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

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

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

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

10 Eusocial bees in particular must collect pollen and nect

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

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

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

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

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

16 Eusocial behavior has arisen in few animal groups, most

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

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

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

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

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

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

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

24 Primitively eusocial bumblebees are uniquely placed to illuminate th

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

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

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

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

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

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

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

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

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

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

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

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

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

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

39 ociated miRNAs occurring relatively early in eusocial evolution.

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

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

42 Eusocial groups contain individuals that forfeit their o

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

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

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

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

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

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

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

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

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

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

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

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

55 omologies in the olfactory pathways of these eusocial Hymenoptera.

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

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

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

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

60 Unlike eusocial insect colonies, human societies do not exhibit

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

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

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

64 Eusocial insect societies produce plastic phenotypes fro

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

66 Several eusocial insect species - with their unique displays of

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

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

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

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

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

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

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

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

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

76 Eusocial insects are characterized by reproductive divis

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

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

79 Genomes of eusocial insects code for dramatic examples of phenotypi

80 Eusocial insects exhibit a remarkable reproductive divis

81 Eusocial insects organize themselves into behavioral cas

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

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

84 Eusocial insects use cuticular hydrocarbons as component

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

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

87 In eusocial insects, genetically identical individuals can

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

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

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

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

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

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

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

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

96 provides another remarkable parallel to the eusocial insects.

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

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

99 positive selection acting on the genomes of eusocial insects.

100 prospects for establishing genetic tools in eusocial insects.

101 ionately large role in adaptive evolution of eusocial insects.

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

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

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

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

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

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

108 olutionary adaptations associated with their eusocial lifestyles.

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

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

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

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

113 the most prominent rapidly evolving genes in eusocial lineages.

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

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

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

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

118 nsights into the early evolution of advanced eusocial organisms.

119 life history characteristics as well as its eusocial organization.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

149 e especially characteristic of the queens of eusocial species.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

165 Eusocial wasps of the family Vespidae are thought to hav

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