Academic literature on the topic 'Pigeons – Behavior'

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Journal articles on the topic "Pigeons – Behavior"

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Sakuma, Takashi, and Tetsumi Moriyama. "THE INTERRELATION BETWEEN PIGEONS’ SCHEDULE-INDUCED AGGRESSIVE BEHAVIOR AND THE RECIPIENTS’ COUNTER-BEHAVIOR." Revista Mexicana de Análisis de la Conducta 45, no. 2 (2019): 483–99. http://dx.doi.org/10.5514/rmac.v45.i2.75579.

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The present experiment was conducted to investigate whether an experimental pigeon's shield-peck responses toward a target pigeon could be induced by a food reinforcement schedule consisting of continuous reinforcement (CRF) and extinction. Further, the interaction between experimental and target pigeons’ shield-peck responses was investigated. The experiment was an ABAB design consisting of alternating phases of nonreinforcement (A) and CRF-extinction (B) of the experimental pigeons' key-peck responses unrelated to their shield-peck responses. The experimental pigeons' shield-peck responses were induced by the CRF-extinction schedule. Further, there were positive correlations between the experimental and the target pigeons' shield-peck responses revealing a similar trend in both their response rates. Thus, the experimental pigeons’ shield-peck responses were controlled by variables including the reinforcement schedule and social stimuli including ontogenic and phylogenic variables derived from their target pigeons. Moreover, the pigeons' responses could be classified as an aggressive behavior derived from the interlocking contingencies of the responses of the pigeons of the dyads.
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Ackerman, Amanda L., and Kennon A. Lattal. "SHAPING COOPERATIVE RESPONDING: A SYSTEMATIC REPLICATION OF DANIEL (1942)." Revista Mexicana de Análisis de la Conducta 45, no. 2 (2019): 417–33. http://dx.doi.org/10.5514/rmac.v45.i2.75575.

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Cooperation between two pigeons was trained in a systematic replication of an earlier study by Daniel (1942) using rats and electric shock avoidance. After both pigeons were trained separately to eat from a food magazine and to stand on a platform located 45 cm from the food magazine, two stimulus lights were added. Different responses of each pigeon were brought under the stimulus control of the lights. In the presence of one light, magazine approach by one of the pigeons was reinforced and in the presence of the other, standing on the platform was reinforced. These functions were reversed for the other pigeon, that is, the light that was the SD for magazine approach for Pigeon A was the SD for the platform response for Pigeon B. When behavior was under stimulus control, the pigeons were placed together in the study space. Across sessions, the lights were removed gradually, transferring stimulus control to the co-actor’s behavior. Thus, the terminal performance was two interlocking response chains: as one pigeon approached the magazine, the other approached the platform, standing on which operated the feeder for up to 7 s. After one pigeon ate for a duration dependent upon the co-actor’s platform standing, the two switched positions. The results are discussed in relation to the definition of social behavior and the role of basic learning principles in social behavior.
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Walcott, C. "Pigeon homing: observations, experiments and confusions." Journal of Experimental Biology 199, no. 1 (1996): 21–27. http://dx.doi.org/10.1242/jeb.199.1.21.

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Homing pigeons can return from distant, unfamiliar release points. Experienced pigeons can do so even if they are transported anesthetized and deprived of outward journey information. Airplane tracking has shown that they make relatively straight tracks on their homeward journey; therefore, pigeons must have some way of determining the home direction at the release site. Manipulating the pigeon's internal clock causes predictable deviations in their flight direction relative to home. When the sun is not visible, such clock shifts have no effect. This result implies a two-step system: the determination of the home direction and the use of a sun compass to fly in that direction. When pigeons cannot see the sun they use a magnetic compass. The use of compass cues to select and maintain a direction of flight is well understood compared with the uncertainty surrounding the nature of the cues used to determine the home direction when pigeons are released at an unfamiliar site. Because they generally home successfully from any direction and distance from the loft, without requiring information gathered on the outward journey, it seems likely that they use some form of coordinate system. Presumably, a displaced pigeon compares the values of some factor at the release site with its remembered value at the home loft. This factor might be olfactory, it might be some feature of the earth's magnetic field or it might be something else. There is some evidence that pigeons may use several cues and that pigeons raised in different lofts under different environmental conditions may prefer to use one cue over another. I believe that it is this flexible use of multiple cues that has led to so much confusion in experiments on pigeon homing.
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Møller, Henrik Devitt, Jazmín Ramos-Madrigal, Iñigo Prada-Luengo, M. Thomas P. Gilbert, and Birgitte Regenberg. "Near-Random Distribution of Chromosome-Derived Circular DNA in the Condensed Genome of Pigeons and the Larger, More Repeat-Rich Human Genome." Genome Biology and Evolution 12, no. 2 (2019): 3762–77. http://dx.doi.org/10.1093/gbe/evz281.

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Abstract Extrachromosomal circular DNA (eccDNA) elements of chromosomal origin are known to be common in a number of eukaryotic species. However, it remains to be addressed whether genomic features such as genome size, the load of repetitive elements within a genome, and/or animal physiology affect the number of eccDNAs. Here, we investigate the distribution and numbers of eccDNAs in a condensed and less repeat-rich genome compared with the human genome, using Columba livia domestica (domestic rock pigeon) as a model organism. By sequencing eccDNA in blood and breast muscle from three pigeon breeds at various ages and with different flight behavior, we characterize 30,000 unique eccDNAs. We identify genomic regions that are likely hotspots for DNA circularization in breast muscle, including genes involved in muscle development. We find that although eccDNA counts do not correlate with the biological age in pigeons, the number of unique eccDNAs in a nonflying breed (king pigeons) is significantly higher (9-fold) than homing pigeons. Furthermore, a comparison between eccDNA from skeletal muscle in pigeons and humans reveals ∼9-10 times more unique eccDNAs per human nucleus. The fraction of eccDNA sequences, derived from repetitive elements, exist in proportions to genome content, that is, human 72.4% (expected 52.5%) and pigeon 8.7% (expected 5.5%). Overall, our results support that eccDNAs are common in pigeons, that the amount of unique eccDNA types per nucleus can differ between species as well as subspecies, and suggest that eccDNAs from repeats are found in proportions relative to the content of repetitive elements in a genome.
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Bancroft, G. Thomas, Reed Bowman, and Richard J. Sawicki. "Rainfall, Fruiting Phenology, and the Nesting Season of White-Crowned Pigeons in the Upper Florida Keys." Auk 117, no. 2 (2000): 416–26. http://dx.doi.org/10.1093/auk/117.2.416.

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AbstractWhite-crowned Pigeons (Columba leucocephala) varied their timing of breeding and nesting intensity in response to variation in production of the four most important fruit species in their breeding-season diet in the upper Florida Keys. From 1988 through 1990, we monitored fruit production year-round in five habitats in which pigeons foraged and monitored all pigeon nests along two transects on Middle Butternut Key. Annually, pigeon breeding was positively correlated with summer rains and with the peak in overall fruit production. However, within the breeding season, only the availability of Metopium toxiferum was positively correlated with rainfall and the number of new clutches initiated. Both the timing and magnitude of breeding varied annually. In 1988, when Metopium was more available, more pigeons nested, the nesting season started earlier and lasted longer, and a large peak in nesting occurred when Metopium fruit ripened. During 1989 and 1990, when the relative availability of Metopium was lower, fewer pigeons nested, the nesting season was shorter, and the seasonal peak in nesting associated with Metopium fruit was reduced or absent. Nesting patterns did not appear to vary with changes in the relative availability of other fruits. White-crowned Pigeons appear to prefer Metopium fruits to other species. Because pigeons do not supplement nestling diets with arthropods, but augment their diets with protein-rich crop milk, they may depend on lipid-rich fruits such as Metopium to provide the energy for breeding and crop-milk production. Metopium fruit production may be influenced by rainfall and climatic conditions, both of which may vary spatially within the range of White-crowned Pigeons in Florida. Evidence that pigeons shift foraging sites when Metopium availability varies emphasizes the need to preserve large tracts of seasonal deciduous forest in the Keys and to protect Metopium trees in suburban areas where they are removed because they cause contact dermatitis in humans.
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Bogach, M., A. Paliy, P. Liulin, et al. "Parasites of domestic and wild pigeons in the south of Ukraine." Biosystems Diversity 29, no. 2 (2021): 135–39. http://dx.doi.org/10.15421/012118.

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Pigeons are closely related to human life and are both a source of food and object for hobbies and sports. Parasitic diseases of birds are the main reason for their growth retardation, reduced productivity and viability. The article presents the results of studying the prevalence of trichomonosis, cestodes and nematodes among the population of wild and domestic pigeons in the south of Ukraine. According to the results of the conducted researches it is established that in the south of Ukraine endoparasitoses of domestic and wild pigeons are quite widespread, and all species of this bird are carriers of Trichomonas gallinae. At the same time, the highest rate of Trichomonas infection was recorded in Columba palambus and C. livia domestica, and the overall infestation of males is higher by 4.4% compared to females. It was determined that domestic pigeons C. livia domestica were infested with trichomonosis (27.5%) and nematodes (Ascaridia columbae, 57.1%), C. palambus – trichomonosis (32.1%) and cestodes (Raillietina spp., 82.4%), Streptopelia turtur – cestodes (Raillietina spp., 12.5%) and S. decaocto – cestodes (Raillietina spp., 71.4%) and nematodes (Heterakis gallinarum, A. columbae – 33.3% and 44.4% respectively). The overall rate of infestation of pigeons with cestodes was 28.4% and the incidence in males was higher by 3.9% compared to females. It was found that the most common species among pigeon cestodes is Raillietina spp. In addition, 22.9% of pigeons are carriers of nematodes (H. gallinarum, A. columbae and Capillaria spp.). Continuous monitoring of pigeon parasites is necessary because they, in most cases, come into contact with other species of poultry and are a source of general invasion. In terms of further research, it would be promising to study the prevalence of helminthic infestation among wild migratory birds.
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IOALE', PAOLO, and DANTE GUIDARINI. "Methods for Producing Disturbances in Pigeon Homing Behaviour by Oscillating Magnetic Fields." Journal of Experimental Biology 116, no. 1 (1985): 109–20. http://dx.doi.org/10.1242/jeb.116.1.109.

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Experiments were performed with homing pigeons treated before release with oscillating magnetic fields produced by small Helmholtz coils placed around the neck and on the head of the pigeon or by larger Helmholtz coils surrounding the cage of the birds. In both types of treatment, which both used a single frequency of about 0.14 Hz, the pigeons' initial orientation was strongly affected when the oscillation of the artificial magnetic field was square-shaped, whereas a triangular or sine-shaped variation had no effect.
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Escobar-Flores, Jonathan G., Mariana Delgado-Férnandez, and Oscar Delgado-González. "First record of Band-tailed Pigeon, Patagioenas fasciata (Columbiformes: Columbidae) in the Sonoran Desert of Baja California." Check List 12, no. 3 (2016): 1880. http://dx.doi.org/10.15560/12.3.1880.

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We report the presence of the Band-tailed Pigeon, which was not previously recorded in the Sonoran Desert in Baja California. The site was 140 km south of the nearest forest. The presence of the pigeon further documents the propensity of Band-tailed Pigeons to wander widely.
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Jacquin, Lisa, Bernard Cazelles, Anne-Caroline Prévot-Julliard, Gérard Leboucher, and Julien Gasparini. "Reproduction management affects breeding ecology and reproduction costs in feral urban Pigeons (Columba livia)." Canadian Journal of Zoology 88, no. 8 (2010): 781–87. http://dx.doi.org/10.1139/z10-044.

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Reproduction management of natural popsulations can have long-term consequences that have to be examined to avoid unwanted side effects. Management policies of urban Pigeons ( Columba livia Gmelin, 1789) include the set up of public Pigeon houses that aim at limiting hatching rate by egg removal. However, long-term consequences of this management method on the ecology of this species are still unknown. In this study we examined how egg removal affected egg-laying cycles of Pigeons by using a powerful method of time-series analysis, the wavelet method. We compared egg-laying cycles in Pigeon houses exposed to different management treatments and found that egg-laying cycles were shorter (4 weeks) in Pigeon houses with egg removal compared with control Pigeon houses without egg removal (11 weeks), suggesting that Pigeons respond to egg-removal pressure by multiplying reproduction attempts. Furthermore, we found that egg quality, an important index of female condition, was negatively affected by egg removal. This result suggests that the observed increase of egg production can lead to an increase of reproductive physiological costs and to a decrease of female condition. This study raises issues about potential consequences of such a management procedure on parasite resistance and health status of urban bird populations.
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Neuringer, Allen. "Choosing to Vary and Repeat." Psychological Science 3, no. 4 (1992): 246–51. http://dx.doi.org/10.1111/j.1467-9280.1992.tb00037.x.

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Can animals choose to vary their behaviors or to repeat them, depending on the rewards they earn for behaving variably versus repetitively? To answer this question, pigeons were rewarded for four-response sequences made to left (L) and right (R) disks. A “varied” sequence differed from each of the previous three sequences, and a “repeated” sequence was the same as some one of the previous three. For example, if a pigeon had generated sequences LLLL. LLLR, and LLRR in that order, then an RRRR sequence in the next trial was defined as a variation, whereas LLLL was a repetition. Two experiments showed that frequencies of varied and repeated sequences depended on the frequencies with which they were reinforced, with a “matching” relationship accounting for the results. It was concluded that pigeons' choices to vary or repeat parallel their choices between simpler response alternatives, a result consistent with the hypothesis that behavioral variability is influenced by its consequences. This finding may help to explain the “voluntary” or “free” nature of operant behavior.
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Dissertations / Theses on the topic "Pigeons – Behavior"

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Sturz, Bradley R. Katz Jeffrey S. "Geometric rule learning by pigeons." Auburn, Ala., 2007. http://repo.lib.auburn.edu/2006%20Fall/Dissertations/STURZ_BRADLEY_52.pdf.

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Lieving, Lori M. "Effects of intertrial interval and d-amphetamine on temporally organized behavior of pigeons." Morgantown, W. Va. : [West Virginia University Libraries], 2002. http://etd.wvu.edu/templates/showETD.cfm?recnum=2418.

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Thesis (M.A.)--West Virginia University, 2002.<br>Title from document title page. Document formatted into pages; contains vii, 54 p. : ill. Includes abstract. Includes bibliographical references (p. 51-54).
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Patton, Tadd B. "Altered features of female pigeons (Columba livia) elicit preference behavior in male pigeons." [Tampa, Fla] : University of South Florida, 2006. http://purl.fcla.edu/usf/dc/et/SFE0001656.

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Cole, Heather J. "Sibling alliances in juvenile feral pigeons." Thesis, McGill University, 1996. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=23878.

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This thesis examines whether juvenile feral pigeons, Columba livia, form sibling alliances when competing for access to a defensible food source. When tested as a flock at a non-depletable column feeder, with room for either one or two birds to feed, siblings associated with each other more often than expected by chance. Frequency of aggression between siblings at these feeders tended to be lower than expected on the basis of their association. Removal experiments showed that sibling presence had a positive effect on relative feeding success at the single column feeder: a juvenile who lost to another juvenile on a one-to-one basis tended, in the presence of its sibling, to lose less badly to, or even beat, that same juvenile. In contrast, presence of the winner's sibling tended not to affect the relative feeding success of competitors. These results support the hypothesis that pigeon siblings form aggressive alliances when competing for food that is defensible.
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Hernandez, Michelle Katz Jeffrey S. "Factors in two-dimensional maze navigation by pigeons." Auburn, Ala, 2008. http://repo.lib.auburn.edu/EtdRoot/2008/SPRING/Psychology/Dissertation/Hernandez_Michelle_24.pdf.

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Elcoro, Mirari. "Delayed disruption of temporally controlled behavior." Morgantown, W. Va. : [West Virginia University Libraries], 2008. https://eidr.wvu.edu/etd/documentdata.eTD?documentid=5793.

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Thesis (Ph. D.)--West Virginia University, 2008.<br>Title from document title page. Document formatted into pages; contains vi, 80 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 73-80).
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Aló, Raquel Moreira. "Effects of alternative-food sources on operant behavior." Morgantown, W. Va. : [West Virginia University Libraries], 2008. https://eidr.wvu.edu/etd/documentdata.eTD?documentid=5810.

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Thesis (Ph. D.)--West Virginia University, 2008.<br>Title from document title page. Document formatted into pages; contains viii, 68 p. : ill. Includes abstract. Includes bibliographical references (p. 66-68).
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Willson, Robert James. "Evidence that pigeons are not lost in space : pigeons perform well at long retention intervals on a modified delayed matching of key location task." Thesis, University of British Columbia, 1988. http://hdl.handle.net/2429/28310.

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The present series of experiments examined pigeons' spatial working memory using two variants of the delayed matching of key location paradigm (Wilkie & Summer, 1982). Exposure to the sample location was extended to 15 min and pecks to this stimulus (S+) produced grain on a variable interval 30-s schedule (the 1 Cue group). For some subjects (the 2 Cues group) both the positive and negative (S-) stimuli were presented during the sample period. In a subsequent test phase subjects were exposed to both the S+ and S- for 1 min. If the subject made more responses to the S+ an additional 15 min of access to the S+ occurred, with grain available on the previous schedule. If more responses were made to the S- the trial terminated and the subject was immediately removed from the apparatus. In the first experiment all subjects performed well with retention intervals of up to 30 s, a level of performance better than previously demonstrated in the delayed matching of key location (Wilkie & Summers, 1982). However, subjects' performance was disrupted when they were removed from the apparatus during the retention interval. Subjects in the 1 Cue group were more severely disrupted than the subjects in the 2 Cues group. Performance improved dramatically when these subjects were subsequently trained and tested on the 2 cues condition. Experiment 2 examined the differences between the 1 cue and 2 cues tasks further. All subjects were run for 30 trials on each task and removed from the apparatus during the retention interval. Performance on the 2 cues task was significantly higher for all subjects. When subjects were switched to the 1 cue task, performance immediately dropped and remained at a low level for all blocks tested. The observed differences probably reflect the operation of transfer appropriate processing (cf. Morris, Bransford, & Franks, 1977), given the similarity between training and testing on the 2 cues task. Experiment 3 used the 2 cues task to examine the performance of pigeons when retention intervals longer than 30 s were imposed between training and testing. The retention interval was incremented in the following stages: 5 min, 15 min, 30 min, 1 hr, 2 hr, 4 hr, 8 hr, 12 hr and 24 hr. Subjects were run until their performance fell below a criterion (70% accuracy or better for a block of 10 trials). When a subject failed to attain criterion within 3 blocks, no further data were collected from that subject. Subjects' upper retention limit varied somewhat, ranging from a minimum of 30 min to a maximum of 24 hr, but the performance of most subjects began to deteriorate at about 4 hr, a level considerably above the upper limit previously demonstrated in other paradigms (30 min-Spetch & Honig, 1988). Experiment 4 was a systematic replication of Experiment 3, using a mixed, rather than an incremental, schedule of retention intervals. Performance was not quite as good. For most subjects performance began to deteriorate at about 2 hr, somewhat sooner than in Experiment 3, but nevertheless higher than the level of performance seen in other paradigms. The results of the present experiments are interpreted in terms of the ecological validity of the procedures employed. The implications of the present studies for the study of "adaptive specializations in cognition" (Sherry, 1984; Sherry & Schacter, 1987), are also discussed, as are the implications for the distinction between reference and working memory.<br>Arts, Faculty of<br>Psychology, Department of<br>Graduate
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Smith, Aaron P. "The Balloon Analogue Risk Task and Behavioral Correlates in Pigeons." UKnowledge, 2015. http://uknowledge.uky.edu/psychology_etds/81.

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Individuals experience risk ubiquitously, but measuring risk taking is difficult. The balloon analogue risk task (BART) was developed in order to assess risk taking through having subjects press a key that accrues reward but also risk losing all reward with each press. In humans, greater responding in this task is associated with other maladaptive risk taking behaviors. The present research modeled this relationship in pigeons due to their previously shown propensity towards risk taking behavior. Experiment 1 used an unsignaled balloon task in which losing could only occur after 5 pecks. Results showed below optimal performance with greater pecks associated with faster acquisition of risk taking in the suboptimal choice task and evidence of modulation by delay discounting measures. Experiment 2 signaled the number of pecks with colors and tested multiple hoppers as a reinforcement modality to increase performance. Results showed only signaling the number of pecks improved performance and was related to performance in the high risk BART task. Both the low and high risk variants were associated with slower suboptimal choice acquisition and again had evidence of modulation by delay discounting measures. Potential shared underlying mechanisms are discussed.
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Johnson, Robert N. "Attention Factors in Temopral Distortion: The Effects of Food Availability on Responses within the Interval Bisection Task." DigitalCommons@USU, 2013. https://digitalcommons.usu.edu/etd/1722.

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There are differences within the timing literature regarding the effects of distracter stimulus presentation within timing tasks. Whereas some researchers have found underestimation (changes in the degree of temporal stimulus control), others have found generalized disruption of timing responses. The purpose of this thesis was to determine the importance of food availability on responses within a time estimation task, using pigeons as subjects. Specifically, it was hypothesized that presenting food access following timing responses after a distracter task would produce underestimation of the target interval, relative to control conditions. Using a 2-parameter function fit to "proportion long" data from the interval bisection task, data revealed a generalized disruption effect of the distracter on timing behavior. Further analysis revealed that presentation of the food following timing responses after the distracter task reduced stimulus control within the timing task, revealing underestimation of the target interval. These findings suggest that the causes of the differences within the timing literature may be based upon differences in procedure.
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Books on the topic "Pigeons – Behavior"

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Vriends, Matthew M. Pigeons: Everything about purchase, care, management, diet, diseases, and behavior of pigeons : with a special chapter, Understanding pigeons. Barron's, 1988.

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Schall, Ulrich. Sensory control of pecking in the pigeon (Columba Livia). Centaurus-Verlagsgesellschaft, 1989.

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Sterner, R. T., and R. D. Thompson. Behavioral-physiological effects of red phosphorus smoke inhalation on two wildlife species: Final report (project summary). U.S. Dept. of Agriculture, Animal and Plant Health Inspection Service, Science and Technology, Denver Wildlife Research Center, 1990.

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Leonard, Jerome Patrick. Nesting and foraging ecology of band-tailed pigeons in western Oregon. 1998.

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Pitts, Raymond C. Effects of amount of food reinforcement on fixed-interval-induced attack in pigeons. 1989.

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Jackson, Kevin D. Token reinforcement, choice, and self-control in pigeons. 1993.

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Nagelhout, Ryan. How Pigeons and Other Animals Sense Magnetic Fields. Powerkids Pr, 2015.

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Hughes, Christine E. Cocaine and food deprivation: Effects on food-reinforced fixed-ratio performance in pigeons. 1991.

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Husak, Douglas. Courses of Conduct. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190683450.003.0009.

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This chapter begins with an argument nearly everyone will reject as unsound. The chapter rejects it too. What is far less obvious, however, is exactly what is wrong with the argument. Despite skeptical challenges from both sides, the chapter tentatively concludes that the best solution to this problem consists in construing some instances of behavior as a course of conduct rather than as a discrete set of acts and omissions. When behavior consists in a course of conduct, it is a complex that consists in both acts and omissions. Attempts to pigeon-hole such behavior as either an act or an omission without regard to the complex in which both play a part are bound to produce philosophical distortion and normative confusion.
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Book chapters on the topic "Pigeons – Behavior"

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Longán, Aida, and Jonathan Buriticá. "Insight in Pigeons." In Encyclopedia of Animal Cognition and Behavior. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-47829-6_2063-1.

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Lamy, Jean-Baptiste. "Artificial Feeding Birds (AFB): A New Metaheuristic Inspired by the Behavior of Pigeons." In Advances in Nature-Inspired Computing and Applications. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-96451-5_3.

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Kiepenheuer, J. "A Further Analysis of the Orientation Behavior of Homing Pigeons Released Within Magnetic Anomalies." In Springer Proceedings in Physics. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71526-6_26.

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Williams, Wendy A. "Pigeon (Columbidae)." In Encyclopedia of Animal Cognition and Behavior. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-47829-6_1202-1.

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Pecchia, Tommaso, Anna Gagliardo, Caterina Filannino, Paolo Ioalè, and Giorgio Vallortigara. "Navigating Through an Asymmetrical Brain: Lateralisation and Homing in Pigeon." In Behavioral Lateralization in Vertebrates. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-30203-9_8.

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Wiltschko, Wolfgang, and Roswitha Wiltschko. "Pigeon Homing: The Effect of Temporary Anosmia on Orientation Behavior." In Chemical Signals in Vertebrates 6. Springer US, 1992. http://dx.doi.org/10.1007/978-1-4757-9655-1_67.

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Bingman, Verner P., Paolo Ioale, Giovanni Casini, and Paola Bagnoli. "Pigeon Homing and the Avian Hippocampal Complex: A Complementary Spatial Behavior Paradigm." In Cognitive Processes and Spatial Orientation in Animal and Man. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3531-0_22.

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Wasserman, Edward A., and Carolyn Rovee-Collier. "Pick the flowers and mind your As and 2s! Categorization by pigeons and infants." In Animal research and human health: Advancing human welfare through behavioral science. American Psychological Association, 2001. http://dx.doi.org/10.1037/10441-017.

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Cesaretti, Giovanni, Claudia Kusmic, and Daniela Musumeci. "Visuomotor Coordination in Behaviour of Pigeons Following Post-Hatching Monocular Experience: An Image Analysis Study." In From Cells to Proteins: Imaging Nature across Dimensions. Springer Netherlands, 2005. http://dx.doi.org/10.1007/1-4020-3616-7_25.

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Ostheim, Joachim, and Werner Rautenberg. "Autonomic and Behavioral Temperature Regulation as a Part of the Response Complex to Food Scarcity in the Pigeon." In Physiology of Cold Adaptation in Birds. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-0031-2_29.

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Conference papers on the topic "Pigeons – Behavior"

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Liu, Xinyu, Jiejie Nie, Yanna Ping, and Hong Wan. "Local field potential oscillations induced by goal-directed behavior of pigeon." In 2017 10th International Congress on Image and Signal Processing, BioMedical Engineering and Informatics (CISP-BMEI). IEEE, 2017. http://dx.doi.org/10.1109/cisp-bmei.2017.8302228.

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Cheng, Shuguan, Mengmeng Li, Haifei Yu, Kun Zhao, Shuo Liu, and Hong Wan. "Decoding Pigeon Behavior Outcomes during Goal-directed Decision Task by WSR Functional Network Analysis*." In 2020 42nd Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) in conjunction with the 43rd Annual Conference of the Canadian Medical and Biological Engineering Society. IEEE, 2020. http://dx.doi.org/10.1109/embc44109.2020.9175413.

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