| P50 | author | Stig A. Walsh | Q56600191 |
| P2093 | author name string | Angela Milner | |
| P2860 | cites work | Mirror-induced behavior in the magpie (Pica pica): evidence of self-recognition | Q21090187 |
| | Cognitive processes associated with sequential tool use in New Caledonian crows | Q21143745 |
| | Kiwi forego vision in the guidance of their nocturnal activities | Q21144765 |
| | Bigger is not always better: when brains get smaller | Q22337114 |
| | Revised nomenclature for avian telencephalon and some related brainstem nuclei | Q22337412 |
| | Do woodpecker finches acquire tool-use by social learning? | Q24522460 |
| | Evolution of consciousness | Q24564383 |
| | A fossil brain from the Cretaceous of European Russia and avian sensory evolution | Q24652825 |
| | Social cognition by food-caching corvids. The western scrub-jay as a natural psychologist | Q24656216 |
| | The anatomical relationships between the avian eye, orbit and sclerotic ring: implications for inferring activity patterns in extinct birds | Q24658036 |
| | Ultraviolet vision and foraging in dip and plunge diving birds | Q24671691 |
| | Ultraviolet vision in birds: what is its function? | Q28244486 |
| | Paleontological evidence to date the tree of life | Q28268884 |
| | The avian nature of the brain and inner ear of Archaeopteryx | Q28275688 |
| | Cognitive adaptations of social bonding in birds | Q28754810 |
| | Inner ear anatomy is a proxy for deducing auditory capability and behaviour in reptiles and birds | Q28754987 |
| | Neuroanatomy of flying reptiles and implications for flight, posture and behaviour | Q29012107 |
| | A Review of the Mongolian Cretaceous Dinosaur Saurornithoides (Troodontidae: Theropoda) | Q29028069 |
| | Developmental differences are correlated with relative brain size in birds: a comparative analysis | Q29544719 |
| | Evolution of Brain Size in the Palaeognath Lineage, with an Emphasis on New Zealand Ratites | Q29997739 |
| | The underestimated role of olfaction in avian reproduction? | Q30480920 |
| | Why are there so few smart mammals (but so many smart birds)? | Q33374690 |
| | Do birds possess homologues of mammalian primary visual, somatosensory and motor cortices? | Q33815196 |
| | Big brains do matter in new environments | Q33936536 |
| | Big brains, enhanced cognition, and response of birds to novel environments | Q33936584 |
| | The visual ecology of avian photoreceptors | Q34317974 |
| | The evolution of cerebrotypes in birds | Q34555907 |
| | The avian muscle spindle | Q35349808 |
| | Brains, innovations and evolution in birds and primates | Q35745951 |
| | Specializations in the lumbosacral vertebral canal and spinal cord of birds: evidence of a function as a sense organ which is involved in the control of walking | Q36383436 |
| | Mammalian and avian neuroanatomy and the question of consciousness in birds | Q36633880 |
| | Parallel tool industries in New Caledonian crows | Q36645499 |
| | Parallel evolution in mammalian and avian brains: comparative cytoarchitectonic and cytochemical analysis | Q37679884 |
| | Avian predators taste-reject aposematic prey on the basis of their chemical defence. | Q40659478 |
| | The evolution of stereopsis and the Wulst in caprimulgiform birds: A comparative analysis | Q42597022 |
| | What is binocular vision for? A birds' eye view | Q43201432 |
| | Relative size of the hyperstriatum ventrale is the best predictor of feeding innovation rate in birds | Q44408665 |
| | Modelling oil droplet absorption spectra and spectral sensitivities of bird cone photoreceptors. | Q45265724 |
| | Secondarily flightless birds or Cretaceous non-avian theropods? | Q45968875 |
| | Quantitative estimates of visual performance features in fossil birds. | Q45993643 |
| | Infrasound responses in the midbrain of the guinea fowl | Q46522528 |
| | Size limitations in semicircular duct systems | Q47263306 |
| | Comparative morphology of the avian cerebellum: II. Size of folia | Q47313699 |
| | Palaeontology: inside the oldest bird brain | Q47326036 |
| | Big birds and their brains: paleoneurology of the New Zealand moa. | Q47736103 |
| | Brain Evolution and Archaeopteryx | Q47769046 |
| | Complex distribution of avian color vision systems revealed by sequencing the SWS1 opsin from total DNA. | Q47950080 |
| | Avian-like attributes of a virtual brain model of the oviraptorid theropod Conchoraptor gracilis. | Q48285359 |
| | Organization of the tectofugal visual pathway in the pigeon: a retrograde transport study | Q48381752 |
| | Memory and the hippocampus in food-storing birds: a comparative approach | Q48411477 |
| | Comparative morphology of the avian cerebellum: I. Degree of foliation | Q48527203 |
| | Evoked cochlear potentials in the barn owl. | Q48619152 |
| | Why some bird brains are larger than others | Q48791328 |
| | Mechanisms of magnetic orientation in birds | Q48882188 |
| | Audiogram, body mass, and basilar papilla length: correlations in birds and predictions for extinct archosaurs. | Q50469899 |
| | Activity of primary auditory neurons in the cochlear ganglion of the emu Dromaius novaehollandiae: spontaneous discharge, frequency tuning, and phase locking. | Q50510335 |
| | Olfaction and behavioral modification in domestic chicks (Gallus domesticus). | Q51222045 |
| | Extraordinary large brains in tool-using New Caledonian crows (Corvus moneduloides). | Q51964652 |
| | A mosaic pattern characterizes the evolution of the avian brain. | Q52088694 |
| | The eyes of oilbirds (Steatornis caripensis): pushing at the limits of sensitivity. | Q52538412 |
| | Chemical compass model of avian magnetoreception. | Q52691055 |
| | Vision and the foraging technique of skimmers (Rynchopidae) | Q54308135 |
| | Functional association of bill morphology and foraging behaviour in calidrid sandpipers | Q55891563 |
| | Forebrain enlargement among nonavian theropod dinosaurs | Q55932533 |
| | Structure and function of hindlimb feathers in Archaeopteryx lithographica | Q56038837 |
| | Avian olfactory navigation: its empirical foundation and conceptual state | Q56158700 |
| | TOOLS AND BRAINS IN BIRDS | Q56172276 |
| | A new pressure sensory mechanism for prey detection in birds: the use of principles of seabed dynamics? | Q56225063 |
| | Avian Vision: A Review of Form and Function with Special Consideration to Birds of Prey | Q56225143 |
| | Feeding innovations and forebrain size in birds | Q56270651 |
| | Ultraviolet Vision in Birds | Q56287563 |
| | Tetrachromacy, oil droplets and bird plumage colours | Q56287564 |
| | Behavioural flexibility predicts species richness in birds, but not extinction risk | Q56942254 |
| | Behavioural flexibility and invasion success in birds | Q56942260 |
| | Visual pigments and oil droplets in the penguin,Spheniscus humboldti | Q57311649 |
| | Olfactory Behavior of Foraging Procellariiforms | Q57482974 |
| | Avian brain evolution: new data from Palaeogene birds (Lower Eocene) from England | Q57591788 |
| | The morphology of the pecten oculi of the ostrich, Struthio camelus | Q58589407 |
| | Smell and Foraging in Shearwaters and Petrels | Q59057053 |
| P304 | page(s) | 282-305 | |
| P577 | publication date | 2011-04-20 | |
| P1476 | title | Evolution of the Avian Brain and Senses | |