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1 and the connections between QS and bacterial sociality.
2 correlate with other self-report measures of sociality.
3 arasite stress and the variables relating to sociality.
4  assumption of the parasite-stress theory of sociality.
5 ain cultural practices promoting assortative sociality.
6 ategies as well as interspecific patterns of sociality.
7  gains and losses of the traits underpinning sociality.
8 ytocin (OT) are key modulators of vertebrate sociality.
9 coordinate their activities and benefit from sociality.
10  and helps explain interspecific patterns of sociality.
11  all of which represent an advanced state of sociality.
12 ology and a key element in understanding our sociality.
13  early learning in the development of female sociality.
14 framework to understand animal space use and sociality.
15 s VT, at least, is associated with levels of sociality.
16  of pathogen transmission that can accompany sociality.
17 the role of trophallaxis in the evolution of sociality.
18 ionship exists between levels of kinship and sociality.
19 reciprocity", that may in part explain human sociality.
20 nd use bacteria to understand the biology of sociality.
21 tutes a paradox of environmental quality and sociality.
22 layed an escalating role in the evolution of sociality.
23 s adaptations to ancestral human small-scale sociality.
24  best support infants with varying levels of sociality.
25  the need for long-term evolution or derived sociality.
26 mon principles in the molecular evolution of sociality.
27 s warfare, in moulding human cooperation and sociality.
28 s of related individuals, and in shaping our sociality.
29 y social species and favour the evolution of sociality.
30 r the cross-generation transmission of human sociality.
31 ial relationships; in others, it facilitates sociality.
32 and community, two elementary forms of human sociality.
33 allowed the expression of contemporary human sociality.
34 tions for epidemic disease spread and animal sociality.
35 in our understanding of the genetic basis of sociality.
36 explain fairness and other features of human sociality.
37 cation and adaptive responses to fluctuating sociality.
38 cal generalism facilitates the transition to sociality.
39 logical and demographic drivers that promote sociality.
40 ity--that may explain the evolution of human sociality.
41 both directions between solitary nesting and sociality [2-5].
42               These discoveries suggest that sociality, a key ungulate strategy to reduce predation-r
43  forces are known to shape the expression of sociality across a broad range of biological taxa, their
44 n sociality, the environmental predictors of sociality across broad geographic and taxonomic scales r
45  societies requires greater knowledge of how sociality affects the performance of whole colonies.
46                             The evolution of sociality and altruism is enigmatic because cooperators
47  at large colony sizes, thus addressing both sociality and colony size range in this social spider.
48 ive evolution most likely related to complex sociality and cooperation.
49 y pathobiology, in which the relationship of sociality and disease transmission can be comparatively
50 d Burmese amber resolves ambiguity regarding sociality and diversity in the earliest ants.
51                                   Thus, both sociality and ecology have played a role in producing th
52 r reveals that no association exists between sociality and encephalization across Carnivora and that
53 er survival, with important implications for sociality and evolution.
54 lturally transmitted behavior coevolved with sociality and extended lifespan in primates.
55  to understand fully the connections between sociality and fitness.
56 avior and the poorly understood link between sociality and fitness.
57 nsitivity and attunement necessary for human sociality and for rearing a human child.
58 ilable data on molecular evolution of insect sociality and highlight key biotic and abiotic factors i
59 neuromodulators involved in human affect and sociality and in disorders like depression and autism.
60 , which predicts a close association between sociality and increased encephalization.
61 ence-sensitive neurons evolve in relation to sociality and indicate that gregarious species accentuat
62 namic social networks in the study of animal sociality and its consequences.
63 fe history traits with these clades, such as sociality and maternal care.
64 mitation may be an early predictor of infant sociality and may help identify infants at risk of neuro
65 ate that under certain conditions, both host sociality and pathogen virulence exhibit continuous cycl
66 s for eight generations were reintroduced to sociality and promiscuity (free mate choice), they adapt
67       We hypothesized a major distinction of sociality and transitivity along dorsal and ventral late
68              In addition, representations of sociality and transitivity features were found more ante
69 ations of action information associated with sociality and transitivity in bilateral LOTC.
70 ect-unrelated versus object-related actions (sociality and transitivity, respectively, hereafter).
71 limits our understanding of the link between sociality and vocal complexity.
72 ductivity of the environment, trophic niche, sociality, and ability to defend a territory.
73 neuropsychological measures of intelligence, sociality, and academic abilities.
74 ening directions for research on inequality, sociality, and aging.
75  has coevolved with enlarged brains, complex sociality, and extended lifespans.
76  of mind, culture and language relate to our sociality, and facilitate the formation and maintenance
77 pothesis that the evolution of large brains, sociality, and long lifespans has promoted reliance on c
78    Such impact is traditionally explained by sociality: ants are the first major group of ground-dwel
79 d by groups of nestmates and the benefits of sociality are retained continuously.
80 size, position in social network, individual sociality) are associated with patterns of gut microbial
81 zation across Carnivora and that support for sociality as a causal agent of encephalization increase
82                                              Sociality based on loose aggregation is followed by a se
83 authors were especially interested in female sociality because adult female birds influence male cour
84 sly argued that language remains embedded in sociality because the motivation to communicate exists o
85 s and rules are crucial for explaining human sociality, but we question the claim of there not being
86                 We propose that titration of sociality by MT represents a phylogenetically deep frame
87 lutionary transition from solitary living to sociality can occur.
88 m their intrinsic interest for understanding sociality, can have significant bearing across many fiel
89 tor in the variation of in-group assortative sociality, cross-nationally and across the United States
90        Human groups maintain a high level of sociality despite a low level of relatedness among group
91                                              Sociality-driven maternal and paternal effects reveal in
92 lutionary approaches and theories focused on sociality, dual inheritance, multilevel selection, and d
93 refore, deciphering the context in which our sociality evolved is invaluable in understanding what ma
94                                 We find that sociality evolves primarily from host generalists, and a
95 jor outstanding problems in the study of how sociality evolves.
96                                   This ultra-sociality figures largely in our success as a species.
97  male phenotypes, and evolves in relation to sociality (flocking vs. territorial) across several rela
98 s can be used to examine the consequences of sociality for genome evolution and gene expression.
99 ease in intelligence may be domain-specific (sociality, for example), and the brain specialization th
100  offer insight in to trends related to human sociality found from research in other fields such as ps
101               For humans and other primates, sociality has adaptive value.
102                                              Sociality has been shown to have adaptive value for greg
103  A second possibility, however, is that once sociality has evolved, subsequent transitions represent
104                                              Sociality has many rewards, but can also be dangerous, a
105                                      Primate sociality has received much attention and its complexity
106 bes, but particularly sophisticated forms of sociality have arisen in the myxobacteria, including gro
107 ity; independent evolutionary transitions in sociality have independent genetic underpinnings.
108  groups; and inter-individual differences in sociality have reported fitness implications in numerous
109                    Current concepts of human sociality highlight a fundamental role of the hypothalam
110 OTC: dorsal LOTC represents actions based on sociality (how much an action is directed to another per
111  effects of body size, habitat structure and sociality identified as determinants of avian escape str
112 vel effects in the origin and maintenance of sociality, illustrate the dynamic nature of equilibria w
113 -stress while devaluing in-group assortative sociality in areas with low levels of parasite-stress.
114  immune repertoire predates the evolution of sociality in bees.
115 sults show that longevity (i) increases with sociality in both sexes and (ii) decreases with male-bia
116                             Although lack of sociality in captivity appears to mediate domestication,
117 ationships between household religiosity and sociality in children sampled from six countries.
118 , encephalization trends are associated with sociality in extant species.
119 tor distributions in the lateral septum, and sociality in female zebra finches was reduced by OT anta
120 es were studied relating to the emergence of sociality in hand-reared cowbirds (Molothrus ater): prox
121 thylenedioxymethamphetamine (MDMA) increases sociality in humans and animals.
122  present evidence of a deep imprint of human sociality in language, observing that (i) the words of n
123 an be used to clarify the extent and form of sociality in natural populations.
124        Because PR interferes with aspects of sociality in other male rodents, PR may eventually be fo
125 ht the adaptive value of large body size and sociality in promoting individual fitness in stochastic
126  higher reproductive flexibility, and higher sociality in species living in more variable climates.
127 e force in the sub-social route to permanent sociality in spiders.
128 ence the independent evolutionary origins of sociality in Synalpheus shrimps.
129 tation that facilitates in-group assortative sociality in the face of high levels of parasite-stress
130  imply that queen pheromones regulate insect sociality in two distinct and complementary ways, i.e.,
131  for the AVP/OT system in several aspects of sociality, including vocal communication and sociospatia
132 s who scored high on Nice had high composite sociality indices (CSI) and stable partner preferences,
133 lution of individual signatures and that the sociality-individuality relationship may be a general ph
134                                              Sociality is a derived trait, and kin discrimination exi
135                                              Sociality is an important component of population struct
136 und in most other birds and mammals: Primate sociality is based on bonded relationships of a kind tha
137                                              Sociality is believed to have evolved as a strategy for
138         This is because in-group assortative sociality is more important for the avoidance of infecti
139 hornhill's (F&T's) parasite-stress theory of sociality is supported largely by correlational evidence
140 roups suggests that the affective meaning of sociality is to some degree a function of social stratif
141 ls that are eusocial, or those with advanced sociality, is reproductive specialization into worker an
142                  We thereby demonstrate that sociality itself can be truly plastic in a hymenopteran.
143                        Our results show that sociality maximizes genotypic diversity, which contradic
144 alian brain evolution and highlight the role sociality may play in driving the evolution of large bra
145  evolutionary discontinuity supporting human sociality might seize on this as an alternative to enjoy
146  dependency dimension - individuality versus sociality - might offer important insights into the dyna
147                                   To evolve, sociality must have some heritable basis, yet the herita
148 ain stable across years, similar to forms of sociality observed in other vertebrates.
149 tion of wild baboons, which demonstrate that sociality of adult females is positively associated with
150                          We investigated the sociality of essential virulence factors (crystal toxins
151 hat cooperation originated from inherent pro-sociality of individuals.
152                 To investigate the impact of sociality on associative learning, we compared the indiv
153 ive value for females, but direct effects of sociality on fitness have never been demonstrated.
154                               The effects of sociality on infant survival are independent of the effe
155 tention has focused on the evolution of host sociality or pathogen virulence separately, few studies
156 sitional populations that can express either sociality or solitary nesting, depending on environmenta
157 STm that influence species-typical levels of sociality or that mediate approach and avoidance.
158 tive symptom measures, self-report scales of sociality, pleasure, and motivation, and coded facial ex
159 a model of primate social evolution, whereby sociality progresses from solitary foraging individuals
160                          We evaluate whether sociality promotes ecological generalism (social conques
161                                              Sociality provides a unique opportunity for animals to a
162                     Yet the genetic basis of sociality remains unclear.
163  of this inter-individual variation in human sociality remains unexplained from a biological perspect
164 F&T) present a model of in-group assortative sociality resulting from differing levels of parasite-st
165                 This may explain why primate sociality seems to be so different from that found in mo
166              Consistent with the notion that sociality should be studied from the perspective of soci
167 des in relation to three separate domains of sociality (social disposition, dyadic relationships, and
168 cal generalism facilitates the transition to sociality (social transition hypothesis) in 38 Synalpheu
169  that resource richness may explain variable sociality, spatial overlap or temporary aggregations of
170 ere there is clear variation in the level of sociality, such as the social insects.
171 g production, and to the genetic benefits of sociality, suggesting that helping was not simply mispla
172 ty in immune complement across a gradient of sociality suggests that a reduced immune repertoire pred
173 ee species characterized by a lower level of sociality than ants and honeybees provide new insights i
174  cooperative behaviors and advanced forms of sociality that depend on pheromone-mediated communicatio
175 ndings support the parasite-stress theory of sociality, that is, the proposal that parasite-stress is
176 as been implicated in species differences in sociality, the environmental predictors of sociality acr
177        Across several independent origins of sociality, the genomes of social hymenopterans share two
178 ccess of both: (a) altruistic forms of human sociality towards unrelated members of one's group; and
179 ify and expand the parasite-stress theory of sociality used to fuel our research presented in the tar
180 l of ectoparasitism, with the net benefit of sociality varying under these different conditions.
181         Contrary to expectations, individual sociality was negatively associated with gut microbial d
182 nterstate analyses that in-group assortative sociality was positively associated with parasite-stress
183 ng of the genetic underpinnings of mammalian sociality, we generated a reference transcriptome for th
184 dorsal LOTC are segregated along features of sociality, whereas action representations in ventral LOT
185  more closely resemble an ancestral state of sociality wherein the phenotype difference between worke
186  intra-regional heterogeneity in assortative sociality, which, we argue, can be better explained by a
187 l novel scenarios, as well as aggression and sociality within familiar and novel social contexts.
188 ral contributor to children's well-being and sociality; yet, the neural basis of coparenting has not

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