| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2005PNAS..102.5460S |
| P356 | DOI | 10.1073/PNAS.0408145102 |
| P932 | PMC publication ID | 556234 |
| P698 | PubMed publication ID | 15784743 |
| P5875 | ResearchGate publication ID | 7949960 |
| P50 | author | Phillip Cassey | Q25991305 |
| Daniel Sol | Q42841230 | ||
| Richard P. Duncan | Q51200192 | ||
| Tim M. Blackburn | Q87879644 | ||
| Louis Lefebvre | Q96105002 | ||
| P2860 | cites work | Killer whale predation on sea otters linking oceanic and nearshore ecosystems | Q28285467 |
| How quickly do brains catch up with bodies? A comparative method for detecting evolutionary lag | Q28766010 | ||
| Social intelligence, innovation, and enhanced brain size in primates | Q30085669 | ||
| Lemur Social Behavior and Primate Intelligence | Q30085672 | ||
| What are big brains for? | Q34046518 | ||
| Covariation between brain size and immunity in birds: implications for brain size evolution. | Q34387976 | ||
| Learning improves growth rate in grasshoppers | Q35078326 | ||
| Brains, innovations and evolution in birds and primates | Q35745951 | ||
| Determinants of establishment success in introduced birds | Q38910977 | ||
| Relative size of the hyperstriatum ventrale is the best predictor of feeding innovation rate in birds | Q44408665 | ||
| Relationship between number of muscles, behavioral repertoire size, and encephalization in mammals | Q47174759 | ||
| A comparative analysis of relative brain size in waterfowl (Anseriformes). | Q47207077 | ||
| Do big-brained animals play more? Comparative analyses of play and relative brain size in mammals | Q47211983 | ||
| Brain architecture and social complexity in modern and ancient birds | Q47363748 | ||
| Cognitive ecology: the evolutionary ecology of information processing and decision making | Q51206506 | ||
| Neocortex size and behavioural ecology in primates | Q51209905 | ||
| Relations between song repertoire size and the volume of brain nuclei related to song: comparative evolutionary analyses amongst oscine birds. | Q52060317 | ||
| Neocortex size predicts deception rate in primates. | Q52088149 | ||
| Recolonizing carnivores and naïve prey: conservation lessons from Pleistocene extinctions. | Q52141536 | ||
| Feeding innovations and forebrain size in birds | Q56270651 | ||
| Behavioural flexibility predicts species richness in birds, but not extinction risk | Q56942254 | ||
| Behavioural flexibility and invasion success in birds | Q56942260 | ||
| Sex, bowers and brains | Q73856024 | ||
| Coevolving avian eye size and brain size in relation to prey capture and nocturnality | Q74170331 | ||
| P433 | issue | 15 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 6 | |
| P304 | page(s) | 5460-5465 | |
| P577 | publication date | 2005-03-22 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Big brains, enhanced cognition, and response of birds to novel environments | |
| P478 | volume | 102 |
| Q57069282 | A comparative analysis of the factors promoting deer invasion |
| Q42592474 | A comparison of success rates of introduced passeriform birds in New Zealand, Australia and the United States |
| Q24675273 | A critique of comparative studies of brain size |
| Q33665661 | A novel strategy to escape a poor habitat: red-necked grebes transfer flightless young to other ponds |
| Q58012151 | A quantitative test of the thermogenesis hypothesis of cetacean brain evolution, using phylogenetic comparative methods |
| Q56604466 | A reassessment of historical records of avian introductions to Australia: no case for propagule pressure |
| Q45383535 | A trade-off between reproductive investment and maternal cerebellum size in a precocial bird |
| Q53178632 | Absolute, not relative brain size correlates with sociality in ground squirrels. |
| Q48177992 | Adaptability and evolution. |
| Q56270793 | Adaptive phenotypic plasticity in an island songbird exposed to a novel predation risk |
| Q40415450 | Adjusting foraging strategies: a comparison of rural and urban common mynas (Acridotheres tristis). |
| Q57155911 | Adjusting risk-taking to the annual cycle of long-distance migratory birds |
| Q30365204 | An approach to incorporate individual personality in modeling fish dispersal across in-stream barriers. |
| Q58785209 | An intraspecific appraisal of the social intelligence hypothesis |
| Q47729370 | Animal innovation defined and operationalized. |
| Q51514656 | Anthropogenic environments exert variable selection on cranial capacity in mammals. |
| Q34841637 | Artificial selection on relative brain size reveals a positive genetic correlation between brain size and proactive personality in the guppy. |
| Q89655624 | Back to the light, coevolution between vision and olfaction in the "Dark-flies" (Drosophila melanogaster) |
| Q34526156 | Behavioral flexibility and problem solving in an invasive bird |
| Q42678142 | Behavioral flexibility positively correlated with relative brain volume in predatory bats |
| Q55259378 | Behavioural changes and the adaptive diversification of pigeons and doves. |
| Q91595674 | Behavioural plasticity is associated with reduced extinction risk in birds |
| Q30990872 | Behavioural responses to human-induced environmental change |
| Q33936536 | Big brains do matter in new environments |
| Q51714555 | Big-brained birds survive better in nature. |
| Q34086939 | Biogeography of species richness gradients: linking adaptive traits, demography and diversification |
| Q30489885 | Bird brains: Does absolute size matter? |
| Q33755870 | Bird species in Mediterranean pine plantations exhibit different characteristics to those in natural reforested woodlands |
| Q89682169 | Birds Drinking Alcohol: Species and Relationship with People. A Review of Information from Scientific Literature and Social Media |
| Q37677488 | Birds introduced in new areas show rest disorders |
| Q28597153 | Brain Mass and Encephalization Quotients in the Domestic Industrial Pig (Sus scrofa) |
| Q58575200 | Brain differences in ecologically differentiated sticklebacks |
| Q28709247 | Brain reorganization, not relative brain size, primarily characterizes anthropoid brain evolution |
| Q57193521 | Brain size and resource specialization predict long-term population trends in British birds |
| Q47390380 | Brain size and the expression of pheomelanin-based colour in birds |
| Q36124401 | Brain size is controlled by the mammalian target of rapamycin (mTOR) in mice |
| Q27323063 | Brain size predicts problem-solving ability in mammalian carnivores. |
| Q101631795 | Brain size, ecology and sociality: a reptilian perspective |
| Q56942219 | Brain size, innovative propensity and migratory behaviour in temperate Palaearctic birds |
| Q28752526 | Brain-size evolution and sociality in Carnivora |
| Q33883105 | Brains and the city: big-brained passerine birds succeed in urban environments |
| Q37870963 | Brains matter, bodies maybe not: the case for examining neuron numbers irrespective of body size |
| Q29542986 | Brains, brawn and sociality: a hyaena's tale |
| Q28681831 | Brains, innovations, tools and cultural transmission in birds, non-human primates, and fossil hominins |
| Q21284022 | Brains, tools, innovation and biogeography in crows and ravens |
| Q35669867 | Breeding system evolution influenced the geographic expansion and diversification of the core Corvoidea (Aves: Passeriformes). |
| Q51468009 | Brood parasitism: a good strategy in our changing world? |
| Q34048622 | Can behavioral and personality traits influence the success of unintentional species introductions? |
| Q34481077 | Can endocranial volume be estimated accurately from external skull measurements in great-tailed grackles (Quiscalus mexicanus)? |
| Q55669324 | Can traits predict species' vulnerability? A test with farmland passerines in two continents |
| Q54035650 | Can you teach an old parrot new tricks? Cognitive development in wild kaka (Nestor meridionalis). |
| Q35033213 | Cellular scaling rules for rodent brains |
| Q46324553 | Climate matching drives spread rate but not establishment success in recent unintentional bird introductions. |
| Q28710016 | Climatic patterns predict the elaboration of song displays in mockingbirds |
| Q34161165 | Coevolution of generalist feeding ecologies and gyrencephalic mushroom bodies in insects |
| Q39439606 | Cognition in an ever-changing world: climatic variability is associated with brain size in Neotropical parrots |
| Q60362688 | Cognitive Buffer Hypothesis, The |
| Q38574167 | Cognitive ecology: ecological factors, life-styles, and cognition |
| Q48778033 | Cognitive skills and bacterial load: comparative evidence of costs of cognitive proficiency in birds |
| Q28743405 | Colloquium paper: gene-culture coevolution in the age of genomics |
| Q43906971 | Colour-variable birds have broader ranges, wider niches and are less likely to be threatened |
| Q30644823 | Commonness and ecology, but not bigger brains, predict urban living in birds |
| Q28657688 | Comparative analysis of classic brain component sizes in relation to flightiness in birds |
| Q34034736 | Comparing determinants of alien bird impacts across two continents: implications for risk assessment and management |
| Q43512471 | Comparison of learning ability and memory retention in altricial (Bengalese finch, Lonchura striata var. domestica) and precocial (blue-breasted quail, Coturnix chinensis) birds using a color discrimination task |
| Q36002573 | Coupling of dispersal and aggression facilitates the rapid range expansion of a passerine bird |
| Q98611607 | Cranial evolution in the extinct Rodrigues Island owl Otus murivorus (Strigidae), associated with unexpected ecological adaptations |
| Q55953907 | DOES DIVING LIMIT BRAIN SIZE IN CETACEANS? |
| Q55373310 | Dark nests and egg colour in birds: a possible functional role of ultraviolet reflectance in egg detectability. |
| Q34063624 | Desiccation risk drives the spatial ecology of an invasive anuran (Rhinella marina) in the Australian semi-desert |
| Q35816119 | Desperate Prawns: Drivers of Behavioural Innovation Vary across Social Contexts in Rock Pool Crustaceans. |
| Q57017795 | Determinants of data deficiency in the impacts of alien bird species |
| Q38045808 | Determinants of inter-specific variation in basal metabolic rate |
| Q55328271 | Determinants of vertebrate invasion success in Europe and North America |
| Q51906065 | Developmental increase of total cell numbers in the murine cerebellum. |
| Q56449844 | Different responses of congeneric consumers to an exotic food resource: who gets the novel resource prize? |
| Q36477493 | Disruptive selection and then what? |
| Q90814086 | Diurnal activity in cane toads (Rhinella marina) is geographically widespread |
| Q56526359 | Do birds understand what's going on in their nests? The experimental test of insight in small passerines |
| Q51165358 | Do smart birds stress less? An interspecific relationship between brain size and corticosterone levels |
| Q30478054 | Does foraging behaviour affect female mate preferences and pair formation in captive zebra finches? |
| Q37514228 | Does invasion success reflect superior cognitive ability? A case study of two congeneric lizard species (Lampropholis, Scincidae). |
| Q36154713 | Does the colonization of new biogeographic regions influence the diversification and accumulation of clade richness among the Corvides (Aves: Passeriformes)? |
| Q51557079 | Early experience and reproductive morph both affect brain morphology in adult male Chinook salmon (Oncorhynchus tshawytscha) |
| Q44775495 | Ecological generalism and behavioural innovation in birds: technical intelligence or the simple incorporation of new foods? |
| Q22066302 | Encephalization is not a universal macroevolutionary phenomenon in mammals but is associated with sociality |
| Q56654627 | Environmental Influences on Neuromorphology in the Non-Native Starling Sturnus vulgaris |
| Q36658635 | Environmental and genetic determinants of innovativeness in a natural population of birds |
| Q99551056 | Environmental variability supports chimpanzee behavioural diversity |
| Q28584610 | Environmental variation and the evolution of large brains in birds |
| Q51011380 | Estimating the repeatability of memories of captured prey formed by Frontinella communis spiders (Araneae: Linyphiidae). |
| Q46884182 | Evidence for sex-specific selection in brain: a case study of the nine-spined stickleback |
| Q28742478 | Evo-devo and brain scaling: candidate developmental mechanisms for variation and constancy in vertebrate brain evolution |
| Q28729956 | Evolution and behavioural responses to human-induced rapid environmental change |
| Q29616594 | Evolution in the social brain |
| Q38572661 | Evolution of cognition |
| Q57591781 | Evolution of the Avian Brain and Senses |
| Q28085575 | Evolutionary Influences of Plastic Behavioral Responses Upon Environmental Challenges in an Adaptive Radiation |
| Q33540171 | Evolutionary divergence in brain size between migratory and resident birds |
| Q37594680 | Evolutionary ecology of intraspecific brain size variation: a review |
| Q35960653 | Evolutionary origins of invasive populations |
| Q51835039 | Evolutionary pressures on primate intertemporal choice. |
| Q57898759 | Experience drives the development of movement-cognition correlations in a butterfly |
| Q46286105 | Exploratory behavior of a native anuran species with high invasive potential. |
| Q33911217 | Exploring or avoiding novel food resources? The novelty conflict in an invasive bird |
| Q51114682 | Expression change in Angiopoietin-1 underlies change in relative brain size in fish |
| Q56031378 | Extinction or Survival? Behavioral Flexibility in Response to Environmental Change in the African Striped Mouse Rhabdomys |
| Q30724550 | Feeding innovations in a nested phylogeny of Neotropical passerines. |
| Q27318233 | Foraging ecology predicts learning performance in insectivorous bats. |
| Q58205755 | Foraging in the tropics: relationships among species’ abundances, niche asymmetries and body condition in an urban avian assemblage |
| Q64447703 | Fundamental bounds on learning performance in neural circuits |
| Q92082233 | Future Directions for Personality Research: Contributing New Insights to the Understanding of Animal Behavior |
| Q38194057 | Genes, evolution and intelligence |
| Q33733834 | Genomic adaptation to agricultural environments: cabbage white butterflies (Pieris rapae) as a case study. |
| Q46442141 | Geographical and taxonomic biases in invasion ecology |
| Q90166465 | Habitat-related differences in song structure and complexity in a songbird with a large repertoire |
| Q35609769 | Handedness- and brain size-related efficiency differences in small-world brain networks: a resting-state functional magnetic resonance imaging study |
| Q30716840 | High individual consistency in fear of humans throughout the adult lifespan of rural and urban burrowing owls |
| Q56923850 | Higher establishment success in specialized parasitoids: support for the existence of trade-offs in the evolution of specialization |
| Q28067639 | How Can We Study the Evolution of Animal Minds? |
| Q36651822 | How does variation in the environment and individual cognition explain the existence of consistent behavioral differences? |
| Q28596897 | How far will a behaviourally flexible invasive bird go to innovate? |
| Q51679207 | Human-related processes drive the richness of exotic birds in Europe. |
| Q56530341 | Hydric balance and locomotor performance of an anuran (Rhinella marina) invading the Australian arid zone |
| Q44639463 | Independent appearance of an innovative feeding behaviour in Antillean bullfinches |
| Q50999875 | Infectious disease, behavioural flexibility and the evolution of culture in primates |
| Q37426117 | Influence of learning on range expansion and adaptation to novel habitats |
| Q33357326 | Influence of personality, age, sex, and estrous state on chimpanzee problem-solving success |
| Q41378780 | Innovation and behavioral flexibility in wild redfronted lemurs (Eulemur rufifrons). |
| Q90282348 | Innovation in wild Barbary macaques (Macaca sylvanus) |
| Q51554207 | Innovative problem solving by wild spotted hyenas. |
| Q40381610 | Innovativeness and the effects of urbanization on risk-taking behaviors in wild Barbados birds. |
| Q36658669 | Innovativeness as an emergent property: a new alignment of comparative and experimental research on animal innovation. |
| Q33883697 | Inter-individual variability in fear of humans and relative brain size of the species are related to contemporary urban invasion in birds. |
| Q36584150 | Introduced Drosophila subobscura populations perform better than native populations during an oviposition choice task due to increased fecundity but similar learning ability |
| Q42000655 | Introduction pathway and climate trump ecology and life history as predictors of establishment success in alien frogs and toads |
| Q56451402 | Invasions cause biodiversity loss and community simplification in vertebrate food webs |
| Q96822121 | Is foraging innovation lost following colonization of a less variable environment? A case study in surface- vs. cave-dwelling Asellus aquaticus |
| Q56490890 | Is propagule size the critical factor in predicting introduction outcomes in passeriform birds? |
| Q47164276 | Is the behavioural divergence between range-core and range-edge populations of cane toads (Rhinella marina) due to evolutionary change or developmental plasticity? |
| Q34119280 | Large brains buffer energetic effects of seasonal habitats in catarrhine primates |
| Q64888409 | Large brains, short life: selection on brain size impacts intrinsic lifespan. |
| Q36053603 | Large-brained birds suffer less oxidative damage |
| Q51051600 | Learning capabilities enhanced in harsh environments: a common garden approach |
| Q26799303 | Life-history evolution in the anthropocene: effects of increasing nutrients on traits and trade-offs |
| Q56448678 | Living on the edge: range edge birds consume novel foods sooner than established ones |
| Q92885977 | Location-level processes drive the establishment of alien bird populations worldwide |
| Q56423235 | Long after the event, or four things we (should) know about bird invasions |
| Q33694397 | Longevity is associated with relative brain size in birds. |
| Q33801916 | Major global radiation of corvoid birds originated in the proto-Papuan archipelago |
| Q37153049 | Maternal effects and range expansion: a key factor in a dynamic process? |
| Q43661123 | Means-end comprehension in four parrot species: explained by social complexity. |
| Q92186172 | Multiphase progenetic development shaped the brain of flying archosaurs |
| Q57094455 | Neural Correlates of Vocal Repertoire in Primates |
| Q56488469 | Niche conservatism in non-native birds in Europe: niche unfilling rather than niche expansion |
| Q56417570 | Non-random patterns and temporal trends (1912-2012) in the transport, introduction and establishment of exotic birds in Spain and Portugal |
| Q51278684 | Nutrition shapes life-history evolution across species. |
| Q98196636 | Of city and village mice: behavioural adjustments of striped field mice to urban environments |
| Q42234037 | On the evolution of brain size in relation to migratory behaviour in birds |
| Q28742197 | Parasitoidism, not sociality, is associated with the evolution of elaborate mushroom bodies in the brains of hymenopteran insects |
| Q56776965 | Parental investment and fecundity, but not brain size, are associated with establishment success in introduced fishes |
| Q42447345 | Patterns of genome size diversity in bats (order Chiroptera). |
| Q35108443 | Patterns of research effort in birds. |
| Q33608343 | Phenotypic plasticity's impacts on diversification and speciation |
| Q38111285 | Phylogenetic analyses: comparing species to infer adaptations and physiological mechanisms |
| Q47781078 | Phylogenetic signal, feeding behaviour and brain volume in Neotropical bats |
| Q46851928 | Physiological flexibility in an avian range expansion |
| Q26863269 | Plasticity-mediated persistence in new and changing environments |
| Q54432594 | Predation pressure shapes brain anatomy in the wild |
| Q60550257 | Predictable evolution towards larger brains in birds colonizing oceanic islands |
| Q56491396 | Predictors of regional establishment success and spread of introduced non-indigenous vertebrates |
| Q90358287 | Propagule pressure does not consistently predict the outcomes of exotic bird introductions |
| Q48325904 | RETRACTED: Large brains and lengthened life history periods in Odontocetes |
| Q35868664 | Rapid loss of antipredatory behaviour in captive-bred birds is linked to current avian invasions |
| Q58279333 | Regional distribution patterns predict bird occurrence in Mediterranean cropland afforestations |
| Q33952100 | Relationship between exercise capacity and brain size in mammals |
| Q99238504 | Renewed Perspectives on the Deep Roots and Broad Distribution of Animal Consciousness |
| Q37339470 | Revisiting the cognitive buffer hypothesis for the evolution of large brains |
| Q46250599 | Seasonality and brain size are negatively associated in frogs: evidence for the expensive brain framework |
| Q51372207 | Sexual selection explains more functional variation in the mammalian major histocompatibility complex than parasitism. |
| Q47313862 | Sexual selection uncouples the evolution of brain and body size in pinnipeds. |
| Q28741372 | Smart moves: effects of relative brain size on establishment success of invasive amphibians and reptiles |
| Q49957985 | Social inhibition and behavioural flexibility when the context changes: a comparison across six primate species |
| Q46317645 | Social makes smart: rearing conditions affect learning and social behaviour in jumping spiders |
| Q21134552 | Spatial sorting drives morphological variation in the invasive bird, Acridotheris tristis |
| Q26851290 | Stereological estimation of total cell numbers in the human cerebral and cerebellar cortex |
| Q38335985 | Studying the evolutionary ecology of cognition in the wild: a review of practical and conceptual challenges. |
| Q42040925 | Taxonomic counts of cognition in the wild |
| Q38684890 | Temperament and problem solving in a population of adolescent guide dogs. |
| Q39074465 | The Ecology of Social Learning in Animals and its Link with Intelligence. |
| Q34735570 | The ability of North Island Robins to discriminate between humans is related to their behavioural type. |
| Q56363503 | The behavioural consequences of translocation: how do invasive cane toads (Rhinella marina) respond to transport and release to novel environments? |
| Q38811686 | The coevolution of innovation and technical intelligence in primates |
| Q56773596 | The comparative analysis of historical alien introductions |
| Q37924641 | The convergent evolution of neural substrates for cognition |
| Q28706830 | The costs and benefits of flexibility as an expression of behavioural plasticity: a primate perspective |
| Q52110450 | The costs of a big brain: extreme encephalization results in higher energetic demand and reduced hypoxia tolerance in weakly electric African fishes. |
| Q57292087 | The degree of altriciality and performance in a cognitive task show correlated evolution |
| Q96576629 | The ecological significance of birds feeding from the hand of humans |
| Q37325901 | The effect of brain size evolution on feeding propensity, digestive efficiency, and juvenile growth |
| Q46346357 | The effect of social learning on avoidance of aposematic prey in juvenile great tits (Parus major). |
| Q33363596 | The evolution of general intelligence |
| Q38799264 | The evolution of intelligence in mammalian carnivores |
| Q28659243 | The evolution of self-control |
| Q26798291 | The extended evolutionary synthesis: its structure, assumptions and predictions |
| Q46378881 | The impact of transportation and translocation on dispersal behaviour in the invasive cane toad |
| Q37358123 | The importance of being active |
| Q101403086 | The influence of early life socialisation on cognition in the domestic pig (Sus scrofa domestica) |
| Q30724547 | The life-history basis of behavioural innovations |
| Q34090444 | The paradox of invasion in birds: competitive superiority or ecological opportunism? |
| Q51720631 | The relationship between migratory behaviour, memory and the hippocampus: an intraspecific comparison. |
| Q35939536 | The reluctant innovator: orangutans and the phylogeny of creativity. |
| Q33881538 | The temporal dependence of exploration on neotic style in birds |
| Q56269026 | The town bird and the country bird: problem solving and immunocompetence vary with urbanization |
| Q57898982 | Time Since Urbanization but Not Encephalisation Is Associated with Increased Tolerance of Human Proximity in Birds |
| Q28601510 | To boldly climb: behavioural and cognitive differences in migrating European glass eels |
| Q35083064 | Tracking changing environments: innovators are fast, but not flexible learners |
| Q40081224 | Triploidy alters brain morphology in pre-smolt Atlantic salmon Salmo salar: possible implications for behaviour |
| Q38408614 | Turtles outsmart rapid environmental change: The role of cognition in navigation |
| Q28754801 | Understanding primate brain evolution |
| Q34363957 | Unraveling the life history of successful invaders. |
| Q36667774 | Urban birds have broader environmental tolerance |
| Q96578741 | Variation in brown rat cranial shape shows directional selection over 120 years in New York City |
| Q56512689 | What determines the impact of alien birds and mammals in Europe? |
| Q49706956 | What factors shape genetic diversity in cetaceans? |
| Q51205260 | What makes specialized food-caching mountain chickadees successful city slickers? |
| Q92888485 | Where and what? Frugivory is associated with more efficient foraging in three semi-free ranging primate species |
| Q36749795 | Why are individuals so different from each other? |
| Q33874848 | Why are there so many explanations for primate brain evolution? |
| Q56774727 | Wild-bird trade and exotic invasions: a new link of conservation concern? |
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