ライフサイエンスコーパス: population growth

1 ation is the most important factor affecting population growth.

2 the predicted number in 2015, accounting for population growth.

3 from non-communicable diseases, were due to population growth.

4 ithin paramecia), thereby facilitating viral population growth.

5 ing of populations and a 25% increase due to population growth.

6 d oxygen is the limiting factor for eukaryal population growth.

7 edators but did not translate into increased population growth.

8 destabilizing social structure and reducing population growth.

9 anges in river flows and flow variability on population growth.

10 ed the negative effect of temperature on the population growth.

11 nships between monthly weather variables and population growth.

12 er and mobility of goods, climate change and population growth.

13 emiological transition and outpaced regional population growth.

14 n and correlations in development can impact population growth.

15 s increase (108 million) was attributable to population growth.

16 ightly between 2005 and 2016, due largely to population growth.

17 acts imply, it was not associated with human population growth.

18 of media, genetics, and stress on microbial population growth.

19 ng of how multiple factors interact to limit population growth.

20 s of mode of phytoplankton mortality, and of population growth.

21 each a conservation objective of 2.3% annual population growth.

22 floaters can coexist only in the process of population growth.

23 lumis in the Balsas River Valley experienced population growth.

24 ibited tumor cell growth, migration, and CSC population growth.

25 the relevant parameters affecting microbial population growth.

26 .4%), population ageing after accounting for population growth (34.6%), and reduction in age-specific

27 three factors, namely an increase because of population growth (38.4%), population ageing after accou

28 Smaller effects are found for population growth (+4.2 Gt) and changes in the compositi

29 the relative strength of factors regulating population growth across stress gradients, but suggests

30 drivers of change in cardiovascular deaths (population growth alone, population growth and aging, an

31 more than 100%) compared with the effect of population growth alone.

32 lobal change had negative effects on species population growth, although species responded to differe

33 ecomposed to quantify change attributable to population growth and ageing.

34 ity but were also positively associated with population growth and aging and negatively associated wi

35 and nonfatal IHD in most regions since 1990, population growth and aging led to a higher global burde

36 diovascular deaths (population growth alone, population growth and aging, and epidemiologic changes i

37 Due to demographic changes, including population growth and aging, the cumulative burden of or

38 able to rising age-specific rates and 21% to population growth and aging.

39 owth data enables accurate quantification of population growth and allows explicit control of effects

40 Links between economic activity, population growth and artificial light are well document

41 Strong positive correlations between population growth and both winter and breeding season te

42 acquire a few key mutations that drive rapid population growth and carcinogenesis.

43 Faced with population growth and changing climate, the next wave of

44 hortage is a deleterious consequence of both population growth and climate change and is one of the m

45 amination of how the tandem effects of human population growth and climate change can disrupt mammali

46 s in crop yield are needed to keep pace with population growth and climate change.

47 This has hampered attempts to model population growth and competition in dynamic environment

48 f 38 bird species finds variable patterns of population growth and declines that broadly correlate wi

49 In the future, population growth and demographic shifts are likely to h

50 y studied (e.g., structural loss), projected population growth and development patterns are unlikely

51 We quantified the effects of a range of population growth and development patterns in California

52 Future population growth and economic development are forecaste

53 males mated with the control female reduced population growth and egg hatching rate, but did not inf

54 were characterized by a substantially slower population growth and evolutionary rates, as well as sma

55 emonstrates that rapid evolution drives both population growth and expansion speed and is thus crucia

56 s decreased, in a MYC-dependent manner, cell population growth and expression of the MYC target gene

57 fe represent a more important driver of mean population growth and fitness of pike than maternal effe

58 r infection in provisioned habitats owing to population growth and food-borne exposure to contaminant

59 Human population growth and global climate change now present

60 ellular abundance of eIF4G and rates of cell population growth and global mRNA translation, with peak

61 ur study offers insight into the dynamics of population growth and impacts of increasing population d

62 e it is associated with both higher rates of population growth and increased morbidity and mortality

63 High productivity thus supports population growth and invasion success, with barriers at

64 rally had positive effects on establishment, population growth and long-term persistence.

65 increasing burden of untreated caries due to population growth and longevity and a significant decrea

66 nfluence of unstable population structure on population growth and mean fitness.

67 otential influence of genetic restoration on population growth and persistence parameters.

68 ing decline will be offset only partially by population growth and population aging such that the pre

69 Nano-PS reduced population growth and reduced chlorophyll concentrations

70 e not known, but are critical for predicting population growth and related degradation of (sub) arcti

71 ood security posed by global climate change, population growth and rising incomes, plant breeders are

72 model, we identify the major determinants of population growth and show that both physiological memor

73 colonizing a novel environment and measured population growth and spread.

74 Lagged correlations between population growth and summer temperature and precipitati

75 t necessarily lead to deleterious impacts on population growth and that negative effects on reproduct

76 ected to respond to climate change and human population growth and these responses may be especially

77 that a fluctuating model - based on repeated population growth and truncation - is more robust than P

78 Understanding how climate change, population growth, and development patterns will affect

79 00 facilitated agricultural intensification, population growth, and settlement expansion across the f

80 nowledge of how year-round factors influence population growth, and the demographic mechanisms throug

81 edicted opposite effects of precipitation on population growth, and the historical models were very p

82 world population, 22.1% was attributable to population growth, and total disability-adjusted life-ye

83 that affluence (per-capita consumption) and population growth are outpacing any improvements in carb

84 however, the spatial patterns of subsequent population growth are unclear.

85 nce of dynamic, species-specific controls on population growth, as could be applied by specialised pa

86 numerical algorithms to show that explosive population growth, as experienced by human populations,

87 th, the expansion dynamics were dominated by population growth at the low-density front, which pulled

88 re significantly increased BPH fecundity and population growth, but suppressed both parameters in lab

89 , predators reduced aphid density by 35% and population growth by 86%.

90 n populations while simultaneously enhancing population growth by improving habitats.

91 Here we examine a general model where population growth can be induced or accelerated by inves

92 derable interdecadal differences observed in population growth coincide with remote Arctic and North

93 ence of improved emissions intensity through population growth, consumption and production structures

94 As population growth continues to outpace development of wa

95 oped a general and robust model of microbial population growth curves using Gaussian process (GP) reg

96 13 ka, which explains five major periods of population growth/decline and ~45% of the population var

97 ding mates can lead to an Allee effect where population growth decreases at low densities.

98 is due mainly to rare alleles, and explosive population growth decreases power.

99 To ensure food security in the face of population growth, decreasing water and land for agricul

100 a convergens) on the mass, number of nymphs, population growth, density and dispersal of aphids (Macr

101 ribe a predator-prey model in which the prey population growth depends on a prey density-dependent fi

102 Virus population growth depends on contacts between viruses an

103 ous coronary intervention (PCI) has outpaced population growth despite declining incidence of myocard

104 gher AVS and porewater DOC but exhibited net population growth despite porewater [Ni] 1.3-1.7x their

105 Although China's coastal population growth did not change following the 1978 econ

106 For future scenarios, we considered population growth, dietary changes, improved feed conver

107 ssing global issue of food insecurity due to population growth, diminishing land and variable climate

108 ce of formidable challenges, including rapid population growth, diverse and often divided ethnic affi

109 colonisation but also to sustain subsequent population growth during early phases of expansion.

110 em-dependent mechanism for limiting parasite population growth during the early stages of an acute bl

111 lineages in the north exhibited a pattern of population growth during the Pleistocene that could be l

112 graphy (reduced extinction risk and enhanced population growth) during the initial stages of invasion

113 concentration, has clear potential to damage population growth dynamics in this species.

114 Global health, population growth, economic development, environmental d

115 Finally, we show that whether lowering population growth entails overall improvements in wellbe

116 ion costs implied by plausible reductions in population growth, finding that large near-term savings

117 Due to population growth, food and energy demands will soon sur

118 alyses provided strong signals of historical population growth for both white marlin and roundscale s

119 oluntary fertility declines and ending world population growth, for changing behavior and adoption of

120 workforce thresholds of 20 per 100 000, the population growth formula (P=0e(rt)) was used and we ass

121 Models projecting population growth from different starting seed densities

122 her, spring biomass is generally higher, but population growth from spring to summer is lower, after

123 underlying coupled dynamics of body mass and population growth has been lacking.

124 Global population growth has caused extensive human-induced env

125 Recent and rapid human population growth has led to an excess of rare genetic v

126 However, human population growth has led to increased pollution, ocean

127 Some theoretical models of population growth, however, predict a broad range of val

128 against those of economic, agricultural and population growth (human development pressures).

129 c phase begin, with evidence for exponential population growth in cultural hotspots, characteristic o

130 The majority of population growth in developing countries will occur in

131 The overall population growth in India explains a greater proportion

132 ency-based tests provided evidence of recent population growth in Malawi and detected potential targe

133 nding and, accordingly, ants increased aphid population growth in meadow but not understory environme

134 lly interpreted as an adaptation to maximise population growth in multi-nutrient environments.

135 Breeder turnover can influence population growth in social carnivores through changes t

136 nstruct the spatiotemporal patterns of human population growth in South America using a newly aggrega

137 Most global population growth in the coming decades is expected to o

138 ithin the last 10 thousand years, with major population growth in the same period, suggesting populat

139 ct biomass, and local conspecific density on population growth in the subsequent year.

140 will be 99%, up to seven times the projected population growth in this group of countries.

141 tress" indicates abiotic factors that reduce population growth), including desert, polar, or high-ele

142 In addition, the recent slowing of population growth indicates that this population may be

143 ax model was fitted to the data on bacterial population growth inhibition at different enrofloxacin c

144 their varying sensitivities to Cu (72-h 50% population growth inhibitions of 8-47 mug Cu/L).

145 actions that can slow and eventually reverse population growth: investing in universal access to repr

146 EW needs locally is critical, as significant population growth is expected in less-developed areas of

147 Meanwhile, population growth is increasing the exposure of human be

148 ose to the carrying capacity K, variation in population growth is more strongly influenced by density

149 Because population growth is multiplicative across time, we intr

150 However, population growth is regulated over the long term by str

151 We also observed that total population growth is transiently maximized at an interme

152 Microbial population growth is typically measured when cells can b

153 Future population growth is uncertain and matters for climate p

154 we found potential for explosive low-density population growth (lambda > 5) and complex density fluct

155 Although local factors, including human population growth, land use change, and water management

156 cceptable risk for copepods at the important population-growth level.

157 lobal food security of stagnating yields and population growth makes increasing crop productivity a c

158 n social group persistence, reproduction and population growth may be greatest when average group siz

159 deling frameworks exist to capture microbial population growth measurements.

160 antially outperforms commonly used microbial population growth models, particularly when modeling gro

161 inflammatory responses, controlled parasite population growth more effectively than naive controls.

162 have reported signatures of recent explosive population growth, notable for an excess of rare genetic

163 The population growth of A. coluzzii followed the first rain

164 Natural range loss limits the population growth of Asian big cats and may determine th

165 ht have a positive effect on recruitment and population growth of black-throated blue warblers if foo

166 er loss on social stability, recruitment and population growth of grey wolves (Canis lupus) in Denali

167 is influences reproductive asynchrony or the population growth of invasive species.

168 ted through climate, is a limiting factor on population growth of sandhill cranes in the RMP, which c

169 mission intensity through its effects on the population growth of the mosquito vector and on pathogen

170 Here we examined the population growth of Vibrio after natural and simulated

171 rld undergoing rapid economic transition and population growth-often with large informal and unregula

172 ct on the number of nymphs, aphid density or population growth on high resistance plants, whereas on

173 ications for understanding the pattern of Bd population growth on individual hosts, as well as popula

174 in skin sloughing patterns could regulate Bd population growth on the skin, and influence subsequent

175 front can arise from either overcompensatory population growth or density-dependent dispersal, both o

176 lt, increases in overall demand due to human population growth or improvement in real income would be

177 s were best explained by marked variation in population growth parameters under different productivit

178 luence on the multi-predator effect on aphid population growth, plant composition had a marked effect

179 By 2050, in the absence of any mitigation, population growth plus higher per capita protein intake

180 the climatic effect most closely related to population growth potential; the colder the winter inhab

181 estimated a spatially explicit landscape of population growth predictions for this endangered specie

182 ures at the wintering grounds lead to higher population growth, primarily through their strong positi

183 ctions among demographic rates contribute to population growth rate (lambda) is key to understanding

184 Population growth rate (lambda) was most affected by var

185 usible distribution of the maximum intrinsic population growth rate (rmax) and compare it to 95 other

186 not only key demographic properties, such as population growth rate and demographic resilience, but a

187 we found a positive relationship between the population growth rate and the number of introduced egg

188 e-history evolution, which drives changes in population growth rate and thus population dynamics, inc

189 ency can decrease-or alternatively the total population growth rate can decrease.

190 The effect of virus on population growth rate depended on virus species and wil

191 hese changes did not propagate to affect the population growth rate due to the small effect of body m

192 pecific fecundity has very limited impact on population growth rate in American crocodiles.

193 tested a core tenet of this hypothesis-that population growth rate is more strongly affected by spec

194 he relative sensitivity of the mean fitness (population growth rate lambda) to different early life i

195 omplex surgical cases will likely match this population growth rate meaning there will be many more s

196 sus was 26.6 million, with an average annual population growth rate of 1.4.

197 s), can explain spatial heterogeneity in the population growth rate of the gypsy moth, Lymantria disp

198 Population growth rate r is determined by a Lotka style

199 h-quality individuals would have much higher population growth rate than a population consisting of l

200 ons and high heterogeneity in elevation, the population growth rate was lowest and the density at whi

201 see text], and the environmental variance in population growth rate, [Formula: see text] Allowing the

202 demographic information allows estimation of population growth rate, as well as projection of future

203 plained 88% of the between-year variation in population growth rate, because it strongly influenced r

204 Population growth rate, estimated from a Leslie-Lefkovit

205 s might not contribute equally to changes in population growth rate, it is essential to examine the e

206 t species worldwide - as measured by in situ population growth rate, its temporal variation and extin

207 Comparisons of estimates of deterministic population growth rate, lambda, and demographic variance

208 fects across treatment years, the cumulative population growth rate, lambdac, and its geometric mean,

209 the impact on daphnid survival also affected population growth rate, with an EC50 of 3.5 mug/L.

210 their rate of recovery from disturbances and population growth rate.

211 the trait at different ages and thus on the population growth rate.

212 title is characterized by the best long-term population growth rate.

213 models and the importance of high potential population growth rate.

214 effect of virus on components of fitness and population growth rate.

215 rate is the only parameter that defines the population growth rate.

216 an, lambdaper-year, the time-averaged annual population growth rate.

217 output and an EC50 value of 73 mg L(-1) for population growth rate.

218 her at the breeding and wintering grounds on population growth rate.

219 as expected, was the most critical stage for population growth rate; however, the survival of younger

220 nd animal populations to simulate stochastic population growth rates (log lambdas ) under different t

221 of demographic compensation on variation in population growth rates across environmental gradients,

222 However, similar population growth rates across generations suggest that

223 re exacerbated in coastal communities, where population growth rates and densities in the United Stat

224 shing effort for devil rays make quantifying population growth rates and extinction risk challenging.

225 e determined how climatic variation affected population growth rates and how these relationships vari

226 sed germination rates, but decreased overall population growth rates by reducing plant survival.

227 Population viability analysis showed that population growth rates declined sharply in response to

228 Population growth rates declined with increased elevatio

229 Analysis of long-term population growth rates documents simultaneous responses

230 snowfall would cause a 2.8-fold increase in population growth rates in Scotch broom and a 3.5-fold i

231 Many climate processes did not affect population growth rates in the predicted direction based

232 experiments (LTREs) for decomposing realised population growth rates into contributions from specific

233 a corresponding demographic model to project population growth rates into the next century.

234 ms with either slow (~0.3%) intrinsic annual population growth rates or a lag in the environmental ca

235 f both sexes evaluate mate availability, but population growth rates tend to be reduced due to surviv

236 eeders in population studies can obscure low population growth rates that should cause management con

237 mera should concentrate efforts on enhancing population growth rates through captive breeding of the

238 story transitions and life-history traits to population growth rates varied among populations and vir

239 Virus did not reduce fruit number, but population growth rates varied among virus treatments an

240 Invader population growth rates were negative only at the modera

241 Even when population growth rates were up to 300% annually, the FM

242 years of field data also showed decreases in population growth rates with elevation and heterogeneity

243 othesis by measuring both short-term (tiller population growth rates) and long-term (17-year survival

244 low life histories, with mean fitness (i.e., population growth rates) more strongly influenced by sur

245 infection can potentially result in reduced population growth rates, but because these effects varie

246 annual reproductive output, and low maximum population growth rates, suggesting they have low produc

247 aptation to a novel environment can increase population growth rates, which also promotes spread.

248 g projection of deterministic and stochastic population growth rates.

249 ate detection probabilities, abundances, and population growth rates.

250 pecies in the short term, which could reduce population growth rates.

251 ation and elevational heterogeneity on local population growth rates.

252 tion sizes; and 3) estimates of post-contact population growth rates.

253 inent-wide "year effects" strongly influence population growth rates.

254 no detectable differences among genotypes in population growth rates.

255 explain most of the evolutionary changes in population growth rates.

256 g and game-hunting has led to high wild boar population growth rates.

257 esearch, the factors determining prehistoric population growth remain uncertain.

258 ople to deadly heat by 2050 under a midrange population growth scenario.

259 cts of precipitation and grass cover on forb population growth showed consistent results for the hist

260 homogeneous and suggests an ubiquitous rapid population growth since the Neolithic revolution.

261 emonstrate that the physical aspects of cell population growth, such as the formation of tight cell c

262 To address this, we propose a model of population growth that includes a new formulation of the

263 table mortality rates, resulting in dramatic population growth that is eventually curtailed by increa

264 rom wildfire nullified pulses of sage-grouse population growth that typically follow years of higher

265 scular disease are increasing as a result of population growth, the aging of populations, and epidemi

266 Because of population growth, the annual number of abortions worldw

267 level for both men and women, but because of population growth, the number of smokers increased signi

268 RRT population will be determined in part by population growth, these results suggest that later dial

269 survival rates always have a large impact on population growth, this decreases with declining increas

270 With population growth, this will increase to between 750 mil

271 to pediatric surgery will continue to exceed population growth through 2030 under two likely scenario

272 e the effects of CDK1 and CKD2 inhibitors on population growth, time-dependent changes in cell cycle

273 the classic Monod model of resource-limited population growth to allow for spatial heterogeneity in

274 ather because aridity reduced sensitivity of population growth to these interactions.

275 for irrigation (blue water footprint) due to population growth (to 2025 and 2050).

276 superoxide has the potential to promote cell population growth under nutrient depravation stress.

277 healthy diets and ecosystems in the face of population growth, urbanisation, and climate change.

278 odels, (ii) determine demographic drivers of population growth using matrix models, and (iii) identif

279 ilaparvata lugens (NlPHF7), on fecundity and population growth via mating.

280 M. persicae population growth was actually reduced on dodder parasit

281 The Late Glacial population growth was fastest during Greenland interstad

282 Initially, population growth was limited at higher temperatures bec

283 We found that warbler population growth was lower following El Nino years (whi

284 Population growth was more strongly affected by four dis

285 tivity, a sensitivity analysis revealed that population growth was most sensitive to changes in adult

286 In addition, while annual population growth was positively correlated with annual

287 exposed to an anti-EsGal1 antibody, symbiont population growth was significantly increased.

288 ver, survival, which has a greater impact on population growth, was little affected by climate variab

289 ationships generally held when influences of population growth were addressed by analyzing per capita

290 accumulation, metal distribution, and algal population growth were measured to elucidate differences

291 ts of climate-driven phenological changes on population growth were not explained by the number of br

292 Significant effects on population growth were observed at the lowest concentrat

293 ion-dependent metal accumulation and reduced population growth were observed in T. weissflogii expose

294 composition, genetic content, and short-term population growth when the individual lost is a breeder.

295 Changes in the climate and population growth will critically impact the future supp

296 ngs-especially for food-imply that projected population growth will undermine protection of the natur

297 wars that followed, coupled with ageing and population growth, will have a major impact on the regio

298 text] Under the classical logistic model of population growth with linear density dependence ([Formu

299 ecades largely due to dietary transition and population growth, with significant impact on climate an

300 collapsed because of centuries of unchecked population growth within a fragile environment.