ライフサイエンスコーパス: nitrogen

1 at resides between Asp-222 and the pyridinyl nitrogen.

2 tion of NO3(-) is anisotropic and minimal on nitrogen.

3 lic exchange of electrons, carbon, and fixed nitrogen.

4 re observed in both bioreactors in excess of nitrogen.

5 removed more than 85% of the total inorganic nitrogen.

6 on of a rosemary extract and packaging under nitrogen.

7 attack by the only weakly nucleophilic amide nitrogen.

8 to the control for creatinine and blood urea nitrogen.

9 arization transfer catalyst to hyperpolarize nitrogen-15 in a variety of molecules with SABRE-SHEATH

10 een a ketone-like oxygen and a pyridine-like nitrogen across the vacancy site.

11 2O accumulation (8.5.3 +/- 0.9% of the total nitrogen added), which was linked to the depletion of C1

12 tional density functional theory methods and nitrogen adsorption methods altogether, for studying the

13 Mass, carbon, and nitrogen allocation to female whorls (pistils and sepals

14 epals) decreased under high density, whereas nitrogen allocation to male organs (stamens) decreased u

15 this cycle, we combined carbon (delta(13)C), nitrogen amino acid (delta(15)NPhe), and Hg isotope (Del

16 tase (ASNS, which converts glutamine-derived nitrogen and aspartate to asparagine) impaired EC sprout

17 trophic organisms, intrinsically linking the nitrogen and carbon cycles.

18 In addition to genes associated with nitrogen and carbon metabolism, a considerable number of

19 u concentration; thus, we propose that these nitrogen and carboxyl functionalities of aromatic compou

20 Liquefied butane pressurized under nitrogen and doped with arsine and a propylene real samp

21 Human urine contains a high concentration of nitrogen and is therefore an interesting source for nutr

22 or novel thieno-fused five- and six-membered nitrogen and oxygen heterocycles such as thieno[3,2-b]py

23 studies of classical examples like molecular nitrogen and oxygen, benzene, naphthalene and their azad

24 Heterogeneous soil resources, such as water, nitrogen and phosphate, also act as signals that shape 3

25 Nitrogen and phosphorus were added at different N:P rati

26 d by excess loading of macronutrients (e.g., nitrogen and phosphorus) from fertilizers, fossil fuels,

27 electivity to HNO over other reactive oxygen/nitrogen and sulfur species.

28 The carbon, nitrogen and sulphur isotope ratios of feed and fillet w

29 ps that are efficient in acquiring and using nitrogen and that can achieve high seed yields with redu

30 ch between the vertical distribution of leaf nitrogen and the light absorption profile.

31 It provided agriculture with reactive nitrogen and ultimately mankind with nourishment for a p

32 man urine contains significant amounts of N (nitrogen) and P (phosphorus); therefore it has been succ

33 lectro)chemical conversions spanning carbon, nitrogen, and oxygen chemistries.

34 ating and -withdrawing groups, halogens, and nitrogen- and oxygen-containing heterocycles, as well as

35 Furthermore, polar (oxygen-, nitrogen-, and sulfur-containing) analytes found in low-

36 udy reports the effect of different doses of nitrogen applied to soil and/or leaves of Syrah and Char

37 cheating when its building blocks carbon or nitrogen are growth-limiting.

38 h the basic ion mobility equation when using nitrogen as drift gas and also agree with a combination

39 ) for positive ionization in both helium and nitrogen as drift gas.

40 oss four trophic modes, proteins involved in nitrogen assimilation and light-independent chlorophyll

41 on of genes encoding high substrate affinity nitrogen assimilation enzymes (GS-GOGAT system) was simi

42 of excessive nitrogen in generalists but for nitrogen assimilation in specialists.

43 f PII phosphorylation that senses carbon and nitrogen assimilation status.

44 se newly formed bound residues contained one nitrogen atom and had a molecular mass between 375 and 5

45 In this Perspective, the "necessary nitrogen atom" is shown to be a versatile high-impact de

46 t and modifiable Lewis acids centered on the nitrogen atom, which provide stable and well-characteriz

47 nds sequentially bearing three all-saturated nitrogen atoms (N-N-N motif).

48 Within marine systems, nitrogen availability is often the limiting factor in th

49 on of fungivore (Folsomia candida) presence, nitrogen availability, and fungal assembly history.

50 n forms are evaluated, as is how they affect nitrogen availability, metabolism and mobilization.

51 In a region of intermediate soil nitrogen availability, the dominant leaf strategy may be

52 anisms to adapt to fluctuating environmental nitrogen availability.

53 Doubly labeled water and urinary nitrogen biomarkers were used to derive estimates of ene

54 l consists of sequential Pd-catalyzed carbon-nitrogen bond formation followed by Lewis acid catalyzed

55 In this process, carbon-nitrogen bond formation proceeds through a key aminium r

56 During GO:Nx synthesis, different nitrogen-bonding species, such as pyrrolic/graphitic-nit

57 Global-scale nitrogen budgets developed to quantify anthropogenic imp

58 is-189 also increase the pKa of the pyridine nitrogen but, more significantly, influence the position

59 mote biotic attack due to low tissue carbon: nitrogen (C : N).

60 Metal-nitrogen-carbon materials prepared via pyrolysis are pro

61 While iron-nitrogen-carbon materials pyrolytically prepared from ZI

62 Organometallic complexes with metal-nitrogen/carbon (M-N/C) coordination are the most import

63 analysis indicates that for both carbon- and nitrogen-centered radicals, which have relatively early

64 ly, which also closely related to soil total nitrogen changes.

65 em sulfonates, sugar derivatives and organic nitrogen compounds.

66 Nitrogen concentration remained almost constant with eac

67 similar in growth-limiting and non-limiting nitrogen concentrations in P. ruminicola 23, whereas E.

68 ing some treatment plants to reduce effluent nitrogen concentrations.

69 precursor gases, such as sulphuric acid and nitrogen- containing highly oxidised organic compounds,

70 ction is compatible with various oxygen- and nitrogen-containing functional groups and afforded the c

71 Benzoannulated nitrogen-containing heterocycles such as indolines, tetr

72 e organic molecules that contain one or more nitrogen-containing moieties, and broadly applicable and

73 centration, and between camera-NDVI and leaf nitrogen content, though weaker relationships between ca

74 Nitrogen contents increased with the progression of puri

75 An examination of the potential nitrogen 'cost' of siderophore production reveals that i

76 est that, in the presence of glucose, carbon/nitrogen cross-talk is likely involved in the response t

77 mium, is an integral component of the marine nitrogen cycle and contributes significant amounts of ne

78 ped to quantify anthropogenic impacts on the nitrogen cycle do not explicitly consider nitrate stored

79 fuelled by chemoautotrophic production and a nitrogen cycle dominated by nitrogen loss processes usin

80 the emergence of a pervasive aerobic marine nitrogen cycle.

81 complete understanding of global carbon and nitrogen cycling and a reduction in the uncertainty of c

82 sults of these incubations shed new light on nitrogen cycling complexity and possible factors underly

83 l factors and anammox was the most sensitive nitrogen cycling pathway responding to variation of the

84 of the microbiome of H. heliophila represent nitrogen cycling taxa that have the potential to contrib

85 lta(15)NNO3 and delta(18)ONO3 to investigate nitrogen cycling.

86 Nitrogen deposition alone increased the soil C input (+2

87 Changes in land use and climate, nitrogen deposition and invasive species are the most im

88 By contrast, trends in climate and nitrogen deposition did not significantly contribute to

89 thropogenic influences of climate change and nitrogen deposition in these systems is critical to impr

90 CO2 concentration, and SO4 and nitrogen deposition on two broadleaf tree species in a t

91 of Marcellus well NOx emissions on regional nitrogen deposition.

92 cing sugars, ethanol, acetic acid, and amino nitrogen did not differ significantly (p<0.05) between c

93 n dioxide (13%), carbon monoxide (0.68%) and nitrogen dioxide (1000 ppm) in air.

94 A new type of nitrogen dioxide (NO2 ) gas sensor based on copper phtha

95 tellite-based measurements of urban form and nitrogen dioxide (NO2) to explore relationships between

96 r (PM10; </=10 mum in aerodynamic diameter), nitrogen dioxide (NO2), and carbon monoxide (CO) and ris

97 whereas among 2,136 boys, sulfur dioxide and nitrogen dioxide exposure in utero, during infancy, and

98 rticle filters, but little change is seen in nitrogen dioxide over the period from 1995 to 2015.

99 proportion, glacier source proportion, total nitrogen, dissolved organic carbon, and pH.

100 ive degree of carbon substrate and amount of nitrogen dopants (i.e., graphitic nitrogen) were modulat

101 ckel nanoparticles encapsulated in few-layer nitrogen-doped graphene (Ni@NC) are synthesized by using

102 uctosyl amino-acid oxidase (FAO) immobilized nitrogen-doped graphene/gold nanoparticles (AuNPs)/fluor

103 elf-assembly technology for the synthesis of nitrogen-doped ordered mesoporous polymers (N-OMPs) is d

104 Nitrogen-doped porous activated carbon monoliths (NDP-AC

105 the CO2 to CO electrocatalysis of metal- and nitrogen-doped porous carbons containing catalytically a

106 cally thin layer-by-layer mesoporous Co3 O4 /nitrogen-doped reduced graphene oxide (N-rGO) nanosheets

107 Thus, nitrogen doping allows the high absorption coefficient o

108 Chitosan-derived, porous nitrogen-enriched carbonaceous carbon nitride catalyst (

109 Here, we show that free ammonia-nitrogen (FAN, which is NH3) altered the glucose ferment

110 pecies richness, precipitation, temperature, nitrogen fertilization (N), and grazing intensity.

111 e formation of infected nodules defective in nitrogen fixation (Fix(-)).

112 ly in the expression of nifH - essential for nitrogen fixation - and could be visualised using marker

113 c interactions can lead to wide variation in nitrogen fixation efficiency, and it is not uncommon tha

114 dicates the potential to estimate biological nitrogen fixation of legume symbioses not only in labora

115 mplete a highly efficient chemical cycle for nitrogen fixation that is mediated by a set of well-char

116 atmosphere, requiring a biologic cycle with nitrogen fixation, nitrification and denitrification.

117 Establishment of symbiotic nitrogen-fixation in legumes is regulated by the plant h

118 production capacity and its role as a model nitrogen fixer.

119 lation to global transcription in the marine nitrogen-fixing cyanobacterium Trichodesmium.

120 legume nodules, rhizobia differentiate into nitrogen-fixing forms called bacteroids, which are enclo

121 n impaired root development and infection by nitrogen-fixing rhizobia.

122 side living plant cells is restricted to the nitrogen-fixing root nodule symbiosis.

123 he symbiotic interaction between legumes and nitrogen-fixing soil bacteria results in a specialized p

124 preconcentration of melamine, a non-protein nitrogen food additive from complex matrices was synthes

125 Mechanistically, glutamine provided nitrogen for asparagine synthesis to sustain cellular ho

126 en cyanide (HCN) as the source of carbon and nitrogen for the synthesis of nucleotide, amino acid and

127 d transient storage of inorganic and organic nitrogen forms are evaluated, as is how they affect nitr

128 s from a coastal environment that assimilate nitrogen from methylamine.

129 rs share metabolomic signatures of perturbed nitrogen handling.

130 psis presents recent amination methods using nitrogen-heteroatom bonds as a powerful and versatile pl

131 Formal hydrogen atom abstraction from the nitrogen-hydrogen bonds in purine nucleosides produces r

132 are utilized mainly for removal of excessive nitrogen in generalists but for nitrogen assimilation in

133 oated by oligolysines to 0.5:1 N:P (ratio of nitrogen in lysine to phosphorus in DNA), are stable in

134 f which requires deprotonation of the indole nitrogen in Trp during its attack on methylcobalamin.

135 oles, and triazoles to provide products with nitrogen incorporated at different sites.

136 at can achieve high seed yields with reduced nitrogen input.

137 put not only reduced the discrepancy between nitrogen inputs and outputs (9.9 kg ha(-1) yr(-1) and 6.

138 eridines is the piperidine ring flip and not nitrogen inversion or rotation about the N-O bond.

139 coli and Salmonella spp. responses to excess nitrogen involve only low substrate affinity enzymes.

140 Critically, the majority of wheat grain nitrogen is derived from amino acids remobilized from ve

141 We find that if the substituted nitrogen is in a meta position relative to both acetylen

142 Furthermore, synglacial sedimentary nitrogen is isotopically heavier than the modern atmosph

143 couple records of ocean redox chemistry with nitrogen isotope ((15)N/(14)N) values from approximately

144 , we measured the naturally occurring stable nitrogen isotope (delta(15) N) patterns that differentia

145 eciation, redox-sensitive trace element, and nitrogen isotope data from a Neoproterozoic (Marinoan) g

146 The interpretation of our nitrogen isotope data in the context of iron speciation

147 mplemented by detection of N2 O released and nitrogen isotope determinations of fern biomass.

148 aroo, while Ruens and Feedlot had the lowest nitrogen isotope values (P</=0.05).

149 reefs across scales by analyzing the stable nitrogen isotopic (delta(15)N) values of the scleractini

150 vational range) and widths of the carbon and nitrogen isotopic niches (which estimates the diversity

151 y Miocene (18-20 Ma) corals exhibit the same nitrogen isotopic ratio offset identified in modern cora

152 reduce ground-layer community-weighted plant nitrogen, leading to the strong stoichiometric convergen

153 Nitrogen levels, particularly under limited situations,

154 On the basis of the reactivity of nitrogen Lewis acids, we prepared, for the first time, c

155 cA enables a more differentiated response to nitrogen limitation and can be advantageous in native ha

156 In contrast, the nitrogen limitation and habitat productivity hypotheses,

157 ption are upregulated by increased salinity, nitrogen limitation and lower temperatures in our model

158 ociated phosphatases are required only under nitrogen limitation condition.

159 ap42-associated phosphatases unresponsive to nitrogen limitation.

160 Under nitrogen-limiting conditions, a fraction of the vegetati

161 The first step to reducing nitrogen load and improving water quality will be contai

162 2O accounted for <1.5% of the incoming total nitrogen load.

163 heric nitrous oxide (N2O) has been linked to nitrogen loading, predicting emissions remains difficult

164 projected future changes in precipitation on nitrogen loading.

165 A second low-lying dark state, involving the nitrogen lone pair (nNpi*), does significantly participa

166 rgies indicated weak interaction between the nitrogen lone pair and proximal radical center in angula

167 production and a nitrogen cycle dominated by nitrogen loss processes using newly available marine oxi

168 Fire-driven carbon and nitrogen losses were substantial in savanna grasslands a

169 In a nitrogen matrix, the cis-to-trans and trans-to-cis conve

170 In cells grown in poor nitrogen medium, the nitrogen permease reactivator kinas

171 ctors had more significant correlations with nitrogen metabolism than physicochemical factors and ana

172 kouts and time-resolved perturbations to the nitrogen metabolism.

173 depleted B. subtilis speD mutant uncovered a nitrogen-, methionine-, and S-adenosylmethionine-suffici

174 ponses of soil fauna, microbial biomass, and nitrogen mineralization shifted from neutral to negative

175 led) due to feedbacks of leaf traits on soil nitrogen mineralization through litter quality.

176 sence tended to reduce microbial biomass and nitrogen mineralization.

177 nk organs and their importance in regulating nitrogen movement in support of metabolism, and vegetati

178 s idea, we coupled an optimality-based plant nitrogen (N) acquisition model with a microbe-focused so

179 ls predict that vertical gradients of foliar nitrogen (N) allocation, increasing from bottom to top o

180 Spatial patterns and temporal trends of nitrogen (N) and phosphorus (P) deposition are important

181 watershed inputs, outputs, and retention for nitrogen (N) and phosphorus (P) in seven subwatersheds o

182 ion, Microcystis populations were under dual nitrogen (N) and phosphorus (P) stress, as genes involve

183 Efficient recycling of subducted sedimentary nitrogen (N) back to the atmosphere through arc volcanis

184 High tissue nitrogen (N) concentrations in N-fixing legumes may be d

185 groups produced root litter that had higher nitrogen (N) content, decomposed faster and resulted in

186 d in water table lowering (WTL) and enhanced nitrogen (N) deposition in Tibetan alpine wetlands.

187 Facing adverse conditions such as nitrogen (N) deprivation, microalgae enter cellular quie

188 Applied nitrogen (N) fertilizer significantly increases the leaf

189 ent that enables direct energy recovery from nitrogen (N) in three steps: (1) ammonium oxidation to n

190 The incorporation of extraneous nitrogen (N) into amino sugars (AS) could reflect the co

191 pinned by a core SDGVM hypothesis that plant nitrogen (N) status is inversely related to increasing c

192 sensor for non-destructive diagnosis of rice nitrogen (N) status.

193 demand for other resources such as water and nitrogen (N), however, the magnitude and direction of ob

194 The level of nitrogen (N), phosphorus (P), zinc (Zn), iron (Fe), and

195 There is increased focus on nitrogen (N)-containing dissolved organic matter (DOM) a

196 e positive charge centralized on the pyridyl nitrogen, N-H(+).

197 analysis exhibited higher reduction of NO to nitrogen (N2) comparing to the predictions by the kineti

198 d higher oxidants (O3) and oxidized reactive nitrogen (N2O5) aloft.

199 sor is used, consistent with the presence of nitrogen neighbors.

200 imized reaction conditions, a broad range of nitrogen nucleophiles and carbon electrophiles are compa

201 d cross-coupling of 1,1-dibromoenamides with nitrogen nucleophiles.

202 cations by the ortho-substituted oxygen and nitrogen nucleophilic groups.

203 d by the pyridyl substituent attached to the nitrogen of the pyridone ring.

204 not the C-6-oxo group, N-1-hydrogen, or N-7-nitrogen, of GDP for the cap formation.

205 the effects of individual chemical forms of nitrogen on magnetic properties.

206 However, the effect of nitrogen on the magnetic properties of graphene has so f

207 rge number of drug or drug-like molecules in nitrogen on the widely available traveling wave IM-MS (T

208 RE) spectroscopy shows hyperfine coupling to nitrogen only when the amide precursor is used, consiste

209 Placebo (nitrogen) or inhaled nitric oxide initiated at 20 ppm wa

210 Adding N2O and N2 effluxes to catchment nitrogen output not only reduced the discrepancy between

211 (-1) yr(-1), respectively), but also between nitrogen outputs from two catchments with different topo

212 comprised a very small portion of the annual nitrogen outputs.

213 or pellet exhaust components (including high nitrogen oxide (NOx), primary particles, or a combinatio

214 hich is of relevance as a catalyst in, e.g., nitrogen oxide emission abatement for environmental prot

215 Atmospheric pollution measurements (nitrogen oxides and particulate matter) were combined wi

216 ste recycling strategy is described in which nitrogen oxides or nitric acid are directly employed in

217 ty approach and 0.5 ppbv by tagging reactive nitrogen oxides.

218 e detection of the common biosignatures from nitrogen-oxygen rich terrestrial-type exoplanets includi

219 ductions in water-soluble organic carbon and nitrogen (p < 0.01) in household air samples.

220 In cells grown in poor nitrogen medium, the nitrogen permease reactivator kinase (Npr1) inhibits TOR

221 ts of three principal fertilizer components (nitrogen, phosphorus and potassium) on the development o

222 Here, we measured carbon, nitrogen, phosphorus, and biomass allocation among flora

223 of these hotspots, and the consequences for nitrogen processing, is still hindered by a paucity of a

224 tion-metal catalysts, ligands and additives, nitrogen-protecting groups, excess reagents and harsh wo

225 In nitrogen, protonated forms of dimethyl methyl phosphonat

226 erolysis liberating an intermediate having a nitrogen radical moiety Fe(III)-N. and a phenoxyl anion.

227 rainfall, soil moisture (SM), the carbon to nitrogen ratio (C/N ratio), soil available phosphorus (S

228 al production of NO and increases oxygen and nitrogen reactive species, and (ii) l-citrulline can rev

229 for biotechnological applications involving nitrogen recovery from urine, and therefore, in this stu

230 key requirement in many processes aiming at nitrogen recovery from urine.

231 de production, carbon dioxide reduction, and nitrogen reduction, where the development of improved ca

232 organic carbon (DOC), chlorophyll, and total nitrogen (reflecting lake sensitivity).

233 CheY, the N-terminal receiver domain of the nitrogen regulation protein NT-NtrC, and the sporulation

234 Anammox processes are increasingly used for nitrogen removal from anaerobic sludge digestion liquor.

235 d with limited plant root systems and poorer nitrogen removal from biofilter effluent.

236 itation/anammox can provide energy-efficient nitrogen removal from the main stream of municipal waste

237 mmox and denitrification suggesting stronger nitrogen removal than upstream sites.

238 d to determine if the ammonia removal, total nitrogen removal, and biomass growth rates at each scale

239 tion, sulfur oxidation, carbon fixation, and nitrogen removal.

240 The nitrogen-removal performance was significantly improved

241 Nitrogen replenishment of nitrogen-starved yeast cells r

242 of the glycolytic genes most affected after nitrogen replenishment.

243 The predicted growth rate under nitrogen-replete and -deplete conditions, as well as the

244 ons are based on a non-hygroscopic dilithium nitrogen-rich salt that serves as both oxidizer and red

245 in is vulnerable to inactivation by reactive nitrogen (RNS) and oxygen species (ROS) that covalently

246 ations reveal that the surface electron-rich nitrogen simultaneously facilitates the initial adsorpti

247 tained on the catalyst dominated with cobalt-nitrogen sites, confirmed by the advanced spectroscopic

248 re widespread in the ocean and are important nitrogen source for bacteria.

249 ecreted waste product but also a fundamental nitrogen source that can support tumor biomass.

250 ile variations in the chemical nature of the nitrogen source were overlooked.

251 lized by the algal endosymbiont as a primary nitrogen source.

252 rbohydrates (glucose, sucrose, fructose) and nitrogen sources (urea, NH4Cl) at various concentrations

253 Anthropogenic nitrogen sources become more important in lower section

254 igestion of various carbon substrates and/or nitrogen sources could alter monomeric saccharide compos

255 Both nitrogen sources stimulated bulk phytoplankton, bacteria

256 as well as the effect of external carbon and nitrogen sources, was thereafter verified.

257 ethods targeting agricultural and stormwater nitrogen sources.

258 ention is being given to reactive oxygen and nitrogen species (RONS), initially generated upon plasma

259 ts were able to scavenge reactive oxygen and nitrogen species (ROS and RNS, respectively), to modulat

260 Plasma-derived reactive oxygen and nitrogen species (ROS/RNS) are assumed the central biolo

261 st transfers electrons to PMS through active nitrogen species and becomes a metastable state of the c

262 copherol is effective scavengers of reactive nitrogen species and prevents DNA bases nitration, what

263 gesting that HDM-induced reactive oxygen and nitrogen species can be neutralized by antioxidants.

264 ) as a "soft" activation agent that deposits nitrogen species exclusively on the surface of commercia

265 sensitivity to reactive oxygen and reactive nitrogen species, as well as increased DNA damage and im

266 An arsine in nitrogen standard was used for optimization and evaluati

267 Nitrogen standards for discharge of wastewater effluent

268 Metabolite patterns were distinct from nitrogen starvation and other abiotic stresses commonly

269 Nitrogen replenishment of nitrogen-starved yeast cells resulted in substantial tra

270 ed with associated acyl chain editing during nitrogen stress, in contrast to an overall decrease in t

271 ntly reported that a variety of couplings of nitrogen, sulfur, oxygen, and carbon nucleophiles with o

272 undance, diversity and cycling of carbon and nitrogen than 'undisturbed' ecosystems, and that even if

273 ) system for determination of total Kjeldahl nitrogen (TKN) was developed for estimating total protei

274 e and contributes significant amounts of new nitrogen to oligotrophic, tropical/subtropical ocean sur

275 reaction conditions that aid coordination of nitrogen to Pd(II), which is rate limiting, and directly

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

277 ial functionalization of the amine and amide nitrogens to rapidly produce diverse analogues.

278 geography, salinity and, to a lesser extent, nitrogen, to be strong determinants of community composi

279 Microbial nitrogen transformation processes such as denitrificatio

280 hat nitrification is a key process governing nitrogen transformation.

281 otential to contribute to a diverse array of nitrogen transformations in the sponge holobiont.

282 Essential functions of nitrogen transporters in source and sink organs and thei

283 s-talk is likely involved in the response to nitrogen upshift.

284 ion metrics were mapped, and loci related to nitrogen uptake and floral organ development were locate

285 l plant and meat protein production have low nitrogen usage efficiencies and high energy needs.

286 ed from the classical "enteric paradigm" for nitrogen utilization.

287 Using a quantum sensor associated with the nitrogen vacancy center in diamond, we experimentally de

288 Coherent manipulation of shallow nitrogen-vacancy (NV) color centers enables the probing

289 A fibre-optic probe that integrates a nitrogen-vacancy (NV) diamond quantum sensor with optica

290 ated by simulating quantum open systems with Nitrogen-Vacancy centers, which has become an increasing

291 s for controlling various coherence times of Nitrogen-Vacancy centers; our method is based on a hybri

292 incorporation into the hydrocarbon chain of nitrogen versus oxygen as a mode of ionization is also d

293 osystems are especially impacted by elevated nitrogen, we investigated controls on N2O production mec

294 % of nitrogen were nonmagnetic; however, once doped at 5.1 at

295 amount of nitrogen dopants (i.e., graphitic nitrogen) were modulated by the calcination temperature.

296 -bonding species, such as pyrrolic/graphitic-nitrogen, were formed by replacing of oxygen-containing

297 orophylls, fresh organic matter, and organic nitrogen, whereas in winter, streams were high in phaeop

298 CA II via an interaction of the acidic ring nitrogen with the CA II active site zinc, as well as two

299 At harvest, 62.6 kg of nitrogen would be sequestered in mussel tissue and shell

300 on/2,3-sigmatropic rearrangement, as well as nitrogen ylide formation followed by azetidine ring expa