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Amodio, P.; Boeckle, M.; Schnell, A.K.; Ostojic, L.; Fiorito, G.; Clayton, N.S. |
![goto web page (via DOI) doi](img/doi.gif)
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Title |
Grow Smart and Die Young: Why Did Cephalopods Evolve Intelligence? |
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Journal Article |
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2018 |
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Trends in Ecology & Evolution |
Abbreviated Journal |
Trends. Ecol. Evol. |
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Intelligence in large-brained vertebrates might have evolved through independent, yet similar processes based on comparable socioecological pressures and slow life histories. This convergent evolutionary route, however, cannot explain why cephalopods developed large brains and flexible behavioural repertoires: cephalopods have fast life histories and live in simple social environments. Here, we suggest that the loss of the external shell in cephalopods (i) caused a dramatic increase in predatory pressure, which in turn prevented the emergence of slow life histories, and (ii) allowed the exploitation of novel challenging niches, thus favouring the emergence of intelligence. By highlighting convergent and divergent aspects between cephalopods and large-brained vertebrates we illustrate how the evolution of intelligence might not be constrained to a single evolutionary route. |
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Elsevier |
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0169-5347 |
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doi: 10.1016/j.tree.2018.10.010 |
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Equine Behaviour @ team @ |
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6508 |
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Author |
Byrne R.W. |
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Title |
The evolution of intelligence |
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Book Chapter |
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1994 |
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Behaviour and Evolution |
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223-265 |
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Cambridge University Press |
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Cambridge,UK |
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P.J.B. Slater and T.R. Halliday |
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Equine Behaviour @ team @ |
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6566 |
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Hofmeester, T.R.; Cromsigt, J.P.G.M.; Odden, J.; Andrén, H.; Kindberg, J.; Linnell, J.D.C. |
![goto web page (via DOI) doi](img/doi.gif)
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Title |
Framing pictures: A conceptual framework to identify and correct for biases in detection probability of camera traps enabling multi-species comparison |
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Journal Article |
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2019 |
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Ecology and Evolution |
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Ecol Evol |
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animal characteristics; detectability; environmental variables; mammal monitoring; reuse of data; trail camera |
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Abstract Obtaining reliable species observations is of great importance in animal ecology and wildlife conservation. An increasing number of studies use camera traps (CTs) to study wildlife communities, and an increasing effort is made to make better use and reuse of the large amounts of data that are produced. It is in these circumstances that it becomes paramount to correct for the species- and study-specific variation in imperfect detection within CTs. We reviewed the literature and used our own experience to compile a list of factors that affect CT detection of animals. We did this within a conceptual framework of six distinct scales separating out the influences of (a) animal characteristics, (b) CT specifications, (c) CT set-up protocols, and (d) environmental variables. We identified 40 factors that can potentially influence the detection of animals by CTs at these six scales. Many of these factors were related to only a few overarching parameters. Most of the animal characteristics scale with body mass and diet type, and most environmental characteristics differ with season or latitude such that remote sensing products like NDVI could be used as a proxy index to capture this variation. Factors that influence detection at the microsite and camera scales are probably the most important in determining CT detection of animals. The type of study and specific research question will determine which factors should be corrected. Corrections can be done by directly adjusting the CT metric of interest or by using covariates in a statistical framework. Our conceptual framework can be used to design better CT studies and help when analyzing CT data. Furthermore, it provides an overview of which factors should be reported in CT studies to make them repeatable, comparable, and their data reusable. This should greatly improve the possibilities for global scale analyses of (reused) CT data. |
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John Wiley & Sons, Ltd |
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2045-7758 |
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doi: 10.1002/ece3.4878 |
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Equine Behaviour @ team @ |
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6518 |
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Hampton, R.R.; Sherry, D.F.; Shettleworth, S.J.; Khurgel, M.; Ivy, G. |
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Title |
Hippocampal volume and food-storing behavior are related in parids |
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Journal Article |
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Year |
1995 |
Publication |
Brain, behavior and evolution |
Abbreviated Journal |
Brain Behav Evol |
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45 |
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54-61 |
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Animals; Appetitive Behavior/*physiology; Birds/*anatomy & histology; Brain Mapping; Evolution; Food Preferences/physiology; Hippocampus/*anatomy & histology; Mental Recall/*physiology; Orientation/*physiology; Predatory Behavior/physiology; Social Environment; Species Specificity |
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The size of the hippocampus has been previously shown to reflect species differences and sex differences in reliance on spatial memory to locate ecologically important resources, such as food and mates. Black-capped chickadees (Parus atricapillus) cached more food than did either Mexican chickadees (P. sclateri) or bridled titmice (P. wollweberi) in two tests of food storing, one conducted in an aviary and another in smaller home cages. Black-capped chickadees were also found to have a larger hippocampus, relative to the size of the telencephalon, than the other two species. Differences in the frequency of food storing behavior among the three species have probably produced differences in the use of hippocampus-dependent memory and spatial information processing to recover stored food, resulting in graded selection for size of the hippocampus. |
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Department of Psychology, University of Toronto, Ontario, Canada |
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0006-8977 |
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PMID:7866771 |
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no |
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refbase @ user @ |
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379 |
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Author |
Houston, A.I.; McNamara, J.M. |
![find record details (via OpenURL) openurl](img/xref.gif)
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Title |
Fighting for food: a dynamic version of the Hawk-Dove game |
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Journal Article |
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Year |
1988 |
Publication |
Evolutionary Ecology |
Abbreviated Journal |
Evol. Ecol. |
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2 |
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51-64 |
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refbase @ user @ |
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750 |
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Author |
Healy,S.; Braithwaite, V |
![find record details (via OpenURL) openurl](img/xref.gif)
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Title |
Cognitive ecology: a field of substance? |
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Journal Article |
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Year |
2000 |
Publication |
Trends in Ecology & Evolution |
Abbreviated Journal |
Trends. Ecol. Evol |
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15 |
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22-26 |
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Cognitive ecology; Neuroethology; Cognition; Ecology; Evolution; Orientation mechanisms |
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In 1993, Les Real invented the label 'cognitive ecology'. This label was intended for work that brought cognitive science and behavioural ecology together. Real's article stressed the importance of such an approach to the understanding of behaviour. At the end of a decade in which more interdisciplinary work on behaviour has been seen than for many years, it is time to assess whether cognitive ecology is a label describing an active field. |
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Division of Biological Sciences, King's Buildings, University of Edinburgh, West Mains Road, Edinburgh, UK EH9 3JT |
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0169-5347 |
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PMID:10603501 |
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refbase @ user @ |
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837 |
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Dellert, B.; Ganslosser, U. |
![find record details (via OpenURL) openurl](img/xref.gif)
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Title |
Experimental alterations of food distribution in two species of captive equids (Equus burchelli and E. hemionus kulan) |
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Journal Article |
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1997 |
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Ethology Ecology & Evolution (EEE) |
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Ethol Ecol Evol |
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9 |
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1-17 |
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n one group each of Plains zebra (six mares, one foal, one subadult) and Asiatic wild asses (seven mares, two foals) at Nuremberg Zoo, food distribution was experimentally changed from clumped (all food in one standard hay rack) to dispersed (one heap per animal). Both groups were characterized by different social structures, which basically remained during the experiment. Plains zebras had an individually structured system of social relationships in a dominance order, wild asses a more egalitarian system without clear-cut rank differences and low frequencies of agonistic interactions. Access to food accordingly was individually (but consistently) different for zebra mares, almost equal for wild ass mares. During the dispersed feeding situation frequencies of agonistic interactions in both species decreased (however non-significantly), individual distances increased but mares also frequently ''visited'' each others' heaps. Feeding time increased for all wild ass mares. Some individuals (in both groups) behaved ''against the trend'' in agonistic behaviour. The results are discussed with regard to food distribution for ungulates in general, and equid social systems. |
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Equine Behaviour @ team @ |
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2292 |
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Author |
Dukas, R. |
![goto web page (via DOI) doi](img/doi.gif)
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Title |
Evolutionary Biology Of Animal Cognition |
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2004 |
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Annual Review of Ecology, Evolution, and Systematics |
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35 |
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347-374 |
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This review focuses on five key evolutionary issues pertaining to animal cognition, defined as the neuronal processes concerned with the acquisition, retention, and use of information. Whereas the use of information, or decision making, has been relatively well examined by students of behavior, evolutionary aspects of other cognitive traits that affect behavior, including perception, learning, memory, and attention, are less well understood. First, there is ample evidence for genetically based individual variation in cognitive traits, although much of the information for some traits comes from humans. Second, several studies documented positive association between cognitive abilities and performance measures linked to fitness. Third, information on the evolution of cognitive traits is available primarily for color vision and decision making. Fourth, much of the data on plasticity of cognitive traits appears to reflect nonadaptive phenotypic plasticity, perhaps because few evolutionary analyses of cognitive plasticity have been carried out. Nonetheless, several studies suggest that cognitive traits show adaptive plasticity, and at least one study documented genetically based individual variation in plasticity. Fifth, whereas assertions that cognition has played a central role in animal evolution are not supported by currently available data, theoretical considerations indicate that cognition may either increase or decrease the rate of evolutionary change. |
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Equine Behaviour @ team @ |
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2970 |
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Author |
Fisher, D.O.; Blomberg, S.P.; Owens, I.P.F. |
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Title |
Convergent Maternal Care Strategies In Ungulates And Macropods |
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Journal Article |
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2002 |
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Evolution |
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56 |
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167-176 |
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Mammals show extensive interspecific variation in the form of maternal care. Among ungulates, there is a dichotomy between species in which offspring follow the mother (“following” strategy) versus species in which offspring remain concealed (“hiding” strategy). Here we reveal that the same dichotomy exists among macropods (kangaroos, wallabies and allies). We test three traditional adaptive explanations and one new life history hypothesis, and find very similar patterns among both ungulates and macropods. The three traditional explanations that we tested were that a “following” strategy is associated with (1) open habitat, (2) large mothers, and (3) gregariousness. Our new life-history hypothesis is that a “following strategy” is associated with delayed weaning, and thus with the “slow” end of the slow-fast mammalian life-history continuum, because offspring devote resources to locomotion rather than rapid growth. Our comparative test strongly supports the habitat structure hypothesis and provides some support for this new delayed weaning hypothesis for both ungulates and macropods. We propose that sedentary young in closed habitats benefit energetically by having milk brought to them. In open habitats, predation pressure will select against hiding. Followers will suffer slower growth to independence. Taken together, therefore, our results provide the first quantitative evidence that macropods and ungulates are convergent with respect to interspecific variation in maternal care strategy. In both clades, differences between species in the form of parental care are due to a similar interaction between habitat, social behavior, and life history. Corresponding Editor: B. Crespi |
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Equine Behaviour @ team @ |
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4252 |
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Author |
Beck, B.B. |
![goto web page (via DOI) doi](img/doi.gif)
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Title |
Chimpocentrism: Bias in cognitive ethology |
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1982 |
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Journal of Human Evolution |
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11 |
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3-17 |
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herring gull; chimpanzee; cognition; tool-use; shell-dropping; mollusk; predation |
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Herring gulls drop hard-shelled mollusks and hermit crab-inhabited molluskan prey in order to break the shells and gain access to the edible interior. A field study of predatory shell dropping on Cape Cod, Massachusetts, U.S.A. showed that the gulls usually drop the same shell repeatedly, orient directly to dropping sites that are invisible from the point at which the mollusks are captured, drop preferentially on hard surfaces, adjust dropping heights to suit the area and elasticity of the substrate, orient directly into the wind while dropping, sever the large defensive cheliped of hermit crabs before consumption, and rinse prey that is difficult to swallow. Proficiency in prey dropping is acquired through dropping objects in play, trial-and-error learning, and perhaps, observation learning.
Observable attributes of predatory shell-dropping support inferences that the gulls are capable of extended concentration, purposefulness, mental representation of spatially and temporally displaced environmental features, cognitive mapping, cognitive modeling, selectivity, and strategy formation. Identical cognitive processes have been inferred to underlie the most sophisticated forms of chimpanzee tool-use.
Advanced cognitive capacities are not restricted to chimpanzees and other pongids, and are not associated uniquely with tool use. The chimpocentric bias should be abandoned, and reconstructions of the evolution of intelligence should be modified accordingly. |
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Equine Behaviour @ team @ |
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4414 |
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