ライフサイエンスコーパス: nitrogen

1 ox process for energy-efficient treatment of nitrogen.

2 imation of crude protein due to chitin-bound nitrogen.

3 n also be formed from an s-block element and nitrogen.

4 diversity effects on stem biomass and canopy nitrogen.

5 organotrophic consortium cycling methane or nitrogen.

6 rients to the bacteria in exchange for fixed nitrogen.

7 up formed by reaction with the cyclic aminal nitrogen.

8 ith bulk stable isotope ratios of carbon and nitrogen.

9 We conducted an in situ whole mature tree nitrogen-15 ((15) N) labeling experiment ((15) NH(4) (+)

10 y regarded as indicating a mantle origin for nitrogen(7-10), in fact represent dominantly air-derived

11 uirements for cell growth and proliferation, nitrogen acquisition and utilization must be tightly reg

12 fertilized plots decreasing in proportion to nitrogen addition-dependent declines in soil pH and loss

13 ces and accounts for the interaction between nitrogen additions and the biochemical processes that co

14 an-induced emissions, which are dominated by nitrogen additions to croplands, increased by 30% over t

15 d exposes more W active sites, optimizes the nitrogen adsorption energy, and facilitates the electroc

16 Materials were characterized using nitrogen adsorption/desorption isotherms, scanning elect

17 ndicated distinct transcriptional responses: nitrogen affects transport of ions such as copper, where

18 180 degrees C and 210 degrees C for 6 h with nitrogen, air or oil as heat-conducting media.

19 and soil pH, but decreased with soil carbon:nitrogen and carbon:nitrogen of microbial biomass.

20 ivated nanostructured metallic precursors in nitrogen and consolidated by spark plasma sintering.

21 y tolerate many donor sites, including basic nitrogen and numerous heterocycles.

22 ermining soil nitrification rate, while soil nitrogen and pH influenced soil nitrification via changi

23 erbivore community alter the ratios at which nitrogen and phosphorus are supplied to plants and test

24 nd associated with growth (respiration rate, nitrogen and phosphorus concentrations, and leaf mass pe

25 Snails in mesocosms enriched with nitrogen and phosphorus had overall higher excretion rat

26 , with lower leaf mass per area, higher leaf nitrogen and phosphorus, faster photosynthetic rates, an

27 root traits, especially root diameter, root nitrogen and specific root length, in driving rhizospher

28 otoionization (APPI)(+)) to characterize the nitrogen and sulfur compounds contained in these samples

29 Ni alloying enables the chemisorption of nitrogen and the lower free-energy change for the *NNH f

30 use, hemoglobin A1c, creatinine, blood urea nitrogen, and estimated glomerular filtration rate.

31 Proteinuria, blood urea nitrogen, and glomerular immune complex deposition were

32 hat competes with denitrification, conserves nitrogen, and minimizes nutrient loss in soils.

33 elative supplies of resources (e.g., carbon, nitrogen, and phosphorus), leading to nonlinear and inte

34 ents namely, ambient (humid) atmosphere, dry nitrogen, and vacuum.

35 Nitrogen- and carbon-containing metabolites have been sh

36 In the wet stream, ammonia and nitrogen are the main products above 120 degrees C.

37 carbons (NACs) with closely-placed graphitic nitrogen as active sites, achieving dihydrogen dissociat

38 Here we report metal-free nitrogen-assembly carbons (NACs) with closely-placed gra

39 increased the abundance of Calvin Cycle and nitrogen assimilation metabolites while suppressing the

40 tively), and long-term shelf stability under nitrogen atmosphere.

41 avorable hyperconjugative donation from each nitrogen atom into neighboring electron-poor sigma bonds

42 the functional groups directly bonded to the nitrogen atom of the ynamides.

43 , bridged bicyclic sultams with a bridgehead nitrogen atom) were outlined, and a number of these comp

44 ionally unreactive C-H bond, proximal to the nitrogen atom, into a versatile chemical entity would be

45 tetrasubstituted carbon atoms attached to a nitrogen atom.

46 able lone-pair repulsion between neighboring nitrogen atoms and maximize the favorable hyperconjugati

47 cids and then volatile carbon species, while nitrogen atoms are oxidized into nitrate ions.

48 Molecular compounds featuring nitrogen atoms are typically regarded as Lewis bases and

49 This strategy couples nitrogen atoms from N(2) with abundant hydrocarbons, and

50 cular mass which often contain oxygen and/or nitrogen atoms in addition to halogens (hHNPs).

51 of nascent carbon atoms and the oxidation of nitrogen atoms into nitro groups.

52 Here, we show that newly introduced nitrogen atoms into the inhibitor scaffold can act as hy

53 With three basic nitrogen atoms that can be protonated, Hoechst can exist

54 uantitative estimates of the basicity of the nitrogen atoms were obtained using conceptual density fu

55 lecules containing internal chains of bonded nitrogen atoms, is of fundamental scientific interest in

56 drogen atoms (H-tpPDI) attached to its imide nitrogen atoms.

57 y by indirect climate effects (e.g., greater nitrogen availability and decreased fungi:bacteria ratio

58 g island-wide surveys of coral bleaching and nitrogen availability within a Bayesian hierarchical mod

59 whose expression is regulated in response to nitrogen availability, but which belong to unknown or hy

60 followed by annealing in 2% hydrogen with a nitrogen balance (2%H(2)-N(2)).

61 Furthermore, we discuss nitrogen-based fuel applications ranging from combustion

62 gress and current research on utilization of nitrogen-based fuels in power applications, covering the

63 Nitrogen-based fuels pose one possible synthetic fuel pa

64 ridge basalts(11), consistent with subducted nitrogen being added to the mantle source.

65 ucial to predicting future changes in marine nitrogen biogeochemistry.

66 ianionic cyanurate ligands linked via silver-nitrogen bonds.

67 Shellfish aquaculture removes nitrogen, but the extent and value of this ecosystem ser

68 Some plants fix atmospheric nitrogen by hosting symbiotic diazotrophic rhizobia or F

69 ntration primary treatment and low carbon-to-nitrogen (C/N) ratio sewage at the secondary biological

70 ams with low chemical oxygen demand (COD) to nitrogen (C/N) ratios.

71 Our finding that excess nitrogen can trigger severe bleaching even under relativ

72 ical relationships with proxies such as leaf nitrogen/chlorophyll content or hyperspectral reflectanc

73 transition metal (M: Fe, Co, or/and Mn) and nitrogen co-doped carbon (M-N-C) catalysts as the most p

74 The effects of argon and nitrogen cold plasma treatments on the lipolytic enzymes

75 ed by a slower conversion to a low-spin iron-nitrogen complex.

76 ort behavior of low molecular weight neutral nitrogen compounds in order to maximize ammonia recovery

77 cement in the periodic table makes catenated nitrogen compounds of interest for development of high-e

78 Nitrogen compounds, fermentable sugars, total phenolic c

79 Change in total dissolved nitrogen concentration, an indication of increased river

80 ion to dimming that gradually increased leaf nitrogen concentration.

81 bit n-type conduction under both ambient and nitrogen conditions; Ni-HAB is found to be ambipolar, wi

82 can play an important role in particular for nitrogen containing functional groups.

83 ding highly toxic iodinated, brominated, and nitrogen-containing DBPs.

84 re unified by the presence of a substituted, nitrogen-containing heterocycle core.

85 ation leads to a great variety of polycyclic nitrogen-containing heterocycles under mild conditions.

86 n to form nitrogen-element bonds en route to nitrogen-containing molecules is a long-standing challen

87 ization of P-phenyl modified phosphorus- and nitrogen-containing phosphaquinolinone heterocycles.

88 The realization of the full potential of nitrogen-containing solid-state materials is limited by

89 d by peat property (bulk density, carbon and nitrogen content), (14) C, (210) Pb and (137) Cs analyse

90 sed with mean annual temperature (MAT), soil nitrogen content, microbial biomass carbon and nitrogen,

91 pecies composition and community-wide foliar nitrogen content.

92 Atomically dispersed and nitrogen coordinated single metal sites (M-N-C, M=Fe, Co

93 has often been attributed to the presence of nitrogen-coordinated, single Ni atom active sites.

94 um oxidation) bacteria are important for the nitrogen cycle in both natural environments and wastewat

95 human influence on ammonia emissions and the nitrogen cycle in the Anthropocene.

96 ow that the effect of subduction on the deep nitrogen cycle may be less important than has been sugge

97 Nitrogenase is a key player in the global nitrogen cycle, as it catalyzes the reduction of dinitro

98 haumarchaeota are important organisms in the nitrogen cycle, but the mechanisms driving their radiati

99 ine N(2) fixation and its role in the global nitrogen cycle.

100 ozoic and ~40% of the Mesoproterozoic ocean, nitrogen cycling dominated.

101 More nitrogen cycling genes were detected in the rare members

102 Microbial functions related to nitrogen cycling showed increased spatial variability un

103 important in understanding marine carbon and nitrogen cycling.

104 e biogeochemical models in simulating global nitrogen cycling.

105 significant consequences for biogeochemical nitrogen cycling.

106 Nitrogen deficiency reduced the average increase to 10%,

107 ed size and yield, likely via the control of nitrogen delivery to the reproductive sinks.

108 derstanding of the implications of increased nitrogen demand to store organic forms of carbon in soil

109 Effects of atmospheric CO(2) fertilization, nitrogen deposition, climate, wildland fire, harvest, an

110 istorical hotspot for atmospheric sulfur and nitrogen deposition, features abundant lakes that are ex

111 (2) , temperature, precipitation regimes and nitrogen deposition, yet few studies evaluate interactio

112 of jasmonic acid, correlating with signs of nitrogen deprivation.

113 (a)pyrene (BaP), sulfur dioxide (SO(2)), and nitrogen dioxide (NO(2)) over two consecutive 24-h sampl

114 try resulted in elevated levels of gas-phase nitrogen dioxide (NO(2)).

115 road traffic day-evening-night noise (Lden); nitrogen dioxide (NO2); and particulate matter (PM) with

116 ltiexposure model identified particulate and nitrogen dioxide air pollution inside the home, urine co

117 each 1-ppb increase in long- and short-term nitrogen dioxide exposure was associated with 3.24 (95%

118 piratory inflammation within the population [Nitrogen Dioxide | American Lung Association].

119 m or 2.5 mum (PM10 and PM2.5, respectively), nitrogen dioxide, ozone, and black carbon.

120 ural gas production and were correlated with nitrogen-dioxide columns at a ratio that is consistent w

121 best explained by species with greater leaf nitrogen dominating upper canopies in mixtures, rather t

122 bers of the NadE family use l-glutamine as a nitrogen donor and are named NadE(Gln) Previous gene nei

123 ivities originate from cooperating graphitic nitrogen dopants induced by the diamine precursors, as d

124 Iron- and nitrogen-doped carbon (Fe-N-C) materials are leading can

125 icate various metal single-atom catalysts on nitrogen-doped carbon (M(1)/CN, M = Pt, Ir, Pd, Ru, Mo,

126 ansition between sulfur and lithium sulfide, nitrogen-doped carbon dots become highly reactive with p

127 ent activity, single iron atoms dispersed on nitrogen-doped carbons (Fe-N-C) have emerged as appealin

128 strated by rational tuning of an assembly of nitrogen-doped nanodiamonds and copper nanoparticles.

129 nalization of coordinated dinitrogen to form nitrogen-element bonds en route to nitrogen-containing m

130 s recent boron examples for the formation of nitrogen-element bonds.

131 Overall, we found that nitrogen enrichment led to an immediate positive increme

132 nced sink capacity in the high light and low nitrogen environment in the field.

133 The growth pressure of the nitrogen feed gas was varied while the growth temperatur

134 Soils amended with nitrogen fertilizer exhibited increased N(2)O production

135 on-farm use as (1) soil amendments to offset nitrogen fertilizer inputs, (2) seed coatings to increas

136 GmVTL1a amino acid substitutions that block nitrogen fixation in Ljsen1 plants reduce iron transport

137 turnover times in the marine subsurface and nitrogen fixation rates in pelagic unicellular cyanobact

138 heavy reliance of the industrial Haber-Bosch nitrogen fixation reaction on fossil fuels, there is a s

139 maturation proteins provided by the NIF (for NItrogen Fixation) assembly machinery.

140 adation-limiting nitrogen through biological nitrogen fixation.

141 proteins play additional roles unrelated to nitrogen fixation.

142 abundance of "centers of calcification" and nitrogen-fixation in GAs.

143 ria have traditionally focused on nodule and nitrogen-fixation phenotypes when hosts are inoculated w

144 f the exopolysaccharide succinoglycan by the nitrogen-fixing bacterium Sinorhizobium meliloti 1021 is

145 ovel form of the heterocyst, the specialized nitrogen-fixing cell of the multicellular cyanobacterium

146 nodulating and nonnodulating species in the nitrogen-fixing clade indicated that the nodulation trai

147 Nitrogen-fixing nodule-inducing bacteria provide nutriti

148 H gene was enriched by a factor of 10 in the nitrogen-fixing reactors (compared to controls) attainin

149 Genetic studies of legume symbiosis with nitrogen-fixing rhizobial bacteria have traditionally fo

150 Nitrogen-fixing root nodulation in legumes challenged wi

151 Nitrogen flushing during ultrasonication process resulte

152 me to engineer a bacterium to deliver a high nitrogen flux to a cereal crop.

153 lar aKG concentrations, thereby sequestering nitrogen from aspartate through glutamic-oxaloacetic tra

154 atio and shift metabolism towards scavenging nitrogen from purines relative to free-living algae.

155 The nitrogen functional chemistry is characterized by C-N do

156 e a 60% linear decrease in volatile reactive nitrogen gas flux (NO(y) = NO, NO(2) , HONO) as ECM tree

157 ped for the conversion from chemically inert nitrogen gas to chiral amino acids, powered by H(2) oxid

158 ffectively treated and converted to harmless nitrogen gas without an external electron donor supply u

159 eatment of ammonia in air with conversion to nitrogen gas without the supply of an extraneous electro

160 orphyrin and amino acid through a main chain nitrogen has been optimized and applied in the synthesis

161 he copper-catalyzed arylation of unsaturated nitrogen heterocycles, known as the Ullmann-Goldberg cou

162 lic adjustments to maintain embryonic carbon/nitrogen homeostasis.

163 mediator substantially weakens the homolytic nitrogen-hydrogen bond strength of a Bronsted acidic ani

164 Pcs with carboxylate functions or quaternary nitrogens (hydrophilic anionic, hydrophilic cationic, am

165 lyzed oxidation of primary C-H bonds beta to nitrogen in an imine of an aliphatic amine, a process th

166 nt exchange and utilization for host-derived nitrogen in the Chlorella genotypes [12, 13] and symbion

167 and stable isotope ratios of Hg, carbon, and nitrogen in the feathers and blood of geolocator-tracked

168 s against mutations that increase carbon and nitrogen incorporation into protein sequences.

169 pared with 0-8 g/d, P < 0.05) and blood urea nitrogen increased with dosage (P = 0.013) and time (P <

170 ext of continuously increasing anthropogenic nitrogen inputs, knowledge of how ammonia oxidation (AO)

171 Importantly, nitrogen interacted with heat stress to increase bleachi

172 verestimate BPE, although models with carbon-nitrogen interactions tend to be more realistic.

173 mework, we tested the hypothesis that excess nitrogen interacts with temperature anomalies to alter c

174 These results suggest that nitrogen is a major driver of the physiological ecology

175 when glutamine, an abundant amino acid when nitrogen is available, binds to the GAF sensory domain o

176 terest in chemical structure and bonding, as nitrogen is uniquely situated in the periodic table to f

177 These data, combined with the carbon and nitrogen isotope contents of the diamonds, indicate that

178 (13)C-carbon and (15)N-nitrogen labeled nutrients are convenient sources of iso

179 Previously, a nitrogen ligand was shown to be involved in coupling a p

180 g root nodulation in legumes challenged with nitrogen-limiting conditions requires infection of the r

181 ts 9% of the total annual Greenwich-specific nitrogen load, 16% of the combined nonpoint sources, 38%

182 ure and other anthropogenic activites (e.g., nitrogen loading) will likely increase CH(4) emissions f

183 Their competition has great implications for nitrogen loss, conservation, and greenhouse gas emission

184 The microbial biomass nitrogen (MBN; total coefficient = 0.19) was nearly of e

185 The properties of catenated nitrogen molecules, molecules containing internal chains

186 ation between the widespread and significant nitrogen (N(2) )-fixing cyanobacterium, UCYN-A and its p

187 by competitive rhizobia that do not maximize nitrogen (N(2)) fixation, resulting in suboptimal yields

188 f greenhouse gases nitrous oxide (N(2)O) and nitrogen (N(2)) in arable soils include high nitrate, mo

189 he Tibetan Plateau to explore the effects of nitrogen (N) addition and rising atmospheric CO(2) conce

190 plant community composition are regulated by nitrogen (N) and phosphorus (P) availability.

191 ii on growth and transcriptome regulation of nitrogen (N) and phosphorus (P) metabolism in winter whe

192 of biologically limiting nutrients, such as nitrogen (N) and phosphorus (P), which can reduce grassl

193 Soil nitrogen (N) availability is critical for grassland func

194 owever, little is known about the role(s) of nitrogen (N) compounds in nectary function.

195 he rhizosphere are an essential link in soil nitrogen (N) cycling and plant N supply.

196 grasslands and their mediated carbon (C) and nitrogen (N) cycling processes at the local scale.

197 The coupling of anoxic nitrogen (N) cycling to the function of HSs as a redox b

198 Anthropogenic nitrogen (N) deposition and resulting differences in eco

199 nditions of chronically elevated atmospheric nitrogen (N) deposition.

200 nd cell-cycle-related gene expression during nitrogen (N) deprivation, and its predicted protein inte

201 rgano-organic interface, showing alkyl C and nitrogen (N) enrichment (by 4 and 7%, respectively).

202 Nitrogen (N) fertilizers can potentially alter spatial d

203 The traditional view holds that biological nitrogen (N) fixation often peaks in early- or mid-succe

204 Biological nitrogen (N) fixation plays an important role in terrest

205 More importantly, soil nitrogen (N) increased in mature deciduous forests throu

206 Optimizing the nitrogen (N) input is crucial to achieving desirable bio

207 all conditions on maize yield, for different nitrogen (N) inputs (0, 80, 160 kg N/ha) for five enviro

208 Nitrogen (N) limits crop yield, and improvement of N nut

209 Human release of reactive nitrogen (N) to the environment has increased 10-fold si

210 e croplands export large amounts of reactive nitrogen (N), which degrades water and air quality and c

211 rite, Allan Hills 84001, preserve indigenous nitrogen(N)-bearing organics by developing a new techniq

212 Reduced forms of nitrogen (NH(x) = ammonia [NH(3)] + ammonium [NH(4) (+)]

213 sulfinyl chlorides in situ with a variety of nitrogen nucleophiles delivers sulfinamides in 32-83% yi

214 Combining sulfinyl nitrenes with carbon and nitrogen nucleophiles enables the synthesis of sulfoximi

215 nterception of ketenimine intermediates with nitrogen nucleophiles such as amines, hydrazines, and TM

216 ubstituted styrenes with internal oxygen and nitrogen nucleophiles undergo oxidative fluorocyclizatio

217 creased with soil carbon:nitrogen and carbon:nitrogen of microbial biomass.

218 found that the soil organic matter and total nitrogen of the + C treatment were 5.2% and 26.6% higher

219 have been compared to heterocycles with two nitrogen or boron atoms, e.g., C(2)B(10)H(12) carboranes

220 esence of an inert, neat buffer gas, usually nitrogen or helium.

221 e many ecological studies focus primarily on nitrogen or protein, and fail to consider carbohydrates,

222 oncentrations of 17 air pollutants including nitrogen oxides (NOX), particulate matter (PM), and comp

223 lters the emission ratios between NMVOCs and nitrogen oxides and hence the ozone chemistry in the eas

224 nt of the blackness of PM(2.5) filters); and nitrogen oxides levels.

225 indicating a negligible long-term impact of nitrogen oxides on the catalytic properties of the model

226 ry and titration of ozone in winter, reduced nitrogen oxides resulted in ozone enhancement in urban a

227 y employing different commercially available nitrogen-, oxygen-, sulfur-, or carbon-based nucleophile

228 ndices of macromolecular distribution, total nitrogen (p < 0.001), and beta-glucan (p < 0.01).

229 m-maximum estimates: 12.2-23.5) teragrams of nitrogen per year (bottom-up) and 16.9 (15.9-17.7) terag

230 bottom-up) and 16.9 (15.9-17.7) teragrams of nitrogen per year (top-down) between 2007 and 2016.

231 US wetlands (about 860 +/- 160 kilotonnes of nitrogen per year) is limited by a spatial disconnect be

232 four decades to 7.3 (4.2-11.4) teragrams of nitrogen per year.

233 ed the effects of adding multiple nutrients (nitrogen, phosphorus and potassium plus nine essential m

234 essential soluble nutrients - particularly, nitrogen, phosphorus and potassium.

235 gging methods incorporating carbon, silicon, nitrogen, phosphorus, and deuterium into NOM are discuss

236 o accelerates the electron transfer from the nitrogen radical intermediate to the Ir(IV) species in t

237 biotic algae also have an elevated carbon-to-nitrogen ratio and shift metabolism towards scavenging n

238 nse to the nutritional status and the carbon/nitrogen ratio of the bacterial cell.

239 h the production of short-chain fatty acids, nitrogen recycling, and amino acid production.

240 ferable to other coastal watersheds pursuing nitrogen reduction goals, both with and without establis

241 approach was employed to quantify and value nitrogen reduction services provided by the shellfish aq

242 The nitrogen-related phosphotransferase system (PTS(Ntr)) of

243 les, e.g. as a transport and storage form of nitrogen, released via endogenous recycling pathways.

244 Cultivated hard clam and eastern oyster nitrogen removal in Greenwich Bay, Connecticut, was valu

245 In this study, a stable nitrogen removal rate (0.13 kg m(-3) day(-1)), together

246 This nitrogen removal represents 9% of the total annual Green

247 s an energy-efficient process for biological nitrogen removal, particularly from wastewater streams w

248 1,2-migration of the organoboron residue to nitrogen, resulting in displacement of 1.[O] and formati

249 Synechococcus that flourishes when iron and nitrogen resupply to surface waters are diminished.

250 little glucose; secreted glutamine and other nitrogen-rich amino acids, indicating active protein bre

251 le bond, length as m-dash]N-Ar5), a class of nitrogen-rich and highly colored compounds, have been kn

252 ground-level NH(3) emissions from composting nitrogen-rich organic waste or post-AD solids.

253 Under nitrogen-rich, carbon-limiting conditions, unphosphoryla

254 PROTEIN 7 (NLP7), a master regulator of the nitrogen signaling pathway in plants.

255 On account of suitable nitrogen sites in COF-DB, the further metalation of COF-

256 trogen content, microbial biomass carbon and nitrogen, soil ammonium, and soil pH, but decreased with

257 nesis and that histidine serves as a crucial nitrogen source during infection.

258 The use of N(2) versus ammonium as nitrogen source during the enrichment process resulted i

259 sides ammonium also glutamine can serve as a nitrogen source under these conditions.

260 cost methodology and allocated by municipal nitrogen source.

261 waste streams is typically considered as the nitrogen source.

262 ther, trimethylsilyl bromide and N(2) as the nitrogen source.

263 vironmental challenge, and diverse watershed nitrogen sources require multifaceted management approac

264 urces, readily prepared azidoformates as the nitrogen sources, and 4-dimethylaminopyridine (DMAP) and

265 n = 156) to explanatory variables describing nitrogen sources, geology, and soil and catchment charac

266 nitrate assimilation in response to various nitrogen sources.

267 Reactive Nitrogen Species (RNS) are a group of bactericidal molec

268 oxyl (OH) and hydroperoxy radicals, oxidized nitrogen species and organic peroxy radicals (RO(2)) in

269 ost insults are reactive oxygen and reactive nitrogen species as well as cellular stress induced by a

270 rs include reactive oxygen species, reactive nitrogen species, and sulfur dioxide.

271 , can also lead to the formation of reactive nitrogen species.

272 tion does not depend on gene expression once nitrogen starvation has set in and occurs indepen-dently

273 Upon nitrogen starvation, Schizosaccharomyces pombe exit the

274 ogical probe of E. coli cell function during nitrogen starvation, we demonstrate that Hfq foci have a

275 he adaptive response of E. coli to long-term nitrogen starvation.

276 ike other CP tags, localize to granules upon nitrogen starvation.

277 sing the ability of T7 phage to replicate in nitrogen-starved bacteria as a biological probe of E. co

278 Cellular nitrogen status modulates phosphorylation when glutamine

279 rom PtsP makes cells "blind" to the cellular nitrogen status.

280 Selective nitrogen substitution into the ortho positions of the ar

281 (TBA) metabolites in the presence of various nitrogen-, sulfur-, or oxygen-containing nucleophiles (e

282 involved in plant responses to environmental nitrogen supply, affecting multiple gene regulatory proc

283 ulfide and by providing degradation-limiting nitrogen through biological nitrogen fixation.

284 scribing the evolution of mantle and surface nitrogen through geological time.

285 ution of soil organic carbon (SOC) and total nitrogen (TN) concentrations in croplands such as switch

286 spheric deposition is an important source of nitrogen to coastal waters.

287 le of silyl radical additions to coordinated nitrogen to form silylamines stands as the lone example

288 d FACE with temperature, drought, ozone, and nitrogen treatments.

289 source (e.g., marine vs terrestrial) and the nitrogen trophic level.

290 n ground-state processes but also highlights nitrogen tunneling and the first example of excited-stat

291 ited oxidation reaction, total volatile base nitrogen (TVBN), peroxide value (PV), malondialdehyde (M

292 lopmental and metabolic processes related to nitrogen use.

293 ing quantum spin magnetometers realized with nitrogen vacancy centres in diamond.

294 orrelations (NCCs) of a system formed by two nitrogen-vacancy (N-V) centers placed in two spatially s

295 Among these, the negatively charged nitrogen-vacancy (NV(-)) defect in diamond is attracting

296 crease bleaching severity up to twofold when nitrogen was high and heat stress was relatively low.

297 Overall, apparent ileal digestibility of nitrogen was similar in vitro and in vivo and the differ

298 Our reactors fixed appreciable quantities of nitrogen with a rate of 11.8 mg N L(-1) day(-1).

299 Substitution of the lactam nitrogen with electronically different groups affords di

300 ubstitution on both the metal (M) and carbon/nitrogen (X) sites presents promising routes for tailori