ライフサイエンスコーパス: coexistence

1 undances contribute substantially to species coexistence.

2 te to a mechanistic understanding of species coexistence.

3 erent dispersal networks can promote species coexistence.

4 n and environmental fluctuations for species coexistence.

5 d a destabilizing effect of GMs on the phase coexistence.

6 equilibrium points characterized by species coexistence.

7 imary role of pathogens in feedback-mediated coexistence.

8 al differences that may facilitate long-term coexistence.

9 pansion may allow lottery effects, promoting coexistence.

10 sk may be a widespread constraint on species coexistence.

11 established, which explicitly explains their coexistence.

12 ies to evolve slow growth to achieve species coexistence.

13 nfall variability was integral to grass-forb coexistence.

14 cture for segregating between neutrality and coexistence.

15 the metric directly linked to plant species coexistence.

16 the storage effect, it was not critical for coexistence.

17 les (NPs) with hexagonal 2H and 3R polytypes coexistence.

18 moderates interaction strengths and promotes coexistence.

19 lating speciation, extinction, and community coexistence.

20 gested clear resource partitioning promoting coexistence.

21 ening competition and thus promoting species coexistence.

22 to regulate droplet dynamics and multiphase coexistence.

23 a modest stabilizing mechanism that promotes coexistence.

24 r effects to improve understandings of plant coexistence.

25 trait plasticity to evaluate its effects on coexistence.

26 emporal partitioning of resources to promote coexistence.

27 ng areas could be another mechanism allowing coexistence.

28 g root neighborhood resource use and species coexistence.

29 ssues to achieve successful conservation and coexistence.

30 e hierarchies across the landscape, leads to coexistence across a much broader range of competitive a

31 tion and promotes sustainable human-wildlife coexistence across large multiple-use landscapes.

32 s encounter-based drivers of consumption and coexistence across systems.

33 same composition, we demonstrate how domain coexistence affects their properties.

34 ype-specific pathogens promote plant species coexistence-albeit less strongly than species-specific p

35 seed predation has profound implications for coexistence among plants because it may enhance or weake

36 ent shade tolerances and the second axis for coexistence among species with the same shade tolerance.

37 ion and temperature, to regions of two-phase coexistence and a region with three-phase coexistence, n

38 elowground strategies in relation to species coexistence and abundance, we assessed four key belowgro

39 l yet currently understudied role in driving coexistence and biodiversity patterns in natural systems

40 in the lysis pattern as a telltale sign for coexistence and co-propagation of bacteria and phages.

41 This could facilitate species coexistence and contribute to the maintenance of high pl

42 Coexistence and food web theory are two cornerstones of

43 quency-dependent feedbacks for plant species coexistence and has generally neglected the consequences

44 d provides a theoretical explanation for the coexistence and interaction of patterns with different s

45 y an exercise in clarifying the semantics of coexistence and neutral theories, but rather reflects ke

46 a mechanistic basis into studies of species coexistence and neutrality.

47 iation rates with distinct opportunities for coexistence and persistence of lineages, shaped by long-

48 s outcomes of mutualistic systems, including coexistence and productivity.

49 vortices and their associated complex-phase coexistence and response under applied electric fields i

50 mber of experiments to predict the outcomes (coexistence and species abundances) of all possible asse

51 olecular dynamics simulations to explore the coexistence and transformation kinetics of these GB phas

52 Here we demonstrate atomic-scale GB phase coexistence and transformations at symmetric and asymmet

53 Species interactions and coexistence are often dependent upon environmental condi

54 Beyond frequent coexistence arising from their high prevalence and share

55 Beyond their frequent coexistence arising from their high prevalence and share

56 models are improving predictions of species coexistence as a function of climate.

57 igher aggressive behaviour may limit species coexistence as they are expected to favour A. oculatus d

58 Several instances of long-term coexistence between donor and patient strains were also

59 by reducing resource competition, promoting coexistence between plant functional groups, which ultim

60 itness benefit when they are rare, promoting coexistence between strains at the population level.

61 ng gap opens along the pocket, revealing the coexistence between superconductivity and antiferromagne

62 ates between high and low, we do not observe coexistence between the species, but rather alternative

63 We use it to evaluate mechanisms promoting coexistence between two congeneric charr that compete fo

64 Long-term coexistence between unicellular cyanobacteria and their

65 to temperature fluctuations maintains their coexistence boundary, highlighting the importance of thi

66 ironmental variability can structure species coexistence by enhancing niche partitioning.

67 gating them may provide deeper insights into coexistence, competitive dynamics, and biodiversity patt

68 mpirical networks, we show that the range of coexistence conditions in mutualistic systems can be ana

69 framework I demonstrate that persistence and coexistence conditions strongly depend on the difference

70 restraint as interactions that contribute to coexistence, consistent with our intuition.

71 Previous studies suggest that continued coexistence depends on relative growth rates: coexistenc

72 tropy disrupts the spatial patterns on which coexistence depends, causing chaotic population fluctuat

73 intertidal food web, partitioning empirical coexistence dynamics.

74 Three coexistence events (two STs simultaneously detected in t

75 5) uncovered a parasitic strategy supporting coexistence, exploiting mosquito nutrients without affec

76 dictions, feedback is more likely to mediate coexistence for pairs of plant species (1) associating w

77 The isotropic and nematic (I + N) coexistence for rod-like colloids is a signature of the

78 Most of the classical theory on species coexistence has been based on species-level competitive

79 Understanding species coexistence has long been a major goal of ecology.

80 How they maintain coexistence has still not been experimentally studied.

81 l studies motivated by an interest in stable coexistence have quantified negative density dependence,

82 but these fitness differences may also favor coexistence if they trade off with competition for other

83 y test if environmental fluctuations enhance coexistence in a California annual grassland.

84 tus, demonstrating that the apparatus allows coexistence in a competitive environment.

85 rough their chemical environment can achieve coexistence in a continuous growth setup (similar to an

86 contribution of local adaptive evolution to coexistence in a landscape of interconnected patches sub

87 traditionally been applied to tests of local coexistence in a narrow range of ecological systems.

88 advances knowledge that can foster peaceful coexistence in a new era defined by globalization and a

89 We first examine coexistence in a theoretical, multitrophic model, adding

90 ial for ecological and evolutionarily stable coexistence in all the models we examined.

91 At the same time, phase-coexistence in chalcogenophosphates may lead to rational

92 ical conditions for stabilisation and stable coexistence in classical competition models.

93 uch shifts is not a prerequisite for species coexistence in competitive communities.

94 er-resource systems and could explain stable coexistence in competitive environments.

95 Coexistence in ecological communities is governed largel

96 effects of structural properties on species coexistence in food webs, and suggest that 'being feasib

97 d demographic mechanisms promoting carnivore coexistence in human-dominated landscapes.

98 itioning is the primary mechanism regulating coexistence in many communities, and our results indicat

99 can be manipulated to alter interactions and coexistence in microbial communities.

100 k is an important driver of biodiversity and coexistence in natural communities.

101 e the links between species interactions and coexistence in natural systems.

102 ic sampling, we find evidence for years-long coexistence in one subject despite adaptive dynamics.

103 We discuss the implications of their coexistence in Stomatopoda, the occurrence of the renifo

104 able to maintain long-term (up to 142 days) coexistence in the laboratory.

105 d again consistent with the model we observe coexistence in the time-averaged dilution rate.

106 litate patterns of resource partitioning and coexistence in these diverse predator communities.

107 oaches that enable stronger tests for stable coexistence-invasibility experiments and model parameter

108 Not knowing what drives this long-term coexistence is a barrier to developing evidence-based st

109 Coexistence is a puzzle because we lack a mechanistic un

110 Promoting human-wildlife coexistence is critical to the long-term conservation of

111 hen interactions are strong, we observe that coexistence is determined primarily by the topology of f

112 oexistence depends on relative growth rates: coexistence is maintained if the slower-growing species

113 nctions, such that the net effect on species coexistence is not clear.

114 y on shared dispersal networks, we find that coexistence is possible on unshared networks, as species

115 Whereas the observation of two-phase coexistence is routinely possible using fluorescence mic

116 of vapor obtained in MD simulation of phase coexistence is used in BKE calculations for consistency

117 connected wilderness is critical to sustain coexistence landscapes.

118 edly, their interaction tends to destabilise coexistence, leading to new insights about the role of b

119 ve niche evolution, diversity-dependence and coexistence limits.

120 This coexistence makes marginally stable proteins ideal tools

121 How species coexistence (mathematical 'feasibility') in food webs em

122 A prominent tree species coexistence mechanism suggests host-specific natural ene

123 nlinearity is a critical if underappreciated coexistence mechanism.

124 ighlights two fluctuation-dependent temporal coexistence mechanisms -the storage effect and relative

125 ity may generally increase the robustness of coexistence mechanisms and be an important component of

126 o all of standard MCT's spatial and temporal coexistence mechanisms, and also process-defined mechani

127 ghting questions on the nature and extent of coexistence mechanisms.

128 ameterise a demographic model, and partition coexistence mechanisms.

129 se coexistence and a region with three-phase coexistence, namely, the liquid-ordered, liquid-disorder

130 We measured the coexistence of 19 combinations of women's anemia, underw

131 el of individual alleles and demonstrate the coexistence of a broad spectrum of genome configurations

132 In this study, the interaction and coexistence of a copiotroph and an oligotroph, isolated

133 to favor proliferation, often promoting the coexistence of a generalist and specialist phenotype.

134 resource-competition models don't allow for coexistence of a large number of species, it was recentl

135 ehavior can be tuned from a mixed state to a coexistence of a liquid-crystalline and a gel, or a liqu

136 Furthermore, the coexistence of a range of nanostructures, from single at

137 The coexistence of abnormal innervation and CMR scar may ide

138 The coexistence of active caspase 3 and EV-A71 protein was o

139 In addition, we identify the coexistence of all three C(4) subtypes of carbon fixatio

140 The coexistence of amyloid-beta (Abeta) plaques and tau neur

141 Liver tissue analysis found the coexistence of an angiogenic process combined with endot

142 stantial plasmid diversity, resulting in the coexistence of antibiotic resistant and sensitive intest

143 lty' incurred by parasitoids leads to stable coexistence of aphids with and without H. defensa and pr

144 ons, under parasitoid pressure, the observed coexistence of aphids with and without protective symbio

145 herefore, in a migrating microbial community coexistence of bacteria and phages implies their co-prop

146 rily maintained by the hosts, explaining the coexistence of bacteria and SGEs.

147 Coexistence of bacteriophages, or phages, and their host

148 The common coexistence of both disorders and the profound related a

149 here is no clear mechanism for the long-term coexistence of both drug-sensitive and resistant strains

150 g selection; hence, the somewhat paradoxical coexistence of both in the same population might be expl

151 of environmental structure enables long-term coexistence of both species via local "pinning" of compe

152 fects during calcination, giving rise to the coexistence of bulk Ti(3+) defects and an ordered mesost

153 as grasses in young habitat types may drive coexistence of closely-related species at high latitudes

154 work is that in situ SEIRAS results show the coexistence of CO(atop) and CO(bridge) as the reaction i

155 The coexistence of comorbidities in patients with CML not on

156 ission electron microscopy images showed the coexistence of compact oligomers, largely consistent wit

157 w that curly-tailed lizards destabilized the coexistence of competing prey species, contrary to the c

158 cognized as an important factor favoring the coexistence of competing species at local scale.

159 ate warming within trophic levels may affect coexistence of competing species, because relative pheno

160 ctions and the potential for persistence and coexistence of competing species.

161 plets is still incomplete, and rules for the coexistence of condensed phases are lacking.

162 ne mechanism of cooperation that permits the coexistence of cooperators and cheaters is an impure pub

163 lds exquisite composition fluctuations and a coexistence of cubic and rhombohedral phases in favor of

164 other phenotypes such as blended reactions (coexistence of cutaneous and respiratory symptoms) or fo

165 l-organic frameworks have high tolerance for coexistence of different metal sizes in their rods and t

166 We demonstrate the coexistence of different microglia phenotypes in ASMko b

167 The first axis allows for coexistence of different shade tolerances and the second

168 The coexistence of different species of large herbivores (un

169 We correspondingly observed coexistence of distinct HSPC subpopulations expressing h

170 Coexistence of ecologically similar species can be maint

171 We argue that this is likely caused by the coexistence of ferromagnetism and geometric frustration

172 educing intra-guild competition and allowing coexistence of four avian predators (snowy owls, glaucou

173 del posited in mammalian cells, in which the coexistence of H3K4me3 and H3K27me3 at developmental pro

174 We aimed to examine the relation of the coexistence of high folate and low vitamin B-12 status w

175 scales are governing the system, namely the coexistence of high- and low-density liquids, which beco

176 tion of stable Ni(I) species and the unusual coexistence of high- and low-spin Co(II) in the pentaden

177 According to the Landau theory, the coexistence of high- and low-temperature phases is therm

178 existing theory does not address the stable coexistence of hundreds of species.

179 HR rats and thus offers new insight into the coexistence of hypertension and concomitant vascular pat

180 The coexistence of immune-mediated inflammatory diseases wit

181 rior species in birth rate, resulting in the coexistence of inferior species.

182 y [fO(2)] conditions and that imposed by the coexistence of iron and wustite) at 1 GPa and 1,400 degr

183 mixture forms a liquid phase (Lalpha) and a coexistence of Lalpha and either gel or ripple phases.

184 The coexistence of large conductivity and robust ferroelectr

185 The coexistence of large monocrystalline diamonds and nanodi

186 shifts of hydrated whole cells indicate the coexistence of linear and cyclic phosphates.

187 e forms a liquid disordered (Ld) phase and a coexistence of liquid ordered (Lo) and either Ld or gel

188 rogresses in a layer-by-layer fashion with a coexistence of liquid-like and solid-like dynamical frac

189 The coexistence of magnetite and elemental iron was found in

190 How the coexistence of many species is maintained is a fundament

191 nt concentrations of nutrients can drive the coexistence of marine copiotrophs and oligotrophs.

192 The coexistence of microbiome and innate immune components i

193 the assumption of trade-offs allows for the coexistence of more species than the number of nutrients

194 Our study highlights the coexistence of morphologic and multiple functional defec

195 Coexistence of multiple ARC-HBR criteria showed additive

196 This suggests the frequent coexistence of multiple breast cancer states within a PD

197 y flux and work efficiency, resulting in the coexistence of multiple functional groups and performing

198 ts that piezoelectric BaTiO(3) NPs display a coexistence of multiple phases with low energy barriers

199 reported in Down syndrome (DS) owing to the coexistence of multiple predisposing factors related to

200 line width is broadened to over 25 nm by the coexistence of multiple reduced-dimensional perovskite d

201 ble chromatin using sequencing confirmed the coexistence of naive and effector-associated epigenetic

202 Understanding long-term coexistence of numerous competing species is a longstand

203 Coexistence of order and fluidity in soft matter often m

204 round shell of trigonal SnS(2) , forcing the coexistence of parallel vdW layering along with unconven

205 w Hampshire in 2017 was driven mainly by the coexistence of phylogenetically diverse antibiotic-resis

206 piezoresponse force microscopy, we revealed coexistence of piezoelectric and non-piezoelectric phase

207 )(1-2x)(SnSe)(x)(SnS)(x) system behaves as a coexistence of point-defect rich solid solution and phas

208 be reserved to highly selected cases, due to coexistence of relevant comorbidities.

209 evidence of effect modification based on the coexistence of reticular pseudodrusen (RPD; adjusted int

210 evidence of effect modification based on the coexistence of reticular pseudodrusen; interaction P = 0

211 eyond a third transition, we further observe coexistence of rheotaxis along the positive and negative

212 SrTiO(3) solid-solution films to realize the coexistence of rhombohedral and tetragonal nanodomains e

213 ith mixtures of nucleotides suggest that the coexistence of ribo- and arabinonucleotides does not imp

214 health-promoting activities, considering the coexistence of several active ingredients from different

215 Our findings support the coexistence of sexual recombination and a one-step opera

216 nce of sex-selective abortion, driven by the coexistence of son preference, readily available technol

217 Coexistence of species requires equalizing mechanisms th

218 The coexistence of superconducting and correlated insulating

219 onocytes and soluble factors, suggesting the coexistence of the counteractive ADCC Abs, in the same A

220 o discuss management challenges posed by the coexistence of the two conditions.

221 ioral and trophic) that could facilitate the coexistence of the two species despite the predominant n

222 llular matrix and the T6SS in modulating the coexistence of the two species on melon plant leaves and

223 The coexistence of these hetero-anions and titanium vacancie

224 with heterogeneous connectivity predicts the coexistence of three types of neurons with distinct func

225 electronic conductivity associated with the coexistence of Ti(4+) and Ti(3+) in Co-Black TNT enables

226 which had been tentatively attributed to the coexistence of trivial two-dimensional electron gas stat

227 Here, the coexistence of two (alpha and beta) phases in wedge-shap

228 chemical shifts are observed, indicating the coexistence of two beta-strand conformations.

229 Atomic-resolution imaging reveals the coexistence of two different structures at Sigma19b GBs

230 The coexistence of two Dyakonov-Voigt surface waves marks a

231 We have further discovered the coexistence of two GB types in hybrid perovskites, one e

232 It makes it possible for coexistence of two independent channels of conductivity

233 re gradient in conditions where they exhibit coexistence of two liquid phases.

234 , DLS and MALDI-TOF a synergic effect of the coexistence of two salivary-PRP fractions (basic-PRPs an

235 o unrecognized dynamical bonding effect: the coexistence of two Sm-B bonding modes within SmB(6) , co

236 ecessary or sufficient conditions for stable coexistence of two species.

237 s as influenced by the chemical and physical coexistence of U with the essential nutrient, phosphorus

238 ans with high mortality rates was enabled by coexistence of variable growth types in a population.

239 ensitive to environmental circumstances, and coexistence only occurs in narrow ranges of conditions.

240 Most work has focused on stable coexistence or assumed ecological neutrality.

241 tiation among competitors facilitates stable coexistence or because equal fitness among neutral speci

242 Niche evolution may drive coexistence or competitive exclusion, and an ability to

243 ge in one competitor, while not changing the coexistence outcome, causes the population trajectories

244 ntibiotic consumption can lead to persistent coexistence over a wide range of treatment coverages, dr

245 ve view of the likelihood of feedback-driven coexistence, partly because of a failure to analyse pair

246 strate how our method helps recover observed coexistence patterns, capture the core dynamics of the s

247 ing such data often fail to recover observed coexistence patterns.

248 Plotting this transition's local coexistence points against the distance from the films'

249 hell-model calculations reproduce this shape coexistence, predicting a rapid transition from spherica

250 ic acid base sequence, control the two-phase coexistence regime, regulate material properties of poly

251 expected to produce ecological drift versus coexistence remains unclear.

252 However, the role of bacterial motility in coexistence remains unexplored experimentally.

253 According to the invasion criterion, stable coexistence requires that all species in a community inc

254 Such mechanisms of coexistence reveal a striking paradox: Connectivity to w

255 Shifts in the phenologies of coexistence species are altering the temporal structure

256 hat PSF may play a key role in plant species coexistence, species invasion, and the phylogenetic dive

257 rocesses, we analyse how temperature affects coexistence, stability and size structure in a tri-troph

258 in some cases, liposomes in the three-phase coexistence state exhibit extreme sensitivity to lateral

259 ch population structure alone cannot support coexistence, suggesting the need for other mechanisms to

260 These aspects include promoting species coexistence, suppressing noncontributors, choosing addit

261 This results in long-term virus-host coexistence that is facilitated by perpetually changing

262 By studying the conditions of species coexistence, the ecological outcomes of cross-feeding in

263 and their consequences on long-term species coexistence, the present study highlights the role of be

264 Heterotrophs also mediated plant coexistence; their removal reduced diversity in naturall

265 Modern coexistence theory (MCT), formalised by Chesson, holds o

266 Here, we integrate modern coexistence theory and food web theory to simultaneously

267 Coexistence theory for two competing species posits that

268 unities is challenging because phenology and coexistence theory have largely proceeded independently.

269 Modern coexistence theory highlights two fluctuation-dependent

270 Modern coexistence theory is increasingly used to explain how d

271 Coexistence theory predicts that historically contingent

272 Contemporary coexistence theory provides a framework for predicting i

273 e extend the empirical application of modern coexistence theory to determine the conditions that prom

274 sms and be an important component of scaling coexistence theory to higher diversity communities.

275 Here, we apply ecological coexistence theory to show how the alignment between dif

276 Using the framework of modern coexistence theory, we found that relative nonlinearity

277 icity are almost completely unknown for most coexistence theory.

278 ss how it fits within the context of current coexistence theory.

279 ncrease, which potentially undermines modern coexistence theory.

280 est carnivores contribute to human-carnivore coexistence through behavioral and demographic mechanism

281 Thus, the dynamics evolve from stable coexistence through niche differentiation to neutral coo

282 story, traits, and environmental factors for coexistence through PSF using a meta-analysis of 1038 pa

283 such feedback and show that it controls both coexistence times and species extinction probabilities.

284 dies, and explore how microbial control over coexistence varies along productivity gradients.

285 ifferences between competing species lead to coexistence versus competitive exclusion.

286 Importantly, coexistence was only lost when the interaction became pa

287 poral population variability on tree species coexistence was usually negative, but sometimes positive

288 The loss of stable coexistence when drought has different effects on the co

289 d species differences are most important for coexistence when multiple processes operate and species

290 ogical models, we explored the potential for coexistence when one cross-feeder became independent.

291 n, relative nonlinearity strongly stabilised coexistence, where Erodium experienced disproportionatel

292 ry niche structure that otherwise stabilized coexistence, which intensified interspecific competition

293 d Daphnia from selection to permit long-term coexistence with a novel predator.

294 ray wolves (Canis lupus) are affected by the coexistence with brown bears (Ursus arctos).

295 Successful primary infection and persistent coexistence with host immune defenses are dependent on t

296 ossible clusters and the nature of its phase coexistence with liquid water could not thus far be unra

297 ruginosa and its phage DMS3vir, we show that coexistence with other human pathogens amplifies the fit

298 at dictate their assembly, substructure, and coexistence with other liquid-like compartments remain e

299 Such close coexistence with plants requires specific adaptations th

300 ecosystem stability and spatial extent; (3) coexistence within and among sites will result in a posi