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1 l care and worker (helper)-based care (e.g., eusociality).
2 could have fueled the initial transitions to eusociality.
3 es a realistic scenario for the evolution of eusociality.
4 ating is a precondition for the evolution of eusociality.
5  evolutionary history and molecular basis of eusociality.
6  having a major role in the evolution of ant eusociality.
7 convergent evolution of novel traits such as eusociality.
8 and almost exclusively so for transitions to eusociality.
9 illion years, close to the origin of termite eusociality.
10  a model organism to study the complexity of eusociality.
11  is essential and causal in the evolution of eusociality.
12 relatedness is important in the evolution of eusociality.
13 uding the evolution of multi-cellularity and eusociality.
14  with the ecological factor that had favored eusociality.
15 neage-specific regulatory features linked to eusociality.
16 n, likely prerequisites for the evolution of eusociality.
17 specific genetic changes to the evolution of eusociality.
18 oretical attempt to explain the evolution of eusociality.
19 ce of eukaryotic cells, multicellularity and eusociality.
20 ay be a consequence, rather than a cause, of eusociality.
21  been considered crucial to the evolution of eusociality.
22 ve coincided with the evolution of honey bee eusociality.
23 ra), representing two independent origins of eusociality.
24 riation in the ecological factors that favor eusociality [10].
25 salient features of these insects, including eusociality [5].
26   Sweat bees have repeatedly gained and lost eusociality, a transition from individual to group repro
27                                         Yet, eusociality also fostered the evolution of social parasi
28  for their siblings is a defining feature of eusociality and a major challenge for evolutionary theor
29 nity in species that differ in the degree of eusociality and coloniality, and suggest that it may als
30 nipulation explanations for the evolution of eusociality and demonstrates that-contrary to current co
31 ing shrimps that exhibit multiple origins of eusociality and extreme interspecific variation in genom
32 s" may be at work in the evolution of insect eusociality and human ultrasociality in relation to agri
33 n of this kind of model for the evolution of eusociality and show that all three of its apparently no
34 nted opportunity to address the evolution of eusociality and the acquisition of lignocellulases at th
35 ses from the emergence of the first cells to eusociality and the economics of nations." In this paper
36 ctive forces impelling the evolution of both eusociality and the soldier caste in termites.
37 stribution of VP immunoreactivity relates to eusociality and the unusual physiology of naked mole-rat
38 rats were likely the first mammals to evolve eusociality, and thus required adaptations to conserve e
39                                     Although eusociality appears to influence TE accumulation, ancest
40 genome features thought to underpin advanced eusociality are also present in bumblebees, indicating a
41 genetic changes involved in the evolution of eusociality are relatively unknown.
42                                     Advanced eusociality arose once in the bees with significant post
43                                              Eusociality based on monandry was thought to be the main
44 factors could have promoted the evolution of eusociality by accelerating and enhancing direct fitness
45 volution across three independent origins of eusociality by sequencing transcriptomes of nine sociall
46 es that-contrary to current consensus belief-eusociality can evolve despite highly promiscuous mating
47                          We demonstrate that eusociality can evolve even if mothers are not strictly
48          Male haploidy, chromosome size, and eusociality can now be excluded as reasons for the high
49 chitecture of this circuit evolves alongside eusociality can open the door to understanding the origi
50                                              Eusociality, defined by overlapping generations, parenta
51 ed and less similar in size, suggesting that eusociality enhances competitive ability and drives comp
52                             The evolution of eusociality, especially how selection would favor steril
53                                              Eusociality evolved independently in diverse taxa, inclu
54                                     Although eusociality evolved independently within several orders
55 ication being that unequivocal evidence that eusociality evolved through the action of kin-selected a
56 e just as important a determinant of whether eusociality evolves.
57 y contradicts notions concerning the role of eusociality for evolutionary success in insects.
58 erged to describe the molecular evolution of eusociality from solitary behavior.
59                             The evolution of eusociality has allowed ants to become one of the most c
60                  In the course of evolution, eusociality has appeared several times independently in
61                                              Eusociality has arisen independently at least 11 times i
62  of division of labour, in lineages in which eusociality has arisen independently, have evolved throu
63 o well-corroborated phylogenies, I show that eusociality has arisen only three times within halictid
64 e early stages of eusocial evolution because eusociality has arisen recently and repeatedly.
65                    Although the evolution of eusociality has been intensively studied, the genetic ch
66                                 Hymenopteran eusociality has been proposed to be associated with the
67                                              Eusociality has been rare in evolution, evidently due to
68                                              Eusociality has convergently evolved multiple times, but
69                                              Eusociality has evolved multiple times across diverse te
70                                              Eusociality has originated numerous times among insects
71                 Advanced social behavior, or eusociality, has been evolutionarily profound, allowing
72 s show that the key pathways associated with eusociality have been under strong selection during the
73 r and degree to which independent origins of eusociality have utilized common genes remain largely un
74 arity in geological time of the emergence of eusociality in ants and other animal phylads; (ii) the p
75                                              Eusociality in ants and termites in the irreversible sta
76                             The evolution of eusociality in ants and termites propelled both insect g
77 sential roles in the origin and evolution of eusociality in ants, through their functional roles in p
78 pertoires suggest that the route to advanced eusociality in bees was mediated by many small changes i
79 tes that provide the earliest indications of eusociality in both insect groups.
80                             The evolution of eusociality in Hymenoptera-encompassing bees, ants, and
81 been the dominant paradigm for understanding eusociality in insects, direct fitness is vital to expla
82 ically to the convergent gains and losses of eusociality in sweat bees.
83  Understanding the origin and maintenance of eusociality in termites has proved problematic, in part,
84                                The origin of eusociality in the Hymenoptera is a question of major in
85 -offs have structured the molecular basis of eusociality in these bees and demonstrate how both direc
86 onies is considered key for the evolution of eusociality in these lineages.
87     Deciphering the genomic underpinnings of eusociality in these marine shrimps has been limited by
88 arliest stages of eusocial evolution because eusociality in these taxa evolved long ago (in the Creta
89                                              Eusociality, in which some individuals reduce their own
90       Second, there is no single road map to eusociality; independent evolutionary transitions in soc
91 hose of the honeybee, a lineage that evolved eusociality independently from ants, and solitary insect
92 ated genes, suggesting that the evolution of eusociality involved major nutritional and reproductive
93                The origin and maintenance of eusociality is a central problem in evolutionary biology
94                                              Eusociality is a distinct form of biological organizatio
95                                              Eusociality is a major evolutionary innovation involving
96                             The evolution of eusociality is a perennial issue in evolutionary biology
97 evolve to be in conflict with the queen, and eusociality is not so difficult to evolve.
98                                The origin of eusociality is often regarded as a change of macroevolut
99                             The evolution of eusociality is one of the major transitions in evolution
100                         In the marine realm, eusociality is only known to have evolved within a clade
101                         One key advantage of eusociality is shared defense of the nest, brood, and st
102 ars that a precondition for the evolution of eusociality is the defence and repeated feeding of offsp
103             A key characteristic of advanced eusociality is the presence of non-reproductive workers.
104                Integral to the definition of eusociality is the presence of reproductive castes, grou
105                                  Conversely, eusociality is widespread in insects, especially the acu
106             Our goal is to determine whether eusociality leads to an accumulation of repetitive eleme
107                  We infer that the advent of eusociality led automatically and unavoidably to selecti
108                               However, their eusociality makes it difficult to use standard forward g
109                                              Eusociality may arise through different mechanisms each
110 ng that the molecular foundations of complex eusociality may have evolved rapidly in less than 20 Ma.
111 s indicate two independent origins of vespid eusociality, once in the clade Polistinae+Vespinae and o
112 involvement of ILPs pathways in invertebrate eusociality or in vertebrate bone physiology, respective
113 nt helping decisions - can determine whether eusociality outperforms other strategies.
114                      Fu et al. inferred that eusociality rarely evolves because it faces a fundamenta
115 "Relatedness, Conflict, and the Evolution of Eusociality" respond to objections raised by Martin Nowa
116 st theories used to explain the evolution of eusociality rest upon two key assumptions: mutations aff
117 e interaction between two common features of eusociality - saturating birth rates and group size-depe
118 eding (bees [Anthophila] and Masarinae), and eusociality (social vespid wasps, ants, and some bees) [
119                                     Advanced eusociality sometimes is given credit for the ecological
120 at monogamy was critical in the evolution of eusociality, strongly supporting the prediction of inclu
121 ransitions towards communal breeding than to eusociality, suggesting that different ecological factor
122   Close kinship may be more a consequence of eusociality than a factor promoting its origin.
123  and independently promotes the evolution of eusociality through adaptive evolution.
124 rts and that species that have reverted from eusociality to solitary living have repeatedly reduced i
125 n played a key role in the origins of insect eusociality, whereas changes in gene composition were mo
126 bolstered by a new model of the evolution of eusociality with novel conclusions that appeared to over
127 ection are linked to key features of complex eusociality, with histone acetylation being implicated i

 
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