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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.
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
47 at large colony sizes, thus addressing both sociality and colony size range in this social spider.
49 y pathobiology, in which the relationship of sociality and disease transmission can be comparatively
52 r reveals that no association exists between sociality and encephalization across Carnivora and that
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.
61 ence-sensitive neurons evolve in relation to sociality and indicate that gregarious species accentuat
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
70 ect-unrelated versus object-related actions (sociality and transitivity, respectively, hereafter).
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
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
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
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
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
97 male phenotypes, and evolves in relation to sociality (flocking vs. territorial) across several rela
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
103 A second possibility, however, is that once sociality has evolved, subsequent transitions represent
106 bes, but particularly sophisticated forms of sociality have arisen in the myxobacteria, including gro
108 groups; and inter-individual differences in sociality have reported fitness implications in numerous
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.
115 sults show that longevity (i) increases with sociality in both sexes and (ii) decreases with male-bia
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
122 present evidence of a deep imprint of human sociality in language, observing that (i) the words of n
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.
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
136 und in most other birds and mammals: Primate sociality is based on bonded relationships of a kind tha
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
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
149 tion of wild baboons, which demonstrate that sociality of adult females is positively associated with
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
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
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
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
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
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.
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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