ライフサイエンスコーパス: intraspecific

1 ained by studies conducted in the context of intraspecific acoustic communication.

2 s to drought stress provides flexibility for intraspecific adaptation to diverse climates.

3 Overall, our results indicate that intraspecific adjustments along the water availability g

4 nderstand the modes of evolution influencing intraspecific allocation of ecologically important funct

5 By comparing inter- and intraspecific allometries, we find that the extreme wing

6 However, comprehensive intraspecific analyses of leaf shape variation across va

7 In intraspecific analyses, we also quantify the degree to w

8 Body size increased with depth at the intraspecific and assemblage levels.

9 symbiotic microorganisms play a key role in intraspecific and interspecific communication; therefore

10 on in the opposite direction, as a result of intraspecific apparent competition mediated via parasite

11 y, we highlight how adopting a quantitative, intraspecific approach generates new avenues for evaluat

12 In order for the intraspecific approach with wild animals to be useful fo

13 Here, we study an intraspecific breakdown of SI and its consequences in No

14 lso discuss the evolutionary implications of intraspecific chemical communication and the mechanisms

15 rmation to describe the various instances of intraspecific chemical communication between conspecific

16 also contains information on other types of intraspecific chemical communication that have not alway

17 tic diversity is an absolute requirement for intraspecific chemical communication.

18 n architectural features and in the level of intraspecific cocoon-type polymorphism.

19 ogy, behaviour, and appearance in studies of intraspecific colour variation and local adaptation.

20 vis canadensis canadensis) routinely conduct intraspecific combat where high energy cranial impacts a

21 tly evolved multiple times in the context of intraspecific communication and predator detection by tr

22 Intraspecific communication between algae has been inves

23 Intraspecific communication is integral to the behaviour

24 used both for attracting client fish and for intraspecific communication.

25 common traits and ecological significance of intraspecific communication.

26 acquisition, self/non-self recognition, and intraspecific communication.

27 h rare, several taxa use venom for agonistic intraspecific competition (e.g. ghost shrimp, Caprella s

28 In Drosophila, intraspecific competition (IC) may cause stress, canniba

29 by contrast, species interactions may reduce intraspecific competition and, thus, the potential for d

30 ies dominating at lower latitudes, to mainly intraspecific competition at the poles.

31 rom four continents, which demonstrates that intraspecific competition between territorial animals ca

32 es, decreasing the ratio of interspecific-to-intraspecific competition by 0.25% for each degree of la

33 sibly as an evolutionary response to greater intraspecific competition for higher quality food.

34 pendent cannibalism as a result of increased intraspecific competition for resources.

35 Following disturbance, intraspecific competition greatly enhanced the extinctio

36 lls into question the emerging paradigm that intraspecific competition has been demonstrated by direc

37 Instead, high intraspecific competition may facilitate the selection f

38 ommon assumption is that within a community, intraspecific competition needs to be relatively strong,

39 By stabilisation, we mean an excess of intraspecific competition relative to interspecific comp

40 ich occurs when stabilizing mechanisms cause intraspecific competition to be stronger than interspeci

41 by partitioning food resources and enhancing intraspecific competition while avoiding agonistic encou

42 us Rossia) were studied to assess inter- and intraspecific competition with niche and diet overlap an

43 ita resource availability (and by extension, intraspecific competition) did not affect the degree of

44 rspecific competition contributes as much as intraspecific competition, consistent with asymmetric co

45 wolf spiders is associated with variation in intraspecific competition, feeding ecology and populatio

46 valuate the strength of interspecific versus intraspecific competition, which combined with informati

47 tits, density regulation is driven mainly by intraspecific competition.

48 adult to juvenile ratio) and the strength of intraspecific competition.

49 ability, feeding rates, and the intensity of intraspecific competition.

50 s in foraging patterns at SCS, likely due to intraspecific competition.

51 e the ecological factors driving IS focus on intraspecific competition.

52 We investigate the effect of nonuniform intraspecific competitions on coexistence and find that

53 Our finding indicates that intraspecific competitions or alternative symmetry-break

54 ation diverge and whether the physiology and intraspecific composition of multistrain populations dif

55 ign with biogeographic boundaries, providing intraspecific concordance between biogeography and phylo

56 c competition influences the transition from intraspecific conflict to cooperation in a facultative c

57 fic competition promotes the transition from intraspecific conflict to cooperation in N. nepalensis v

58 ifferences were likely due to pQBR57's lower intraspecific conjugation rate in P. putida By contrast,

59 s from this study, we propose that verifying intraspecific conservation in vaccine or drug target can

60 host groups and account for both inter- and intraspecific contact.

61 However, we further show that intraspecific cooperation enables beetles to outcompete

62 However, such intraspecific cooperation entails risks, as fusion can t

63 pirical research on interspecific as well as intraspecific cooperation.

64 ocused on how it influences the evolution of intraspecific cooperation.

65 e expansions of populations with and without intraspecific cooperativity.

66 eralized form of Kleiber's law incorporating intraspecific, correlated variations of nutrient-uptake

67 y industrial doubled haploid pipelines using intraspecific crosses to in vivo haploid inducer males d

68 theory for two competing species posits that intraspecific density dependence should be stronger than

69 for the preponderance of mechanisms causing intraspecific density dependence, will provide an incomp

70 Intraspecific density had the strongest effect on the st

71 We ask how interspecific and intraspecific density-dependent interactions relate to p

72 environmental conditions might be generating intraspecific differences in cognitive abilities.

73 Our results revealed strong intraspecific differences in the tolerance of D. galeata

74 versity and invasibility could depend on any intraspecific differences of the invader that may alter

75 ion patterns may require an understanding of intraspecific differentiation in invasive species and it

76 ell volume within each species, we find that intraspecific distributions of cell volume and metabolic

77 in many species contain genes important for intraspecific divergence and speciation, yet mechanisms

78 ime variation is a main factor driving rapid intraspecific divergence in B. distachyon, although it i

79 Since intraspecific divergence is often the first step toward

80 Here, we investigate factors driving intraspecific divergence within a HDM alpine species Sal

81 hese factors are likely important drivers of intraspecific divergence within Cushion willow and possi

82 High intraspecific divergences were found in 34% of the speci

83 he HEC were found to contain a high level of intraspecific divergent migration, including partial mig

84 understanding of the broader implications of intraspecific diversification because comparative analys

85 ehavioural phenotypes and can favour further intraspecific diversification in life-history traits in

86 This analysis of B. gracilis intraspecific diversity across spatial scales will impro

87 ary dynamics have shown that the presence of intraspecific diversity affects community structure and

88 plants, and none of them have focused on the intraspecific diversity and evolution of their plastid g

89 By comparing intraspecific diversity and interspecific divergence, we

90 This intraspecific diversity is captured in immense natural h

91 A correlation between recombination rate and intraspecific diversity is in part owing to a higher mut

92 Many bacterial species show high intraspecific diversity of autoinducer-receptor alleles,

93 s, and where coexistence, in return, lowered intraspecific diversity of the host population.

94 ersity than higher latitude species and that intraspecific diversity showed evidence of greater persi

95 Here, we quantify how intraspecific diversity, via cultivars, changes global p

96 phenomenon and locally modifies patterns in intraspecific diversity.

97 y by facilitating challenging conditions for intraspecific dominance, whereas stasis tends to homogen

98 impact, contributing to local adaptation and intraspecific ecological diversification.

99 latum, but at a reduced strength compared to intraspecific effects alone.

100 ore the relative importance of phylogenetic, intraspecific, experimental and ecological factors to wa

101 We geminated intraspecific F1 seeds of Euphrates Poplar individually

102 rs and bite scars suggest significantly more intraspecific fighting among these experimental populati

103 Large intraspecific functional trait variation strongly impact

104 c plasticity vs. local adaptation-underlying intraspecific functional trait variation.

105 ty and identifying landscape barriers, using intraspecific genetic data and quantification of landsca

106 ct psocids was significantly higher than the intraspecific genetic distance according to the barcodin

107 this challenge and examined patterns of its intraspecific genetic diversity across Cuba.

108 By examining patterns of both inter- and intraspecific genetic diversity in mouse lemur species f

109 effects of land use and human density on the intraspecific genetic diversity of 17 082 species of bir

110 larger geographic ranges would have greater intraspecific genetic diversity than more restricted spe

111 For intraspecific genetic diversity, however, we lack even b

112 c differentiation and their integration with intraspecific genetic structure have been underexplored

113 Moreover, they show that intraspecific genetic variability can be as important as

114 Theory predicts that intraspecific genetic variation can increase the complex

115 Taken together, our results indicate that intraspecific genetic variation can play a key role in s

116 and attention has focused on exploiting the intraspecific genetic variation within a crop [Hajjar et

117 anning for representing adaptive and neutral intraspecific genetic variation.

118 ers, to investigate the extent of inter- and intraspecific genomic rearrangements and variation in re

119 However, the impacts of intraspecific genotypic diversity in these studies are u

120 ated recombination rate variation in a large intraspecific hybrid population (named HEB-25) derived f

121 Intraspecific hybrid zones involving long-lived woody sp

122 Intraspecific hybridization and polyploidy exacerbate th

123 nterspecific hybrids matched MEGs in fertile intraspecific hybrids.

124 our understanding remains largely limited to intraspecific impacts.

125 r, the proposed role of certain compounds as intraspecific infochemicals appears questionable.

126 cruitment of four myrmecochore species among intraspecific interaction treatments of each ant species

127 Interestingly, intraspecific interactions also appear to act at a short

128 nserved across two body sites whereas strong intraspecific interactions are much more conserved, rang

129 ionately positive, whereas almost all strong intraspecific interactions are negative.

130 Intraspecific interactions are then concentrated within

131 jority of empirical studies, the strength of intraspecific interactions is estimated by using simple

132 Intraspecific interactions may therefore be an important

133 Such intraspecific interactions need to be understood in orde

134 coustic transceivers to study the inter- and intraspecific interactions of sand tiger sharks Carchari

135 stabilizing mechanisms that enhance negative intraspecific interactions versus interspecific ones.

136 coexisting cells could be regulated through intraspecific interactions.

137 obial diversity on plant fitness trade-offs, intraspecific-interactions, and soil nutrient dynamics i

138 Here, we show a unique crop response to intraspecific interference, whereby neighboring sunflowe

139 In humans and chimpanzees, most intraspecific killing occurs during coalitionary intergr

140 revalence of cytonuclear interactions at the intraspecific level remains poorly investigated.

141 oided by other carnivores, especially at the intraspecific level, most likely to reduce exposure to p

142 invasions but are rarely investigated at the intraspecific level.

143 heir habitat conditions on interspecific and intraspecific levels in various hydraulic parameters.

144 Intraspecific mean log scores ranged from 1.786 to 2.584

145 However, the factors governing intraspecific microbiome variability are underexplored a

146 First, intraspecific microbiota variation is consistently less

147 10% of the cases, compared with 42% for the intraspecific mixtures.

148 s selected by prior tests to have a range of intraspecific natural heat tolerance.

149 s the dominance of superior competitors, and intraspecific niche variation reduces species-level nich

150 e families in plants, but the true extent of intraspecific NLR diversity has been unclear.

151 Intraspecific olfactory signals known as pheromones play

152 ic overlap of foraging areas was higher than intraspecific overlap.

153 Further, we show that comparing intraspecific patterns of trait variation across ranges,

154 We examined intraspecific phenotypic variation in freeze resistance

155 into how unique habitat characteristics and intraspecific phenotypic variation may allow pikas to ex

156 the oak genome and of oak interspecific and intraspecific phenotypic variation will improve our abil

157 oses, we sampled extensively to estimate the intraspecific phylogenetic pattern of the Chinese mole s

158 Almost 30 y ago, the field of intraspecific phylogeography laid the foundation for spa

159 Specifically, intraspecific phytochemical changes associated with vert

160 Our results suggest that intraspecific phytochemical diversity structures herbivo

161 This highlights the importance of conserving intraspecific plant diversity.

162 We show that over 90% of the intraspecific plant taxa found in a literature search ar

163 ibranchs, and suggest further exploration of intraspecific plasticity versus evolutionary changes in

164 We analyze inter- and intraspecific plastid comparative genomics and phylogeno

165 We quantified intraspecific ploidy diversity, heterogeneity in diversi

166 truction of transmission events reveals that intraspecific PLVA transmission has occurred among panth

167 um to evaluate: (1) the relationship between intraspecific polyploid frequency and species diversific

168 Our study emphasises the role of intraspecific polyploid frequency combined with ecologic

169 dy the scale at which water-use traits alter intraspecific population yields.

170 In addition to intraspecific recombination, this study showed that rece

171 over historic time-scales for understanding intraspecific response to climate change.

172 The same data set reveals that intraspecific responses to climate variation do not mirr

173 Intraspecific richness increased plant root productivity

174 effects are driving some of the responses to intraspecific richness.

175 s, we found size-temperature interactions in intraspecific scaling of metabolic rate to be common.

176 e first time, we were able to closely follow intraspecific selection within an artificial population

177 are widely studied as a fine-tuned system of intraspecific sexual communication that reinforces inter

178 ting upper canopies in mixtures, rather than intraspecific shifts in canopy structure or chemistry.

179 likely functioned in substrate matching and intraspecific signaling.

180 Experimental evidence for intraspecific size-structured responses in prey populati

181 While foraging, animals can form inter- and intraspecific social signalling networks to avoid simila

182 short timescales through selection from the intraspecific standing stock, indicating the potential f

183 nubilalis mitochondrial genomes contained 82 intraspecific substitution and insertion/deletion mutati

184 We conducted an intraspecific target-neighbor pot experiment with Androp

185 This result for the young age of intraspecific taxa is consistent with the earlier observ

186 arely include the divergence times of sister intraspecific taxa, and when they do little is said abou

187 A Bayesian analysis of intraspecific taxon ages indicates that indeed these tax

188 m functioning, and consistent with models of intraspecific territoriality.

189 solutions) could be useful model systems for intraspecific tests of the universal ecological response

190 irds (2008-2011) we demonstrate a shift from intraspecific to interspecific transmission that along w

191 genic mutants became highly resistant to two intraspecific toxins, the S-pyocins AP41 and S1.

192 tory and the leaf economics spectrum explain intraspecific trait changes across global spatiotemporal

193 Despite growing evidence for intraspecific trait differences, it remains unclear unde

194 Intraspecific trait variability (ITV) maintains function

195 Intraspecific trait variability has important consequenc

196 Intraspecific trait variation along latitudinal gradient

197 his review discusses sources and patterns of intraspecific trait variation and their consequences for

198 ce across the gradient, indicating that high intraspecific trait variation belowground may facilitate

199 an extraction of living resources can reduce intraspecific trait variation by, for example, causing t

200 Here we explore the consequences of intraspecific trait variation for coexistence in two- an

201 models can allow a stronger consideration of intraspecific trait variation if the necessary data are

202 Intraspecific trait variation is caused by genetic and p

203 Yet intraspecific trait variation is inconsistent and hard t

204 rowth contributes to demographic parameters, intraspecific trait variation is likely to play a key ro

205 Thus, considering the evolution of intraspecific trait variation is necessary for reliable,

206 Intraspecific trait variation is widespread in nature, y

207 Additionally, the degree of intraspecific trait variation was positively correlated

208 ently have often overlooked the influence of intraspecific trait variation, which can profoundly alte

209 n the S. solidus population, suggesting that intraspecific variability can affect the assembly of par

210 ions, suggesting that failure to account for intraspecific variability can result in overestimation o

211 among locations, and shows the importance of intraspecific variability in mediating eco-evolutionary

212 berry clones and served to explain the great intraspecific variability in mulberry secondary metaboli

213 three Pinaceae) we quantified the inter- and intraspecific variability of a set of traits along a wat

214 consumed vegetable, we dissected the natural intraspecific variability of tocochromanols in tomato fr

215 unt of variability for most traits, although intraspecific variability was also relevant.

216 ficient wings in 12 species and a further 10 intraspecific variants, including three co-mimetic pairs

217 ed forest tree species, the understanding of intraspecific variation among populations and their resp

218 d demonstrates asymmetry in the magnitude of intraspecific variation among species is critical for un

219 We compare amounts of intraspecific variation and covariation between cranial

220 Sexual dimorphisms fuel significant intraspecific variation and evolutionary diversification

221 aridity gradients, yet little is known about intraspecific variation and its drivers.

222 on modelling are characterized by continuous intraspecific variation and trait-environmental relation

223 trophic (MH) species, we explored inter- and intraspecific variation as well as selective constraints

224 The intraspecific variation contributed to approximately one

225 e phylogenetic relatedness among species and intraspecific variation could contribute to the observed

226 response of species to climate change ignore intraspecific variation due to local adaptation.

227 ely fast and possess unusually low levels of intraspecific variation during postnatal development.

228 structure was detected, also suggesting that intraspecific variation exists at mtMutS in Chrysogorgia

229 cle phenotypes to species-level ecology, but intraspecific variation has remained largely unexplored.

230 Significant intraspecific variation in A is known to exist in variou

231 of the first to link migratory strategy and intraspecific variation in body shape.

232 In fact, we find similar amounts of intraspecific variation in both species, but no covariat

233 C3 -gm , little is currently known about the intraspecific variation in C4 -gm or its responsiveness

234 Understanding the evolution of inter and intraspecific variation in cognitive abilities is one of

235 the X-linked M/LWS opsin gene have produced intraspecific variation in color vision.

236 ce of the first two mechanisms, we find that intraspecific variation in competitive ability increases

237 step toward this goal is determining whether intraspecific variation in coral metabolite profiles can

238 distribution models account for the role of intraspecific variation in determining responses to anti

239 worldwide; however, factors responsible for intraspecific variation in disease resistance remain unc

240 T. castaneum and T. confusum) to examine how intraspecific variation in dispersal behaviour and commu

241 process, independent of community context or intraspecific variation in dispersal behaviour.

242 Recognition of the importance of intraspecific variation in ecological processes has been

243 Intraspecific variation in ecologically important traits

244 nge of fish species and identify patterns of intraspecific variation in energy storage, and use these

245 Our characterization of intraspecific variation in expression dynamics suggests

246 Examinations of intraspecific variation in g(sn) as a function of climat

247 ld help parameterize models that account for intraspecific variation in global change predictions, an

248 e consequential for the host [16] or whether intraspecific variation in host traits can alter the tra

249 We conclude that intraspecific variation in isoprenoid-mediated photoprot

250 aldulensis subsp. camaldulensis to partition intraspecific variation in leaf functional traits to gen

251 Intraspecific variation in leaf traits arises similarly

252 For the first time, these data illustrate intraspecific variation in metabolomic profiles for cora

253 ies of species coexistence, the magnitude of intraspecific variation in nature is forcing ecologists

254 Here we review the current data on intraspecific variation in recombination rate and discus

255 rmore, the relative magnitudes of inter- vs. intraspecific variation in resource use are rarely consi

256 While intraspecific variation in sensory systems has been docu

257 a pace-of-life syndrome describes inter- and intraspecific variation in several life-history traits a

258 nderthals and recent humans demonstrate high intraspecific variation in shape covariation.

259 requires us to identify the genes underlying intraspecific variation in signals and responses and to

260 results demonstrate how detailed studies of intraspecific variation in suites of traits along enviro

261 h genomes are stably maintained, we analyzed intraspecific variation in the mitochondrial genome of S

262 We address the extent of intraspecific variation in the regulation of a mutually

263 We present evidence of intraspecific variation in the use of adhesive toe pads

264 Non-human animals sometimes show marked intraspecific variation in their cognitive abilities tha

265 Even less is known about intraspecific variation in tissues other than stems, des

266 ork highlights the importance of considering intraspecific variation in trait-based ecology and demon

267 ive approach that considers the magnitude of intraspecific variation in traits and growth as it relat

268 We hypothesized that intraspecific variation in vulnerability in leaves and s

269 Intraspecific variation in water potential at which 50%

270 Here we incorporate intraspecific variation into a common model of competiti

271 rsal, dispersal syndromes and more generally intraspecific variation into studies predicting the impa

272 Intraspecific variation is at the core of evolutionary t

273 earance, and it is known that, despite rare, intraspecific variation is caused by seasonality, epigen

274 lthough biologists have long recognized that intraspecific variation is consequential to an animals'

275 However, when intraspecific variation is heritable, allowing for the p

276 This intraspecific variation is likely the result of genetic

277 d establish that the genetic architecture of intraspecific variation is quite similar to that of the

278 ecific manners but the influence of pathogen intraspecific variation is rarely studied.

279 ies, the only strong effect of non-heritable intraspecific variation is to reduce expected species ri

280 e played by most organismal traits and their intraspecific variation is unknown.

281 rliest-diverging dinosaurs, anomalously high intraspecific variation is widespread but then is lost i

282 Intraspecific variation maintained in natural population

283 to overexploitation, deciphering patterns of intraspecific variation may also enable recognition of p

284 ces associated with invasion history-related intraspecific variation of the non-native species.

285 cies and its mean metabolic rate, neglecting intraspecific variation of these 2 traits.

286 erging empirical interests in the effects of intraspecific variation on species diversity.

287 alternative site fidelity strategies driving intraspecific variation remain poorly understood and hav

288 between species-level clades was 10%, while intraspecific variation was 30 times lower (0.36%).

289 Intraspecific variation within MH Ericaceae ranges from

290 hood of coexistence is in general reduced by intraspecific variation, except when the species have al

291 t ecological models and theories incorporate intraspecific variation, review existing data sources th

292 nes on when it is most important to consider intraspecific variation, such as when trait variation is

293 While there was substantial intraspecific variation, there was some evidence for hos

294 ory shapes the interspecific relatedness and intraspecific variation, which has a profound influence

295 seek to identify the mechanisms maintaining intraspecific variation.

296 changing environments and the maintenance of intraspecific variation.

297 Insights into intraspecific variations in early life-stages may furthe

298 surrounding this species may be reflected in intraspecific variations in photosynthetic behavior.

299 Our findings underline the fact that intraspecific variations in sensitivity to precipitation

300 at allows measuring the relative strength of intraspecific versus interspecific competition in domina