ライフサイエンスコーパス: maxima

1 alysis of variance of joint angle minima and maxima.

2 er interglacials and their preceding glacial maxima.

3 6 nm) blue-shifts in excitation and emission maxima.

4 g primordia, overlapping with auxin response maxima.

5 particularly subsurface ammonium and nitrite maxima.

6 sical sigma-hole region with one or even two maxima.

7 significant (100 nm) blue shifts in emission maxima.

8 ty in the timing and magnitude of the summer maxima.

9 esonant character of the trapping efficiency maxima.

10 tern North Atlantic prevailed during glacial maxima.

11 shifting (+40 nm) of its excitation/emission maxima.

12 and the noradrenergic systems, are at their maxima.

13 the same area and thickness at the resonance maxima.

14 verning the hitherto unknown CHF enhancement maxima.

15 isogenic cells may display multiple distinct maxima.

16 ming covariance to emphasize coincident peak maxima.

17 oincident bacterial productivity and biomass maxima.

18 an alternation of positive and negative ECD maxima.

19 ing a fitness landscape characterized by two maxima.

20 rganizer that interprets wound-induced auxin maxima.

21 ere connected to the mainland during glacial maxima.

22 y and a bathochromic shift of the absorption maxima.

23 st-generated movement amplitude and velocity maxima.

24 yes with red-shifted absorbance and emission maxima.

25 carbon dioxide concentrations during glacial maxima.

26 ains to escape from suboptimal local fitness maxima.

27 gnificant difference in the excimer emission maxima (475-510 nm; Stokes shifts 125-160 nm or 7520-896

28 In the upper ocean, a Pb concentration maxima (64-113 pmol kg(-1)) extended throughout the enti

29 rgy equalled or exceeded measured historical maxima across the US West Coast, corresponding to anomal

30 The Bathycoccus overlapped more often with maxima along Line-P for BI (10 667 +/- 1299 copies ml(-1

31 open ocean basins, Arctic MeHg concentration maxima also occur in the pycnocline waters, but at much

32 ochromically shifted absorption and emission maxima and a higher photoluminescence quantum yield comp

33 Our data cover multiple insolation maxima and are therefore an important benchmark for test

34 zone and coincided with secondary NO(2) (-) maxima and available NH(4) (+) .

35 e report high-quality genome sequences of C. maxima and C. moschata and provide evidence supporting a

36 26 Mya and 3 Mya, the estimated date when C. maxima and C. moschata diverged.

37 Sequential Eimeria maxima and C. perfringens challenges significantly induc

38 , but sour orange is an F1 hybrid of pure C. maxima and C. reticulata parents, thus implying that wil

39 easuring several features of local intensity maxima and classifying them with a supervised random for

40 the case of cultivars belonging to Cucurbita maxima and Cucurbita pepo species, while a slight increa

41 ding the molecules from the intensity of the maxima and exposing them only to the lower intensities (

42 tial for regulating formation of auxin local maxima and gradients.

43 approximately 100 nm in localized absorption maxima and increased electron affinities.

44 We suggest that glacial maxima and lowering of sea level caused anomalous meltin

45 by matching seasonal SST and skeletal Sr/Ca maxima and minima in modern corals.

46 ily oscillations in current with the current maxima and minima occurring during daylight hours.

47 Surprisingly, we find that the maxima and minima of the lateral force are not produced

48 minima of the voltage responses against the maxima and minima of the stimuli.SIGNIFICANCE STATEMENT

49 s obtained in the literature by plotting the maxima and minima of the voltage responses against the m

50 th two in-plane easy axes shows well-defined maxima and minima that can serve as two binary logic sta

51 able to observe alternations of conductance maxima and minima with gate voltage.

52 magnetoresistance oscillatory extrema, i.e., maxima and minima, disappear rather asymmetrically with

53 movment, experienced semidiurnal temperature maxima and minima.

54 How auxin maxima and MP direct initiation of flower primordia is p

55 re associated with changes in auxin activity maxima and PIN localization.

56 5-50.5 ka and 37.5-33 ka that lead obliquity maxima and precession minima.

57 oles display remarkably red-shifted emission maxima and pronounced positive solvochromicity, spanning

58 si0 yield more symmetric profiles with broad maxima and slow, uniform propagation of twist.

59 nts over the Indo-Pacific Ocean during solar maxima and the following 1-2 y.

60 from annual field surveys indicated that S. maxima and the hybrid were more susceptible to bleaching

61 on between the spectral position of the LSPR maxima and the maximum enhancement factor (EF).

62 low-type relationship between the absorption maxima and the thermal isomerization rate suggesting a l

63 side chains, (c) blue-shifted Qy absorption maxima, and (d) a sigmoid-shaped circular dichroism spec

64 s in the 27, 54, and 108 nm channels exhibit maxima, and at 0.1 mM NaCl, the electroosmotic mobility

65 ed oils (PSO) from Cucurbita pepo, Cucurbita maxima, and Cucurbita moschata cultivated in Brazil.

66 Auxin polar transport, local maxima, and gradients have become an important model sys

67 have different thermal stability, absorption maxima, and quantum yields.

68 ed shift in both the absorption and emission maxima, and the effect became especially noteworthy in t

69 as intensity changes, shifts in fluorescence maxima, and variations in lifetimes, among many others.

70 ger vertical gold segments large absorptance maxima appear in 3p-periodic designs due to E-field enha

71 shows a complex behavior whereby additional maxima are developed at field dependent angles.

72 or the generation of the secondary lightning maxima are discussed based on the presence and potential

73 Instead, the maxima are shifted along the great circle of the sphere

74 ve markers like first- and second-derivative maxima are used.

75 n epistasis, and the number of local fitness maxima, are distorted in the inferred landscape.

76 phase slips of the CDW, and that dissipation maxima arise from hysteretic behaviour of the CDW phase

77 al studies, LET-dependencies with pronounced maxima around 100-200 keV/mum occur on nanometre scale f

78 could facilitate effective utilization of E. maxima as an oral antidiabetic drug or functional food i

79 rowth depends on PIN1-mediated lateral auxin maxima as well as subsequent internal auxin drainage and

80 Similarly, exposure to air temperature maxima associated with delayed fledging, reduced fledgli

81 Activation maxima associated with visuospatial and mnemonic process

82 n rates, we derive energy distributions with maxima at 2.06 +/- 0.13/1.88 +/- 0.11 eV and widths of 0

83 es were characterized by excitation/emission maxima at 270/315nm, (310, 370)/455nm, and 430/(550, 680

84 cted by LFP with strong transient absorption maxima at 390 nm.

85 num we identified three ACRs with absorption maxima at 485, 545, and 590 nm, indicating color-sensiti

86 conformations, having their (0,0) absorption maxima at 489 and 522 nm, respectively.

87 , which leads to derivatives with absorption maxima at 503, 587, and 668 nm, respectively.

88 iven proton pumps that absorb visible light (maxima at 520-540 nm).

89 ket that creates spectral sensitivities with maxima at 590 to 610 nm, the most red-shifted channelrho

90 luciferases exhibit NIR bioluminescence with maxima at 670 nm and 720 nm, respectively.

91 ndicator (GECI) with excitation and emission maxima at 678 and 704 nm, respectively.

92 orescence in the near-infrared with emission maxima at 691-700 nm.

93 WMG1 and WMG2 show absorption maxima at around 800 nm, which favors tissue penetration

94 The excess sorption isotherms show maxima at bulk CO(2) densities of approximately 0.15 g/c

95 aped cells, Pom1 kinase forms gradients with maxima at cell poles.

96 We report here on electron transfer rate maxima at donor-acceptor separations of 30.6 A, observed

97 fulvic acids to the hydrophobic surface with maxima at moderate doses, while O3 decreased their sorpt

98 ane lipids showed similar distributions with maxima at the chemocline.

99 Both sigmai and DeltaHf,ox show maxima at x=0.15 and 0.20 for the singly and doubly dope

100 transmission minima and the sharp resonance maxima bear a strong resemblance to the extraordinary op

101 rC leads to relatively low energy absorption maxima between 350 and 550 nm in THF with high absorptio

102 wavelengths longer than 500 nm and emission maxima between 620 and 660 nm.

103 gene expression and localized auxin activity maxima, both of which are known to promote leaflet forma

104 cells competent to respond to auxin hormone maxima by giving rise to new organs.

105 ifts of both the absorption and fluorescence maxima by more than 120 and 213 nm, respectively.

106 ana is estimated to be closely related to C. maxima, C. heterophylla var. thunbergii and the Colurnae

107 axis, tend to exhibit regularly spaced local maxima, called "domes", separated by steep troughs.

108 ttle as 1 degrees C above the average summer maxima can cause the breakdown of this symbiosis, termed

109 revealed the formation of two new absorption maxima characteristic of Cob(I)alamin.

110 We were able to identify all C. maxima chromosomes in the same metaphase cells using mul

111 These reactive dyes exhibit absorption maxima close to 450 nm and emission above 600 nm.

112 and antiphase (half-period lag, so consumer maxima coincide with minima of the resource species).

113 tribution of DNRA rates and diatom abundance maxima coincided, suggesting that DNRA was the main ener

114 s, lower flashiness response, and lower flow maxima compared to similarly developed watersheds in lan

115 res reached or exceeded the long-term summer maxima, coral growth during summer periods was equal to,

116 dorsolateral prefrontal cortex (dlPFC; local maxima corrected to P </= 0.001).

117 These results suggest that E. maxima could be a natural source of potent antioxidants

118 formation, as well as time-resolved peak and maxima count for longitudinal strain and axial deformati

119 For all study species, critical thermal maxima (CT(MAX) > 20 degrees C) far exceeded the stream

120 Infection reduced the critical thermal maxima (CTmax) of hosts by up to 4 degrees C.

121 rovides a specific context to auxin response maxima culminating in leaf primordia initiation.

122 lections from one progenitor species, Citrus maxima, cultivated mandarins are introgressions of C. ma

123 Deep Chlorophyll Maxima (DCMs) are subsurface peaks in chlorophyll-a conc

124 varieties belonging to the species Cucurbita maxima Duch. and Cucurbita pepo L.

125 whereas proxies of export production exhibit maxima during ice age terminations.

126 as a mechanism for maintaining proper auxin maxima during leaf margin morphogenesis.

127 The colony experienced five population maxima during the Holocene.

128 entrations and maxima urine corresponding to maxima dust for the pairs bis(1,3-dichloro-2-propyl) pho

129 tophysical properties, namely the absorption maxima, emission maxima, Stokes shifts, vibronic progres

130 alyses (also in Brassica napus and Cucurbita maxima) employing complementary electrophysiological app

131 ivities are nonlinear with temperatures, the maxima equal kappamax/kappamin, where two extremes denot

132 ochromic shifts in its fluorescence emission maxima following compression, a composite containing a m

133 ng; a surprising result given that the daily maxima for control and NTW scenarios were identical.

134 Although maxima for denitrification and nitrification occur at op

135 d of pumpkin flesh 'Melon Yellow' (Cucurbita maxima) fortification with calcium.

136 e range of 530-535 nm and full-width at half-maxima (fwhm) of <25 nm are particularly desirable for a

137 A model of range expansions during glacial maxima (GM) for cold-adapted species is generally accept

138 d from each individual test (EEG-fMRI global maxima [GM]/ESI maximum) and from the combination of bot

139 Auxin maxima have been shown to maintain meristematic activity

140 diterranean coast; and earlier soil moisture maxima have led to earlier winter floods in western Euro

141 flux through the nanowire and corresponding maxima (having magnitudes of almost a conductance quantu

142 ariability and levels in excess of permitted maxima highlighted the importance of monitoring vegetabl

143 lower detection limit of 7x10(-9)M, current maxima (Imax) of 92.55microA and Michaelis-Menten (Km) c

144 ximum that is hidden among many poorer local maxima in a search space.

145 ison, with calcium present, glutamate showed maxima in adsorption at both low and high pH, whereas ly

146 These pigments exhibit absorption maxima in between 532-550 nm and 457-485 nm, respectivel

147 o reproduce the trend of observed absorption maxima in both A1 and A2 rhodopsins, reveal a Barlow-typ

148 Here we report on the existence of maxima in CHF enhancement at intermediate texture densit

149 ed dose-response curves were identified with maxima in either the nanomolar or low micromolar NAADP c

150 resolved harmonics are represented by local maxima in firing rates along the tonotopic axis, has bee

151 nstrated curtailed sexual reproduction of E. maxima in HS chickens.

152 nd V lateral root primordia; decreased auxin maxima in indole-3-acetic acid (IAA)-treated root apical

153 began in April 2018, showed two surface flow maxima in June 2018 and May 2019, and terminated followi

154 ement, suggesting the existence of a line of maxima in kappaT (LMkappaT).

155 in glioblastoma tumor cells, has absorption maxima in NIR region, and showed similar therapeutic eff

156 rcritical liquid-gas transition is marked by maxima in response functions that define a line emanatin

157 ne domains in TEM images and new diffraction maxima in selected area electron diffraction patterns.

158 a choice of performing the search for local maxima in six dimensions on |T(A)|(2), |T*|(2), or k.

159 Two distinct maxima in sulfate reduction rates, of similar orders of

160 were characterized by intensity trends with maxima in the 1990s, reflecting intensified human activi

161 We find several anomalies: maxima in the adiabatic compressibility and nonmonotonic

162 on irradiation of either of their absorption maxima in the blue and red regions.

163 efflux carrier concentrates auxin into local maxima in the epidermis, which position incipient leaf o

164 ure auxin accumulation into highly localized maxima in the fruit valves.

165 is high ruggedness, however, all the fitness maxima in the landscapes are evolutionarily accessible f

166 ere shifted to the left and displayed larger maxima in the mutants.

167 tters with adjustable photoluminescence (PL) maxima in the range of 530-535 nm and full-width at half

168 tution allows modulation of their absorption maxima in the range of 693-805 nm and photophysical prop

169 uence of the formation of sigma-holes, i.e., maxima in the surface electrostatic potential (VS,max),

170 The theory predicts maxima in the TC-concentration dependence indeed observe

171 where Fe(III), U(VI), and FeRB were at their maxima in the vicinity of the injection wells.

172 photoreceptor density, with additional local maxima in which densities were highest.

173 method, the estimated expansion range (smear maxima) in cases was 800-4,400.

174 rties, including substituent-sensitive Soret maxima indicative of ligand noninnocence, strong fluores

175 dy was to investigate the pathogenesis of E. maxima infection in broiler chickens under heat stress (

176 ental effect of HS on the pathogenesis of E. maxima infection in broilers.

177 he aspect ratio (AR) dependence of LSPR band maxima inherently provides an ideal multiplex mechanism.

178 ultivated mandarins are introgressions of C. maxima into the ancestral mandarin species Citrus reticu

179 Regions of import and export maxima into the Arctic are identified along the Arctic C

180 the KwaZulu-Natal province during precession maxima is driven by a combination of increased local eva

181 The shallow MeHg maxima just below the productive surface layer possibly

182 d on cubes of two pumpkin species (Cucurbita maxima L. var. Delica and Cucurbita moschata Duchesne va

183 large separation (70 nm) in their absorption maxima (lambda(max)) and a 2.5-fold increase in molar ex

184 ce resonances (SLRs) with full-width at half-maxima linewidths as narrow as 4 nm from arrays of Au, A

185 The maxima local CO2 fluxes were 36.4 +/- 10.5 and -14.0 +/-

186 electronic structure, with the valence band maxima located away from any particular high-symmetry di

187 (F) ca. 0.4) are observed for emissions with maxima longer than 600 nm in solvents of moderate polari

188 nce quantum yields of up to 0.2 for emission maxima longer than 600 nm.

189 Each of these maxima may be associated with a subpopulation of a parti

190 bly directed by the formation of local auxin maxima, may explain fruit-shape diversification in the B

191 f auxin gradients and the formation of auxin maxima/minima most likely involve the regulation of both

192 nvironment on the corresponding fluorescence maxima must parallel that of D0 absorption spectra.

193 per-binding protein that displays absorbance maxima near 411, 581, and 721 nm and is monomeric in sol

194 s of NO turnover and N2 O production reached maxima near O2 half-saturation constant concentration (2

195 The maxima occur at the (five-dimensional) surfaces of seven

196 tics, unique periodically varying minima and maxima occur throughout the photoacoustic signal power s

197 from transects and time-series, Ostreococcus maxima occurred in the North Pacific coastal upwelling f

198 id growth of the ash cloud, while the second maxima occurred near the time of a deadly pyroclastic de

199 Phi exhibits Aharonov-Bohm oscillations with maxima occurring alternately at half-integer or integer

200 ion bands exhibited large Stokes shifts with maxima occurring at 553 nm for 1-N, 518 nm for 2-N, 508

201 ow spectral response with full-width at half maxima of <20 nm.

202 llent band separation between the absorbance maxima of (E)- and (Z)-isomers in the UV or visible regi

203 oderate to strong fluorescence with emission maxima of 362-554 nm.

204 n pulses were generated with full width half maxima of 417 fs for DNA and 323 fs for DNA-CTMA thin-so

205 200 nm), which exhibited electroluminescence maxima of 455, 480, and 525 nm, respectively.

206 ressure-induced displacement of the emission maxima of a solvatochromic fluorophore (7-diethylamino-3

207 PTTP exhibits maxima of absorption at 507 nm and of emission at 725 nm

208 chromic shifts of 10-15 nm of the absorption maxima of anilines in frozen samples compared to those i

209 red at 600 +/- 30 nm with full-width at half maxima of ca. 200 nm upon ultraviolet light excitation a

210 While 1D profiles showed apparent coincident maxima of Co, Mn, and Fe, 2D images revealed mutually ex

211 shifts, i.e., differences in the absorption maxima of colorless and colored forms, observed for a ra

212 hape of the morphogenic field, causing local maxima of epithelial signals, in particular Shh, at the

213 gth, and the intrinsic fluorescence emission maxima of its single tryptophan blue shifts considerably

214 can be determined by detecting variations in maxima of local fluorescence intensity over time.

215 ift the absorption and fluorescence emission maxima of rhodamine dyes to longer wavelengths.

216 rately reproduce the experimental absorption maxima of rhodopsin and the red, green, and blue color p

217 Altogether, 13 significant local maxima of SF rate for a pair of ethylenes are identified

218 Sharp maxima of some metals in the vertical 1D profiles of GB

219 Whereas maxima of the average drift velocity can be interpreted

220 rences on subdiffraction scales requires the maxima of the intensity pattern to exceed the threshold

221 n spring and autumn correspond to the annual maxima of the organic carbon content (r = 0.56; p = 0.00

222 The maxima of the Ra/Ba intensity ratio distribution histogr

223 We find that the lines connecting the maxima of the response functions converge on approaching

224 olo[3,2,1-jk]carbazole, whereas the emission maxima of the sulfur derivatives is shifted from 375 to

225 The absorption maxima of these chromophores shift predominantly due to

226 linity levels and regular summer temperature maxima of up to approximately 35 degrees C that kill con

227 modynamic consequence of the line of density maxima of water, or emanate from a critical point termin

228 of the vertical ice-shelf deflection reaches maxima of ~1 m at the lake centres, declining to zero at

229 t balance, with these traits achieving their maxima on different diet compositions, giving the appear

230 e. redox potentials, absorption and emission maxima or fluorescence quantum yields, of the synthesize

231 ankton bloom results in transient subsurface maxima or pulses in the sinking mass flux.

232 ropic but nodeless and that they exhibit gap maxima oriented orthogonally in momentum space.

233 ility without affecting the dyes' absorption maxima originates from the twisted geometry of the N-ary

234 Texas and New Mexico, methane columns showed maxima over regions with the highest natural gas product

235 Emission maxima over the series ranged from 595 to 730 nm.

236 With absorption maxima overlapping with the wavelengths of common commer

237 of their physical properties show minima or maxima parallel to the alignment direction.

238 ce was characterised by the critical thermal maxima parameter (CTM50) of the cucumber beetle (Diabrot

239 From these maxima, PIN1 transports auxin into internal tissues alon

240 Conversely, C. maxima PSO showed highest oxidative stability and total

241 ng probes for all nine chromosomes in Citrus maxima (Pummelo).

242 The redox reaction maxima, R(max) and Delta(max) from SEED-R and SEED-I, re

243 These probes had absorbance/emission maxima ranging from 367/454 to 546/576 nm and represent

244 ds as high as 0.89 in toluene, with emission maxima ranging from 474 to 495 nm in the solid state.

245 tum yields of up to phi = >4%, with emission maxima ranging from 725 to 820 nm.

246 taining ~3 x 10(9) kg of ice on average with maxima reaching ~10(10) kg.

247 rigation grape samples when the fluorescence maxima region of catechin and epicatechin, and resveratr

248 Cu depth profiles showing retention of input maxima related to fallout and local industrial discharge

249 ifted (D380E, lambdamax = 533 nm) absorption maxima relative to the wild-type protein (lambdamax = 52

250 ere, we show that the dgt mutant lacks auxin maxima relevant to priming and specification of lateral

251 n, the thermodynamic response functions show maxima reminiscent of the critical divergence.

252 ft coral bleaching was examined in Sinularia maxima, S. polydactyla, and their hybrid S. maxima x pol

253 reads incorporated with pomelo fruit (Citrus maxima) segments.

254 Chromatographic peak maxima (serving as the retention time, tR) above a user

255 ed fluorosolvatochromism, hence the emission maxima shift from 468 nm (8-hydroxybenzo[b]quinolizinium

256 0% molar ratio copper, the photoluminescence maxima shift from 947 to 1067 nm, with excitation at 360

257 ion generated 70 GR variants with absorption maxima shifted by up to +/-80nm, extending the protein's

258 haped extension-rotation profiles with sharp maxima shifted toward positive or negative rotations, de

259 shoot apical meristem (SAM) following auxin maxima signals; however, little is known about the under

260 However, driving LFS at auxin response maxima sites using the DR5 promoter fails to fully rescu

261 nd stable FRs with a broad range of emission maxima spanning from cyan to red.

262 ties, namely the absorption maxima, emission maxima, Stokes shifts, vibronic progressions, extinction

263 opulation size change since the last glacial maxima, suggesting that these populations are not as sta

264 was consistently higher (50%) during glacial maxima than during interglacials.

265 transport results in the formation of auxin maxima that have a key role in developmental patterning.

266 the CalFluors, these probes possess emission maxima that range from green to far red wavelengths, and

267 ntially between the boronic acids, with rate maxima that varied over 6 orders of magnitude.

268 er than the shifts in excitation or emission maxima that would enable precise quantitation through ra

269 d with two Eimeria species, E. tenella or E. maxima, that preferentially infect the cecum and jejunum

270 lations towards environment-specific fitness maxima through acquisition of positively selected traits

271 During glacial maxima throughout that period, species in Europe with te

272 haviors, even at temperatures below critical maxima, tipping the balance in favor of the parasite.

273 mental investigation, we attribute the three maxima to the Fermi energy optimization, band convergenc

274 sites, PCB concentrations showed subsurface maxima (tropical Atlantic Ocean -800 m, North Atlantic -

275 e produces different far-red to nIR emission maxima up to lambda(max)=706 nm with different Fluc muta

276 periments, splashes combined to reach higher maxima (up to 61.7 cm; linear-by-quadratic surface model

277 s were observed in the fluorescence emission maxima upon increasing the solvent polarity.

278 spectral shift at the distinct plasmon band maxima upon specific binding.

279 ns between urine and dust concentrations and maxima urine corresponding to maxima dust for the pairs

280 consistently higher in females and circadian maxima varied by up to 10 h with respect to sex.

281 lymerization resulting in the secondary rate maxima was observed for the hydrophilic-rich mimic.

282 agents for diploid (Riverside) and triploid (Maxima) watermelon seeds.

283 were observed in AgNP-treated Riverside and Maxima watermelons, respectively.

284 stability, hypsochromic shift of absorption maxima wavelengths of initial and cyclic forms, and high

285 For precession maxima, we infer significantly enhanced rainfall in the

286 The absorption maxima were 665 and 704 nm, while the emission maxima we

287 xima were 665 and 704 nm, while the emission maxima were 717 and 719 nm for 3C and 3D, respectively.

288 4 h after consumption while, in plasma, peak maxima were achieved 2 h after intake.

289 Critical thermal maxima were estimated, and ecological niches delineated

290 o [1,4] dioxine (eckol) (3) isolated from E. maxima were evaluated for antiradical and alpha-glucosid

291 chloroform and THF solution the fluorescence maxima were in the range of 440-465 nm, and quantum yiel

292 mer precipitation such that two distinct GPP maxima were separated by a period of foresummer drought.

293 luorescence excitation, and emission spectra maxima when compared to unsubstituted [6]helicene.

294 Surprisingly, we found three power factor maxima when doping Bi with Pb.

295 ly affects the position of UV-vis absorption maxima, which can be tuned in a broad range of 100 nm by

296 e in the sample is repeatedly exposed to the maxima, which exacerbates bleaching.

297 ses, rounding out the TC (n) dome, the three maxima with accompanying superconducting gaps emerging c

298 ly during Heinrich stadials close to glacial maxima with increased ice coverage, probably as a result

299 llele-specific expression analysis in the C. maxima x C. moschata interspecific F1 hybrid and their t

300 maxima, S. polydactyla, and their hybrid S. maxima x polydactyla.