Programme Overviews
Plenary Speakers ---- Symposia List ---- Symposia & Oral Sessions ---- Poster Sessions
Symposia & Oral session (PDF version).
Check the list and visit to the session that you find it interesting. We cover a wide range of subjects that will contribute to understanding of the latest issues of ornithology.
Symposia & Oral Sessions
Presentation Type | Time | Room | Session Theme | Session Staritng Time |
Paper Title | Session ID |
---|---|---|---|---|---|---|
Tuesday, 19-Aug | ||||||
Concurrent Symposia | 10:00-12:00 | Room 2 | S07 To understand what birds actually see: toward a newer synthesis of visual perception and methods to study coloration |
10:03 | Understanding and Quantifying the Colour Patterns of Birds | s07-1k |
10:30 | Colour to birds and to humans: why is it so different? | s07-2k | ||||
10:57 | Using multispectral imaging to study bird coloration | s07-3 | ||||
11:19 | Color characteristics of delayed plumage maturation in the male Red-flanked Bluetail Tarsiger cyanurus. | s07-4 | ||||
11:41 | A novel method for quantifying egg patterns using HLAC | s07-5 | ||||
Room 3 | S11 Invasive species and Pacific island bird conservation |
10:03 | The Endemic Amami Jay (Garrulus lidthi), invasive Small Indian Mongoose, and other alien organisms : a 21st century investigation of island aliens for improved ecosystem management | s11-1k | ||
10:30 | Population Viability Analysis for Swinhoe’s Storm Petrels on Chilbal-do Islet, Korea | s11-2k | ||||
10:57 | Impact of invasive predators on Okinawa and Guam Rails | s11-3 | ||||
11:19 | Behavioural changes in an invasive parasitic fly and its avian hosts, the Darwin’s finches. | s11-4 | ||||
11:41 | The spread of the Spur-winged Plover (Vanellus miles novaehollandiae) in New Zealand | s11-5 | ||||
Room 4 | S12 Evolution and behavioral adaptation of waterbirds flying in the air and in the water |
10:03 | Locomotor transitions in birds: the evolution of wing propelled diving as a case study in parsing patterns of character evolution associated with acquisition of a novel locomotor mode | s12-1k | ||
10:30 | Comparative analyses of swim speed in marine vertebrates | s12-2k | ||||
10:57 | Is the evolution of avian locomotion driven by biomechanics or physiology? | s12-3 | ||||
11:19 | Why do penguins inhale before diving? | s12-4 | ||||
11:41 | Functional morphology of wing musculature of extinct flightless Mancalline Auks (Alcidae, Mancallinae) | s12-5 | ||||
Room 5 | S42 Nutritional satisfaction: new perspectives on how birds acquire necessary energy and nutrients |
10:03 | Nutritional wisdom: How do birds balance their food choices with the dynamics of fluctuating nutrient needs? | s42-1k | ||
10:30 | Biofilm grazing: missing link in shorebird ecology (satisfaction from “snot”) | s42-2k | ||||
10:57 | The importance of salt-tolerance in the energetic trade-offs of migratory Dark-bellied Brent Geese | s42-3 | ||||
11:19 | Geese surfing the green wave: a comparison of three flyways differing in predictability | s42-4 | ||||
11:41 | Interference competition in a sexually dimorphic shorebird: prey behaviour explains why the dominant sex suffers and the subordinate does not | s42-5 | ||||
Room 6 | S15 Social complexity, vocal communication and cooperation |
10:03 | Learn for life: teaching predator recognition boosts survival of inexperienced individuals in a group-living bird species | s15-1k | ||
10:30 | Vocal communication and cooperation in socially-complex species | s15-2k | ||||
10:57 | Heterospecific responses to mobbing calls | s15-3 | ||||
11:19 | Female counter-singing: complex social networks and song learning abilities in New Zealand Bellbirds (Anthornis melanura) | s15-4 | ||||
11:41 | Mobbing calls of Japanese great tits signal predator type to both parents and offspring | s15-5 | ||||
Room 7 | S10 Physiological factors influencing migratory strategies |
10:03 | The stress of stopping over: oxidative stress associated with long-duration flights and its implications for the ecology of migrants at stopover sites | s10-1k | ||
10:30 | Hormonal regulation of the fuel metabolism in migrating birds | s10-2k | ||||
10:57 | Corticosterone and migratory fueling in Northern Wheatears facing different barrier crossings | s10-3 | ||||
11:19 | Physiological strategies for stopover in migrating songbirds after barrier crossing in spring | s10-4 | ||||
Room 8 | S16 Radar Aeroecology |
10:03 | Studying ecosystem connectivity with radar – recent findings and future perspectives. | s16-1k | ||
10:30 | Recent and on-going advancements in radar aeroecology: A physicist’s perspective | s16-2k | ||||
10:57 | Continental-scale radar monitoring of the aerial movements of animals | s16-3 | ||||
11:19 | Weather radar observations of bird stopover distributions along the northern Gulf coast of Mexico during spring migration | s16-4 | ||||
11:41 | Convergent Patterns of Long-distance Nocturnal Migration in Passerines and Moths | s16-5 | ||||
Room 9 | S20 Avian nest predation: New perspectives |
10:03 | Nest predation influences on life history strategies | s20-1k | ||
10:30 | Acoustic communication, surveillance and eavesdropping by young under the risk of predation | s20-2k | ||||
10:57 | Adaptive breeding site selection in the face of nest predation: Is it for the birds? | s20-3 | ||||
11:19 | Nest survival in Arctic-breeding shorebirds in relation to activity of predators and nest site characteristics | s20-4 | ||||
11:41 | Blackbird (Turdus merula) nestlings treated with corticosterone or testosterone fail to respond to the risk of nest predation | s20-5 | ||||
Concurrent Oral Sessions | 16:30-18:00 | Room 2 | o03 Cognition & Signalling |
16:30 | Individual differences in taste perception & dietary wariness in European Starlings: causes and consequences | o03-1 |
16:48 | Olfactory signalling in a highly divergent species complex: the Crimson Rosella (Platycercus elegans) | o03-2 | ||||
17:06 | Hotshots and Hotspots: local spatial heterogeneity in life-history variation and signal content of UV structural colours in a socially monogamous passerine | o03-3 | ||||
17:24 | Effect of a fluctuating environment on multimodal signals | o03-4 | ||||
17:42 | The Colour of an Entire Avifauna: Understanding Chromatic Variability of Australian Birds | o03-5 | ||||
Room 3 | o02 Bird-human interactions |
16:30 | Listening to nature’s views | o02-1 | ||
16:48 | Relating species traits to extinction risk from the pet bird trade in Southeast Asia | o02-2 | ||||
17:06 | Antarctic seabirds as indicators of anthropogenic influences | o02-3 | ||||
17:24 | Understanding attacks by Kea (Nestor notabilis), an endemic high country parrot, on sheep in New Zealand | o02-4 | ||||
17:42 | Factors affecting bycatch of Black-Browed Albatross and Wandering Albatross: relationship between distribution and bycatch probabilities | o02-5 | ||||
Room 4 | o05 Conservation Techniques |
16:30 | Applications of unmanned vehicle systems to bird studies | o05-1 | ||
16:48 | At-sea experiment to evaluate the effectiveness of multiple mitigation measures on pelagic longline operations in the western North Pacific | o05-2 | ||||
17:06 | A world review of seabird translocation and social attraction projects | o05-3 | ||||
17:24 | Use of marine radar to evaluate collision risk of migrants with wind turbines | o05-4 | ||||
17:42 | Translocation of Asian houbara bustards (Chlamydotis macqueenii): current knowledge, constraints and future directions | o05-5 | ||||
Room 5 | o08 Evolution |
16:30 | The evolution of sweet taste perception in a nectar-feeding bird | o08-1 | ||
16:48 | Macroevolutionary processes in non-passeriform birds (Aves) at the global scale. | o08-2 | ||||
17:06 | Tracing the evolution of casque ornamentation in hornbills | o08-3 | ||||
17:24 | Is density-dependent diversification in North American wood warblers an artifact of species delimitation? | o08-4 | ||||
17:42 | Forelimb disparity of water birds in a phylogenetic context | o08-5 | ||||
Room 6 | o04 Community Ecology 1 |
16:30 | Hierarchical community models for analysing species- and density-area relationships | o04-1 | ||
16:48 | Do long term patterns of bird assemblage dynamics imply interspecific competition? Null model analyses of species associations. | o04-2 | ||||
17:06 | Abiotic versus biotic constraints on the elevational distributions of Andean birds. | o04-3 | ||||
17:24 | Population and community-level niche conservatism in antbirds (Thamnophilidae) along a tropical elevational gradient | o04-4 | ||||
17:42 | Contrasting avian community transitions from lowland to submontane forest on a variety of Bornean mountains | o04-5 | ||||
Room 7 | o06 Reproductive Behaviour |
16:30 | When a male changes his ways: sex differences in feeding behaviour in the Pied Flycatcher | o06-1 | ||
16:48 | Male Daito white-eyes improve nest positioning skills by learning the threat of two nest predators | 06-2 | ||||
17:06 | Microhabitat selection in ground nesting birds | o06-3 | ||||
17:24 | Solving a paradox: context-dependent effects of maternal testosterone in the Rock Pigeon (Columba livia) and its causes and consequences | o06-4 | ||||
17:42 | Provisioning behaviour correlates with the reactive-proactive personality axis among Great Tits in the wild | o06-5 | ||||
Room 8 | o01 Biogeography & Paleontology |
16:30 | Evolution of wing-propelled diving in the Pan-Alcidae: integration of phylogeny, fossils, bone histology and endocranial anatomy | o01-1 | ||
16:48 | Exploring moving range edges in parapatric distributed passerines: of climate, genes and biotic interactions | o01-2 | ||||
17:06 | An overview of the diversity and relationships of the mihirungs (Aves: Dromornithidae), enigmatic giant flightless fowl of Australia | o01-3 | ||||
17:24 | Gondwanian relationships of the Early Eocene bird fauna of Australia | o01-4 | ||||
17:42 | Biogeography of the Neotropical genus Malacoptila (Aves: Bucconidae) support the influence of Andean uplift and the reconfiguration of the Amazon basin as primary triggers of speciation | o01-5 | ||||
Room 9 | o07 Dispersal |
16:30 | Shorter natal dispersal distances at higher population densities in the Great Tit (Parus Major) in both time and space | o07-1 | ||
16:48 | Can population-specific variation in spatio-temporal migration patterns increase our understanding of dispersal in migrants? | o07-2 | ||||
17:06 | Discrete choice modeling of natal dispersal: “Choosing” where to breed from a finite set of fragmented areas | o07-3 | ||||
17:24 | Extreme weather events influence reproduction and trigger extraordinary movements of Brown Dipper Cinclus pallasii in Taiwan | o07-4 | ||||
17:42 | Long-distance dispersal results in a large-scale metapopulation of caspian terns in western North America | o07-5 | ||||
Wednesday, 20-Aug | ||||||
Concurrent Symposia | 10:00-12:00 | Room 2 | S01 The avifauna of the Sino-Himalayas: history, ecology, (no?) future. |
10:03 | Past, extant and future diversification patterns of Sino-Himalayan passerines | s01-1k |
10:30 | Phylogeographical patterns of birds in response to the Quaternary environmental changes on the Tibetan Plateau and adjacent regions | s01-2k | ||||
10:57 | The Sino-Himalayan avifauna (S-HA) as a high power species pool for colonizing nearby regions, mainly north/eastwards, in the course of Pleistocene glacial/interglacial alterations | s01-3 | ||||
11:19 | The drivers of a mid-elevation peak in bird diversity of the eastern Himalayas, India | s01-4 | ||||
11:41 | Interactions between climate, competition, and habitat in limiting Himalayan bird distributions | s01-5 | ||||
Room 3 | S02 Rice fields as a model system for studying bird ecology and conservation. |
10:03 | A history of ecological studies of birds in rice fields | s02-1k | ||
10:30 | Avian responses to heterogeneity in rice fields at local, landscape and macro scales | s02-2k | ||||
10:57 | The recent decline of heron populations in Italy and the changes in rice cultivation practice | s02-3 | ||||
11:19 | Rice farming and duck interactions: looking at possible mutual benefits by testing post-harvest practices and duck densities | s02-4 | ||||
11:41 | Does Alternate Wetting and Drying have an impact on birds in rice fields? |
s02-5 | ||||
Room 4 | S22 Sensory and molecular genetics mechanisms of migratory traits |
10:03 | Sensory mechanisms of long-distance navigation in migratory songbirds: a recent advance | s22-1k | ||
10:30 | Genomic analyses of a migratory divide between two subspecies of the Willow Warbler Phylloscopus trochilus | s22-2k | ||||
10:57 | Hierarchy of compass cues in migrating passerines: what is the role of the stellar compass? | s22-3 | ||||
11:19 | Disentangling the behavioural and physiological mechanisms of magnetic compass orientation and polarized light sensitivity in birds | s22-4 | ||||
11:41 | Structure and function of the two avian senses for direction and intensity of the geomagnetic field | s22-5 | ||||
Room 5 | S26 Plasticity in birdsong production |
10:03 | Peripheral mechanisms for birdsong diversity | s26-1k | ||
10:30 | Neural basis for adaptive adjustment of temporal structure in song of Bengalese Finches | s26-2k | ||||
10:57 | Lateralization of song production and implications for song plasticity in Bengalese Finches | s26-3 | ||||
11:19 | How vocal plasticity facilitates communication in birds | s26-4 | ||||
11:41 | Involvement of the songbird song system in reproductive behaviour | s26-5 | ||||
Room 6 | S23 Avian brood parasitism - novel findings and new puzzles |
10:03 | Geographic morph-ratio cline in a host species with egg color polymorphism: selection gradient versus gene flow | s23-1k | ||
10:30 | The evolvability of mimetic egg patterns: a new perspective | s23-2k | ||||
10:57 | Absence of host aggression towards brood parasites in a multiple -cuckoo parasite system, China | s23-3 | ||||
11:19 | Sex and seasonal differences in cognition in Brown-headed Cowbirds (Molothrus ater) | s23-4 | ||||
11:41 | Do Shining Cuckoos mimic the odours of their host? | s23-5 | ||||
Room 7 | S14 Neural plasticity and the waxing and waning of cognition in birds |
10:03 | Seasonal change in the avian brain: energy, trade-offs, and remodelling | s14-1k | ||
10:30 | Variation in cognitive ability: causes and confounds | s14-2k | ||||
10:57 | Transient transcriptomic profiling of pre-singing adult female Canary brain at the onset of testosterone treatment | s14-3 | ||||
11:19 | Changes in preferential response for a mate’s call in the budgerigar, a monogamous parrot (Melopsittacus undulatus) | s14-4 | ||||
11:41 | Gonad-dependent and gonad-independent regulation of neural and behavioural plasticity in songbirds | s14-5 | ||||
Room 8 | S43 Ecological immunology at 30: a midlife crisis or newfound opportunity? |
10:03 | Antimicrobial functions of avian eggshells in an ecological context. | s43-1k | ||
10:30 | Linking gut microbiota composition to life-history and individual quality of arctic-breeding shorebirds | s43-2k | ||||
10:57 | Body condition and immune status as potential risk factors for avian influenza virus infection in migratory birds | s43-3 | ||||
11:19 | Decision to breed in tropical Red-capped Lark (calandrella cinerea) is a balance between reproduction and adequate immune defense against disease | s43-4 | ||||
Room 9 | S05 Recent advances in the study of Psittaciformes: breeding biology, population ecology and phylogeography. |
10:03 | Breeding biology and conservation of old world Psittaciformes | s05-1k | ||
10:30 | Phylogeography: its development in recent years and relevance to parrots | s05-2k | ||||
10:57 | Impact of invasive species on parrots – case studies in New Caledonia and Wallis & Futuna Archipelago | s05-3 | ||||
11:19 | Beak and feather disease virus in a wild parrot species complex (Platycercus elegans): host predictors of prevalence and effects on breeding biology | s05-4 | ||||
11:41 | Reproduction in Blue-throated Macaws: factors limiting the recovery of a critically threatened parrot under intense management. | s05-5 | ||||
Concurrent Oral Sessions | 16:30-18:00 | Room 2 | o09 Community Ecology 2 |
16:30 | Temporal partitioning to avoid soundspace overlap by bird communities | o09-1 |
16:48 | Quantifying forest vertical structure to determine bird habitat quality in the Greenbelt Corridor, Denton, Texas | o09-2 | ||||
17:06 | Consequences of land use change for breeding birds at the German Coast | o09-3 | ||||
17:24 | Shorebirds in a tropical bay: what resources support their food webs? | o09-4 | ||||
17:42 | Bird community responses to vegetation cover and structural heterogeneity | o09-5 | ||||
Room 3 | o14 Global Change |
16:30 | Post-war changes in rice farming and egrets in Japan | o14-1 | ||
16:48 | Responses of the Chinese bulbul in life history traits to urbanization: the role of food and nest predation | o14-2 | ||||
17:06 | Birds, body size and climate change | o14-3 | ||||
17:24 | Fynbos endemic birds are vulnerable to extinction due to global warming | o14-4 | ||||
17:42 | Decline of urban House Sparrows in relation to local and landscape factors | o14-5 | ||||
Room 4 | o11 Evolutionary Ecology |
16:30 | Modeling maintenance of egg polymorphism over a geographic scale | o11-1 | ||
16:48 | The importance of early-life environmental stress on total phenotypic variation | o11-2 | ||||
17:06 | Changing phenology when phenotypic plasticity does not suffice: evidence for evolution in action? | o11-3 | ||||
17:24 | The spatial scale of selection and the evolution of phenotypic plasticity in seasonal timing | o11-4 | ||||
17:42 | The genomics of a wild passerine bird, the Great Tit Parus major and its application for quantitative traits | o11-5 | ||||
Room 5 | o15 Hormones & Stress |
16:30 | Molecular cloning and seasonal expression of corticosterone receptors in the diencephalon of Eurasian Tree Sparrows (Passer montanus) | o15-1 | ||
16:48 | Hormonal correlates of photoperiod induced seasonal life history states in the migratory Black-headed Bunting | o15-2 | ||||
17:06 | Climate-induced environmental variation in yolk hormone levels in Great Tits | o15-3 | ||||
17:24 | Geographic variation in clutch size and stress response along a latitudinal gradient in the Thorn-tailed Rayadito (Aphrastura spinicauda), a Patagonian furnariid | o15-4 | ||||
17:42 | Effects of social status and oxidative stress on antioxidant allocation and sperm quality in a passerine bird | o15-5 | ||||
Room 6 | o13 Sexual Behaviour 2 |
16:30 | Do phenotypic and ejaculate quality reflect siring success in the Collared Flycatcher? | o13-1 | ||
16:48 | Superior performance of extra-pair offspring may result from genotype-by-environment interactions | o13-2 | ||||
17:06 | Flirty females? The role of female song in Malurus cyaneus | o13-3 | ||||
17:24 | Broad-sense” sexual conflict: the evolution of female sexual autonomy and theoretical implications for the evolution of morphology and complex behavior in birds | o13-4 | ||||
17:42 | Females insure against infertility of their mates: an empirical test of the fertility insurance hypothesis in a wild bird population | o13-5 | ||||
Room 7 | o10 Conservation 1 |
16:30 | Conservation values of variously managed off-reserve forests for avifaunal communities in lowland Nepal | o10-1 | ||
16:48 | Bird community at Gunung Halimun Salak National Park: an important endemic bird area in Java, Indonesia | o10-2 | ||||
17:06 | Large-scale changes in birdlife and landscape - winners and losers in Germany over the past 25 years | o10-3 | ||||
17:24 | Interrelationship of bird species richness and habitat features during breeding and nonbreeding seasons in Indian Himalayas - a conservation approach | o10-4 | ||||
17:42 | The cost-effectiveness of bird conservation in agricultural landscapes | o10-5 | ||||
Room 8 | o12 Population Structure |
16:30 | Distinguishing the effects of selection from demographic history in the genetic variation of two Old World flycatchers | o12-1 | ||
16:48 | Hybrid zones and clines as sources of novelty in a parrot species complex: implications for speciation and conservation | o12-2 | ||||
17:06 | Admixture as a factor in diversification in Wallacean bird assemblages | o12-3 | ||||
17:24 | The origin and trend of the common magpie in Japan: Microsatellite analysis of old and new introduced populations | o12-4 | ||||
17:42 | Comparative phylogeography of the entire understorey bird community in a sky island reveals differential impacts of island structure on population structure | o12-5 | ||||
Room 9 | o16 Life history |
16:30 | Cumulative delays from pre-breeding stages affect breeding chronology and performance in a migratory seabird | o16-1 | ||
16:48 | Carry-over effects and individual variations in corticosterone level, at-sea behaviour and reproductive success in a small pelagic seabird, the Manx shearwater | o16-2 | ||||
17:06 | Individual variation in resource allocation strategies in the lesser black-backed gull | o16-3 | ||||
17:24 | Timing of moult is regulated by an intrinsic schedule in the Pied Flycatcher (Ficedula hypoleuca) | o16-4 | ||||
17:42 | The effects of nest predation risk on parental investment and reproductive success. | o16-5 | ||||
Thursday, 21-Aug | ||||||
Concurrent Symposia | 10:00-12:00 | Room 2 | S34 Effects of radiation on birds and other organisms: Chernobyl, Fukushima and beyond |
10:03 | Chernobyl, Fukushima and other hot places: biological consequences of nuclear accidents for avifauna | s34-1k |
10:30 | Effects of radiation exposure on species diversity and population density of birds at Fukushima | s34-2k | ||||
10:57 | Radioactive contamination of nest materials of Eurasian Tree Sparrows due to the Fukushima nuclear accident | s34-3 | ||||
11:19 | Fukushima radiation exposure & effects in birds | s34-4 | ||||
Room 3 | S17 Avian Phylogeography in East Asia |
10:03 | Avian phylogeography in East Asia: current status and future directions | s17-1k | ||
10:30 | Japanese islands may have contributed to the rich species diversity of East Asian birds: results of DNA barcoding | s17-2k | ||||
10:57 | Assessing the biogeographic impact of the ‘Tanaka-Kaiyong line’ in Southwest China: a comparison of avian community compositions and phylogeographic patterns | s17-3 | ||||
11:19 | The Utility of Microfluidics PCR Libraries and Other Next-generation Sequencing Approaches in Avian Phylogeography: A Case Study for Light-vented (Pycnonotus sinensis) and Taiwan Bulbuls (Pycnonotus taivanus) | s17-4 | ||||
11:41 | Phylogeography and population genomics of a wide-ranging bird in Eurasia, the Common Pheasant Phasianus colchicus | s17-5 | ||||
Room 4 | S25 Developmental stress beyond bird song: Can early life stressors engineer physiology and behavior for harsh environments? |
10:03 | Adult phenotypes after developmental stress: assessing costs and benefits with fitness metrics | s25-1k | ||
10:30 | Understanding developmental stress: integrating brain, physiology and behaviour | s25-2k | ||||
10:57 | Do Telomeres Shorten in Response to Early Life Stress? | s25-3 | ||||
11:19 | The importance of the postnatal context for the study of prenatal effects | s25-4 | ||||
11:41 | The physio-behavioral phenotype: hypothalmo-pituitary-adrenal axis responsiveness and the timid-to-bold continuum in Florida Scrub-Jays | s25-5 | ||||
Room 5 | S39 Ethno-ornithology: Birds, Culture & Conservation |
10:03 | Ethno-ornithology and environmental ethics in the southernmost forests of the world | s39-1k | ||
10:30 | Ornithophilia, ornithophobia: encounters and dialogues in the human landscape | s39-2k | ||||
10:57 | The bird people: Jívaro traditional beliefs, ecological knowledge, and conservation of birds in the Peruvian Amazon | s39-3 | ||||
11:19 | The bird trade in Taiwan: an analysis of an Eastern pathway to biological invasions | s39-4 | ||||
11:41 | Tiritiri Matangi Island, New Zealand: inspiring environmental stewardship though interactions with birds | s39-5 | ||||
Room 6 | S27 Non-native birds as natural experiments: ecological and evolutionary change during biological invasions. |
10:03 | Niche changes during biological invasions: prevalence, drivers and consequences | s27-1k | ||
10:30 | Effects of contrasting evolutionary life histories on genetic variation and immune function in birds: a test using populations of endemic and invasive parakeets on Mauritius. | s27-2k | ||||
10:57 | Common Starlings in South Africa: alien, but not invasive? | s27-3 | ||||
11:19 | Feral Greylag Geese – why do they fare so well? | s27-4 | ||||
11:41 | Status of an invasive species, the Red-billed Leiothrix and negative impact on native species in Japan | s27-5 | ||||
Room 7 | S31 Birds in space: is individual variation relevant? |
10:03 | Evolutionary feedback loops: population cycles as both a cause and consequence of individual variation in behavior | s31-1k | ||
10:30 | Spatial behaviour in the Great Tit: exploration, personality and dispersal | s31-2k | ||||
10:57 | Adaptive behavioural variation in social environments | s31-3 | ||||
11:19 | Does immobility in a novel environment predict breeding performance: a study of Great Tits in two different habitats | s31-4 | ||||
Room 8 | S33 Departure decisions in nocturnal migrants |
10:03 | Departure decisions in nocturnally migrating songbirds: when, in which direction, and why? | s33-1k | ||
10:30 | Nocturnal departure decisions of individuals at ecological barriers | s33-2k | ||||
10:57 | Departure and flight behavior of migrants facing a large water crossing | s33-3 | ||||
11:19 | Optimal wind selectivity and flight orientation on departure among avian migrants – dependencies on prevailing wind conditions and flight distances | s33-4 | ||||
11:41 | Physiological conditions influence stopover decision in short-distance migrants | s33-5 | ||||
Room 9 | S48 Physiological mechanisms underlying individual variation in life-history traits |
10:03 | Individual variation in workload during parental care: can we detect a physiological signature of quality or cost of reproduction? | s48-1k | ||
10:30 | Mechanisms underlying individual variation in ageing and mortality: the importance of early life | s48-2k | ||||
10:57 | Mechanisms underlying individual variation in timing of breeding | s48-3 | ||||
11:19 | Individual variation in corticosterone responses and the ability of birds to cope with environmental change | s48-4 | ||||
11:41 | Insulin–like growth factor 1 drives life-history evolution in passerine birds | s48-5 | ||||
Concurrent Oral Sessions | 16:30-18:00 | Room 2 | o17 Conservation 2 |
16:30 | Ecological correlates of vulnerability to fragmentation in forest birds on inundated subtropical land-bridge islands | o17-1 |
16:48 | Facultative cooperative breeding in Cabanis’s greenbul (Phyllastrephus cabanisi) in relation to cloud forest fragmentation | o17-2 | ||||
17:06 | Mesopredator release: impacts on previously unaffected components of a seabird population | o17-3 | ||||
17:24 | Variation in the role of tree decay to promote cavity nester biodiversity in the World Wide Cavity Nest Web | o17-4 | ||||
17:42 | Variable food supplies and introduced predators set a complex ecological trap for a facultative migratory bird. | o17-5 | ||||
Room 3 | o19 Migration 1 |
16:30 | Going the distance: Shared duration and destination of overwintering in pairs of Scopoli’s shearwaters (Calonectris diomedea) | o19-1 | ||
16:48 | The role of endogenous rhythm in movements of facultative migrants | o19-2 | ||||
17:06 | To be at the right place at the right time – individual timing of annual life history events by a trans-Sahara migrant | o19-3 | ||||
17:24 | Dispersion, route fidelity and within-pair coordination: the mysterious migration of the Atlantic Puffin | o19-4 | ||||
17:42 | Time to move: Nomadic Black Swans (Cygnus atratus) in arid Australia following La Niña floods | o19-5 | ||||
Room 4 | o22 Physiology |
16:30 | Seasonal changes in responsiveness of the photoperiodic response system to long day length in the subtropical tree sparrow | o22-1 | ||
16:48 | Numerical demonstration of inspiratory aerodynamic valving in Japanese Quail | o22-2 | ||||
17:06 | Winter thermoregulatory strategies of a small, solitary-roosting bird, the Rufous Treecreeper (Climacteris rufa) | o22-3 | ||||
17:24 | Circadian rhythm of neurotranmitters and neuromodulators in central and peripheral tissues of a migratory song bird | o22-4 | ||||
Room 5 | o20 Parasites & immunity |
16:30 | The effect of hen flea infestation on the status and intensity of infection with malaria parasites in the Blue Tit | o20-1 | ||
16:48 | Genetic background helps understanding immunocompetence, growth and survival in House Sparrows | o20-2 | ||||
17:06 | Does environmental microbial community composition drive maternal immune investment in avian eggs? | o20-3 | ||||
17:24 | Long antibody persistence and transgenerational transfer of immunity in a long-lived vertebrate | o20-4 | ||||
17:42 | Dynamics of a plumage ecosystem | o20-5 | ||||
Room 6 | o21 Phylogeography & Phylogenetics |
16:30 | Comparative phylogeography of widespread Palearctic corvid birds | o21-1 | ||
16:48 | Phylogeography of Phasianus colchinus Linnaeus, 1758 inferred from mitochondrial and nuclear genes in Iranian plateau | o21-2 | ||||
17:06 | Resolving the puzzling evolutionary background of Blue Tits (Cyanistes spp.) on the Canary Islands, in Africa, and in Europe | o21-3 | ||||
17:24 | Phylogeography and bioacoustic variation of Southeast Asian bulbuls (Aves: Pycnonotidae) | o21-4 | ||||
17:42 | Into and out of the tropics: the generation of the latitudinal gradient among New World passerine birds | o21-5 | ||||
Room 7 | o23 Population Ecology |
16:30 | Population limitation in a migratory songbird with variable recruitment: direct and indirect effects of nest depredation and weather on reproductive success | o23-1 | ||
16:48 | Predicting small-scale variation in Great Tit breeding phenology using remotely-sensed satellite data | o23-2 | ||||
17:06 | When early birds do not get the worm: habitat heterogeneity modulates the breeding performance of a raptor under changing climate | o23-3 | ||||
17:24 | Undermatching swallow distributions at large scales due to perceptual constraints | o23-4 | ||||
17:42 | Age dependent reproductive success and seasonal change of adult survival of Japanese Rock Ptarmigan | o23-5 | ||||
Room 8 | o18 Social Interactions |
16:30 | Within-song type variation facilitates neighbour-stranger discrimination in a bird with a small repertoire size | o18-1 | ||
16:48 | Sharing mates and nestboxes is associated with female “friendship” in European Starlings Sturnus vulgaris | o18-2 | ||||
17:06 | Song sharing in neighbouring and non-neighbouring territorial male Pied Bush Chats | o18-3 | ||||
17:24 | Social organization in the flightless Kagu, a bird endemic to New Caledonia | o18-4 | ||||
17:42 | Can birds negotiate hatching time via acoustic communication? | o18-5 | ||||
Room 9 | o24 Evolutionary Morphology |
16:30 | Postglacial colonization and diversification of the Jungle Crow in its north-eastern frontier as revealed by comparative morphological analysis | o24-1 | ||
16:48 | Ecological and phylogenetic significance of the scleral ring in diving aquatic birds | o24-2 | ||||
17:06 | Walkings, from birds to dinosaurs. | o24-3 | ||||
17:24 | The morphological and developmental evolution of asymmetrical flight feathers | o24-4 | ||||
17:42 | Fossil Insight into the Evolution of Penguins | o24-5 | ||||
Saturday, 23-Aug | ||||||
Concurrent Symposia | 10:00-12:00 | Room 2 | S28 Avian cognition in natural populations |
10:03 | Cognition, ecology, and evolution in wild Great Tits (Parus major) | s28-1k |
10:30 | Do Mexican Jays choose peanuts by listening to the sounds produced by handling the nuts? – field experiments. | s28-2k | ||||
10:57 | What determines vehicle avoidance behaviour in birds? | s28-3 | ||||
11:19 | Sibling Communication in barn owls: role of cognition and social interaction | s28-4 | ||||
11:41 | Physical cognition in wild-caught New Caledonian crows | s28-5 | ||||
Room 3 | S04 Birds and agroecosystems: experiences from the tropics |
10:03 | Identifying areas of high-value for bird conservation and restoration of diversity in the Brazilian Southeastern region | s04-1k | ||
10:30 | Bird functional diversity and ecosystem services in tropical forests, agroforests and agricultural areas | s04-2k | ||||
10:57 | The conservation importance of agroforests and tree plantations for forest birds in the Malay Archipelago | s04-3 | ||||
11:19 | Bird functional diversity changes in tropical dry forest: comparison among a forest patch, silvopastoral systems and pastures | s04-4 | ||||
11:41 | Potentiality of Indigenous Agroforestry Systems with reference to bird diversity in the Sikkim Himalayas, India | s04-5 | ||||
Room 4 | S45 Avian phylogenetics: advances in understanding of Old World passerine evolution |
10:03 | What’s a warbler? Phylogeny of the Old World “Sylviidae” complex | s45-1k | ||
10:30 | What can we learn from the molecular systematics, phylogeography, and speciation genetics of Taiwanese birds? | s45-2k | ||||
10:57 | Molecular systematics and diversification of the Asian scimitar babblers (Timaliidae, Aves) | s45-3 | ||||
11:19 | Speciation in Eurasian Wagtails (Aves: Motacilla): inferring phylogeny, delimiting species, and estimating gene flow using RAD-seq data. | s45-4 | ||||
11:41 | Diversification and the adaptive radiation of the Parrotbills in Asia | s45-5 | ||||
Room 5 | S38 Evolutionary Morphology of Birds: New Methods and Concepts |
10:03 | The interdependent evolution of the flight, feeding, respiratory and vocalization apparatus in birds: advances in 3D visualization and animation | s38-1k | ||
10:30 | Analysis of morphology and functions of jaw apparatus of Vietnamese Passerine birds (Passeriformes; Aves) helps us to specify their trophic adaptations and systematic position | s38-2k | ||||
10:57 | The songbird syrinx morphome: a three-dimensional, high-resolution, interactive morphological map of the Zebra Finch vocal organ | s38-3 | ||||
11:19 | Peculiarities of deep dorsal thigh muscles in moa (Aves, Dinornithiformes) | s38-4 | ||||
11:41 | The pelvic system of birds and the origin of flight | s38-5 | ||||
Room 6 | S29 The value of long-term ringing data in ornithology |
10:03 | Possibilities of long-term monitoring of birds by Rybachy-type funnel traps | s29-1k | ||
10:30 | The value of long-term ringing data in the light of environmental change | s29-2k | ||||
10:57 | Latitudinal differences in long-term migratory change in the Willow Warbler (Phylloscopus trochilus) | s29-3 | ||||
11:19 | An ultra-rich, but homogenized, biodiversity hot-spot: a long-term study using ringing data at Eilat, Israel | s29-4 | ||||
11:41 | Combining migration counts from several sites – a way to improve population monitoring by ringing stations | s29-5 | ||||
Room 7 | S30 Ecophysiology of Circannual and Long-term Timing Mechanisms: Recent Advances |
10:03 | Multi-year consistency of individual migration timing in Bar-tailed Godwits | s30-1k | ||
10:30 | Ecophysiology of the circannual clock in Spotted Munia, Lonchura punctulata | s30-2k | ||||
10:57 | Do earlier birth dates in Pied flycatchers allow for rapid adaptation of laying to climate change? | s30-3 | ||||
11:19 | Avian annual temporal organization in a warming world | s30-4 | ||||
11:41 | Role of photoperiod and circannual rhythms in the control of seasonal events in food specialists Cardueline finches (Fringillidae) | s30-5 | ||||
Room 8 | S21 Avian Neurosteroids: Biosynthesis and Biological Action |
10:03 | Biosynthesis and biological action of pineal allopregnanolone in birds | s21-1k | ||
10:30 | Biosynthesis and biological action of estrogen at the synapse in birds | s21-2k | ||||
10:57 | Gonadotropin-inhibitory hormone inhibits socio-sexual behaviors by increasing neuroestrogen synthesis in the male quail | s21-3 | ||||
11:19 | Delayed onset and irregular cycles of oviposition in female chicken chimera grafted with male brain | s21-4 | ||||
11:41 | Neural regulation of seasonality in Palaearctic-Indian night-migratory songbirds | s21-5 | ||||
Room 9 | S47 Patterns and mechanisms of metabolic flexibility in birds |
10:03 | Environmental, ecological and mechanistic drivers of seasonal metabolic flexibility in birds | s47-1k | ||
10:30 | Seasonal metabolic adjustments in southern African birds | s47-2k | ||||
10:57 | Effects of temperature and photoperiod on energy metabolism and thermoregulation in Chinese Bulbuls Pycnonotus sinensis | s47-3 | ||||
11:19 | Water availability mitigates the effects of extended fasting in Zebra Finches | s47-4 | ||||
11:41 | When body temperature is increasing; potential constraints to work rate. | s47-5 | ||||
Concurrent Oral Sessions | 16:30-18:00 | Room 2 | o28 Sexual Behaviour 1 |
16:30 | Parental food provisioning strategy in relation to brood sex ratio in the Black-billed Magpie: an experimental study | o28-1 |
16:48 | A behavioural correlate of extra-pair paternity in Blue Tits Cyanistes caeruleus | o28-2 | ||||
17:06 | Breeding habitats and song structures shed light on evolutionary mechanisms of tinamou (Tinamidae, Tinamiformes) sexual dimorphisms | o28-3 | ||||
17:24 | A Genetic Approach to Understanding the Mating System of Greater Rheas | o28-4 | ||||
Room 3 | o25 Conservation of migratory birds |
16:30 | Migratory waterbird research and monitoring in the East-Asian Australasian Flyway – essential for conservation or fiddling while Rome burns? | o25-1 | ||
16:48 | Shorebird foraging ecology in Australia: anthropogenic vs natural supratidal habitats. | o25-2 | ||||
17:06 | Global patterns in the conservation of migratory birds | o25-3 | ||||
17:24 | Ecology of migratory shorebirds in Australia’s ephemeral wetlands | o25-4 | ||||
17:42 | Effects of the Great East Japan Earthquake on the wintering distribution of Brent Geese | o25-5 | ||||
Room 4 | o31 Song |
16:30 | Song structure and organization in California Thrashers (Toxostoma redivivum) | o31-1 | ||
16:48 | Non-gradual vocal development through the stage of voice breaking in three species of Auks (Alcidae, Charadriiformes). | o31-2 | ||||
17:06 | Song discrimination before song learning in free-living sparrows: implications for learning and evolution | o31-3 | ||||
17:24 | The plasticity of song learning as revealed by a cross-fostering and a multiple tutor experiments in Bengalese Finches. | o31-4 | ||||
17:42 | A possible trade-off between song and a cognitive metric in a songbird | o31-5 | ||||
Room 5 | o26 Migration 2 |
16:30 | Radar studies of flight speed and migration patterns of nocturnal passerine migrants in relation to light and topography | o26-1 | ||
16:48 | Migratory movement of Streaked Shearwaters Calonectris leucomelas | o26-2 | ||||
17:06 | Colonization of migratory Oriental Honey-buzzards in Taiwan reveals fast evolution of migration without a genetic basis | o26-3 | ||||
17:24 | Migration of the Common Cuckoo Cuculus canorus and reactions to displacement followed with satellite telemetry | o26-4 | ||||
17:42 | Individual consistency in migratory behaviour in Atlantic shearwaters and petrels | o26-5 | ||||
Room 6 | o27 Disease |
16:30 | Factors driving rapid changes in virulence of the bacterial pathogen Mycoplasma gallisepticum in house finches Haemorhous mexicanus. | o27-1 | ||
16:48 | Experimental infectivity trials reveal adaptation by song sparrow hosts to local strains of Plasmodium | o27-2 | ||||
17:06 | The effect of spatially varying seasonality on the epidemiology of Avian Influenza | o27-3 | ||||
17:24 | Testing the role of migratory birds in the spread of zoonotic disease | o27-4 | ||||
17:42 | Emerging infectious disease selects for darker plumage coloration in Greenfinches | o27-5 | ||||
Room 7 | o32 Species conservation |
16:30 | Response of a declining wood warbler to forest treatments: Preliminary results from a 100-year study | o32-1 | ||
16:48 | Conservation and restoration of tern colonies in North America | o32-2 | ||||
17:06 | Threats to Lilian’s Lovebird Agapornis lilianae in Malawi: disease, predators & waterhole poisoning | o32-3 | ||||
17:24 | Determination of the nutrient requirements of kiwi (Apteryx spp.): a model for the development of synthetic diets for captive- held species | o32-4 | ||||
17:42 | Factors affecting Saltmarsh and Seaside Sparrow reproductive success in New York City, NY, USA: implications for tidal marsh management action plans in urban areas. | o32-5 | ||||
Room 8 | o30 Functional Morphology |
16:30 | Habitat fragmentation as an evolutionary force shaping bird wings | o30-1 | ||
16:48 | Estimating bending mechanics of extant and fossil penguin contour feathers | o30-2 | ||||
17:06 | Structural color production in avian eggshells? | o30-3 | ||||
17:24 | The morphology of the bill tip organ in Anseriformes | o30-4 | ||||
17:42 | The evolution of crypsis in nightjars (Caprimulgidae) | o30-5 | ||||
Room 9 | o29 Foraging Patterns |
16:30 | How food predictability affects foraging routines of Griffon Vultures | o29-1 | ||
16:48 | Wintering hotpots of Short-tailed Shearwaters, and their prey distribution, in the Bering and Arctic Seas | o29-2 | ||||
17:06 | Aeroecology of post-breeding Purple Martins (Progne subis): distribution, abundance and trophic impact | o29-3 | ||||
17:24 | Effects of social context on foraging behavior of participants in mixed-species flocks across space | o29-4 | ||||
17:42 | Foraging behaviour of Adélie Penguins throughout the Antarctic winter | o29-5 | ||||
Sunday, 24-Aug | ||||||
Concurrent Symposia | 10:00-12:00 | Room 2 | S06 Avian reintroductions in changing environments |
10:03 | Avian translocations to modified habitats: from Reintroduction to Conservation Introduction | s06-1k |
10:30 | Avian reintroduction into socio-ecological production landscapes: lessons from case studies | s06-2k | ||||
10:57 | Reintroduction and ecology of the Oriental white stork Ciconia boyciana - Coexistence between humans and birds in Japan | s06-3 | ||||
11:19 | A lesson for life: is it possible to prepare release candidates in captivity to their post-release environment? A case study in Grey Partridge | s06-4 | ||||
11:41 | Using Habitat Suitability Models for conservation translocations: empirical investigations within the reinforcement program of Houbara Bustard | s06-5 | ||||
Room 3 | S46 Recent insights on sexual selection from avian models |
10:03 | Aesthetic evolution by mate choice: Darwin’s really dangerous idea | s46-1k | ||
10:30 | Are female extra-pair matings sexually selected? Testing non-adaptationist hypotheses in house sparrows | s46-2k | ||||
10:57 | How does plasticity of sexually selected traits in birds influence their evolution? | s46-3 | ||||
11:19 | Evolution of courtship dance in Estrildid finches | s46-4 | ||||
11:41 | What do we really know about the role of colour signalling in a model species? Blue Tit plumage research as a case study of impediments to progress in evolutionary biology | s46-5 | ||||
Room 4 | S40 Turning the tide for East Asia’s migratory shorebirds |
10:03 | Conserving migratory shorebirds in a rapidly changing world | s40-1k | ||
10:30 | Migratory shorebirds in the Yellow Sea: status, threats, and conservation | s40-2k | ||||
10:57 | Simultaneous decreases in shorebird summer survival suggest a flyway at risk | s40-3 | ||||
11:19 | Conserving Southeast Asian shorebirds in natural and anthropogenic habitats: an ecological and economic analysis | s40-4 | ||||
11:41 | International Cooperation in Migratory Waterbird Research and Conservation in the East-Asian Australasian Flyway | s40-5 | ||||
Room 5 | S35 Lifelong individual development as an important component of life history |
10:03 | Causes and consequences of ontogenetic change in birds | s35-1k | ||
10:30 | Adaptive responses over the lifetime to ecological and social adversity in infancy | s35-2k | ||||
10:57 | Differences in the rate of improvement in reproductive performance of long-lived and shorter-lived Tree Swallows in New York, USA | s35-3 | ||||
11:19 | How does reproductive effort influence telomere length in the Blue Tit? | s35-4 | ||||
11:41 | Within-individual approach to sex ratio variation in breeding Common Terns: does experience matter? | s35-5 | ||||
Room 6 | S37 Genomes and the evolution of modern birds |
10:03 | Generating a bird genome resource: insights in the avian Tree Of Life, complex traits, and genome evolution. | s37-1k | ||
10:30 | Conserved non-exonic elements: a new class of marker in avian phylogenomics | s37-2k | ||||
10:57 | Retroposon insertions are genome-wide witnesses of incomplete lineage sorting during the radiation of Neoaves | s37-3 | ||||
11:19 | Regulatory mechanisms of the singing-related genome of songbirds | s37-4 | ||||
11:41 | Avian Genomics: Current Status and Future Opportunities | s37-5 | ||||
Room 7 | S13 Avian dispersal: Implications for speciation, community build-up and migration |
10:03 | A movement ecology approach for studying avian dispersal processes and patterns and their evolutionary and biogeographical consequences | s13-1k | ||
10:30 | Individual responses of trans-equatorial migrants to seasonal variation in regional resources across continents | s13-2k | ||||
10:57 | Dynamic migration, drought and drones | s13-3 | ||||
11:19 | Combining GPS tracking with genotyping techniques to study connectivity of Mediterranean Osprey populations. | s13-4 | ||||
11:41 | Comparative evolution of the rails (Aves: Rallidae) in Australasia: phylogeography analysis of supertramp species | s13-5 | ||||
Room 8 | S24 Fire regimes and bird population responses. |
10:03 | Effects of fire regimes on bird populations in foothill forests of the Great Dividing Range in eastern Victoria, Australia. | s24-1k | ||
10:30 | Fire and Mediterranean bird communties: the complex role of global change in novel forest systems. | s24-2k | ||||
10:57 | Pyrodiversity begets biodiversity: the influence of mosaic burning on bird assemblages across multiple spatial scales | s24-3 | ||||
11:19 | Wildfire, stable unpredictability, and the evolution of cooperative-breeding in the Florida Scrub-Jay | s24-4 | ||||
11:41 | How does fire affect bird migration? | s24-5 | ||||
15:00-17:00 | Room 2 | S41 Persistent organic pollutants - lasting problems and new aspects in migratory birds. |
15:03 | The Black Stork – a New “Kid on the (Contamination) Stage” – New and / or Previously Unnoticed Aspects of DDE Impact | s41-1k | |
15:27 | Monitoring of contaminants and their effects in the Common Guillemot | s41-2k | ||||
15:57 | Fifty years after Silent spring: temporal and latitudinal trends of DDE in North American birds over the last three decades | s41-3 | ||||
16:19 | Effects of contaminants on reproduction in the White-tailed Sea Eagle Effects of contaminants on reproduction in the White- tailed Sea Eagle | s41-4 | ||||
16:41 | Focal bird species in neotropical soybean and rice fields for pesticide registration purposes | s41-5 | ||||
Room 3 | S44 New finds and old bones - integrative palaeornithology for the 21st century |
15:03 | Early evolution of birds: perspectives from new fossil discoveries in China | s44-1k | ||
15:27 | Fossils, molecular calibrations, and the divergence of crown group birds | s44-2k | ||||
15:57 | Mid-Cenozoic avifaunas and their bearing on the evolution of extant lineages: an example from the Miocene of Europe | s44-3 | ||||
16:19 | Demise of the giants: the role of the biological drivers for the flightless, wing-propelled divers | s44-4 | ||||
16:41 | Fossil evidence for the evolution of the avian hyo-lingual feeding | s44-5 | ||||
Room 4 | S08 Why Birds Matter: Birds’ Ecological Functions, Ecosystem Services, and Value to Society. |
15:03 | An overview of ecosystem services provided by birds | s08-1k | ||
15:27 | Nutrient dynamics and nutrient cycling by birds: Implications from an East Asian perspective | s08-2k | ||||
15:57 | The role of dabbling ducks in the dispersal of plant seeds | s08-3 | ||||
16:19 | Estimation of pest control by Great Tits with application of a nest finder system at artificial nestboxes in Hongneung Experimental Forest, Korea | s08-4 | ||||
16:41 | Input of ornithogenic nitrogen into paddy fields near a breeding colony of the great cormorants, and its contributions for rice crops | s08-5 | ||||
Room 5 | S36 Colour polymorphisms |
15:03 | The adaptive value of melanin-based color morphs: a role for the melanocortin system. | s36-1k | ||
15:27 | Redneck wonderland: maintenance of plumage colour diversity in a parrot species complex | s36-2k | ||||
15:57 | Amount of variation in multiple colouration traits within populations on a large spatial scale in the Pied Flycatcher (Ficedula hypoleuca) | s36-3 | ||||
16:19 | Causes and consequences of plumage polymorphism in the Common Buzzard Buteo buteo | s36-4 | ||||
16:41 | The Niche Expansion Hypothesis: a novel hypothesis to explain the maintenance of polymorphism for species with bi-parental care. | s36-5 | ||||
Room 6 | S03 Light in the darkness: how does artificial night lighting influence bird behaviour and ecology? |
15:03 | Lighting up the forest – what is the impact of artificial light on breeding birds? | s03-1k | ||
15:27 | The effects of light pollution on daily and seasonal rhythms of songbirds: a mechanistic perspective | s03-2k | ||||
15:57 | Waterfowl utilize different habitat at night: implications for conservation. | s03-3 | ||||
16:19 | Effects of artificial night lighting on the timing of dawn and dusk singing in common songbirds | s03-4 | ||||
16:41 | Effect of artificial lighting of roosting female Blue Tits on their breeding behavior | s03-5 | ||||
Room 7 | S09 Vocal communication and vocal control in sub-oscine and oscine passerines. |
15:03 | Vocal control regions of sub-oscine passerines | s09-1k | ||
15:27 | Vocal communication in two sub-oscine species from Amazonia, Brazil | s09-2k | ||||
15:57 | Pattern and neural control of unlearned vocalizations in the Zebra Finch Taeniopygia guttata. | s09-3 | ||||
16:19 | Integrating song and radio telemetry tracking with playback experiments, to infer intra- and inter-sexual relationships in a Neotropical terrestrial insectivore, Formicarius moniliger. | s09-4 | ||||
16:41 | Individual, population, and geographical variation in advertising song of some passerine bird species | s09-5 |