ライフサイエンスコーパス: intraspecific

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

2 by chance in both forests, reflecting strong intraspecific aggregation.

3 abundances of individuals, as well as their intraspecific aggregations, in driving differences in bi

4 c mortality and explored the factors driving intraspecific aggression in the prey-rich northern area

5 Our results indicate that density-dependent intraspecific aggression is a major driver of adult wolf

6 ulated adult survival through an increase in intraspecific aggression, independent of prey availabili

7 N-ethyl palythine (= aplysiapalythine B)--as intraspecific alarm cues for sea hares (Aplysia californ

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

9 Finally, we conducted intraspecific analyses of malaria prevalence as a functi

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

11 include quantifying the magnitude of evolved intraspecific and clade-level variation in niches and un

12 across carnivores and lizards, and with both intraspecific and interspecific approaches, we consisten

13 ve been shown to play an outstanding role in intraspecific and interspecific communication systems wi

14 ence in pollinator-mediated and above-ground intraspecific and interspecific competition between two

15 The role of intraspecific and interspecific interactions in structur

16 ty, presence of pheromone trails, along with intraspecific and interspecific interactions outside the

17 ur methods enable unprecedented meiosis-free intraspecific and interspecific introgression of select

18 reaction data showed massive and significant intraspecific and interspecific variation as well as gen

19 tive analysis of these sequences both at the intraspecific and the interspecific levels have revealed

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

21 We characterize the development of several intraspecific Arabidopsis (Arabidopsis thaliana) F1 hybr

22 s well as homologous recombination events in intraspecific Arabidopsis hybrids using a set of transge

23 hat these indole ascarosides serve as potent intraspecific attraction and aggregation signals for her

24 r mouse chromosome, we produced a 103-member intraspecific backcross panel that segregated for jal, a

25 all vs large trait variation associated with intraspecific barley diversity and interspecific weed di

26 success is important for the maintenance of intraspecific biodiversity.

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

28 Intraspecific brood parasitism has been reported in arou

29 so cheat on individuals of the same species (intraspecific brood parasitism).

30 ss whether sterility barriers are related to intraspecific changes in genome size, indicating major g

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

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

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

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

35 to serve a previously undocumented role, as intraspecific chemical cues.

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

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

38 Intraspecific communication between algae has been inves

39 Intraspecific communication is integral to the behaviour

40 Geckos use vocalizations for intraspecific communication, but little is known about t

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

42 common traits and ecological significance of intraspecific communication.

43 Indeed, we observed intraspecific competition among sympatric strains in a n

44 es that spatial structure can subtly mediate intraspecific competition and the effects of natural ene

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

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

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

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

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

50 eshold responses in biophysical processes to intraspecific competition for limiting resources manifes

51 Following disturbance, intraspecific competition greatly enhanced the extinctio

52 These results support a model of intraspecific competition in nematode dauer formation.

53 Reducing intraspecific competition increases carrying capacities,

54 grei are consistent with the hypothesis that intraspecific competition is more important than predati

55 Intraspecific competition leads to a unique strategic eq

56 Instead, high intraspecific competition may facilitate the selection f

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

58 Our analysis also illustrates why intraspecific competition should not be the presumed mec

59 Intraspecific competition was thus the dominant biotic i

60 These allorecognition phenomena mediate intraspecific competition, support allotypic diversity,

61 s on the manner in which temperature affects intraspecific competition.

62 urces were depleted as a result of increased intraspecific competition.

63 rent sized food items and therefore minimize intraspecific competition.

64 resent and thereby reducing the intensity of intraspecific competition.

65 t restated by Cooke et al. in the context of intraspecific competition.

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

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

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

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

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

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

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

73 gaster and D. simulans and compare them with intraspecific control crosses of D. melanogaster.

74 pirical research on interspecific as well as intraspecific cooperation.

75 e expansions of populations with and without intraspecific cooperativity.

76 sex was independently validated in a second, intraspecific cross (A. mexicanum).

77 In contrast to the intraspecific cross, we discover that interspecific hybr

78 We confirm previous reports showing that intraspecific crosses are characterized by derepression

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

80 Intraspecific density had the strongest effect on the st

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

82 We investigated the genetic basis of intraspecific differences in the naked valley in D. mela

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

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

85 introgression could explain both the reduced intraspecific differentiation around mac-1 and the high

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

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

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

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

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

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

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

93 By comparing intraspecific diversity and interspecific divergence, we

94 vulgaris and found unprecedented amounts of intraspecific diversity for plant mitochondrial DNA (mtD

95 ue to its tropical origin, demonstrates high intraspecific diversity in cold-tolerance.

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

97 f individuals (i.e. genotypes), and yet such intraspecific diversity is rarely considered when invest

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

99 salamandra), a species that displays unique intraspecific diversity of reproductive strategies, to a

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

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

102 rabidopsis thaliana were sequenced to assess intraspecific diversity, phylogenetic relationships, and

103 phenomenon and locally modifies patterns in intraspecific diversity.

104 We estimated intraspecific DNA sequence variation by analyzing 50 gen

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

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

107 gically important than more commonly studied intraspecific effects.

108 g even in recently diverged genotypes due to intraspecific epiallelic variation.

109 f allele-specific imprinting correlated with intraspecific epigenetic variation at a TE.

110 acks on North Uist show almost unprecedented intraspecific evolution of body size that has taken plac

111 We geminated intraspecific F1 seeds of Euphrates Poplar individually

112 We developed three intraspecific F2 populations with parents that carried t

113 choice by (usually) females create important intraspecific filters for reproductive success, so that

114 This study demonstrates intraspecific food competition through active disruption

115 site relationships, a feature that may limit intraspecific gene flow or range expansions of closely r

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

117 s occurred within the last 4 millennia, with intraspecific genetic diversity arising within the last

118 However, studies of intraspecific genetic diversity have used genotypes vary

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

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

121 s is a highly divergent clade with extensive intraspecific genetic diversity.

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

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

124 Theory predicts that intraspecific genetic variation can increase the complex

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

126 tionary history, as revealed by contemporary intraspecific genetic variation, can provide valuable in

127 anning for representing adaptive and neutral intraspecific genetic variation.

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

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

130 ly used taxonomic units to formally describe intraspecific geographic variation in morphological trai

131 potential physiological basis underlying the intraspecific habitat differentiation among plants of di

132 Viral phylogeny, geographic location, intraspecific host density, and parrot community diversi

133 pecific crosses were also upregulated in the intraspecific hybrid met1XWT or meaXWT, in which the mut

134 Intraspecific hybrid zones involving long-lived woody sp

135 Intraspecific hybridization and polyploidy exacerbate th

136 ybrids fit into three categories: inter- and intraspecific hybrids involving the taxa of Fallopia sec

137 In intraspecific hybrids of Arabidopsis thaliana, genome-wi

138 nterspecific hybrids matched MEGs in fertile intraspecific hybrids.

139 Evidence in support of the intraspecific hypothesis has been accumulating for ants

140 n scenario for the parasite, whereas (2) the intraspecific hypothesis postulates that the parasite ev

141 our understanding remains largely limited to intraspecific impacts.

142 Intraspecific incompatibility in the soil bacterium Myxo

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

144 Intraspecific interactions are then concentrated within

145 nts is critical for teasing apart inter- and intraspecific interactions in aboveground and belowgroun

146 Intraspecific interactions may therefore be an important

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

148 raction strengths are weak compared with the intraspecific interactions.

149 coexisting cells could be regulated through intraspecific interactions.

150 Intraspecific interference reduces long-term pest suppre

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

152 This first intraspecific investigation of C4 evolutionary ecology s

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

154 ction is much greater than predicted from an intraspecific 'late ontogenetic' model of dwarfism in wh

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

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

157 invasions but are rarely investigated at the intraspecific level.

158 ting rampant copy-number polymorphism at the intraspecific level.

159 on in the composition of whole venoms at the intraspecific level.

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

161 Since data on intraspecific litter size variation are often sparse, it

162 Intraspecific male-male aggression, which is important f

163 Intraspecific mean log scores ranged from 1.786 to 2.584

164 First, intraspecific microbiota variation is consistently less

165 10% of the cases, compared with 42% for the intraspecific mixtures.

166 gical similarity among species and extensive intraspecific morphological diversity.

167 we report a previously unrecognized type of intraspecific multi-locus genetic variation that has bee

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

169 Intraspecific olfactory signals known as pheromones play

170 ales, from the base of the plant kingdom, to intraspecific or hybridization events associated with re

171 Two major intraspecific patterns of adult size variation are plast

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

173 Intraspecific phenotypic variation can strongly impact c

174 We examined intraspecific phenotypic variation in freeze resistance

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

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

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

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

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

180 tion often omit competitive interactions and intraspecific plasticity, but here both are essential to

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

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

183 Self-incompatibility (SI)--intraspecific pollen recognition systems that allow plan

184 the relationship between alleles underlying intraspecific polymorphism and interspecific divergence

185 ent in the common ancestor gave rise to both intraspecific polymorphism and interspecific divergence.

186 egulatory sites than expected from levels of intraspecific polymorphism, suggestive of positive selec

187 blematic because the usual methods, based on intraspecific polymorphisms, can be thwarted by difficul

188 There is a general assumption that intraspecific populations originating from relatively ar

189 nt size classes of the same species of prey (intraspecific prey responses).

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

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

192 t facilitation, which is dependent on strong intraspecific responses from one or more prey species.

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

194 s of the rising component of within-species (intraspecific) responses reveals that 87% are fit well b

195 Intraspecific richness increased plant root productivity

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

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

198 dicted from a model of dwarfing based on the intraspecific scaling of the mainland ancestor.

199 ecause these animals exhibit highly variable intraspecific scaling relationships for metabolic rate a

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

201 We tested whether intraspecific sexual size dimorphism of mammalian carniv

202 ic reproductive barrier may be linked to the intraspecific SI mechanism.

203 59) inclusivity for Y. pestis and consistent intraspecific signal transduction levels.

204 s lack eyes, there is no sexual selection or intraspecific signaling for coloration, providing an ide

205 likely functioned in substrate matching and intraspecific signaling.

206 dies of C. elegans aggregation behaviors, no intraspecific signals promoting attraction or aggregatio

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

208 positive density dependence (Allee effects), intraspecific social aggregation and area sensitivity in

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

210 Two selective pressures, intraspecific spatial competition between whole colonies

211 ather-daughter inbreeding and high levels of intraspecific strife, including the unexpected behavior

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

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

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

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

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

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

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

219 n of experience-dependent processes from the intraspecific to the interspecific domain.

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

221 Intraspecific trade-offs between growth and defense are

222 The consideration of intraspecific trait variability improved the detection o

223 ecent studies have shown that accounting for intraspecific trait variation (ITV) may better address m

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

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

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

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

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

229 Intraspecific trait variation is widespread in nature, y

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

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

232 FINDINGS: We investigated interspecific and intraspecific transmission routes, by comparing African

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

234 ay need to be considered in order to explain intraspecific variability in cooperative behaviors, and

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

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

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

238 Sexual dimorphisms fuel significant intraspecific variation and evolutionary diversification

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

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

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

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

243 ogeny of ciliates, the few studies assessing intraspecific variation have largely relied on just a si

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

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

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

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

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

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

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

251 Intraspecific variation in ecologically important traits

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

253 ults emphasize the importance of considering intraspecific variation in future climate change scenari

254 Intraspecific variation in genotypically determined trai

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

256 Examining intraspecific variation in growth and function in relati

257 a of 60 nasal microbiomes, and this revealed intraspecific variation in growth inhibition and that in

258 We assess the intraspecific variation in growth responses to nonlocal

259 We investigated intraspecific variation in imprinting, coupled with anal

260 We conclude that intraspecific variation in isoprenoid-mediated photoprot

261 Effects of intraspecific variation in keystone species have been sh

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

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

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

265 While intraspecific variation in sensory systems has been docu

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

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

268 Ultimately, intraspecific variation in social behavior has different

269 Knowledge of intraspecific variation in symbioses may aid in understa

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

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

272 crobiomes, it will be crucial to account for intraspecific variation in the traits that mediate speci

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

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

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

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

277 There was, however, considerable residual intraspecific variation indicating that other, more loca

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

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

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

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

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

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

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

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

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

287 Intraspecific variation ranged from low diversity in C.

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

289 selection provided by hosts, but also to the intraspecific variation that facilitates shifts between

290 polymorphism introduces a remarkable type of intraspecific variation that may be widespread.

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

292 paratively little attention has been paid to intraspecific variation with less drastic effects.

293 Intraspecific variation within MH Ericaceae ranges from

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

295 or whether inadequate allowance was made for intraspecific variation, in particular with reference to

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

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

298 changing environments and the maintenance of intraspecific variation.

299 usive, can be informed by the examination of intraspecific variation.

300 early defined barcode gap between inter- and intraspecific variation.