ライフサイエンスコーパス: eusocial

1 a wide range of life styles from solitary to eusocial.

2 tion were more relevant for lineage-specific eusocial adaptations.

3 Though Cretaceous stem-group ants were eusocial and adaptively diverse, we hypothesize that the

4 Helpers in primitively eusocial and cooperatively breeding animal societies for

5 arison of orthologous gene promoters between eusocial and solitary species revealed significant regul

6 ts is adaptive, perhaps tailoring hearing to eusocial and subterranean lifestyles.

7 The observed differences between the eusocial and the solitary bee species may reflect differ

8 Although all ants are eusocial, and display a variety of complex and fascinati

9 mpact of sleep deprivation on signaling in a eusocial animal.

10 s and rates of molecular evolution in marine eusocial animals.

11 forced sterility/coercion of conspecifics in eusocial animals; sex-change suppression in sequential h

12 e, lethal hazards in sexes and castes of the eusocial bee Bombus terrestris and in sexes of the solit

13 cene (ca. 45 million years ago) diversity of eusocial bee lineages.

14 Eusocial bees in particular must collect pollen and nect

15 Eusocial bees inhabit a wide range of environments and t

16 Colony defense in other eusocial bees is less well understood, but enough inform

17 data from acorn woodpeckers and primitively eusocial bees potentially can account for many of the hi

18 liponini), a mainly tropical group of highly eusocial bees, present an intriguing variety of well-des

19 female mating frequencies in 267 species of eusocial bees, wasps, and ants.

20 se plays an important role in the biology of eusocial bees.

21 Eusocial behavior has arisen in few animal groups, most

22 Similar to eusocial behavior, biparental care leads to greater broo

23 etic clade, thus implying a single origin of eusocial behavior.

24 family is required for all major aspects of eusocial behavior.

25 nipulation by nest mates in the evolution of eusocial behavior.

26 inking the expression of a termite gene with eusocial behavior; they illustrate the connection betwee

27 uticular hydrocarbons important in mediating eusocial behaviour.Cuticular hydrocarbons (CHC) mediate

28 Here we show that workers of a eusocial bumble bee (Bombus terrestris) enter unrelated,

29 Dufour's gland secretion in the primitively eusocial bumble bee Bombus impatiens signals information

30 t bee, Megalopta genalis, and the obligately eusocial bumble bee, Bombus impatiens.

31 e caste-associated miRNAs in the primitively eusocial bumblebee Bombus terrestris.

32 Primitively eusocial bumblebees are uniquely placed to illuminate th

33 For apid bees, including eusocial bumblebees, core members of the adult gut micro

34 However, despite neatly showing eusocial colonies as arenas where selection at the gene

35 Honey bees live in large eusocial colonies in which a single queen is responsible

36 Naked mole-rats live in large eusocial colonies that are characterized by exceptional

37 f social complexity, from solitary living to eusocial colonies, and thus are exemplary for studies of

38 In eusocial colonies, group size may have similar effects o

39 f conflicts over sex-ratio production within eusocial colonies.

40 r levels of biological organization, such as eusocial colonies.

41 lved to serve the functional requirements of eusocial communication.

42 ving arrangements - ranging from solitary to eusocial communities - has revealed that medication beha

43 We find that evolution of increased eusocial complexity in Apis proceeds via increases in th

44 These eusocial Cretaceous taxa diverged from extant lineages p

45 pollinators, they overlook the diversity of eusocial dynamics and multi-kingdom interactions.

46 s, provide insights into the early stages of eusocial evolution because eusociality has arisen recent

47 provide insights into the earliest stages of eusocial evolution because eusociality in these taxa evo

48 fying adaptive molecular changes involved in eusocial evolution in insects is important for understan

49 or developing inferences regarding the early eusocial evolution of ants and termites.

50 ial organization, and suggest that models of eusocial evolution should be extended to include neglect

51 modulating social behaviour and suggest that eusocial evolution was facilitated by alteration of the

52 eages and discuss potential common themes of eusocial evolution, as well as challenges and prospects

53 thways in B. terrestris, suggesting that, in eusocial evolution, the caste-associated role of individ

54 To investigate how miRNAs affect caste in eusocial evolution, we used deep sequencing and Northern

55 espidae), which is a model system for insect eusocial evolution.

56 versals are common in the earliest stages of eusocial evolution.

57 ociated miRNAs occurring relatively early in eusocial evolution.

58 oup selection is the strong binding force in eusocial evolution; individual selection, the strong dis

59 Eusocial groups contain individuals that forfeit their o

60 ves and sterile workers differentiate within eusocial groups has long been a core issue in sociobiolo

61 nces in glomerular numbers are higher in the eusocial honeybee and a sexual dimorphism of the relativ

62 ing these new genomes to those of the highly eusocial honeybee Apis mellifera and other Hymenoptera,

63 es, with higher rates measured in the highly eusocial honeybee than the primitively social bumblebee.

64 In the advanced eusocial honeybee, Apis mellifera, studies suggest that

65 mason bees, whereas it is clearly present in eusocial honeybees and stingless bees.

66 pathway in queens, workers, and males of the eusocial hornet Vespa velutina.

67 cal identification of a sex pheromone in the eusocial hornets.

68 In eusocial Hymenoptera (ants, bees and wasps), queen and w

69 In some eusocial Hymenoptera (ants, bees and wasps), workers can

70 Social parasites are common among eusocial Hymenoptera and exhibit a wide range of distinc

71 The complex social organization of eusocial Hymenoptera relies on sophisticated olfactory c

72 aste-associated miRNAs from outside advanced eusocial Hymenoptera, so providing evidence for caste-as

73 odea) and compare them with similar data for eusocial Hymenoptera, to better identify commonalities a

74 omologies in the olfactory pathways of these eusocial Hymenoptera.

75 It is therefore a paradox that two thirds of eusocial hymenopteran insects appear to be exclusively m

76 riking reproductive patterns in large-colony eusocial Hymenopteran species, from the loss of worker c

77 ground-dwelling predatory insects to become eusocial, increasing efficiency of tasks and establishin

78 genome-wide maps of chromatin structure in a eusocial insect and found that gene-proximal changes in

79 onally characterized in termites, the oldest eusocial insect clade.

80 Collective behaviour by eusocial insect colonies is typically achieved through m

81 Unlike eusocial insect colonies, human societies do not exhibit

82 The honeybee (Apis mellifera) is a eusocial insect displaying a pronounced age-dependent di

83 ative and evolutionary genomics in different eusocial insect groups (bees, ants, wasps, and termites)

84 Eusocial insect queens exhibit some of the most extreme

85 Eusocial insect reproductive females show strikingly lon

86 e greatest plasticity is found in the simple eusocial insect societies in which individuals retain th

87 Eusocial insect societies produce plastic phenotypes fro

88 heromone communication is the cornerstone of eusocial insect societies since it mediates the social h

89 t and reach their most complex expression in eusocial insect societies.

90 placed to illuminate the evolution of highly eusocial insect societies.

91 Several eusocial insect species - with their unique displays of

92 matically different strategy in thousands of eusocial insect species in which colonies are started by

93 Genomic applications to the study of eusocial insect species, in particular, have led to seve

94 the differential life histories of these two eusocial insect species.

95 ons of methylation in eggs and sperm in this eusocial insect species.

96 the first accurate estimate of drifting in a eusocial insect: 56% of females drifted in a natural pop

97 Eusocial-insect colonies display emergent cognitive-like

98 volution of extreme cooperation, as found in eusocial insects (those with a worker caste), is potenti

99 Nest drifting in eusocial insects (where workers move between nests) pres

100 s comprise one lineage of the triumvirate of eusocial insects and experienced their early diversifica

101 in humans and other vertebrates, policing in eusocial insects and partner choice in mutualisms betwee

102 e the world's most conspicuous and important eusocial insects and their diversity, abundance, and ext

103 d per capita brood production in primitively eusocial insects and why only one of the five major line

104 Eusocial insects are characterized by reproductive divis

105 particularly intriguing for some species of eusocial insects because they display exceptionally high

106 The spectacular success of eusocial insects can be attributed to their sophisticate

107 Genomes of eusocial insects code for dramatic examples of phenotypi

108 Eusocial insects divide labor between reproductive and n

109 Ants and other eusocial insects emit and receive chemical signals to co

110 Eusocial insects exhibit a remarkable reproductive divis

111 However, the reproductive queen in eusocial insects exhibits a much longer life span than t

112 Studies in eusocial insects have argued for its role in caste devel

113 Studies in eusocial insects have shown that juvenile hormone (JH) i

114 Division of labor in reproduction in eusocial insects is governed by delicate and context- de

115 Nests of ecosystem-dominant eusocial insects like ants and termites offer stable, nu

116 Eusocial insects organize themselves into behavioral cas

117 Morphologically distinct worker castes of eusocial insects specialize in different tasks.

118 Such communication is especially critical in eusocial insects such as honey bees and ants, where coop

119 Stingless bees-a diverse group of highly eusocial insects that includes managed species, varies i

120 Eusocial insects use cuticular hydrocarbons as component

121 The evolution of sterile worker castes in eusocial insects was a major problem in evolutionary the

122 s fully specialised in reproduction (as with eusocial insects).

123 iate the interactions between individuals in eusocial insects, but the sensory receptors for CHCs are

124 In eusocial insects, genetically identical individuals can

125 lationship is particularly true for advanced eusocial insects, including ants, bees, and wasps, whose

126 Eusocial insects, including ants, some bees, some wasps,

127 In eusocial insects, individual variation and its influence

128 mmals, DNA methylation in insects, including eusocial insects, is enriched in gene bodies of actively

129 Some, such as eusocial insects, may use agonistic behavior to partitio

130 In many facultatively eusocial insects, offspring need continuous care during

131 In most eusocial insects, only the queen can transmit genetic in

132 Together, our results show that, as in eusocial insects, reproductive division of labor in mole

133 Advanced eusocial insects, such as ants, termites, and corbiculat

134 In contrast, primitively eusocial insects, such as halictid bees, provide insight

135 altruism as that found in sterile castes of eusocial insects.

136 provides another remarkable parallel to the eusocial insects.

137 location is key to the ecological success of eusocial insects.

138 re, including carnivores, bats, primates and eusocial insects.

139 d may function similarly as it does in other eusocial insects.

140 ergone a massive expansion in ants and other eusocial insects.

141 ers that resemble the caste systems found in eusocial insects.

142 positive selection acting on the genomes of eusocial insects.

143 prospects for establishing genetic tools in eusocial insects.

144 ionately large role in adaptive evolution of eusocial insects.

145 iscuity, revealing a novel benefit of it for eusocial insects.

146 life history transitions from a cooperative, eusocial life history to exploitative social parasitism

147 omes, morphology, venoms, and parasitoid and eusocial life styles.

148 dation (and vice versa) and from solitary to eusocial life, we inferred the phylogeny and divergence

149 t symbionts with their hosts, favored by the eusocial lifestyle of honey bees, might have promoted th

150 s reflect adaptation to a unique hypoxic and eusocial lifestyle that collectively may contribute to t

151 es and wasps), where it is associated with a eusocial lifestyle.

152 rgence, there are striking differences among eusocial lifestyles, ranging from species living in smal

153 olutionary adaptations associated with their eusocial lifestyles.

154 various solitary insects to examine whether eusocial lineages share distinct features of genomic org

155 ignature of accelerated evolution across all eusocial lineages studied, as well as unique sets of 173

156 ness, is ancestral for all eight independent eusocial lineages that we investigated.

157 ion specific to either highly or primitively eusocial lineages, respectively.

158 the most prominent rapidly evolving genes in eusocial lineages.

159 The evolutionary changes from solitary to eusocial living in vertebrates and invertebrates are ass

160 he naked mole-rat Heterocephalus glaber is a eusocial mammal exhibiting extreme longevity (37-year li

161 arities between worker transcriptomes of the eusocial mammal, the naked mole-rat H. glaber, with orth

162 xts will see an increase in the frequency of eusocial nesting as warming temperatures accelerate deve

163 A hallmark of animals that are eusocial, or those with advanced sociality, is reproduct

164 f sleep has been ascribed to a truly social (eusocial) organism in the context of its society.

165 Eusocial organisms typically live in colonies with one r

166 ation of other biological characteristics of eusocial organisms, when accounts based on phylogenetic

167 rld's most diverse and ecologically dominant eusocial organisms.

168 nsights into the early evolution of advanced eusocial organisms.

169 life history characteristics as well as its eusocial organization.

170 males drifted in a natural population of the eusocial paper wasp Polistes canadensis, exceeding previ

171 "workers" in north temperate colonies of the eusocial paper wasp Polistes fuscatus disappear within a

172 Subjects were eusocial paper wasps from queen and worker castes of 10

173 on of ecological keystone insects, including eusocial, phytophagous, and parasitoid lineages, occurre

174 impacts on non-target organisms, even for a eusocial pollinator species in which colony size may buf

175 Lower termites express a unique form of eusocial polyphenism in that totipotent workers can diff

176 Hornets are large eusocial predatory wasps with a highly developed olfacto

177 at (Heterocephalus glaber) is a subterranean eusocial rodent with a markedly long lifespan and resist

178 Naked mole-rats are eusocial rodents that live in large subterranean colonie

179 However, communities containing eusocial shrimp - which cooperatively defend territories

180 The complete mitochondrial genome of the eusocial shrimp Synalpheus microneptunus will contribute

181 Here, we report, for a eusocial shrimp Synalpheus microneptunus, a complete mit

182 It includes solitary, eusocial, socially parasitic, and an exceptionally high

183 more important for shaping conflicts within eusocial societies than for explaining its origins [6, 1

184 ion of labor is a defining characteristic of eusocial societies, but individual larvae will maximize

185 (Dinoponera quadriceps) that live in simple eusocial societies.

186 and behaviors regulating the formation of a eusocial society.

187 more recently has it become clear that many eusocial species also regularly reproduce thelytokously,

188 Paradoxically, queens of several eusocial species are extremely promiscuous, a derived be

189 However, eusocial species are far less common and have much less

190 e times across diverse terrestrial taxa, and eusocial species fundamentally shape many terrestrial ec

191 ogenetically informed analyses, we find that eusocial species have larger genomes with more transposa

192 Mechanisms of disease control used by eusocial species include antibiotic glandular secretions

193 ary trajectories of caste differentiation in eusocial species is a major goal of sociobiology.

194 gically specialized castes are well known in eusocial species like ants and termites, but castes have

195 in a nest or other protected cavity, and so eusocial species must be able to exploit a predator-safe

196 Thus, all eusocial species of Hymenoptera are contained within two

197 Consistent with this idea, eusocial species of sponge-dwelling Synalpheus shrimps f

198 In different insect lineages, for example, eusocial species show both positive and negative associa

199 In all eusocial species studied, thelytoky probably has a nucle

200 of social strategies, from fungus thieves to eusocial species to communities assembled by attraction

201 ploid sex determination mechanisms, which in eusocial species usually require heterozygosity for fema

202 n selection theory to explain the biology of eusocial species, independently of ploidy, and add suppo

203 In eusocial species, the sex ratio of helpers varies from f

204 trajectory between primitively and advanced eusocial species, which have, respectively, relatively u

205 e (Vespinae+Polistinae), which includes most eusocial species.

206 e especially characteristic of the queens of eusocial species.

207 r host breadth and higher abundance than non-eusocial species.

208 ns in early ontogeny should be restricted to eusocial species.

209 inated food resources by a limited number of eusocial species.

210 We studied how communities of tropical, eusocial stingless bees (Apidae: Meliponini) disassemble

211 Naked mole-rats are highly vocal, eusocial, subterranean rodents with, counterintuitively,

212 ngs uncover multi-layered mechanisms shaping eusocial superorganism microbiomes, from host biology to

213 sible for the growth and reproduction of the eusocial superorganism.

214 maturation in the males of the facultatively eusocial sweat bee, Megalopta genalis, and the obligatel

215 proximate mechanisms of caste development in eusocial taxa can reveal how social species evolved from

216 icidae) represent one of the most successful eusocial taxa in terms of both their geographic distribu

217 In facultatively eusocial taxa, offspring can choose whether to found new

218 , with a comparative study across all sexual eusocial taxa.

219 During the Cretaceous, eusocial termites, bees, and vespid wasps also first app

220 Reversals from eusocial to solitary behavior have occurred as many as 1

221 n diversity, leaving today only two advanced eusocial tribes comprising less than 2% of the total bee

222 anatory framework for caste evolution in the eusocial wasp genus Polistes (Vespidae), which is a mode

223 classic social insect model, the primitively eusocial wasp Polistes dominulus.

224 studying gene expression in the primitively eusocial wasp Polistes metricus.

225 Colonies of the primitively eusocial wasp Ropalidia marginata consist of a single eg

226 ylogenetic hypothesis of Vespidae places the eusocial wasps (subfamilies Stenogastrinae, Polistinae,

227 Eusocial wasps of the family Vespidae are thought to hav

228 rise to different behavioral phenotypes in a eusocial worker caste.