Literatura académica sobre el tema "Passerine songs"

AbstractBirds with songs having two or more acoustically distinct elements can arrange them either rigidly (i.e., in the same sequence) or flexibly. Flexible song syntax can be achieved either by varying the number of repetitions of elements or by combining elements in different ways. Combinatorial syntax has been documented only in the songs of oscine passerines and in one nonpasserine, but not in the suboscine passerines. Dawn and day songs of a tyrant flycatcher, the Flammulated Attila (Attila flammulatus), were recorded in Costa Rica. Flexible syntax was noted in both dawn and day song. Attilas not only varied the number of repetitions of their song elements but also combined elements in various ways. This appears to be the first reported case of combinatorial song syntax in a suboscine species.

We ask whether rates of evolution in traits important for reproductive isolation vary across a latitudinal gradient, by quantifying evolutionary rates of two traits important for pre-mating isolation—avian syllable diversity and song length. We analyse over 2500 songs from 116 pairs of closely related New World passerine bird taxa to show that evolutionary rates for the two main groups of passerines—oscines and suboscines—doubled with latitude in both groups for song length. For syllable diversity, oscines (who transmit song culturally) evolved more than 20 times faster at high latitudes than in low latitudes, whereas suboscines (whose songs are innate in most species and who possess very simple song with few syllable types) show no clear latitudinal gradient in rate. Evolutionary rates in oscines and suboscines were similar at tropical latitudes for syllable complexity as well as for song length. These results suggest that evolutionary rates in traits important to reproductive isolation and speciation are influenced by latitude and have been fastest, not in the tropics where species diversity is highest, but towards the poles.

Abstract Across populations, animals that inhabit areas with high anthropogenic noise produce vocalizations that differ from those inhabiting less noisy environments. Such patterns may be due to individuals rapidly adjusting their songs in response to changing noise, but individual variation is seldom explored. Therefore, we tested the hypothesis that male house wrens (Troglodytes aedon) immediately adjust their songs according to changing noise and that social context further modifies responses. We recorded songs, quantified noise, and defined social context within pairs as female fertile status and between males as number of conspecific neighbors. We used a reaction-norm approach to compare song trait intercepts (between-male effects) and slopes (within-male effects) as a function of noise. Individuals immediately adjusted song duration in response to changing noise. How they achieved adjustments varied: some sang shorter and others longer songs with greater noise, and individuals varied in the extent to which they adjusted song duration. Variation in song duration could be affected by competition as between-male noise levels interacted with number of neighbors to affect syllable duration. Neither within- nor between-male noise effects were detected for frequency traits. Rather, males with fertile mates sang lower-frequency songs and increased peak frequency with more neighbors. Among males, social context but not noise affected song frequency, whereas temporal structure varied between and within individuals depending on noise and social factors. Not all males adjusted signals the same way in response to noise, and selection could favor different levels of variation according to noise.

Anthropogenic noise, now common to many landscapes, can impair acoustic communication for many species, yet some birds compensate for masking by noise by altering their songs. The phylogenetic distribution of these noise-dependent signal adjustments is uncertain, and it is not known whether closely related species respond similarly to noise. Here, we investigated the influence of noise on habitat occupancy rates and vocal frequency in two congeneric vireos with similar song features. Noise exposure did not influence occupancy rates for either species, yet song features of both changed, albeit in different ways. With increases in noise levels, plumbeous vireos ( Vireo plumbeus ) sang shorter songs with higher minimum frequencies. By contrast, grey vireos ( Vireo vicinior ) sang longer songs with higher maximum frequencies. These findings support the notion that vocal plasticity may help some species occupy noisy areas, but because there were no commonalities among the signal changes exhibited by these closely related birds, it may be difficult to predict how diverse species may modify their signals in an increasingly noisy world.

The songs of oscine passerine birds vary on many spatial scales, reflecting the actions of diverse evolutionary pressures. Here we examine the songs of Cisticola erythrops , which effectively signal species identity across a geographical area spanning 6500 km in sub-Saharan Africa. Selection for species identification should promote stability in song traits, while sexual selection and geographical segregation should promote diversity. Cisticola erythrops share syllable types across the entire range of species and structure songs similarly, but individuals sing highly variable songs through improvisational recombination of syllables. Patterns of syllable use change gradually across the range of the species and do not show distinct breaks at subspecies boundaries. The acoustic properties of the most common syllable type also change gradually with distance. The results illustrate how songs can be simultaneously species-specific and highly variable at an individual level. At a larger level, patterns of variation indicate that cultural drift has generated song diversity through an isolation by distance mechanism.

Birdsong is one of the most complex signals in the animal world, as it may consist of many different sounds grouped according to certain rules. Singing acts as a distant signal, indicating, e.g., the species and gender identity of the singer. However, territorial songbirds also use singing as an interactive social signal during territorial disputes, as well while interacting with female. In these contexts, males vary the type and timing of their songs to convey graded information about their motivational state, and those variations can play a role in communication. In this review, we considered how male songbirds vary their singing in territorial context. To study such variations, researchers usually simulated territorial intrusion by broadcasting conspecific singing in territories, including singing modified in a manner necessary for the researcher. For comparison, we considered briefly how singing vary in intersexual context. The author of the paper focuses on the role of singing complexity in communication. Therefore, not all known context-dependent changes in singing are considered, but only those related to “complexity”: the diversity of song/sound types and the transitional patterns of different song/sound types in the course of singing. Our review has shown that males change their singing when they detect environmental changes such as the appearance of a female or a competitor as follows: 1) song rate increases, 2) syllable rate increases, 3) song-type switching rate increases, 4) song-type diversity increases (i.e., the observed repertoire size), and 5) longer and more complex songs are predominantly used. In some species, the song bout organization may also change, but the data is still scarce. Typically, one or more, but not all the aforementioned acoustic behaviors have been found in a given song-bird species. All these behaviors (tactics) come down to a single strategy, namely: maximizing the acoustic diversity over a short period of time (e.g., several minutes), that is, increasing the number of different song and/or note types. The proximate causes of how the increased acoustic diversity work in the territorial competition context might lie in a sensory, or perceptual bias of the receiver. Namely, habituation should occur to repeated presentation of the same song type faster than to presentation of different song types. Therefore, by vocalizing more diversely, males more effectively influence the signal recipient’s behavior.

In most passerine species, an individual bird sings multiple song types to be combined into non-random song sequences. Because of this non-randomness, stereotype sequences of several or even dozens of song types appear in the vocalization of some species. Passerine birds acquire songs through some learning process while imitating other individuals. Song sharing is well known in songbirds and is a consequence of the song learning. Apparently, above the song type level, transitions between song types may be also shared. However, we still do not know exactly, how long are those song sequencies a bird can memorize? We analyze song sequence sharing in Radde’s warbler. Each song of this species consists of a dozen of short notes and lasts 1 s. In many males, the identity of the next song type in a sequence can be predicted on the basis of the previous song type (linear syntax). We found that males can share (i.e. memorize) song sequences from no more than 5 song types. Individual repertoires included up to 40 song types. Therefore, the ability of memorizing song sequences are rather limited in Radde’s warbler, as shared song sequences were rather short in comparison with the total size of the repertoire.

AbstractIn this study the effects of bird size, genus, habitat, song community and geographical distribution on song structure and singing behaviour of some passcrine species in northern Europe were simultaneously studied. Most species tend to improve their long distance song propagation in their specific habitat and song community. Song propagation correlates strongest with the use of low-pitched elements but not all birds are able to use these because of size limitation. In forest habitats whistles and modulated elements were used to improve song propagation. In open habitats high-pitched elements as well as repeated and trilled syllables were often used for better propagation of acoustic information. In song communities with a great number of species, the birds reduce song interference by other singers, by singing short songs and using modulated elements and long intersong pauses. When the birds greatly profit from effective long distance song propagation, like in northern areas with only short time for pair formation, the birds can segregate in singing time by using the light nights for singing. In these communities with low numbers of species the birds have been freed from song interference and have long songs and short intersong pauses and they can increase in this way their singing rate. The effect of song community on song length, intersong pause and the use of modulated elements in the song is stronger than that of habitat. The effect of the song community increases towards the north.

AbstractRecent studies have shown that female passerine birds give more sexual displays for songs of their mates than for songs of other males. The present study aimed to determine to what extent familiarisation with a song may account for females' song preferences. Ten female canaries were paired with a male during 3 days before egg laying; females were subsequently left alone to incubate and rear their young. Females were subjected to the familiarisation procedure when nestlings were 9 days old, until they were 17 days old. During the familiarisation period, twice a day, each female was successively exposed to the playback of three successive song records: (a) The mate song (M), a song frequently emitted by their previous sexual partner; when this song was played back, females were concurrently exposed to the sight of their previous mate. (b) The song of a non-mate accompanied by the sight of the mate (NMAS), a song emitted by a non-mate male; when this song was played back, females were also exposed to the sight of their previous mate. (c) The song of a non-mate not accompanied by the sight of the mate (NMNAS). At the end of this familiarisation period, the sexual preferences of the females for these songs were studied. Sexual responses were elicited by the emission of the M, NMAS and NMNAS songs, without male presentation. We analysed the total number of copulation solicitation displays (CSDs) elicited by each song. Females displayed more for M song than for NMAS or NMNAS songs. Eight of the 10 females gave at least half of their displays to M song. In a separate experiment, females without reproductive experience with the males failed to present a preference for any of these songs. Taken together, these results strongly suggest that mate recognition is not a mere effect of familiarisation with songs but is closely associated with previous reproductive experience. Song preferences that develop as a result of association with a particular male may be important in the maintenance of pair bonds and could influence future copulation acceptance with this mate.

An undue focus on Temperate Zone oscines (songbirds or passerines) has led to a geographical bias in interpretation of song frmnction and evolution. This bias led initially to relatively simplistic theories of the ftmnction of bird song with vocalizations divided into 'songs' and 'calls'. Songs were complex, learned vocalizations, given by males in the breeding season, thnctioning in territory defence and mate attraction and stimulation. Calls, on the other hand, were simple innate vocalizations serving more immediate needs such as begging for food and raising an alarm. Female song, where it occurred, was considered an aberration. Further studies suggested that complex songs were associated with mate attraction functions while simpler songs were associated with territory defence. However it became apparent that the distinction between songs and calls was not nearly so clear-cut and the supposed connection between complexity and function in song was questioned. Moreover it was realised that female song could not be dismissed as a mere aberration. Another problem was the ftmnction of the dawn chorus, where research had failed to find a consistent, all-encompassing explanation. Since most studies had been done on Northern Hemisphere songbirds, it was becoming clear that the geographical focus needed to be broadened. The life histories of Northern Hemisphere TemperateZone songbirds are very different from those in many other regions. In contrast to the situation in this zone, maintenance of year-round territory, territory defence by both male and female, life-long social monogamy and extensive female vocalization are widespread in tropical, subtropical and Southern Hemisphere regions. Recently it has been suggested that more intensive studies of vocalizations in these regions might help clariQi some of these issues and consequently an endemic Australian passerine was chosen for the current study. The study focused on the vocalizationsof the grey butcherbird Cracticus torquatus Artamidae, which displays the life history features described above. The main study population was located in the Brisbane suburbs of Rainworth and Bardon. Additional data were gathered from other Brisbane suburbs and bushland sites within the city and at Lake Broadwater near Dalby, Queensland. Vocalizations were initially recorded electronically and analysed using Canary sound editing program. Vocalization data were supplemented using an aural recording method, which was independently checked for reliability. Behavioural data including posture during vocalizations and interactions with other birds were also gathered. Initial investigationsrevealed the existence of two main categories of vocalizations - those given by the family group during the day, all year round and those given at dawn by males during the breeding season. For the focal study populations, group vocalizations were studied throughout the year over several years, however the song given at dawn by males during the breeding season proved to be quite complex and three birds from three territories in the main study area were chosen as case studies. Recordings were made of the vocalizations of the three case study birds over three breeding seasons. Starting and fmishing times (with respect to civil twilight) were recorded in order to determine both changes in song bout duration and starting time throughout the breeding season. Additional birds from the same area, from the other Brisbane suburbs and from the bushland sites were studied to check the validity of conclusions drawn from the case studies. The results of the investigations revealed a vocalization structure that contrasted strongly with the simple picture of bird song drawn from study ofNorthernHemisphere Temperate Zone passerines. The vocalizations given during the day, often referred to as the 'song' of this species, were very different from the early dawn song given by the male during the breeding season. This latter appeared to be song sensu stricto according to the paradigms developed for Northern Hemisphere birds. The thytime vocalizations, however, fitted neither the classic definition of 'song' nor the classic definition of 'call'. This relatively long-term study revealed different starting time patterns and periodicity for thy vocalizations and male breeding season song. Day vocalizations commenced at a fairly constant time with respect to civil twilight throughoutthe year but breeding season song started progressively earlier from the beginning through to the middle of the season then progressively later till the end of the season. Relative finishing time of breeding song however remained constant so that the duration of breeding season song gradually increased then decreased paralleling the change in starting times. A consequence of the two distinct classes of vocalizations was that there were essentially two distinct 'dawn choruses'. One, consisting of group vocals, was sung all year round; the other was given by males singing 'breeding season' song. Since there was no reason the expect that a single function would necessarily be ascribed to both choruses, this raised the possibility that some of the confusion surrounding the ftinction and nature of the 'dawn chorus' originated from a failure to recognize the existence of two such choruses. Variation in time and space showed ifirther differences between the two vocalization classes. The breeding song of each male was distinctly different from that of his neighbours and there was a marked change in the repertoire of any individual from one year to the next. In marked contrast, daytime vocalization repertoires of neighbouring groups were virtually indistinguishable and changed little from year to year. These findings, together with information from recent literature, suggested that the two song classes had a different ontogeny, function and possibly evolution. It was proposed that territory declaration was the function of dawn singing by grey butcherbird family groups but that the function most consistent with adult male dawn song was attraction of females for extra-pair copulations. It was suggested that chorusing itself was to some extent an accidental by-product of the advantage to the individual or group of singing at dawn although a recently proposed function, the social dynamics function, could not be ruled out. Further differences from the Northern Hemisphere situation were detected in subsong. First, subsong was given by birds in their first year and also by adult males. The finding of subsong in adult males was not without precedent as it has been documented previously for a small number of passerines, especially those that change repertoire from year to year. Subsong in young (first year) birds, however, was unusual in that birds practised in small groups rather than in the complete isolation usually associated with subsong. Moreover they did not practise adult male song but instead practised group daytime vocalizations. It was suggested that it was important for birds to learn to sing in company for the important task of group territory defence. Further investigation of the literature and observations during the present study revealed similar vocalization classes and behaviours in other members of the Artamidae and other endemic Australasian taxa. These literature investigations also revealed that the possession two song vocalization classes was quite widespread although they tended to be restricted (but not exclusive) to males rather than found in males and females. These findings led to furtherresearch into the significanceofAustraliain the evolution of songbirds, the role of co-operative breeding in Australianpasserines, and finally to an hypothesis for a possible origin of male bird song. It is suggested that male song arose in a social environment where the male and female were in frequent vocal communication. If the tendency to seek extra-pair copulations (EPCs) and female choice had already been incorporated into the suite of passerine behaviours, it would be necessary to avoid the mate during such activities and the male would need to advertise with a signal distinct from group vocalizations. Early dawn, with poor light conditions, could be a favourable time for these activities. Thus it is proposed that the ancestral condition was with all group members singing most vocalisations, the intermediate situation was similar to that in the grey butcherbird and the 'advanced' condition was where female and other group member vocalizations (other than calls) have dropped out and only male song remains.

An undue focus on Temperate Zone oscines (songbirds or passerines) has led to a geographical bias in interpretation of song function and evolution. This bias led initially to relatively simplistic theories of the function of bird song with vocalizations divided into 'songs' and 'calls'. Songs were complex, learned vocalizations, given by males in the breeding season, functioning in territory defence and mate attraction and stimulation. Calls, on the other hand, were simple innate vocalizations serving more immediate needs such as begging for food and raising an alarm. Female song, where it occurred, was considered an aberration. Further studies suggested that complex songs were associated with mate attraction functions while simpler songs were associated with territory defence. However it became apparent that the distinction between songs and calls was not nearly so clear-cut and the supposed connection between complexity and function in song was questioned. Moreover it was realised that female song could not be dismissed as a mere aberration. Another problem was the function of the dawn chorus, where research had failed to find a consistent, all-encompassing explanation. Since most studies had been done on Northern Hemisphere songbirds, it was becoming clear that the geographical focus needed to be broadened. The life histories of Northern Hemisphere Temperate Zone songbirds are very different from those in many other regions. In contrast to the situation in this zone, maintenance of year-round territory, territory defence by both male and female, life-long social monogamy and extensive female vocalization are widespread in tropical, subtropical and Southern Hemisphere regions. Recently it has been suggested that more intensive studies of vocalizations in these regions might help clarify some of these issues and consequently an endemic Australian passerine was chosen for the current study. The study focused on the vocalizations of the grey butcherbird Cracticus torquatus Artamidae, which displays the life history features described above. The main study population was located in the Brisbane suburbs of Rainworth and Bardon. Additional data were gathered from other Brisbane suburbs and bushland sites within the city and at Lake Broadwater near Dalby, Queensland. Vocalizations were initially recorded electronically and analysed using Canary sound editing program. Vocalization data were supplemented using an aural recording method, which was independently checked for reliability. Behavioural data including posture during vocalizations and interactions with other birds were also gathered. Initial investigations revealed the existence of two main categories of vocalizations - those given by the family group during the day, all year round and those given at dawn by males during the breeding season. For the focal study populations, group vocalizations were studied throughout the year over several years, however the song given at dawn by males during the breeding season proved to be quite complex and three birds from three territories in the main study area were chosen as case studies. Recordings were made of the vocalizations of the three case study birds over three breeding seasons. Starting and finishing times (with respect to civil twilight) were recorded in order to determine both changes in song bout duration and starting time throughout the breeding season. Additional birds from the same area, from the other Brisbane suburbs and from the bushland sites were studied to check the validity of conclusions drawn from the case studies. The results of the investigations revealed a vocalization structure that contrasted strongly with the simple picture of bird song drawn from study of Northern Hemisphere Temperate Zone passerines. The vocalizations given during the day, often referred to as the 'song' of this species, were very different from the early dawn song given by the male during the breeding season. This latter appeared to be song sensu stricto according to the paradigms developed for Northern Hemisphere birds. The daytime vocalizations, however, fitted neither the classic definition of 'song' nor the classic definition of 'call'. This relatively long-term study revealed different starting time patterns and periodicity for day vocalizations and male breeding season song. Day vocalizations commenced at a fairly constant time with respect to civil twilight throughout the year but breeding season song started progressively earlier from the beginning through to the middle of the season then progressively later till the end of the season. Relative finishing time of breeding song however remained constant so that the duration of breeding season song gradually increased then decreased paralleling the change in starting times. A consequence of the two distinct classes of vocalizations was that there were essentially two distinct 'dawn choruses'. One, consisting of group vocals, was sung all year round; the other was given by males singing 'breeding season' song. Since there was no reason the expect that a single function would necessarily be ascribed to both choruses, this raised the possibility that some of the confusion surrounding the function and nature of the 'dawn chorus' originated from a failure to recognize the existence of two such choruses. Variation in time and space showed further differences between the two vocalization classes. The breeding song of each male was distinctly different from that of his neighbours and there was a marked change in the repertoire of any individual from one year to the next. In marked contrast, daytime vocalization repertoires of neighbouring groups were virtually indistinguishable and changed little from year to year. These findings, together with information from recent literature, suggested that the two song classes had a different ontogeny, function and possibly evolution. It was proposed that territory declaration was the function of dawn singing by grey butcherbird family groups but that the function most consistent with adult male dawn song was attraction of females for extra-pair copulations. It was suggested that chorusing itself was to some extent an accidental by-product of the advantage to the individual or group of singing at dawn although a recently proposed function, the social dynamics function, could not be ruled out. Further differences from the Northern Hemisphere situation were detected in subsong. First, subsong was given by birds in their first year and also by adult males. The finding of subsong in adult males was not without precedent as it has been documented previously for a small number of passerines, especially those that change repertoire from year to year. Subsong in young (first year) birds, however, was unusual in that birds practised in small groups rather than in the complete isolation usually associated with subsong. Moreover they did not practise adult male song but instead practised group daytime vocalizations. It was suggested that it was important for birds to learn to sing in company for the important task of group territory defence. Further investigation of the literature and observations during the present study revealed similar vocalization classes and behaviours in other members of the Artamidae and other endemic Australasian taxa. These literature investigations also revealed that the possession two song vocalization classes was quite widespread although they tended to be restricted (but not exclusive) to males rather than found in males and females. These findings led to further research into the significance of Australia in the evolution of songbirds, the role of co-operative breeding in Australian passerines, and finally to an hypothesis for a possible origin of male bird song. It is suggested that male song arose in a social environment where the male and female were in frequent vocal communication. If the tendency to seek extra-pair copulations (EPCs) and female choice had already been incorporated into the suite of passerine behaviours, it would be necessary to avoid the mate during such activities and the male would need to advertise with a s
Thesis (PhD Doctorate)
Doctor of Philosophy (PhD)
Australian School of Environmental Studies
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The aim of this study was to understand the function of song and its role in the speciation process in a duetting Neotropical passerine, the gray-breasted wood-wren (Henicorhina leucophrys). This species lives in the dense understory of mid-elevation cloudforests throughout the Andes and up into southern Mexico. Gray-breasted wood-wrens sing sex-specific songs, either as solos or as complex duets, with the male and female of a mated pair alternating their songs with variable degrees of coordination. Males sing more than 50 different song types, while females sing at least 15-20 song types. Duets are initiated by males and females at equal rates. Using playback experiments simulating intrusions by paired and single birds, I show that males and females sing to advertise their partner’s mated status and to repel potential rivals. These results show that duets reflect conflict between the sexes rather than cooperation between the pair. I studied song variation in two subspecies of the gray-breasted wood-wren which occupy different habitats in the Ecuadorian Andes. I found that the subspecies sing significantly different songs and showed that these differences are driven by acoustic differences in their preferred habitats – loud cicada choruses in the habitat occupied by one subspecies have caused that subspecies to sing at a lower frequency in order to be heard over the noise. Where the two subspecies come into secondary contact, their songs are more different from each other than in areas where they do not meet. This suggests that there is a cost to mating with the wrong subspecies and that selection has driven the songs apart in order to prevent such an occurrence. This result provides the first convincing case of character displacement in bird song and strong evidence that song divergence acts as a barrier to gene flow between these two subspecies.

Birdsong is one of the most astounding natural sounds which profoundly shaped our evolutionary thinking since the 19th century. Despite a strong interest in birdsong for over 100 years, our understanding of birdsong ecology and evolution over large spatial and phylogenetic scales is still very fragmentary. Answering many basic questions requires a global synthesis covering vast diversity of extant bird species and adoption of multidisciplinary approaches. In presented dissertation thesis, my co-workers and I have explored important patterns in macroecology and macroevolution of song in passerines (Order: Passeriformes), the most diverse and widespread bird order. We have focused on three key song phenomena: (1) song complexity, (2) song frequency and (3) the presence of song in female birds. We have exploited birdsong "big data" available on public citizen science databases and other open sources in order to fill several important gaps in the current knowledge. These data were analysed by a combination of phylogenetically-informed cross-species analyses and spatial macroecological approaches. Since the publication of Darwin's seminal work, elaborated songs are generally agreed to be the result of sexual selection. We developed a simple but reliable song complexity metric to explore a global diversity in...

Recent classifications of Australian birds have been limited to lists of "species" which are inadequate as biodiversity indicators. The Directory of Australian Birds: Passerines fills a huge gap in ornithological knowledge by separating out and listing not only 340 species of song-birds but also the 720 distinct regional forms. Covering about half the national bird fauna, the Directory provides science and the community with baseline information about what bird it is and where it lives in an Australia-wide context. Identity is taken down to the level of distinct regional population. No other compendium on Australian birds does this.

Birds are excellent animal models in studies of cognition, neuroplasticity, neuroendocrinology, and sex differences in behavior. Experiments with diverse avian species have revealed a potent modulation of neuroanatomy and complex brain function by steroids, both during development and adulthood. This chapter describes some of the foundational and more recent developments in the estrogenic modulation of spatial memory function, as well as related studies regarding effects of the steroid on auditory discrimination and memory for song in passerines. More specifically, the chapter describes the evolution of our understanding of how locally synthesized and rapidly acting estradiol modulates higher cognitive functions in this varied and important vertebrate class, as well as the mechanisms whereby this synaptic aromatization may underlie the learning and retention of these behaviors.