| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/BIES.201500166 |
| P698 | PubMed publication ID | 27174816 |
| P50 | author | Niclas Kolm | Q42649752 |
| Wouter van der Bijl | Q51156820 | ||
| P2860 | cites work | Encephalization is not a universal macroevolutionary phenomenon in mammals but is associated with sociality | Q22066302 |
| A critique of comparative studies of brain size | Q24675273 | ||
| Brain size predicts problem-solving ability in mammalian carnivores. | Q27323063 | ||
| Arms races between and within species | Q28237790 | ||
| Brain size affects the behavioural response to predators in female guppies (Poecilia reticulata) | Q28637566 | ||
| Comparative analysis of classic brain component sizes in relation to flightiness in birds | Q28657688 | ||
| The evolution of self-control | Q28659243 | ||
| What is comparable in comparative cognition? | Q28728252 | ||
| Parasitoidism, not sociality, is associated with the evolution of elaborate mushroom bodies in the brains of hymenopteran insects | Q28742197 | ||
| Brain-size evolution and sociality in Carnivora | Q28752526 | ||
| Understanding primate brain evolution | Q28754801 | ||
| Mating system and brain size in bats | Q28767958 | ||
| Both social and ecological factors predict ungulate brain size | Q28767973 | ||
| Neocortex size as a constraint on group size in primates | Q29026453 | ||
| Linked regularities in the development and evolution of mammalian brains | Q29615651 | ||
| Evolution in the social brain | Q29616594 | ||
| Stepwise evolution of stable sociality in primates | Q30085655 | ||
| Sociality, ecology, and relative brain size in lemurs | Q30085660 | ||
| Overall brain size, and not encephalization quotient, best predicts cognitive ability across non-human primates. | Q30085664 | ||
| Social brains, simple minds: does social complexity really require cognitive complexity? | Q30085665 | ||
| Lemur Social Behavior and Primate Intelligence | Q30085672 | ||
| Brain size as a driver of avian escape strategy | Q30407450 | ||
| Neocortex evolution in primates: the "social brain" is for females | Q30442289 | ||
| Primate brain architecture and selection in relation to sex. | Q33284258 | ||
| Individual recognition in mice mediated by major urinary proteins | Q33956363 | ||
| Are bigger brains better? | Q34020215 | ||
| The evolution of cerebrotypes in birds | Q34555907 | ||
| Revisiting social recognition systems in invertebrates | Q34638641 | ||
| Artificial selection on relative brain size reveals a positive genetic correlation between brain size and proactive personality in the guppy. | Q34841637 | ||
| Comparative support for the expensive tissue hypothesis: Big brains are correlated with smaller gut and greater parental investment in Lake Tanganyika cichlids | Q35035118 | ||
| A larger brain confers a benefit in a spatial mate search learning task in male guppies | Q35218065 | ||
| Chimpanzee and felid diet composition is influenced by prey brain size | Q35701531 | ||
| Brain size affects female but not male survival under predation threat | Q36364641 | ||
| Artificial selection on relative brain size in the guppy reveals costs and benefits of evolving a larger brain | Q36592964 | ||
| Individual recognition: it is good to be different | Q36955362 | ||
| The evolution of isocortex | Q38564538 | ||
| Gregariousness increases brain size in ungulates | Q38701523 | ||
| Primate socioecology at the crossroads: past, present, and future | Q39566435 | ||
| Predator-prey interactions, flight initiation distance and brain size | Q40922756 | ||
| The evolution of relative brain size in marsupials is energetically constrained but not driven by behavioral complexity. | Q40947294 | ||
| A comparative analysis of brain size in relation to foraging ecology and phylogeny in the Chiroptera | Q44205982 | ||
| Individual recognition in ant queens. | Q45926720 | ||
| Evidence for coevolution of sociality and relative brain size in three orders of mammals | Q47267796 | ||
| Brain architecture and social complexity in modern and ancient birds | Q47363748 | ||
| The social brain hypothesis and its implications for social evolution | Q47584427 | ||
| Environmental complexity and social organization sculpt the brain in Lake Tanganyikan cichlid fish | Q48227005 | ||
| Neocortex size and behavioural ecology in primates. | Q51209905 | ||
| Distributed cognition and social brains: reductions in mushroom body investment accompanied the origins of sociality in wasps (Hymenoptera: Vespidae). | Q51350095 | ||
| Social fishes and single mothers: brain evolution in African cichlids. | Q51678893 | ||
| Big-brained birds survive better in nature. | Q51714555 | ||
| Learning your own strength: winner and loser effects should change with age and experience. | Q51918629 | ||
| Neocortex size predicts deception rate in primates. | Q52088149 | ||
| Visual signals of individual identity in the wasp Polistes fuscatus. | Q52597924 | ||
| Disentangling evolutionary cause-effect relationships with phylogenetic confirmatory path analysis. | Q53343866 | ||
| The Expensive-Tissue Hypothesis: The Brain and the Digestive System in Human and Primate Evolution | Q54299945 | ||
| Schooling preferences for familiar fish vary with group size in a wild guppy population | Q54432860 | ||
| Predator Inspection Behaviour Covaries With Schooling Tendency Amongst Wild Guppy, Poecilia Reticulata, Populations in Trinidad | Q54432873 | ||
| The evolution of female social relationships in nonhuman primates | Q56689787 | ||
| Evolution of Primate Social Systems | Q56771057 | ||
| Evolution of fighting behaviour: Decision rules and assessment of relative strength | Q57649217 | ||
| Assessments of fighting ability need not be cognitively complex | Q57930792 | ||
| Long-term memory of individual neighbours in a migratory songbird | Q59068608 | ||
| Large body and small brain and group sizes are associated with predator preferences for mammalian prey | Q59185136 | ||
| Social bonds in birds are associated with brain size and contingent on the correlated evolution of life-history and increased parental investment | Q59185143 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | predation | Q170430 |
| social brain | Q51289154 | ||
| P304 | page(s) | 568-577 | |
| P577 | publication date | 2016-05-13 | |
| P1433 | published in | BioEssays | Q4914614 |
| P1476 | title | Why direct effects of predation complicate the social brain hypothesis: And how incorporation of explicit proximate behavioral mechanisms might help | |
| P478 | volume | 38 |
| Q92624888 | Annual variation in predation risk is related to the direction of selection for brain size in the wild |
| Q101631795 | Brain size, ecology and sociality: a reptilian perspective |
| Q93182418 | Grow Smart and Die Young: Why Did Cephalopods Evolve Intelligence? |
| Q37619919 | Increased juvenile predation is not associated with evolved differences in adult brain size in Trinidadian killifish (Rivulus hartii). |
| Q33637828 | Meat and Nicotinamide: A Causal Role in Human Evolution, History, and Demographics |
| Q54432594 | Predation pressure shapes brain anatomy in the wild |
| Q51278694 | Predator-driven brain size evolution in natural populations of Trinidadian killifish (Rivulus hartii). |
| Q46340239 | Simulated predator stimuli reduce brain cell proliferation in two electric fish species, Brachyhypopomus gauderio and Apteronotus leptorhynchus. |
| Q55395180 | Sociality does not drive the evolution of large brains in eusocial African mole-rats. |
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