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Author | Valero, A.; Byrne, R. | ||||
Title | Spider monkey ranging patterns in Mexican subtropical forest: do travel routes reflect planning? | Type | Journal Article | ||
Year | 2007 | Publication | Animal Cognition | Abbreviated Journal | Anim. Cogn. |
Volume | 10 | Issue | 3 | Pages | 305-315 |
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Abstract | Although it is well known that frugivorous spider monkeys (Ateles geoffroyi yucatanensis) occupy large home ranges, travelling long distances to reach highly productive resources, little is known of how they move between feeding sites. A 11 month study of spider monkey ranging patterns was carried out at the Otochma’ax Yetel Kooh reserve, Yucatán, Mexico. We followed single individuals for as long as possible each day and recorded the routes travelled with the help of a GPS (Global Positioning System) device; the 11 independently moving individuals of a group were targeted as focal subjects. Travel paths were composed of highly linear segments, each typically ending at a place where some resource was exploited. Linearity of segments did not differ between individuals, and most of the highly linear paths that led to food resources were much longer than the estimate visibility in the woodland canopy. Monkeys do not generally continue in the same ranging direction after exploiting a resource: travel paths are likely to deviate at the site of resource exploitation rather than between such sites. However, during the harshest months of the year consecutive route segments were more likely to retain the same direction of overall movement. Together, these findings suggest that while moving between feeding sites, spider monkeys use spatial memory to guide travel, and even plan more than one resource site in advance. | ||||
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Call Number | Equine Behaviour @ team @ | Serial | 3363 | ||
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Author | Cantlon, J.F.; Brannon, E.M. | ||||
Title | How Much Does Number Matter to a Monkey (Macaca mulatta)? | Type | Journal Article | ||
Year | 2007 | Publication | Journal of Experimental Psychology: Animal Behavior Processes | Abbreviated Journal | |
Volume | 33 | Issue | 1 | Pages | 32-41 |
Keywords | numerical cognition; Weber's law; nonhuman primates; numerosity | ||||
Abstract | Although many animal species can represent numerical values, little is known about how salient number is relative to other object properties for nonhuman animals. In one hypothesis, researchers propose that animals represent number only as a last resort, when no other properties differentiate stimuli. An alternative hypothesis is that animals automatically, spontaneously, and routinely represent the numerical attributes of their environments. The authors compared the influence of number versus that of shape, color, and surface area on rhesus monkeys' (Macaca mulatta) decisions by testing them on a matching task with more than one correct answer: a numerical match and a nonnumerical (color, surface area, or shape) match. The authors also tested whether previous laboratory experience with numerical discrimination influenced a monkey's propensity to represent number. Contrary to the last-resort hypothesis, all monkeys based their decisions on numerical value when the numerical ratio was favorable. | ||||
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Notes | Approved | no | |||
Call Number | Equine Behaviour @ team @ | Serial | 2891 | ||
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Author | Hirsch, B.T. | ||||
Title | Costs and benefits of within-group spatial position: a feeding competition model | Type | Journal Article | ||
Year | 2007 | Publication | The Quarterly review of biology | Abbreviated Journal | Q Rev Biol |
Volume | 82 | Issue | 1 | Pages | 9-27 |
Keywords | Animals; Competitive Behavior/*physiology; Dominance-Subordination; Feeding Behavior/*physiology/*psychology; Population Dynamics; Predatory Behavior/*physiology | ||||
Abstract | An animal's within-group spatial position has several important fitness consequences. Risk of predation, time spent engaging in antipredatory behavior and feeding competition can all vary with respect to spatial position. Previous research has found evidence that feeding rates are higher at the group edge in many species, but these studies have not represented the entire breadth of dietary diversity and ecological situations faced by many animals. In particular the presence of concentrated, defendable food patches can lead to increased feeding rates by dominants in the center of the group that are able to monopolize or defend these areas. To fully understand the tradeoffs of within-group spatial position in relation to a variety of factors, it is important to be able to predict where individuals should preferably position themselves in relation to feeding rates and food competition. A qualitative model is presented here to predict how food depletion time, abundance of food patches within a group, and the presence of prior knowledge of feeding sites affect the payoffs of different within-group spatial positions for dominant and subordinate animals. In general, when feeding on small abundant food items, individuals at the front edge of the group should have higher foraging success. When feeding on slowly depleted, rare food items, dominants will often have the highest feeding rates in the center of the group. Between these two extreme points of a continuum, an individual's optimal spatial position is predicted to be influenced by an additional combination of factors, such as group size, group spread, satiation rates, and the presence of producer-scrounger tactics. | ||||
Address | Department of Anthropology, Stony Brook University Stony Brook, New York 11794, USA. BTHIRSCH@IC.SUNYSB.EDU | ||||
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Language | English | Summary Language | Original Title | ||
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ISSN | 0033-5770 | ISBN | Medium | ||
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Notes | PMID:17354992 | Approved | no | ||
Call Number | refbase @ user @ | Serial | 803 | ||
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Author | Croneya, C.C. | ||||
Title | Group size and cognitive processes | Type | Journal Article | ||
Year | 2007 | Publication | Applied Animal Behaviour Science | Abbreviated Journal | Appl. Anim. Behav. Sci. |
Volume | 103 | Issue | 3-4 | Pages | 15-228 |
Keywords | Group size; Social complexity; Social learning; Cognitive processes | ||||
Abstract | Animal group sizes may exert important effects on various cognitive mechanisms. Group size is believed to exert pressures on fundamental brain structures that correlate with the increased social demands placed on animals living in relatively large, complex and dynamic social organizations. There is strong experimental evidence connecting social complexity, social learning and development of other cognitive abilities in a broad range of wild and domesticated animal species. In particular, group size seems to have significant effects on animals? abilities to derive concrete and abstract relationships. Here, we review the literature pertaining to cognitive processes and behaviours of various animal species relative to group size, with emphasis on social learning. It is suggested that understanding the relationship between group size and cognition in animals may yield practical animal management benefits, such as housing and conservation strategies, and may also have implications for improved animal welfare. |
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Corporate Author | Ruth C. Newberryb | Thesis | |||
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Notes | Approved | no | |||
Call Number | refbase @ user @ | Serial | 277 | ||
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Author | Naug, D.; Arathi, H.S. | ||||
Title | Sampling and decision rules used by honey bees in a foraging arena | Type | Journal Article | ||
Year | 2007 | Publication | Animal Cognition | Abbreviated Journal | Anim. Cogn. |
Volume | 10 | Issue | 2 | Pages | 117-124 |
Keywords | Animals; Bees/*physiology; *Choice Behavior; Cooperative Behavior; *Feeding Behavior; Flight, Animal | ||||
Abstract | Animals must continuously choose among various available options to exploit the most profitable resource. They also need to keep themselves updated about the values of all available options, since their relative values can change quickly due to depletion or exploitation by competitors. While the sampling and decision rules by which foragers profitably exploit a flower patch have attracted a great deal of attention in theory and experiments with bumble bees, similar rules for honey bee foragers, which face similar foraging challenges, are not as well studied. By presenting foragers of the honey bee Apis cerana with choice tests in a foraging arena and recording their behavior, we investigate possible sampling and decision rules that the foragers use to choose one option over another and to track other options. We show that a large part of the sampling and decision-making process of a foraging honey bee can be explained by decomposing the choice behavior into dichotomous decision points and incorporating the cost of sampling. The results suggest that a honey bee forager, by using a few simple rules as part of a Bayesian inference process, is able to effectively deal with the complex task of successfully exploiting foraging patches that consist of dynamic and multiple options. | ||||
Address | Department of Biology, Colorado State University, Fort Collins, CO 80523, USA. dhruba@lamar.colostate.edu | ||||
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Language | English | Summary Language | Original Title | ||
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ISSN | 1435-9448 | ISBN | Medium | ||
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Notes | PMID:16941157 | Approved | no | ||
Call Number | Equine Behaviour @ team @ | Serial | 2441 | ||
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Author | Meschan, E.M.; Peham, C.; Schobesberger, H.; Licka, T.F. | ||||
Title | The influence of the width of the saddle tree on the forces and the pressure distribution under the saddle | Type | Journal Article | ||
Year | 2007 | Publication | The Veterinary Journal | Abbreviated Journal | |
Volume | 173 | Issue | 3 | Pages | 578-584 |
Keywords | Saddle fit; Kinematics; Kinetics; Pressure; Saddletree | ||||
Abstract | As there is no statistical evidence that saddle fit influences the load exerted on a horse's back this study was performed to assess the hypothesis that the width of the tree significantly alters the pressure distribution on the back beneath the saddle. Nineteen sound horses were ridden at walk and trot on a treadmill with three saddles differing only in tree width. Kinetic data were recorded by a sensor mat. A minimum of 14 motion cycles were used in each trial. The saddles were classified into four groups depending on fit. For each horse, the saddle with the lowest overall force (LOF) was determined. Saddles were classified as “too-narrow” if they were one size (2 cm) narrower than the LOF saddle, and “too-wide” if they were one size (2 cm) wider than the LOF saddle. Saddles two sizes wider than LOF saddles were classified as “very-wide”. In the group of narrow saddles, the pressure in the caudal third (walk 0.63 N/cm2 +/- 0.10; trot 1.08 N/cm2 +/- 0.26) was significantly higher compared to the LOF saddles (walk 0.50 N/cm2 +/- 0.09; trot 0.86 N/cm2 +/- 0.28). In the middle transversal third, the pressure of the wide saddles (walk 0.73 N/cm2 +/- 0.06; trot 1.52 N/cm2 +/- 0.19) and very-wide saddles (walk 0.77 N/cm2 +/- 0.06; trot 1.57 N/cm2 +/- 0.19) was significantly higher compared to LOF saddles (walk 0.65 N/cm2 +/- 0.10/ 0.63 N/cm2 +/- 0.11; trot 1.33 N/cm2 +/- 0.22/1.27 N/cm2 +/- 0.20). This study demonstrates that the load under poorly fitting saddles is distributed over a smaller area than under properly fitting saddles, leading to potentially harmful pressures peaks. | ||||
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Call Number | Admin @ knut @ | Serial | 4349 | ||
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Author | Pain, S. | ||||
Title | Inner Representations and Signs in Animals | Type | Book Chapter | ||
Year | 2007 | Publication | Introduction to Biosemiotics | Abbreviated Journal | |
Volume | Issue | Pages | 409-455 | ||
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Abstract | At the beginning of the twentieth century, behaviourists like John B. Watson (1878-1958) changed the focus of attention from the inside of the brain (mentalism and introspection then being the main trend in psychology at the time) to the outside (Watson, 1913). They believed that we could learn nearly everything about animals and humans by studying their performance in learning experiments, and this was both measurable and verifiable. Today in the first decade of the twenty-first century, there has been a return to the inside. The neurosciences seek physiological explanations and connections between external behaviour and the neural mechanisms within the nervous system. With the revolution in magnetic resonance imaging (MRI) technology researchers are now able to visually represent neural activity. Other researchers have developed mathematical models and programs to visualise the patterns created in the periphery prior to central integration The author in this paper would like to distinguish these descriptive forms of representation from actual representations, i.e., those of which the animal is actually aware or conscious. Why does an animal sometimes make perceptual mistakes? (Case Study I “The Turtle and the Plastic Bag”). Is there more to dispositions? (Case Study II: “Taking Representation for a Walk. Argos and the Fake Daniel Dennett”). How is prey represented to an animal? (Case Study III “Representation of Prey in the Jellyfish/Herring Predator-Prey Dyad”). Does a simple animal feel pain or suffer? (Case Study IV: A Can of Worms. The Earthworm as Bait) It will be argued on the basis of contemporary biosemiotic research that animals (including both vertebrates and invertebrates) represent environmental information internally, and these representations can be subdivided into i.) primary or peripheral representation and ii.) central representation which are quantitative and qualitative respectively. Sensory information is conveyed via signals, these are received as stimuli then transduced into internal signals (see Theoretical Framework). At this stage the animal is not aware of the quality of the information as it has not yet been integrated or processed in a ganglionic complex. One can describe the properties of this pre-integrated information as quantitative and syntactical i.e., spatial and temporal ordering of incoming signals and their relations. The sign which is the smallest unit of qualitative representation arises only after integration of information from two or more discrete sensory modalities. These findings have repercussions for current models of animal learning and behaviour, especially in lower invertebrates (the principal subject of this paper); they also challenge the development of robots based on so-called simple systems | ||||
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Call Number | Equine Behaviour @ team @ | Serial | 3102 | ||
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Author | Paramastri, Y.; Royo, F.; Eberova, J.; Carlsson, H.-E.; Sajuthi, D.; Fernstrom, A.-L.; Pamungkas, J.; Hau, J. | ||||
Title | Urinary and fecal immunoglobulin A, cortisol and 11-17 dioxoandrostanes, and serum cortisol in metabolic cage housed female cynomolgus monkeys (Macaca fascicularis) | Type | Journal Article | ||
Year | 2007 | Publication | Journal of Medical Primatology | Abbreviated Journal | |
Volume | 36 | Issue | 6 | Pages | 355-364 |
Keywords | cortisol; cynomolgus monkey; immunoglobulin A; long tailed macaque; Macaca fascicularis; metabolism cage | ||||
Abstract | Background and methods Quantitative enzyme-immunoassays of urinary and fecal immunoglobulin A (IgA), cortisol and 11-17-dioxoandrostanes (11,17-DOA), and serum cortisol in eight metabolic-cage-housed female cynomolgus monkeys were performed. The monkeys were divided into two groups, B and NB. Group B animals were blood sampled every 6 hours, whereas Group NB animals were not handled/blood sampled. Results No differences were recorded between the amounts of feces and urine excreted by the two groups. Group B animals excreted more urinary cortisol than did Group NB animals indicating that restraint-blood sampling resulted in a stress response. Excreted amounts of IgA and 11,17-DOA (urine and feces) did not differ between the groups. Conclusions Urinary cortisol was a reliable marker of the stress associated with repeated blood sampling. Declining amounts of excreted urinary cortisol indicated that cynomolgus monkeys acclimated quickly to repeated blood sampling in metabolism cages. Within and between animal variation in amounts of feces voided demonstrated the importance of expressing fecal markers as ‘amounts excreted per time unit per kg body weight’ rather than just measuring the concentrations in fecal samples. | ||||
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Publisher | Blackwell Publishing Ltd | Place of Publication | Editor | ||
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ISSN | 1600-0684 | ISBN | Medium | ||
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Notes | Approved | no | |||
Call Number | Equine Behaviour @ team @ | Serial | 5854 | ||
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Author | Elfman, L.; Brannstrom, J.; Smedje, G. | ||||
Title | Detection of Horse Allergen around a Stable | Type | Journal Article | ||
Year | 2007 | Publication | Abbreviated Journal | Int Arch Allergy Immunol | |
Volume | 145 | Issue | 4 | Pages | 269-276 |
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Abstract | Background: Integrating horse stables with built-up areas may lead to conflicts. Dispersion of horse allergen may become a health risk for allergic people. The aim was to measure the dispersion of horse allergen around a stable, considering wind speed and direction and vegetation. The disturbance of staff at a workplace nearby a stable was investigated. Methods: Air sampling was performed around a stable (32 horses) at distances of 50-500 m in all directions. Sampling was done with a pump and an IOM sampler. Samples were collected at 50 points during all seasons. Horse allergen levels were determined using ELISA. Disturbance by horses was studied with a questionnaire handed to the employees in an office near the stable. Results: The median horse allergen level at the stable entrance was 316 U/m(3), in the horse fields 40 U/m(3) and in the whole source area 16 U/m(3), which declined to <2 U/m(3) at about 50 m from the source area. Downwind of the prevailing winds low levels of horse allergen (2-4 U/m(3)) could sometimes be detected at up to 500 m. The staff, including those allergic to horses, managed to tolerate horses close to the workplace. Conclusions: At low winds horse allergen spread in ambient air about 50 m from the stable and horse fields. At higher winds low allergen levels were sometimes found in open areas up to 500 m from the source area. These levels were similar to those found in the office after moving away from the stable area. The employees did not report more symptoms of allergy or asthma while working close to the stable compared to after the move. Copyright (c) 2007 S. Karger AG, Basel. | ||||
Address | Department of Medical Sciences, Occupational and Environmental Medicine, Uppsala University Hospital, Uppsala, Sweden | ||||
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Language | English | Summary Language | Original Title | ||
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ISSN | 1423-0097 | ISBN | Medium | ||
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Notes | PMID:18025788 | Approved | no | ||
Call Number | Equine Behaviour @ team @ | Serial | 4357 | ||
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Author | Ajie, B.C.; Pintor, L.M.; Watters, J.; Kerby, J.L.; Hammond, J.I.; Sih, A. | ||||
Title | A framework for determining the fitness consequences of antipredator behavior | Type | Journal Article | ||
Year | 2007 | Publication | Behavioral Ecology | Abbreviated Journal | Behav. Ecol. |
Volume | 18 | Issue | 1 | Pages | 267-270 |
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Abstract | Behavioral ecologists have long been interested in understanding the adaptive value of antipredator behavior (Sih 1987Go; Lima and Dill 1990Go; Lima 1998Go). A recent review by Lind and Cresswell (2005)Go, however, noted some important difficulties with quantifying the fitness consequences of antipredator behaviors. In essence, Lind and Cresswell suggest that most studies do not provide strong evidence on the adaptive value of antipredator behavior because they do not consider 1) trade-offs between antipredator and reproductive performance, 2) the abilities of organisms to avoid fitness losses associated with constraints on focal traits by employing behavioral alternatives (behavioral compensation), and 3) the effects of behavioral defenses at different stages of the predation sequence. The authors rightfully assert that an understanding of these issues can only be accomplished by measuring multiple traits and fitness components (i.e., survival and reproduction). Nevertheless, the question of how to integrate such data into | ||||
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Notes | 10.1093/beheco/arl064 | Approved | no | ||
Call Number | Equine Behaviour @ team @ | Serial | 4087 | ||
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