Abstract is: Learning & Behavior is a quarterly peer-reviewed scientific journal published by Springer Science+Business Media on behalf of the Psychonomic Society. The journal was established in 1973 as Animal Learning and Behavior, obtaining its current title in 2003. The founding editor-in-chief was Abram Amsel, the current editor is Jonathan Crystal (Indiana University). The journal covers research into fundamental processes underlying learning and behavior in animals (including humans).
scientific journal | Q5633421 |
P6981 | ACNP journal ID | 12036 |
2283784 | ||
2477134 | ||
2599930 | ||
P8375 | Crossref journal ID | 79344 |
118745 | ||
230386 | ||
P1250 | Danish Bibliometric Research Indicator (BFI) SNO/CNO | 347 |
P1609 | Dialnet journal ID | 10458 |
P1058 | ERA Journal ID | 6504 |
P646 | Freebase ID | /m/0123kj0p |
P236 | ISSN | 0033-3131 |
0090-4996 | ||
1532-5830 | ||
1543-4494 | ||
1543-4508 | ||
2197-9952 | ||
P1277 | JUFO ID | 62539 |
P1144 | Library of Congress Control Number (LCCN) (bibliographic) | 2003212080 |
P4730 | Mir@bel journal ID | 20814 |
P1055 | NLM Unique ID | 0360135 |
0357415 | ||
101155056 | ||
P243 | OCLC control number | 890337525 |
P856 | official website | http://www.springer.com/psychology/psychology+general/journal/13420 |
P10283 | OpenAlex ID | V16559285 |
P3181 | OpenCitations bibliographic resource ID | 186123 |
318868 | ||
318883 | ||
P8104 | Paperity journal ID | 84955 |
P1156 | Scopus source ID | 12030 |
55116 | ||
37190 | ||
P5983 | Springer journal ID | 13420 |
P1240 | Danish Bibliometric Research Indicator level | 1 | |
P571 | inception | 1973-01-01 | |
P8875 | indexed in bibliographic review | Scopus | Q371467 |
Science Citation Index Expanded | Q104047209 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | neuroscience | Q207011 |
P123 | publisher | Springer Science+Business Media | Q176916 |
P1476 | title | Learning and Behavior |
Q51958208 | "Artificial grammar learning" in pigeons: a preliminary analysis. |
Q48216827 | "Counting" by pigeons: discrimination of the number of biologically relevant sequential events |
Q38768318 | "Zeroing" in on mathematics in the monkey brain |
Q52046453 | A behavior systems view of the organization of multiple responses during a partially or continuously reinforced interfood clock. |
Q60326241 | A behavioral field approach to instrumental learning in the rat: I. Partial reinforcement effects and sex differences |
Q34217240 | A bottlenose dolphin discriminates visual stimuli differing in numerosity |
Q59199960 | A chimpanzee’s (Pan troglodytes) long-term retention of lexigrams |
Q51832190 | A common error term regulates acquisition but not extinction of causal judgments in people. |
Q51927374 | A comparative approach to cue competition with one and two strong predictors. |
Q52113511 | A comparison between elemental and compound training of cues in retrospective revaluation. |
Q44826822 | A comparison of the aversive and female attractant properties of urine from dominant and subordinate male mice |
Q50788112 | A configural theory of attention and associative learning. |
Q50593446 | A delay-specific differential outcomes effect in delayed matching to sample. |
Q86637629 | A derived transformation of emotional functions using self-reports, implicit association tests, and frontal alpha asymmetries |
Q51889984 | A differential-outcome effect in pigeons using spatial hedonically nondifferential outcomes. |
Q50453232 | A differential-outcomes effect using hedonically nondifferential outcomes with delayed matching to sample by pigeons. |
Q90320266 | A dimensional summation account of polymorphous category learning |
Q92830232 | A fish eye view of the mirror test |
Q43818501 | A history of morphine-induced taste aversion learning fails to affect morphine-induced place preference conditioning in rats |
Q48285207 | A landmark blocks searching for a hidden platform in an environment with a distinctive shape after extended pretraining |
Q43264838 | A learned flavor preference persists despite the extinction of conditioned hedonic reactions to the cue flavors |
Q41090035 | A long-term study of the impulsive choices of Lewis and Fischer 344 rats |
Q120714390 | A method for producing avoidance behavior in the turtle |
Q46434096 | A mixed design reveals that glucose moieties facilitate extinction of a conditioned taste aversion in rats |
Q89450927 | A new approach to understanding canine social cognition |
Q52147699 | A new direction for grid cells. |
Q41478294 | A new tool-using bird to crow about. |
Q38744532 | A pathway for spatial memory encoding |
Q113202182 | A quantitative genetic analysis of change in open-field behavior of mice |
Q52242474 | A role of stimulus compounds in eliciting responses: relatively spaced extinction following massed acquisition |
Q60512383 | A serial effect in time estimation |
Q30997933 | A signal detection analysis of contingency data |
Q129744607 | A special issue honoring Ken Cheng: navigating animal minds |
Q93043736 | A special issue in honour of Stephen Lea - a true comparative psychologist |
Q61661283 | A test for dominance of cues during maze learning by toads |
Q51799261 | A test of Rescorla and Wagner's (1972) prediction of nonlinear effects in contingency learning. |
Q53111232 | A time course analysis of satiety-induced instrumental outcome devaluation. |
Q48559310 | Abram Amsel (1922-2006) in memoriam |
Q113999481 | Absolute time estimates as a function of complexity and interruption of melodies |
Q50537355 | Abstract numerical discrimination learning in rats. |
Q38839185 | Accumbens D2: Raters of the Loss Outcome |
Q50700872 | Acquired equivalence and generalized suppression in a virtual reality environment. |
Q52002529 | Acquisition and extinction of conditioned nicotine analgesic tolerance. |
Q52022036 | Acquisition and extinction of facilitation in the C57BL/6J mouse. |
Q50075537 | Acquisition and retention of conditioned aversions to context and taste in laboratory mice |
Q114881985 | Acquisition of behavioral control by the auditory features of an imprinting object |
Q48491939 | Acquisition of schedule-induced polydipsia by rats in proximity to upcoming food delivery |
Q125799195 | Acquisition of the same/different concept by an African Grey parrot (Psittacus erithacus): Learning with respect to categories of color, shape, and material |
Q81323628 | Acquisition with partial and continuous reinforcement in pigeon autoshaping |
Q35782698 | Action imitation in birds |
Q130121613 | Active and passive waiting in impulsive choice: Effects of fixed-interval and fixed-time delays |
Q91872600 | Addition and subtraction by honeybees |
Q38077508 | Adjunctive behaviors are operants |
Q50516788 | Adolescent rats fail to demonstrate a LiCl-induced pre-exposure effect: Implications for the balance of drug reward and aversion in adolescence. |
Q47587143 | Adult humans' understanding of support relations: an up-linkage replication |
Q67854210 | Affiliation and aggression in rats |
Q113202192 | Aggression and open field behavior in male mice |
Q44188128 | Alternating exposure to two compound flavors creates inhibitory associations between their unique features |
Q59938918 | Alternative accounts are preferable to value transfer theory: Commentary on Dorrance, Kaiser, and Zentall (1998) |
Q115783036 | Altruistic behavior in the albino rat |
Q114881925 | Among-individual differences in auditory and physical cognitive abilities in zebra finches |
Q34499504 | Amount of training effects in representation-mediated food aversion learning: no evidence of a role for associability changes |
Q46887180 | An analysis of visual oddity concept learning in a California sea lion (Zalophus californianus). |
Q104204111 | An attempt to demonstrate magnetic compass orientation in two species of mammals |
Q51918246 | An attention-modulated associative network. |
Q41234308 | An avian perspective on simulating other minds |
Q38213929 | An easy-to-hard effect after nonreinforced preexposure in a sweetness discrimination |
Q46098076 | An elemental model of retrospective revaluation without within-compound associations |
Q51954199 | An empirical analysis of the super-latent inhibition effect. |
Q51833834 | An exploration of the feature-positive effect in adult humans. |
Q50992786 | An instance theory of associative learning. |
Q43567754 | Analogical reasoning in baboons (Papio papio): flexible reencoding of the source relation depending on the target relation. |
Q51955340 | Analysis of a trial-spacing effect with relatively long intertrial intervals. |
Q81196025 | Animal Learning & Behavior has consistently published high-quality and important articles |
Q51889828 | Animal memory: the contribution of generalization decrement to delayed conditional discrimination retention functions. |
Q92032736 | Animal procrastination: Pigeons choose to defer experiencing an aversive gap or a peck requirement |
Q113202196 | Animal-experimenter interaction and open-field behavior: The rat |
Q46881813 | Anxiolytic-like effect of ejaculation upon frustration |
Q91015861 | Any reward will do: Effects of a reverse-reward contingency on size preference with pet dogs (Canis lupus familiaris) |
Q98947753 | Anybody watching? How others affect helpful actions |
Q38905743 | Apes have eyes to the future |
Q47141443 | Apes perform like infants in false-belief tasks |
Q47753256 | Apes track false beliefs but might not understand them |
Q90648501 | Appetitive conditioning task in a shuttle box and its comparison with the active avoidance paradigm |
Q48562959 | Appetitive latent inhibition in rats: now you see it (sign tracking), now you don't (goal tracking). |
Q42868925 | Applicability to foraging simulation of a reinforcement schedule controlling the response energy of pigeons |
Q114576363 | Approach tendency and threat display as related to social status of Siamese fighting fish,Betta splendens |
Q35782713 | Approaches to the study of traditional behaviors of free-living animals |
Q56394709 | Are chimpanzees "stuck" on their "selves" in video? |
Q38389756 | Artificial grammar learning in pigeons |
Q92105887 | Asking for help: Do dogs take into account prior experiences with people? |
Q114109617 | Assessing human performance during contingency changes and extinction tests in reversal-learning tasks |
Q91073001 | Assessing object-recognition memory in rats: Pitfalls of the existent tasks and the advantages of a new test |
Q35185597 | Assessing power PC. |
Q50496878 | Assessment of progressively delayed prompts on guided skill learning in rats. |
Q50193298 | Associations and hallucinations in mice and men. |
Q44536712 | Associative foundation of causal learning in rats. |
Q34976497 | Associative learning and elemental representation: II. Generalization and discrimination |
Q51856001 | Associative learning phenomena in the snail (Helix aspersa): conditioned inhibition. |
Q89629918 | Associative models fail to characterize transitive inference performance in rhesus monkeys (Macaca mulatta) |
Q93021291 | Associative structure of conditioned inhibition produced by inhibitory perceptual learning treatment |
Q37347312 | Associative structure of integrated temporal relationships |
Q50170365 | Associative structure of second-order conditioning in humans. |
Q51981601 | Associatively activated representations of food events resemble food outcome expectancies more closely than they resemble food-based memories. |
Q50559456 | Associatively mediated stopping: Training stimulus-specific inhibitory control. |
Q50576403 | Asymmetry in the discrimination of quantity by rats: The role of the intertrial interval. |
Q48376984 | Attention and salience in associative blocking |
Q50697578 | Attention as an acquisition and performance variable (AAPV). |
Q49720559 | Attention toward contexts modulates context-specificity of behavior in human predictive learning: Evidence from the n-back task |
Q51943217 | Attentional changes in blocking are not a consequence of lateral inhibition. |
Q45143699 | Attenuation of the intermittent punishment effect: the effect of interpolated punishment and nonreward trials |
Q113693478 | Attribute dimensions and patterns of trait inferences |
Q114881960 | Auditory delayed discriminations by the dolphin: Nonequivalence with delayed-matching performance |
Q114881967 | Auditory matching-to-sample in monkeys (Cebus apella) |
Q30431993 | Auditory proactive interference in monkeys: the roles of stimulus set size and intertrial interval |
Q98507131 | Auditory sentence comprehension in children with cochlear implants after simple visual discrimination training with specific auditory-visual consequences |
Q114881964 | Auditory short-term memory in the budgerigar (Melopsittacus undulatus) |
Q51890523 | Aversive, appetitive and flavour avoidance responses in the presence of contextual cues. |
Q52309415 | Avoidance differences between rats and gerbils |
Q51018836 | Avoidance of interspecific mating in female Syrian hamsters is stronger toward familiar than toward unfamiliar heterospecific males. |
Q90716883 | Awareness of danger inside the egg: Evidence of innate and learned predator recognition in cuttlefish embryos |
Q48986780 | Bayesian approaches to associative learning: from passive to active learning |
Q52046469 | Behavioral and associative effects of differential outcomes in discrimination learning. |
Q34644216 | Behavioral contrast redux |
Q51030253 | Behavioral expression of learned fear in rats is appropriate to their age at training, not their age at testing. |
Q89643117 | Behavioral flexibility: A review, a model, and some exploratory tests |
Q109039233 | Behavioral mechanisms underlying vocal communication in nonhuman primates |
Q33691082 | Behavioral momentum and relapse of extinguished operant responding. |
Q43076755 | Behavioral momentum and resurgence: Effects of time in extinction and repeated resurgence tests |
Q88528343 | Behavioral synchronization and affiliation: Dogs exhibit human-like skills |
Q120714426 | Behaviorally determined dark adaptation functions in the turtle, Pseudemys |
Q47799158 | Benzodiazepine administration prevents the use of error-correction mechanisms during fear extinction. |
Q62092023 | Bidirectional associations |
Q63953551 | Bidirectional avoidance by mice as a function of CS, US, and apparatus variables |
Q50219222 | Bigger brains may make better problem-solving carnivores |
Q62092020 | Biological significance attenuates overshadowing, relative validity, and degraded contingency effects |
Q97428977 | Biotremology in arthropods |
Q30489885 | Bird brains: Does absolute size matter? |
Q34458441 | Blocking between landmarks during 2-D (touchscreen) and 3-D (ARENA) search tasks with pigeons. |
Q30417808 | Blocking in autoshaped lever-pressing procedures with rats |
Q50670109 | Blocking in human causal learning is affected by outcome assumptions manipulated through causal structure. |
Q120714394 | Body temperature change in the snapping turtle (Chelydra serpentina) |
Q50607591 | Boosting weakened synapses to treat Alzheimer's disease. |
Q47330409 | Bumblebees at work in an emotion-like state |
Q44855578 | CS-US interval determines the transition from overshadowing to potentiation with flavor compounds |
Q36983680 | CS-US temporal relations in blocking |
Q36408221 | CS-duration and partial-reinforcement effects counteract overshadowing in select situations |
Q97428983 | Can a dog be spontaneous? |
Q40431146 | Can squirrel monkeys (Saimiri sciureus) plan for the future? Studies of temporal myopia in food choice |
Q29304582 | Can your dog read your mind? Understanding the causes of canine perspective taking |
Q57022493 | Canine cognition |
Q46433732 | Capuchin monkeys can make and use stone tools |
Q40400379 | Causal and predictive-value judgments, but not predictions, are based on cue-outcome contingency |
Q115290406 | Cause, development, function, and evolution: Toward a behavioral ecology of rescue behavior in ants |
Q86526249 | Central amygdala lesions inhibit pontine nuclei acoustic reactivity and retard delay eyeblink conditioning acquisition in adult rats |
Q120714419 | Cerebral lesions and climbing suppression in the turtle |
Q51870269 | Changes in attention to an irrelevant cue that accompanies a negative patterning [corrected] discrimination. |
Q36915296 | Changes in inhibition during differential eyeblink conditioning with increased training |
Q115337453 | Changes in neuronal activity in the cochlear nucleus as a function of classical and instrumental conditioning |
Q52102431 | Changes in stimulus salience as a result of stimulus preexposure: evidence from aversive and appetitive testing procedures. |
Q113202190 | Changes in the open field behavior of female golden hamsters |
Q50597098 | Characteristics of retrograde amnesia for CS preexposure. |
Q41871375 | Characteristics of the lithium-mediated proximal US-preexposure effect in flavor-aversion conditioning |
Q115484379 | Chemocommunication among prey and predator species |
Q81323623 | Chemosensory conditioning in molluscs: I. Failure of contextual conditioning in Hermissenda |
Q36021011 | Chemosensory conditioning in molluscs: II. A critical review |
Q38667360 | Chimpanzee food preferences, associative learning, and the origins of cooking |
Q46153613 | Chimpanzees, cooking, and a more comparative psychology |
Q59265998 | Chlordiazepoxide and the determinants of negative contrast |
Q48140979 | Choice and goal-directed behavior in preschool children |
Q51067773 | Circadian-temporal context and latent inhibition of conditioned taste aversion: Effect of restriction in the intake of the conditioned taste stimulus. |
Q120714400 | Classical and avoidance conditioning of the nictitating membrane in frogs (Rana pipiens) and toads (Bufo Americanus) |
Q52304661 | Classical conditioning of the rabbit nictitating membrane response: effects of reinforcement schedule on response maintenance and resistance to extinction. |
Q120714391 | Climbing suppression: Passive avoidance in the turtle |
Q47768695 | Cocaine preexposure enhances sexual conditioning and increases resistance to extinction in male Japanese quail |
Q90954304 | Coffee time: Low caffeine dose promotes attention and focus in zebrafish |
Q109039235 | Cognition in the African Grey parrot: Preliminary evidence for auditory/vocal comprehension of the class concept |
Q97428310 | Cognitive control of working memory but not familiarity in rhesus monkeys (Macaca mulatta) |
Q39220766 | Cognitive theories as reinforcement history surrogates: the case of likelihood ratio models of human recognition memory |
Q37236167 | Cognitive versus stimulus-response theories of learning |
Q50476332 | Color vision in the giant panda (Ailuropoda melanoleuca). |
Q50443857 | Comparative approaches to same/different abstract-concept learning. |
Q50421445 | Comparing cognition by integrating concept learning, proactive interference, and list memory |
Q48531668 | Comparing demand functions when different price manipulations are used: does unit price help? |
Q96826439 | Comparing pet and detection dogs (Canis familiaris) on two aspects of social cognition |
Q36271443 | Comparing the context specificity of extinction and latent inhibition |
Q51924826 | Comparison of auditory and visual conditioning stimuli in delay eyeblink conditioning in healthy young adults. |
Q46794839 | Comparison of spatial learning in the partially baited radial-arm maze task between commonly used rat strains: Wistar, Spargue-Dawley, Long-Evans, and outcrossed Wistar/Sprague-Dawley |
Q52042633 | Competence and performance in causal learning. |
Q52102435 | Competition among spatial cues in a naturalistic food-carrying task. |
Q44631131 | Competition between ethanol-induced reward and aversion in place conditioning |
Q58853788 | Concept identification strategies used for positive and negative instances |
Q48174104 | Concurrent VR VI schedules: Primacy of molar control of preference and molecular control of response rates |
Q51889793 | Concurrent extinction does not render appetitive conditioning context specific. |
Q51799209 | Concurrent schedules of wheel-running reinforcement: choice between different durations of opportunity to run in rats. |
Q52113509 | Concurrent-chain performance in transition: effects of terminal-link duration and individual reinforcers. |
Q46876947 | Conditioned avoidance responses survive contingency degradation in the garden slug, Lehmannia valentiana |
Q46582318 | Conditioned context aversion learning in the laboratory mouse |
Q45177485 | Conditioned inhibition and the UCS-CS interval |
Q52113512 | Conditioned inhibitory effects of discriminated Pavlovian training with food in rats depend on interactions of search modes, related repertoires, and response measures. |
Q36485465 | Conditioned suppression is an inverted-U function of footshock intensity |
Q114109629 | Conditioning in garter snakes: Aversion to palatable prey induced by delayed illness |
Q52002524 | Conditioning of tentacle lowering in the snail (Helix aspersa): acquisition, latent inhibition, overshadowing, second-order conditioning, and sensory preconditioning. |
Q44924566 | Conditioning-specific reflex modification of the rabbit (Oryctolagus cuniculus) nictitating membrane response is sensitive to context |
Q44898303 | Conditioning-specific reflex modification of the rabbit (Oryctolagus cuniculus) nictitating membrane response: US intensity effects |
Q50596599 | Configural integration of temporal and contextual information in rats: Automated measurement in appetitive and aversive preparations. |
Q114576348 | Conformity as a function of experimentally induced minority and majority competence |
Q33632067 | Conserving and managing animals that learn socially and share cultures |
Q103837636 | Conspecific presence, but not pilferage, influences pinyon jays' (Gymnorhinus cyanocephalus) caching behavior |
Q108898676 | Constraints on vocal production learning in budgerigars (Melopsittacus undulates) |
Q50435413 | Context modulation of learned attention deployment |
Q50595623 | Contextual control of conditioning is not affected by extinction in a behavioral task with humans. |
Q51943209 | Contextual control of first- and second-learned excitation and inhibition in equally ambiguous stimuli. |
Q34039456 | Contextual control of operant behavior: evidence for hierarchical associations in instrumental learning |
Q50451876 | Contextual control over equivalence and nonequivalence explains apparent arbitrary applicable relational responding in accordance with sameness and opposition. |
Q51790602 | Contextual modulation of attention in human category learning. |
Q36216579 | Contiguity and covariation in human causal inference |
Q58369786 | Contrast and value: Beyond the work ethic effect. A reply to Zentall (2008) |
Q51890521 | Contrasting AAC and ABC renewal: the role of context associations. |
Q113202189 | Contrasting effects of group housing and isolation on subsequent open field exploration in laboratory rats |
Q40400373 | Contrasting predictive and causal values of predictors and of causes. |
Q97535732 | Convergent evolution of complex cognition: Insights from the field of avian cognition into the study of self-awareness |
Q67388084 | Copulatory behavior and nest building behavior of wild house mice (Mus musculus) |
Q64945682 | Copulatory behavior of Mongolian gerbils (Meriones unguiculatus). |
Q51786304 | Counting absolute numbers of items, from 1 to 8, in pigeons. |
Q39432006 | Creating a common terminology for play behavior to increase cross-disciplinary research |
Q97547452 | Cross-modal tactile-visual neural representations in bumble bees |
Q57243536 | Cross-modality contrast: Exteroceptive context habituation enhances taste neophobia and conditioned taste aversions |
Q90583372 | Cues Associated with Alternative Reinforcement During Extinction Can Attenuate Resurgence of an Extinguished Instrumental Response |
Q50191585 | Data archiving for animal cognition research: report of an NIMH workshop |
Q51854150 | Deactivation and reactivation of the inhibitory power of a conditioned inhibitor: testing the predictions of an attentional-associative model. |
Q83430167 | Decision making by humans in a behavioral task: do humans, like pigeons, show suboptimal choice? |
Q50513665 | Delay discounting in rhesus monkeys: equivalent discounting of more and less preferred sucrose concentrations. |
Q114881966 | Delayed matching of visual materials by a bottlenosed dolphin aided by auditory symbols |
Q41898200 | Delayed matching to sample: reinforcement has opposite effects on resistance to change in two related procedures |
Q114576336 | Dependency of the spectral reflectance curves of the Munsell color chips |
Q48356231 | Deprivation level and choice in pigeons: a test of within-trial contrast. |
Q120714398 | Depth vision in monocular frogs |
Q50770292 | Derived relations and generalized alteration of preferences. |
Q102381323 | Designer receptor inhibition suggests mechanism for monkey Theory of Mind |
Q44918824 | Determinants of ejaculatory failure in the copulatory behavior of cactus mice (Peromyscus eremicus) |
Q51977803 | Determinants of range effects in face recognition. |
Q89643125 | Development of point following behaviors in shelter dogs |
Q35782717 | Development, direction, and damage limitation: social learning in domestic fowl |
Q51947856 | Differences in taste-potentiated odor aversions with O+/OT+ versus OT+/O+ conditioning: Implications for configural associations. |
Q115337447 | Different neuronal responses in the cochlear nucleus of a cat during classical and instrumental conditioning |
Q114576343 | Different nocturnal activity patterns of Peromyscus californicus and Peromyscus erenicus in lunar lighting |
Q36614457 | Differential reinforcement and resistance to change of divided-attention performance. |
Q91758848 | Directed forgetting in rats: Evidence for active memory control? |
Q50440795 | Discrimination and representation of relative numerosity in a bisection task by pigeons |
Q81401416 | Discrimination blocking: acquisition versus performance deficits in human contingency learning |
Q61661287 | Discrimination learning and extinction in toads1 |
Q51899511 | Discrimination learning in humans: role of number and complexity of rules. |
Q89643121 | Discrimination of artificial starry sky by pigeons |
Q60134014 | Discrimination of geons by pigeons: The effects of variations in surface depiction |
Q52119792 | Discrimination of individual vocalizations by black-capped chickadees (Poecile atricapilla). |
Q43871894 | Discrimination of what, when, and where is not based on time of day. |
Q113250636 | Discrimination training and reversal in groups of honey bees |
Q61820882 | Discrimination-reversal skills in squirrel monkeys: The reversal index and the reversal-acquisition ratio compared |
Q36723193 | Discriminative properties of the reinforcer can be used to attenuate the renewal of extinguished operant behavior. |
Q52029505 | Discriminative stimuli that follow the absence of reinforcement are preferred by pigeons over those that follow reinforcement. |
Q52029496 | Disruption of latent inhibition by interpolation of task-irrelevant stimulation between preexposure and conditioning. |
Q51902742 | Disruption of temporal discrimination and the choose-short effect. |
Q50420727 | Distance and direction, but not light cues, support response reversal learning |
Q35782723 | Distinguishing social and asocial learning using diffusion dynamics |
Q114576342 | Diurnal and nocturnal sleep stage patterns following sleep deprivation |
Q47180907 | Divergences in learning and memory among wild zebrafish: Do sex and body size play a role? |
Q48380985 | Divided attention and the matching law: sample duration affects sensitivity to reinforcement allocation |
Q52002531 | Divided attention performance and the matching law. |
Q44768340 | Do adjustments in search behavior depend on the precision of spatial memory? |
Q34337010 | Do monkeys choose to choose? |
Q36428217 | Do pigeons prefer information in the absence of differential reinforcement? |
Q39395427 | Does chess instruction improve mathematical problem-solving ability? Two experimental studies with an active control group. |
Q42038264 | Does satiation close the open economy? |
Q90970781 | Dogs do not demonstrate a human-like bias to defer to communicative cues |
Q52094795 | Domestic pigeons (Columba livia) discriminate between photographs of individual pigeons. |
Q51764238 | Domestic pigeons (Columba livia) discriminate between photographs of male and female pigeons. |
Q91712376 | Domesticated dogs (Canis familiaris) tend to follow repeated deceptive human cues even when food is visible |
Q51977804 | Dynamic object recognition in pigeons and humans. |
Q52022045 | Dynamics of temporal discrimination. |
Q115290413 | Early cold stress and emotional reactivity in BALB/c mice: A brief note on Schaefer’s temperature hypothesis |
Q95376328 | Editorial |
Q95553785 | Editorial |
Q60922976 | Effect of age on discrimination learning, reversal learning, and cognitive bias in family dogs |
Q56454651 | Effect of attitude similarity-dissimilarity on the utilization of additional stimulus inputs in judgments of interpersonal attraction |
Q113693467 | Effect of context on ratings of personality traits |
Q51889459 | Effect of extended training on generalization of latent inhibition: an instance of perceptual learning. |
Q113693482 | Effect of group size on avoidance learning in zebra fish,Brachydanio rerio (Pisces: Cyprinidae) |
Q113693473 | Effect of monetary rewards on an insight learning task |
Q50693418 | Effect of odor preexposure on acquisition of an odor discrimination in dogs. |
Q48216849 | Effect of outcome valence on positive and negative patterning in human causal reasoning |
Q113202179 | Effect of presence of an imprinted object on response of ducklings in an open field and when exposed to a fear stimulus |
Q51993062 | Effect of required response force on rats' performance on a VI+ schedule of reinforcement. |
Q59265957 | Effect of taste context and ambient context changes on successive negative contrast |
Q90070868 | Effect of the number of training trials on the event-related potential correlates of equivalence relations |
Q51955342 | Effect on subsequent fixed-interval schedule performance of prior exposure to ratio and interval schedules of reinforcement. |
Q114881987 | Effects of auditory stress on grooming dominance in the rat |
Q114881988 | Effects of changeover contingencies on auditory stimulus control of two responses |
Q51943965 | Effects of context exposure during conditioning on conditioned taste aversions. |
Q47660607 | Effects of effort and difficulty on human preference for a stimulus: Investigation of the within-trial contrast |
Q33676672 | Effects of forced movements on learning: Findings from a choice reaction time task in rats |
Q52008945 | Effects of forced-choice runway variations on rats' T-maze serial pattern learning. |
Q52309393 | Effects of habituation on threat display and dominance establishment in the Siamese fighting fish, Betta splendens. |
Q113693479 | Effects of hints and interpolated activity on solution of an insight problem |
Q52046456 | Effects of identical context on visual pattern recognition by pigeons. |
Q52102433 | Effects of postconditioning inflation on odor + taste compound conditioning. |
Q51979890 | Effects of preexposure and retention interval placement on latent inhibition and perceptual learning in a choice-maze discrimination task. |
Q51924829 | Effects of pretraining on acquisition of novel configural discriminations in human predictive learning. |
Q113202205 | Effects of preweaning injections of adrenalin on later open field behavior of rats |
Q114109623 | Effects of prey movement and background on predatory behavior of chameleons |
Q43825752 | Effects of proximal unconditioned stimulus preexposure on ingestional aversions learned as a result of taste presentation following drug treatment |
Q36954015 | Effects of reinforcer delay and variability in a successive-encounters procedure |
Q51890518 | Effects of response-independent stimuli on fixed-interval and fixed-ratio performance of rats: a model for stressful disruption of cyclical eating patterns. |
Q48491932 | Effects of runway shift and stay rules on rats' serial pattern learning in the T-maze |
Q114576335 | Effects of shock, ego-threat, and neutral conditions on affective experience during paired-associates learning |
Q60500062 | Effects of social isolation and crowding upon active-avoidance performance in the rat |
Q51850690 | Effects of the amount of acquisition and contextual generalization on the renewal of instrumental behavior after extinction. |
Q113202176 | Effects of two types of feeding on the weight and open-field behavior of rats |
Q43908307 | Elemental representation and configural mappings: combining elemental and configural theories of associative learning |
Q52098698 | Elemental versus configural perception in a people-present/people-absent discrimination task by pigeons |
Q56271146 | Elements of syntax in the systems of three language-trained animals |
Q52309410 | Elimination of self-punitive behavior with a novel stimulus and safety signal |
Q114881958 | Embryonic auditory experience and maternal call recognition |
Q50239014 | Emergent relations in pigeons following training with temporal samples |
Q113202191 | Emotionality ratings and open-field behavior |
Q39575578 | Empathy in prairie voles: Is this the consolation prize? |
Q50648176 | Enhancement and reduction of associative retroactive cue interference by training in multiple contexts. |
Q50621851 | Enhancement of equivalence class formation by pretraining discriminative functions. |
Q89566399 | Enhancing "self-control": The paradoxical effect of delay of reinforcement |
Q48532656 | Enumeration of briefly presented items by the chimpanzee (Pan troglodytes) and humans (Homo sapiens). |
Q92836839 | Episodic time in the brain: A new world order |
Q94949586 | Erratum to Gershman and Niv (2012), Learning & Behavior, 40, 255-268 |
Q87193917 | Erratum to: An elemental model of retrospective revaluation without within-compound associations |
Q114881972 | Erratum to: Auditory matching-to-sample in monkeys(Cebus apella) |
Q43863820 | Erratum to: Learned predictiveness effects following single-cue training in humans. |
Q50435641 | Erratum to: Relationship between individual and group learning in a marine teleost: A case study with sea bass under self-feeding conditions |
Q88149641 | Erratum to: Renewal of extinguished instrumental responses: independence from Pavlovian processes and dependence on outcome value |
Q85383073 | Erratum to: the goldfish conditioned withdrawal preparation: effects of some basic methodological variables |
Q109667212 | Estimating on the fly: The approximate number system in rufous hummingbirds (Selasphorus rufus) |
Q115484378 | Ethological analysis of predator avoidance by the paradise fish (Macropodus opercularis L.): II. Key stimuli in avoidance learning |
Q51955346 | Evaluating conditioning of related and unrelated stimuli using a compound test. |
Q44019935 | Evaluating the TD model of classical conditioning |
Q30420309 | Evaluating the logic of perspective-taking experiments |
Q52116778 | Evaluation and development of a connectionist theory of configural learning. |
Q51867726 | Evaluation of bidirectional interstimulus interval (ISI) shift in auditory delay eye-blink conditioning in healthy humans. |
Q57464283 | Even bees know zero is less than one |
Q58853782 | Evidence for a two-process theory of problem solving |
Q114106026 | Evidence for distinct serial processes in animals: The multiplicative-factors method |
Q50616735 | Evidence for online processing during causal learning. |
Q44301407 | Evidence for social learning in wild lemurs (Lemur catta). |
Q49154493 | Evidence for the interchangeability of an avoidance behavior and a negative occasion setter |
Q36216583 | Evidence for the role of higher order reasoning processes in cue competition and other learning phenomena |
Q96158707 | Evidence of learning and memory in the juvenile dwarf cuttlefish Sepia bandensis |
Q89706673 | Evidence that novel flavors unconditionally suppress weight gain in the absence of flavor-calorie associations |
Q58853785 | Evidence that ‘thinking aloud’ constitutes an externalization of inner speech |
Q51951404 | Evolution of an elemental theory of Pavlovian conditioning. |
Q120714408 | Excretory electrolytes and habituation in the turtle |
Q47327787 | Expanding the definitional criteria for imaginative play: Contributions of sociocultural perspectives |
Q37772369 | Experimental identification of social learning in wild animals |
Q37772372 | Experimental studies of animal social learning in the wild: Trying to untangle the mystery of human culture |
Q50788109 | Exploring a latent cause theory of classical conditioning. |
Q92423609 | Exploring individual and social learning in jackdaws (Corvus monedula) |
Q97532860 | Exploring the impact of coherence (through the presence versus absence of feedback) and levels of derivation on persistent rule-following |
Q44734933 | Exploring the limits of spatial memory in rats, using very large mazes |
Q92389735 | Exploring the potential impact of relational coherence on persistent rule-following: The first study |
Q114881949 | Exposure learning of auditory stimuli by rats |
Q91538617 | Exposure to maternal odor enhances intake of a taste that mimicks the sensory attributes of ethanol |
Q41817802 | Extended exposure to environmental cues, but not to sucrose, reduces sucrose cue reactivity in rats |
Q51896422 | Extinction and blocking of conditioned inhibition in human causal learning. |
Q52088394 | Extinction and retraining of simultaneous and successive flavor conditioning. |
Q51859919 | Extinction context as a conditioned inhibitor. |
Q50532157 | Extinction in multiple contexts: Effects on the rate of extinction and the strength of response recovery. |
Q91265322 | Extinction of a Pavlovian-conditioned inhibitor leads to stimulus-specific inhibition |
Q52014438 | Extinction of a saccharin-lithium association: assessment by consumption and taste reactivity. |
Q52309409 | Extinction of a taste aversion in the absence of the consummatory response |
Q36581803 | Extinction of chained instrumental behaviors: Effects of consumption extinction on procurement responding. |
Q51943211 | Extinction of conditioned inhibition: effects of different outcome continua. |
Q44905162 | Extinction produces context inhibition and multiple-context extinction reduces response recovery in human predictive learning. |
Q48627221 | Extinction revisited: similarities between extinction and reductions in US intensity in classical conditioning of the rabbit's nictitating membrane response |
Q36592546 | Extinction with multiple excitors |
Q52991175 | Face facts: Even nonhuman animals discriminate human faces. |
Q93021277 | Facilitation and retardation of flavor preference conditioning following prior exposure to the flavor conditioned stimulus |
Q48305282 | Factors moderating blocking in human place learning: the role of task instructions. |
Q51962755 | Failure to obtain value enhancement by within-trial contrast in simultaneous and successive discriminations. |
Q88498972 | Fake snakes uncover chimpanzees' mind-reading ability |
Q52008948 | Family resemblances facilitate formation and expansion of functional equivalence classes in pigeons. |
Q113202202 | Fear level and rats’ open-field activity and defecation |
Q51272777 | Fearfulness in female and male cats |
Q50657478 | Feature-positive discriminations during a spatial-search task with humans. |
Q56535380 | Feline indolence: Cats prefer free to response-produced food |
Q68918706 | Female odors evoke ultrasounds from male mice |
Q51896426 | First- and second-order configural sensitivity for greeble stimuli in baboons. |
Q51947854 | Flattening generalization gradients, context, and perceptual learning. |
Q46104259 | Flavor avoidance learning based on missing calories but not on palatability reduction. |
Q46875549 | Flavor evaluative conditioning and contingency awareness |
Q51983744 | Flavor-evaluative conditioning is unaffected by contingency knowledge during training with color-flavor compounds. |
Q39228530 | Flexible goal imitation: Vicarious feedback influences stimulus-response binding by observation |
Q114881970 | Frequency range size and the frequency range constraint in auditory perception by European starlings (Sturnus vulgaris) |
Q50980562 | Frustration and sexual behavior in male rats. |
Q53241764 | Gambling in rhesus macaques (Macaca mulatta): The effect of cues signaling risky choice outcomes. |
Q50786622 | Generalization decrements: further support for flexibility in stimulus processing. |
Q51924827 | Generalization of causal efficacy judgments after evaluative learning. |
Q115028543 | Generalization of visual matching and delayed matching by a California sea lion (Zalophus californianus) |
Q50879808 | Genetic analysis of tonic immobility in young Japanese quail (Coturnix coturnix japonica). |
Q114023478 | Geometrical representation of serial order in working memory |
Q43427980 | Get out of the corner: Inhibition and the effect of location type and number on perceptron and human reorientation. |
Q51742693 | Global undernutrition during gestation influences learning during adult life |
Q62495677 | Grid-like units help deep learning agent to navigate |
Q111896365 | Habituation in the polychaete Hesperonoë adventor |
Q47745788 | Habituation, latent inhibition, and extinction |
Q122459369 | Hatching behavior of the chick (Callus domesticus): Plasticity of the rotatory component |
Q50317385 | Hearing is believing: Birds learn fear. |
Q113693483 | Higher reliability and closer relationship between open-field test measures on aggregation data |
Q51031628 | History effects on induced and operant variability. |
Q46330574 | How New Caledonian crows solve novel foraging problems and what it means for cumulative culture. |
Q46574823 | How comparative psychology can shed light on human evolution: Response to Beran et al.'s discussion of "Cognitive capacities for cooking in chimpanzees". |
Q51918232 | How do adult humans compare with New Caledonian crows in tool selectivity? |
Q34322748 | How do apes ape? |
Q39525072 | How does the ecological foraging behavior of desert kangaroo rats (Dipodomys deserti) relate to their behavior on radial mazes? |
Q38809819 | How lost "passenger" ants find their way home |
Q99596102 | How to make smoke without fire. Minds are not (just) trainable machines |
Q51936397 | Human and animal perceptual learning: some common and some unique features. |
Q92718416 | Human and pigeon suboptimal choice |
Q52102430 | Human causality judgments and response rates on DRL and DRH schedules of reinforcement. |
Q47375775 | Human cumulative culture in the laboratory: Effects of (micro) population size |
Q92389743 | Human free-operant performance varies with a concurrent task: Probability learning without a task, and schedule-consistent with a task |
Q50523788 | Human nonverbal discrimination of relative and absolute number. |
Q50592724 | Human performance on random ratio and random interval schedules, performance awareness and verbal instructions. |
Q46881811 | Humidity as an aversive stimulus in learning in Drosophila melanogaster |
Q109667206 | Hummingbirds modify their routes to avoid a poor location |
Q50780920 | Hyperbolic discounting of delayed social interaction. |
Q37772370 | Identifying teaching in wild animals |
Q83011824 | Identity concept formation during visual multiple-choice matching in a harbor seal (Phoca vitulina) |
Q92214232 | Imagery in wild birds: Retrieval of visual information from referential alarm calls |
Q22336969 | Imitative learning in Japanese quail (Coturnix japonica) using the bidirectional control procedure |
Q61820871 | Immunization and helplessness phenomena in the rat in a nonaversive situation |
Q46616910 | Impact of brief or extended extinction of a taste aversion on inhibitory associations: evidence from summation, retardation, and preference tests. |
Q50313103 | Impact of intervening learning on resurgence in humans with Autism Spectrum Disorders |
Q46316476 | Impact of stimulus format and reward value on quantity discrimination in capuchin and squirrel monkeys |
Q46774037 | Implicit learning in cotton-top tamarins (Saguinus oedipus) and pigeons (Columba livia). |
Q114881952 | Imprinting or exposure learning in rats given early auditory stimulation |
Q50657187 | In a daily time-place learning task, time is only used as a discriminative stimulus if each daily session is associated with a distinct spatial location. |
Q38162766 | In search of consolidation of short-term memory in nonhuman animals. |
Q91712371 | In what sense are dogs special? Canine cognition in comparative context |
Q88913312 | Incidental spatial memory in the domestic dog (Canis familiaris) |
Q39278523 | Individual differences in learning predict the return of fear |
Q51936394 | Individual differences: either relational learning or item-specific learning in a same/different task. |
Q91712361 | Individual performance across motoric self-regulation tasks are not correlated for pet dogs |
Q57125410 | Inequity aversion in dogs: a review |
Q92894460 | Influence of seeing a red face during the male-male encounters of mosquito-specialist spiders |
Q54623439 | Influences of social isolation during development on sexual behavior of the rat |
Q52089377 | Influences of social learning on mate-choice decisions. |
Q35782727 | Information and aggression in fishes |
Q52014432 | Initial-link duration and acquisition of preference in concurrent chains. |
Q104111582 | Innovative problem solving in macaws |
Q39714236 | Instrumental electrodermal conditioning in the monkey (Cebus albifrons): Acquisition and long-term retention |
Q36411943 | Integrating Tinbergen's inquiries: Mimicry and play in humans and other social mammals. |
Q52113507 | Integration and representation in rats' serial pattern learning in the T-maze. |
Q51042337 | Integration of cardiac responses to serial stimuli after Pavlovian conditioning in rats. |
Q33757010 | Integration of spatial relationships and temporal relationships in humans |
Q50614768 | Inter-response-time reinforcement and relative reinforcer frequency control choice. |
Q81323632 | Interaction of retention interval with CS-preexposure and extinction treatments: symmetry with respect to primacy |
Q35762209 | Interactions between retroactive-interference and context-mediated treatments that impair pavlovian conditioned responding |
Q51022118 | Interactions of numerical and temporal stimulus characteristics on the control of response location by brief flashes of light. |
Q46202614 | Interactive effects of the probability of the cue and the probability of the outcome on the overestimation of null contingency. |
Q114881963 | Interference and auditory short-term memory in the bottlenosed dolphin |
Q58853794 | Interpretation of information that an instance is positive or negative in concept identification |
Q39519322 | Intertrial unconditioned stimuli differentially impact trace conditioning |
Q47411236 | Interval timing under a behavioral microscope: Dissociating motivational and timing processes in fixed-interval performance |
Q60941578 | Intervening activity and the retention of meaningful verbal material |
Q114881926 | Intra-individual variation in the songs of humpback whales suggests they are sonically searching for conspecifics |
Q42115769 | Intradimensional vs. extradimensional transfer in the discriminative learning of goldfish and pigeons |
Q50050359 | Investigating the balance between goal-directed and habitual control in experimental and real-life settings |
Q47375798 | Investigating the impact of observation errors on the statistical performance of network-based diffusion analysis |
Q114914351 | Involvement of the neural social behaviour network during social information acquisition in zebra finches (Taeniopygia guttata) |
Q92672800 | Is symmetry inference an essential component of language? |
Q98611864 | It's not just the animals that are STRANGE |
Q129208704 | Jumping spiders: An exceptional group for comparative cognition studies |
Q47640660 | Latent inhibition in flavor-preference conditioning: effects of motivational state and the nature of the reinforcer. |
Q43094822 | Latent inhibition of conditioned disgust reactions in rats |
Q39881929 | Learned predictiveness effects following single-cue training in humans |
Q44320125 | Learned suppression of photopositive tendencies in Drosophila melanogaster |
Q51951405 | Learning and the wisdom of the body. |
Q48562975 | Learning by pigeons playing against tit-for-tat in an operant prisoner's dilemma |
Q92830193 | Learning is negatively associated with strength of left/right paw preference in wild grey squirrels (Sciurus carolinensis) |
Q45907474 | Learning of colonial odor in the ant Cataglyphis niger (Hymenoptera; Formicidae). |
Q51927377 | Learning of contingent relationships. |
Q38646581 | Learning to play: A review and theoretical investigation of the developmental mechanisms and functions of cetacean play |
Q50582369 | Learning to write without writing: writing accurate descriptions of interactions after learning graph-printed description relations. |
Q29036236 | Learning with prolonged delay of reinforcement |
Q30479615 | Learning-related shifts in generalization gradients for complex sounds. |
Q36489930 | Level of deprivation does not affect degree of discounting in pigeons |
Q46696009 | Light stimulus change evokes an activity response in the rat. |
Q120714392 | Light-contingent operant behavior in the turtle |
Q79757992 | Limits of dynamic object perception in pigeons: dynamic stimulus presentation does not enhance perception and discrimination of complex shape |
Q58853789 | Logical and empirical thinking in a problem solving task |
Q52029512 | Looking for inhibition of return in pigeons. |
Q44927496 | Magnetic compass orientation in C57BL/6J mice |
Q48905698 | Maintenance of responding when reinforcement becomes delayed. |
Q46921389 | Male-female associations in the domestic guinea pig |
Q51010225 | Massive preexposure and preexposure in multiple contexts attenuate the context specificity of latent inhibition. |
Q80116075 | Matching-to-sample in pigeons: in the absence of sample memory, sample frequency is a better predictor of comparison choice than the probability of reinforcement for comparison choice |
Q93043752 | Measuring response inhibition with a continuous inhibitory-control task |
Q50086526 | Measuring the "transfer of meaning" through members of equivalence classes merged via a class-specific reinforcement procedure |
Q29029280 | Mechanisms for turn alternation in woodlice (Porcellio scaber): The role of bilaterally asymmetrical leg movements |
Q61659648 | Mediated responding on a multiple-choice test-only list following the acquisition of a double-function list |
Q58599483 | Memories of emotional expressions in horses |
Q51998904 | Memory priming and trial spacing effects in Pavlovian learning. |
Q44128098 | Memory span for heterospecific individuals' odors in an ant, Cataglyphis cursor |
Q92950330 | Mental imagery in animals: Learning, memory, and decision-making in the face of missing information |
Q93021284 | Metacognition in dogs: Do dogs know they could be wrong? |
Q52841335 | Methodological-conceptual problems in the study of chimpanzees' folk physics: how studies with adult humans can help. |
Q92775229 | Mickey Mouse's negative affect facing mistakes |
Q46548207 | Microstructural analysis of conditioned and unconditioned responses to maltodextrin |
Q39416467 | Microstructural analysis of negative anticipatory contrast: A reconsideration of the devaluation account. |
Q92669952 | Midsession reversal learning by pigeons: Effect on accuracy of increasing the number of stimuli associated with one of the alternatives |
Q36472742 | Midsession reversal learning: why do pigeons anticipate and perseverate? |
Q37641805 | Midsession reversals with pigeons: visual versus spatial discriminations and the intertrial interval |
Q87328657 | Midsession shifts in reward probability and the control of behavioral variability |
Q50788104 | Modeling attention in associative learning: two processes or one? |
Q51890525 | Modeling imitation and emulation in constrained search spaces. |
Q79757994 | Modeling unidimensional categorization in monkeys |
Q46232377 | Modulation of an activity response with associative and nonassociative fear in the rat: a lighting differential influences the form of defensive behavior evoked after fear conditioning |
Q51852044 | Modulation of attention in discrimination learning: the roles of stimulus relevance and stimulus-outcome correlation. |
Q52011452 | Monkey auditory list memory: tests with mixed and blocked retention delays. |
Q51810099 | More but not less uncertainty makes adult humans' tool selections more similar to those reported with crows. |
Q88990572 | More evidence that less is better: Sub-optimal choice in dogs |
Q47739087 | Mothering matters: Maternal style predicts puppies' future performance |
Q91073006 | Motivation to run measured by progressive ratio tests: Failure to support the addiction hypothesis for rats |
Q60503040 | Motivational control after extended instrumental training |
Q38498109 | Multiple determinants of transfer of evaluative function after conditioning with free-operant schedules of reinforcement |
Q51951410 | Multiple-pair training enhances transposition in pigeons. |
Q56522052 | Music discriminations by carp (Cyprinus carpio) |
Q28596107 | Name that tune: Melodic recognition by songbirds |
Q51826699 | Narrowing down the conditions for extinction of Pavlovian feature-positive discriminations in humans. |
Q50760345 | Natural category discrimination in chimpanzees (Pan troglodytes) at three levels of abstraction. |
Q52098690 | Negative priming and occasion setting in an appetitive Pavlovian procedure. |
Q59702116 | Neophobia in wild and laboratory mice |
Q38638070 | New perspectives in gaze sensitivity research |
Q51950471 | No evidence for overshadowing or facilitation of spatial pattern learning by visual cues. |
Q92508588 | No evidence that footedness in pheasants influences cognitive performance in tasks assessing colour discrimination and spatial ability |
Q56002876 | Noise-induced changes in calls of the Japanese quail |
Q114023479 | Nonhuman primates learn adjacent dependencies but fail to learn nonadjacent dependencies in a statistical learning task with a salient cue |
Q36216574 | Nonnormative discounting: there is more to cue interaction effects than controlling for alternative causes |
Q43631572 | Nonreinforced flavor exposure attenuates the effects of conditioned taste aversion on both flavor consumption and cue palatability |
Q44523000 | Normalization between stimulus elements in a model of Pavlovian conditioning: showjumping on an elemental horse. |
Q57151825 | North American river otters (Lontra canadensis) discriminate between 2D objects varying in shape and color |
Q91501176 | Novel flexibility of social learning in dog puppies |
Q92289202 | Novel methodology to assess vocal learning in nature |
Q47220539 | Numbers and brains. |
Q114881973 | Numerical discrimination by rats using sequential auditory stimuli |
Q55919899 | Object permanence in cats and dogs |
Q123278573 | On a conjecture of Bush and Mosteller |
Q44320123 | On the determinants of induction in responding for sucrose when food pellet reinforcement is upcoming |
Q51860365 | On the hunt for the gene of perspective taking: pitfalls in methodology. |
Q35583207 | On the nature of CS and US representations in Pavlovian learning |
Q60054669 | One-trial associative memory: comparison of food-storing and nonstoring species of birds |
Q50942344 | Ontogenetic forgetting of stimulus attributes. |
Q52309419 | Ontogeny of persistence: immediate extinction effects in preweanling and weanling rats |
Q113202175 | Open field behavior of C57BL/6J mice as a function of age, experience, and prenatal maternal stress |
Q113202195 | Open field behavior of the Mongolian gerbil |
Q113202177 | Open-field activity and exploratory behavior |
Q113202180 | Open-field activity of retinal regenerate C3H mice: Further evidence of some visual capacities |
Q113202194 | Open-field behavior in mice: Analysis of maternal effects by means of ovarian transplantation |
Q113202193 | Open-field behavior in mice: Effect of test illumination |
Q113202178 | Open-field behavior in mice: Genetic analysis of repeated measures |
Q113202203 | Open-field behavior of C3H mice: Effect of early handling, field illumination, and age at testing |
Q113202184 | Open-field behavior of C3H mice: Effect of size and illumination of field |
Q113202185 | Open-field behavior of C57BL/6J mice: Effect of illumination, age, and number of test days |
Q50879813 | Open-field behavior of wild and domestic Norway rats |
Q122963379 | Open-field behavior of young chicks (Gallus gallus): Antipredatory responses, social reinstatement motivation, and gender effects |
Q35834241 | Operant avoidance learning in crayfish, Orconectes rusticus: Computational ethology and the development of an automated learning paradigm |
Q120714393 | Operant rate in the turtle as a function of temperature |
Q52008957 | Operant variability when reinforcement is delayed. |
Q37772367 | Opportunities and constraints when studying social learning: Developmental approaches and social factors |
Q41478355 | Optimisation of cognitive performance in rodent operant (touchscreen) testing: Evaluation and effects of reinforcer strength. |
Q89161725 | Orienting asymmetries and physiological reactivity in dogs' response to human emotional faces |
Q48229828 | Orthographic processing in animals: Implications for comparative psychologists |
Q93043747 | Outcome expectancy and suboptimal risky choice in nonhuman primates |
Q44734936 | Outcome-specific conditioned inhibition in Pavlovian backward conditioning |
Q37344411 | Overshadowing and CS duration: counteraction and a reexamination of the role of within-compound associations in cue competition. |
Q50786273 | Overshadowing and associability change: examining the contribution of differential stimulus exposure. |
Q51873333 | Overshadowing and blocking between landmark learning and shape learning: the importance of sex differences. |
Q52309413 | Overshadowing and stimulus intensity |
Q51958210 | Overshadowing as a function of trial number: dynamics of first- and second-order comparator effects. |
Q50774048 | Overshadowing of geometric cues by a beacon in a spatial navigation task. |
Q89172444 | Parallel overinterpretation of behavior of apes and corvids |
Q48143366 | Partial reinforcement and latent inhibition effects on stimulus-outcome associations in flavor preference conditioning |
Q114109615 | Partial reinforcement effects on acquisition and extinction of a conditioned taste aversion |
Q51947853 | Partial reinforcement effects on learning and extinction of place preferences in the water maze. |
Q39659126 | Pattern Cue and Visual Cue Competition in a Foraging Task by Rats |
Q93032865 | Perception and the metaphysics of information |
Q51936403 | Perceptions of perceptual learning. Editorial. |
Q30376284 | Perceptual learning and representational learning in humans and animals. |
Q51936400 | Perceptual learning in human and nonhuman animals: a search for common ground. |
Q50493925 | Perceptual learning transfer in an appetitive Pavlovian task. |
Q39255783 | Perceptual learning with tactile stimuli in rodents: Shaping the somatosensory system |
Q38038535 | Performance factors in associative learning: assessment of the sometimes competing retrieval model |
Q51887188 | Pigeon and human performance in a multi-armed bandit task in response to changes in variable interval schedules. |
Q50527971 | Pigeons exhibit higher accuracy for chosen memory tests than for forced memory tests in duration matching-to-sample. |
Q51898572 | Pigeons learn to answer the question "where did you just peck?" and can report peck location when unexpectedly asked. |
Q89643128 | Pigeons process actor-action configurations more readily than bystander-action configurations |
Q50753981 | Pigeons rank-order responses to temporally sequential stimuli. |
Q51972901 | Pigeons' memory for sequences of light flashes when gap duration is an unreliable discriminative cue. |
Q51943213 | Pigeons' memory for time: assessment of the role of subjective shortening in the duration-comparison procedure. |
Q97675209 | Pigeons' midsession reversal: Greater magnitude of reinforcement on the first half of the session leads to improved accuracy |
Q36785132 | Pigeons' use of cues in a repeated five-trial-sequence, single-reversal task |
Q114881977 | Pigeons’ memory for empty time intervals marked by visual or auditory stimuli |
Q114881983 | Pigeons’ memory for event duration: Differences between visual and auditory signals |
Q120714431 | Place and cue learning in turtles |
Q51970989 | Place versus response learning in rats. |
Q114914363 | Plasticity in the hippocampal formation of shorebirds during the wintering period: Stereological analysis of parvalbumin neurons in Actitis macularius |
Q112765494 | Poison avoidance and patch (location) selection in rats |
Q60723893 | Polymorphic response patterns under frequency-dependent selection |
Q113202186 | Postexposition administration of d-amphetamine impairs the habituation of rats to an open field |
Q52108978 | Postinjection suppression of drinking is modified by the presence of conditioned contextual cues: implications for both anticipatory and posttreatment nausea in humans. |
Q48107744 | Posttraining flavor exposure in hungry rats after simultaneous conditioning with a nutrient converts the CS into a conditioned inhibitor |
Q42036523 | Potentiation and overshadowing between landmarks and environmental geometric cues |
Q46719880 | Potentiation of taste and extract stimuli in conditioned flavor preference learning |
Q30477348 | Practice effects in the absolute judgment of frequency |
Q50643077 | Pre-exposure enhances recovery of conditioned responding after extinction. |
Q91838636 | Precrastination: The fierce urgency of now |
Q51523662 | Predicting shifts in generalization gradients with perceptrons. |
Q48634876 | Preference and resistance to change in concurrent variable-interval schedules |
Q51924832 | Preference for 50% reinforcement over 75% reinforcement by pigeons. |
Q48320123 | Preference for rewards that follow greater effort and greater delay |
Q56444189 | Preference reversal and delayed reinforcement |
Q46899146 | Preliminary evidence for color stimuli discrimination in the Asian small-clawed otter (Aonyx cinerea). |
Q51889792 | Preserved nodal number effects under equal reinforcement. |
Q113693477 | Prey selection in naive Elaphe obsoleta (Squamata: serpentes) — A reappraisal |
Q50442397 | Prior beliefs influence symmetrical or asymmetrical generalizations in human causal learning. |
Q47557860 | Proactive interference by cues presented without outcomes: Differences in context specificity of latent inhibition and conditioned inhibition. |
Q47838243 | Proactive interference of open field on consummatory successive negative contrast. |
Q50576704 | Procedure for preventing response strain on random interval schedules with a linear feedback loop. |
Q114881959 | Processing of complex auditory stimuli (tunes) by rats and monkeys (Cebus apella) |
Q50709020 | Processing of conflicting and redundant stimulus information by pigeons. |
Q48491946 | Processing of empty and filled time intervals in pigeons |
Q115484377 | Prolonged exposure to conspecific and predator odors reduces fear reactions to these odors during subsequent prod-shock tests |
Q51057798 | Prospective and retrospective timing by pigeons. |
Q33746300 | Protection from extinction provided by a conditioned inhibitor. |
Q52102438 | Protection from extinction. |
Q39519331 | Quantitative analysis of local-level resurgence |
Q91364315 | Questioning the developmental effects of group size on cognitive abilities |
Q104758597 | Rainbow trout discriminate 2-D photographs of conspecifics from distracting stimuli using an innovative operant conditioning device |
Q53511397 | Raising the bar on studying cultural evolution. |
Q91838632 | Rapid eye movement density during REM sleep in dogs (Canis familiaris) |
Q51983739 | Rats acquire a low-response-cost daily time-place task with differential amounts of food. |
Q90934033 | Rats can replay episodic memories of past odors |
Q50780918 | Rats exhibit asymmetrical retention functions for hedonic and nonhedonic samples in many-to-one symbolic delayed matching to sample. |
Q39121101 | Rats in a levered T-maze task show evidence of time-place discriminations in two different measures |
Q89224993 | Rats respond where it counts |
Q51962749 | Rats show preference for delayed rewards on the radial maze. |
Q36688842 | Rats' choices between one and two delayed reinforcers |
Q46696422 | Rats' midsession reversal performance: the nature of the response |
Q52002534 | Rats' performance on an interval time-place task: increasing sequence complexity. |
Q113202183 | Rats’ performance on repeated tests in the open field as a function of age |
Q56115976 | Rats’ responses to a moving object related to food or water: A behavior-systems analysis |
Q51998910 | Reaction time signatures of discriminative processes: differential effects of stimulus similarity and incentive. |
Q125124391 | Reaction to novelty as a behavioral assay of recognition memory in homing pigeons and Japanese quail |
Q44550793 | Reactions of selectively bred strains of rats to a cat. |
Q57451023 | Recall of three-item sequences by pigeons |
Q58839658 | Recency/primacy ratio: A short test of task orientation |
Q47369800 | Reciprocal altruism in rats: Why does it occur? |
Q91063333 | Reciprocity: Different behavioural strategies, cognitive mechanisms and psychological processes |
Q64387428 | Recoding as a function of chunking and meaningfulness |
Q52088397 | Recognition of static and dynamic images of depth-rotated human faces by pigeons. |
Q52098688 | Recovery effects after extinction in the Morris swimming pool navigation task |
Q50933667 | Recovery of conditioned fear by a single postextinction shock: effect of similarity of shock contexts and of time following extinction. |
Q48491958 | Recovery of the rabbit's conditioned nictitating membrane response without direct reinforcement after extinction |
Q91230565 | Red is the new orange: Nonlinguistic categorical color perception |
Q50651632 | Reducing the feature positive effect by alerting people to its existence. |
Q84834936 | Reevaluating canine perspective-taking behavior |
Q120714401 | Reflex “training” in frogs |
Q50582375 | Regularities in responding during performance of a complex choice task. |
Q54223306 | Reinforcement of schedule-induced drinking in rats by lick-contingent shortening of food delivery. |
Q64977996 | Relationship between behavioral measures of anxiety and latent inhibition in mature rats. |
Q50949356 | Relationship between cooperation in an iterated prisoner's dilemma game and the discounting of hypothetical outcomes. |
Q46390519 | Relationship between individual and group learning in a marine teleost: A case study with sea bass under self-feeding conditions |
Q48127126 | Relationship between the rewarding and aversive effects of morphine and amphetamine in individual subjects |
Q90220079 | Relative reinforcer rates determine pigeons' attention allocation when separately trained stimuli are presented together |
Q46392665 | Release from proactive interference in rat spatial working memory |
Q48380970 | Remembering as discrimination in delayed matching to sample: discriminability and bias |
Q50743617 | Remembering: the role of extraneous reinforcement. |
Q60512374 | Reminiscence in recognition memory for faces |
Q50155359 | Removing but not adding elements of a context affects generalization of instrumental responses |
Q51983746 | Renewal after overexpectation. |
Q34691360 | Renewal after the extinction of free operant behavior |
Q44020631 | Renewal of extinguished instrumental responses: independence from Pavlovian processes and dependence on outcome value |
Q92508595 | Reorientation by features and geometry: Effects of healthy and degenerative age-related cognitive decline |
Q52108975 | Representation of time in time-place learning. |
Q48273265 | Representations of single and compound stimuli in negative and positive patterning. |
Q51962745 | Required pecking and refraining from pecking alter judgments of time by pigeons. |
Q52113505 | Research productivity in animal learning from 1953 to 2000. |
Q52022043 | Resistance to interference in complex negative patterning. |
Q114576347 | Resistance to threat |
Q91054734 | Response and place learning in crayfish spatial behavior |
Q100472124 | Response of male and female domestic chicks to change in the number (quantity) of imprinting objects |
Q52029514 | Response rate is not an effective mediator of learned stimulus equivalence in pigeons. |
Q120714424 | Response rate of turtles to fixed ratio reinforcement |
Q48562968 | Response stability and variability induced in humans by different feedback contingencies |
Q60530192 | Response to stimulus relations by a dog (Canis lupus familiaris) |
Q46032032 | Response variability in pigeons in a Pavlovian task. |
Q61820868 | Response-contingent sensory change in a causally structured environment |
Q51962752 | Response-cost punishment with pigeons: further evidence of response suppression via token loss. |
Q45394464 | Response-food delay gradients for lever pressing and schedule-induced licking in rats |
Q50584976 | Response-independent outcomes impact response rates and judgments of control differentially depending on rate of response-dependent outcomes. |
Q80771093 | Resurgence of behavior during extinction depends on previous rate of response |
Q33650962 | Resurgence of instrumental behavior after an abstinence contingency |
Q49906735 | Retention period differentially attenuates win-shift/lose-stay relative to win-stay/lose-shift performance in the rat. |
Q126099411 | Rethinking syntax: A commentary on E. Kako’s “Elements of syntax in the systems of three language-trained animals” |
Q49873718 | Retrieval practice after multiple context changes, but not long retention intervals, reduces the impact of a final context change on instrumental behavior. |
Q50885457 | Retrograde amnesia for extinction: similarities with amnesia for original acquisition memories. |
Q37684633 | Retrospective revaluation of associative retroactive cue interference. |
Q50641516 | Revaluation of geometric cues reduces landmark discrimination via within-compound associations. |
Q62092018 | Reversal from blocking in humans as a result of posttraining extinction of the blocking stimulus |
Q92739806 | Reversal training facilitates acquisition of new learning in a Morris water maze |
Q89397308 | Revisiting the famous farm foxes: A psychological perspective |
Q50798208 | Revisiting the role of within-compound associations in cue-interaction phenomena. |
Q48273242 | Reward contrast in delay and probability discounting |
Q52682877 | Reward devaluation disrupts latent inhibition in fear conditioning. |
Q51293093 | Reward magnitude and shock variables (continuity and intensity) in shuttlebox-avoidance learning |
Q51912959 | Rhesus monkeys (Macaca mulatta) select Arabic numerals or visual quantities corresponding to a number of sequentially completed maze trials. |
Q56443090 | Role of physical attractiveness in impression formation |
Q36818552 | Role of the discriminative properties of the reinforcer in resurgence |
Q37452564 | Roles of attention in perceptual learning from perspectives of psychophysics and animal learning |
Q50465389 | Roles of context in acquisition of human instrumental learning: Implications for the understanding of the mechanisms underlying context-switch effects. |
Q50060571 | Rotational stress influences sensitized, but not habituated, exploratory behaviors in the woodlouse, Porcellio scaber |
Q50075543 | Running-based pica and taste avoidance in rats |
Q51970986 | Sample and comparison location as factors in matching acquisition, transfer, and acquired equivalence. |
Q51958213 | Savings in classical conditioning in the rabbit as a function of extended extinction. |
Q51934569 | Scalar effects in the visual discrimination of numerosity by pigeons. |
Q46773279 | Sea lions' (Zalophus californianus) use of human pointing gestures as referential cues |
Q91501172 | Searching images and the meaning of alarm calls |
Q50611477 | Second-order conditioning of LiCl-induced gaping with flavor and contextual cues. |
Q35053543 | Secondary extinction in Pavlovian fear conditioning |
Q115484376 | Selective habituation of defensive behavior: Evidence for predator-prey synchrony |
Q92894456 | Selective overimitation in dogs |
Q46200835 | Selective reinstatement of instrumental performance depends on the discriminative stimulus properties of the mediating outcome |
Q113202174 | Sensory regulation of open-field activity in mice: Visual stimulation and discontinuous development |
Q46043662 | Sensory-specific associations in flavor-preference reversal learning |
Q57804425 | Separate brain areas for processing human and dog faces as revealed by awake fMRI in dogs (Canis familiaris) |
Q114576341 | Sequential dependencies and children’s stimulus alternation |
Q50569725 | Serial discrimination reversal learning in pigeons as a function of intertrial interval and delay of reinforcement. |
Q50485479 | Serial discrimination reversal learning in pigeons as a function of signal properties during the delay of reinforcement. |
Q51826696 | Serial overshadowing of taste aversion learning by stimuli preceding the target taste. |
Q51977386 | Serial position effects in social transmission of food preference. |
Q51857821 | Serial position effects in social transmission of food preference: retention/demonstration intervals. |
Q50552451 | Sex differences after environmental enrichment and physical exercise in rats when solving a navigation task. |
Q113202197 | Sex differences in the activity wheel and open field as a function of fetal x-irradiation |
Q67388079 | Sexual excitation function of hamster vaginal scretion |
Q67388081 | Sexual excitation function of hamster vaginal secretion |
Q44915637 | Sexually dimorphic extinction of a conditioned taste aversion in rats |
Q29397978 | Shock to a conspecific as an aversive stimulus |
Q114881974 | Short-term memory for visual and auditory stimuli in pigeons |
Q60512378 | Short-term memory: Are item and position information stored independently? |
Q46434100 | Sign-tracking (autoshaping) in rats: a comparison of cocaine and food as unconditioned stimuli |
Q40450977 | Signaling a change in cue-outcome relations in human associative learning. |
Q47177989 | Simians in the Shape School: A comparative study of executive attention |
Q58853779 | Similarities between memory for visually perceived relations and comparative sentences |
Q90324942 | Similarity between an unfamiliar human and the owner affects dogs' preference for human partner when responding to an unsolvable problem |
Q40400386 | Simulations of a modified SOP model applied to retrospective revaluation of human causal learning |
Q50527975 | Simultaneous discrimination reversal learning in pigeons and humans: anticipatory and perseverative errors. |
Q52119791 | Simultaneous temporal and spatial processing. |
Q50532154 | Single-trial evaluative conditioning can be moderated by instructed forgetting. |
Q90396434 | Smarter through group living: A response to Smulders |
Q89543053 | Smarter through group living? |
Q52089379 | Social and asocial cues about new food: cue reliability influences intake in rats. |
Q46883425 | Social and nonsocial category discriminations in a chimpanzee (Pan troglodytes) and American black bears (Ursus americanus). |
Q48273254 | Social effects on spatial choice in the radial arm maze |
Q29030261 | Social encounters in two prosimian species: Galago crassicaudatus and Nycticebus coucang |
Q98611865 | Social factors in bird-song development: Learning to sing with friends and rivals |
Q89629923 | Social housing enhances acquisition of task set independently of environmental enrichment: A longitudinal study in the Barnes maze |
Q113202181 | Social isolation in young rats: Effects of cage size on open-field behavior |
Q35782736 | Social learning about predators: a review and prospectus |
Q51625812 | Social learning in New Caledonian crows. |
Q89689828 | Social learning in great white pelicans (Pelecanus onocrotalus): A preliminary study |
Q47375810 | Social learning research outside the laboratory: How and why? |
Q35782693 | Social learning strategies |
Q46325463 | Social play as joint action: A framework to study the evolution of shared intentionality as an interactional achievement |
Q47555007 | Social tolerance in not-so-social pumas |
Q35782730 | Social transmission of courtship behavior and mating preferences in brown-headed cowbirds, Molothrus ater |
Q51947850 | Social working memory: Memory for another rat's spatial choices can increase or decrease choice tendencies. |
Q35782705 | Socially biased learning in monkeys |
Q52006541 | Socially transmitted food preferences can be used to study long-term memory in rats. |
Q33354212 | Solving Pavlov's puzzle: attentional, associative, and flexible configural mechanisms in classical conditioning |
Q51890515 | Some determinants of second-order conditioning. |
Q110632213 | Some evidence supporting Nuttin’s explanation of spread of effect |
Q48512071 | Some observations and remembrances of Kenneth W. Spence |
Q52309416 | Some tests of the additivity (autoshaping) theory of behavioral contrast |
Q92836854 | Sometimes a stick might just be a stick |
Q37139637 | Spacing extinction trials alleviates renewal and spontaneous recovery |
Q52046459 | Spatial configuration and list learning of proximally cued arms by rats in the enclosed four-arm radial maze. |
Q54163098 | Spatial integration with rats. |
Q56032222 | Spatial pattern learning in the radial arm maze |
Q51931220 | Spatial patterns and memory for locations. |
Q43592305 | Special issue on computational models of classical conditioning guest editors' introduction |
Q88128593 | Specificity and flexibility of social influence on spatial choice |
Q114881946 | Spontaneous alternation and middle ear disease |
Q46602139 | Spontaneous alternation behavior in Paramecium |
Q51970994 | Spontaneous recovery after reversal and partial reinforcement. |
Q51855688 | Spontaneous recovery and ABC renewal from retroactive cue interference. |
Q48442875 | Spontaneous recovery from overexpectation |
Q48951965 | Spontaneous recovery varies inversely with the training-extinction interval |
Q38447388 | Stable individual differences on developmental tasks in young yellow-crowned parakeets, Cyanoramphus auriceps |
Q48137930 | Statistical learning of action: the role of conditional probability |
Q91597145 | Sticks and stones: Associative learning alone? |
Q38395191 | Still searching for the engram |
Q42217111 | Stimuli associated with the cancellation of food and its cues enhance eating but display negative incentive value |
Q48174122 | Stimuli that signal the absence of reinforcement are paid more attention than are irrelevant stimuli |
Q50301227 | Stimuli with identical contextual functions taught independently become functionally equivalent |
Q62092026 | Stimulus competition in the absence of compound conditioning |
Q81196035 | Stimulus control in fixed interfood intervals |
Q51799861 | Stimulus control in multiple temporal discriminations. |
Q114109621 | Stimulus control of prey attack in naive rat snakes: A species duplication |
Q114109618 | Stimulus control of the prey attack response in naive garter snakes |
Q114881945 | Stimulus factors in auditory identification learning |
Q50100192 | Stimulus preexposure speeds or slows subsequent acquisition of associative learning depending on learning test procedures and response measure |
Q51998906 | Stimulus salience and asymmetric forgetting in the pigeon. |
Q46881818 | Stimulus specificity of concurrent recovery in the rabbit nictitating membrane response |
Q113202200 | Strain differences in open-field behavior of the rat |
Q38369685 | Strategic interactions: Games of the Ju|'hoan |
Q60359290 | Strike-induced chemosensory searching in Old World vipers and New World pit vipers |
Q33349448 | Studying children's social learning experimentally "in the wild". |
Q51847223 | Suboptimal choice in nonhuman animals: rats commit the sunk cost error. |
Q120714404 | Subproblem analysis of discrimination shift learning in the turtle (Chrysemys picta picta) |
Q44320127 | Superlatent inhibition and spontaneous recovery: differential effects of pre- and postconditioning CS-alone presentations after long delays in different contexts |
Q51927376 | Surprise and change: variations in the strength of present and absent cues in causal learning. |
Q60147294 | Symmetrical and asymmetrical sources of variance in temporal generalization |
Q50780495 | Symmetrical generalization decrements: configural stimulus processing in human contingency learning. |
Q115028537 | Tactual discrimination of size and shape by a California sea lion (Zalophus californianus) |
Q50421756 | Taking an insect-inspired approach to bird navigation. |
Q92830199 | Taking pigeons to heart: Birds proficiently diagnose human cardiac disease |
Q125289968 | Taming the boojum: Being theoretical about peculiarities of learning |
Q125289976 | Taming the boojum: Being theoretical about peculiarities of learning |
Q41465629 | Target-absent controls in blocking experiments with rats |
Q52116780 | Target-defining features in a "people-present/people-absent" discrimination task by pigeons. |
Q47419810 | Task-specific modulation of adult humans' tool preferences: number of choices and size of the problem |
Q46434093 | Taste + odor interactions in compound aversion conditioning |
Q128490669 | Taste aversion learning during successive negative contrast |
Q34217248 | Taste avoidance and taste aversion: evidence for two different processes |
Q38712741 | Temporal discounting of aversive consequences in rats |
Q50143821 | Temporal discrimination of alternate days in rats |
Q52113513 | Temporal discrimination using different feature--target intervals in classical conditioning of the rabbit's nictitating membrane response. |
Q80771100 | Temporal generalization and peak shift in humans |
Q38618398 | Temporal integration and instrumental conditioned reinforcement. |
Q52098694 | Temporal integration and temporal backward associations in human and nonhuman subjects |
Q46101875 | Temporal integration in Pavlovian appetitive conditioning in rats |
Q50707319 | Test order effects in simultaneous protocols. |
Q52089380 | Testing social learning in a wild mountain parrot, the kea (Nestor notabilis). |
Q33357063 | Testing the limits of optimality: the effect of base rates in the Monty Hall dilemma |
Q113032629 | Testing the memory reconsolidation hypothesis in a fear extinction paradigm: The effects of ecological and arbitrary stimuli |
Q50484215 | Testing the scalar expectancy theory (SET) and the learning-to-time model (LeT) in a double bisection task. |
Q51887834 | Testing the translational-symmetry hypothesis of abstract-concept learning in pigeons. |
Q47731868 | The Monty Hall dilemma with pigeons: No, you choose for me. |
Q51993064 | The basic tastants in aversion conditioning: evidence for sensory preconditioning and not potentiation. |
Q64081858 | The bottlenosed dolphin’s (Tursiops truncatus) understanding of gestures as symbolic representations of its body parts |
Q45836722 | The criterion-calibration model of cue interaction in contingency judgments |
Q89147082 | The curiously long absence of cooking in evolutionary thought |
Q114576338 | The dependency of intermediate size problem responses upon sets in human Ss |
Q38374339 | The derived generalization of thought suppression |
Q114106027 | The determinants of random choice |
Q113693472 | The determination of trait redundancy in personality impression formation |
Q125287950 | The development of the concept of artistic style: A free classification study |
Q45324378 | The differential expression of male sexual behavior in the Lewis, Fischer and Sprague-Dawley rat strains |
Q45910669 | The dual role of the context in postpeak performance decrements resulting from extended training. |
Q61979701 | The effect of a pratfall on increasing interpersonal attractiveness |
Q50476258 | The effect of encoding conditions on learning in the prototype distortion task. |
Q50689066 | The effect of filled and empty intervals on clock and memory processes in pigeons. |
Q51827589 | The effect of mindfulness on extinction and behavioral resurgence. |
Q52098696 | The effect of rate of reinforcement and time in session on preference for variability |
Q114109626 | The effect of relative prey size on the ingestion behavior of rodent-eating snakes |
Q120714415 | The effect of schedules of reinforcement upon the response rates of turtles |
Q37139881 | The effect of subadditive pretraining on blocking: limits on generalization. |
Q51904263 | The effect of task structure on diffusion dynamics: Implications for diffusion curve and network-based analyses. |
Q114881982 | The effect of the controllability of auditory discriminative stimuli in the performance of go/no-go discriminations by pigeons |
Q40450986 | The effectiveness of inhibitors in human predictive judgments depends on the strength of the positive predictor. |
Q114914382 | The effects of an alien stimulus on reminiscence in pursuit rotor performance |
Q50753985 | The effects of differential outcomes and different types of consequential stimuli on 7-year-old children's discriminative learning and memory. |
Q114109624 | The effects of feeding experience on the response to prey-object extracts in rat snakes |
Q57913315 | The effects of isolation rearing on exploration in the rat |
Q113202199 | The effects of open-field size on activity in the Mongolian gerbil |
Q50531614 | The effects of pool shape manipulations on rat spatial memory acquired in the Morris water maze. |
Q48397049 | The effects of rapid eye movement sleep deprivation and recovery on spatial reference memory of young rats |
Q45087120 | The effects of response cost and species-typical behaviors on a daily time-place learning task |
Q114576337 | The effects of threat and attraction on interpersonal bargaining |
Q45063281 | The evolutionary significance of pretend play: Two-year-olds' interpretation of behavioral cues |
Q42734306 | The fate of redundant cues: Further analysis of the redundancy effect |
Q51991047 | The fine-grained spatial abilities of three seed-caching corvids. |
Q48501402 | The geometric module in the rat: independence of shape and feature learning in a food finding task |
Q39005999 | The goldfish conditioned withdrawal preparation: effects of some basic methodological variables |
Q120714411 | The immobility reaction in leopard frogs (Rana pipiens) as a function of noise-induced fear |
Q50655212 | The impact of context relevance during extinction learning. |
Q37772368 | The importance of history in definitions of culture: Implications from phylogenetic approaches to the study of social learning in chimpanzees |
Q48627228 | The influence of a distractor during compound preexposure on latent inhibition. |
Q46336734 | The influence of breed and environmental factors on social and solitary play in dogs (Canis lupus familiaris). |
Q52739499 | The influence of light deprivation on implantation in the rat. |
Q35554446 | The influence of multiple temporal memories in the peak-interval procedure |
Q38223733 | The influence of partner cues on the extinction of causal judgments in people |
Q52008952 | The influence of temporal spacing on time-place discrimination. |
Q46612166 | The influences of guiding cues on motor skill autonomy in rats |
Q50760079 | The informational value of contexts affects context-dependent learning. |
Q51871813 | The learning of basic-level categories by pigeons: the prototype effect, attention, and effects of categorization. |
Q93274809 | The midsession reversal task: A theoretical analysis |
Q129799067 | The mosaic structure of the mammalian cognitive map |
Q51951409 | The nature of discrimination learning in pigeons. |
Q51951407 | The nature of the response in Simon discriminations by pigeons. |
Q52659002 | The neuroscience of perceptual categorization in pigeons: A mechanistic hypothesis. |
Q35983972 | The oddity preference effect and the concept of difference in pigeons |
Q96688482 | The paradoxical performance by different species on the ephemeral reward task |
Q33262881 | The pattern of responding after extensive extinction |
Q114881993 | The perception of time relations in auditory tempo discrimination |
Q52108982 | The pigeon's discrimination of visual entropy: a logarithmic function. |
Q120714412 | The primacy effect of the first feeding experience in the snapping turtle |
Q113202211 | The principle of aggregation in psychobiological correlational research: An example from the open-field test |
Q46325458 | The processing of positional information in a two-item sequence limits the emergence of symmetry in baboons (Papio papio), but not in humans (Homo sapiens). |
Q50580782 | The promise of cyborg intelligence. |
Q49146286 | The propositional approach to associative learning as an alternative for association formation models |
Q46336161 | The psychological significance of play with imaginary companions in early childhood |
Q91431289 | The push and pull of dopamine in cue-reward learning |
Q48531685 | The relation of multiple-schedule behavioral contrast to deprivation, time in session, and within-session changes in responding |
Q43450564 | The relative effectiveness of an inanimate stimulus and a live surrogate during imprinting in Japanese quail, Coturnix coturnix japonica |
Q53481140 | The rewarding effects of number and surface area of food in rats. |
Q120714405 | The righting reflex in turtles: A description and comparison |
Q91785859 | The road ahead for sunk costs |
Q91344192 | The role of category density in pigeons' tracking of relevant information |
Q51955344 | The role of comparison in perceptual learning: effects of concurrent exposure to similar stimuli on the perceptual effectiveness of their unique features. |
Q92836846 | The role of context in animal memory |
Q51955338 | The role of extramaze cues in spontaneous alternation in a plus-maze. |
Q52029500 | The role of habituation of the response to LiCl in the US-preexposure effect. |
Q43094825 | The role of injection cues in the production of the morphine preexposure effect in taste aversion learning |
Q51918239 | The role of keypecking during filled intervals on the judgment of time for empty and filled intervals by pigeons. |
Q51947593 | The role of sensory preconditioning in memory retrieval by preverbal infants. |
Q81196039 | The role of temporal variables in inhibition produced through extinction |
Q35889980 | The role of test context in latent inhibition of conditioned inhibition: Part of a search for general principles of associative interference |
Q42722873 | The role of within-compound associations in learning about absent cues |
Q48054697 | The roles of the anterior cingulate cortex and its dopamine receptors in self-paced cost-benefit decision making in rats. |
Q37452571 | The search for symmetry: 25 years in review |
Q47859337 | The transfer of social exclusion and inclusion functions through derived stimulus relations. |
Q48634886 | The value hypothesis and acquisition of preference in concurrent chains |
Q93020275 | The whole is equal to the sum of its parts: Pigeons (Columba livia) and crows (Corvus macrorhynchos) do not perceive emergent configurations |
Q51858513 | Theory of mind in dogs: is the perspective-taking task a good test? |
Q34203500 | Theory of mind in dogs?: examining method and concept. |
Q58599489 | Thought control with the dopamine transient |
Q113202204 | Time of day effects on learning and open field activity |
Q52088396 | Time-course of control by specific stimulus features and relational cues during same-different discrimination training. |
Q97532853 | Time-of-day affects the amount rats run during daily sessions in activity wheels |
Q56701039 | Time-of-day discrimination by pigeons,Columba livia |
Q52088391 | Time-place learning in the eight-arm radial maze. |
Q52098693 | Timing in retroactive interference |
Q50491401 | Timing of interfering events in one-trial serial overshadowing of a taste aversion. |
Q38618410 | Timing with opportunity cost: concurrent schedules of reinforcement improve peak timing. |
Q90434086 | Timmy's in the well: Empathy and prosocial helping in dogs |
Q93021298 | To peck or not peck: Which do pigeons prefer? |
Q115484370 | Tonic immobility as a reaction to predation: Artificial eyes as a fear stimulus for chickens |
Q49947905 | Tool use in Goffin's cockatoos: Shape/frame matching |
Q90970776 | Tools of engagement: Information seeking in chimpanzees |
Q98396297 | Towards a resolution of some outstanding issues in transitive research: An empirical test on middle childhood |
Q99618196 | Towards describing scenes by animals: Pigeons' ordinal discrimination of objects varying in depth |
Q44918577 | Trace and long-delay fear conditioning in the developing rat. |
Q48882394 | Tracking of the expected time to reinforcement in temporal conditioning procedures. |
Q89523634 | Tracking of unpredictable moving stimuli by pigeons |
Q50582372 | Training order and structural location of meaningful stimuli: effects on equivalence class formation. |
Q50309960 | Training reinforcement rates, resistance to extinction, and the role of context in reinstatement. |
Q113693471 | Trait similarity and trait evaluation as correlates of attraction |
Q50541270 | Transcription inhibitors prevent amnesia induced by NMDA antagonist-mediated impairment of memory reconsolidation. |
Q50621849 | Transfer of absolute and relative predictiveness in human contingency learning. |
Q40626127 | Transfer of control between causal predictive judgments and instrumental responding. |
Q50195065 | Transfer of discriminative control during stimulus fading conducted without reinforcement |
Q51812943 | Transfer of judgments of control to a target stimulus and to novel stimuli through derived relations. |
Q115028524 | Transfer of visual identity matching-to-sample in two california sea lions (zalophus californianus) |
Q52242475 | Transient variations in responding to Pavlovian conditioned stimuli have implications for the mechanisms of "priming" |
Q52046467 | Transposition in pigeons: reassessing Spence (1937) with multiple discrimination training. |
Q52088392 | Trial number and compound stimuli temporal relationship as joint determinants of second-order conditioning and conditioned inhibition. |
Q64883033 | Truth is in the eye of the beholder: Perception of the Müller-Lyer illusion in dogs. |
Q59699686 | Twenty-four hour retention by neonates of an habituated heart rate response |
Q114881944 | Two choice discrimination learning as a function of stimulus similarity along an auditory intensity dimension |
Q51890508 | Two components of responding in Pavlovian lick suppression. |
Q52309420 | Two-choice conditional discrimination performance of pigeons as a function of reward expectancy, prechoice delay, and domesticity |
Q48235644 | Two-factor theory, the actor-critic model, and conditioned avoidance |
Q46042590 | Two-item same-different concept learning in pigeons |
Q50186210 | Ultimate and proximate mechanisms of reciprocal altruism in rats |
Q41765247 | Understanding dog cognition by functional magnetic resonance imaging |
Q114914357 | Understanding hippocampal neural plasticity in captivity: Unique contributions of spatial specialists |
Q46269049 | Understanding social decision-making from another species' perspective |
Q87161655 | Underwater observations of dolphin reactions to a distressed conspecific |
Q48183412 | Unraveling sources of stimulus control in a temporal discrimination task |
Q51993066 | Use of a single-code/default strategy by pigeons to acquire duration sample discriminations. |
Q44642440 | Using action dynamics to assess competing stimulus control during stimulus equivalence testing. |
Q46062929 | Using the reassignment procedure to test object representation in pigeons and people |
Q51829457 | Variations on variability: effects of display composition on same-different discrimination in pigeons. |
Q51829169 | Varied but not necessarily random: human performance under variability contingencies is affected by instructions. |
Q51936402 | Varieties of perceptual learning. |
Q67367400 | Visual cliff performance in 10 species of muroid rodents |
Q114576351 | Visual discrimination learning and memory in nocturnal prosimians |
Q47798107 | Visual discrimination learning in the fire-bellied toad Bombina orientalis |
Q114881951 | Visual discrimination learning: Interactions of auditory input pattern, articulation, and instructions |
Q43575266 | Visual observing by rhesus monkeys: some relationships with social dominance rank |
Q60205119 | Vocal displays under water by the gray seal, the harbor seal,. and the stellar sea lion |
Q113250634 | Vocal flexibility in a eusocial rodent |
Q114881956 | Vocalization correlated with self-induced changes in visual-auditory contact between mated Japanese quail |
Q51890511 | Waiting to decide helps in the face of probabilistic uncertainty but not delay uncertainty. |
Q51943218 | What are association formation models? |
Q91606002 | What influences a pet dog's first impression of a stranger? |
Q38857021 | What is play fighting and what is it good for? |
Q50516784 | What is timed in a fixed-interval temporal bisection procedure? |
Q57804429 | What makes a landmark effective in adolescent and adult rats? Sex and age differences in a navigation task |
Q48577355 | What makes a landmark effective? Sex differences in a navigation task |
Q48161159 | When it looks and walks like an ant. |
Q35661593 | When more is less: extending training of the blocking association following compound training attenuates the blocking effect |
Q109039236 | Who is crying wolf? Seasonal effect on antipredator response to age-specific alarm calls in common ravens, Corvus corax |
Q50734478 | Why don't guiding cues always guide in behavior chains? |
Q41969356 | Win-stay and win-shift lever-press strategies in an appetitively reinforced task for rats. |
Q98207205 | With a little help from my (Psittacidae) friends |
Q30839912 | Within-group relationships and lack of social enhancement during object manipulation in captive Goffin's cockatoos (Cacatua goffiniana) |
Q47708143 | Within-subjects assessment of the within-compound associations resulting from intermixed and blocked preexposure schedules. |
Q53155768 | Within-trial contrast: when you see it and when you don't. |
Q89450930 | Would dogs copy irrelevant actions from their human caregiver? |
Q57987740 | “P-R” differences in intact cockroaches as a function of testing interval |
Q56446338 | “Primary memory”: The effects of redundancy upon digit repetition |
Learning & Behavior | wikipedia |
Search more.