Abstract is: Ludwig Huber (Juli 25, 1964 in Neunkirchen, Austria) is an Austrian zoologist and a comparative cognitive biologist cognitive biologist at the Messerli Research Institute at the University of Veterinary Medicine Vienna, where he is co-founder head of the Unit of Comparative Cognition.His research is focused on the experimental and comparative study of animal cognition, and he has worked with a wide variety of species, including pigeons, dogs, kea, and marmosets.
| human | Q5 |
| P646 | Freebase ID | /m/0g9vbjy |
| P227 | GND ID | 1247641198 |
| P269 | IdRef ID | 259725412 |
| P213 | ISNI | 0000000371568966 |
| P244 | Library of Congress authority ID | nb2004008274 |
| P691 | NL CR AUT ID | xx0123518 |
| P496 | ORCID iD | 0000-0002-0217-136X |
| P3368 | Prabook ID | 2170960 |
| P1153 | Scopus author ID | 7102868913 |
| P214 | VIAF ID | 149427854 |
| P10832 | WorldCat Entities ID | E39PBJrKWy7hwVfqtdGfMR48YP |
| P27 | country of citizenship | Austria | Q40 |
| P69 | educated at | University of Vienna | Q165980 |
| P108 | employer | Charles University | Q31519 |
| University of Vienna | Q165980 | ||
| P734 | family name | Huber | Q1755469 |
| Huber | Q1755469 | ||
| Huber | Q1755469 | ||
| P735 | given name | Ludwig | Q14159020 |
| Ludwig | Q14159020 | ||
| P106 | occupation | zoologist | Q350979 |
| university teacher | Q1622272 | ||
| biologist | Q864503 | ||
| P21 | sex or gender | male | Q6581097 |
| Q58745659 | A Modified Feature Theory as an Account of Pigeon Visual Categorization |
| Q58745674 | A Modified Feature Theory as an Account of Pigeon Visual Categorization |
| Q58746061 | A case of quick problem solving in birds: string pulling in keas, Nestor notabilis |
| Q52051972 | A new learning paradigm elicits fast visual discrimination in pigeons. |
| Q30840658 | Adopt, ignore, or kill? Male poison frogs adjust parental decisions according to their territorial status |
| Q30374991 | Aging effects on discrimination learning, logical reasoning and memory in pet dogs. |
| Q30846105 | Aging of Attentiveness in Border Collies and Other Pet Dog Breeds: The Protective Benefits of Lifelong Training |
| Q36565824 | Animal logics: decisions in the absence of human language |
| Q58746007 | Attention in common marmosets: implications for social-learning experiments |
| Q51903161 | Automatic imitation in dogs. |
| Q51900565 | Big brains are not enough: performance of three parrot species in the trap-tube paradigm. |
| Q48727064 | Brains are not just neurons. Comment on "Toward a computational framework for cognitive biology: unifying approaches from cognitive neuroscience and comparative cognition" by Fitch |
| Q30578705 | Brief owner absence does not induce negative judgement bias in pet dogs |
| Q61698383 | Can early temperament tests predict behavioral tendencies in dog puppies? |
| Q57022493 | Canine cognition |
| Q52177206 | Categorical learning in pigeons: the role of texture and shape in complex static stimuli. |
| Q39178612 | Choice of conflict resolution strategy is linked to sociability in dog puppies |
| Q47590115 | Cognitive Aging in Dogs |
| Q58745693 | Cold-Blooded Cognition: Reptilian Cognitive Abilities |
| Q58746016 | Common marmosets (Callithrix jacchus) do not utilize social information in three simultaneous social foraging tasks |
| Q58745962 | Cooperation in Keas: Social and Cognitive Factors |
| Q51946508 | Discrimination of face-like patterns in the giant panda (Ailuropoda melanoleuca). |
| Q37253645 | Discrimination of familiar human faces in dogs (Canis familiaris). |
| Q47253131 | Do capuchin monkeys use weight to select hammer tools? |
| Q36488667 | Do owners have a clever hans effect on dogs? Results of a pointing study |
| Q50960194 | Does the A-not-B error in adult pet dogs indicate sensitivity to human communication? |
| Q52020447 | Does the use of natural stimuli facilitate amodal completion in pigeons? |
| Q58745556 | Dog Imitation and Its Possible Origins |
| Q33697016 | Dogs (Canis familiaris) can learn to attend to connectivity in string pulling tasks |
| Q28257031 | Dogs can discriminate emotional expressions of human faces |
| Q33840434 | Dogs demonstrate perspective taking based on geometrical gaze following in a Guesser-Knower task |
| Q42205985 | Dogs imitate selectively, not necessarily rationally: reply to. |
| Q28654429 | Dogs learn to solve the support problem based on perceptual cues |
| Q33697024 | Dogs' attention towards humans depends on their relationship, not only on social familiarity |
| Q21135607 | Dogs' expectation about signalers' body size by virtue of their growls. |
| Q30412881 | Dogs' use of the solidity principle: revisited |
| Q51000725 | Domestic dogs (Canis familiaris) flexibly adjust their human-directed behavior to the actions of their human partners in a problem situation. |
| Q59328946 | Effect of Age and Dietary Intervention on Discrimination Learning in Pet Dogs |
| Q52098698 | Elemental versus configural perception in a people-present/people-absent discrimination task by pigeons |
| Q34046690 | Evidence of heterospecific referential communication from domestic horses (Equus caballus) to humans |
| Q58745734 | Evolution of cognition: A comparative approach |
| Q30504030 | Female but not male dogs respond to a size constancy violation |
| Q27339498 | Flexibility in problem solving and tool use of kea and New Caledonian crows in a multi access box paradigm |
| Q30010561 | Flexible compensation of uniparental care: female poison frogs take over when males disappear |
| Q50579954 | Gaze following in the red-footed tortoise (Geochelone carbonaria). |
| Q58745744 | Have we met before? Pigeons recognise familiar human faces |
| Q30010537 | Honest signaling in domestic piglets (Sus scrofa domesticus): vocal allometry and the information content of grunt calls |
| Q57307784 | How Dogs Perceive and Understand Us |
| Q51903882 | How do keas (Nestor notabilis) solve artificial-fruit problems with multiple locks? |
| Q45020238 | How to solve a mechanical problem: the relevance of visible and unobservable functionality for kea. |
| Q58064854 | Hunting strategies in wild common marmosets are prey and age dependent |
| Q21144443 | Imitation as faithful copying of a novel technique in marmoset monkeys |
| Q30837815 | Individual and group level trajectories of behavioural development in Border collies |
| Q21131723 | Inference by Exclusion in Goffin Cockatoos (Cacatua goffini). |
| Q51963022 | Inferential reasoning by exclusion in pigeons, dogs, and humans. |
| Q27324756 | Inhibitory Control, but Not Prolonged Object-Related Experience Appears to Affect Physical Problem-Solving Performance of Pet Dogs |
| Q37432914 | Kea (Nestor notabilis) consider spatial relationships between objects in the support problem |
| Q58745851 | Kea, Nestor notabilis, produce dynamic relationships between objects in a second-order tool use task |
| Q48448471 | Lateralized cognition: asymmetrical and complementary strategies of pigeons during discrimination of the "human concept". |
| Q37564328 | Lifespan development of attentiveness in domestic dogs: drawing parallels with humans |
| Q52022263 | Limited spread of innovation in a wild parrot, the kea (Nestor notabilis). |
| Q79757992 | Limits of dynamic object perception in pigeons: dynamic stimulus presentation does not enhance perception and discrimination of complex shape |
| Q35211525 | Long-term fidelity of foraging techniques in common marmosets (Callithrix jacchus) |
| Q30853136 | Measures of Dogs' Inhibitory Control Abilities Do Not Correlate across Tasks |
| Q38981968 | Navigating a tool end in a specific direction: stick-tool use in kea (Nestor notabilis). |
| Q48436118 | Obey or not obey? Dogs (Canis familiaris) behave differently in response to attentional states of their owners |
| Q52092388 | Object permanence in common marmosets (Callithrix jacchus). |
| Q64061941 | Oviposition and father presence reduce clutch cannibalism by female poison frogs |
| Q34253540 | Part-based and configural processing of owner's face in dogs |
| Q52596430 | Personality traits in companion dogs-Results from the VIDOPET. |
| Q51983042 | Picture-object recognition in pigeons: evidence of representational insight in a visual categorization task using a complementary information procedure. |
| Q50504301 | Picture-object recognition in the tortoise Chelonoidis carbonaria. |
| Q58745860 | Pigeons can discriminate group mates from strangers using the concept of familiarity |
| Q50748811 | Pigeons discriminate objects on the basis of abstract familiarity. |
| Q52098834 | Pigeons use item-specific and category-level information in the identification and categorization of human faces. |
| Q30010642 | Production and perception rules underlying visual patterns: effects of symmetry and hierarchy |
| Q34443771 | Push or pull: an experimental study on imitation in marmosets |
| Q50515849 | Radial-arm-maze behavior of the red-footed tortoise (Geochelone carbonaria). |
| Q30376606 | Reasoning by exclusion in the kea (Nestor notabilis). |
| Q51930659 | Representational insight in pigeons: comparing subjects with and without real-life experience. |
| Q51987770 | Selective imitation in domestic dogs. |
| Q30362819 | Sex-specific offspring discrimination reflects respective risks and costs of misdirected care in a poison frog. |
| Q30413308 | Social attention in keas, dogs, and human children |
| Q28648189 | Social cognition and the evolution of language: constructing cognitive phylogenies |
| Q58746105 | Social contact influences the response of infant marmosets towards novel food |
| Q56555142 | Social factors determine cooperation in marmosets |
| Q51791574 | Social influences on the development of foraging behavior in free-living common marmosets (Callithrix jacchus). |
| Q58746158 | Social learning affects object exploration and manipulation in keas, Nestor notabilis |
| Q51938049 | Social learning and mother's behavior in manipulative tasks in infant marmosets. |
| Q46841848 | Social learning by imitation in a reptile (Pogona vitticeps). |
| Q42076654 | Social learning in a non-social reptile (Geochelone carbonaria). |
| Q52116780 | Target-defining features in a "people-present/people-absent" discrimination task by pigeons. |
| Q36230418 | Task Differences and Prosociality; Investigating Pet Dogs' Prosocial Preferences in a Token Choice Paradigm |
| Q27674706 | Technical intelligence in animals: the kea model |
| Q52089380 | Testing social learning in a wild mountain parrot, the kea (Nestor notabilis). |
| Q47778847 | The ALDB box: automatic testing of cognitive performance in groups of aviary-housed pigeons |
| Q30385346 | The Processing of Human Emotional Faces by Pet and Lab Dogs: Evidence for Lateralization and Experience Effects |
| Q51800941 | The Vienna comparative cognition technology (VCCT): an innovative operant conditioning system for various species and experimental procedures. |
| Q30485536 | The absence of reward induces inequity aversion in dogs |
| Q30417402 | The advantage of objects over images in discrimination and reversal learning by kea, Nestor notabilis |
| Q37578832 | The effect of brumation on memory retention |
| Q58745924 | The effect of ostensive cues on dogs’ performance in a manipulative social learning task |
| Q33831600 | The evolution of imitation: what do the capacities of non-human animals tell us about the mechanisms of imitation? |
| Q27317064 | The importance of the secure base effect for domestic dogs - evidence from a manipulative problem-solving task |
| Q21090074 | The maintenance of traditions in marmosets: individual habit, not social conformity? A field experiment |
| Q33863950 | The predictive value of early behavioural assessments in pet dogs--a longitudinal study from neonates to adults |
| Q90927360 | The repeatability of cognitive performance: a meta-analysis |
| Q51043772 | The role of skin-related information in pigeons' categorization and recognition of humans in pictures. |
| Q33881538 | The temporal dependence of exploration on neotic style in birds |
| Q30588414 | The use of a displacement device negatively affects the performance of dogs (Canis familiaris) in visible object displacement tasks. |
| Q58745986 | Tolerated mouth-to-mouth food transfers in common marmosets |
| Q50468266 | Touchscreen performance and knowledge transfer in the red-footed tortoise (Chelonoidis carbonaria). |
| Q30405120 | Training for eye contact modulates gaze following in dogs |
| Q27674700 | True imitation in marmosets |
| Q41765247 | Understanding dog cognition by functional magnetic resonance imaging |
| Q61698386 | Understanding of size constancy in dogs: a new approach to account for novelty effects |
| Q59403474 | Utilising dog-computer interactions to provide mental stimulation in dogs especially during ageing |
| Q61698376 | Validity of ealy behavioral assessments in dogs – A longitudinal study |
| Q58745997 | Visual categorization of natural stimuli by domestic dogs |
| Q47761091 | Vocal Conditioning in Kea Parrots (Nestor notabilis). |
| Q30840092 | What Are the Ingredients for an Inequity Paradigm? Manipulating the Experimenter's Involvement in an Inequity Task with Dogs |
| Q27346258 | What you see is what you get? Exclusion performances in ravens and keas |
| Q47858079 | Where is the evidence for general intelligence in nonhuman animals? |
| Arabic (ar / Q13955) | لودفيغ هوبر | wikipedia |
| Egyptian Arabic (arz / Q29919) | لودفيج هوبر | wikipedia |
| Ludwig Huber (Biologe) | wikipedia | |
| Ludwig Huber (biologist) | wikipedia |
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