ライフサイエンスコーパス: sociality

1 y social species and favour the evolution of sociality.

2 r the cross-generation transmission of human sociality.

3 ial relationships; in others, it facilitates sociality.

4 and community, two elementary forms of human sociality.

5 allowed the expression of contemporary human sociality.

6 tions for epidemic disease spread and animal sociality.

7 in our understanding of the genetic basis of sociality.

8 explain fairness and other features of human sociality.

9 cation and adaptive responses to fluctuating sociality.

10 logical and demographic drivers that promote sociality.

11 ity--that may explain the evolution of human sociality.

12 correlate with other self-report measures of sociality.

13 nism underlying male- versus female-directed sociality.

14 arasite stress and the variables relating to sociality.

15 assumption of the parasite-stress theory of sociality.

16 ain cultural practices promoting assortative sociality.

17 ategies as well as interspecific patterns of sociality.

18 gains and losses of the traits underpinning sociality.

19 ytocin (OT) are key modulators of vertebrate sociality.

20 has always been a central component of human sociality.

21 coordinate their activities and benefit from sociality.

22 and helps explain interspecific patterns of sociality.

23 all of which represent an advanced state of sociality.

24 ology and a key element in understanding our sociality.

25 early learning in the development of female sociality.

26 framework to understand animal space use and sociality.

27 s VT, at least, is associated with levels of sociality.

28 of pathogen transmission that can accompany sociality.

29 the role of trophallaxis in the evolution of sociality.

30 ionship exists between levels of kinship and sociality.

31 reciprocity", that may in part explain human sociality.

32 sensilla confirm hypotheses of their complex sociality.

33 es that repeatedly underpin the evolution of sociality.

34 ic is a defining and ancient aspect of human sociality.

35 ariation in key functional traits, including sociality.

36 ge is restricted to species with a degree of sociality.

37 s crucial for understanding the evolution of sociality.

38 le phylogenetic patterns in the evolution of sociality.

39 o play an important role in the evolution of sociality.

40 social recognition memory without affecting sociality.

41 y can be used to advance research into human sociality.

42 nderstanding constraints on the evolution of sociality.

43 enough to explain patterns in interspecific sociality.

44 major transitions, such as the evolution of sociality.

45 ges that have a great positive impact on pro-sociality.

46 and the connections between QS and bacterial sociality.

47 cal generalism facilitates the transition to sociality.

48 effect on animals across multiple levels of sociality.

49 nd use bacteria to understand the biology of sociality.

50 tutes a paradox of environmental quality and sociality.

51 layed an escalating role in the evolution of sociality.

52 s adaptations to ancestral human small-scale sociality.

53 best support infants with varying levels of sociality.

54 the need for long-term evolution or derived sociality.

55 mon principles in the molecular evolution of sociality.

56 s warfare, in moulding human cooperation and sociality.

57 s of related individuals, and in shaping our sociality.

58 It has been suggested that bee sociality(14) and diet(15) affect bee foraging ranges, b

59 both directions between solitary nesting and sociality [2-5].

60 t), (2) territorial pair versus family group sociality, (3) large versus small maximum flock size, an

61 er harsh environments drive the evolution of sociality [6] or, alternatively, whether sociality facil

62 These discoveries suggest that sociality, a key ungulate strategy to reduce predation-r

63 forces are known to shape the expression of sociality across a broad range of biological taxa, their

64 n sociality, the environmental predictors of sociality across broad geographic and taxonomic scales r

65 show that in the wild, different degrees of sociality across populations are associated with differe

66 tionships, making life-history important for sociality across taxonomic scales.

67 societies requires greater knowledge of how sociality affects the performance of whole colonies.

68 The evolution of sociality and altruism is enigmatic because cooperators

69 Furthermore, sociality and behaviour can also shape space use, and su

70 at large colony sizes, thus addressing both sociality and colony size range in this social spider.

71 ive evolution most likely related to complex sociality and cooperation.

72 elderly dominants and support the idea that sociality and delayed senescence are positively self-rei

73 Many investigations into sociality and disease may nevertheless be subject to cry

74 y pathobiology, in which the relationship of sociality and disease transmission can be comparatively

75 d Burmese amber resolves ambiguity regarding sociality and diversity in the earliest ants.

76 Thus, both sociality and ecology have played a role in producing th

77 r reveals that no association exists between sociality and encephalization across Carnivora and that

78 er survival, with important implications for sociality and evolution.

79 lturally transmitted behavior coevolved with sociality and extended lifespan in primates.

80 to understand fully the connections between sociality and fitness.

81 avior and the poorly understood link between sociality and fitness.

82 nsitivity and attunement necessary for human sociality and for rearing a human child.

83 Here, we explore the relationship between sociality and genome architecture in Synalpheus snapping

84 ilable data on molecular evolution of insect sociality and highlight key biotic and abiotic factors i

85 neuromodulators involved in human affect and sociality and in disorders like depression and autism.

86 , which predicts a close association between sociality and increased encephalization.

87 ence-sensitive neurons evolve in relation to sociality and indicate that gregarious species accentuat

88 namic social networks in the study of animal sociality and its consequences.

89 fe history traits with these clades, such as sociality and maternal care.

90 mitation may be an early predictor of infant sociality and may help identify infants at risk of neuro

91 ate that under certain conditions, both host sociality and pathogen virulence exhibit continuous cycl

92 s for eight generations were reintroduced to sociality and promiscuity (free mate choice), they adapt

93 ion has been fundamental to understand human sociality and social evolution more broadly.

94 explored the relationship between individual sociality and the order of behavioural acquisition.

95 We hypothesized a major distinction of sociality and transitivity along dorsal and ventral late

96 In addition, representations of sociality and transitivity features were found more ante

97 ations of action information associated with sociality and transitivity in bilateral LOTC.

98 ect-unrelated versus object-related actions (sociality and transitivity, respectively, hereafter).

99 limits our understanding of the link between sociality and vocal complexity.

100 ductivity of the environment, trophic niche, sociality, and ability to defend a territory.

101 neuropsychological measures of intelligence, sociality, and academic abilities.

102 ening directions for research on inequality, sociality, and aging.

103 with genetic correlations between boldness, sociality, and antipredator morphology, as expected, bei

104 l adaptations such as flight, metamorphosis, sociality, and chemoperception.

105 er, many behavioural paradigms are devoid of sociality, and commonly-used social spontaneous recognit

106 mediate spatial navigation, decision-making, sociality, and creativity evolved, in part, to enable su

107 with age; and those dependent on migration, sociality, and cultural transmission for survival.

108 hensive long-term dataset of their behavior, sociality, and ecology.

109 has coevolved with enlarged brains, complex sociality, and extended lifespans.

110 of mind, culture and language relate to our sociality, and facilitate the formation and maintenance

111 its (body size, phenology, nesting location, sociality, and foraging choice) and prevalence of trypan

112 pothesis that the evolution of large brains, sociality, and long lifespans has promoted reliance on c

113 ng of the relation between moral obligation, sociality, and stancetaking in interaction.

114 ocieties fragment, the workings of multitier sociality, and the significance of cooperation.

115 l behaviours and three alternate measures of sociality, and whether the LPS effect differs by kinship

116 Such impact is traditionally explained by sociality: ants are the first major group of ground-dwel

117 d by groups of nestmates and the benefits of sociality are retained continuously.

118 size, position in social network, individual sociality) are associated with patterns of gut microbial

119 s might depend on the type of behaviour, how sociality as a biological trait is defined (e.g. network

120 zation across Carnivora and that support for sociality as a causal agent of encephalization increase

121 Sociality based on loose aggregation is followed by a se

122 ween them, these create a form of multilevel sociality based on strong versus weak ties similar to th

123 authors were especially interested in female sociality because adult female birds influence male cour

124 sly argued that language remains embedded in sociality because the motivation to communicate exists o

125 Sociality before breeding was connected with patterns of

126 ile revealing that the relative influence of sociality, breeding experience and local ecology are dyn

127 m the ventral tegmental area (VTA) regulates sociality, but the ongoing, unstructured nature of free

128 s and rules are crucial for explaining human sociality, but we question the claim of there not being

129 e to consider the multidimensional nature of sociality by explicitly examining social associations ac

130 We propose that titration of sociality by MT represents a phylogenetically deep frame

131 utism spectrum disorder (ASD) development of sociality can be impaired.

132 lutionary transition from solitary living to sociality can occur.

133 m their intrinsic interest for understanding sociality, can have significant bearing across many fiel

134 s and, if so, whether other aspects of early sociality contribute to this difference.

135 tor in the variation of in-group assortative sociality, cross-nationally and across the United States

136 Human groups maintain a high level of sociality despite a low level of relatedness among group

137 When the consequences of sociality differ depending on the state of individual an

138 Sociality-driven maternal and paternal effects reveal in

139 lutionary approaches and theories focused on sociality, dual inheritance, multilevel selection, and d

140 ediary mechanism with broad consequences for sociality (e.g., group structure, functioning), ecology

141 Animal sociality emerges from individual decisions on how to ba

142 n size, potentially rendering transitions to sociality "evolutionarily dead-ends." We addressed this

143 When sociality evolved and in which groups remain open questi

144 refore, deciphering the context in which our sociality evolved is invaluable in understanding what ma

145 rodents (Muridae: Hydromyini) and show that sociality evolves only under harsh conditions of low rai

146 We find that sociality evolves primarily from host generalists, and a

147 jor outstanding problems in the study of how sociality evolves.

148 of sociality [6] or, alternatively, whether sociality facilitates the invasion of harsh environments

149 This ultra-sociality figures largely in our success as a species.

150 male phenotypes, and evolves in relation to sociality (flocking vs. territorial) across several rela

151 s can be used to examine the consequences of sociality for genome evolution and gene expression.

152 ease in intelligence may be domain-specific (sociality, for example), and the brain specialization th

153 offer insight in to trends related to human sociality found from research in other fields such as ps

154 mosignals may sustain the transfer of infant sociality from the mother-infant bond to life within soc

155 More importantly, this study shows that sociality has a key role in the resilience of population

156 For humans and other primates, sociality has adaptive value.

157 Intense sociality has been a catalyst for human culture and civi

158 les of oxytocin and vasopressin in mammalian sociality has been shaped by seminal vole research that

159 Sociality has been shown to have adaptive value for greg

160 mparative genomic study in spiders, in which sociality has evolved independently at least 23 times, b

161 A second possibility, however, is that once sociality has evolved, subsequent transitions represent

162 Sociality has many rewards, but can also be dangerous, a

163 Primate sociality has received much attention and its complexity

164 bes, but particularly sophisticated forms of sociality have arisen in the myxobacteria, including gro

165 ity; independent evolutionary transitions in sociality have independent genetic underpinnings.

166 groups; and inter-individual differences in sociality have reported fitness implications in numerous

167 y suited for investigating the links between sociality, health, longevity and reproductive success.

168 e use empirical observations to test whether sociality helps animals cross busy roads.

169 Current concepts of human sociality highlight a fundamental role of the hypothalam

170 we consider the demographic consequences of sociality, highlight a historic bias favoring studies of

171 OTC: dorsal LOTC represents actions based on sociality (how much an action is directed to another per

172 This sociality, however, cannot be fully explained by the can

173 effects of body size, habitat structure and sociality identified as determinants of avian escape str

174 vel effects in the origin and maintenance of sociality, illustrate the dynamic nature of equilibria w

175 k a consolidation of the mechanisms by which sociality impacts reproduction.

176 -stress while devaluing in-group assortative sociality in areas with low levels of parasite-stress.

177 immune repertoire predates the evolution of sociality in bees.

178 sults show that longevity (i) increases with sociality in both sexes and (ii) decreases with male-bia

179 Although lack of sociality in captivity appears to mediate domestication,

180 ationships between household religiosity and sociality in children sampled from six countries.

181 , encephalization trends are associated with sociality in extant species.

182 tor distributions in the lateral septum, and sociality in female zebra finches was reduced by OT anta

183 estigated the links between neuroanatomy and sociality in free-ranging rhesus macaques.

184 es were studied relating to the emergence of sociality in hand-reared cowbirds (Molothrus ater): prox

185 ping a comprehensive understanding of animal sociality in human-modified landscapes is especially imp

186 thylenedioxymethamphetamine (MDMA) increases sociality in humans and animals.

187 Any defects of sociality in individuals diagnosed with autism spectrum

188 present evidence of a deep imprint of human sociality in language, observing that (i) the words of n

189 an be used to clarify the extent and form of sociality in natural populations.

190 Because PR interferes with aspects of sociality in other male rodents, PR may eventually be fo

191 ht the adaptive value of large body size and sociality in promoting individual fitness in stochastic

192 higher reproductive flexibility, and higher sociality in species living in more variable climates.

193 e force in the sub-social route to permanent sociality in spiders.

194 ence the independent evolutionary origins of sociality in Synalpheus shrimps.

195 ight thing to do" does not only increase pro-sociality in the choice immediately after, but also in s

196 tation that facilitates in-group assortative sociality in the face of high levels of parasite-stress

197 imply that queen pheromones regulate insect sociality in two distinct and complementary ways, i.e.,

198 hinos and the importance of depredation, not sociality, in the evolution of eavesdropping [4, 7].

199 for the AVP/OT system in several aspects of sociality, including vocal communication and sociospatia

200 s who scored high on Nice had high composite sociality indices (CSI) and stable partner preferences,

201 lution of individual signatures and that the sociality-individuality relationship may be a general ph

202 Sociality is a derived trait, and kin discrimination exi

203 ature of the relationship between vision and sociality is a particular visual sensitivity to social e

204 In some taxa, sociality is accompanied by a transition from outcrossin

205 Sociality is an important component of population struct

206 und in most other birds and mammals: Primate sociality is based on bonded relationships of a kind tha

207 Sociality is believed to have evolved as a strategy for

208 ionship between infant survival and maternal sociality is confounded by previously underappreciated v

209 Human sociality is governed by two types of social norms: inju

210 Human sociality is grounded in the dynamic coordination of ind

211 ferences in the effects of oxytocin on human sociality is limited because of the predominance of all-

212 This is because in-group assortative sociality is more important for the avoidance of infecti

213 pendent changes in social behavior, maternal sociality is no longer positively associated with infant

214 Sociality is probably an evolutionarily labile trait tha

215 hornhill's (F&T's) parasite-stress theory of sociality is supported largely by correlational evidence

216 A hallmark of bacterial sociality is that groups can coordinate cooperative acti

217 roups suggests that the affective meaning of sociality is to some degree a function of social stratif

218 ls that are eusocial, or those with advanced sociality, is reproductive specialization into worker an

219 We thereby demonstrate that sociality itself can be truly plastic in a hymenopteran.

220 t coevolutionary relationships between human sociality, language and teaching have likely been fundam

221 tion is assumed to underlie the evolution of sociality, many vertebrates-including nearly half of all

222 Our results show that sociality maximizes genotypic diversity, which contradic

223 alian brain evolution and highlight the role sociality may play in driving the evolution of large bra

224 not significantly impair helping but reduced sociality measures, indicating that helping does not rel

225 k two interconnected questions: (a) how does sociality mediate vulnerability to climate change, and (

226 evolutionary discontinuity supporting human sociality might seize on this as an alternative to enjoy

227 dependency dimension - individuality versus sociality - might offer important insights into the dyna

228 longevity, egg mass relative to female mass, sociality, migration status and time to fledge were amon

229 avior and the neurobiological foundations of sociality more broadly, our understanding of the ant ner

230 ress uncovering the genomic underpinnings of sociality, much less is known about how social living af

231 To evolve, sociality must have some heritable basis, yet the herita

232 ain stable across years, similar to forms of sociality observed in other vertebrates.

233 tion of wild baboons, which demonstrate that sociality of adult females is positively associated with

234 We investigated the sociality of essential virulence factors (crystal toxins

235 hat cooperation originated from inherent pro-sociality of individuals.

236 ns display a lifelong preoccupation with the sociality of moral obligation.

237 for significant behavioural modifications in sociality of southern pig-tailed macaques visiting Malay

238 It would appear that the sociality of the African wild dog is dependent upon the

239 To investigate the impact of sociality on associative learning, we compared the indiv

240 ive value for females, but direct effects of sociality on fitness have never been demonstrated.

241 The effects of sociality on infant survival are independent of the effe

242 cross the orthogonal dimension was lower for sociality only in adolescents.

243 y those involved in sensorimotor processing, sociality or cognition, may reveal features that are eit

244 tention has focused on the evolution of host sociality or pathogen virulence separately, few studies

245 sitional populations that can express either sociality or solitary nesting, depending on environmenta

246 STm that influence species-typical levels of sociality or that mediate approach and avoidance.

247 of ID MMEs and host characteristics, such as sociality or trophic level, but ID MMEs did occur more f

248 ntibodies and tested whether host phylogeny, sociality, or diet influence viral prevalence and divers

249 a hallmark of animals with higher levels of sociality, our findings in a species considered solitary

250 Importantly, our results suggest that sociality plays a role in safe movements around anthropo

251 tive symptom measures, self-report scales of sociality, pleasure, and motivation, and coded facial ex

252 rtant in many ecological processes including sociality, predation and disease transmission.

253 Findings provide non-invasive evidence that sociality predicts vocal phenotype in a wild great ape.

254 a model of primate social evolution, whereby sociality progresses from solitary foraging individuals

255 We evaluate whether sociality promotes ecological generalism (social conques

256 Sociality provides a unique opportunity for animals to a

257 ortance of resource optimization afforded by sociality (rather than resource abundance per se) in sha

258 ancestral ground plan (a genetic toolkit for sociality) regulates caste differentiation across levels

259 Assessing the physiological costs of sociality remains challenging due to complex interaction

260 Yet the genetic basis of sociality remains unclear.

261 of this inter-individual variation in human sociality remains unexplained from a biological perspect

262 disasters affect disease risk via changes in sociality remains unexplored in animal populations.

263 Advanced sociality requires not just nestmate cooperation and spe

264 F&T) present a model of in-group assortative sociality resulting from differing levels of parasite-st

265 This may explain why primate sociality seems to be so different from that found in mo

266 Consistent with the notion that sociality should be studied from the perspective of soci

267 des in relation to three separate domains of sociality (social disposition, dyadic relationships, and

268 cal generalism facilitates the transition to sociality (social transition hypothesis) in 38 Synalpheu

269 that resource richness may explain variable sociality, spatial overlap or temporary aggregations of

270 a social dilemma: the evolutionarily-stable sociality strategy (ESS) is distinct from the collective

271 ere there is clear variation in the level of sociality, such as the social insects.

272 g production, and to the genetic benefits of sociality, suggesting that helping was not simply mispla

273 ty in immune complement across a gradient of sociality suggests that a reduced immune repertoire pred

274 ee species characterized by a lower level of sociality than ants and honeybees provide new insights i

275 cooperative behaviors and advanced forms of sociality that depend on pheromone-mediated communicatio

276 nct from the collective optimum-the level of sociality that would be best for all individuals.

277 ndings support the parasite-stress theory of sociality, that is, the proposal that parasite-stress is

278 as been implicated in species differences in sociality, the environmental predictors of sociality acr

279 Across several independent origins of sociality, the genomes of social hymenopterans share two

280 pressures, challenging static models linking sociality to cognition.

281 ccess of both: (a) altruistic forms of human sociality towards unrelated members of one's group; and

282 nts (body parts, scenes, movements, objects, sociality, transitivity) and three control models (dista

283 elation to key life-history characteristics (sociality, trophic level, habitat breadth) and environme

284 Evolutionary explanations for mammalian sociality typically center on inclusive-fitness benefits

285 , but an explicit account of the dynamics of sociality under selection pressure imposed by contagion

286 ify and expand the parasite-stress theory of sociality used to fuel our research presented in the tar

287 l of ectoparasitism, with the net benefit of sociality varying under these different conditions.

288 Contrary to expectations, individual sociality was negatively associated with gut microbial d

289 nterstate analyses that in-group assortative sociality was positively associated with parasite-stress

290 Furthermore, the level of suppression in sociality was positively correlated with that of stereot

291 ng of the genetic underpinnings of mammalian sociality, we generated a reference transcriptome for th

292 Host phylogeny and sociality were not significantly associated with HA anti

293 Gender and sociality were relatively inconsequential, although high

294 dorsal LOTC are segregated along features of sociality, whereas action representations in ventral LOT

295 xed groups, and present evidence that 'loose sociality', whereby individuals do not form fixed groups

296 more closely resemble an ancestral state of sociality wherein the phenotype difference between worke

297 but a mechanism underpinned by more complex sociality, which could be carried over to other behaviou

298 intra-regional heterogeneity in assortative sociality, which, we argue, can be better explained by a

299 l novel scenarios, as well as aggression and sociality within familiar and novel social contexts.

300 ral contributor to children's well-being and sociality; yet, the neural basis of coparenting has not