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1 mes (prisoner's dilemma, snowdrift, and hawk-dove).
2 re finally committing to a decision (hawk or dove).
3  cattle and others (e.g., pets - cats, dogs, doves).
4 ptom within the duration window specified in DOVE.
5 natal cortex of lizard, turtle, chicken, and dove.
6 forebrain and in the cortices of chicken and dove.
7 s with ability below the critical level play Dove.
8 re (eCQM) was developed and used to quantify DOVE.
9 awks that acquiesce to punishment by playing dove.
10 enerates aerodynamic force during takeoff in doves.
11 blers and nidopallium caudolateral in turtle doves.
12 tral trigeminal structures in hatchling ring doves.
13 th and 8-month) and adult (1-year to 8-year) doves.
14 nd drawings from the American painter Arthur Dove (1880-1946).
15 sical diel vertical migration, the porpoises dove 24-37% deeper at night and the frequency of deep di
16                      After lunch at 14:30 he dove again (third dive of the day) during which time itc
17 s, representing the prisoner's dilemma, hawk-dove and coordination classes of games, in structured po
18                    Here, we combine the hawk-dove and prisoner's dilemma games to model the effects o
19 cies which ranged from 18.5 to 33.8 for ring doves and 7.9 to 14.8 for Japanese koi.
20 -magnification) model was calibrated in ring doves and Japanese koi using matched data on dietary ass
21  input in songbirds, which is not present in doves and pigeons that vocalize with a closed beak, may
22 inate, with one playing Hawk and one playing Dove, and with conflicts in which both animals play Hawk
23                      House sparrows and rock doves are potential free-ranging sentinel species for WN
24 n repeated Prisoner's Dilemma, Chicken (Hawk-Dove), Battle of the Sexes, and Leader games.
25 ent study, the ontogeny of mast cells in the dove brain was followed by using three markers: acidic t
26  In the avian reproductive model of the rock dove (Columba livia), we characterized the transcript co
27 ing lice," are both parasites of pigeons and doves (Columbiformes).
28 ls in the medial habenula of sexually active doves compared with controls.
29                                              DOVE eCQM rates using the greater than 24-hour definitio
30 n all-cause mortality support the use of the DOVE eCQM tool to guide quality improvement efforts at i
31 tricted doves than Prl-treated, food-clamped doves even though response rates were similar on VI sche
32  and the melanocortin-4 receptor in the ring dove feeding behavior.
33 ection with Voxel-based deep neural nEtwork (DOVE) for evaluating protein docking models.
34                              We analyze hawk-dove game and prisoner's dilemma introducing social pena
35 vior in two types of chicken games (the hawk-dove game and the snowdrift game) but not in the prisone
36   We illustrate this in relation to the hawk-dove game by showing that three different mechanisms, ea
37 ition that the mixed equilibrium of the Hawk-Dove game captures important aspects of many animal inte
38                                     The hawk-dove game has proved to be an important tool for underst
39 he cognitive model into an evolutionary hawk-dove game in order to investigate Trivers' and Ramachand
40            We consider a version of the Hawk-Dove game in which an animal knows its own fighting abil
41 stability than is found in the standard Hawk-Dove game in which there are no differences in ability o
42 s such as the Prisoner's Dilemma or the Hawk-Dove game on graphs.
43 e how the Hawk and Dove strategies in a Hawk-Dove game spread in a population represented by a random
44 tegy, which punishes hawkishness in the hawk-dove game with defection in the prisoner's dilemma, can
45 chnique works for a simple example (the Hawk-Dove game) where an analytic solution is known, and prov
46                      In Maynard Smith's Hawk-Dove game, for example, Selten's result restricts attent
47 l known model of animal aggression, the Hawk-Dove game, to incorporate the possibility of eavesdroppe
48 ecies contest a resource by playing the hawk-dove game.
49      As a specific example we study the Hawk-Dove game.
50 multi-player extension of the classical Hawk-Dove game.
51 ated asymmetric Battle of the Sexes and Hawk-Dove games, to explore how cognitive and social skills r
52 epeated Prisoner's Dilemma and Chicken (Hawk-Dove) games lead to the emergence of genes coding for sy
53 nt from that observed in seeds obtained from dove gizzards, indicating that seed passage through coug
54 relating to production, the multiplayer Hawk-Dove (HD) dilemma is a commons dilemma focusing on the f
55                                     The hawk-dove (HD) game, as defined by Maynard Smith, allows for
56 ther lice (Columbicola) and their pigeon and dove hosts (Columbiformes).
57          The prevalence of ovarian cancer in DOVE is 10 times that of large screening trials, prompti
58 katiels is acutely concave, whereas that for doves is intermediate in shape and shows higher mass-spe
59                                  Prl-treated doves learned the key-pecking response when food intake
60 isk assessment into a novel HAWK (high risk)/DOVE (low risk) patient grouping, intensivist/hospitalis
61 ce Raman are complementary methods, TRSF and DOVE methods are complementary to coherent Raman methods
62           Here I extend Maynard Smith's hawk-dove model of animal conflict to explore the logic of a
63             We first extend the classic hawk-dove model of the evolution of animal aggression to cons
64 taxa; specifically adapting the classic Hawk-Dove model to consider conflict decisions made by groups
65 ategy only occurred in 2010/2011, when birds dove more and deeper, suggesting limited prey resources.
66 rl elevated pecking rates in food-restricted doves on a variable-interval (VI) reinforcement schedule
67                                      Using a dove prism, a simple single axis optical train may be em
68 ly, with "m" total internal reflections in a Dove prism, MRSFG signal is approximately m times that o
69 nances using excitation light coupled into a Dove prism.
70 agation geometry was adopted and trapezoidal Dove prisms were used as sample substrates.
71                                          The DOVE rate using the greater than 72-hour definition was
72                    The primary outcomes were DOVE rates and 30-day all-cause mortality by time to dia
73  of delayed VTE diagnosis, consistently high DOVE rates and associated increases in all-cause mortali
74                                              DOVE rates were calculated using thresholds of greater t
75                                              Doves reduce the angle of attack of their wing mid-downs
76 gnificance of adult neurogenesis in the ring dove remains to be determined.
77 line; the first reduction coincided with the dove's attainment of adult physical size (about 3 months
78 op-of-canopy height with thousands of Planet Dove satellite images into a random forest machine learn
79         To evaluate a protein docking model, DOVE scans the protein-protein interface of the model wi
80  laboratory-infected birds but not from rock dove serum samples.
81                                Food-deprived doves showed a fourfold increase in the number of AGRP-i
82 rds and parrots, as well as in the brains of dove species as examples of close vocal nonlearning rela
83 r presents the first electronically resonant DOVE spectra and demonstrates the capabilities for analy
84 y comparing electronically resonant TRSF and DOVE spectra with each other and with infrared absorptio
85 cy (TRSF) and doubly vibrationally enhanced (DOVE) spectroscopies are examples of a recently develope
86  as members of the dominant species who play dove, splitting the resource when facing other dominant
87  an example, we investigate how the Hawk and Dove strategies in a Hawk-Dove game spread in a populati
88 ouse sparrow (Passer domesticus) and spotted dove (Streptopelia chinensis) in particular.
89 gth sensitive opsin 1 (SWS1) of the laughing dove (Streptopelia senegalensis), the current study conf
90 tin (Prl) increases food consumption in ring doves (Streptopelia risoria) and may promote the hyperph
91 measured changes in feeding behavior in ring doves (Streptopelia risoria) following intracerebroventr
92 ls (Nymphicus hollandicus) and ringed turtle-doves (Streptopelia risoria).
93 arblers (Acrocephalus scirpaceus) and turtle doves (Streptopelia turtur), caught in Israel while retu
94 urogenesis occurs in a nonsongbird, the ring dove (Streptoplia risoria), and whether it persists to o
95 The ongoing Diagnosing Ovarian Cancer Early (DOVE) Study in Montreal, Quebec, Canada, provides diagno
96 le were 2-3 times greater in food-restricted doves than Prl-treated, food-clamped doves even though r
97       William Smith introduces the wild rock dove, the ancestor of domestic and feral pigeons.
98           Larger birds, mainly from St Paul, dove to deeper depths, spent more time in the Bering Sea
99        He traveled by boat to the dive site, dove twice and then ate lunch at 12:30 on the diving boa
100             In this study, using female ring doves, we recorded neuronal activity from hypothalamic n
101 dule and supported continued responding when doves were returned to ad-lib feeding.
102  promote the hyperphagia exhibited by parent doves when provisioning young.
103 ting the resource when facing other dominant doves while continuing to surrender the resource to domi
104 months old) and the second occurred when the dove would normally attain reproductive fitness (about 1
105 ially consumed by their main prey, the Eared Dove Zenaida auriculata.

 
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