ライフサイエンスコーパス: seasonal

1 terionella formosa have a broad variation in seasonal abundance leading to the possibility that diato

2 hypothesis that differences in the timing of seasonal activity are driven by differences in the rate

3 However, shifts in seasonal activity patterns, or phenology, may also have

4 The timing of dormancy is therefore a key seasonal adaptation, and it evolves rapidly with changin

5 To unveil them, here we have analyzed seasonal adjustment of the photosynthetic machinery of S

6 nial rhinitis symptoms and positive SPT with seasonal allergens only (discrepant group) were subjecte

7 e kinetics in a panel study of subjects with seasonal allergic rhinitis (SAR) and subjects without al

8 y samples were collected from 40 adults with seasonal allergic rhinitis at baseline and at 4, 8, 16,

9 ice, and outcome assessment in patients with seasonal allergic rhinitis.

10 Th2 cytokines are characteristic features of seasonal allergic rhinitis.

11 Ragweed frequently causes seasonal allergies in North America and Europe.

12 of population importance, characterized the seasonal and circadian use, and identified snow cover as

13 coupling-may have implications for improving seasonal and decadal predictions and managing the climat

14 es between the surveillance populations, the seasonal and genotypic associations between sporadic cas

15 While seasonal and intraseasonal variability can also create c

16 reas with high vegetation complexity on both seasonal and lifetime scales.

17 glutination inhibition activity against both seasonal and pandemic H1N1 influenza strains.

18 ral flexibility animals need for adapting to seasonal and unpredictable habitats.

19 xity within their home range, on short-term (seasonal) and long-term (lifetime) scales and estimated

20 Seasonal animal movement among disparate habitats is a f

21 y-monthly) timescales and reduces on longer (seasonal-annual) scales.

22 Influenza B virus (IBV) undergoes seasonal antigenic drift more slowly than influenza A vi

23 ion and freezing, we conducted an exhaustive seasonal assessment of photosynthesis (gas exchange, lim

24 We found models that used seasonal averaging could grossly overestimate infection

25 By analyzing a 35-year dataset of seasonal biomass dynamics of a Tibetan alpine grassland,

26 al coupling between vegetation greenness and seasonal bird migration within North America.

27 urements, and a predictive model to simulate seasonal canopy color dynamics.

28 pare eDNA detection against well-established seasonal changes in blacktip shark (Carcharhinus limbatu

29 We demonstrate that at winter-dormant sites, seasonal changes in canopy color can be used to predict

30 live within different environments, adapt to seasonal changes in diet and maintain performance throug

31 ed significant among-individual variation in seasonal changes in reproduction, which is necessary for

32 Migrations allow animals to track seasonal changes in resources, find mates, and avoid har

33 Seasonal changes in the color of evergreen forest canopi

34 trinsic but result from passive responses to seasonal changes in the environment experienced by repro

35 t different maturation stages to investigate seasonal changes in the phenolic compounds profile and i

36 12.3 mumol m(-2) s(-1) , which suggests that seasonal changes in V(cmax,25C) are consistent with opti

37 d the world continuously adjust to daily and seasonal changes in wave and tide conditions, which are

38 ated by the circadian clock and can adapt to seasonal changes of day length.

39 Overall, the obtained results suggest the seasonal changes of polyphenolic composition and bioacti

40 In Alpine regions changes in seasonal climatic parameters, such as temperature, rainf

41 s have established marine protected areas or seasonal closures to recover these overfished stocks.

42 Seasonal co-occurrences (alignment of seasonal peaks) an

43 We determine the krill seasonal contribution to POC flux in terms of faecal pel

44 tuitary gonadal axis, may be involved in the seasonal control of camel's reproduction.

45 confirmed highly potent neutralization of a seasonal coronavirus; however, no cross-neutralization o

46 ens during infection by SARS-CoV-2 and three seasonal coronaviruses (HCoV-OC43, HCoV-NL63, and HCoV-2

47 ttern observed among other preexisting human seasonal coronaviruses (sCoVs).

48 irus infections, including influenza and the seasonal coronaviruses that cause colds, serum antibodie

49 s infection (SARS-CoV-2, SARS-CoV, MERS-CoV, seasonal coronaviruses).

50 ors required for infection by SARS-CoV-2 and seasonal coronaviruses, we designed a focused high-cover

51 EM41B) for infection by SARS-CoV-2 and three seasonal coronaviruses.

52 Here we describe the epidemiology of seasonal CoVs (sCoVs) and other cocirculating viruses in

53 By identifying key seasonal cues found in the native range of the cereal mo

54 t photoperiod and low temperature, the major seasonal cues heralding winter, suppress branching by si

55 ent to disrupt the ability of flies to sense seasonal cues, thereby altering the extent of female rep

56 te whether the placenta may be influenced by seasonal cues.

57 investigate the net carbon dioxide (CO(2) ) seasonal cycle and its climatic and environmental contro

58 processes in dictating the evolution of the seasonal cycle in biomass.

59 We find that the isotopic seasonal cycle in this region is driven by a shift in mo

60 cooling mode is determined by changes in the seasonal cycle of Arctic sea-ice that are forced by orbi

61 lengths and timings, which would affect the seasonal cycle of atmospheric radiocarbon concentrations

62 imple temperature-based model to predict the seasonal cycle of canopy greenness, and we show that the

63 The seasonal cycle of respiratory viral diseases has been wi

64 We investigate the seasonal cycle of strong NIW events and find that despit

65 re budget analysis shows that these enhanced seasonal cycles are associated with similar amplificatio

66 IT prescriptions in two different successive seasonal cycles were compared with non-AIT patients who

67 Moreover, our multi-seasonal data indicate that environmental stressors may

68 Finally, we show how seasonal day-length, after-effects to light entrainment

69 In contrast, seasonal decline of photosynthetic activity and cessatio

70 d project population models that account for seasonal demographic covariation using a latent variable

71 nction through physical activity and cure of seasonal depression with phototherapy.

72 significant recovery in algal growth before seasonal dieback began in autumn.

73 ters microclimate, but little is known about seasonal differences and microclimate variance.

74 orested landscapes during autumn, suggesting seasonal differences in habitat function and highlightin

75 and) to identify Hg methylation hotspots and seasonal differences in MeHg cycling unique to Arctic ec

76 l community composition, whereas significant seasonal differences in stream chemistry were observed.

77 atures of vaccine response as well as marked seasonal differences.

78 cessful case studies focusing on endemic and seasonal diseases such as influenza and dengue.

79 Robust shifts in seasonal drought are most apparent during the cool seaso

80 advances understanding of g(s) dynamics over seasonal drought, and identifies a practical, trait-base

81 Across Amazon forests, mean LAI, LAI seasonal dynamics and leaf traits vary with soil moistur

82 vailability with other critical resources on seasonal dynamics of ecosystem productivity remains larg

83 We characterize the seasonal dynamics of NSC in relation to the aboveground

84 Seasonal dynamics of NSC were synchronous between wood t

85 There was a dominant seasonal effect on the drinking water microbiomes at all

86 l shifts in GRD socio-behavioural states and seasonal effects on resource partitioning, respectively.

87 ntermediate-host modeling, or by restricting seasonal effects through use of yearly averaging.

88 ast coast of Australia were investigated for seasonal endocrine changes associated with reproduction.

89 eet migratory and reproductive costs through seasonal energy intake.

90 is are still needed to enable short-term and seasonal energy storage in the form of liquid fuels.

91 ereby facilitating adaptation to diurnal and seasonal environmental changes.

92 Here, we assess the seasonal environmental drivers and predictability of Afr

93 y to other large herbivores living in highly seasonal environments elsewhere.

94 and underestimate control outcomes in highly seasonal environments.

95 ized to understand population persistence in seasonal environments.

96 ating how tri-trophic food chains persist in seasonal environments.

97 H1N1 influenza A viruses (IAVs) have caused seasonal epidemics since 1977.

98 le for up to 650,000 deaths per year through seasonal epidemics, and pandemics have caused tens of mi

99 in advance and can be generalized to provide seasonal estimates of regional and global fire risk.

100 balance, highlight their contribution to the seasonal evolution of sea surface temperature, and discu

101 Despite evidence of seasonal export of MeHg from the HCC, annual loads indic

102 Seasonal export of MeHg was evidenced by increases in mo

103 incur daily (e.g. tropical mountains) and/or seasonal extremes in temperature (e.g. temperate/contine

104 Seasonal faunal migrations have been hypothesized to occ

105 In many perennial plants, seasonal flowering is primarily controlled by environmen

106 self-initiated behavioral changes during the seasonal flu.

107 ation has been used to control the spread of seasonal flu; however, the virus continues to evolve and

108 increasing latitude because larger-amplitude seasonal fluctuations generate more opportunities for sp

109 aged concentrations that are not affected by seasonal fluctuations in air quality.

110 e low temperatures, high salinity, and broad seasonal fluctuations in light conditions.

111 In addition, there was consistent seasonal fluctuations in relative genetic diversity.

112 gainst Bd correspond with infection risk and seasonal fluctuations in temperature and humidity.

113 a focus for accelerated research to improve seasonal forecasts through multidecadal climate projecti

114 rd to savanna-forest transition and tropical seasonal forest regions in response to increased forest

115 s facilitating integration of branching with seasonal growth control in perennial trees.

116 How branching is coordinated with seasonal growth is poorly understood.

117 bodies are protective in prophylaxis against seasonal H1N1 viruses in mice.

118 performed for LPAIV strains in comparison to seasonal H3N2 and avian H3N8.

119 5N1, H6N1, H11N9, an avian H3N8, and a human seasonal H3N2 subtype.

120 nmental cue synchronizing rhythms of life in seasonal habitats.

121 ll expose alpine species adapted to a highly seasonal, harsh environment to novel environmental condi

122 he Kruger National Park to investigate their seasonal home range differences and habitat preferences.

123 land use change, the duration and extent of seasonal host-seeking activity increases in northern Cal

124 We identified seasonal human coronaviruses, influenza viruses and rhin

125 ds against BIRFLU was further confirmed with seasonal IAVs (A/California/04/2009 H1N1 and A/Wyoming/3

126 declining, and we project a mean decrease in seasonal ice duration of 6.10 +/- 0.08 days per 1- degre

127 shift from thick, multiyear ice to thinner, seasonal ice with higher biological productivity.

128 Seasonal IIV could not induce seroprotective antibodies

129 Seasonal IIVs did not induce seroprotective antibodies (

130 creasingly threatened by climate change with seasonal implications for photosynthesis and forest grow

131 t for China, whereas sCoVs tended to be less seasonal in China and in tropical sites.

132 ic BMPCs 4 weeks after immunization with the seasonal inactivated influenza vaccine, but numbers retu

133 ting cluster IV A(H3N2)v vaccine and several seasonal inactivated influenza vaccines (IIVs) in adults

134 Seasonal influenza A viruses of humans evolve rapidly du

135 Globally, these phenomena are observed with seasonal influenza and with the current coronavirus dise

136 Seasonal influenza carrying key hemagglutinin (HA) head

137 ethnic disparities in vaccination rates for seasonal influenza exist.

138 Our findings characterize seasonal influenza hospitalizations among pregnant women

139 model, we simulate transmission dynamics of seasonal influenza in England from 2012 to 2018.

140 r burden than the 2009 influenza pandemic or seasonal influenza in terms of hospitalization and morta

141 to currently circulating strains.IMPORTANCE Seasonal influenza infection remains a major cause of di

142 Seasonal influenza is an annual occurrence, but it is th

143 of the public health and economic impact of seasonal influenza on pregnant women.

144 ipants in 15 European countries during three seasonal influenza seasons, allocated 1629 to usual care

145 ccine containing 15 mug of each of the three seasonal influenza strains for that year, as a single do

146 Seasonal influenza vaccination in humans primarily stimu

147 Seasonal influenza vaccination with either LAIV4 or IIV3

148 We sought to determine the seasonal influenza vaccine effectiveness (VE) against la

149 study there was no evidence to suggest that seasonal influenza vaccine was associated with major mal

150 Seasonal influenza vaccines lack efficacy against drifte

151 Seasonal influenza vaccines prevent influenza-related il

152 hould be specifically dedicated to improving seasonal influenza vaccines while developing entirely ne

153 Here, we review the history of seasonal influenza vaccines, describe challenges associa

154 ly in the MF59 adjuvant, a component in some seasonal influenza vaccines, in stockpiled, emulsion-bas

155 Seasonal influenza virus infections cause mild illness i

156 In healthy adults, seasonal influenza virus infections result in mild disea

157 Seasonal influenza virus is a common cause of acute lowe

158 Seasonal influenza virus is associated with high morbidi

159 Although seasonal influenza viruses circulate globally, preventio

160 erica: respiratory syncytial virus (RSV) and seasonal influenza.

161 How these two forcings affect the seasonal intensity and characteristics of monsoonal prec

162 Our analysis indicates complex seasonal interactions of underlying C cycle processes in

163 ent observations have suggested large, rapid seasonal intrusions of water into the upper atmosphere,

164 Poyang Lake is a typical seasonal lake linked to the Yangtze River and is signifi

165 ce, we examined transcriptome changes during seasonal leaf senescence in Populus trichocarpa Nisquall

166 urce for identification of genes involved in seasonal leaf senescence in trees, and informs efforts t

167 ing time and senescence to create a range of seasonal life-history syndromes.

168 ition activity against a panel of historical seasonal-like and pandemic-like H1N1 influenza viruses.

169 opes in the Cb, Sa, or Sb antigenic sites of seasonal-like and pandemic-like wild-type or COBRA HA an

170 productivity, assuming simple changes in the seasonal magnitude of phytoplankton division rates.

171 Seasonal malaria chemoprevention (SMC) is a novel strate

172 Seasonal malaria chemoprevention (SMC) is now widely dep

173 Children that received seasonal malaria chemoprevention had fewer malaria episo

174 In the current study, the impact of seasonal malaria chemoprevention on malaria-induced immu

175 ose that P. falciparum virulence in areas of seasonal malaria transmission is regulated so that the p

176 Evolutionary theories of seasonal migration generally assume that the costs of lo

177 ed for long-distance movement and 2) loss of seasonal migration is associated with reductions in fore

178 n groups expressing one of the four distinct seasonal migration patterns) of Chinook salmon (Oncorhyn

179 Changes in the phenology of seasonal migrations between the breeding and wintering g

180 fraction of the fish assemblage may conduct seasonal migrations in this region, and propose seasonal

181 in both the downslope and reciprocal upslope seasonal migratory movements that characterize altitudin

182 Here we use field surveys to demonstrate seasonal mismatches in the exposure of marine consumers

183 rs that contribute to the pathophysiology of seasonal mood variations.

184 The seasonal movement of animals has been linked to seasonal

185 ecutive nasal allergen challenges (NAC) with seasonal (NAC-S) and perennial allergens (NAC-P).

186 al (wintering quarters/breeding grounds) and seasonal (nonbreeding/breeding periods) MeHg exposures.

187 Ray parenchyma fraction (RPF) and seasonal NSC dynamics were quantified for 12 conifers an

188 f the Southern Ocean to potential changes in seasonal nutrient and light availability suggests that a

189 al Vietnam are governed by the timing of the seasonal onset and withdrawal of the Intertropical Conve

190 We show that the seasonal onset of photosynthetic activity as determined

191 sociated with the severity of infection with seasonal or avian influenza virus.

192 me coronavirus 2 (SARS-CoV-2) could recur as seasonal outbreaks, a circulating pattern observed among

193 on private vs. communal land, on farms with seasonal pans (temporary, shallow wetlands) and perennia

194 rk for 34 forest sites in North America, the seasonal pattern of sensitivities of net ecosystem produ

195 ules and microbes that demonstrate different seasonal patterns in insulin sensitive and insulin resis

196 we address this knowledge gap by identifying seasonal patterns of Al and their drivers in 16 rivers a

197 tency was also found for (a) the diurnal and seasonal patterns of fluxes and (b) the ecosystem functi

198 Seasonal patterns of life history in salmon are used to

199 As climate change transforms seasonal patterns of temperature and precipitation, germ

200 These seasonal patterns of warming and cooling have significan

201 The different molecules group into two major seasonal patterns which correlate with peaks in late spr

202 al peaks) and synchronization (similarity of seasonal patterns) of infections are noted, yet rarely e

203 Trends in survival revealed divergent seasonal patterns, which were similar across age-classes

204 active P (SRP) with no discernable annual or seasonal patterns.

205 d media use; and (2) signal intensity of the seasonal peak in searches.

206 Annual seasonal peaks changing from PeV-A1 to PeV-A3 were obser

207 ic approach to evaluate the co-occurrence of seasonal peaks using a combination of L-moments, seasona

208 Seasonal co-occurrences (alignment of seasonal peaks) and synchronization (similarity of seaso

209 gamation of multiple pathogens with variable seasonal phasing and attack rates, most existing process

210 tion, which is predominately associated with seasonal photoperiodic variation.

211 Our analysis reveals seasonal phytoplankton accumulation ('blooming') events

212 ions between the magnitude of WA(deep) , the seasonal plasticity of WA(deep) , midday leaf water pote

213 African Bicyclus butterflies show strong seasonal polyphenism in a suite of phenotypic and life-h

214 Increases in projected seasonal precipitation variation in already highly varia

215 se, in general, projects an increase in mean seasonal precipitation, runoff, and streamflow.

216 dening) the low-frequency variability of the seasonal precursors into the decadal-scale variance of t

217 tors are further identified to determine the seasonal predictability of fire activity in Africa.

218 Successful seasonal prediction of fire activity over these fire-pro

219 Our study highlights this important seasonal process and shows spring greenhouse gas emissio

220 ng toward diversified farming, and consuming seasonal produce.

221 te hypersensitivity (IBH) is the most common seasonal pruritic allergic dermatitis of horses occurrin

222 olonged desiccation in semiarid regions with seasonal rainfall.

223 tween the 1990s and 2010s, adult female (AF) seasonal ranges more than doubled in spring and summer a

224 gether with changes in polar bear movements, seasonal ranges, body condition, and reproductive metric

225 hat highly dynamic structural and functional seasonal rearrangements of the photosynthetic apparatus

226 hat C. limbatus eDNA detection follows known seasonal residency patterns consistently over 2 years of

227 onditions on H. kamschatkana are mediated by seasonal resource identity.

228 We recruited 29 patients with atopic seasonal rhinoconjunctivitis and performed a longitudina

229 fe health requires a deeper understanding of seasonal rhythms in host-pathogen interactions.

230 d and social behavior.SIGNIFICANCE STATEMENT Seasonal rhythms influence emotion and sociability.

231 possibly linked to the ocean freeze-up and a seasonal rise in ozone.

232 th the consequences of the Earth's daily and seasonal rotation.

233 A temporal trade-off observed at the seasonal scale was influenced by the phenology of the sp

234 At monthly or seasonal scales, less common birds experienced decreases

235 Nordic Seas during cold stadials and reduced seasonal sea ice conditions during warmer interstadials.

236 and threshold response between an extensive seasonal sea ice cover in the Nordic Seas during cold st

237 tively linked to ipRGC function (chronotype, seasonal sensitivity, presence of a photic sneeze reflex

238 Model results suggest that the observed seasonal seroprevalence dynamics can be best explained b

239 Observed seasonal seroprevalence patterns were compared with thos

240 time, or in relation to SST or slope of the seasonal shift in diet from principal to secondary prey.

241 erved patterns are indicative of an adaptive seasonal shift in parental investment in response to a d

242 ication during winter will be exacerbated by seasonal shifts in their resources.

243 Seasonal snail control, implemented alone, was less effe

244 Here we assessed the seasonal spatial organization of Serengeti lions and Yel

245 use projections for California coupled with seasonal species distribution models to explore the resp

246 T PA mutants appears relatively unaltered in seasonal subtypes warranting surveillance for its dissem

247 how the magnitude and direction of changing seasonal suitability differs regionally across Californi

248 thermal regions using objective analysis of seasonal surface temperature dynamics from satellite obs

249 rgy system planners and operators anticipate seasonal surpluses or shortfalls and take precautionary

250 We analyzed the temporal trends in seasonal survival of yellow-bellied marmots (Marmota fla

251 Understanding of disease seasonal synchronization is essential for developing rel

252 ronounced changes in hydroclimate, including seasonal temperatures in specific Mediterranean regions

253 atoms as a feasible methodology to constrain seasonal timelines in forensics.

254 We showed that proper intra-seasonal timing of control measures could make marked im

255 identifying nine major clusters based on the seasonal timing of gene expression, and variation in beh

256 The seasonal timing of seed germination determines a plant's

257 A seasonal transmission environment including seasonal var

258 Disruptions to the seasonal transmission patterns of these diseases may hav

259 phenology had a significant influence on NSC seasonal trends, there was no clear trade-off between NS

260 interventions will likely be needed despite seasonal trends.

261 tial for large compositional differences and seasonal turnover across ecotones.

262 rmula: see text]O emissions can be traced to seasonal upwelling in the tropical ocean and winter mixi

263 We then use seasonal V(cmax,25C) field measurements from 10 sites ac

264 Natural influenza virus infections and seasonal vaccinations often do not confer broadly neutra

265 or age and prior LAIV (n = 436), inactivated seasonal vaccine (n = 100), or (H1N1)pdm09 vaccine (n =

266 Seasonal vaccines are often ineffective and escape mutan

267 from this study improve the understanding of seasonal variability in mercury transport through and tr

268 ly reflecting streamflow conditions, and (3) seasonal variability in particulate IHg loading at the i

269 sonal migrations in this region, and propose seasonal variability in surface ocean primary production

270 i (AMF), the diversity of plant partners and seasonal variability in trophic exchanges between the sy

271 ence (occurrence, abundance, fidelity, inter-seasonal variance and age) and performance (body conditi

272 Overall, the model explains about 83% of the seasonal variation in C3 plant V(cmax,25C) across the 10

273 lity-based approach can accurately reproduce seasonal variation in canopy photosynthetic potential, a

274 We then investigated experimentally whether seasonal variation in daylength causally influences brai

275 sonal movement of animals has been linked to seasonal variation in ecological productivity, and it ha

276 unraveling the mechanisms that regulate the seasonal variation in GEP across a network of eight Euro

277 henology constituted a key predictor for the seasonal variation in GEP and further acted as a distinc

278 s suggest that the MOR system might underlie seasonal variation in human mood and social behavior.

279 s suggest that the MOR system might underlie seasonal variation in human mood and social behavior.SIG

280 To resolve spatial and seasonal variation in species' response, we use a unique

281 We found significant seasonal variation in TDD and/or PDD for all but four sp

282 Seasonal variation in the age distribution of influenza

283 the ability of optimality theory to explain seasonal variation in V(cmax) has not been fully investi

284 ever, the ability to predict its spatial and seasonal variation is constrained by the lack of a therm

285 Seasonal variation makes Schistosoma transmission less s

286 seasonal transmission environment including seasonal variation of snail population density and human

287 This study reports the effects of seasonal variation on the total polyphenol and flavonoid

288 ly varying socioemotional functions, but its seasonal variation remains elusive with no previously re

289 ly varying socioemotional functions, but its seasonal variation remains elusive.

290 ability in humans and rats shows significant seasonal variation, which is predominately associated wi

291 Much of the seasonal variations in global [Formula: see text]O emiss

292 ngth, after-effects to light entrainment and seasonal variations in light sensitivity in the mammalia

293 Here, we report more than 1000 seasonal variations in omics analytes and clinical measu

294 Seasonal variations in viral community composition were

295 nd an ICPMS/MS system were used to study the seasonal variations of total arsenic and all species kno

296 Seasonal variations were noticed among different genotyp

297 Both neuronal populations display opposed seasonal variations with more Kp neurons and less RFRP-3

298 xity of the environment, combined with their seasonal variations, drive the fate of metastable ENMs.

299 o increase SSTs and the frequency of extreme seasonal weather events, epizootics causing MMEs are lik

300 We assimilated a seasonal wing color phenotype in a naturally plastic pop