy (31P MRS)

23 Phosphorus, a critical environmental pollutant, is effec

24 Here we present a compilation of phosphorus abundances in marine sedimentary rocks spanni

25 ch intermittent iron limitation of microbial phosphorus acquisition provides an additional facet in t

26 xtracellular enzymes needed for nitrogen and phosphorus acquisition than in C-acquisition enzymes, re

27 ry growth of dicotyledonous species improves phosphorus acquisition.

28 Phosphorus allocation decreased by half in pistils under

29 A phosphorus allotrope that has not been observed so far,

30 he latter reaction is the first example of a phosphorus analog of the Buchner ring expansion reaction

31 own phenyldioxophosphorane, the long elusive phosphorus analogue of nitrobenzene.

32 aulic loads, with iron removing >70% soluble phosphorus and aluminum <40% (P values of 0.0035-0.0143)

33 ds with cyclohexyl or phenyl substituents on phosphorus and benzyl or phenyl substituents on nitrogen

34 monstration of seagrass-derived rhizospheric phosphorus and iron mobilization explains why seagrasses

35 We show that tropical seagrasses mobilize phosphorus and iron within their rhizosphere via plant-i

36 and fecundability, a greater consumption of phosphorus and lactose was associated with slightly high

37 bundance of biologically important nutrients phosphorus and nickel across the Archean-Proterozoic bou

38 an regions where iron is more accessible but phosphorus and nitrogen are less.

39 ne through addition across the electrophilic phosphorus and nucleophilic N-methylanilide sites in a c

40 but ancient soils record the mobilization of phosphorus and other elements by organic acids in weathe

41 resolution down to approximately 2.5 mum for phosphorus and platinum in HCT116 colon cancer spheroids

42 terval, 0.03-0.11), whereas changes in serum phosphorus and potassium concentrations were not differe

43 endosperm protein (REP), which contains less phosphorus and potassium than soy and casein proteins, a

44 e principal fertilizer components (nitrogen, phosphorus and potassium) on the development of potted r

45 Phosphorus and S concentrations in animal feeds ranged f

46 eco-friendly method for indirect determining phosphorus and sulfur in animal feed by ion chromatograp

47 ntake, in addition to appreciable content of phosphorus and zinc.

48 is with two-thirds of land plants, providing phosphorus and/or N in exchange for carbon.

49 Here, we measured carbon, nitrogen, phosphorus, and biomass allocation among floral whorls i

50 irect reaction of zirconium powders with red phosphorus, and characterized by XRD, SEM, XPS, XRF, SAE

51 al organic carbon, reduction of nitrogen and phosphorus, and concentration changes of soluble ions.

52 lated with higher levels of serum magnesium, phosphorus, and lower AKP level.

53 (Hordeum vulgare) under suboptimal nitrate, phosphorus, and potassium availability.

54 pended solids, chemical oxygen demand, total phosphorus, and total nitrogen were 85%, 65%, 80% and 33

55 owth by up to 52%, 73%, and 41% in nitrate-, phosphorus-, and potassium-limiting conditions, respecti

56 Our study paves the way for black phosphorus applications in infrared photonics and optoel

57 bandgap tuning properties in intrinsic black phosphorus, arising from the strong interlayer electroni

58 We demonstrate printed black phosphorus as a passive switch for ultrafast lasers, sta

59 chemical vapor transport and reaction of red phosphorus at 500 degrees C.

60 amino) carbene (cAAC) stabilized monoanionic phosphorus atom in the form of lithium phosphinidene [cA

61 s using a single step with a base-stabilized phosphorus atom.

62 The CA.M network is aligned with rows of phosphorus atoms and forms large domains which passivate

63 these phases results from the motions of the phosphorus atoms and the hydrogen atoms bound to them.

64 onfiguration assigned to labeled stereogenic phosphorus atoms on the basis of synthesis.

65 ondary growth is an adaptive response to low phosphorus availability and merits investigation as a po

66 ht on potential effects of climate change on phosphorus availability to grassland vegetation.

67 osphorus ratios in response to low dissolved phosphorus availability.

68 igh phosphorus intake may result in positive phosphorus balance and correlate with renal calcificatio

69 beta-aminophosphines having both carbon- and phosphorus-based chirality centers is described.

70 ps is presented, and a comparison to related phosphorus-based systems is offered.

71 Denitrification leads to the occurrence of phosphorus-bearing, N-depleted surface waters, which enc

72 phorus burial before that time was linked to phosphorus biolimitation, resulting in elemental stoichi

73 s carbon and other elements source (sulphur, phosphorus, boron and iron), and porous g-C3N4 as both t

74 Lately rediscovered orthorhombic black phosphorus (BP) exhibits promising properties for near-

75 2D black phosphorus (BP) nanomaterials are presented as a deliver

76 tra-low contact resistance few-layered black phosphorus (BP) transistor with metallic PGex contacts f

77 he limited stability of the surface of black phosphorus (BP) under atmospheric conditions is a signif

78 PM) effect for solution dispersions of black phosphorus (BP).

79 PTAs such as graphene, Au, MoS2 , and black phosphorus (BP).

80 passivation of mechanically exfoliated black phosphorus (BP).

81 se leads us to propose that limited marginal phosphorus burial before that time was linked to phospho

82 der is a kind of biocompatible material, red phosphorus can be used to produce safety matches, organo

83 ponse, and reduced secondary growth improves phosphorus capture from low-phosphorus soil.

84 bolic costs, increases root length, improves phosphorus capture, and increases shoot biomass in low-p

85 euphotic zone was not correlated to nitrogen:phosphorus cellular quotas.

86 that the reaction involves dissociation of a phosphorus centered radical (stabilized by the peri-back

87 selective synthesis of compounds with chiral phosphorus centers remains an unsolved problem.

88 on of a free-standing, flexible nitrogen and phosphorus co-doped hierarchically porous graphitic carb

89 entire brain utilizing a dual-tuned, proton-phosphorus coil to minimize subject movement.

90 Y) to soil extracts, allowing us to separate phosphorus components in the second domain based on thei

91 s (leaf dry mass per area, leaf nitrogen and phosphorus concentration, and wood density) collectively

92 However, the fate of dissolved inflow phosphorus concentrations in these systems is unknown.

93 species-specific adaptation to oligotrophic phosphorus concentrations, control elemental particle ra

94 ndicators of phosphorus limitation including phosphorus concentrations, phosphorus to nitrogen, and c

95 creases by 3-6 degrees C at low nitrogen and phosphorus concentrations.

96 ns from summer mean total nitrogen and total phosphorus concentrations.

97 were used to investigate the partitioning of phosphorus (concentrations of 2.5-3.5 mg/L, >80% was in

98 rrent understanding of root responses to low phosphorus conditions and will emphasize the importance

99 pear to be tensioned differently compared to phosphorus congeners.

100 at has not been observed so far, ring-shaped phosphorus consisting of alternate P8 and P2 structural

101 merization of styrene with designer boron or phosphorus containing monomers.

102 pectroscopic characterization of the heavier phosphorus-containing analogue of isocyanic acid (HPCO),

103 Butyrophilin 3A1 (BTN3A1) binds small phosphorus-containing molecules, which initiates transme

104 be released, affording P4 in the case of the phosphorus-containing species, and elemental arsenic in

105 InsPs contributed 32-55% of the organic phosphorus content and 20-38% of the total phosphorus co

106 proton transport, and a requirement of high phosphorus content for the rapid growth in the "growth r

107 c phosphorus content and 20-38% of the total phosphorus content in the meal.

108 , 27% greater root length, 78% greater shoot phosphorus content, and 68% greater shoot mass than geno

109 , 32% greater root length, 58% greater shoot phosphorus content, and 80% greater shoot mass than geno

110 s process reduced the copper, potassium, and phosphorus content, but had little effect on other trace

111 on failed for a forest soil with low organic phosphorus content.

112 is still limited to soils with high organic phosphorus content.

113 ut Earth's history and therefore whether the phosphorus cycle has consistently modulated biospheric p

114 lso suggests that a fundamental shift in the phosphorus cycle may have occurred during the late Prote

115 ed effort to reconstruct the dynamics of the phosphorus cycle over the past 3.5 billion years, it rem

116 ant interplay between oceanic zinc, iron and phosphorus cycles.

117 ng the coupling between oceanic nitrogen and phosphorus cycles.

118 ligible oxygen diffusion is able to maintain phosphorus cycling activity associated with the enrichme

119 Phosphorus cycling exerts significant influence upon soi

120 Our results shed light on black phosphorus degradation which can aid future passivation

121 ameter controlling biomass growth, increased phosphorus demand but thresholds that suggest P limitati

122 mation, we have used neutral high-generation phosphorus dendrimers bearing 48 (G3) or 96 (G4) bisphos

123 ether, these data suggest that neutral G3-G4 phosphorus dendrimers have strong potential applications

124 ere, we present data indicating that neutral phosphorus dendrimers show impressive antiinflammatory a

125 Phosphorus depletion in E. coli after reaction with AMZ,

126 th headspace gas chromatography and nitrogen-phosphorus detection.

127 phospholipids in soybean lecithin samples by phosphorus determination using high-resolution continuum

128 survive the scarcity of dissolved inorganic phosphorus (DIP), and alkaline phosphatase (AP) has been

129 le the previously known alpha form and black phosphorus display the more common chair conformation fo

130 Elemental phosphorus displays an impressive number of allotropes w

131 ion of the electron-nuclear spin states of a phosphorus donor that can be controlled by microwave ele

132 The ability to utilize dissolved organic phosphorus (DOP) is important for phytoplankton to survi

133 ders interactions among C (carbon), N and P (phosphorus), driven by a new reconstruction of historica

134 In order to sustain the native vitamin B1 phosphorus esters, sample preparation is crucial.

135 Each few-layer black phosphorus exhibits a thickness-dependent unique infrare

136 nfluence of trees on stormwater nitrogen and phosphorus export across 19 urban watersheds in Minneapo

137 ses are nutrient-limited owing to the strong phosphorus fixation capacity of carbonate-rich sediments

138 Phosphorus flame retardants and plasticizers (PFRs) are

139 We combine novel high-frequency phosphorus flux data from three representative catchment

140 The ratio of dissolved nitrogen:phosphorus fluxes into the euphotic zone was not correla

141 and the ability to efficiently extract soil phosphorus, for example Carex appressa, are, thus, recom

142 io (the atomic ratio of carbon, nitrogen and phosphorus found in phytoplankton).

143 ters of water treated, to remove 70% soluble phosphorus from eutrophic waters with 0.35 g m(-3) solub

144 ion, which promotes the outward diffusion of phosphorus from the compound nanocrystals of palladium p

145 oading of macronutrients (e.g., nitrogen and phosphorus) from fertilizers, fossil fuels, and human an

146 PBDE) congeners, 19 other brominated FRs, 11 phosphorus FRs (PFRs), 2 Dechlorane-Plus (DP) isomers, a

147 Research on black phosphorus has been experiencing a renaissance over the

148 White phosphorus has now been filled into single-wall carbon n

149 Phosphorene, a single atomic layer of black phosphorus, has recently emerged as a new two-dimensiona

150 The phosphorus in 3% CLWMS decreased with increasing pH and

151 to 0.5:1 N:P (ratio of nitrogen in lysine to phosphorus in DNA), are stable in low salt and up to ten

152 Under low phosphorus in greenhouse mesocosms, genotypes with reduc

153 uperconductivity could be achieved for black phosphorus in its normal orthorhombic form, despite seve

154 ained almost constant with each cycle, while phosphorus in the effluent increased by 1 mg/L and 3 mg/

155 understanding of the composition of organic phosphorus in the environment.

156 rms of the movement of electron density from phosphorus in the HOMO of PCO(-) to sulfur in the HOMO o

157 n is the immediate primary fate of dissolved phosphorus in the system (up to 57% of input P).

158 to mobilize the essential nutrients iron and phosphorus in their rhizosphere via multiple biogeochemi

159 Here, the authors demonstrate a stable black phosphorus ink suitable for printed ultrafast lasers and

160 Here we show a black phosphorus ink that can be reliably inkjet printed, enab

161 icultural changes (e.g., 20-80% reduction in phosphorus inputs).The impact of climate change on phosp

162 High phosphorus intake can cause vascular and renal calcifica

163 s, recent research raises concerns that high phosphorus intake could have detrimental effects on heal

164 , and death, limited data exist linking high phosphorus intake directly to adverse clinical outcomes.

165 tive studies are needed to determine whether phosphorus intake is a modifiable risk factor for kidney

166 Small studies in human suggest that high phosphorus intake may result in positive phosphorus bala

167 suggested that La2O3 converted intracellular phosphorus into LaPO4.

168 Recently rediscovered black phosphorus is a layered semiconductor with promising ele

169 Black phosphorus is a two-dimensional material of great intere

170 Phosphorus is abundant in the food supply of developed c

171 Black phosphorus is also known to be a superconductor under hi

172 Although phosphorus is an essential nutrient required for multipl

173 Black phosphorus is an infrared layered material.

174 terning and layer-by-layer thinning of black phosphorus is demonstrated with conductive atomic-force-

175 -specific discrepancy in GSA response to low phosphorus is mirrored by similar differences in growth

176 Following encapsulation, the printed black phosphorus is stable against long-term (> 30 days) oxida

177 Although serum phosphorus is strongly associated with cardiovascular di

178 The macronutrient phosphorus is thought to limit primary productivity in t

179 tions and with inversion of configuration at phosphorus, is a key step in this process.

180 try, which are composed of simple cubic like phosphorus layers capped with hydrogen atoms and layers

181 egatively charged hydrogen atoms capping the phosphorus layers.

182 eactive protein level, hemoglobin A1c level, phosphorus level, troponin T level, log N-terminal pro-B

183 experiments show that Pth4 can alter calcium/phosphorus levels and affect expression of genes involve

184 etyl enamides, for which a new C2 -symmetric phosphorus ligand is designed.

185 In this study we analyze indicators of phosphorus limitation including phosphorus concentration

186 billion years, it remains uncertain whether phosphorus limitation persisted throughout Earth's histo

187 Poorer litter quality and greater phosphorus limitation towards the equator may restrict d

188 is driven mainly by nitrogen and less so by phosphorus limitation.

189 e effect of climate change on average winter phosphorus loads (predicted increase up to 30% by 2050s)

190 Phosphorus losses from land to water will be impacted by

191 s fall between those of alpha-GeSe and black phosphorus, making beta-GeSe a promising candidate for f

192 philic carbon atoms and the structure of the phosphorus moiety.

193 y (HR-CS GF MAS) via molecular absorption of phosphorus monoxide.

194 Black phosphorus nanosheets (BPs) show great potential for var

195 how the chemical features of the high-energy phosphorus-nitrogen bond shape the dominant position of

196 of SP-C and cholesterol by deuterium NMR and phosphorus NMR and by electron spin resonance.

197 l-plane thermal conductivities of thin black phosphorus obtained from a new four-probe measurement ex

198 a transistor channel made of flakes of black-phosphorus or InAs nanowires.

199 n compared with the wild type in response to phosphorus or nitrogen starvation.

200 ailability, but the opposite was true in low phosphorus or potassium availability.

201 ers accelerates dissociation of the unloaded phosphorus-oxygen bond orthogonal to the pulling axis, w

202 2 -fixing tropical trees would have distinct phosphorus (P) acquisition strategies allowing them to e

203 on the biogeochemistry of carbon (C), N, and phosphorus (P) across different terrestrial ecosystems.

204 Here, we test how nitrogen (N) and phosphorus (P) affect Rdark and its relationship with ph

205 Uncertainty exists over the importance of N, phosphorus (P) and molybdenum (Mo) availability in contr

206 roles of total carbon (C), nitrogen (N) and phosphorus (P) availabilities and ratios, together with

207 Phosphorus (P) availability in soils limits crop yields

208 We show that phosphorus (P) competition and allelopathy by the microb

209 temperature influence soil nitrogen (N) and phosphorus (P) concentrations and their stoichiometry is

210 Phosphorus (P) deficiency limits plant growth and yield.

211 erns and temporal trends of nitrogen (N) and phosphorus (P) deposition are important for quantifying

212 In soils, phosphorus (P) exists in numerous organic and inorganic

213 nimizing the consumption of nitrogen (N) and phosphorus (P) fertilizers.

214 particular, we noted a 24.3-fold increase in phosphorus (P) flux between pre-European and modern sedi

215 rganic, occluded, adsorbed, and precipitated phosphorus (P) forms, which differ depending on soil for

216 fungi and rely on this symbiosis to scavenge phosphorus (P) from soil.

217 on the potentially growth-limiting nutrient phosphorus (P) had not to our knowledge been analyzed gl

218 ers, the ratios of silicon (Si)/nitrogen (N)/phosphorus (P) have changed dramatically as anthropogeni

219 Nitrogen (N) and phosphorus (P) have key roles in leaf metabolism, result

220 Excess Phosphorus (P) in agriculture is causing serious environ

221 outputs, and retention for nitrogen (N) and phosphorus (P) in seven subwatersheds of the Mississippi

222 Phosphorus (P) is an essential nutrient for living organ

223 Phosphorus (P) is one of the essential nutrients for pla

224 Molecular mechanisms of phosphorus (P) limitation are of great interest for unde

225 in Panama to inform model representation of phosphorus (P) limitation of tropical forest productivit

226 orus inputs).The impact of climate change on phosphorus (P) loss from land to water is unclear.

227 nsport (Jmax )), leaf mass, nitrogen (N) and phosphorus (P) per unit leaf area (Ma , Na and Pa , resp

228 gen deficiency and in turn promotes sediment phosphorus (P) release (A).

229 However, CANDO does not currently target phosphorus (P) removal.

230 populations were under dual nitrogen (N) and phosphorus (P) stress, as genes involved in scavenging o

231 medium containing Phi, as the sole source of phosphorus (P), can serve as an effective and efficient

232 ical cycles of carbon (C), nitrogen (N), and phosphorus (P), resulting in shifting stoichiometry that

233 The level of nitrogen (N), phosphorus (P), zinc (Zn), iron (Fe), and copper (Cu) in

234 d transporting carbon (C), nitrogen (N), and phosphorus (P).

235 NR2) experimental nutrient (nitrogen [N] and phosphorus [P]) additions to five forest streams.

236 nutrient enrichment experiment (nitrogen, N; phosphorus, P; potassium, K).

237 guests that may be used in this way is white phosphorus (P4 ), whose inherent reactivity towards oxyg

238 monotonic decreases in leaf water (LWC) and phosphorus (Pmass ) contents and an increase in leaf mas

239 The contents and properties of soil organic phosphorus (Po) largely drive ecosystem productivity wit

240 gions, a proportion of the dissolved organic phosphorus pool can be accessed by microbes employing a

241 Phosphorus quantification and nondestructive X-ray compu

242 of ground-layer plant community nitrogen to phosphorus ratios across all regions.

243 itrogen ratios and increased their carbon-to-phosphorus ratios in response to low dissolved phosphoru

244 und lower litter quality and higher nitrogen:phosphorus ratios in the tropics.

245 c populations tended to have lower carbon-to-phosphorus ratios than single cell cyanobacterial groups

246 ad range of cellular carbon- and nitrogen-to-phosphorus ratios.

247 We place our phosphorus record in a quantitative biogeochemical model

248 transporters has implications for the marine phosphorus redox cycle, and might aid the use of phosphi

249 ple functions for oxygen controlled-release, phosphorus removal and less impact on water pH.

250 when grown on 10-CW; meanwhile, nitrogen and phosphorus removal efficiencies rose to 86.8 +/- 1.1% (p

251 Maximum soluble phosphorus removals of 70-80% were observed in mixed bat

252 Approximately 60% of the phosphorus retained in the filter media was recovered in

253 n the upper 20 cm of the columns showed high phosphorus retention.

254 The electronic band structure of phosphorus-rich GaNxPyAs1-x-y alloys (x 0.025 and y >/

255 o nitrogen ratio (C/N ratio), soil available phosphorus (SAP), soil NH4(+)-N, soil NO3(-)N, abovegrou

256 work and find that a combination of enhanced phosphorus scavenging in anoxic, iron-rich oceans and a

257 cular practical importance because algae aid phosphorus sequestration from wastewater and the thus en

258 rm for printed devices.Atomically thin black phosphorus shows promise for optoelectronics and photoni

259 A distinct diel phosphorus signal was observed under low flow conditions

260 ncentrations of PM10-2.5 mass, copper, zinc, phosphorus, silicon, and endotoxin, using land-use regre

261 Plant storage was found to be the dominant phosphorus sink (64% on average).

262 aces capped by additional partially occupied phosphorus sites.

263 growth improves phosphorus capture from low-phosphorus soil.

264 capture, and increases shoot biomass in low-phosphorus soil.

265 precipitation effectively removed increased phosphorus solubilized by acidification at the end of se

266 t aid the use of phosphite as an alternative phosphorus source in biotechnological, industrial and ag

267 f methane in the upper, aerobic ocean, where phosphorus-starved microbes catabolize methylphosphonate

268 ereoselective method for the installation of phosphorus-stereogenic phosphoramidates to nucleosides t

269 the field and greenhouse confirm that, under phosphorus stress, resource allocation is shifted from s

270 as a response to changes in regional excess phosphorus supply due to sea level-driven variations in

271 uld contribute 80% of winter total dissolved phosphorus (TDP) loading in this watershed ( approximate

272 s significant amounts of N (nitrogen) and P (phosphorus); therefore it has been successfully used as

273 In the field under low phosphorus, these genotypes had 43% smaller root cross-s

274 urements indicate that PMMA passivated black phosphorus thin film flakes can stay pristine for a peri

275 nanocrystals is the effective extraction of phosphorus through an oxidation reaction, which promotes

276 uggested based on boron, silicon, germanium, phosphorus, tin, and metal di-chalcogenides.

277 itation including phosphorus concentrations, phosphorus to nitrogen, and carbon ratios, oxygen isotop

278 linear models for total nitrogen (TN), total phosphorus (TP), stoichiometry (TN:TP), and Chl.

279 ensemble of future climate simulations, two phosphorus transfer models of contrasting complexity and

280 tilization of the lithium phosphinidene as a phosphorus transfer reagent for a wide range of organic

281 impact of projected climate change on future phosphorus transfers, and to assess what scale of agricu

282 Omegamum, which is the lowest value in black phosphorus transistors without degradation of ION/IOFF r

283 amics and role of these polymers crucial for phosphorus uptake and storage.

284 lation of specific Pht1 transcripts and high phosphorus uptake by mycorrhizal plants.

285 and -external fungal structures, mycorrhizal phosphorus uptake, and accumulation of transcripts encod

286 system, using (33) P to quantify mycorrhizal phosphorus uptake.

287 ere, we spatially Raman map exfoliated black phosphorus using confocal fast-scanning technique at dif

288 mitant formation of benzene from an unstable phosphorus(V) intermediate, yielding (C5 Me5 )2 Th[kappa

289 Phosphorus was immobilized employing insoluble La2O3 to

290 Phosphorus was introduced as scalar to compensate for di

291 mide; Dipp: 2,6-diisopropylphenyl) and white phosphorus was revisited.

292 half in pistils under drought, while stamen phosphorus was unaffected by environment.

293 Furthermore, leveraging a 10 nm-thick black phosphorus, we continuously tune its bandgap from approx

294 aging of O2, pH, iron, sulfide, calcium, and phosphorus, we found that tropical seagrasses are able t

295 Nitrogen and phosphorus were added at different N:P ratios using incr

296 rphous solid granules containing calcium and phosphorus were pervasive in the mitochondrial matrices

297 y of mechanically exfoliated few-layer black phosphorus, with thickness ranging from 2 to 15 layers a

298 m eutrophic waters with 0.35 g m(-3) soluble phosphorus would include 5-17.5 USD electricity costs an

299 presence of a hydrogen acceptor, such as the phosphorus ylide, when combined with the alkylidene comp

300 nd Mg(+2) QTLs, twenty-seven QTLs for tissue Phosphorus, Zinc, Iron, Manganese, Copper, Sulphur and B