Abstract is: Behavioral Ecology is a bimonthly peer-reviewed scientific journal published by Oxford University Press on behalf of the . The journal was established in 1990.
| scientific journal | Q5633421 |
| P6981 | ACNP journal ID | 2477235 |
| 915594 | ||
| P8375 | Crossref journal ID | 5065 |
| P1250 | Danish Bibliometric Research Indicator (BFI) SNO/CNO | 15572 |
| P1058 | ERA Journal ID | 3206 |
| P646 | Freebase ID | /m/0nb0dwv |
| P8903 | HAL journal ID | 11075 |
| P1160 | ISO 4 abbreviation | Behav. Ecol. |
| P236 | ISSN | 1045-2249 |
| 1465-7279 | ||
| P7363 | ISSN-L | 1045-2249 |
| P1277 | JUFO ID | 52215 |
| P4730 | Mir@bel journal ID | 21080 |
| P1055 | NLM Unique ID | 9426330 |
| P243 | OCLC control number | 41963900 |
| P856 | official website | http://beheco.oupjournals.org |
| http://beheco.oxfordjournals.org | ||
| P10283 | OpenAlex ID | S121360315 |
| P3181 | OpenCitations bibliographic resource ID | 55413 |
| P7662 | Scilit journal ID | 85747 |
| P1156 | Scopus source ID | 13151 |
| P4616 | UniProt journal ID | 3064 |
| P495 | country of origin | United Kingdom | Q145 |
| P1240 | Danish Bibliometric Research Indicator level | 1 | |
| 2 | |||
| P571 | inception | 1990-01-01 | |
| P8875 | indexed in bibliographic review | Scopus | Q371467 |
| Science Citation Index Expanded | Q104047209 | ||
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | ecology | Q7150 |
| P123 | publisher | Oxford University Press | Q217595 |
| P1476 | title | Behavioral Ecology |
| Q36701398 | "Parasite-induced aposematism" protects entomopathogenic nematode parasites against invertebrate enemies |
| Q115543282 | Gammarus pulexshow a grouping response to conspecific injury cues but not to predator kairomones |
| Q59891451 | A bee or not a bee: an experimental test of acoustic mimicry by hoverflies |
| Q34060906 | A behavioral mechanism underlying ecological divergence in the malaria mosquito Anopheles gambiae |
| Q128095759 | A benefit to providing information? Flower size cues, plant attractiveness, and plant visit length |
| Q53417109 | A case for considering individual variation in diel activity patterns. |
| Q29303912 | A case of mental time travel in ant-following birds? |
| Q60549946 | A chorus of color: hierarchical and graded information content of rapid color change signals in chameleons |
| Q29302967 | A commitment model of reproductive inhibition in cooperatively breeding groups |
| Q55966932 | A comparative analysis of the evolution of variation in appearance of eggs of European passerines in relation to brood parasitism |
| Q115538203 | A comparative study of activity levels in larval anurans and response to the presence of different predators |
| Q115414499 | A comparative study of the function of heterospecific vocal mimicry in European passerines |
| Q57529355 | A context-dependent induction of natal habitat preference in a generalist herbivorous insect |
| Q113393727 | A dynamic model of group-size choice in the coral reef fish Dascyllus albisella |
| Q57269619 | A farewell to Bonferroni: the problems of low statistical power and publication bias |
| Q115787891 | A game-theoretical model of kleptoparasitic behavior in an urban gull (Laridae) population |
| Q35218065 | A larger brain confers a benefit in a spatial mate search learning task in male guppies |
| Q109745478 | A link between heritable parasite resistance and mate choice in dung beetles |
| Q107099628 | A longitudinal study of dominance and aggression in greylag geese (Anser anser) |
| Q36701391 | A lover or a fighter? Opposing sexual selection pressures on men's vocal pitch and facial hair |
| Q55277700 | A marker of biological ageing predicts adult risk preference in European starlings, Sturnus vulgaris. |
| Q56421621 | A mechanism for cryptic female choice in chinook salmon |
| Q112806639 | A meta-analysis of correlated behaviors with implications for behavioral syndromes: relationships between particular behavioral traits |
| Q112855595 | A meta-analysis of factors influencing the strength of mate-choice copying in animals |
| Q112806649 | A meta-analysis of the group-size effect on vigilance in mammals |
| Q60384404 | A meta-analytic castle built on sand? A comment on Roca et al |
| Q59256270 | A multi-level approach to quantify speed-accuracy trade-offs in great tits (Parus major) |
| Q115543241 | A multilevel society of herring-eating killer whales indicates adaptation to prey characteristics |
| Q60490580 | A multivariate analysis of phenotype and paternity in male harbor seals, Phoca vitulina, at Sable Island, Nova Scotia |
| Q109041135 | A mutual understanding? Interspecific responses by birds to each other's aerial alarm calls |
| Q129749346 | A new trophic specialization buffers a top predator against climate-driven resource instability |
| Q115414536 | A novel evolutionary pattern of reversed sexual dimorphism in fairy wrens: implications for sexual selection |
| Q54284208 | A parasite in wolf's clothing: hawk mimicry reduces mobbing of cuckoos by hosts |
| Q115543386 | A pigheaded compromise: do competition and predation explain variation in warthog group size? |
| Q56999593 | A place for behavior in ecological epigenetics |
| Q129558552 | A pollen fatty acid enhances learning and survival in bumblebees |
| Q62006927 | A possible case of contemporary selection leading to a decrease in sexual plumage dimorphism in a grassland-breeding shorebird |
| Q57236814 | A prison effect in a wild population: a scarcity of females induces homosexual behaviors in males |
| Q55892800 | A prudent hoarder: effects of long-term hoarding in the European nuthatch, Sitta europaea |
| Q115414522 | A quantitative genetics approach to validate lab- versus field-based behavior in novel environments |
| Q115544010 | A rare predator exploits prey escape behavior: the role of tail-fanning and plumage contrast in foraging of the painted redstart (Myioborus pictus) |
| Q60393663 | A receiver bias for red predates the convergent evolution of red color in widowbirds and bishops |
| Q113821480 | A reevaluation of the logic of pilferage effects, predation risk, and environmental variability on avian energy regulation: the critical role of time budgets |
| Q59197847 | A sex-specific behavioral syndrome in a wild passerine |
| Q109041166 | A songbird mimics different heterospecific alarm calls in response to different types of threat |
| Q128144077 | A superb solo, or a deviant duet? Overlapping songs in superb fairy-wrens |
| Q57669777 | A survey of the statistical power of research in behavioral ecology and animal behavior |
| Q60502026 | A tale of 2 signals: signal mimicry between aposematic species enhances predator avoidance learning |
| Q56156790 | A taste for novelty in invading house sparrows, Passer domesticus |
| Q113035189 | A test of alternative hypotheses for kin recognition in cannibalistic tiger salamanders |
| Q113035026 | A test of the dear enemy hypothesis in female New Zealand bellbirds (Anthornis melanura): female neighbors as threats |
| Q56269921 | A test of the good-genes-as-heterozygosity hypothesis using red-winged blackbirds |
| Q113035159 | A test of the risk allocation hypothesis: tadpole responses to temporal change in predation risk |
| Q113034963 | A test of the sexy-sperm and good-sperm hypotheses for the evolution of polyandry |
| Q56656961 | A theory of mate choice based on heterozygosity |
| Q57438204 | A trade-off between natural and sexual selection underlies diversification of a sexual signal |
| Q58486880 | A trait-based approach to understand the evolution of complex coalitions in male mammals |
| Q113275629 | Absence of nepotism toward imprisoned young queens during swarming in the honey bee |
| Q30053488 | Acceptance by the splendid fairy-wren of parasitism by Horsfield's bronze-cuckoo: further evidence for evolutionary equilibrium in brood parasitism |
| Q114896875 | Accuracy of song syntax learning and singing consistency signal early condition in zebra finches |
| Q115414437 | Achromatic plumage brightness predicts stress resilience and social interactions in tree swallows (Tachycineta bicolor) |
| Q57205981 | Achromatic plumage reflectance predicts reproductive success in male black-capped chickadees |
| Q113821406 | Acoustic and visual stimuli combined promote stronger responses to aerial predation in fish |
| Q60336919 | Acoustic communication in zebra finches signals when mates will take turns with parental duties |
| Q29041537 | Acoustic cues alter perceived sperm competition risk in the field cricket Teleogryllus oceanicus |
| Q58790827 | Acoustic experience influences male and female pre- and postcopulatory behaviors in a bushcricket |
| Q112806646 | Acoustic preferences and localization performance of blood-sucking flies (Corethrella Coquillett) to túngara frog calls |
| Q129150999 | Acoustic stability in hyrax snorts: vocal tightrope-walkers or wrathful verbal assailants? |
| Q115787911 | Activity patterns of urban red foxes (Vulpes vulpes) reduce the risk of traffic-induced mortality |
| Q56270793 | Adaptive phenotypic plasticity in an island songbird exposed to a novel predation risk |
| Q56766524 | Adjusting to a toxic invader: native Australian frogs learn not to prey on cane toads |
| Q27304568 | Adjustment of costly extra-group paternity according to inbreeding risk in a cooperative mammal |
| Q37529949 | Adult helpers increase the recruitment of closely related offspring in the cooperatively breeding rifleman |
| Q128462001 | Adult nutritional stress decreases oviposition choosiness and fecundity in female butterflies |
| Q113275631 | Advantages and disadvantages of large colony size in a halictid bee: the queen's perspective |
| Q112560473 | Aerial attack strategies of hawks hunting bats, and the adaptive benefits of swarming |
| Q60255331 | Aerial dispersal plasticity under different wind velocities in a salt marsh wolf spider |
| Q90635580 | Affiliation history and age similarity predict alliance formation in adult male bottlenose dolphins |
| Q59160250 | African ungulates recognize a locally extinct native predator |
| Q58039033 | Against the odds? Nestling sex ratio variation in green-rumped parrotlets |
| Q115543382 | Agamas exhibit behavioral syndromes: bolder males bask and feed more but may suffer higher predation |
| Q60456520 | Age, parasites, and condition affect humoral immune response in tropical pythons |
| Q60466671 | Age- and sex-specific response to population density and sex ratio |
| Q56552444 | Age- and tactic-related paternity success in male African elephants |
| Q56093895 | Age-dependent health status and song characteristics in the barn swallow |
| Q57266119 | Age-related decrease in male reproductive success and song quality in Drosophila montana |
| Q59298816 | Aggression in Columbian ground squirrels: relationships with age, kinship, energy allocation, and fitness |
| Q56040772 | Aggression, dominance, and mating success among capybara males (Hydrochaeris hydrochaeris) |
| Q59197880 | Aggressive Ural owl mothers recruit more offspring |
| Q115543242 | Aggressive jumping spiders make quicker decisions for preferred prey but not at the cost of accuracy |
| Q129947911 | Aggressive spiders make the wrong decision in a difficult task |
| Q123141302 | Agonistic communication between males of a zaprochiline katydid (Orthoptera: Tettigoniidae) |
| Q109041181 | Alarm calls of a cooperative bird are referential and elicit context-specific antipredator behavior |
| Q109041139 | Alarm calls of tufted titmice convey information about predator size and threat |
| Q123760286 | Allee effects drive the coevolution of cooperation and group size in high reproductive skew groups |
| Q125973248 | Allo-preening is linked to vocal signature development in a wild parrot |
| Q53417120 | Allopreening in birds is associated with parental cooperation over offspring care and stable pair bonds across years. |
| Q60054621 | Alternative behavioral measures of postconflict affiliation |
| Q115543829 | Alternative forms of competition and predation dramatically affect habitat selection under foraging--predation-risk trade-offs |
| Q56288568 | Alternative reproductive strategies in the white-throated sparrow: behavioral and genetic evidence |
| Q104879199 | Alternative reproductive tactics and lifetime reproductive success in a polygynandrous mammal |
| Q116847083 | Alternative reproductive tactics in female horseshoe crabs |
| Q128109102 | Alternative reproductive tactics shape within-species variation in behavioral syndromes |
| Q113035121 | Altitudinal variation in sexual dimorphism: a new pattern and alternative hypotheses |
| Q125855471 | American black bears perceive the risks of crossing roads |
| Q121010044 | Among-population covariation between sperm competition and ejaculate expenditure in frogs |
| Q58820867 | Amphibians’ response to the lunar synodic cycle—a review of current knowledge, recommendations, and implications for conservation |
| Q129265733 | An androgenic endocrine disruptor alters male mating behavior in the guppy (Poecilia reticulata) |
| Q33583276 | An arms race between producers and scroungers can drive the evolution of social cognition |
| Q56391379 | An evolutionarily stable strategy for aggressiveness in feeding groups |
| Q112556378 | An evolutionary model of sensitive periods when the reliability of cues varies across ontogeny |
| Q27304563 | An experimental conflict of interest between parasites reveals the mechanism of host manipulation |
| Q124880439 | An experimental field test of female defense in territorial male collared lizards |
| Q115414453 | An experimental test of duet function in a fairy-wren (Malurus) with moderate cuckoldry rates |
| Q112222968 | An experimental test of the Westermarck effect: sex differences in inbreeding avoidance |
| Q104868594 | An experimental test to separate the effects of male age and mating history on female mate choice |
| Q61458472 | An intimidating ornament in a female pipefish |
| Q111168796 | An invasive amphibian drives antipredator responses in two prey at different trophic positions |
| Q90635602 | Analysis of direct and indirect genetic effects in fighting sea anemones |
| Q104101944 | Analysis of within-individual variation in extrapair paternity in blue tits (Cyanistes caeruleus) shows low repeatability and little effect of changes in neighborhood |
| Q115414451 | Ant recognition cue diversity is higher in the presence of slavemaker ants |
| Q57517247 | Anthropogenic food patches and association patterns of Tursiops truncatus at Lampedusa island, Italy |
| Q128683556 | Anthropogenic increases in nutrients alter sexual selection dynamics: a case study in butterflies |
| Q60504685 | Anthropogenic noise disrupts mate searching in Gryllus bimaculatus |
| Q60319840 | Antipredator behavior in blackbirds: habituation complements risk allocation |
| Q125370614 | Antipredator behavior: escape flights on a landscape slope |
| Q60557289 | Antipredator calls of tufted titmice and interspecific transfer of encoded threat information |
| Q115543841 | Antipredator defense as a limited resource: unequal predation risk in broods of an insect with maternal care |
| Q125902913 | Antipredator escape distances of common and threatened birds |
| Q63000266 | Aposematic coloration, luminance contrast, and the benefits of conspicuousness |
| Q115543260 | Aposematic signals in North American black widows are more conspicuous to predators than to prey |
| Q59024293 | Aposematism in the burying beetle? Dual function of anal fluid in parental care and chemical defense |
| Q63379871 | Applying Lanchester’s laws to the interspecific competition of coral reef fish |
| Q58486840 | Applying the coalitionary-traits metric: sociality without cooperation in male yellow-bellied marmots |
| Q115543216 | Aquatic prey use countershading camouflage to match the visual background |
| Q125358567 | Are 2D space-use analyses adapted to animals living in 3D environments? A case study on a fish shoal |
| Q114633535 | Are bird species that vocalize at higher frequencies preadapted to inhabit noisy urban areas? |
| Q60508670 | Are females in good condition better able to cope with costly males? |
| Q56942159 | Are innovative species ecological generalists? A test in North American birds |
| Q57205983 | Are least flycatcher (Empidonax minimus) clusters hidden leks? |
| Q57716008 | Are queen ants inhibited by their own pheromone? Regulation of productivity via negative feedback |
| Q109041199 | Are signals of aggressive intent less honest in urban habitats? |
| Q58486473 | Are social attributes associated with alarm calling propensity? |
| Q60299113 | Are there benefits to being born asynchronously: an experimental test in a social lizard |
| Q104206494 | Area-restricted search by the plains pocket gopher (Geomys bursarius) in tallgrass prairie habitat |
| Q128848214 | Arena size modulates functional responses via behavioral mechanisms |
| Q112806644 | Armament under direct sexual selection does not exhibit positive allometry in an earwig |
| Q114633539 | Artificial light at night alters activity, body mass, and corticosterone level in a tropical anuran |
| Q56093528 | Artificial night lighting rather than traffic noise affects the daily timing of dawn and dusk singing in common European songbirds |
| Q60337256 | Artificial ornaments manipulate intrinsic male quality in wild-caught zebra finches (Taeniopygia guttata) |
| Q127773222 | Artificial selection on walking distance suggests a mobility-sperm competitiveness trade-off |
| Q123258223 | Assessing reliance on vector navigation in the long-distance oceanic migrations of green sea turtles |
| Q113034993 | Assessing the developmental stress hypothesis in the context of a reaction norm |
| Q57269616 | Assessing the function of house sparrows' bib size using a flexible meta-analysis method |
| Q56387830 | Assessing “false” alarm calls by a drongo (Dicrurus paradiseus) in mixed-species bird flocks |
| Q115543551 | Assessment of local predation risk: the role of subthreshold concentrations of chemical alarm cues |
| Q112806635 | Associative learning of flowers by generalist bumble bees can be mediated by microbes on the petals |
| Q128339495 | Assortative interactions revealed in a fission–fusion society of Australian humpback dolphins |
| Q58486476 | Asymmetric eavesdropping between common mynas and red-vented bulbuls |
| Q57220226 | Asymmetric larval mobility and the evolutionary transition from siblicide to nonsiblicidal behavior in parasitoid wasps |
| Q60481759 | Asymmetry in size, shape, and color impairs the protective value of conspicuous color patterns |
| Q58643622 | Asynchronous hatching in a nonavian species: a test of the hurry-up hypothesis |
| Q61762072 | Attraction of a predator to chemical information related to nonprey: when can it be adaptive? |
| Q114592027 | Attraction to conspecific eggs may guide oviposition site selection in a solitary insect |
| Q105613058 | Attractiveness is positively related to World Cup performance in male, but not female, biathletes |
| Q56803302 | Attractiveness of women's body odors over the menstrual cycle: the role of oral contraceptives and receiver sex |
| Q115543749 | Auditory prey location in a pause—travel predator: search height, search time, and attack range of Tengmalm's owls (Aegolius funereus) |
| Q111168908 | Australian house geckos are more aggressive than a globally successful invasive Asian house gecko |
| Q60368994 | Availability of nonpigmentary antioxidant affects red coloration in gulls |
| Q56211781 | Avian prey-dropping behavior. I. The effects of prey characteristics and prey loss |
| Q56211782 | Avian prey-dropping behavior. II. American crows and walnuts |
| Q56689020 | Avoidance of aposematic prey in European tits (Paridae): learned or innate? |
| Q115543286 | Avoiding predators in a fluctuating environment: responses of the wood warbler to pulsed resources |
| Q52603707 | Avoiding the misuse of BLUP in behavioural ecology. |
| Q60393656 | Background colour matching increases with risk of predation in a colour-changing grasshopper |
| Q59300101 | Barn swallow antipredator behavior covaries with melanic coloration and predicts survival |
| Q63378996 | Battle of the sexes: a multi-male mating strategy helps lionesses win the gender war of fitness |
| Q63431252 | Beards augment perceptions of men's age, social status, and aggressiveness, but not attractiveness |
| Q113275623 | Bees learn preferences for plant species that offer only pollen as a reward |
| Q60311503 | Begging and cowbirds: brood parasites make hosts scream louder |
| Q56228273 | Begging and the risk of predation in nestling birds |
| Q60566050 | Begging for a better future: how far can behavioral ecologists go without specifying mechanisms? |
| Q60566053 | Begging in the absence of parents: a “quick on the trigger” strategy to minimize costly misses |
| Q59663604 | Behavioral adaptation of Pallas's squirrels to germination schedule and tannins in acorns |
| Q59256273 | Behavioral and morphological responses to perceived predation risk: a field experiment in passerines |
| Q110792808 | Behavioral and physiological consequences of nest predation pressure for larval fish |
| Q59845496 | Behavioral and physiological responses to male handicap in chick-rearing black-legged kittiwakes |
| Q113275627 | Behavioral attributes influence annual mating success more than morphological traits in male collared lizards |
| Q60463607 | Behavioral changes associated with a population density decline in the facultatively social red fox |
| Q56379264 | Behavioral changes in tadpoles after multigenerational exposure to an invasive intraguild predator |
| Q57718712 | Behavioral coexistence and feeding efficiency drive niche partitioning in European avian scavengers |
| Q56767771 | Behavioral consequences of plant invasion: an invasive plant alters rodent antipredator behavior |
| Q57236638 | Behavioral consistency and the resolution of sexual conflict over parental investment |
| Q110532035 | Behavioral diversity is maintained by a conditional strategy in a freshwater zooplankton |
| Q58832961 | Behavioral dominance between female color morphs of a Lake Victoria cichlid fish |
| Q56593187 | Behavioral drivers of communal roosting in a songbird: a combined theoretical and empirical approach |
| Q59594793 | Behavioral ecology and genomics: new directions, or just a more detailed map? |
| Q115414464 | Behavioral ecology and the successful integration of function and mechanism |
| Q60236451 | Behavioral ecology of odometric memories in desert ants: acquisition, retention, and integration |
| Q58317559 | Behavioral interference and facilitation in the foraging cycle shape the functional response |
| Q57254112 | Behavioral plasticity in larval reef fish: orientation is influenced by recent acoustic experiences |
| Q125759569 | Behavioral plasticity in nest residency compensates for inbreeding depression in male prairie voles |
| Q64922549 | Behavioral responses by an apex predator to urbanization. |
| Q113821426 | Behavioral responses of a sex-role reversed pipefish to a gradient of perceived predation risk |
| Q34532685 | Behavioral responses of wolves to roads: scale-dependent ambivalence |
| Q60564255 | Behavioral responses to changing environments |
| Q114633532 | Behavioral responses vary with prey species in the social spider, Stegodyphus sarasinorum |
| Q56933844 | Behavioral shifts associated with reproduction in garter snakes |
| Q121084492 | Behavioral strategies and signaling in interspecific aggressive interactions in gray tree frogs |
| Q60432502 | Behavioral syndrome over the boundaries of life—carryovers from larvae to adult damselfly |
| Q57003481 | Behavioral syndromes influence mating systems: floater pairs of a lizard have heavier offspring |
| Q119525377 | Behavioral syndromes vary among geographically distinct populations in a reptile |
| Q113035002 | Behavioral syndromes: carryover effects, false discovery rates, and a priori hypotheses |
| Q58486842 | Behavioral types as predictors of survival in Trinidadian guppies (Poecilia reticulata) |
| Q59620287 | Behavioral, demographic, and environmental correlates of extrapair fertilizations in eastern bluebirds, Sialia sialis |
| Q113034919 | Behavioral, energetic, and color trait integration in male guppies: testing the melanocortin hypothesis |
| Q59225097 | Beneficial effects of group size on oxidative balance in a wild cooperative breeder |
| Q56806191 | Benefits of foundress associations in the paper wasp Polistes dominulus: increased productivity and survival, but no assurance of fitness returns |
| Q57228575 | Benefits of recruitment in honey bees: effects of ecology and colony size in an individual-based model |
| Q60534357 | Better the devil you know? How familiarity and kinship affect prey responses to disturbance cues |
| Q57277749 | Better to be bimodal: the interaction of color and odor on learning and memory |
| Q60502378 | Between- and within-individual variation in activity increases with water temperature in wild perch |
| Q115543439 | Beware of bats, beware of birds: the auditory responses of eared moths to bat and bird predation |
| Q126566808 | Beyond the group: how food, mates, and group size influence intergroup encounters in wild bonobos |
| Q57087295 | Bidirectional communication system in katydids: the effect on chorus structure |
| Q124843342 | Bill morphology and neutral genetic structure both predict variation in acoustic signals within a bird population |
| Q56096291 | Bills as daggers? A test for sexually dimorphic weapons in a lekking hummingbird |
| Q105612870 | Biological market effects predict cleaner fish strategic sophistication |
| Q30559344 | Biparental incubation patterns in a high-Arctic breeding shorebird: how do pairs divide their duties? |
| Q35024901 | Biparental incubation-scheduling: no experimental evidence for major energetic constraints. |
| Q125768329 | Birds associate species-specific acoustic and visual cues: recognition of heterospecific rivals by male blackcaps |
| Q30473602 | Birds flee en mass from New Year's Eve fireworks |
| Q58202951 | Birds living near airports advance their dawn chorus and reduce overlap with aircraft noise |
| Q58486891 | Birdsong tuned to the environment: green hylia song varies with elevation, tree cover, and noise |
| Q60190994 | Birth sex ratios relate to mare condition at conception in Kaimanawa horses |
| Q56953859 | Black holes, mate retention, and the evolution of ungulate leks |
| Q113821445 | Black-and-white plumage in male pied flycatchers (Ficedula hypoleuca) reduces the risk of predation from sparrowhawks (Accipiter nisus) during the breeding season |
| Q101631695 | Blue tail and striped body: why do lizards change their infant costume when growing up? |
| Q125812992 | Body condition and food shapes group dispersal but not solitary dispersal in a social spider |
| Q101631697 | Body size and evolution of motion dazzle coloration in lizards |
| Q56882394 | Body size and sex allocation in simultaneously hermaphroditic animals |
| Q115543344 | Body spot coloration of a nocturnal sit-and-wait predator visually lures prey |
| Q63916260 | Body stores persist as fitness correlate in a long-distance migrant released from food constraints |
| Q60264401 | Bolder stickleback fish make faster decisions, but they are not less accurate |
| Q57738454 | Boldness affects foraging decisions in barnacle geese: an experimental approach |
| Q30449848 | Boldness behavior and stress physiology in a novel urban environment suggest rapid correlated evolutionary adaptation |
| Q57030821 | Boldness-aggression syndromes can reduce population density: behavior and demographic heterogeneity |
| Q61306763 | Both the past and the present affect risk-sensitive decisions of foraging rufous hummingbirds |
| Q113182302 | Bowers on the savanna: display courts and mate choice in a lekking widowbird |
| Q113035176 | Breeding colonies as information centers: a reappraisal of information-based hypotheses using the producer--scrounger game |
| Q92838730 | Breeding success but not mate choice is phenotype- and context-dependent in a color polymorphic raptor |
| Q54046488 | Breeding synchronization facilitates extrapair mating for inbreeding avoidance |
| Q60550261 | Breeding systems, climate, and the evolution of migration in shorebirds |
| Q58614263 | Bright nights and social interactions: a neglected issue |
| Q59300115 | Brood size, telomere length, and parent-offspring color signaling in barn swallows |
| Q57233937 | Brooding, provisioning, and compensatory care in the cooperatively breeding acorn woodpecker |
| Q113275634 | Built to change: dominance strategy changes with life stage in a primitively eusocial bee |
| Q56156933 | Bumble bees (Bombus terrestris) store both food and information in honeypots |
| Q125406616 | Bumblebee flower constancy and pollen diversity over time |
| Q57228447 | Bumblebees utilize floral cues differently on vertically and horizontally arranged flowers |
| Q56930335 | Burrow fractal dimension and foraging success in subterranean rodents: a simulation |
| Q35419499 | By any name, female-female competition yields differential mating success |
| Q123361589 | Cadmium does not affect post-hatching maternal care or early offspring development in earwigs |
| Q128187389 | Calling in the heat: the zebra finch incubation call depends on heat AND reproductive stage—a comment on McDiarmid et al. 2018 |
| Q111935150 | Calling in the heat: the zebra finch “incubation call” depends on heat but not reproductive stage |
| Q55072577 | Camouflaging moving objects: crypsis and masquerade. |
| Q60502036 | Can experienced birds select for Müllerian mimicry? |
| Q56593179 | Can information sharing explain recruitment to food from communal roosts? |
| Q61781981 | Can males detect the strength of sperm competition and presence of genital plugs during mate choice? |
| Q125927526 | Can mixed singing facilitate coexistence of closely related nightingale species? |
| Q115414518 | Can native predators be used as a stepping stone to reduce prey naivety to novel predators? |
| Q113821494 | Can nest predation and predator type explain variation in dispersal of adult birds during the breeding season ? |
| Q110030187 | Can ultraviolet cues function as aposematic signals? |
| Q60426762 | Cannibalism, competition, and costly care in the plainfin midshipman fish,Porichthys notatus |
| Q125723911 | Cape buffalo (Syncerus caffer caffer) social dynamics in a flood-pulsed environment |
| Q58814730 | Cape honeybees, Apis mellifera capensis, police worker-laid eggs despite the absence of relatedness benefits |
| Q57193789 | Capital or income breeding? A theoretical model of female reproductive strategies |
| Q114093526 | Captivating color: evidence for optimal stimulus design in a polymorphic prey lure |
| Q60577829 | Caribbean damselfish with varying territory quality: correlated behaviors but not a syndrome |
| Q60162669 | Carotenoid status signaling in captive and wild red-collared widowbirds: independent effects of badge size and color |
| Q60318443 | Carotenoid-based status signaling by females in the tropical streak-backed oriole |
| Q59117631 | Caste-specific symbiont policing by workers of Acromyrmex fungus-growing ants |
| Q126338274 | Categorical perception in animal communication and decision-making |
| Q115543302 | Caterpillar hair as a physical barrier against invertebrate predators |
| Q91272714 | Causes and consequences of intraspecific variation in animal responses to anthropogenic noise |
| Q113821197 | Cautious versus desperado males: predation risk affects courtship intensity but not female choice in a wolf spider |
| Q57614473 | Certainty of paternity and paternal effort in the collared flycatcher |
| Q58399581 | Chacma baboon mating markets: competitor suppression mediates the potential for intersexual exchange |
| Q115787906 | Change in flight initiation distance between urban and rural habitats following a cold winter |
| Q60465914 | Change in sex pheromone expression by nutritional shift in male cockroaches |
| Q115543343 | Changes in antipredator vigilance over time caused by a war of attrition between predator and prey |
| Q128178605 | Changing of the guard: mixed specialization and flexibility in nest defense (Tetragonisca angustula) |
| Q57260814 | Changing philosophies and tools for statistical inferences in behavioral ecology |
| Q60525579 | Cheating workers with large activated ovaries avoid risky foraging |
| Q30047801 | Chemical communication in an archaic anuran amphibian |
| Q58492485 | Chemical espionage on species-specific butterfly anti-aphrodisiacs by hitchhiking Trichogramma wasps |
| Q113821337 | Chemical footprints mediate habitat selection in co-occurring aphids |
| Q58643693 | Chemical stimuli from parents trigger larval begging in burying beetles |
| Q129501019 | Chemically mediated sexual signals restrict hybrid speciation in a flea beetle |
| Q29028758 | Chic chicks: the evolution of chick ornamentation in rails |
| Q56773197 | Choice processes in multialternative decision making |
| Q121030670 | Choosy females and indiscriminate males: mate choice in mixed populations of sexual and hybridogenetic water frogs (Rana lessonae, Rana esculenta) |
| Q56039027 | Chromatic and achromatic vision: parameter choice and limitations for reliable model predictions |
| Q113821378 | Chronic predation risk affects prey escape abilities through behavioral and physiological changes |
| Q30410809 | Cicadas impact bird communication in a noisy tropical rainforest |
| Q63360948 | Cleaner fish cause predators to reduce aggression toward bystanders at cleaning stations |
| Q63360784 | Cleaner fish coloration decreases predation risk in aggressive fangblenny mimics |
| Q64937170 | Cleaner personality and client identity have joint consequences on cleaning interaction dynamics. |
| Q61986379 | Cleaning in pairs enhances honesty in male cleaning gobies |
| Q58890582 | Closer clutch inspection—quicker egg ejection: timing of host responses toward parasitic eggs |
| Q113035163 | Clutch size variation in the Nazca booby: a test of the egg quality hypothesis |
| Q52603699 | Cognition, personality, and stress in budgerigars, Melopsittacus undulatus. |
| Q114093529 | Cold winters have morph-specific effects on natal dispersal distance in a wild raptor |
| Q113393720 | Collective aggressiveness of an ecosystem engineer is associated with coral recovery |
| Q92209562 | Collective behavior and colony persistence of social spiders depends on their physical environment |
| Q56837706 | Collective decision making in guppies: a cross-population comparison study in the wild |
| Q60319928 | Collective detection in escape responses of temporary groups of Iberian green frogs |
| Q92838738 | Collective responses to heterospecifics emerge from individual differences in aggression |
| Q59416381 | Colony genetic structure in a facultatively eusocial hover wasp |
| Q111264304 | Colony personality and plant health in the Azteca-Cecropia mutualism |
| Q29544255 | Colony structure and reproduction in the ant, Leptothorax acervorum |
| Q34767410 | Colony variation in the collective regulation of foraging by harvester ants |
| Q125755289 | Color Change from male-mimic to Gynomorphic: a New Aspect of Signaling Sexual Status in Damselflies (Odonata, Zygoptera) |
| Q57228390 | Color discrimination is not just limited by photoreceptor noise: a comment on Olsson et al |
| Q112806634 | Color lures in orb-weaving spiders: a meta-analysis |
| Q30495143 | Color signal information content and the eye of the beholder: a case study in the rhesus macaque |
| Q60459677 | Coloration of chicks modulates costly interactions among family members |
| Q57699094 | Colorful male guppies do not provide females with fecundity benefits |
| Q113034980 | Comb size and color relate to sperm quality: a test of the phenotype-linked fertility hypothesis |
| Q57888095 | Comment on Moffett: "Supercolonies of billions in an invasive ant: What is a society?" |
| Q60299026 | Comment on “Intrasexual competition among females: evidence for sexual selection” by Kimberly Rosvall |
| Q56031541 | Common waxbills use carnivore scat to reduce the risk of nest predation |
| Q126094729 | Communal and efficient movement routines can develop spontaneously through public information use |
| Q56593175 | Communal life: honest signaling and the recruitment center hypothesis |
| Q59547116 | Comparative effects of urban development and anthropogenic noise on bird songs |
| Q59835886 | Comparative manipulation of predation risk in incubating birds reveals variability in the plasticity of responses |
| Q60578502 | Comparative transitive and temporal orderliness in dominance networks |
| Q28602968 | Comparing pre- and post-copulatory mate competition using social network analysis in wild crickets |
| Q60550131 | Competition and brood reduction: testing alternative models of clutch-size evolution in parasitoids |
| Q124802742 | Competition between wild herbivores: reintroduced red deer and Apennine chamois |
| Q59621255 | Competition level determines compensatory growth abilities |
| Q63975770 | Competitor density cues for habitat quality facilitating habitat selection and investment decisions |
| Q115039433 | Complex adaptations in a multivariate trait: a comment on Caro et al. |
| Q60304659 | Complexity and behavioral ecology |
| Q128130490 | Conception risk affects in-pair and extrapair desire similarly: a comment on Shimoda et al. (2018) |
| Q37132165 | Conclusions beyond support: overconfident estimates in mixed models |
| Q128215002 | Condition dependence of (un)predictability in escape behavior of a grasshopper species |
| Q113034923 | Condition-dependent foraging strategies in a coastal seabird: evidence for the rich get richer hypothesis |
| Q56505304 | Condition-dependent resource value affects male–male competition in the blue–black grassquit |
| Q125628361 | Condition-dependent sexual reproduction is driven by benefits, not costs of sex |
| Q113275624 | Conditional helping and evolutionary transitions to eusociality and cooperative breeding |
| Q125462788 | Conditional indirect genetic effects of caregivers on brood in the clonal raider ant |
| Q114093531 | Conditional natal dispersal provides a mechanism for populations tracking resource pulses after fire |
| Q56083371 | Conditions favoring anticipatory and reactive displays deflecting predatory attack |
| Q113035142 | Conflict between sexes in the water strider, Gerris lacustris: a test of two hypotheses for male guarding behavior |
| Q128277464 | Conformity in the collective: differences in hunger affect individual and group behavior in a shoaling fish |
| Q57232175 | Confusion of predators does not rely on specialist coordinated behavior |
| Q115543485 | Consequences of complex signaling: predator detection of multimodal cues |
| Q104868630 | Consequences of natal philopatry for reproductive success and mate choice in an Alpine rodent |
| Q53417134 | Consequences of sibling rivalry vary across life in a passerine bird. |
| Q57455191 | Consistency of animal social networks after disturbance |
| Q127492451 | Consistent female preference for rare and unfamiliar male color patterns in wild guppy populations |
| Q112806651 | Consistent mixing of near and distant resources in foraging bouts by the solitary mason bee Osmia lignaria |
| Q58387771 | Consistent waves of collective vigilance in groups using public information about predation risk |
| Q113821511 | Conspecific nest parasitism is associated with inequality in nest predation risk in the common goldeneye (Bucephala clangula) |
| Q111593551 | Conspecifics enhance egg production in an egg-carrying bug |
| Q54158318 | Conspicuousness, not eye mimicry, makes "eyespots" effective antipredator signals |
| Q60319843 | Conspicuousness-dependent antipredatory behavior may counteract coloration differences in Iberian rock lizards |
| Q56286686 | Constraints on control: factors influencing reproductive success in male mandrills (Mandrillus sphinx) |
| Q113821420 | Constrating short-term and long-term effects of predation risk on consumer habitat use and resources |
| Q113390265 | Contact with caterpillar hairs triggers predator-specific defensive responses |
| Q112806645 | Contemporary sexual selection on sexually dimorphic traits in the ambush bug Phymata americana |
| Q128628787 | Contest dynamics and assessment strategies in combatant monkey beetles (Scarabaeidae: Hopliini) |
| Q60311451 | Context-, phenotype-, and kin-dependent natal dispersal of barn swallows (Hirundo rustica) |
| Q109315028 | Context-dependent coloration of prey and predator decision making in contrasting light environments |
| Q130119496 | Context-dependent costs and benefits of a heterospecific nesting association |
| Q104872663 | Context-dependent effects of carotenoid supplementation on reproduction in zebra finches |
| Q57669293 | Context-dependent male mate choice: the effects of competitor presence and competitor size |
| Q61696559 | Context-dependent mate choice in relation to social composition in green swordtails Xiphophorus helleri |
| Q61050668 | Context-dependent relationship between a composite measure of men’s mate value and ejaculate quality |
| Q128288130 | Context-dependent strategies of food allocation among offspring in a facultative cooperative breeder |
| Q115039445 | Context-dependent trait covariances: how plasticity shapes behavioral syndromes |
| Q129894529 | Context-specific learning and its implications for social learning |
| Q59197860 | Context-specific repeatability of personality traits in a wild bird: a reaction-norm perspective |
| Q115543664 | Contrasting parental color morphs increase regularity of prey deliveries in an African raptor |
| Q113821223 | Contrasting risks from different predators change the overall nonlethal effects of predation risk |
| Q56690161 | Convergent song preferences between female field crickets and acoustically orienting parasitoid flies |
| Q30051807 | Cooperation and competition in two forest monkeys |
| Q29304292 | Cooperation, conflict, and coevolution in the attine ant-fungus symbiosis |
| Q109041205 | Cooperative bird discriminates between individuals based purely on their aerial alarm calls |
| Q115543947 | Cooperatively breeding Arabian babblers call differently when mobbing in different predator-induced situations |
| Q60331496 | Coordinated parental provisioning is related to feeding rate and reproductive success in a songbird |
| Q57596570 | Coral bleaching and habitat degradation increase susceptibility to predation for coral-dwelling fishes |
| Q113821356 | Correction to: Female-biased sex ratios in urban centers create a “fertility trap” in 
post-war Finland |
| Q57269598 | Corrections for "Assessing the function of house sparrows' bib size using a flexible meta-analysis method [Behav Ecol 18: 831-840]" |
| Q124173866 | Correlates of reproductive success within alternative mating tactics of the common shrew |
| Q57614369 | Correlates of the occurrence of inbreeding in a wild bird population |
| Q115039436 | Corrigendum to: Male–male behavioral interactions drive social-dominance mediated differences in ejaculate traits |
| Q126837738 | Corrigendum to: ‘Demographic processes in animal networks are a question of time: a comment on Shizuka and Johnson’ by Adriana A. Maldonado-Chaparro and Damien R. Farine |
| Q60264389 | Corrigendum to: ‘Reciprocity and conditional cooperation between great tit parents’ by Rufus A. Johnstone, Andrea Manica, Annette L. Fayet, Mary Caswell Stoddard, Miguel A. Rodriguez-Gironés and Camilla A. Hinde. 25: 216–222 |
| Q115543667 | Corrigendum to: “Predator and prey activity levels jointly influence the outcome of long-term foraging bouts” (2013) 24:1205–1210, doi:10.1093/beheco/art052 |
| Q128056048 | Corrigendum: A mathematical model of aggressive mimicry |
| Q129920234 | Corrigendum: Reply to Sherratt and Holen: Goldilocks and the half-empty glass |
| Q60376520 | Corrigendum: Social conflict and costs of cooperation in meerkats are reflected in measures of stress hormones |
| Q130180374 | Corrigendum: Women’s emotional and sexual attraction to men across the menstrual cycle |
| Q60336978 | Corticosterone triggers high-pitched nestlings’ begging calls and affects parental behavior in the wild zebra finch |
| Q35024910 | Cortisol in mother's milk across lactation reflects maternal life history and predicts infant temperament |
| Q58202991 | Cosmetic enhancement of signal coloration: experimental evidence in the house finch |
| Q115039454 | Cost of an elaborate trait: a trade-off between attracting females and maintaining a clean ornament |
| Q60442172 | Costly interactions between the sexes: combined effects of male sexual harassment and female choice? |
| Q59599306 | Costs and benefits of colony aggregation in the social wasp, Polistes annularis |
| Q112806640 | Costs of elaborate weapons in a rhinoceros beetle: how difficult is it to fly with a big horn? |
| Q104872607 | Costs of long-term carrying of extra mass in a songbird |
| Q30053308 | Countershading enhances crypsis with some bird species but not others |
| Q92209568 | Counting crows: population structure and group size variation in an urban population of crows |
| Q56268713 | Courtship as an honest indicator of male parental quality in the bicolor damselfish, Stegastes partitus |
| Q30484568 | Courtship attention in sagebrush lizards varies with male identity and female reproductive state |
| Q30049339 | Courtship displays and coloration as indicators of safety rather than of male quality : the safety assurance hyposthesis |
| Q60529037 | Courtship in long-legged flies (Diptera: Dolichopodidae): function and evolution of signals |
| Q56690154 | Courtship song's role during female mate choice in the field cricket Teleogryllus oceanicus |
| Q130180585 | Criteria for studies of dear enemy and nasty neighbor effects: a comment on Christensen and Radford |
| Q113275621 | Cross-activity of honeybee queen mandibular pheromone in bumblebees provides evidence for sensory exploitation |
| Q60439620 | Cue choice and spatial learning ability are affected by habitat complexity in intertidal gobies |
| Q59024938 | Current brood size and residual reproductive value predict offspring desertion in the burying beetle Nicrophorus vespilloides |
| Q60463587 | Curse of the black spot: spotting negatively correlates with fitness in black grouseLyrurus tetrix |
| Q52603704 | Cut your losses: self-amputation of injured limbs increases survival. |
| Q62924876 | Cuticular hydrocarbons as potential kin recognition cues in a subsocial spider |
| Q57206055 | DNA fingerprinting reveals relation between tail ornaments and cuckoldry in barn swallows, Hirundo rustica |
| Q56209667 | Daily body mass regulation in dominance-structured coal tit (Parus ater) flocks in response to variable food access: a laboratory study |
| Q29037352 | Danger may enhance communication: predator calls alert females to male displays |
| Q41118110 | Dazzle camouflage, target tracking, and the confusion effect. |
| Q115414500 | Deactivation of dietary wariness through experience of novel food |
| Q129272078 | Dead or alive? Sexual conflict and lethal copulatory interactions in long-jawed Tetragnatha spiders |
| Q105613060 | Dear enemies or nasty neighbors? Causes and consequences of variation in the responses of group-living species to territorial intrusions |
| Q57607647 | Dear enemy phenomenon in the leaf-cutting ant Acromyrmex lobicornis: behavioral and genetic evidence |
| Q57251819 | Death comes suddenly to the unprepared: singing crickets, call fragmentation, and parasitoid flies |
| Q115543244 | Deceiving predators: linking distraction behavior with nest survival in a ground-nesting bird |
| Q61781977 | Deception down under: is Australia a hot spot for deception? |
| Q60498480 | Deception with honest signals: signal residuals and signal function in snapping shrimp |
| Q115543462 | Deceptive color signaling in the night: a nocturnal predator attracts prey with visual lures |
| Q54293728 | Deceptive use of alarm calls by male swallows, Hirundo rustica: a new paternity guard |
| Q60297582 | Decoy presentations as a means to manipulate the risk of extrapair copulation: an experimental study in a semicolonial raptor, the Montagu's harrier (Circus pygargus) |
| Q115787890 | Decreased vigilance or habituation to humans? Mechanisms on increased boldness in urban animals |
| Q126663641 | Defense against outside competition is linked to cooperation in male–male partnerships |
| Q96762561 | Defense against predators incurs high reproductive costs for the aposematic moth Arctia plantaginis |
| Q58486663 | Defensive and social aggression: repeatable but independent |
| Q125877860 | Delayed dispersal in western bluebirds: teasing apart the importance of resources and parents |
| Q60578568 | Demographic consequences of sexual selection in the long-tailed manakin |
| Q104872614 | Demographic processes in animal networks are a question of time: a comment on Shizuka and Johnson |
| Q60466679 | Density, social information, and space use in the common lizard (Lacerta vivipara) |
| Q60467372 | Density-dependent mating tactic expression is linked to stress hormone in Woodhouse's toad |
| Q58088939 | Despite reproductive interference, the net outcome of reproductive interactions among spider mite species is not necessarily costly |
| Q58388029 | Determinants of local and migratory movements of Great Lakes double-crested cormorants |
| Q113035113 | Determinants of offspring sex in kangaroos: a test of multiple hypotheses |
| Q60463597 | Determinants of yearling male lekking effort and mating success in black grouse (Tetrao tetrix) |
| Q58839067 | Determining interaction rules in animal swarms |
| Q58311829 | Determining the fitness consequences of antipredation behavior |
| Q113821418 | Developmental stability and predation success in an insect predator-prey system |
| Q60430747 | Developmental stressors that impair song learning in males do not appear to affect female preferences for song complexity in the zebra finch |
| Q57446716 | Diet affects ejaculate traits in a lizard with condition-dependent fertilization success |
| Q104368733 | Diet and provisioning rate differ predictably between dispersing and philopatric pied flycatchers |
| Q56996114 | Diet of intraguild predators affects antipredator behavior in intraguild prey |
| Q113178637 | Diet selection in birds: trade-off between energetic content and digestibility of seeds |
| Q115414515 | Dietary carotenoid pigments and immune function in a songbird with extensive carotenoid-based plumage coloration |
| Q104368912 | Dietary carotenoids affect the development of individual differences and behavioral plasticity |
| Q56420975 | Dietary protein selection in a free-ranging urban population of common myna birds |
| Q126302700 | Dietary vitamin D in female rock lizards induces condition-transfer effects in their offspring |
| Q67223558 | Differences in combinatorial calls among the 3 elephant species cannot be explained by phylogeny |
| Q56441404 | Differences in neophobia between cane toads from introduced and native populations |
| Q60501983 | Different reactions to aposematic prey in 2 geographically distant populations of great tits |
| Q113821230 | Differential effects of food availability and nest predation risk on avian reproductive strategies |
| Q115543420 | Differential effects of structural complexity on predator foraging behavior |
| Q56213556 | Differential grooming rate and tick load of territorial male and female impala, Aepyceros melampus |
| Q117788686 | Differential parasitism of native and invasive widow spider egg sacs |
| Q125823142 | Differential persistence favors habitat preferences that determine the distribution of a reef fish |
| Q113821194 | Differential predation drives the geographical divergence in multiple traits in aposematic frogs |
| Q61762089 | Direct and indirect cues of predation risk influence behavior and reproduction of prey: a case for acarine interactions |
| Q63885731 | Direct fitness benefits and kinship of social foraging groups in an Old World tropical babbler |
| Q60502019 | Direction and strength of selection by predators for the color of the aposematic wood tiger moth |
| Q59238963 | Direction matching for sparse movement data sets: determining interaction rules in social groups |
| Q115543303 | Direction of approach by predators and flight initiation distance of urban and rural populations of birds |
| Q115414521 | Discoid decorations function to shield juvenile Argiope spiders from avian predator attacks |
| Q115414502 | Discrete genetic variation in mate choice and a condition-dependent preference function in the side-blotched lizard: implications for the formation and maintenance of coadapted gene complexes |
| Q126121478 | Discrimination behavior mediates foraging quality versus quantity trade-offs: nut choice in wild rodents |
| Q128439728 | Disentangling the costs of male harassment and the benefits of polyandry for females |
| Q104206499 | Dispersal and new colony formation in wild naked mole-rats: evidence against inbreeding as the system of mating |
| Q126014161 | Dispersal and prepupation behavior of Chilean sympatric Drosophila species that breed in the same site in nature |
| Q113035149 | Dispersion of greater prairie chicken nests in relation to lek location: evaluation of the hot-spot hypothesis of lek evolution |
| Q115039412 | Disrupting information alters the behavioral response to a mutual signal trait in both sexes of Nicrophorus (Coleoptera: Silphidae) burying beetles |
| Q130149123 | Disruptive sexual selection on male body size in the polyphenic black scavenger fly Sepsis thoracica |
| Q128126089 | Distinguishing explanations for cycle shifts: a response to Shirazi et al |
| Q113821191 | Distracted decision makers: ship noise and predation risk change shell choice in hermit crabs |
| Q115543337 | Distress calls in tufted titmice (Baeolophus bicolor): are conspecifics or predators the target? |
| Q57579412 | Distress calls reflect poxvirus infection in lesser short-toed lark Calandrella rufescens |
| Q60315932 | Disturbance across an ecosystem boundary drives cannibalism propensity in a riparian consumer |
| Q115543464 | Do 3-D predators attack the margins of 2-D selfish herds? |
| Q59822411 | Do birds differentially distribute antimicrobial proteins within clutches of eggs? |
| Q58311851 | Do energetic demands constrain incubation scheduling in a biparental species? |
| Q61050617 | Do exaggerated sexual swellings function in female mating competition in primates? A comparative test of the reliable indicator hypothesis |
| Q113035171 | Do female pied flycatchers seek extrapair copulations with familiar males? A test of the incomplete knowledge hypothesis |
| Q59845520 | Do females trade copulations for food? An experimental study on kittiwakes (Rissa tridactyla) |
| Q56094929 | Do hoverflies (Diptera: Syrphidae) sound like the Hymenoptera they morphologically resemble? |
| Q61780135 | Do male golden egg bugs carry eggs they have fertilized? A microsatellite analysis |
| Q59464022 | Do male ornaments signal immunity in the common yellowthroat? |
| Q36733532 | Do men's faces really signal heritable immunocompetence? |
| Q60528951 | Do molt-migrant songbirds optimize migration routes based on primary productivity? |
| Q57551793 | Do mothers bias offspring sex ratios in carotenoid-rich environments? |
| Q60481714 | Do polyandrous pygmy grasshopper females obtain fitness benefits for their offspring? |
| Q113821216 | Do scatter hoarders trade off increased predation risks for lower rates of cache pilferage? |
| Q104368765 | Do sex-specific densities affect local survival of free-ranging great tits? |
| Q36056173 | Do the benefits of polyandry scale with outbreeding? |
| Q115543490 | Do the multiple defense chemicals of visually distinct species enhance predator learning? |
| Q127347597 | Do vampire bats groom others based on need? |
| Q128744338 | Do wolf spiders’ egg-sacs emit tactochemical signals perceived by mothers? |
| Q128722849 | Do zombie ant fungi turn their hosts into light seekers? |
| Q113034934 | Does antiparasite behavior improve with experience? An experimental test of the priming hypothesis |
| Q113034914 | Does bat response to traffic noise support the misleading cue hypothesis? |
| Q112574183 | Does brain size affect mate choice? An experimental examination in pygmy halfbeaks |
| Q117215740 | Does city life reduce neophobia? A study on wild black-capped chickadees. |
| Q113178644 | Does developmental environment affect sexual conflict? An experimental test in the seed beetle |
| Q61930396 | Does hatching failure breed infidelity? |
| Q130035825 | Does multiple paternity explain phenotypic variation among offspring in wild boar? |
| Q115543468 | Does predator swamping promote synchronous emergence of turtle hatchlings among nests? |
| Q57566021 | Does the presence of an odd individual affect group choice? |
| Q60562908 | Does water velocity influence optimal escape behaviors in stream insects? |
| Q58776324 | Dominance rank and boldness predict social attraction in great tits |
| Q56456071 | Dominance status and carcass availability affect the outcome of sperm competition in burying beetles |
| Q37090331 | Drivers and fitness consequences of dispersive migration in a pelagic seabird |
| Q127702390 | Drought decreases cooperative sentinel behavior and affects vocal coordination in meerkats |
| Q115414487 | Dual function of seminal substances for mate guarding in a ground beetle |
| Q56020464 | Duets defend mates in a suboscine passerine, the warbling antbird (Hypocnemis cantator) |
| Q57246362 | Dusk light environment optimizes visual perception of conspecifics in a crepuscular horned beetle |
| Q61375074 | Dying young and living fast: variation in life history across English neighborhoods |
| Q91437403 | Dynamic conflict among heterogeneous groups: a comment on Christensen and Radford |
| Q121096007 | Dynamic properties of the advertisement calls of gray tree frogs: patterns of variability and female choice |
| Q30657187 | Dynamics of among-individual behavioral variation over adult lifespan in a wild insect |
| Q56827871 | Early interactions with adults mediate the development of predator defenses in guppies |
| Q124852311 | Early social experience shapes female mate choice in guppies |
| Q57940522 | Early weaning in bighorn sheep, Ovis canadensis affects growth of males but not of females |
| Q60557297 | Eastern chipmunks increase their perception of predation risk in response to titmouse alarm calls |
| Q113035086 | Ecological and behavioral correlates of coloration in artiodactyls: systematic analyses of conventional hypotheses |
| Q113275625 | Ecological and genetic distribution of eusociality: the case for kin selection |
| Q59162297 | Ecological and social determinants of birth intervals in baboons |
| Q104352729 | Ecological context determines the choice between prey of different salinities |
| Q114896877 | Ecological correlates of song learning in song sparrows |
| Q56445206 | Ecological cues, gestation length, and birth timing in African buffalo (Syncerus caffer) |
| Q115041127 | Ecological drivers of variation in tool-use frequency across sea otter populations |
| Q113178643 | Ecology of fear and its effect on seed dispersal by a neotropical rodent |
| Q58791036 | Economics of mate choice at leks: do female waxmoths pay costs for indirect genetic benefits? |
| Q111631551 | Ectothermic vertebrates are too cool to care: a response to comments on Beekman et al |
| Q115543342 | Educated predators make strategic decisions to eat defended prey according to their toxin content |
| Q58423810 | Effect of an ectoparasite on lay date, nest-site choice, desertion, and hatching success in the great tit (Pants major) |
| Q57735775 | Effect of color vision phenotype on the foraging of wild white-faced capuchins, Cebus capucinus |
| Q30388014 | Effect of competitive cues on reproductive morphology and behavioral plasticity in male fruitflies. |
| Q113034957 | Effect of flower visual angle on flower constancy: a test of the search image hypothesis |
| Q60521722 | Effect of parasite-induced behavioral alterations on juvenile development |
| Q115543422 | Effect of predation risk, body size, and habitat characteristics on emigration decisions in mallards |
| Q114633534 | Effect of prey personality depends on predator species |
| Q115543258 | Effectiveness of social information used by seabirds searching for unpredictable and ephemeral prey |
| Q37387367 | Effects of age and experience on contest behavior in the burying beetle, Nicrophorus vespilloides |
| Q35024906 | Effects of age, size, and mating history on sex role decision of a simultaneous hermaphrodite |
| Q59835900 | Effects of ambient temperature on avian incubation behavior |
| Q115543438 | Effects of autotomy and regeneration on detection and capture of prey in a generalist predator |
| Q104206491 | Effects of begging on growth rates of nestling chicks |
| Q57206042 | Effects of breeding density, synchrony, and experience on extrapair paternity in tree swallows |
| Q113821382 | Effects of chronic and acute predation risk on sexual ornamentation and mating preferences |
| Q59211124 | Effects of cortisol administration on cooperative behavior in meerkat helpers |
| Q129631435 | Effects of experimental anthropogenic noise on avian settlement patterns and reproductive success |
| Q115543560 | Effects of food value, predation risk, and pilferage on the caching decisions of Dipodomys merriami |
| Q58726249 | Effects of foraging and sexual selection on ecomorphology of a fish with alternative reproductive tactics |
| Q60297512 | Effects of human activity on physiological and behavioral responses of an endangered steppe bird |
| Q54046851 | Effects of intra- and interspecific brood parasitism on a precocial host, the canvasback, Aythya valisineria |
| Q57671693 | Effects of juvenile infection on adult immunity and secondary sexual characters in a wolf spider |
| Q57827750 | Effects of load-lightening and delayed extrapair benefits on the fitness consequences of helping behavior |
| Q91755393 | Effects of manipulated levels of predation threat on parental provisioning and nestling begging |
| Q57614282 | Effects of neighbor familiarity on reproductive success in the great tit (Parus major) |
| Q56689021 | Effects of novelty and gregariousness in survival of aposematic prey |
| Q127936127 | Effects of ovarian fluid on sperm traits and its implications for cryptic female choice in zebrafish |
| Q129802782 | Effects of past mating behavior versus past ejaculation on male mate choice and male attractiveness |
| Q60439713 | Effects of predation pressure on the cognitive ability of the poeciliid Brachyraphis episcopi |
| Q113182301 | Effects of predation risk and group dynamics on white-tailed deer foraging behavior in a longleaf pine savanna |
| Q113821505 | Effects of predation risk on diurnal mass dynamics and foraging routines of yellowhammers (Emberiza citrinella) |
| Q113821207 | Effects of predation risk on group size, vigilance, and foraging behavior in an African ungulate community |
| Q60242949 | Effects of predator behavior and proximity on risk assessment by Columbian black-tailed deer |
| Q114093517 | Effects of resource availability on the web structure of female western black widows: is the web structure constrained by physiological trade-offs? |
| Q56601653 | Effects of resource holding potential and resource value on tenure at nest sites in sand gobies |
| Q56882398 | Effects of risk assessment, predator behavior, and habitat on escape behavior in Columbian black-tailed deer |
| Q56386383 | Effects of sex, body size, temperature, and location on the antipredator tactics of free-ranging gartersnakes (Thamnophis sirtalis, Colubridae) |
| Q59185257 | Effects of simultaneous polyandry on offspring fitness in an African tree frog |
| Q57196930 | Effects of trail gradient on leaf tissue transport and load size selection in leaf-cutter ants |
| Q57705935 | Effects of water-level fluctuations on the littoral benthic fish community in lakes: a mesocosm experiment |
| Q127855792 | Egg discrimination is mediated by individual differences in queen olfactory responsiveness and boldness |
| Q123161477 | Egg ejection risk and hatching asynchrony predict egg mass in a communally breeding cuckoo, the Greater Ani (Crotophaga major) |
| Q54046165 | Egg puncturing by the brood parasitic Greater Honeyguide and potential host counteradaptations |
| Q112667125 | Egg size and reproductive allocation in eusocial thrips |
| Q111896245 | Egg trading in the simultaneously hermaphroditic polychaete worm Ophryotrocha gracilis (Huth) |
| Q124173852 | Ejaculate allocation under varying sperm competition risk in the house mouse, Mus musculus domesticus |
| Q58042134 | Ejaculate size, second male size, and moderate polyandry increase female fecundity in a seed beetle |
| Q54045233 | Elaborate ornaments are costly to maintain: evidence for high maintenance handicaps |
| Q60330325 | Elevated spring testosterone increases parasite intensity in male red grouse |
| Q126202582 | Elevation-related difference in serial reversal learning ability in a nonscatter hoarding passerine |
| Q56432241 | Emasculation to plug up females: the significance of pedipalp damage in Nephila fenestrata |
| Q60333569 | Endogenous testosterone is not associated with the trade-off between paternal and mating effort |
| Q123111971 | Energetic cost of behavioral thermoregulation in turtle embryos |
| Q114152181 | Environment and mate attractiveness in a wild insect |
| Q60564290 | Environment-dependent use of mate choice cues in sticklebacks |
| Q29399453 | Environmental and social influences on calling effort in the prairie mole cricket (Gryllotalpa major) |
| Q128494390 | Environmental constraints on size-dependent signaling affects mating and rival interactions |
| Q52603717 | Environmental heterogeneity and population differences in blue tits personality traits. |
| Q61474623 | Environmental interference: impact of acoustic noise on seismic communication and mating success |
| Q113821372 | Environmental variability as a predictor of behavioral flexibility in urban environments |
| Q56999601 | Epigenetics for behavioral ecologists |
| Q109231173 | Equivalent effect of UV coloration and vibratory signal on mating success in a jumping spider |
| Q59238980 | Estrous synchrony in a nonseasonal breeder: adaptive strategy or population process? |
| Q57199238 | European barn swallows use melanin pigments to color their feathers brown |
| Q56940647 | Evading invaders: the effectiveness of a behavioral response acquired through lifetime exposure |
| Q62064602 | Everybody needs somebody: unequal parental effort in little penguins |
| Q55924129 | Evidence for MHC-correlated perfume preferences in humans |
| Q60264393 | Evidence for conditional cooperation: a response to Schlicht et al |
| Q115787886 | Evidence for differing trajectories of songs in urban and rural populations |
| Q129197165 | Evidence for dominant males but not choosy females in an insular rock iguana |
| Q115543190 | Evidence for nonconsumptive effects from a large predator in an ungulate prey? |
| Q57272253 | Evidence for the signaling function of egg color in the pied flycatcher Ficedula hypoleuca |
| Q61502491 | Evidence versus speculation on the validity of methods for measuring masculinity preferences: comment on Scott et al |
| Q56210175 | Evolution of alternative mating tactics: conditional versus mixed strategies |
| Q56953886 | Evolution of black grouse leks: female preferences benefit males in larger leks |
| Q63646422 | Evolution of defense against depletion of local food resources in a mechanistic foraging model |
| Q37599184 | Evolution of elaborate parental care: phenotypic and genetic correlations between parent and offspring traits. |
| Q61609305 | Evolution of female mating preferences in stalk-eyed flies |
| Q56675007 | Evolution of parental roles in provisioning birds: diet determines role asymmetry in raptors |
| Q56391373 | Evolutionarily stable stealing: game theory applied to kleptoparasitism |
| Q58717117 | Evolving through day and night: origin and diversification of activity pattern in modern primates |
| Q57483665 | Exaggerated rostra as weapons and the competitive assessment strategy of male giraffe weevils |
| Q33650904 | Examination of prior contest experience and the retention of winner and loser effects. |
| Q94560363 | Experience modulates an insect's response to anthropogenic noise |
| Q115543243 | Experience with predators shapes learning rules in larval amphibians |
| Q91437426 | Experimental cross-fostering of eggs reveals effects of territory quality on reproductive allocation |
| Q104873000 | Experimental evidence for a causal effect of pair-bond duration on reproductive performance in oystercatchers (Haematopus ostralegus) |
| Q57669389 | Experimental evidence for a seasonal shift in the strength of a female mating preference |
| Q104872904 | Experimental evidence for interference competition in oystercatchers, Haematopus ostralegus. I. Captive birds |
| Q104872907 | Experimental evidence for interference competition in oystercatchers, Haematopus ostralegus. II. Free-living birds |
| Q30577689 | Experimental evidence of impacts of an invasive parakeet on foraging behavior of native birds. |
| Q57272249 | Experimental evidence that egg color indicates female condition at laying in a songbird |
| Q90446384 | Experimental field evidence that out-group threats influence within-group behavior |
| Q55895447 | Experimental manipulation of maternal effort produces differential effects in sons and daughters: implications for adaptive sex ratios in the blue-footed booby |
| Q115543660 | Experimental predator intrusions in a cooperative breeder reveal threat-dependent task partitioning |
| Q113821405 | Experimental shelter-switching shows shelter type alters predation on caterpillars (Hesperiidae) |
| Q113035030 | Experimental support for the makeup hypothesis in nestling tawny owls (Strix aluco) |
| Q126096911 | Experimental traffic noise attracts birds during the breeding season |
| Q91755378 | Experimentally induced antipredator responses are mediated by social and environmental factors |
| Q56442031 | Experiments with Elasmucha grisea L. (Heteroptera: Acanthosomatidae): does a female parent bug lay as many eggs as she can defend? |
| Q59599262 | Exploiting new terrain: an advantage to sociality in the slime mold Dictyostelium discoideum |
| Q37529954 | Exploration is dependent on reproductive state, not social state, in a cooperatively breeding bird |
| Q56971845 | Exploration of environmental changes relates to lifestyle |
| Q57699052 | Exploring simultaneous allocation to mating effort, sperm production, and body growth in male guppies |
| Q61954700 | Exposing the behavioral gambit: the evolution of learning and decision rules |
| Q125564431 | Exposure to elevated temperature during development affects bumblebee foraging behavior |
| Q57699063 | Expression of pre- and postcopulatory traits under different dietary conditions in guppies |
| Q126672245 | Extra-pair mating opportunities mediate parenting and mating effort trade-offs in a songbird |
| Q93012983 | Extrapair mating and the strength of sexual selection: insights from a polymorphic species |
| Q56432242 | Extrapair paternity and egg hatchability in tree swallows: evidence for the genetic compatibility hypothesis? |
| Q108685638 | Extrapair paternity and genetic similarity—we are not quite there yet: a response to comments on Arct et al |
| Q55969751 | Extrapair paternity and the evolution of bird song |
| Q58376764 | Extrapair paternity and the opportunity for sexual selection in long-distant migratory passerines |
| Q57206488 | Extrapair paternity in Mediterranean blue tits: socioecological factors and the opportunity for sexual selection |
| Q58867292 | Extrapair paternity in an insular population of house sparrows after the experimental introduction of individuals from the mainland |
| Q56210342 | Extrapair paternity in the great tit (Parus major): a test of the “good genes” hypothesis |
| Q98224097 | Extraterritorial forays by great tits are associated with dawn song in unexpected ways |
| Q61781984 | Extreme short-term repeatability of male courtship performance in a tropical orb-web spider |
| Q57486436 | Eye for an eyespot: how iridescent plumage ocelli influence peacock mating success |
| Q30529630 | Eyespot display in the peacock butterfly triggers antipredator behaviors in naïve adult fowl |
| Q128124216 | Facing death together: heterospecific aggregations of blowfly larvae evince mutual benefits |
| Q114093527 | Factors influencing dispersal initiation and timing in a facultative cooperative breeder |
| Q54642899 | Facultative paternal investment in the polyphenic beetle Onthophagus taurus: the role of male morphology and social context |
| Q56387734 | Facultative response to a kleptoparasite by the cooperatively breeding pied babbler |
| Q117472151 | Failed despots and the equitable distribution of fitness in a subsidized species |
| Q60487931 | False feeding: the trade-off between chick hunger and caregivers needs in cooperative crows |
| Q60398514 | Familiarity mediates equitable social associations in guppies |
| Q60299079 | Family conflict and the evolution of sociality in reptiles |
| Q108685640 | Family living: an overlooked but pivotal social system to understand the evolution of cooperative breeding |
| Q113821400 | Fast food in the city? Nomadic flying-foxes commute less and hang around for longer in urban areas |
| Q115787892 | Fat and happy in the city: Eastern chipmunks in urban environments |
| Q115543245 | Fear of the human “super predator” far exceeds the fear of large carnivores in a model mesocarnivore |
| Q30494096 | Feeding decisions of eastern bluebirds are situationally influenced by fledgling plumage color |
| Q37090324 | Feeding habitat quality and behavioral trade-offs in chimpanzees: a case for species distribution models |
| Q57236881 | Feeding preferences in 2 disjunct populations of tiger snakes, Notechis scutatus (Elapidae) |
| Q126567706 | Female Assamese macaques bias their affiliation to paternal and maternal kin |
| Q30475609 | Female Lincoln's sparrows modulate their behavior in response to variation in male song quality |
| Q58643627 | Female Soay sheep do not adjust their maternal care behaviour to the quality of their home range |
| Q29398540 | Female and male Texas cichlids (Herichthys cyanoguttatum) do not fight by the same rules |
| Q60430739 | Female androgen levels--what are the selective pressures in birds? A comment on Goymann and Wingfield |
| Q57605244 | Female anoles display less but attack more quickly than males in response to territorial intrusions |
| Q61954711 | Female assessment: cheap tricks or costly calculations? |
| Q59464156 | Female choice and male humoral immune response in the lekking great snipe (Gallinago media) |
| Q60308884 | Female choice for optimal combinations of multiple male display traits increases offspring survival |
| Q67235674 | Female choice for related males in wild red-backed toadlets (Pseudophryne coriacea) |
| Q115414513 | Female collared flycatchers learn to prefer males with an artificial novel ornament |
| Q59447059 | Female eviction, abortion, and infanticide in banded mongooses (Mungos mungo): implications for social control of reproduction and synchronized parturition |
| Q115543818 | Female greater wax moths reduce sexual display behavior in relation to the potential risk of predation by echolocating bats |
| Q56429097 | Female hunger can explain variation in cannibalistic behavior despite male sacrifice in redback spiders |
| Q56287980 | Female mate choice and male red coloration in a natural three-spined stickleback (Gasterosteus aculeatus) population |
| Q113178638 | Female mating preferences for male morphological traits used in species and mate recognition in the Mexican sailfin mollies, Poecilia velifera and Poecilia petenensis |
| Q113821192 | Female mosquitoes disperse further when they develop under predation risk |
| Q57699088 | Female ornamentation and directional male mate preference in the rock sparrow |
| Q129856441 | Female ornamentation is associated with elevated aggression and testosterone in a tropical songbird |
| Q58791125 | Female pheromonal chorusing in an arctiid moth, Utetheisa ornatrix |
| Q56209835 | Female plumage spottiness signals parasite resistance in the barn owl (Tyto alba) |
| Q29304871 | Female praying mantids use sexual cannibalism as a foraging strategy to increase fecundity |
| Q115414509 | Female preference for complex/novel signals in a spider |
| Q56639664 | Female preference for fast-rate, high-pitched calls in Hermann's tortoises Testudo hermanni |
| Q56287850 | Female preference for male color is necessary and sufficient for assortative mating in 2 cichlid sister species |
| Q115414440 | Female preference for novel males constrains the contemporary evolution of assortative mating in guppies |
| Q115414531 | Female preference function related to precedence effect in an amphibian anuran (Alytes cisternasii): tests with non-overlapping calls |
| Q115414534 | Female preference functions based on call duration in the gray tree frog (Hyla versicolor) |
| Q56690157 | Female preferences for acoustic and olfactory signals during courtship: male crickets send multiple messages |
| Q57064982 | Female preferences for facial masculinity are probably not adaptations for securing good immunocompetence genes |
| Q56213636 | Female reproductive success in bottlenose dolphins (Tursiops sp.): life history, habitat, provisioning, and group-size effects |
| Q24657465 | Female reproductive synchrony predicts skewed paternity across primates |
| Q60442642 | Female reproductive tactics in a sex-role reversed pipefish: scanning for male quality and number |
| Q57561624 | Female sexual selection in light of the Darwin–Bateman paradigm |
| Q57955151 | Female signals enhance the efficiency of mate assessment in satin bowerbirds (Ptilonorhynchus violaceus) |
| Q58771211 | Female sociality and kin discrimination in brood parasitism: unrelated females fight over egg laying |
| Q126862569 | Female solo song and duetting are associated with different territoriality in songbirds |
| Q122643470 | Female túngara frogs elicit more complex mating signals from males |
| Q120913021 | Female túngara frogs vary in commitment to mate choice |
| Q113821407 | Female-biased sex ratios in urban centers create a “fertility trap” in post-war Finland |
| Q60551099 | Female-solicited extrapair matings in Humboldt penguins fail to produce extrapair fertilizations |
| Q60308881 | Female-specific ornamentation predicts offspring quality in the striped plateau lizard, Sceloporus virgatus |
| Q57257583 | Females as mobile resources: communal roosts promote the adoption of lek breeding in a temperate bat |
| Q105940259 | Females call the shots: breeding dispersal and divorce in blue tits |
| Q60277422 | Females decide whether size matters: plastic mate preferences tuned to the intensity of male–male competition |
| Q60551839 | Females increase egg deposition in favor of large males in the rainbowfish, Melanotaenia australis |
| Q127515625 | Females of a cannibalistic spider control mutilation of their genitalia by males |
| Q57009343 | Fetal sex ratio variation in the highly polygynous Himalayan tahr: evidence for differential male mortality |
| Q128622869 | Fighting in rounds: males of a neotropical cricket switch assessment strategies during contests |
| Q112736036 | Fighting over defense chemicals disrupts mating behavior |
| Q107989364 | Fine-scale habitat selection limits trade-offs between foraging and temperature in a grassland bird |
| Q115543493 | Fine-scale substrate use by a small sit-and-wait predator |
| Q125261794 | Fire-driven behavioral response to smoke in a Mediterranean lizard |
| Q57579451 | First evidence of sex differences in the duration of avian embryonic period: consequences for sibling competition in sexually dimorphic birds |
| Q114633541 | First explorations: ontogeny of central place foraging directions in two tropical seabirds |
| Q56551796 | Fitness consequences of cannibalism in the fall armyworm, Spodoptera frugiperda |
| Q56689054 | Fitness consequences of helping behavior in the western bluebird |
| Q58486923 | Fitness consequences of personality: a meta-analysis |
| Q55934104 | Fitness costs and benefits of cowbird egg ejection by gray catbirds |
| Q128610426 | Fitness costs of mating with preferred females in a scramble mating system |
| Q115543198 | Flash behavior increases prey survival |
| Q60298741 | Flesh flies regulate the consumption of 3 macronutrients to maximize lifespan and egg production |
| Q113821239 | Flexible alarm calling in meerkats: the role of the social environment and predation urgency |
| Q60483568 | Flexible alternative mating tactics by New Zealand giraffe weevils |
| Q115543271 | Flexible color learning in an invertebrate predator:Habronattusjumping spiders can learn to prefer or avoid red during foraging |
| Q30010561 | Flexible compensation of uniparental care: female poison frogs take over when males disappear |
| Q127440443 | Flexible polyandry in female flies is an adaptive response to infertile males |
| Q29040626 | Flexible social structure of a desert rodent, Rhombomys opimus: philopatry, kinship, and ecological constraints |
| Q28674350 | Flight calls signal group and individual identity but not kinship in a cooperatively breeding bird |
| Q60430772 | Flight, fitness, and sexual selection: a response |
| Q113821190 | Flirting with danger: predation risk interacts with male condition to influence sexual display |
| Q129150311 | Floral community predicts pollinators’ color preference: implications for Batesian floral mimicry |
| Q57638533 | Flower signal variability overwhelms receptor-noise and requires plastic color learning in bees |
| Q58486852 | Flush early and avoid the rush: a general rule of antipredator behavior? |
| Q115041122 | Food abundance, prey morphology, and diet specialization influence individual sea otter tool use |
| Q118180492 | Food availability and offspring demand influence sex-specific patterns and repeatability of parental provisioning |
| Q57651275 | Food availability and offspring sex in a monogamous seabird: insights from an experimental approach |
| Q124852331 | Food availability and parasite infection influence mating tactics in guppies (Poecilia reticulata) |
| Q125321124 | Food availability modulates differences in parental effort between dispersing and philopatric birds |
| Q56875250 | Food division in the Arabian babbler nest: adult choice or nestling competition? |
| Q105612864 | Food limitation increases aggression in juvenile meerkats |
| Q61546922 | Food resources, chemical signaling, and nest mate recognition in the ant Formica aquilonia |
| Q61956957 | Food sharing: a model of manipulation by harassment |
| Q60254996 | Food stress during juvenile and maternal development shapes natal and breeding dispersal in a spider |
| Q61609095 | Food-sharing vampire bats are more nepotistic under conditions of perceived risk |
| Q58317575 | Foraging among cannibals and kleptoparasites: effects of prey size on pike behavior |
| Q61761950 | Foraging behavior of egg parasitoids exploiting chemical information |
| Q56171572 | Foraging dynamics of bumble bees: correlates of movements within and between plant species |
| Q34159746 | Foraging for carotenoids: do colorful male hihi target carotenoid-rich foods in the wild? |
| Q109041156 | Foraging guild influences dependence on heterospecific alarm calls in Amazonian bird flocks |
| Q109041160 | Foraging in groups allows collective predator detection in a mammal species without alarm calls |
| Q115414449 | Foraging sparrows exhibit individual differences but not a syndrome when responding to multiple kinds of novelty |
| Q58489745 | Foraging strategies as a function of season and rank among wild female chimpanzees (Pan troglodytes) |
| Q113821417 | Foraging to balance conflicting demands: novel insights from grasshoppers under predation risk |
| Q60488348 | Forewing pigmentation predicts migration distance in wild-caught migratory monarch butterflies |
| Q56047501 | Forum |
| Q60465910 | Frequently mated males have higher protein preference in German cockroaches |
| Q115414460 | Frugivorous bats evaluate the quality of social information when choosing novel foods |
| Q115414511 | Function of being colorful in web spiders: attracting prey or camouflaging oneself? |
| Q115414455 | Function of copulatory plugs in house mice: mating behavior and paternity outcomes of rival males |
| Q115414505 | Function of pair duets in the eastern whipbird: cooperative defense or sexual conflict? |
| Q104368915 | Functional relations between body mass and risk-taking behavior in wild great tits |
| Q127745869 | Further mismeasures of animal contests: a new framework for assessment strategies |
| Q114633531 | Game of webs: species and web structure influence contest outcome in black widow spiders |
| Q127435519 | Game theory models of animal contests: are we at a standstill?: a comment on Chapin et al. |
| Q55922754 | Gape coloration reliably reflects immunocompetence of barn swallow (Hirundo rustica) nestlings |
| Q115414435 | Gender-related behaviors: evidence for a trade-off between sexual functions in a hermaphrodite |
| Q63379872 | Gene expression shifts in yellow-bellied marmots prior to natal dispersal |
| Q125289994 | Generalization in mate-choice copying in humans |
| Q90446460 | Generalization of learned preferences covaries with behavioral flexibility in red junglefowl chicks |
| Q56935479 | Genetic analysis of the mating system and opportunity for sexual selection in northern water snakes (Nerodia sipedon) |
| Q60560964 | Genetic and plastic components of divergent male intersexual behavior in Misty lake/stream stickleback |
| Q115414477 | Genetic diversity, colony chemical phenotype, and nest mate recognition in the ant Formica fusca |
| Q56020427 | Genetic evidence for kin-based female social structure in common eiders (Somateria mollissima) |
| Q94560368 | Genetic monogamy despite frequent extrapair copulations in "strictly monogamous" wild jackdaws |
| Q56019183 | Genetic monogamy in blue-headed vireos and a comparison with a sympatric vireo with extrapair paternity |
| Q125663110 | Genetic relatedness and sex predict helper provisioning effort in the cooperatively breeding noisy miner |
| Q124969568 | Genetic relatedness delineates the social structure of southern Australian bottlenose dolphins |
| Q108685642 | Genetic similarity between mates predicts extrapair paternity—a meta-analysis of bird studies |
| Q60337020 | Genetic similarity is broadly associated with genetic polyandry in birds: a comment on Arct et al |
| Q60162775 | Genetic variation in worker temporal polyethism and colony defensiveness in the honey bee, Apis mellifera |
| Q123153231 | Genetic, prenatal, and postnatal correlates of dispersal in hatchling fence lizards (Sceloporus occidentalis) |
| Q29543232 | Genital damage in the orb-web spider Argiope bruennichi (Araneae: Araneidae) increases paternity success |
| Q91437419 | Genomic analysis of MHC-based mate choice in the monogamous California mouse |
| Q113347182 | Geographic variation in dispersal of western burrowing owl (Athene cunicularia hypugaea) populations across North America |
| Q36455875 | Geometric analysis of macronutrient selection in breeds of the domestic dog, Canis lupus familiaris |
| Q57435546 | Get off my lawn: increased aggression in urban song sparrows is related to resource availability |
| Q56332796 | Get smart: native mammal develops toad-smart behavior in response to a toxic invader |
| Q116041962 | Glow-worm larvae bioluminescence (Coleoptera: Lampyridae) operates as an aposematic signal upon toads (Bufo bufo) |
| Q117194735 | Glow-worm larvae bioluminescence (Coleoptera: Lampyridae) operates as an aposematic signal upon toads (Bufo bufo) |
| Q128119571 | Gone with the rain: negative effects of rainfall on male reproductive success in a nest-building arachnid |
| Q57607616 | Gone with the wind: short- and long-term responses of leaf-cutting ants to the negative effect of wind on their foraging activity |
| Q128611894 | Great spotted cuckoos disregard information on conspecific breeding success while parasitizing magpie hosts |
| Q126577111 | Great spotted cuckoos show dynamic patterns of host selection during the breeding season. The importance of laying stage and parasitism status of magpie nests |
| Q63437929 | Greater precision, not parsimony, is the key to testing the peri-ovulation spandrel hypothesis: a response to comments on Havliček et al. 2015 |
| Q56688665 | Green symphonies or wind in the willows? Testing acoustic communication in plants |
| Q28681675 | Green symphonies: a call for studies on acoustic communication in plants |
| Q112586832 | Gregariousness, foraging effort, and affiliative interactions in lactating bonobos and chimpanzees |
| Q56389380 | Ground squirrel sociality and the quest for the ‘holy grail’: does kinship influence behavioral discrimination by juvenile Columbian ground squirrels? |
| Q56268439 | Group defense by colony-founding queens in the fire ant Solenopsis invicta |
| Q58486493 | Group size affects social relationships in yellow-bellied marmots (Marmota flaviventris) |
| Q113821448 | Group size and predation risk in colonial web-building spiders: analysis of attack abatement mechanisms |
| Q126063050 | Group size and social status affect scent marking in dispersing female meerkats |
| Q56391344 | Group size effect caused by food competition in nutmeg mannikins (Lonchura punctulata) |
| Q29308499 | Group stability and homing behavior but no kin group structures in a coral reef fish |
| Q60564262 | Habitat alteration influences male signalling effort in the Australian desert goby |
| Q57742162 | Habitat assessment by parasitoids: mechanisms for patch use behavior |
| Q113821327 | Habitat change alters the expression and efficiency of a female ornament |
| Q60566041 | Habitat choice and complex decision making in a trap-building predator |
| Q115414520 | Habitat complexity and complex signal function – exploring the role of ornamentation |
| Q121306362 | Habitat disturbance alters color contrast and the detectability of cryptic and aposematic frogs |
| Q112341232 | Habitat features and colony characteristics influencing ant personality and its fitness consequences |
| Q115543186 | Habitat geometry and limited perceptual range affect habitat choice of a trap-building predator |
| Q60298868 | Habitat saturation promotes delayed dispersal in a social reptile |
| Q60483559 | Habitat selection in a deceptive predator: maximizing resource availability and signal efficacy |
| Q109041124 | Habitat structure and alarm call dialects in Gunnison's prairie dog (Cynomys gunnisoni) |
| Q115543472 | Habitat use and movements of plains zebra (Equus burchelli) in response to predation danger from lions |
| Q111376723 | Habitat-dependent acoustic divergence affects playback response in urban and forest populations of the European blackbird |
| Q60631297 | Habitat-mediated effects of diurnal and seasonal migration strategies on juvenile salmon survival |
| Q121359205 | Habitat-specific constraints on induced hatching in a treefrog with reproductive mode plasticity |
| Q115787896 | Habituation to human disturbance is faster in urban than rural house sparrows |
| Q56880111 | Hatching asynchrony in the house wren, Troglodytes aedon: a test of the brood-reduction hypothesis |
| Q59197876 | Hatching asynchrony is an individual property of female Ural owls which improves nestling survival |
| Q122924580 | Hatching asynchrony, nestling competition, and the cost of interspecific brood parasitism |
| Q123273372 | Hatching hierarchy but not egg-related effects governs behavioral phenotypes in gull chicks |
| Q59746856 | Hatching order and size-dependent mortality in relation to brood sex ratio composition in chinstrap penguins |
| Q122722586 | Hatching order explains an extrapair chick advantage in western bluebirds |
| Q115543284 | Hawk models, hawk mimics, and antipredator behavior of prey |
| Q104680252 | Heat wave effects on the behavior and life-history traits of sedentary antlions |
| Q113821249 | Heat-conserving postures hinder escape: a thermoregulation–predation trade-off in wintering birds |
| Q60331540 | Helpers increase long-term but not short-term productivity in cooperatively breeding long-tailed tits |
| Q55967707 | Helping opportunities and space segregation in cooperatively breeding cichlids |
| Q98612738 | Heritability and correlations among learning and inhibitory control traits |
| Q58486926 | Heterospecific eavesdropping in a nonsocial species |
| Q60557291 | Heterospecific information about predation risk influences exploratory behavior |
| Q55919115 | Heterospecific mating preferences for a feather ornament in least auklets |
| Q58486498 | Heterospecific nonalarm vocalizations enhance risk assessment in common mynas |
| Q63372833 | Hidden Markov analysis describes dive patterns in semiaquatic animals |
| Q61781973 | Hidden in plain orange: aposematic coloration is cryptic to a colorblind insect predator |
| Q115543315 | Hide and seek: properties of prey and background patterns affect prey detection by blue tits |
| Q59846184 | Hiding in plain sight: a study on camouflage and habitat selection in a slow-moving desert herbivore |
| Q90635548 | Hierarchically embedded interaction networks represent a missing link in the study of behavioral and community ecology |
| Q117215741 | High background risk induces risk allocation rather than generalized neophobia in the fathead minnow |
| Q56228698 | High frequency of polyandry in a lek mating system |
| Q129903139 | High male density favors maintenance over reproduction in a butterfly |
| Q57655575 | High resource valuation fuels “desperado” fighting tactics in female jumping spiders |
| Q115041137 | Honest advertisement and song output during the dawn chorus of black-capped chickadees |
| Q109041154 | Honest begging: expanding from Signal of Need |
| Q109041146 | Honest begging: signals of need, quality, and/or hunger? |
| Q109041126 | Honest signaling of cooperative intentions |
| Q113034033 | Honeybee guards do not use food-derived odors to recognize non-nest mates: a test of the Odor Convergence hypothesis |
| Q111264303 | Horizontal partner exchange does not preclude stable mutualism in fungus-growing ants |
| Q54642898 | Horn polyphenism in the beetle Onthophagus taurus: larval diet quality and plasticity in parental investment determine adult body size and male horn morphology |
| Q55953334 | Host life-history strategies and the evolution of chick-killing by brood parasitic offspring |
| Q59241014 | Host location by visual and olfactory floral cues in an oligolectic bee: innate and learned behavior |
| Q60442164 | Host species of a sexual-parasite do not differentiate between clones of Amazon mollies |
| Q113275622 | How a generalist bee achieves high efficiency of pollen collection on diverse floral resources |
| Q105612856 | How and why are some species so smart? A comment on Rowe and Healy |
| Q56084291 | How colorful are birds? Evolution of the avian plumage color gamut |
| Q127876860 | How demographic processes shape animal social networks |
| Q56769968 | How depth alters detection and capture of buried prey: exploitation of sea turtle eggs by mongooses |
| Q109041176 | How do biparental species optimally provision young when begging is honest? |
| Q59394335 | How does a diurnal hawkmoth find nectar? Differences in sensory control with a nocturnal relative |
| Q109041164 | How does honest costly signaling work? |
| Q60302155 | How good does our map of knowledge have to be?: comment on Berger-Tal et al |
| Q57273093 | How much should reproduction cost? |
| Q55328266 | How partnerships end in guillemots Uria aalge: chance events, adaptive change, or forced divorce? |
| Q58803721 | How site fidelity leads to individual differences in the foraging activity of harvester ants |
| Q125389677 | How size and conspicuousness affect the efficacy of flash coloration |
| Q58299364 | Human behavioral ecology and its evil twin |
| Q58292590 | Human behavioral ecology: current research and future prospects |
| Q59162168 | Human observers impact habituated samango monkeys’ perceived landscape of fear |
| Q59221889 | Human perception of fighting ability: facial cues predict winners and losers in mixed martial arts fights |
| Q63437874 | Human preference for masculinity differs according to context in faces, bodies, voices, and smell |
| Q104368916 | Human recreation reduces clutch size in great tits Parus major regardless of risk-taking personality |
| Q60564299 | Human-induced water turbidity alters selection on sexual displays in sticklebacks |
| Q61306675 | Hummingbirds choose not to rely on good taste: information use during foraging |
| Q56228279 | Humoral immunocompetence correlates with date of egg-laying and reflects work load in female tree swallows |
| Q61556835 | Hungry females show stronger mating preferences |
| Q115543408 | Hunting efficiency and predation risk shapes the color-associated foraging traits of a predator |
| Q58317520 | Ice cover alters the behavior and stress level of brown trout Salmo trutta |
| Q59845487 | Identifying the selective pressures underlying offspring sex-ratio adjustments: a case study in a wild seabird |
| Q57275166 | If everything is special, is anything special? A response to comments on Bailey et al |
| Q104368803 | Immediate and carry-over effects of perceived predation risk on communication behavior in wild birds |
| Q130195638 | Immigrant song: males and females learn songs after dispersal in a tropical bird |
| Q57267707 | Immigration and dispersal are key determinants of cultural diversity in a songbird population |
| Q129129640 | Immune challenge induces terminal investment at an early breeding stage in female zebra finches |
| Q56267809 | Immune challenge mediates vocal communication in a passerine bird: an experiment |
| Q60311568 | Immune response covaries with corticosterone plasma levels under experimentally stressful conditions in nestling barn swallows (Hirundo rustica) |
| Q58486859 | Immune system activation affects song and territorial defense |
| Q110035469 | Immunocompetence and resource holding potential in the damselfly, Calopteryx virgo L |
| Q113034949 | Immunocompetence handicap hypothesis in tree frog: trade-off between sexual signals and immunity? |
| Q59198808 | Impact of chronic noise exposure on antipredator behavior: an experiment in breeding house sparrows |
| Q125388818 | Impact of food predictability on social facilitation by foraging scavengers |
| Q56931125 | Impacts of mussel invasions on the prey preference of two native predators |
| Q41118085 | Imperfect past and present progressive: beak color reflects early-life and adult exposure to antigen |
| Q60119989 | Implications of fidelity and philopatry for the population structure of female black-tailed deer |
| Q113275639 | Implications of senescence patterns for the evolution of age polyethism in eusocial insects |
| Q125911565 | Improved nutritional status may promote an “asset protection” reproductive strategy in male rock lizards |
| Q127320569 | In a noisy world, some animals are more equal than others: a response to comments on Harding et al. |
| Q105612853 | In search of the Darwinian Holy Trinity in cognitive evolution: a comment on Croston et al |
| Q57669353 | Inbreeding and measures of immune function in the cricket Teleogryllus commodus |
| Q125906658 | Inbreeding depression in male traits and preference for outbred males in Poecilia reticulata |
| Q56455455 | Inbreeding is reduced by female-biased dispersal and mating behavior in Ethiopian wolves |
| Q120969613 | Incest avoidance, extrapair paternity, and territory quality drive divorce in a year-round territorial bird |
| Q59757734 | Inclusive fitness and reproductive strategies in dwarf mongooses |
| Q41828683 | Increased host aggression as an induced defense against slave-making ants |
| Q115543659 | Increased male mating success in the presence of prey and rivals in a sexually cannibalistic mantis |
| Q56783788 | Increased parental care cost for nest-guarding fish in a lake with hyperabundant nest predators |
| Q60557286 | Increased perception of predation risk to adults and offspring alters avian reproductive strategy and performance |
| Q56450132 | Increasing sexual ornamentation during a biological invasion |
| Q59256351 | Increasing vulnerability to predation increases preference for the scrounger foraging tactic |
| Q115543333 | Incubating females use dynamic risk assessment to evaluate the risk posed by different predators |
| Q128787898 | Incubation temperature and social context affect the nest exodus of precocial ducklings |
| Q60459100 | Indicators of development as sexually selected traits: the developmental stress hypothesis in context |
| Q58307343 | Indicators of physiological stress and the elaboration of sexual traits in the collared flycatcher |
| Q59000084 | Individual attributes and self-organizational processes affect dominance network structure in pukeko |
| Q58311785 | Individual behavior and survival: the roles of predator avoidance, foraging success, and vigilance |
| Q125607540 | Individual differences exceed species differences in the movements of a river fish community |
| Q115787901 | Individual flexibility in nocturnal activity reduces risk of road mortality for an urban carnivore |
| Q60439625 | Individual personality traits influence group exploration in a feral guppy population |
| Q57049349 | Individual quality and reproductive effort mirrored in white wing plumage in both sexes of south polar skuas |
| Q104352367 | Individual shifts toward safety explain age-related foraging distribution in a gregarious shorebird |
| Q126174037 | Individual signatures outweigh social group identity in contact calls of a communally nesting parrot |
| Q61821029 | Individual variation and the source-sink group dynamics of extra-group paternity in a social mammal |
| Q58832966 | Individual variation in male mating preferences for female coloration in a polymorphic cichlid fish |
| Q56434506 | Individual variation in predator behavior and demographics affects consumption of non-native prey |
| Q59212909 | Individual, nightly, and seasonal variation in calling behavior of the gray tree frog, Hyla versicolor: implications for energy expenditure |
| Q56972659 | Inducible defense behavior of an anuran tadpole: cue-detection range and cue types used against predator |
| Q60516479 | Inferring activity budgets in wild animals to estimate the consequences of disturbances |
| Q113821241 | Influence of immediate predation risk by lions on the vigilance of prey of different body size |
| Q113178635 | Influence of phenotypic and social traits on dispersal in a family living, tropical bird |
| Q113821424 | Influence of prey foraging posture on flight behavior and predation risk: predators take advantage of unwary prey |
| Q58471272 | Influence of social dominance rank on diet quality of pronghorn females |
| Q58317547 | Influences of environmental cues, migration history, and habitat familiarity on partial migration |
| Q60233805 | Information for patch assessment: a field investigation with black-chinned hummingbirds |
| Q60255131 | Information use and density-dependent emigration in an agrobiont spider |
| Q61655385 | Inhibition of optimal behavior by social transmission in the guppy depends on shoaling |
| Q115543148 | Innate antipredator behavior can promote infection in fish even in the absence of predators |
| Q115414432 | Innovative consumers: ecological, behavioral, and physiological predictors of responses to novel food |
| Q60557356 | Innovative problem solving in nonhuman animals: the effects of group size revisited |
| Q57031799 | Insect personality depends on environmental conditions |
| Q56211407 | Insular tammar wallabies (Macropus eugenii) respond to visual but not acoustic cues from predators |
| Q57034349 | Insularization effects on acoustic signals of 2 suboscine Amazonian birds |
| Q56780128 | Integrating animal behavior and conservation biology: a conceptual framework |
| Q56942113 | Integrating behavior into life-history theory: a comment on Wong and Candolin |
| Q61502778 | Integrating fundamental and formant frequencies in women’s preferences for men’s voices |
| Q57063853 | Integrating network analysis, sensor tags, and observation to understand shark ecology and behavior |
| Q129684867 | Inter- and intraspecific female behavioral plasticity drive temporal niche segregation in two Tribolium species |
| Q113821433 | Interacting effects of predation risk and male and female density on male/female conflicts and mating dynamics of stream water striders |
| Q56502939 | Interaction rate informs harvester ant task decisions |
| Q61503011 | Interactions between masculinity–femininity and apparent health in face preferences |
| Q60362683 | Interactive effects of yolk testosterone and carotenoid on prenatal growth and offspring physiology in a precocial bird |
| Q113035053 | Interference competition between coyotes and raccoons: a test of the mesopredator release hypothesis |
| Q60466659 | Interindividual variability in habitat use: evidence for a risk management syndrome in roe deer? |
| Q60658755 | Internal acoustic structuring in pied babbler recruitment cries specifies the form of recruitment |
| Q36701402 | Internest food sharing within wood ant colonies: resource redistribution behavior in a complex system |
| Q128781735 | Interspecific aggression among parapatric and sympatric songbirds on a tropical elevational gradient |
| Q63975840 | Interspecific analysis of vehicle avoidance behavior in birds |
| Q115041129 | Interspecific dominance relationships and hybridization between black-capped and mountain chickadees |
| Q115543992 | Intraflock variation in the speed of escape-flight response on attack by an avian predator |
| Q115543417 | Intraguild predation, thermoregulation, and microhabitat selection by snakes |
| Q126020144 | Intrapopulation variation in the behavioral responses of dwarf mongooses to anthropogenic noise |
| Q58832960 | Intrasexual competition and throat color evolution in female three-spined sticklebacks |
| Q34637258 | Intrasexual competition in females: evidence for sexual selection? |
| Q29039778 | Intrasexual selection and group spawning in quacking frogs (Crinia georgiana) |
| Q56783793 | Intraspecific competition influences the symmetry and intensity of aggression in the Argentine ant |
| Q127355134 | Intraspecific variation in animal responses to anthropogenic noise through long-term monitoring: a comment on Harding et al. |
| Q117788684 | Invasive shrubs modify rodent activity timing, revealing a consistent behavioral rule governing diel activity |
| Q126307236 | Investigating social and environmental predictors of natal dispersal in a cooperative breeding bird |
| Q113275632 | Iridescence untwined: honey bees can separate hue variations in space and time |
| Q57230037 | Iridescent structurally based coloration of eyespots correlates with mating success in the peacock |
| Q61439962 | Is a proactive mum a good mum? A mother’s coping style influences early fawn survival in roe deer |
| Q59197899 | Is extrapair mating random? On the probability distribution of extrapair young in avian broods |
| Q123166718 | Is hatching asynchrony beneficial for the brood? |
| Q60658773 | Is information from both quality signaling and social recognition really redundant? A comment on Sheehan and Bergman |
| Q55894623 | Is male germ line control creating avenues for female choice? |
| Q58643784 | Is male plumage reflectance correlated with paternal care in bluethroats? |
| Q52603702 | Is male rhesus macaque facial coloration under intrasexual selection? |
| Q115543799 | Isolation from mammalian predators differentially affects two congeners |
| Q59185181 | Isolation rearing does not constrain social plasticity in a family-living lizard |
| Q60501986 | Item Response Trees: a recommended method for analyzing categorical data in behavioral studies |
| Q117788677 | It’s a trap! Invasive common mynas learn socially about control-related cues |
| Q56420968 | It’s a trap: sampling bias due to animal personality is not always inevitable |
| Q109667217 | It’s not all about temperature: breeding success also affects nest design |
| Q105612858 | Jackdaw nestlings can discriminate between conspecific calls but do not beg specifically to their parents |
| Q52802186 | Joint care can outweigh costs of nonkin competition in communal breeders. |
| Q58418583 | Juvenile infection and male display: testing the bright male hypothesis across individual life histories |
| Q93013013 | Juvenile social experience generates differences in behavioral variation but not averages |
| Q109667219 | Juvenile socio-ecological environment shapes material technology in nest-building birds |
| Q113821412 | Kalahari skinks eavesdrop on sociable weavers to manage predation by pygmy falcons and expand their realized niche |
| Q120689672 | Keeping the Virgin in her niche: a commentary on Richardson and Zuk |
| Q113821344 | Kin do not always help: testing multiple hypotheses on nest feeding in a cooperatively breeding bird |
| Q62564639 | Kin recognition and incest avoidance in a group-living insect |
| Q62075117 | Kin recognition in the larvae of a solitary insect: the cue is in the plug |
| Q129126049 | Kin selection and allocare in sperm whales |
| Q56020656 | Kin selection does not explain male aggregation at leks of 4 manakin species |
| Q29544490 | Kin selection, relatedness, and worker control of reproduction in a large-colony epiponine wasp, Brachygastra mellifica |
| Q113347181 | Kinship and association in a highly social apex predator population, killer whales at Marion Island |
| Q115041132 | Kinship and sociality in coastal river otters: are they related? |
| Q104206412 | Kinship in colonial tuco-tucos: evidence from group composition and population structure |
| Q57669355 | Know thine enemy’s neighbor: neighbor size affects floaters’ choice of whom to fight |
| Q124822614 | Knowing your habitat: linking patch-encounter rate and patch exploitation in parasitoids |
| Q56050386 | Koala bellows and their association with the spatial dynamics of free-ranging koalas |
| Q57043747 | Lack of floral constancy by bee fly pollinators: implications for ethological isolation in an African daisy |
| Q57018097 | Lack of inbreeding avoidance in the Argentine ant Linepithema humile |
| Q57270744 | Landscape and anthropogenic features influence the use of auditory vigilance by mule deer |
| Q59185136 | Large body and small brain and group sizes are associated with predator preferences for mammalian prey |
| Q120689670 | Larval and adult experience and ecotype affect oviposition behavior in a niche-expanding butterfly |
| Q60568349 | Larval competition risk shapes male–male competition and mating behavior in an anuran |
| Q129702500 | Larval pheromones act as colony-wide regulators of collective foraging behavior in honeybees |
| Q60319788 | Latency to flee from an immobile predator: effects of predation risk and cost of immobility for the prey |
| Q115039449 | Laterality in foraging phalaropes promotes phenotypically assorted groups |
| Q58006279 | Lateralization in refuge selection in Podarcis hispanica at different hierarchical levels |
| Q56452976 | Leachates from an invasive shrub causes risk-prone behavior in a larval amphibian |
| Q115543263 | Learning about aposematic prey |
| Q114641690 | Leave me alone: solitary females attract more mates in a nocturnal insect |
| Q57955121 | Lekking satin bowerbird males aggregate with relatives to mitigate aggression |
| Q105952191 | Leks in ground-displaying birds: hotspots or safe places? |
| Q60564266 | Lessons for a changing world: a response to comments on Wong and Candolin |
| Q60541039 | Let the most motivated win: resource value components affect contest outcome in a parasitoid wasp |
| Q37332056 | Lethal combat and sex ratio evolution in a parasitoid wasp |
| Q37627055 | Lethal combat over limited resources: testing the importance of competitors and kin. |
| Q57159457 | Letter from the Editors |
| Q113035102 | Let’s keep alternative hypotheses on the table: a response to comments on Schubert et al. |
| Q57649147 | Life-history analysis of the Trivers and Willard sex-ratio problem |
| Q115039414 | Life-history and behavioral trait covariation across 3 years in Temnothorax ants |
| Q59394420 | Light intensity limits foraging activity in nocturnal and crepuscular bees |
| Q113821331 | Light received by embryos promotes postnatal junior phenotypes in a seabird |
| Q28740956 | Linking amphibian call structure to the environment: the interplay between phenotypic flexibility and individual attributes |
| Q60506496 | Linking foraging behavior to lifetime reproductive success for an insect parasitoid: adaptation to host distributions |
| Q55980439 | Lion population dynamics: do nomadic males matter? |
| Q58488477 | Litter size and fetal sex ratio adjustment in a highly polytocous species: the wild boar |
| Q115543167 | Little to fear: largest lizard predator induces weak defense responses in ungulate prey |
| Q60262962 | Live and let die: why fighter males of the ant Cardiocondyla kill each other but tolerate their winged rivals |
| Q56448678 | Living on the edge: range edge birds consume novel foods sooner than established ones |
| Q115543296 | Local enhancement in a seabird: reaction distances and foraging consequence of predator aggregations |
| Q104368758 | Local offspring density and sex ratio affect sex allocation in the great tit |
| Q60187640 | Location and group size influence decisions in simulated intergroup encounters in banded mongooses |
| Q129208767 | Locomotory mimicry in ant-like spiders |
| Q57199233 | Long tails matter in sugarbirds—positively for extrapair but negatively for within-pair fertilization success |
| Q115543470 | Long-lasting mobbing of the pied flycatcher increases the risk of nest predation |
| Q128744229 | Long-term dynamics of phenotype-dependent dispersal within a wild bird population |
| Q126038916 | Longer breeding dispersal than natal dispersal in the ortolan bunting |
| Q60362964 | Losing the last feather: feather loss as an antipredator adaptation in birds |
| Q128590850 | Love them all: mothers provide care to foreign eggs in the European earwig Forficula auricularia |
| Q56228485 | Low frequency of extrapair paternity in the polygynous great reed warbler, Acrocephalus arundinaceus |
| Q60287815 | Low light reflectance may explain the attraction of birds to defoliated trees |
| Q129744267 | Low sex drive and choosy females: fungal infections are a reproductive downfall for male house flies |
| Q125800492 | MHC-associated mate choice under competitive conditions in captive versus wild Tasmanian devils |
| Q115787893 | Macronutrient selection of free-ranging urban Australian white ibis (Threskiornis moluccus) |
| Q129922415 | Macronutrient signature of dietary generalism in an ecologically diverse primate in the wild |
| Q113821365 | Made-up mouths with preen oil reveal genetic and phenotypic conditions of starling nestlings |
| Q59746736 | Magpies do not desert after prolonging the parental care period: an experimental study |
| Q59485995 | Maintenance of androdioecy in the freshwater shrimp Eulimnadia texana: sexual encounter rates and outcrossing success |
| Q128228971 | Maintenance of deceptive gifts in a natural spider population: ecological and demographic factors |
| Q55881822 | Major histocompatibility complex genes, symmetry, and body scent attractiveness in men and women |
| Q115543281 | Malaria parasites, immune challenge, MHC variability, and predator avoidance in a passerine bird |
| Q60442264 | Male Sailfin mollies (Poecilia latipinna) copy the mate choice of other males |
| Q60393694 | Male Seychelles warblers use territory budding to maximize lifetime fitness in a saturated environment |
| Q112177671 | Male age, mating probability, and progeny fitness in the bulb mite |
| Q113035057 | Male and female cooperatively breeding fish provide support for the “Challenge Hypothesis” |
| Q57669693 | Male attractiveness covaries with fighting ability but not with prior fight outcome in house crickets |
| Q57272348 | Male biased sex ratio reduces the fecundity of one of three female morphs in a polymorphic damselfly |
| Q56058455 | Male bimaturism and reproductive success in Sumatran orang-utans |
| Q113035015 | Male chickadees match neighbors interactively at dawn: support for the social dynamics hypothesis |
| Q56932936 | Male choice of mates and mating resources in the rose bitterling (Rhodeus ocellatus) |
| Q62383041 | Male competition and female choice interact to determine mating success in the bluefin killifish |
| Q129149838 | Male courtship behaviors and female choice reduced during experimental starvation stress |
| Q56506203 | Male courtship pheromones as indicators of genetic quality in an arctiid moth (Utetheisa ornatrix) |
| Q60514587 | Male decisions or female accessibility? Spatiotemporal patterns of extra pair paternity in a songbird |
| Q105952194 | Male display areas in exploded leks: the importance of food resources for male mating success |
| Q60119845 | Male dominance and immunocompetence in a field cricket |
| Q56690159 | Male dominance influences pheromone expression, ejaculate quality, and fertilization success in the Australian field cricket, Teleogryllus oceanicus |
| Q57669360 | Male fiddler crabs defend multiple burrows to attract additional females |
| Q60384833 | Male green frogs lower the pitch of acoustic signals in defense of territories: a possible dishonest signal of size? |
| Q56001554 | Male harassment influences female movements and associations in Grevy's zebra (Equus grevyi) |
| Q126320529 | Male harassment leads to fitness costs for females by disrupting oviposition site preferences |
| Q115039416 | Male mate choice based on female coloration in a lizard: the role of a juvenile trait |
| Q94560351 | Male mate choice for large gravid spots in a livebearing fish |
| Q57699136 | Male mating behavior and ejaculate expenditure under sperm competition risk in the eastern mosquitofish |
| Q57308970 | Male mating strategies and the mating system of great-tailed grackles |
| Q113821514 | Male mating strategies under predation risk: do females call the shots? |
| Q59024994 | Male morph predicts investment in larval immune function in the dung beetle, Onthophagus taurus |
| Q126199978 | Male morphological variation and the determinants of body size in two Otiteselline fig wasps |
| Q57614405 | Male ornamentation, timing of breeding, and cost of polygyny in the collared flycatcher |
| Q114633533 | Male phenotypic diversity experienced during ontogeny mediates female mate choice in guppies |
| Q29395321 | Male preference and female cues: males assess female sexual maturity and mating status in a web-building spider |
| Q58393363 | Male quality, dominance rank, and mating success in free-ranging rhesus macaques |
| Q56020646 | Male rank and optimal lek size |
| Q125762475 | Male reed buntings do not adjust parental effort in relation to extrapair paternity |
| Q114641663 | Male reproductive adjustments to an introduced nest predator |
| Q59117856 | Male reproductive investment and queen mating-frequency in fungus-growing ants |
| Q122884783 | Male reproductive senescence as a potential source of sexual conflict in a beetle |
| Q56935491 | Male reproductive success and sexual selection in northern water snakes determined by microsatellite DNA analysis |
| Q126162858 | Male rock lizards may compensate reproductive costs of an immune challenge affecting sexual signals |
| Q60428985 | Male size predicts extrapair paternity in a socially monogamous bird with extreme sexual size dimorphism |
| Q59835843 | Male songbirds provide indirect parental care by guarding females during incubation |
| Q122740810 | Male sperm expenditure under sperm competition risk and intensity in quacking frogs |
| Q126123702 | Male spiders reduce pre- and postmating sexual investment in response to sperm competition risk |
| Q56051076 | Male spotted hyenas (Crocuta crocuta) queue for status in social groups dominated by females |
| Q58488429 | Male survival patterns do not depend on male allocation to sexual competition in large herbivores |
| Q113035181 | Male-biased sex ratio in litters of Alpine marmots supports the helper repayment hypothesis |
| Q60575695 | Males do not always switch females when presented with a better reproductive option |
| Q113178632 | Males evolve to be more harmful under increased sexual conflict intensity in a seed beetle |
| Q58768008 | Males mate with multiple females to increase offspring numbers in a nursery web spider |
| Q109041132 | Males perceive honest information from female released sex pheromone in a moth |
| Q115039441 | Male–male behavioral interactions drive social-dominance-mediated differences in ejaculate traits |
| Q112806650 | Male–male contest limits the expression of assortative mate preferences in a polymorphic poison frog |
| Q109296716 | Mammalian nest predator feces as a cue in avian habitat selection decisions |
| Q125340491 | Manipulated sex ratios alter group structure and cooperation in the brown-headed nuthatch |
| Q30378983 | Manipulating carer number versus brood size: complementary but not equivalent ways of quantifying carer effects on offspring. |
| Q58232748 | Manipulation of male attractiveness induces rapid changes in avian maternal yolk androgen deposition |
| Q56235067 | Manipulations of male parental investment in polygynous pied flycatchers, Ficedula hypoleuca |
| Q53417115 | Marginal predation: do encounter or confusion effects explain the targeting of prey group edges? |
| Q91272716 | Marriage stability in a pastoralist society |
| Q115414474 | Mass Fluctuations Suggest Different Functions of Bimodal Foraging Trips in a Central-place Forager |
| Q113034989 | Mate change in a socially monogamous mammal: evidences support the “forced divorce” hypothesis |
| Q60303814 | Mate choice and courtship signal differentiation promotes speciation in an Amazonian frog |
| Q35611107 | Mate choice and genetic monogamy in a biparental, colonial fish |
| Q63437947 | Mate choice copying and mate quality bias: different processes, different species |
| Q129477053 | Mate choice driven by genome in an allopolyploid fish complex |
| Q61954714 | Mate choice for cognitive traits: a review of the evidence in nonhuman vertebrates |
| Q60570953 | Mate choice for genetic quality: a test of the heterozygosity and compatibility hypotheses in a lek-breeding bird |
| Q61458483 | Mate choice in lekking sage grouse revisited: the roles of vocal display, female site fidelity, and copying |
| Q52330538 | Mate choice in sticklebacks reveals that immunogenes can drive ecological speciation. |
| Q61954728 | Mate choice in the face of costly competition |
| Q59199719 | Mate choice or harassment avoidance? A question of female control at the lek |
| Q113393722 | Mate choice plasticity in a coral reef fish |
| Q57021081 | Mate choice, operational sex ratio, and social promiscuity in a wild population of the long-snouted seahorse Hippocampus guttulatus |
| Q56050305 | Mate feeding, offspring investment, and sexual differences in katydids (Orthoptera: Tettigoniidae) |
| Q60277485 | Mate preference for multiple cues: interplay between male and nest size in the sand goby, Pomatoschistus minutus |
| Q56020655 | Mate retention, harassment, and the evolution of ungulate leks |
| Q113821425 | Mate-choice copying under predation risk in the Trinigadian guppy (Poecilia reticulata) |
| Q129673205 | Mate-copying for a costly variant in Drosophila melanogaster females |
| Q58279482 | Mate-feeding has evolved as a compensatory energetic strategy that affects breeding success in birds |
| Q60337266 | Maternal adjustment of parental effort in relation to mate compatibility affects offspring development |
| Q36140334 | Maternal age at maturation underpins contrasting behavior in offspring |
| Q60311532 | Maternal allocation of androgens and antagonistic effects of yolk androgens on sons and daughters |
| Q57063297 | Maternal and additive genetic effects contribute to variation in offspring traits in a lizard |
| Q113821408 | Maternal and personal information mediates the use of social cues about predation risk |
| Q57940053 | Maternal condition and offspring sex ratio in polygynous ungulates: a case study of bighorn sheep |
| Q58643655 | Maternal effects and female manipulation: a response to comments on Paquet and Smiseth |
| Q58643680 | Maternal effects as a mechanism for manipulating male care and resolving sexual conflict over care |
| Q56638203 | Maternal effects on offspring social status in spotted hyenas |
| Q58200667 | Maternal immune factors and the evolution of secondary sexual characters |
| Q113821411 | Maternal predation risk increases offspring’s exploration but does not affect schooling behavior |
| Q129278657 | Maternal presence facilitates plasticity in offspring behavior: insights into the evolution of parental care |
| Q60337171 | Maternal stress to partner quality is linked to adaptive offspring sex ratio adjustment |
| Q115414481 | Maternal yolk testosterone in canary eggs: toward a better understanding of mechanisms and function |
| Q125891507 | Maternally derived androgens and antioxidants in bird eggs: complementary but opposing effects? |
| Q126329965 | Maternity uncertainty in cobreeding beetles: females lay more and larger eggs and provide less care |
| Q130120112 | Mating and/or social system to explain territorial responses: a comment on Christensen and Radford |
| Q61546963 | Mating for convenience or genetic diversity? Mating patterns in the polygynous ant Plagiolepis pygmaea |
| Q60490367 | Mating order and reproductive success in male Columbian ground squirrels (Urocitellus columbianus) |
| Q111593548 | Mating rate and fitness in female bean weevils |
| Q55880589 | Mating success in lekking males: a meta-analysis |
| Q57007075 | Mating system and intrapatch mobility delay inbreeding in fragmented populations of a gecko |
| Q57768695 | Mating system, sexual dimorphism, and the opportunity for sexual selection in a territorial ungulate |
| Q115039427 | Mating traits are phenotypically but not genetically correlated to fitness |
| Q61306449 | Measuring cognition will be difficult but worth it: a response to comments on Rowe and Healy |
| Q115543360 | Measuring marginal predation in animal groups |
| Q30054148 | Measuring mating competition correctly: available evidence supports operational sex ratio theory |
| Q61306456 | Measuring variation in cognition |
| Q56933805 | Mechanisms and consequences of sexual conflict in garter snakes (Thamnophis sirtalis, Colubridae) |
| Q115414445 | Mechanisms of reciprocity and diversity in social networks: a modeling and comparative approach |
| Q115414495 | Mechanosensory function for facial ornamentation in the whiskered auklet, a crevice-dwelling seabird |
| Q60311460 | Melanic coloration differentially predicts transfer of immune factors to eggs with daughters or sons |
| Q112748509 | Memory extinction and spontaneous recovery shaping parasitoid foraging behavior |
| Q115543153 | Mesopredators change temporal activity in response to a recolonizing apex predator |
| Q113821410 | Metabolic and behavioral adaptations of greater white-toothed shrews to urban conditions |
| Q114093511 | Microhabitat complexity influences fear acquisition in fathead minnows |
| Q113821427 | Microhabitat use and behavior of voles under weasel and raptor predation risk: predator facilitation? |
| Q56269919 | Microsatellite identification of extrapair sires in a socially monogamous warbler |
| Q60525891 | Migrant and resident birds adjust antipredator behavior in response to social information accuracy |
| Q121737279 | Migration cues and timing in leatherback sea turtles |
| Q59216472 | Migration strategy of a flight generalist, the Lesser Black-backed Gull Larus fuscus |
| Q63360909 | Mimicry in coral reef fish: how accurate is this deception in terms of color and luminance? |
| Q113035050 | Mimicry in hoverflies (Diptera: Syrphidae): a field test of the competitive mimicry hypothesis |
| Q60462644 | Mixing nutrients mitigates the intake constraints of a plant toxin in a generalist herbivore |
| Q57260816 | Modeling rule-based behavior: habitat selection and the growth-survival trade-off in larval cod |
| Q115543169 | Modeling the functional link between movement, feeding activity, and condition in a marine predator |
| Q60562887 | Modeling the role of stage-structured agonistic interactions in ontogenetic habitat shifts |
| Q59394212 | Models for a colorful reality?: a response to comments on Olsson et al |
| Q60438664 | Models of optimal foraging and resource partitioning: deep corollas for long tongues |
| Q57893306 | Modification of the visual background increases the conspicuousness of golden-collared manakin displays |
| Q63347974 | Monandry and polyandry as alternative lifestyles in a butterfly |
| Q108065867 | Monitoring starvation risk: adjustments of body reserves in greenfinches (Carduelis Chloris L.) during periods of unpredictable foraging success |
| Q60658823 | Monogamous dominant pairs monopolize reproduction in the cooperatively breeding pied babbler |
| Q57596592 | Monogamy when there is potential for polygyny: tests of multiple hypotheses in a group-living fish |
| Q98224100 | Monotocy and the evolution of plural breeding in mammals |
| Q129369823 | More than kin: subordinates foster strong bonds with relatives and potential mates in a social bird |
| Q113275630 | Morphological and behavioral defenses in dragonfly larvae: trait compensation and cospecialization |
| Q126624964 | Morphological and physiological consequences of a dietary restriction during early life in bats |
| Q59086696 | Mortal combat and competition for oviposition sites in female pollinating fig wasps |
| Q58873514 | Mortality by moonlight: predation risk and the snowshoe hare |
| Q59621269 | Mothers adjust egg size to helper number in a cooperatively breeding cichlid |
| Q63975877 | Mother–offspring conflicts, hormone signaling, and asymmetric ownership of information |
| Q60311522 | Mouth coloration of nestlings covaries with offspring quality and influences parental feeding behavior |
| Q60475581 | Movement decisions in natural catastrophes: how a flying scavenger deals with a volcanic eruption |
| Q115543275 | Multicomponent deceptive signals reduce the speed at which predators learn that prey are profitable |
| Q104368796 | Multidimensional environmental predictors of variation in avian forest and city life histories |
| Q56048793 | Multilevel social organization and space use in reticulated giraffe (Giraffa camelopardalis) |
| Q115543369 | Multimodal mixed messages: the use of multiple cues allows greater accuracy in social recognition and predator detection decisions in the mosquitofish, Gambusia holbrooki |
| Q112288702 | Multiple constraints on urban bird communication: both abiotic and biotic noise shape songs in cities |
| Q93013002 | Multiple environmental cues impact habitat choice during nocturnal homing of specialized reef shrimp |
| Q57063317 | Multiple mating in a lizard increases fecundity but provides no evidence for genetic benefits |
| Q128616527 | Multiple mating is linked to social setting and benefits the males in a communally rearing mammal |
| Q63437889 | Multiple motives in women's preferences for masculine male faces: comment on Scott et al |
| Q56211907 | Multiple sexual ornaments in satin bowerbirds: ultraviolet plumage and bowers signal different aspects of male quality |
| Q113821323 | Multiple views on animal coloration: a comment on Postema et al |
| Q113090871 | Multisensory integration facilitates perceptual restoration of an interrupted call in a species of frog |
| Q58486801 | Multisensory perception in uncertain environments |
| Q58673152 | Multistate estimates of survival and movement in relation to colony size in the sociable weaver |
| Q115543371 | Multitasking and eavesdropping in cotton rats foraging under predation risk |
| Q123396373 | Mutual mate choice in the potbellied seahorse (Hippocampus abdominalis) |
| Q115039429 | Mutual mate preferences and assortative mating in relation to a carotenoid-based color trait in blue tits |
| Q127439265 | Natal conditions, lifespan and lifetime reproductive success of European blackbirds |
| Q60466668 | Natal dispersal correlates with behavioral traits that are not consistent across early life stages |
| Q57040615 | Natal dispersal, interactions among siblings and intrasexual competition |
| Q92838763 | Natal habitat and sex-specific survival rates result in a male-biased adult sex ratio |
| Q60546344 | Natal philopatry in passerine birds: genetic or ecological influences? |
| Q126081673 | Natural and anthropogenic sounds reduce song performance: insights from two emberizid species |
| Q56700621 | Natural variation in the sexually selected feather ornaments of crested auklets (Aethia cristatella) does not predict future survival |
| Q63976294 | Navigating infection risk during oviposition and cannibalistic foraging in a holometabolous insect |
| Q109047637 | Necessity creates opportunities for chimpanzee tool use |
| Q126096978 | Necessity or capacity? Physiological state predicts problem-solving performance in house sparrows |
| Q27304577 | Negotiation of territorial boundaries in a songbird |
| Q62273518 | Negotiation over offspring care?—a positive response to partner-provisioning rate in great tits |
| Q56212765 | Negotiation over offspring care—how should parents respond to each other's efforts? |
| Q113035096 | Negotiations over parental care: a test of alternative hypotheses in the clown anemonefish |
| Q126027718 | Neighbor-stranger discrimination by song in a suboscine bird, the alder flycatcher, Empidonax alnorum |
| Q125620597 | Nest and mate choice in the red bishop (Euplectes orix) : female settlement rules |
| Q62556885 | Nest defensibility decreases home-range size in central place foragers |
| Q58045941 | Nest desertion by a cowbird host: an antiparasite behavior or a response to egg loss? |
| Q122713129 | Nest material preferences in wild hazel dormice Muscardinus avellanarius : testing predictions from optimal foraging theory |
| Q105940261 | Nest ornamentation in blue tits: is feather carrying ability a male status signal? |
| Q57534903 | Nest predation risk explains variation in avian clutch size |
| Q113821200 | Nest predation risk, but not demography, drives dynamics of conspecific brood parasitism |
| Q30524611 | Nest site and weather affect the personality of harvester ant colonies |
| Q115414525 | Nest site limitation and colony takeover in the ant Leptothorax nylanderi |
| Q56169705 | Nest size affects clutch size and the start of incubation in magpies: an experimental study |
| Q57272216 | Nest size and aromatic plants in the nest as sexually selected female traits in blue tits |
| Q59746902 | Nest size predicts the effect of food supplementation to magpie nestlings on their immunocompetence: an experimental test of nest size indicating parental ability |
| Q59835882 | Nest-site preference and maternal effects on offspring growth |
| Q125383462 | Nestling and adult sparrows respond differently to conspecific dialects |
| Q115543405 | Nestling begging increases predation risk, regardless of spectral characteristics or avian mobbing |
| Q60311425 | Nestling sex and plumage color predict food allocation by barn swallow parents |
| Q60436019 | Nestmate recognition in the unicolonial ant Formica paralugubris |
| Q104206498 | New colony formation in the "highly inbred" eusocial naked mole-rat: outbreeding is preferred |
| Q130019138 | Niche separation, ontogeny, and heterospecific alarm responses in centrarchid sunfish |
| Q56002477 | No benefits of polyandry to female green turtles |
| Q60331516 | No direct fitness benefits of helping in a cooperative breeder despite higher survival of helpers |
| Q58867414 | No effect of parental quality or extrapair paternity on brood sex ratio in the blue tit (Parus caeruleus) |
| Q60337095 | No evidence for deception over allocation to brood care in a cooperative bird |
| Q59464102 | No evidence for inbreeding avoidance in a great reed warbler population |
| Q57236979 | No evidence for inbreeding avoidance through active mate choice in red-billed gulls |
| Q58643576 | No evidence for parent–offspring competition in the burying beetle Nicrophorus vespilloides |
| Q128200257 | No immediate or future extra costs of raising a virulent brood parasite chick |
| Q59594827 | No kin discrimination in female mate choice of a parasitoid with complementary sex determination |
| Q62022825 | No peace for estrous topi cows on leks |
| Q113178634 | No phenotypic signature of acoustic competition in songs of a tropical cricket assemblage |
| Q58707102 | No risk, no gain: effects of crop raiding and genetic diversity on body size in male elephants |
| Q120214917 | No signs of behavioral evolution of threespine stickleback following northern pike invasion |
| Q115543532 | Nocturnal anti-predator adaptations in eared and earless Nearctic Lepidoptera |
| Q37333983 | Non-random brood mixing suggests adoption in a colonial cichlid |
| Q115414533 | Non-warning odors trigger innate color aversions--as long as they are novel |
| Q63437945 | Nonindependent mate choice in monogamy |
| Q113393724 | Nonindependent mating in a coral reef damselfish: evidence of mate choice copying in the wild |
| Q60362950 | Nonlinear effects of group size on the success of wolves hunting elk |
| Q60331416 | Non–nest mate discrimination and clonal colony structure in the parthenogenetic ant Cerapachys biroi |
| Q37264753 | Not leaving home: grandmothers and male dispersal in a duolocal human society |
| Q115787898 | Not so sexy in the city: urban birds adjust songs to noise but compromise vocal performance |
| Q115414527 | Novel cost of a sexually selected trait in the rubyspot damselfly Hetaerina americana: conspicuousness to prey |
| Q58486572 | Novel effects of monitoring predators on costs of fleeing and not fleeing explain flushing early in economic escape theory |
| Q60343738 | Novel environment exploration and home range size in starlings Sturnus vulgaris |
| Q115414456 | Novel mate preference through mate-choice copying in zebra finches: sexes differ |
| Q115414523 | Novel sources of (co)variation in nestling begging behavior and hunger at different biological levels of analysis |
| Q55933436 | Nowhere to hide: pumas, black bears, and competition refuges |
| Q56212669 | Number of eyespots and their intimidating effect on naïve predators in the peacock butterfly |
| Q56506198 | Nuptial gift in the spider Pisaura mirabilis maintained by sexual selection |
| Q56506208 | Nuptial gifts protect male bell crickets from female aggressive behavior |
| Q60366347 | O2 replenishment to fish nests: males adjust brood care to ambient conditions and brood development |
| Q112607409 | Ocean warming increases availability of crustacean prey via riskier behavior |
| Q64989301 | Odor alters color preference in a foraging jumping spider. |
| Q115414446 | Odor is linked to adrenocortical function and male ornament size in a colonial seabird |
| Q60560499 | Odor preference in house mice: influences of habitat heterogeneity and chromosomal incompatibility |
| Q129065607 | Offspring dispersal ability covaries with nest-site choice |
| Q113035146 | Offspring retention in the Siberian jay {Perisoreus infaustus): the prolonged brood care hypothesis |
| Q57220303 | Offspring size-number strategy in the bethylid parasitoid Laelius pedatus |
| Q60534359 | Olfactory cues of habitats facilitate learning about landscapes of fear |
| Q123436600 | Olfactory cues of large carnivores modify red deer behavior and browsing intensity |
| Q58261325 | Olfactory mate recognition in a sympatric species pair of three-spined sticklebacks |
| Q56047498 | Olfactory recognition of predators by nocturnal lizards: safety outweighs thermal benefits |
| Q104206492 | On the cost of begging vocalization: implications of vigilance |
| Q104206490 | On the evolution of group-living in the New World cursorial hystricognath rodents |
| Q56287175 | On the intersexual selection for spurs in the ring-necked pheasant |
| Q109041150 | On the meaning of hunger and behavioral control in the evolution of honest begging |
| Q115543455 | On the spot: the absence of predators reveals eyespot plasticity in a marine fish |
| Q113821361 | On the strategic learning of signal associations |
| Q125372358 | On the use of private versus social information in oviposition site choice decisions by Drosophila melanogaster females |
| Q128215005 | Once an optimist, always an optimist? Studying cognitive judgment bias in mice |
| Q56212786 | Open-cell parasitism shapes maternal investment patterns in the Red Mason bee Osmia rufa |
| Q60433397 | Operational sex ratio in newts: field responses and characterization of a constituent chemical cue |
| Q57234011 | Opportunity of parentage and nest destruction in polygynandrous acorn woodpeckers, Melanerpes formidvorus |
| Q125628446 | Opposing effects of group size on reproduction and survival in African wild dogs |
| Q113275633 | Optimal distributions of central-place foragers: honey bee foraging in a mass flowering crop |
| Q104873014 | Optimal foraging on perilous prey: risk of bill damage reduces optimal prey size in oystercatchers |
| Q129165923 | Optimal foraging or surplus killing: selective consumption and discarding of salmon by brown bears |
| Q115543359 | Optimal foraging theory predicts diving and feeding strategies of the largest marine predator |
| Q56268910 | Optimal group positioning after a predator attack: the influence of speed, sex, and satiation within mobile whirligig swarms |
| Q58478956 | Optimal hunting conditions drive circalunar behavior of a diurnal carnivore |
| Q59118056 | Optimal mating strategies in nonterritorial ungulates: a general model tested on muskoxen |
| Q129487973 | Optimal sperm length for high siring success depends on forehead patch size in collared flycatchers |
| Q64998133 | Organization enhances collective vigilance in the hovering guards of Tetragonisca angustula bees. |
| Q98224109 | Out in the open: behavior's effect on predation risk and thermoregulation by aposematic caterpillars |
| Q34429224 | Overlapping signals in banded wrens: long-term effects of prior experience on males and females |
| Q113034930 | Overlapping vocalizations produce far-reaching choruses: a test of the signal enhancement hypothesis |
| Q114633542 | Overriding the oddity effect in mixed-species aggregations: group choice by armored and nonarmored prey |
| Q115543456 | Oviposition behavior partitions aquatic landscapes along predation and nutrient gradients |
| Q125880687 | Pace-of-life in a social insect: behavioral syndromes in ants shift along a climatic gradient |
| Q56060600 | Pack social dynamics and inbreeding avoidance in the cooperatively breeding red wolf |
| Q125018192 | Pair bonds, reproductive success, and rise of alternate mating strategies in a social carnivore |
| Q105612891 | Pairs of cleaner fish prolong interaction duration with client reef fish by increasing service quality |
| Q60638018 | Pale by comparison: competitive interactions between signaling female glow-worms |
| Q60119431 | Parasite infection in a central sensory organ of fish does not affect host personality |
| Q115543300 | Parasite- and predator-induced maternal effects in the great tit ( Parus major ) |
| Q113275641 | Parasites delay worker reproduction in bumblebees: consequences for eusociality |
| Q126229637 | Parasites physically block host copulation: a potent mechanism of parasite-mediated sexual selection |
| Q56268739 | Parasitic spawning in sand gobies: an experimental assessment of nest-opening size, sneaker male cues, paternity, and filial cannibalism |
| Q104206495 | Parasitism and group size in social animals: a meta-analysis |
| Q56686600 | Parentage and the evolution of parental behavior |
| Q104206493 | Parental aggression in black-capped chickadees |
| Q127773643 | Parental care buffers against effects of ambient temperature on offspring performance in an insect |
| Q60277252 | Parental coordination with respect to color polymorphism in a crater lake fish |
| Q116847084 | Parental effects on early development: testing for indirect benefits of polyandry |
| Q53278666 | Parental investment in Tibetan populations does not reflect stated cultural norms. |
| Q128902871 | Parental overproduction allows siblicidal bird to adjust brood size to climate-driven prey variation |
| Q113821438 | Parental provisioning and predation risk in rhinoceros auklets (Cerorhinca monocerata): effects on nestling growth and fledging |
| Q54294051 | Parental-care parasitism: how do unrelated offspring attain acceptance by foster parents? |
| Q37090336 | Paroxetine exposure skews litter sex ratios in mice suggesting a Trivers-Willard process |
| Q115414470 | Partial incubation and its function in great tits (Parus major)—an experimental test |
| Q111895207 | Partner fidelity and egg reciprocation in the simultaneously hermaphroditic polychaete worm Ophryotrocha diadema |
| Q60466663 | Partners’ personality types and mate preferences: predation risk matters |
| Q127339381 | Partner’s age, not social environment, predicts extrapair paternity in wild great tits (Parus major) |
| Q90649078 | Past and present resource availability affect mating rate but not mate choice in Drosophila melanogaster |
| Q56981179 | Patch density determines movement patterns and foraging efficiency of large herbivores |
| Q56391362 | Patch exploitation in a producer-scrounger system: test of a hypothesis using flocks of spice finches (Lonchura punctulata) |
| Q57742185 | Patch leaving decision rules and the Marginal Value Theorem: an experimental analysis and a simulation model |
| Q113821348 | Patch quality and habitat fragmentation shape the foraging patterns of a specialist folivore |
| Q115543476 | Patch use, apprehension, and vigilance behavior of Nubian Ibex under perceived risk of predation |
| Q34417405 | Paternal care and the evolution of exaggerated sexual swellings in primates |
| Q60535581 | Paternal effects on access to resources in a promiscuous primate society |
| Q60543861 | Paternity costs from polyandry compensated by increased fecundity in the hide beetle |
| Q57939207 | Paternity in eastern grey kangaroos: moderate skew despite strong sexual dimorphism |
| Q56689074 | Pathogen disgust predicts women’s preferences for masculinity in men’s voices, faces, and bodies |
| Q115039446 | Pathways linking female personality with reproductive success are trait- and year-specific |
| Q63360751 | Pattern edges improve predator learning of aposematic signals |
| Q57655600 | Pattern of sperm transfer in redback spiders: implications for sperm competition and male sacrifice |
| Q57205991 | Patterns of extrapair mating in relation to male dominance status and female nest placement in black-capped chickadees |
| Q61552136 | Patterns of song evolution and sexual selection in the oropendolas and caciques |
| Q29543435 | Paying to stay or paying to breed? Field evidence for direct benefits of helping behavior in a cooperatively breeding fish |
| Q111165616 | Perceived risk structures the space use of competing carnivores |
| Q90447729 | Perceived threat to paternity reduces likelihood of paternal provisioning in house wrens |
| Q113821475 | Perch selection by singing chaffinches: a better view of surroundings and the risk of predation |
| Q58486897 | Peripheral obstructions influence marmot vigilance: integrating observational and experimental results |
| Q59024837 | Personal immunity versus social immunity |
| Q60331580 | Personality affects mate choice: bolder males show stronger audience effects under high competition |
| Q128442649 | Personality and social foraging tactic use in free-living Eurasian tree sparrows (Passer montanus) |
| Q58311768 | Personality constraints versus flexible antipredation behaviors: how important is boldness in risk management of redshanks (Tringa totanus) foraging in a natural system? |
| Q110532063 | Personality does not predict individual niche variation in a freshwater fish |
| Q60337025 | Personality in the wild zebra finch: exploration, sociality, and reproduction |
| Q60119569 | Personality pace-of-life hypothesis: testing genetic associations among personality and life history |
| Q60777712 | Personality predicts behavioral flexibility in a fluctuating, natural environment |
| Q56481934 | Personality traits are related to ecology across a biological invasion |
| Q60343747 | Personality traits in wild starlings: exploration behavior and environmental sensitivity |
| Q57063871 | Personality-dependent spatial ecology occurs independently from dispersal in wild burbot (Lota lota) |
| Q114093518 | Personality-mediated speed-accuracy tradeoffs in mating in a 17-year periodical cicada |
| Q29039203 | Persuasive companions can be wrong: the use of misleading social information in nutmeg mannikins |
| Q98224104 | Phenotypic flexibility in background-mediated color change in sticklebacks |
| Q110615302 | Phenotypic plasticity in fluctuating environments: consequences of the lack of individual optimization |
| Q110615301 | Phenotypic plasticity of larval retreat design in a net-spinning caddisfly |
| Q115414529 | Phenotypic selection and function of reproductive behavior in the subsocial bug Elasmucha putoni (Heteroptera: Acanthosomatidae) |
| Q58814693 | Pheromonal predisposition to social parasitism in the honeybee Apis mellifera capensis |
| Q113035021 | Philopatry in prairie voles: an evaluation of the habitat saturation hypothesis |
| Q104206409 | Philopatry, kin clusters, and genetic relatedness in a population of woodrats (Neotoma macrotis) |
| Q36200152 | Photorefractoriness and energy availability interact to permit facultative timing of spring breeding |
| Q96762555 | Physical and social cues shape nest-site preference and prey capture behavior in social spiders |
| Q57772804 | Physiological conditions and genetic controls of phaeomelanin pigmentation in nestling barn swallows |
| Q60514564 | Pied flycatcher nestlings incur immunological but not growth begging costs |
| Q90581791 | Pipefish embryo oxygenation, survival, and development: egg size, male size, and temperature effects |
| Q115414450 | Plasticity in social communication and its implications for the colonization of novel habitats |
| Q113821352 | Plasticity of snowy plover incubation behaviors in response to risks of nest predation |
| Q115543154 | Playback of predator calls inhibits and delays dawn singing in a songbird community |
| Q130077755 | Plover parents care more for young of the opposite sex |
| Q57955144 | Plumage brightness predicts male mating success in the lekking golden-collared manakin, Manacus vitellinus |
| Q58466813 | Plumage color manipulation has no effect on social dominance or fitness in zebra finches |
| Q125055159 | Pollinators adjust their behavior to presence of pollinator-transmitted pathogen in plant population |
| Q113275638 | Polyandry and paternity affect disease resistance in eusocial wasps |
| Q55953229 | Polyandry, sperm competition, and reproductive success in mice |
| Q59413677 | Polygynandry in a red fox population: implications for the evolution of group living in canids? |
| Q110615303 | Population density, body size, and phenotypic plasticity of brood size in a burying beetle |
| Q117788687 | Population differences in the effect of context on personality in an invasive lizard |
| Q129748917 | Population turnover, behavioral conservatism, and rates of cultural evolution |
| Q125705996 | Population-level personalities in zebrafish: aggression-boldness across but not within populations |
| Q35218069 | Populations, pools, and peccaries: simulating the impact of ecosystem engineers on rainforest frogs |
| Q60393654 | Positioning behavior according to individual color variation improves camouflage in novel habitats |
| Q57589952 | Positive effects of an invasive shrub on aggregation and abundance of a native small rodent |
| Q115543341 | Possible top-down control of solitary bee populations by ambush predators |
| Q57190991 | Post-breeding dispersal by female red squirrels (Tamiasciurus hudsonicus): the effect of local vacancies |
| Q114633538 | Post-fledging behavioral ecology of migratory songbirds: how do fledgling activity rates vary across species? |
| Q105315266 | Postcopulatory consequences of female mate choice in a fish with alternative reproductive tactics |
| Q61887070 | Postcopulatory mechanisms of inbreeding avoidance in the island endemic hihi (Notiomystis cincta) |
| Q115543492 | Potential risks of olfactory signaling: the effect of predators on scent marking by beavers |
| Q115543611 | Pouncing spider, flying mosquito: blood acquisition increases predation risk in mosquitoes |
| Q63362623 | Practical models for publishing replications in behavioral ecology: a comment on Ihle et al |
| Q60016607 | Pre- and postdispersal seed predation by rodents: balance of food and safety |
| Q60331512 | Predation and kin-structured populations: an empirical perspective on the evolution of cooperation |
| Q115543823 | Predation and the evolution of prey behavior: an experiment with tree hole mosquitoes |
| Q115543600 | Predation by red-jointed fiddler crabs on congeners: interaction between body size and positive allometry of the sexually selected claw |
| Q60564241 | Predation cost of a sexual signal in the threespine stickleback |
| Q56001737 | Predation costs associated with parental care in the golden egg bug Phyllomorpha laciniata (Heteroptera: Coreidae) |
| Q113821500 | Predation risk affects trade-off between nest guarding and foraging in Seychelles warblers |
| Q115543355 | Predation risk and jumping behavior in Pseudopaludicola aff. falcipes tadpoles |
| Q113821414 | Predation risk and mating behavior: the responses of moths to bat-like ultrasound |
| Q113821419 | Predation risk and social interference as factors influencing habitat selection in two species of stream-dwelling waterstriders |
| Q113821193 | Predation risk drives the expression of mobbing across bird species |
| Q113821409 | Predation risk increases intraspecific heterogeneity in white-tailed deer diel activity patterns |
| Q115543431 | Predation risk of whole-clutch filial cannibalism in a tropical skink with maternal care |
| Q113821389 | Predation risk shapes the use of conflicting personal risk and social safety information in guppies |
| Q60503525 | Predation risk, host immune response, and parasitism |
| Q113821386 | Predation shapes behavioral lateralization: insights from an adaptive radiation of livebearing fish |
| Q113821199 | Predation shapes the movement of a well-defended species, the North American porcupine, even when nutritionally stressed |
| Q113821440 | Predation, sensitivity, and sex: why female black rhinoceroses outlive males |
| Q37084839 | Predator and prey activity levels jointly influence the outcome of long-term foraging bouts |
| Q115543678 | Predator defense is shaped by risk, brood value and social group benefits in a cooperative breeder |
| Q115543494 | Predator detection and avoidance by starlings under differing scenarios of predation risk |
| Q59256330 | Predator escape tactics in birds: linking ecology and aerodynamics |
| Q115543629 | Predator exposure alters female mate choice in the green swordtail |
| Q115543316 | Predator exposure leads to a short-term reversal in female mate preferences in the green swordtail, Xiphophorus helleri |
| Q56047499 | Predator lethality, optimal escape behavior, and autotomy |
| Q115543780 | Predator preference for brightly colored males in the guppy: a viability cost for a sexually selected trait |
| Q115543910 | Predator search pattern and the strength of interference through prey depression |
| Q115543879 | Predator versus prey: on aerial hunting and escape strategies in birds |
| Q56020097 | Predator-elicited visual signal: why the turquoise-browed motmot wag-displays its racketed tail |
| Q55982347 | Predator-induced plasticity in nest visitation rates in the Siberian jay (Perisoreus infaustus) |
| Q115543442 | Predator-induced reductions in nest visitation rates are modified by forest cover and food availability |
| Q115543368 | Predator-induced stress changes parental feeding behavior in pied flycatchers |
| Q115543502 | Predators, reproductive parasites, and the persistence of poor males on leks |
| Q105758488 | Predators’ consumption of unpalatable prey does not vary as a function of bitter taste perception |
| Q57651269 | Predictable food supplies induce plastic shifts in avian scaled body mass |
| Q58486938 | Predicted fitness consequences of threat-sensitive hiding behavior |
| Q58486957 | Predicted fitness consequences of threat-sensitive hiding behavior |
| Q113821429 | Predicting group size in primates: foraging costs and predation risks |
| Q58389800 | Predicting multiple behaviors from GPS radiocollar cluster data |
| Q60474857 | Predicting translocation outcomes with personality for desert tortoises |
| Q56454718 | Preference for human male body hair changes across the menstrual cycle and menopause |
| Q126096626 | Preferred males are not always good providers: female choice and male investment in tree crickets |
| Q113821195 | Prenatal exposure to predation affects predator recognition learning via lateralization plasticity |
| Q60550260 | Presence of mammalian predators decreases tolerance to human disturbance in a breeding shorebird |
| Q61954721 | Previous experiences shape adaptive mate preferences |
| Q115414537 | Prey attraction as a possible function of the silk decoration of the uloborid spider Octonoba sybotides |
| Q113821204 | Prey body size mediates the predation risk associated with being "odd" |
| Q115543326 | Prey escorting behavior and possible convergent evolution of foraging recruitment mechanisms in an invasive ant |
| Q56473821 | Prey handling performance facilitates competitive dominance of an invasive over native keystone ant |
| Q57232172 | Prey jitters; protean behaviour in grouped prey |
| Q60510142 | Prey naiveté in an introduced prey species: the wild rabbit in Australia |
| Q115543370 | Prey or predator? Body size of an approaching animal affects decisions to attack or escape |
| Q56813951 | Primate copulation calls and postcopulatory female choice |
| Q58222634 | Primates adjust movement strategies due to changing food availability |
| Q63437870 | Priming men with different contest outcomes modulates their dominance perceptions |
| Q58486501 | Prioritizing conservation behavior research: a comment on Wong and Candolin |
| Q127592372 | Problems with repeated contests: a comment on Chapin et al |
| Q35053234 | Progressive parenting behavior in wild golden lion tamarins |
| Q56169298 | Prolactin and helping in birds: has natural selection strengthened helping behavior? |
| Q56485752 | Prolonged offspring dependence and cooperative breeding in birds |
| Q56235200 | Prospecting behavior and the influenceof forest cover on natal dispersal in aresident bird |
| Q55922898 | Prospecting in a solitary breeder: chick production elicits territorial intrusions in common loons |
| Q55895437 | Protandry and sexual dimorphism in trans-Saharan migratory birds |
| Q125849020 | Protandry models and their application to salmon |
| Q62518212 | Protein content of diets dictates the daily energy intake of a free-ranging primate |
| Q118561687 | Proteomics in behavioral ecology |
| Q104368739 | Provisioning tactics of great tits (Parus major) in response to long-term brood size manipulations differ across years |
| Q57065281 | Proximate and ultimate causes of dispersal in the Iberian lynx Lynx pardinus |
| Q105952696 | Proximate and ultimate causes of natal dispersal in the great bustard Otis tarda |
| Q127684801 | Proximate causes of avian protandry differ between subspecies with contrasting migration challenges |
| Q129208220 | Prudent behavior rather than chemical deception enables a parasite to exploit its ant host |
| Q59447062 | Pup escorting in the communal breeding banded mongoose: behavior, benefits, and maintenance |
| Q57159378 | Quality of breeding territory mediates the influence of paternal quality on sex ratio bias in a free-living bird population |
| Q62273514 | Quality, need, or hunger; begging the question |
| Q115787889 | Quantifying human presence in a heterogeneous urban landscape |
| Q113821181 | Quantifying the structure and dynamics of fish shoals under predation threat in three dimensions |
| Q115414478 | Quantitative genetic variation in courtship song and its covariation with immune function and sperm quality in the field cricket Teleogryllus oceanicus |
| Q63975847 | Quantitative genetics and fitness consequences of neophilia in zebra finches |
| Q60472940 | Queen pheromone: contraceptive or a queen presence signal?—A comment on Holman |
| Q130067268 | Queen pheromones and reproductive division of labor: a meta-analysis |
| Q129980201 | Queen pheromones out of context: a comment on Holman |
| Q129984239 | Queen pheromones under scrutiny: a comment on Holman |
| Q129885306 | Queen pheromones, colony odors, and better science: a comment on Holman |
| Q56268450 | Queen recruitment in a multiple-queen population of the fire ant Solenopsis invicta |
| Q37347195 | Queen reproductive state modulates pheromone production and queen-worker interactions in honeybees |
| Q109255703 | Queen succession conflict in the paper wasp Polistes dominula is mitigated by age-based convention |
| Q57699036 | Quick-change artists: male guppies pay no cost to repeatedly adjust their sexual strategies |
| Q54143297 | Quorum sensing by encounter rates in the ant Temnothorax albipennis |
| Q56456091 | RETRACTED: Fiery frills: carotenoid-based coloration predicts contest success in frillneck lizards |
| Q115543237 | Rain, predators, and spider sociality: a manipulative experiment |
| Q37003020 | Randomized or fixed order for studies of behavioral syndromes? |
| Q56805500 | Rank and colony defense against conspecifics in a facultatively eusocial hover wasp |
| Q125123790 | Rate of intersexual interactions affects injury likelihood in Tasmanian devil contact networks |
| Q37229946 | Rates of agonism among female primates: a cross-taxon perspective |
| Q59649960 | Reactions of hand-reared and wild-caught predators toward warningly colored, gregarious, and conspicuous prey |
| Q112806647 | Reciprocal pilferage and the evolution of food-hoarding behavior |
| Q104206414 | Reciprocal territorial responses of parapatric African sunbirds: species-level asymmetry and intraspecific geographic variation |
| Q60264424 | Reciprocity and conditional cooperation between great tit parents |
| Q113290475 | Red foxes avoid apex predation without increasing fear |
| Q55893755 | Red-billed oxpeckers: vampires or tickbirds? |
| Q124933051 | Redder isn’t always better: cost of carotenoids in Chinook salmon eggs |
| Q60503025 | Redhead reproductive strategy choices: a dynamic state variable model |
| Q126775667 | Reduced cooperative behavior as a cost of high testosterone in a lekking passerine bird |
| Q29038952 | Reduced reproductive effort in male field crickets infested with parasitoid fly larvae |
| Q57237191 | Reduction in site fidelity with smaller spatial scale may suggest scale-dependent information use |
| Q113821415 | Refuge sites of voles under owl predation risk: priority of dominant individuals? |
| Q113275640 | Regulation of worker activity in a primitively eusocial wasp, Ropalidia marginata |
| Q56336112 | Relatedness and altruism in Polistes wasps |
| Q126030060 | Relationship of visual and olfactory signal parameters in a food-deceptive flower mimicry system |
| Q52330541 | Relative advantages of dichromatic and trichromatic color vision in camouflage breaking. |
| Q57940106 | Relative allocation to horn and body growth in bighorn rams varies with resource availability |
| Q121848343 | Reliable acoustic cues for female mate preference in a katydid (Scudderia curvicauda, Orthoptera: Tettigoniidae) |
| Q59162256 | Remotely sensed productivity, regional home range selection, and local range use by an omnivorous primate |
| Q113035092 | Repeatability is the first step in a broader hypothesis test: a comment on Stuber et al. |
| Q52603712 | Repeatable and heritable behavioural variation in a wild cooperative breeder. |
| Q56780124 | Replacement female house sparrows regularly commit infanticide: gaining time or signaling status? |
| Q60331494 | Replication in behavioural ecology: a comment on Ihle et al |
| Q58790836 | Reproduction and immunity trade-offs constrain mating signals and nuptial gift size in a bushcricket |
| Q56807038 | Reproduction in foundress associations of the social wasp, Polistes carolina: conventions, competition, and skew |
| Q128109086 | Reproductive aging and pace-of-life syndromes: more active females age faster |
| Q60333753 | Reproductive asynchrony and population divergence between two tropical bird populations |
| Q127440709 | Reproductive conflict resolution in cooperative breeders |
| Q61927283 | Reproductive consequences of natal dispersal in a highly philopatric seabird |
| Q58489678 | Reproductive energetics in free-living female chimpanzees (Pan troglodytes schweinfurthii) |
| Q60302865 | Reproductive monopoly enforced by sterile police workers in a queenless ant |
| Q55967705 | Reproductive parasitism of broodcare helpers in a cooperatively breeding fish |
| Q29013415 | Reproductive promiscuity in the splendid fairy-wren: effects of group size and auxiliary reproduction |
| Q61547188 | Reproductive sharing among queens in the ant Formica fusca |
| Q124875853 | Reproductive skew and the evolution of conflict resolution: a synthesis of transactional and tug-of-war models |
| Q60546246 | Reproductive skew, costs, and benefits of cooperative breeding in female wood mice (Apodemus sylvaticus) |
| Q56227014 | Reproductive specialization in multiple-queen colonies of the ant Formica exsecta |
| Q58867514 | Reproductive success of polygynous male corn buntings (Miliaria calandra) as confirmed by DNA fingerprinting |
| Q29030656 | Reproductive success of solitarily and communally nesting white-footed mice and deer mice |
| Q56430252 | Reproductive timing in a lekking mammal: male fallow deer getting ready for female estrus |
| Q126565793 | Reproductive workers insufficiently signal their reproductive ability in a paper wasp |
| Q63379896 | Research credibility: the devil is in the details: a comment on Ihle et al |
| Q56971431 | Residency and a Broad Feeding Spectrum are Related to Extensive Spatial Exploration in Parrots* |
| Q59197837 | Residual correlations, and not individual properties, determine a nest defense boldness syndrome |
| Q61696513 | Resource availability and life-history origin affect competitive behavior in territorial disputes |
| Q58643616 | Resource availability, but not polyandry, influences sibling conflict in a burying beetle Nicrophorus vespilloides |
| Q56391381 | Resource defense in a group-foraging context |
| Q60298888 | Resource distribution mediates social and mating behavior in a family living lizard |
| Q35053229 | Resource quality or competition: why increase resource acceptance in the presence of conspecifics? |
| Q34159758 | Resource redistribution in polydomous ant nest networks: local or global? |
| Q115039425 | Resource-dependent investment in male sexual traits in a viviparous fish |
| Q54377391 | Response to comments on "Do men's faces really signal heritable immunocompetence?" |
| Q60578498 | Response to comments on the dynamics of network dynamics |
| Q55952599 | Response to conspecific and heterospecific alarm calls in mixed-species bird flocks of a Sri Lankan rainforest |
| Q58292586 | Response: how much you need to engage with mechanism depends on what you are trying to do |
| Q59238973 | Responses of vervet monkeys in large troops to terrestrial and aerial predator alarm calls |
| Q129518077 | Responsible sharing of articles published in Behavioral Ecology |
| Q115543152 | Retention of learned predator recognition in embryonic and juvenile rainbow trout |
| Q112806642 | Rethinking birdsong evolution: meta-analysis of the relationship between song complexity and reproductive success |
| Q59185190 | Retraction |
| Q114093519 | Retraction to: Spider aggressiveness determines the bidirectional consequences of host–inquiline interactions |
| Q114590579 | Revealed by conspicuousness: distractive markings reduce camouflage |
| Q61930404 | Revisiting the evidence for inbreeding avoidance in zebra finches |
| Q113821189 | Revisiting the functional response in habitat selection for large herbivores: a matter of spatial variation in resource distribution? |
| Q115414430 | Risk assessment and the use of novel shortcuts in spatial detouring tasks in jumping spiders |
| Q115543434 | Risk effects in elk: sex-specific responses in grazing and browsing due to predation risk from wolves |
| Q96762559 | Risk exposure trade-offs in the ontogeny of sexual segregation in Antarctic fur seal pups |
| Q113178633 | Risk of cache pilferage determines hoarding behavior of rodents and seed fate |
| Q113035184 | Risk taking during parental care: a test of the harm-to-offspring hypothesis |
| Q117826073 | Risky business: males choose more receptive adults over safer subadults in a cannibalistic spider |
| Q55954212 | Risky mate search and male self-sacrifice in redback spiders |
| Q57655587 | Risky mate search and mate preference in the golden orb-web spider (Nephila plumipes) |
| Q30407064 | Rival male chemical cues evoke changes in male pre- and post-copulatory investment in a flour beetle. |
| Q60331584 | Rival presence leads to reversible changes in male mate choice of a desert dwelling ungulate |
| Q115543257 | Road noise causes earlier predator detection and flight response in a free-ranging mammal |
| Q115787897 | Roads are no barrier for dispersing red squirrels in an urban environment |
| Q59941027 | Roads elicit negative movement and habitat-selection responses by wolverines (Gulo gulo luscus) |
| Q115543587 | Rodent foraging is affected by indirect, but not by direct, cues of predation risk |
| Q115414512 | Rufous-tailed jacamars and aposematic butterflies: do older birds attack novel prey? |
| Q59210478 | Saami reindeer herders cooperate with social group members and genetic kin |
| Q59485343 | Safer sex with feeding females: sexual conflict in a cannibalistic spider |
| Q126188954 | Salamander climbing behavior varies among species and is correlated with community composition |
| Q121289595 | Same-sex sexual behavior in birds: expression is related to social mating system and state of development at hatching |
| Q57277760 | Scent marking by otters (Lutra lutra): signaling the use of resources |
| Q115543593 | Scent marking by voles in response to predation risk: a field-laboratory validation |
| Q63437957 | Scent-marking by male mice under the risk of predation |
| Q62022290 | Scent-marking displays provide honest signals of health and infection |
| Q60550142 | Seasonal dynamic shifts in patch exploitation by parasitic wasps |
| Q60442220 | Seasonal plasticity in male mating preferences in sailfin mollies |
| Q115543227 | Seasonal variation in behavioral thermoregulation and predator avoidance in a small mammal |
| Q30484565 | Seismic signal dominance in the multimodal courtship display of the wolf spider Schizocosa stridulans Stratton 1991. |
| Q60501968 | Selection for multicomponent mimicry: equal feature salience and variation in preferred traits |
| Q63672129 | Selection of interdependent choice of 2 complementary resources |
| Q129029662 | Selective attention by priming in host search behavior of 2 generalist butterflies |
| Q112035696 | Selective disappearance does not underlie age-related changes in trait repeatability in red squirrels |
| Q127718230 | Self-deception in nonhuman animals: weak crayfish escalated aggression as if they were strong |
| Q54288431 | Self-organized aerial displays of thousands of starlings: a model |
| Q112806652 | Self-organized asymmetries in ant foraging: a functional response to food type and colony needs |
| Q53417105 | Selfish partners: resource partitioning in male coalitions of Asiatic lions. |
| Q109267091 | Sentinel dominance status influences forager use of social information |
| Q129077071 | Sequential choices using signal detection theory can reverse classical predictions |
| Q33583287 | Sequential male mate choice under sperm competition risk |
| Q112297908 | Sequential organization of birdsong: relationships with individual quality and fitness |
| Q60298476 | Sequential settlement and site dependence in a migratory raptor |
| Q55882264 | Serial monogamy increases reproductive success in men but not in women |
| Q56212794 | Sex allocation in a facultatively polygynous ant: between-population and between-colony variation |
| Q63975768 | Sex allocation in response to local resource competition over breeding territories |
| Q60777727 | Sex allocation in response to paternal attractiveness in the zebra finch |
| Q59037539 | Sex allocation within broods: the intrabrood sharing-out hypothesis |
| Q60311423 | Sex and stress: a comment on Moore et al |
| Q56268909 | Sex and the selfish herd: sexual segregation within nonmating whirligig groups |
| Q57065633 | Sex change evolution and cost of reproduction |
| Q113393726 | Sex change in either direction by growth-rate advantage in the monogamous coral goby, Paragobiodon echinocephalus |
| Q122909841 | Sex differences in embryo development periods and effects on avian hatching patterns |
| Q57651306 | Sex ratio and male sexual characters in a population of blue tits, Parus caeruleus |
| Q59117865 | Sex ratio variation in the bumblebee Bombus terrestris |
| Q113178640 | Sex, drugs and mating role: testosterone-induced phenotype-switching in Galapagos marine iguanas |
| Q126344438 | Sex, synchrony, and skin contact: integrating multiple behaviors to assess pathogen transmission risk |
| Q60562600 | Sex-biased juvenile dispersal is adaptive but does not create genetic structure in island lizards |
| Q58478912 | Sex-ratio variation and reproductive costs in relation to density in a forest-dwelling population of red deer (Cervus elaphus) |
| Q56882395 | Sex-role reversal revisited: choosy females and ornamented, competitive males in a pipefish |
| Q115543793 | Sex-specific differences in reindeer calf behavior and predation vulnerability |
| Q125587869 | Sex-specific effects of size and condition on timing of natal dispersal in kangaroo rats |
| Q58479918 | Sex-specific parental strategies according to the sex of offspring in the Adélie penguin |
| Q60459680 | Sex-specific phenotypes and metabolism-related gene expression in juvenile sticklebacks |
| Q60441443 | Sex-specific thermal constraints on fiddler crab behavior |
| Q113178647 | Sexes of a monomorphic species differ in preference for mates with a novel trait |
| Q60119860 | Sexual advertisement and immune function in an arachnid species (Lycosidae) |
| Q60483557 | Sexual cannibalism in a facultative parthenogen: the springbok mantis (Miomantis caffra) |
| Q115414485 | Sexual coercion in Panorpa scorpionflies?—The function of the notal organ reconsidered |
| Q56657515 | Sexual dimorphism in a feeding apparatus is driven by mate choice and not niche partitioning |
| Q60550837 | Sexual harassment in heterogeneous landscapes can mediate population regulation in a grasshopper |
| Q60442226 | Sexual harassment in live-bearing fishes (Poeciliidae): comparing courting and noncourting species |
| Q58478891 | Sexual segregation in Eurasian wild sheep |
| Q126118397 | Sexual segregation in Indo-Pacific bottlenose dolphins is driven by female avoidance of males |
| Q110032376 | Sexual selection and condition dependence of courtship display in three species of horned dung beetles |
| Q115414538 | Sexual selection and tail streamers in the barn swallow: appropriate tests of the function of size-dimorphic long tails |
| Q113821340 | Sexual selection for flight performance in hummingbirds |
| Q63830243 | Sexual selection in honey bees: colony variation and the importance of size in male mating success |
| Q110032378 | Sexual selection in the wolf spider Hygrolycosa rubrofasciata: female preference for drum duration and pulse rate |
| Q56853293 | Sexual signaling under predation: attractive moths take the greater risks |
| Q115543357 | Sexual signals, risk of predation and escape behavior |
| Q56518892 | Sexual swelling in mandrills (Mandrillus sphinx): a test of the reliable indicator hypothesis |
| Q127483417 | Sexually opposite effects of testosterone on mating success in wild rock hyrax |
| Q37264758 | Sexually selected sentinels? Evidence of a role for intrasexual competition in sentinel behavior |
| Q114939583 | Sexually size dimorphic brains and song complexity in passerine birds |
| Q113821205 | Shaping the antipredator strategy: flexibility, consistency, and behavioral correlations under varying predation threat |
| Q113821202 | Shifts in movement behavior of spawning fish under risk of predation by land-based consumers |
| Q114093525 | Shoaling in the Trinidadian guppy: costs, benefits, and plasticity in response to an ambush predator |
| Q127108686 | Shorebird feeding specialists differ in how environmental conditions alter their foraging time |
| Q113821235 | Short timescale rate maximization by gulls and implications for predation on size-structured prey |
| Q28602361 | Short-term and delayed effects of mother death on calf mortality in Asian elephants |
| Q126091086 | Short-term social dynamics following anthropogenic and natural disturbances in a free-living mammal |
| Q57699127 | Should I stay or should I go? Female brood desertion and male counterstrategy in rock sparrows |
| Q61954725 | Should attractive males have more sons? |
| Q60277434 | Should females prefer males with elaborate nests? |
| Q111725222 | Show me you care: female mate choice based on egg attendance rather than male or territorial traits |
| Q57220248 | Siblicide and life-history evolution in parasitoids |
| Q60566009 | Signal residuals during shell fighting in hermit crabs: can costly signals be used deceptively? |
| Q63379915 | Signaler and receiver boldness influence response to alarm calls in eastern chipmunks |
| Q62058689 | Signaling by decorating webs: luring prey or deterring predators? |
| Q121364717 | Silence is sexy: soundscape complexity alters mate choice in túngara frogs |
| Q112664034 | Silent listeners: can preferences of eavesdropping midges predict their hosts’ parasitism risk? |
| Q121438157 | Silver spoon effects of hatching order in an asynchronous hatching bird |
| Q127459147 | Simplifying our understanding of contests: a comment on Chapin et al |
| Q61930379 | Simulated hatching failure predicts female plasticity in extra-pair behavior over successive broods |
| Q115414466 | Singing in Africa: no evidence for a long supposed function of winter song in a migratory songbird |
| Q115787902 | Singing in the city: high song frequencies are no guarantee for urban success in birds |
| Q60459103 | Singing to impress: the importance of developmental stress |
| Q114093521 | Site fidelity increases reproductive success by increasing foraging efficiency in a marine predator |
| Q37623375 | Size and competitive mating success in the yeast Saccharomyces cerevisiae |
| Q129133680 | Size and contrast increase the divertive effect of eyespots |
| Q36775801 | Size and heterozygosity influence partner selection in the Formosan subterranean termite. |
| Q113393721 | Size matters: male and female mate choice leads to size-assortative pairing in a coral reef cardinalfish |
| Q114588941 | Size-dependent aggression towards kin in a cannibalistic species |
| Q114093514 | Size-dependent microhabitat selection by masquerading prey |
| Q125728582 | Size-dependent patterns of diel vertical migration: smaller fish may benefit from faster ascent |
| Q115543804 | Size-dependent predation by snakes: selective foraging or differential prey vulnerability? |
| Q113178639 | Size-dependent trait-mediated indirect interactions among sea urchin herbivores |
| Q59256318 | Slow explorers take less risk: a problem of sampling bias in ecological studies |
| Q58045856 | Small-scale demographic structure suggests preemptive behavior in a flocking shorebird |
| Q112748508 | Smart mating: the cognitive ability of females influences their preference for male cognitive ability |
| Q88702387 | Social and ecological drivers of reproductive seasonality in geladas |
| Q34159751 | Social and ecological factors influencing offspring survival in wild macaques |
| Q107099636 | Social and life-history correlates of hormonal partner compatibility in greylag geese (Anser anser) |
| Q112743915 | Social and physical environment independently affect oviposition decisions in Drosophila |
| Q60376533 | Social conflict and costs of cooperation in meerkats are reflected in measures of stress hormones |
| Q114939577 | Social conflict in ant larvae: egg cannibalism occurs mainly in males and larvae prefer alien eggs |
| Q128880564 | Social context affects thermoregulation but not activity level during avian immune response |
| Q130034997 | Social context alters host behavior and infection risk |
| Q38202046 | Social context of shell acquisition in Coenobita clypeatus hermit crabs |
| Q57247650 | Social environment and reproductive interference affect reproductive success in the frog Rana latastei |
| Q104368922 | Social experiences shape behavioral individuality and within-individual stability |
| Q60658778 | Social foraging strategies and acquisition of novel foraging skills in cooperatively breeding Arabian babblers |
| Q114093523 | Social information use about novel aposematic prey depends on the intensity of the observed cue |
| Q124295651 | Social integration predicts survival in female white-faced capuchin monkeys |
| Q57237184 | Social interactions generate mutually reinforcing selection for male aggression in Lake Eyre dragons |
| Q55128141 | Social interactions predict genetic diversification: an experimental manipulation in shorebirds. |
| Q30049161 | Social mating systems and extrapair fertilizations in passerine birds |
| Q36477835 | Social pairing of Seychelles warblers under reduced constraints: MHC, neutral heterozygosity, and age. |
| Q121030691 | Social plasticity in choosiness in green tree frogs, Hyla cinerea |
| Q57649088 | Social stability and daily body mass gain in great tits |
| Q61050718 | Social transmission of maladaptive information in the guppy |
| Q61896048 | Sociality across species: spatial proximity of newborn bats promotes heterospecific social bonding |
| Q126160504 | Sociality and asociality in white-nosed coatis (Nasua narica): foraging costs and benefits |
| Q115041133 | Sociality and signaling activity modulate information flow in river otter communication networks |
| Q58486976 | Sociality in New World hystricognath rodents is linked to predators and burrow digging |
| Q56873937 | Sociality in river otters: cooperative foraging or reproductive strategies? |
| Q34449204 | Socially mediated polyandry: a new benefit of communal nesting in mammals. |
| Q90446392 | Socio-ecological conditions and female infidelity in the Seychelles warbler |
| Q125789953 | Socio-ecological factors shape the opportunity for polygyny in a migratory songbird |
| Q56945800 | Sociospatial structuration of alternative breeding strategies in a color polymorphic raptor |
| Q114093516 | Something in the wind: the influence of wind speed and direction on African lion movement behavior |
| Q115787894 | Song adjustments by an open habitat bird to anthropogenic noise, urban structure, and vegetation |
| Q56168849 | Song and immunological condition in male barn swallows (Hirundo rustica) |
| Q114896874 | Song bout length is indicative of spatial learning in European starlings |
| Q58311448 | Song discrimination suggests premating isolation among sympatric indigobird species and host races |
| Q30496499 | Song matching, overlapping, and switching in the banded wren: the sender's perspective. |
| Q115543500 | Song post exposure, song features, and predation risk |
| Q129973256 | Song recognition and heterospecific associations between 2 fairy-wren species (Maluridae) |
| Q114152187 | Song varies with latitude, climate, and species richness in a Neotropical bird |
| Q33789003 | Songbird chemosignals: volatile compounds in preen gland secretions vary among individuals, sexes, and populations |
| Q115543402 | Sophisticated early life lessons: threat-sensitive generalization of predator recognition by embryonic amphibians |
| Q109041143 | Sound familiar? Acoustic similarity provokes responses to unfamiliar heterospecific alarm calls |
| Q123093156 | Sounds of senescence: male swamp sparrows respond less aggressively to the songs of older individuals |
| Q91272719 | Sources of intraspecific variation in the collective tempo and synchrony of ant societies |
| Q105427722 | Space use by animals on the urban fringe: interactive effects of sex and personality |
| Q34060900 | Spatial autocorrelation: an overlooked concept in behavioral ecology |
| Q115414469 | Spatial decoupling of song and plumage generates novel phenotypes between 2 avian subspecies |
| Q113821209 | Spatial ecology of perceived predation risk and vigilance behavior in white-faced capuchins |
| Q117215750 | Spatial learning overshadows learning novel odors and sounds in both predatory and frugivorous bats |
| Q35624495 | Spatial movements and social networks in juvenile male song sparrows |
| Q60018274 | Spatial positioning in the selfish herd |
| Q57235654 | Spatial variation in food availability predicts extrapair paternity in the arctic fox |
| Q60487923 | Spatiotemporal variation of host use in a brood parasite: the role of the environment |
| Q52603709 | Specialists and generalists coexist within a population of spider-hunting mud dauber wasps. |
| Q128502851 | Specialization reduces foraging effort and improves breeding performance in a generalist bird |
| Q115543835 | Specialized predation on plataspid heteropterans in a coccinellid beetle: adaptive behavior and responses of prey attended or not by ants |
| Q54432762 | Species and population differences in social recognition between fishes: a role for ecology? |
| Q126123540 | Species divergence in offspring begging and parental provisioning is linked to nutritional dependency |
| Q61745132 | Species identity cues: possibilities for errors during vibrational communication on plant stems |
| Q56382846 | Species replacement reduces community participation in avian antipredator groups |
| Q60246871 | Species- and sex-specific adjustments of movement behavior to landscape heterogeneity in butterflies |
| Q115543522 | Specific color sensitivities of prey and predator explain camouflage in different visual systems |
| Q59265122 | Spectral niche segregation and community organization in a tropical cricket assemblage |
| Q30484562 | Sperm investment in male meadow voles is affected by the condition of the nearby male conspecifics. |
| Q59117672 | Sperm length evolution in the fungus-growing ants |
| Q110615304 | Sperm phenotypic plasticity in a cichlid: a territorial male's counterstrategy to spawning takeover |
| Q56210088 | Sperm precedence in monarch butterflies (Danaus plexippus) |
| Q112806638 | Spider aggressiveness determines the bidirectional consequences of host-inquiline interactions |
| Q126091483 | Spinner dolphins in a remote Hawaiian atoll: social grouping and population structure |
| Q60435988 | Split sex ratios in the social Hymenoptera: a meta-analysis |
| Q125902997 | Spontaneous nongenetic variation of group size creates cheater-free groups of social microbes |
| Q127702988 | Squaring the information triangle: a comment on Chapin et al |
| Q115543474 | State-dependent decision making: educated predators strategically trade off the costs and benefits of consuming aposematic prey |
| Q55970352 | State-dependent male mating tactics in the grey seal: the importance of body size |
| Q130042735 | Statistically testing the role of individual learning and decision-making in trapline foraging |
| Q115543228 | Steller’s jays assess and communicate about predator risk using detection cues and identity |
| Q60467380 | Steroid hormone profiles and relative body condition of calling and satellite toads: implications for proximate regulation of behavior in anurans |
| Q56484036 | Stinging spines protect slug caterpillars (Limacodidae) from multiple generalist predators |
| Q57237204 | Strategic male mate choice minimizes ejaculate consumption |
| Q56267840 | Strategic paternity assurance in the sex-role reversed Eurasian dotterel (Charadrius morinellus): behavioral and genetic evidence |
| Q56017914 | Strategic sperm allocation and a Coolidge effect in an externally fertilizing species |
| Q60430734 | Stress and sexual traits: why are there no clear relationships? A comment on Moore et al |
| Q60430766 | Stress, resource allocation, and mortality |
| Q113035193 | Stress, testosterone, and the immunoredistribution hypothesis |
| Q113034985 | Stress-induced sex ratios in ground squirrels: support for a mechanistic hypothesis |
| Q63241322 | Stripes for warning and stripes for hiding: spatial frequency and detection distance |
| Q53417138 | Striving for transparent and credible research: practical guidelines for behavioral ecologists. |
| Q104872940 | Strong but variable associations between social dominance and clutch sex ratio in a colonial corvid |
| Q105940386 | Strong evidence for selection for larger brood size in a great tit population |
| Q126357674 | Strong sexual selection despite spatial constraints on extrapair paternity |
| Q60548754 | Structural and melanin coloration indicate parental effort and reproductive success in male eastern bluebirds |
| Q112271141 | Structural equation modeling reveals determinants of fitness in a cooperatively breeding bird |
| Q114093520 | Studying predator foraging mode and hunting success at the individual level with an online videogame |
| Q113178642 | Substrate type affects caching and pilferage of pine seeds by chipmunks |
| Q57269558 | Sugar-free extrapair mating: a comment on Arct et al |
| Q57018636 | Superb fairy-wren males aggregate into hidden leks to solicit extragroup fertilizations before dawn |
| Q109041187 | Superb fairy-wrens respond more to alarm calls from mate and kin compared to unrelated individuals |
| Q56873712 | Supercolonies of billions in an invasive ant: What is a society? |
| Q58461321 | Suppressed breeding in the field vole (Microtus agrestis): an adaptation to cyclically fluctuating predation risk |
| Q62088230 | Survival benefits and divergence of predator-induced behavior between pumpkinseed sunfish ecomorphs |
| Q128087073 | Symmetrical discrimination despite weak song differentiation in 2 suboscine bird sister species |
| Q61503136 | Symmetry and sexual dimorphism in human faces: interrelated preferences suggest both signal quality |
| Q126555001 | Sympatric wren-warblers partition acoustic signal space and song perch height |
| Q60481358 | Systematic evidence synthesis as part of a larger process: a response to comments on Berger-Tal et al |
| Q60481370 | Systematic reviews and maps as tools for applying behavioral ecology to management and policy |
| Q61502935 | Taller men are less sensitive to cues of dominance in other men |
| Q60658845 | Task partitioning increases reproductive output in a cooperative bird |
| Q38996417 | Task switching is associated with temporal delays in Temnothorax rugatulus ants |
| Q60398556 | Teaching behavior is responsive and costly in fairy-wrens though the time course needs to be defined |
| Q56873716 | Teams in animal societies |
| Q29030335 | Temperature affects operational sex ratio and intensity of male-male competition: an experimental study of sand gobies, Pomatoschistus minutus |
| Q36701381 | Temperature can shape a cline in polyandry, but only genetic variation can sustain it over time. |
| Q58416538 | Temporal activity patterns of predators and prey across broad geographic scales |
| Q56387311 | Temporal habitat shift of a polymorphic newt species under predation risk |
| Q52330532 | Temporal migration patterns and mating tactics influence size-assortative mating in Rana temporaria. |
| Q64298847 | Temporal plasticity in habitat selection criteria explains patterns of animal dispersal |
| Q60399016 | Temporal variability in a multicomponent trait: nuptial coloration of female two-spotted gobies |
| Q113821413 | Temporally variable predation risk and fear retention in Trinidadian guppies |
| Q115543760 | Tendency to inspect predators predicts mortality risk in the guppy (Poecilia reticulata) |
| Q34060895 | Terminal investment and senescence in rhesus macaques (Macaca mulatta) on Cayo Santiago |
| Q57190995 | Territorial bequeathal by red squirrel mothers |
| Q56688636 | Territorial male bullfrogs (Rana catesbeiana) do not assess fighting ability based on size-related variation in acoustic signals |
| Q125663232 | Territorial male color predicts agonistic behavior of conspecifics in a color polymorphic species |
| Q57699128 | Territorial male gobies respond aggressively to sneakers but do not adjust their sperm expenditure |
| Q114896873 | Territorial song sparrows tolerate juveniles during the early song-learning phase |
| Q58310271 | Territory quality drives intraspecific patterns of extrapair paternity |
| Q128723581 | Testes size increases with sperm competition risk and intensity in bony fish and sharks |
| Q113035081 | Testing a new version of the size-advantage hypothesis for sex change: sperm competition and size-skew effects in the bucktooth parrotfish, Sparisoma radians |
| Q125584477 | Testing for cryptic female choice in monarch butterflies |
| Q126126498 | Testing predictions of foraging theory for a sit-and-wait forager, Anolis gingivinus |
| Q113035047 | Testing the beneficial acclimation hypothesis: temperature effects on mating success in a butterfly |
| Q113035107 | Testing the niche differentiation hypothesis in wild capuchin monkeys with polymorphic color vision |
| Q55980560 | Testing the sexy son hypothesis--a research framework for empirical approaches |
| Q113035139 | Testosterone effects on the immune system and parasite infestations in the barn swallow (Hirundo rustica): an experimental test of the immunocompetence hypothesis |
| Q57566237 | Testosterone production, sexually dimorphic morphology, and digit ratio in the dark-eyed junco |
| Q60320062 | Testosterone supplementation in subordinate, small male lizards: consequences for aggressiveness, color development, and parasite load |
| Q60117750 | Testosterone, immunocompetence, and honest sexual signaling in male red grouse |
| Q57955097 | Tests of the kin selection model of mate choice and inbreeding avoidance in satin bowerbirds |
| Q113035155 | Tests of the mate-guarding hypothesis for social monogamy: male snapping shrimp prefer to associate with high-value females |
| Q55883968 | Thanatosis as an adaptive male mating strategy in the nuptial gift–giving spider Pisaura mirabilis |
| Q56228690 | The Social Implications of traditional use of lek sites in the ruff Philomachus pugnax |
| Q56235189 | The adaptive significance of stealing in a marine bird and its relationship to parental quality |
| Q125554299 | The advantage of starving: success in cannibalistic encounters among wolf spiders |
| Q56424862 | The aggressive personality of an introduced fish affects foraging behavior in a polymorphic newt |
| Q56436651 | The art of choice: predation risk changes interspecific competition between freshwater amphipods |
| Q55870981 | The behavioral ecology of threshold evolution in a polyphenic beetle |
| Q64910079 | The behavioral origins of novelty: did increased aggression lead to scale-eating in pupfishes? |
| Q126259246 | The behavioral trade-off between thermoregulation and foraging in a heat-sensitive species |
| Q113035198 | The beneficial sexually transmitted microbe hypothesis of avian copulation |
| Q30367329 | The benefits of being toxic to deter predators depends on prey body size. |
| Q56485637 | The benefits of costly signaling: Meriam turtle hunters |
| Q113821416 | The benefits of stealing from a predator: foraging rates, predation risk, and intraspecific aggression in the kleptoparasitic spider Argyrodes antipodiana |
| Q113034968 | The biparental care hypothesis for the evolution of monogamy: experimental evidence in an amphibian |
| Q60337395 | The blue tit's song is an inconsistent signal of male condition |
| Q61956783 | The bounds of rationality and cognitive building blocks |
| Q56213272 | The carotenoid beta-carotene enhances facial color, attractiveness and perceived health, but not actual health, in humans |
| Q113034945 | The chimeric embryo hypothesis as a mechanism of avian sex ratio manipulation: a reply to Szász and Rosivall |
| Q113034942 | The chimeric embryo hypothesis as a mechanism of avian sex ratio manipulation? Comment on Tagirov and Rutkowska: Figure 1 |
| Q60564271 | The complexity of fish communication in human-disturbed environments: a comment on Radford et al |
| Q56688115 | The complexity of male reproductive success: effects of nutrition, morphology, and experience |
| Q60570952 | The composition, stability, and kinship of reproductive coalitions in a lekking bird |
| Q55920176 | The confusion effect—from neural networks to reduced predation risk |
| Q115414514 | The cost of dispersal: predation as a function of movement and site familiarity in ruffed grouse |
| Q60398563 | The cost of teaching embryos in superb fairy-wrens |
| Q60549547 | The cost of virulence: an experimental study of egg eviction by brood parasitic chicks |
| Q91272721 | The costs and benefits of decentralization and centralization of ant colonies |
| Q56442463 | The costs of autotomy and regeneration in animals: a review and framework for future research |
| Q127970652 | The costs of competition: injury patterns in 2 Asian colobine monkeys |
| Q56040937 | The definition of eusociality |
| Q115543366 | The degree of response to increased predation risk corresponds to male secondary sexual traits |
| Q56689068 | The description of mate choice |
| Q30486733 | The deterrent effect of bird song in territory defense |
| Q29392262 | The development of behavioral defenses: a mechanistic analysis of vulnerability in red-eyed tree frog hatchlings |
| Q105612865 | The development of foraging microhabitat preferences in meerkats |
| Q60430749 | The developmental stress hypothesis: a special case of the evolution of condition-dependent sexual traits |
| Q113035043 | The discounting-by-interruptions hypothesis: model and experiment |
| Q110031519 | The discrimination of alternative male morphologies |
| Q115543415 | The distribution of unequal predators across food patches is not necessarily (semi)truncated |
| Q60578500 | The dynamics of animal social networks: analytical, conceptual, and theoretical advances |
| Q58884000 | The ecology of conception and pregnancy failure in wild baboons |
| Q61956934 | The economic basis of cooperation: tradeoffs between selfishness and generosity |
| Q54294042 | The economics of nestmate killing in avian brood parasites: a provisions trade-off |
| Q56769966 | The educated prey: consequences for exploitation and control |
| Q57669379 | The effect of competitor presence and relative competitive ability on male mate choice |
| Q112806637 | The effect of experimental design on the measurement of mate choice: a meta-analysis |
| Q30047865 | The effect of partial brood loss on male desertion in a cichlid fish: an experimental test |
| Q56168836 | The effect of tail streamer length on aerodynamic performance in the barn swallow |
| Q56269918 | The effectiveness of mate guarding by male black-throated blue warblers |
| Q116977407 | The effects of familiarity and mating experience on mate choice in mosquitofish, Gambusia holbrooki |
| Q126124189 | The effects of habitat- and diet-based cues on association preferences in three-spined sticklebacks |
| Q114093512 | The effects of microhabitat specialization on mating communication in a wolf spider |
| Q57669326 | The effects of neighbor familiarity and size on cooperative defense of fiddler crab territories |
| Q59270503 | The effects of predation risk from crab spiders on bee foraging behavior |
| Q115543327 | The effects of recruitment to direct predator cues on predator responses in meerkats |
| Q57216881 | The effects of social network position on the survival of wild Barbary macaques,Macaca sylvanus |
| Q125566662 | The effects of stress and glucocorticoids on vocalizations: a test in North American red squirrels |
| Q112806643 | The effects of wind on trap structural and material properties of a sit-and-wait predator |
| Q58311847 | The energetic costs of egg heating constrain incubation attendance but do not determine daily energy expenditure in the pectoral sandpiper |
| Q56066709 | The evolution and function of pattern diversity in snakes |
| Q113035207 | The evolution of bill coloration and plumage dimorphism supports the transference hypothesis in dabbling ducks |
| Q54045411 | The evolution of communal roosting in birds: origin and secondary losses |
| Q56269180 | The evolution of cryptic spider silk: a behavioral test |
| Q56288564 | The evolution of imperfect mimicry |
| Q56806950 | The evolution of lateralized foot use in parrots: a phylogenetic approach |
| Q60670655 | The evolution of paternity and paternal care in birds |
| Q56534586 | The evolution of progressive provisioning |
| Q55970358 | The evolution of reproductive systems in pinnipeds |
| Q55932426 | The evolution of soldier reproduction in social thrips |
| Q127863447 | The evolution of two types of play |
| Q56535388 | The evolution of vocal alarm communication in rodents |
| Q56953914 | The evolutionarily stable strategy for secondary sexual characters |
| Q57002607 | The expression of dietary conservatism in solitary and shoaling 3-spined sticklebacks Gasterosteus aculeatus |
| Q56019923 | The fear of unseen predators: ground squirrel tail flagging in the absence of snakes signals vigilance |
| Q58486623 | The flush early and avoid the rush hypothesis holds after accounting for spontaneous behavior |
| Q113178645 | The foraging behavior of granivorous rodents and short-term apparent competition among seeds |
| Q60430774 | The function and evolution of the tail streamer in hirundines |
| Q115414482 | The function of contrasting pelage markings in artiodactyls |
| Q115414524 | The function of extrapair paternity in blue tits and great tits: good genes or fertility insurance? |
| Q115414528 | The function of long tails in female barn swallows (Hirundo rustica): an experimental study |
| Q60430671 | The growth benefits of aggressive behavior vary with individual metabolism and resource predictability |
| Q122538198 | The habitat connectivity hypothesis of escape in urban woodland birds |
| Q29027490 | The heterospecific habitat copying hypothesis: can competitors indicate habitat quality? |
| Q113275628 | The honeybee queen influences the regulation of colony drone production |
| Q125023225 | The impact of food availability on risk-induced trait responses in prey |
| Q114896876 | The impact of learning foster species' song on the evolution of specialist avian brood parasitism |
| Q126075878 | The importance of phenotypic defectors in stabilizing reciprocal altruism |
| Q60658757 | The importance of understanding costs and benefits: a comment on Christensen and Radford |
| Q115543487 | The influence of conspecifics and predation risk on the vigilance of elk (Cervus elaphus) in Yellowstone National Park |
| Q58817099 | The influence of ecology on sociality in the killer whale (Orcinus orca) |
| Q112806653 | The influence of environmental conditions on cache recovery and cache pilferage by yellow pine chipmunks (Tamias amoenus) and deer mice (Peromyscus maniculatus) |
| Q129899817 | The influence of environmental variance on the evolution of signaling behavior |
| Q58706979 | The influence of forage, protected areas, and mating prospects on grouping patterns of male elephants |
| Q113821454 | The influence of nest predation on mating strategies under polygyny |
| Q57649122 | The influence of predation risk on threat display in great tits |
| Q56518138 | The influence of water velocity on the display behavior of male guppies, Poecilia reticulata |
| Q113821395 | The interaction between ambush predators, search patterns of herbivores, and aggregations of plants |
| Q115414447 | The interface of ecological novelty and behavioral context in the formation of ecological traps |
| Q60331383 | The logic of hypersocial colonies |
| Q127215890 | The long view on demographic effects on social networks: a response to comments on Shizuka and Johnson |
| Q58771333 | The long-term consequences of egg predation |
| Q62382984 | The meaning of melanin, carotenoid, and pterin pigments in the bluefin killifish, Lucania goodei |
| Q114633536 | The mere presence of cuckoos in breeding area alters egg-ejection decisions in Daurian redstarts |
| Q121577938 | The mixed-species chorus as public information: túngara frogs eavesdrop on a heterospecific |
| Q120839781 | The nature of privilege: intergenerational wealth in animal societies |
| Q56686601 | The origin of parental care in birds: a reassessment |
| Q61661117 | The parental investment model and minimum mate choice criteria in humans |
| Q115543662 | The performance of permutations and exponential random graph models when analyzing animal networks |
| Q125822544 | The position of eyespots and thickened segments influence their protective value to caterpillars |
| Q57237218 | The predation cost of female resistance |
| Q115543311 | The presence of neighbors influences defense against predators in a cooperatively breeding cichlid |
| Q115039411 | The problem of measuring trait-preference correlations without disrupting them |
| Q123162023 | The refractory period of female katydids (Orthoptera: Tettigoniidae): sexual conflict over the remating interval? |
| Q127855465 | The relationship of body condition, superoxide dismutase, and superoxide with sperm performance |
| Q58771341 | The relative effect of parasites and social status on sperm traits in Arctic charr |
| Q57655571 | The relative importance of RHP and resource quality in contests with ownership asymmetries |
| Q104206407 | The relative importance of size and asymmetry in sexual selection |
| Q56228692 | The resident's dilemma: a female choice model for the evolution of alternative mating strategies in lekking male ruffs (Philomachus pugnax) |
| Q57002635 | The response of fish to novel prey: evidence that dietary conservatism is not restricted to birds |
| Q115543384 | The responses of prey fish to temporal variation in predation risk: sensory habituation or risk assessment? |
| Q56288157 | The role of avoidance learning in an aggressive mimicry system |
| Q37229951 | The role of beginner's luck in learning to prefer risky patches by socially foraging house sparrows |
| Q114093524 | The role of behavioral type composition on resource use and growth of a juvenile predator |
| Q56953880 | The role of females in influencing mating patterns |
| Q60535313 | The role of motor diversity in foraging innovations: a cross-species comparison in urban birds |
| Q113821486 | The role of predation risk in stopover habitat selection in migrating bramblings, Fringilla montifringilla |
| Q60264429 | The role of previous social experience on risk-taking and leadership in three-spined sticklebacks |
| Q60631403 | The role of serotonin in the modulation of cooperative behavior |
| Q58389834 | The secret sex lives of sage-grouse: multiple paternity and intraspecific nest parasitism revealed through genetic analysis |
| Q60566048 | The sexual signals of the East-Mediterranean barn swallow: a different swallow tale |
| Q115414458 | The shape of preference functions and what shapes them: a comment on Edward |
| Q56502938 | The short-term regulation of foraging in harvester ants |
| Q129574487 | The shortfall of sociality: group-living affects hunting performance of individual social spiders |
| Q60384352 | The signal in noise: acoustic information for soundscape orientation in two North American tree frogs |
| Q115543178 | The significance of prey avoidance behavior for the maintenance of a predator color polymorphism |
| Q63437930 | The spandrels of Santa Barbara? A new perspective on the peri-ovulation paradigm |
| Q113821198 | The sparrow and the hawk: aggressive signaling under risk of predation |
| Q57309981 | The strength of postcopulatory sexual selection within natural populations of field crickets |
| Q55878561 | The swaying behavior ofExtatosoma tiaratum: motion camouflage in a stick insect? |
| Q56269026 | The town bird and the country bird: problem solving and immunocompetence vary with urbanization |
| Q121210811 | The transmission of advertisement calls in Central American frogs |
| Q63361205 | The ultimate effect of being cleaned: does ectoparasite removal have reproductive consequences for damselfish clients? |
| Q60895447 | The unequal variance t-test is an underused alternative to Student's t-test and the Mann–Whitney U test |
| Q114592023 | The use and relative importance of intraspecific and interspecific social information in a bird community |
| Q125824742 | The value of information in floral cues: bumblebee learning of floral size cues |
| Q115543620 | The waiting game: a "battle of waits" between predator and prey |
| Q111894648 | The worm re-turns: hiding behavior of a tube-dwelling marine polychaete, Serpula vermicularis |
| Q57592636 | Then versus now: effect of developmental and current environmental conditions on incubation effort in birds |
| Q126119892 | Thermal stress affects patch time allocation by preventing forgetting in a parasitoid wasp |
| Q111631552 | Thermodynamic constraints and the evolution of parental provisioning in vertebrates |
| Q56384998 | Thick eggshells of brood parasitic cowbirds protect their eggs and damage host eggs during laying |
| Q60511501 | Threat sensitive adjustment of aggression by males and females in a biparental cichlid |
| Q34532678 | Thrips domiciles protect larvae from desiccation in an arid environment |
| Q115543298 | Time scales of associating food and odor by predator communities in the field |
| Q56432895 | To boldly go where no goby has gone before: boldness, dispersal tendency, and metabolism at the invasion front |
| Q125443947 | To eat, or not to eat: a phantom decoy affects information-gathering behavior by a free-ranging mammalian herbivore |
| Q57940546 | To lek or not to lek: mating strategies of male fallow deer |
| Q58776309 | To sing or not to sing: seasonal changes in singing vary with personality in wild great tits |
| Q60415585 | To trill or not to trill? Territorial response to a heterospecific vocal trait in male collared doves, Streptopelia decaocto |
| Q57579335 | Tonic immobility is a measure of boldness toward predators: an application of Bayesian structural equation modeling |
| Q57232177 | Toward an individual-level understanding of vigilance: the role of social information |
| Q105612859 | Toward wild psychometrics: linking individual cognitive differences to fitness |
| Q90635552 | Towards a comparative approach to the structure of animal personality variation |
| Q121775026 | Trade-off in short- and long-distance communication in tungara (Physalaemus pustulosus) and cricket (Acris crepitans) frogs |
| Q57409007 | Trade-offs between energy maximization and parental care in a central place forager, the sea otter |
| Q63437897 | Trade-offs between markers of absolute and relative quality in human facial preferences |
| Q59024535 | Trade-offs between personal immunity and reproduction in the burying beetle, Nicrophorus vespilloides |
| Q125995857 | Trade-offs between postcopulatory riding and mate location in the blue milkweed beetle |
| Q57245982 | Trade-offs in lactation and milk intake by competing siblings in a fluctuating environment |
| Q55180459 | Transparent and credible practices under the microscope: a response to comments on Ihle et al. |
| Q115414490 | Trapline foraging by bumble bees: V. Effects of experience and priority on competitive performance |
| Q109667238 | Traplining in hummingbirds: flying short-distance sequences among several locations |
| Q57607638 | Trash to treasure: leaf-cutting ants repair nest-mound damage by recycling refuse dump materials |
| Q59028266 | Traveling or stopping of migrating birds in relation to wind: an illustration for the osprey |
| Q113821335 | Triparental ageing in a laboratory population of an insect with maternal care |
| Q60430047 | Trophic dimorphism in alternative male reproductive morphs of the acarid mite Sancassania berlesei |
| Q60777714 | Ultraviolet crown coloration in female blue tits predicts reproductive success and baseline corticosterone |
| Q60502057 | Ultraviolet reflection and predation risk in diurnal and nocturnal Lepidoptera |
| Q60264490 | Unavoidable limits on group size in a body size-based linear hierarchy |
| Q60319807 | Uncertainty about future predation risk modulates monitoring behavior from refuges in lizards |
| Q128978115 | Uncoordinated dances associated with high reproductive success in a crane |
| Q59238969 | Understanding antagonism: a comment on Sheehan and Bergman |
| Q61814220 | Unexploited females and unreliable signals of male quality in a Malawi cichlid bower polymorphism |
| Q60354051 | Unmasking Zorro: functional importance of the facial mask in the Masked Shrike (Lanius nubicus) |
| Q60557354 | Unraveling the key to innovative problem solving: a test of learning versus persistence |
| Q61781995 | Unraveling the true complexity of costly color signaling |
| Q60337040 | Unrelated helpers neither signal contributions nor suffer retribution in chestnut-crowed babblers |
| Q60549948 | Urban and colorful male house finches are less aggressive |
| Q115543336 | Urban areas as refuges from predators and flight distance of prey |
| Q115787903 | Urban habitats and feeders both contribute to flight initiation distance reduction in birds |
| Q60544734 | Urban-associated drivers of song variation along a rural–urban gradient |
| Q125899306 | Urbanization and individual differences in exploration and plasticity |
| Q125388278 | Use of California bay foliage by wood rats for possible fumigation of nest-borne ectoparasites |
| Q60490041 | Using playback of territorial calls to investigate mechanisms of kin discrimination in red squirrels |
| Q115543770 | Utilization of different prey type patches in the Ural owl(Strix uralensis): a sit-and-wait predator |
| Q37090328 | Variable ecological conditions promote male helping by changing banded mongoose group composition |
| Q110125357 | Variable mode of estrus affects female decision for multiple mating |
| Q60658857 | Variable postfledging care in a cooperative bird: causes and consequences |
| Q123125916 | Variance in lifetime reproductive success of male polar bears |
| Q33893676 | Variance in male lifetime reproductive success and estimation of the degree of polygyny in a primate |
| Q115414457 | Variation and selection on preference functions: a comment on Edward |
| Q105613061 | Variation in group territorial behavior: a response to comments on Christensen and Radford |
| Q122191230 | Variation in nuptial gift quality in bush crickets (Orthoptera: Tettigoniidae) |
| Q128683763 | Variation in the condition-dependence of individual sexual traits in male eastern mosquitofish, Gambusia holbrooki |
| Q57237209 | Variation in the effect of repeated intrusions on calling behavior in a territorial toadlet |
| Q115414519 | Varied female and male courtship behavior facilitated the evolution of a novel sexual signal |
| Q114093513 | Vegetation structure mediates a shift in predator avoidance behavior in a range-edge population |
| Q57706875 | Vertical bars on male Xiphophorus multilineatus: a signal that deters rival males and attracts females |
| Q112806636 | Viability selection by invertebrate predators in the polyphenic black scavenger fly Sepsis thoracica |
| Q57655579 | Vibratory communication in the jumping spider Phidippus clarus: polyandry, male courtship signals, and mating success |
| Q111376724 | Vigilance and predation of a forest-living bird species depend on large-scale habitat structure |
| Q115543404 | Vigilance and predator detection vary between avian species with different visual acuity and coverage |
| Q57067391 | Vigilance does not covary with group size in an island population of silvereyes (Zosterops lateralis) |
| Q56505305 | Vigor and skill in the acrobatic mating displays of a Neotropical songbird |
| Q113034032 | Vireo song repertoires and migratory distance: three sexual selection hypotheses fail to explain the correlation |
| Q37627040 | Virginity and the clutch size behavior of a parasitoid wasp where mothers mate their sons |
| Q109041127 | Visual obstruction, but not moderate traffic noise, increases reliance on heterospecific alarm calls |
| Q60481822 | Visual predators impose correlational selection on prey color pattern and behavior |
| Q115543654 | Visual recognition and coevolutionary history drive responses of amphibians to an invasive predator |
| Q59278403 | Vocal behavior predicts reproductive success in a teleost fish |
| Q109041209 | Vocal characteristics of prairie dog alarm calls across an urban noise gradient |
| Q30407655 | Vocal fundamental and formant frequencies are honest signals of threat potential in peripubertal males |
| Q98238548 | Volatile fatty acid and aldehyde abundances evolve with behavior and habitat temperature in Sceloporus lizards |
| Q124833483 | W. D. Hamilton and the evolution of sociality |
| Q112806641 | Walking the line: search behavior and foraging success in ant species |
| Q34532669 | Wall lizards display conspicuous signals to conspecifics and reduce detection by avian predators. |
| Q56451698 | Wary invaders and clever natives: sympatric house geckos show disparate responses to predator scent |
| Q60802455 | Wasp behavior leads to uniform parasitism of a host available only a few hours per year |
| Q56267788 | Waste management in the leaf-cutting ant Atta colombica |
| Q60060557 | Water-seeking behavior in insects harboring hairworms: should the host collaborate? |
| Q30499362 | Water-seeking behavior in worm-infected crickets and reversibility of parasitic manipulation. |
| Q61954695 | We can study how mechanisms evolve without knowing the rules of chess or the workings of the brain |
| Q55872328 | Wealth modifies relationships between kin and women's fertility in high-income countries |
| Q59394344 | What a hawkmoth remembers after hibernation depends on innate preferences and conditioning situation |
| Q115543459 | What best explains vigilance in elk: characteristics of prey, predators, or the environment? |
| Q57062859 | What decision rules might pink-footed geese use to depart on migration? An individual-based model |
| Q115543246 | What do predators do? A response to comments on Skelhorn et al. |
| Q127776647 | What have we recently learned about song learning and social interactions? |
| Q113035061 | What hypothesis tests are not: a reply to Johnson |
| Q113035064 | What hypothesis tests are not: a response to Colegrave and Ruxton |
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