ライフサイエンスコーパス: maxima

1 tern North Atlantic prevailed during glacial maxima.

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

3 and the noradrenergic systems, are at their maxima.

4 the same area and thickness at the resonance maxima.

5 verning the hitherto unknown CHF enhancement maxima.

6 isogenic cells may display multiple distinct maxima.

7 ming covariance to emphasize coincident peak maxima.

8 oincident bacterial productivity and biomass maxima.

9 an alternation of positive and negative ECD maxima.

10 ing a fitness landscape characterized by two maxima.

11 NbN stripes and result in local absorptance maxima.

12 all taxa of invertebrates during the thermal maxima.

13 n the adenylyl cyclase CyaG from Arthrospira maxima.

14 s were most abundant at the deep chlorophyll maxima.

15 alysis of variance of joint angle minima and maxima.

16 nsiderations and the relative payoff between maxima.

17 he adjacent continental shelf during glacial maxima.

18 cane sugars at yields near their theoretical maxima.

19 nce at ambient pressure of two specific heat maxima.

20 hat particle size can be inferred from shift maxima.

21 er interglacials and their preceding glacial maxima.

22 6 nm) blue-shifts in excitation and emission maxima.

23 g primordia, overlapping with auxin response maxima.

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

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

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

27 esonant character of the trapping efficiency maxima.

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

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

30 Ecklonia maxima, a brown alga which grows abundantly on the west

31 flavonols except kaempferol have absorption maxima above 440nm and so readings at 420nm are erroneou

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

33 ins, deformations, long-range forces, energy maxima, adhesion minima, as well as the instability (whe

34 mechanisms in the EFP of pumpkin (Cucurbita maxima) after leaf damage.

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

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

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

38 Differences in narB subgroup abundance maxima and abundance patterns support the view that subg

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

40 26 Mya and 3 Mya, the estimated date when C. maxima and C. moschata diverged.

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

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

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

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

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

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

47 ns, and mismatches by the change of emission maxima and intensities of fluorescence and that can be a

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

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

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

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

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

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

54 movment, experienced semidiurnal temperature maxima and minima.

55 erate a triphasic tuning curve with distinct maxima and minima.

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

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

58 5-50.5 ka and 37.5-33 ka that lead obliquity maxima and precession minima.

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

60 s (ROS) with tunable excitation and emission maxima and sensitivity to endogenously produced H(2)O(2)

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

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

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

64 We conducted studies on pumpkin (Cucurbita maxima) and cucumber (Cucumis sativus) to determine the

65 asurements are the number of observed peaks (maxima) and peak standard deviation in the regions and t

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

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

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

69 All fluorophore emission maxima, and nearly all absorption maxima were significan

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

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

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

73 of the cultivars belonging to the species C. maxima are characterised by a higher content of fatty ac

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

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

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

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

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

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

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

81 icient separation of absorbance and emission maxima, as well as for excitation with conventional two-

82 Activation maxima associated with visuospatial and mnemonic process

83 e basis of the shift in the batho absorption maxima at 10 K [lambda(max) band (native) = 544 +/- 2 nm

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

85 ) to form a low-spin complex with UV-visible maxima at 362, 418, and 537 nm and when reduced to ferro

86 rrinoid-containing proteins, with absorbance maxima at 370 and 420 nm and a band of broad absorbance

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

88 and 537 nm and when reduced to ferrous gave maxima at 424, 527, and 559 nm.

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

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

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

92 broad absorbance between 450 and 600 nm with maxima at 525, 490, and 550 nm.

93 d absorption band in the visible region with maxima at 540 and 610 nm and redox potentials E(1/2)(0/+

94 is, had absorbance and fluorescence emission maxima at 566 and 574 nm, respectively.

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

96 e range 660-710 nm and fluorescence emission maxima at 680-740 nm.

97 protein (iRFP) with excitation and emission maxima at 690 nm and 713 nm, respectively.

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

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

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

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

102 from <0.045 to 0.12, 1.82, and 12.8 g/h with maxima at highest temperatures and shortest residence ti

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

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

105 ncreased after the onset of light, exhibited maxima at the end of the day, and decreased during the n

106 The model predicts the location of density maxima at the locus of a near-constant fraction of the l

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

108 s before, with intense electronic absorption maxima at ~410 and 760 nm.

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

110 t for luteolin and orientin, have absorption maxima below 400nm.

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

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

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

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

115 mboo (Phyllostachys nuda), squash (Cucurbita maxima), castor bean (Ricinus communis), and tomato (Sol

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

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

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

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

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

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

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

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

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

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

126 rom the hematophagous insects Dipetalogaster maxima (DMAV) and Triatoma infestans (TIAV) were express

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

128 duction rates of A. sulfonivorans showed two maxima due to its pleomorphic growth lifecycle.

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

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

131 The colony experienced five population maxima during the Holocene.

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

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

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

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

136 Although maxima for denitrification and nitrification occur at op

137 transfer strengthened at glacial ice-volume maxima for every glacial-interglacial transition, with m

138 fluorescent nucleobase probes with emission maxima from 379 to 419 nm and fluorescence quantum yield

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

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

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

142 em proteins, C. maxima phloem protein 16, C. maxima GTP-binding protein, and C. maxima phosphoinositi

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

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

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

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

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

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

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

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

151 cle, with a female maxima in July and a male maxima in December.

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

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

154 female for most of the cycle, with a female maxima in July and a male maxima in December.

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

156 using a new statistical test that focuses on maxima in orbital forcing.

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

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

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

160 ize distribution either flat or with a small maxima in the accumulation mode (0.5-2 mum).

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 the biaryls was used for tuning of emission maxima in the broad range of 366-565 nm.

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

165 al pattern, with hourly PM(10) concentration maxima in the evening (7 pm-midnight) and in the morning

166 At the heat capacity maxima in the mixtures, the domain size distributions ch

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

168 (Na(+)) and oxygen (O(+)), exhibit distinct maxima in the northern magnetic-cusp region, indicating

169 yurethane hydrogel D4 and feature absorption maxima in the range 660-710 nm and fluorescence emission

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

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

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

173 nulls of the CD signals were coincident with maxima in the UV spectrum, consistent with exciton coupl

174 wo or more minima in the conduction band (or maxima in the valence band) in momentum space, and if it

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

176 seasonal variability of cell abundance, with maxima in the warm oligotrophic gyres of the Indian and

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

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

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

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

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

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

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

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

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

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

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

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

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

192 , including how the experimental cyclization maxima, observed at DNA lengths that are not an integral

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

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

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

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

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

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

199 concentration transients that had an average maxima of 4.5 +/- 1.1 muM (n = 6 animals, 3-4 injections

200 a terminal alkyne group and having emission maxima of 410-670 nm.

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

202 200 nm), which exhibited electroluminescence maxima of 455, 480, and 525 nm, respectively.

203 minescence emission spectra, which displayed maxima of 479-528 and 518-574 nm, respectively.

204 The dyes have absorbance maxima of 603-697 nm in the window where the solar spect

205 Shifting the absorption and emission maxima of a fluorophore into the visible region increase

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 The absorption maxima of Az48W* display an approximately 23 nm hypsochr

210 ng from 526 to 545 nm, dovetailing well with maxima of channelrhodopsin-2 derivatives ranging from 46

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 Maxima of persistent organic pollutant (POP) concentrati

216 ine-v, which further red-shifts the emission maxima of Renilla luciferases by 35 nm.

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

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

219 Whereas maxima of the average drift velocity can be interpreted

220 These values are very close to the emission maxima of the corresponding ions in solution, indicating

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

222 orresponding to dynamically accessible local maxima of the maximum productivity of the ecosystem.

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

224 rmined pyrite oxidation rates coincided with maxima of the pyrite content, total cell counts, and MPN

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

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

227 in a 95 nm difference between the absorption maxima of the two forms, and (ii) induction of a structu

228 The absorption maxima of these chromophores shift predominantly due to

229 The maxima of these delta-like events are reliably detected,

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

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

232 ures as low as 120 degrees C with conversion maxima of ~45% higher than that achieved with Pt.

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

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

235 erent slopes, directions, and times at which maxima or minima occur.

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

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

238 Africa, reaching up to 2500 ng L(-1), while maxima over the continent of about 2000 ng L(-1) occurre

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

240 With absorption maxima overlapping with the wavelengths of common commer

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

242 ents revealed that three phloem proteins, C. maxima phloem protein 16, C. maxima GTP-binding protein,

243 n using as bait the NCAP, pumpkin (Cucurbita maxima) PHLOEM PROTEIN16 (Cm-PP16).

244 in 16, C. maxima GTP-binding protein, and C. maxima phosphoinositide-specific phospholipase-like prot

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

246 phycobiliproteins of Arthrospira (Spirulina) maxima protect renal cells against mercury-caused oxidat

247 as eIF5A was recently detected in Cucurbita maxima (pumpkin) phloem sap.

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

249 ve rise to chimeric variants with absorption maxima ranging from 526 to 545 nm, dovetailing well with

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

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

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

253 was observed as seen by the red-shift in ECL maxima relative to their corresponding photoluminescence

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

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

256 hloem P-protein plugs from squash (Cucurbita maxima) represent cucurbit members of the SEO family.

257 lex is based on a phloem RBP named Cucurbita maxima RNA-binding protein 50 (CmRBP50), a member of the

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

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

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

261 0% molar ratio copper, the photoluminescence maxima shift from 947 to 1067 nm, with excitation at 360

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

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

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

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

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

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

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

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

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

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

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

273 ocarpus longan, Litchi chinensis, and Citrus maxima, the Taiwanese endemic plant Aglaia formosana, an

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

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

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

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

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

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

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

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

282 m pathway of the symplasmic loader Cucurbita maxima was found to be well coupled with the SECCC.

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

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

285 In Pinctada margaritifera and Pinctada maxima, we identified 80 shell matrix proteins, among wh

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

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

288 The maxima were observed in Santa Monica Bay when sampling t

289 hods of computational chemistry the emission maxima were reproduced with a satisfactory degree of acc

290 roduction, PFAS concentration and deposition maxima were shifted about 30 years toward the past and s

291 e emission maxima, and nearly all absorption maxima were significantly red-shifted when compared to P

292 rmore, phloem exudates of pumpkin (Cucurbita maxima) were analyzed.

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

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

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

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

297 nally, fractions of the salivary gland of D. maxima with native DMAV contain Cu(2+) and display metal

298 rom the wavelengths of UV/Visible absorption maxima with solute H-bond parameters obtained from the f

299 itation profiles for Az48W* exhibit distinct maxima within the absorption envelope.

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