Wiley

Journal of Avian Biology

Published by Wiley and Nordic Society Oikos

Online ISSN: 1600-048X

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Print ISSN: 0908-8857

Disciplines: General life sciences

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112 reads in the past 30 days

Locations of study sites. (a) The dotted line marks the approximate breeding range of the taiga bean goose in Finland. Hollow circles show the trapping sites and filled circles are the release sites. The solid square denotes the location of the aviary geese were kept in until release. (b) Schematic depiction of the experiment and hypothesized outcomes. The black line, connecting hollow (breeding area) and filled (moult site) triangles, shows an approximate normal moult migration route. A hollow inverted triangle shows an example of a displacement site. In outcome 1 (red dotted line), displaced one‐year‐old birds compensate for displacement and fly directly to the correct moulting grounds (‘goal‐area navigation'). In outcome 2 (orange dotted line), displaced birds migrate the same length and in the same direction as wild control birds and end up in a correspondingly shifted moulting area marked with a filled inverted triangle (‘clock and compass navigation'). Outcome 3 (blue arrows), displaced birds fail to migrate and randomly disperse around the release site.
Tracks of control groups. (a) Moult migration route of the four wild control birds from trapping (hollow triangles) sites to moulting sites in Novaya Zemlya (filled triangles). (b) Track of the only procedural control bird that executed moult migration. Three procedural control birds (Y29, Y37, Y33) moulted at or near the release site and thus are not plotted on the map. The black line shows the moult migration route of Y38 from the release site (hollow triangle) to the moult site (filled triangle) in Novaya Zemlya.
Tracks of translocated one‐year‐old taiga bean geese from their release sites to their moulting sites. (a) Tracks of birds that moulted in Finland. (b) Tracks of birds that moulted in Russia. Hollow triangles mark release sites and solid triangles the moulting sites.
Efficiency of travel coefficient from the release site to the moulting site. The y‐axis shows the ratio of the total travel distance (km) over the great circle distance (km) from the release site to the moulting site for three different treatment groups. Translocated birds reached moulting grounds through much less efficient routes than the other two groups (F2 = 8.82, p = 0.004). Letters denote statistically different groups according to the post hoc HSD Tukey test (Alpha = 0.5).
Translocation experiment of taiga bean geese Anser fabalis provides evidence for oblique social learning of moult migration

November 2024

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112 Reads

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Aims and scope


Journal of Avian Biology is an open access outlet for innovative, hypothesis-driven research on the biology of birds, with a particular emphasis on ecological, evolutionary and behavioural studies.
We welcome submissions that study avian biology across all levels of ecological organization, from organisms and populations to communities and ecosystems. As a Nordic Society Oikos journal, we advocate research that is fair, openly accessible and reproducible.

Recent articles


Nonmetric multidimensional scaling ordinations for the Bray–Curtis dissimilarity matrix, demonstrating clear separation in the composition of the polar metabolic profile. Eurasian blackcap (A) and lesser whitethroat (B) at the three different stopover sites.
Differences in vital polar metabolites in the Eurasian blackcap (A) and lesser whitethroat (B) among the three different stopover sites, as detected in SIMPER analyses. Different letters account for significant differences. Within boxes, horizontal lines indicate the median; black dots show the mean; box boundaries indicate the interquartile range; whiskers indicate the minimum and maximum.
Differences in relative intensity of total TAG in the Eurasian blackcap (A) and lesser whitethroat (B) and total PUFA TAG in the Eurasian blackcap (C) and lesser whitethroat (D) among the three different stopover sites. Different letters account for significant differences. Within boxes, horizontal lines indicate the median; black dots show the mean; box boundaries indicate the interquartile range; whiskers indicate the minimum and maximum.
Differences in relative intensity of β‐hydroxybutyric acid (BUTY) in the Eurasian blackcap (A) and lesser whitethroat (B) among the three different stopover sites. Different letters account for significant differences. Within boxes, horizontal lines indicate the median; black dots show the mean; box boundaries indicate the interquartile range; whiskers indicate the minimum and maximum.
The suggested fate of protein catabolism and elevated plasma glucose during and post long‐endurance flights. Free amino acids are delivered to the liver through the bloodstream. These amino acids are then used to produce glucose using gluconeogenesis. Lactic acid is maintained as a result of anaerobic conditions. The alanine cycle is maintained for the disposal of the ammonium group through the uric acid cycle. The lack of NAD+ is compensated via the malate and glycerol shuttles. High plasma glucose can also facilitate repair mechanisms for increased oxidative stress.
Comparative analysis of the plasma metabolome of migrating passerines: novel insights into stopover metabolism
  • Article
  • Full-text available

December 2024

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11 Reads

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Weronika Jasinska

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Leah Rosental

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Ofer Ovadia

During long‐distance migration, many birds experience periods of either prolonged fasting (during endurance flights) or extensive feeding (during stopovers). Despite decades of research on avian metabolism during migration, many questions have remained unanswered, as such research mainly focused on targeted metabolites and fat metabolism. Here, we examined the plasma‐metabolome of two migrating passerine species before they crossed the Sahara Desert. Birds were sampled at two sites populated by Pistacia trees bearing fat‐rich fruits and at an additional site dominated by blooming Eucalyptus trees. The blood samples were analyzed using both GC‐MS and LC‐MS, using an untargeted approach. Examination of metabolic pathways activated during stopovers indicated a crucial role for cycling glucose through the Cori and Cahill cycles in resting and recovery processes. This novel perspective, conducted on free‐ranging birds, suggests the evolution of avian insulin resistance due to factors such as endurance exercise, fasting, and a preference for fatty acid oxidation during migration, akin to cell trauma recovery. We detected significant inter‐site variations in birds' polar and lipophilic metabolic profiles. We interpret the differences in the polar metabolites to be associated with the physiological state of the birds, with birds that are considered to have landed during the night prior to capture showing different metabolic profiles compared to birds that have spent more time at the stopover site. In contrast, distinctions in the lipophilic profiles of birds were associated with variations in the primary food source that was available to them in the different sites. This study underscores the challenge of interpreting commonly used indicators for assessing migrating birds' physiological state, which was predominantly derived from lipid metabolism in complex ecological systems.


Annual cycles of adult black terns (a), adult common terns (b) and one juvenile common tern (c) from breeding sites in southernmost Sweden, as recorded by geolocators. Each horizontal bar shows the estimated cycle for each individual and year (1 Jul–30 Jun; Supporting information). Some individuals were tracked during several successive years (or part of year) as indicated at the logger code for each horizontal bar. The common tern with logger code F080 was tracked during two annual cycles followed by continued tracking during a third year with a new logger (T855). RED = in breeding area, GREEN = travel between breeding area and NW Africa (Canary Isl., Mauretania), southwards in autumn and northwards in spring. BLUE = travel between NW Africa and non‐breeding range, southwards in autumn and northwards in spring. YELLOW = in main non‐breeding area. GREY = arrival date in non‐breeding area could not be estimated during the autumn equinox period for three individuals of black terns (4 journeys) with non‐breeding quarters north of the equator (see text). For the juvenile common tern (c), the RED periods at the end of the first year and beginning of the second year do not reflect a stay in the Swedish breeding area but instead at an African northern summer area (Fig. 3 and text). The adjoining periods in BLUE show the travel periods between the northern summer area and the main non‐breeding quarters (at South Africa).
Estimated locations (based on light‐level geolocator data) for adult black terns (9 individuals, 11 journeys), and adult common terns (6 individuals, 9 journeys) during four monthly/bimonthly periods (Aug, Nov, Feb and Apr/May, respectively). For each species, daily locations are shown for all individuals and journeys combined to illustrate the overall migration pattern for the study population. Geographic locations, as estimated from geolocator data, are given in separate maps for each individual and journey in Supporting information. Background maps were created using ArcGIS® software (Esri).
Estimated locations for one juvenile common tern during three periods of non‐breeding and over‐summering in Africa (during the birds' initial twenty months of its life; see Fig. 1). a) Nov 2013 to Mar 2014, b) Jun to Aug 2014, and c) Nov 2014 to Jan 2015. Background maps were created using ArcGIS® software (Esri).
Migration of black terns Chlidonias niger and common terns Sterna hirundo between south Sweden and the Atlantic coast of Africa

December 2024

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16 Reads

Light‐level geolocators were used to record the annual migration cycles of black terns Chlidonias niger (9 individuals, 11 journeys) and common terns Sterna hirundo (7 individuals, 11 journeys) breeding in southernmost Sweden. The black terns used two different non‐breeding (Oct–Mar) regions along the Atlantic coast of Africa, either north of the equator between Senegal and Liberia (3 individuals) or south of the equator between Gabon and northern Namibia (5 individuals). All the common terns travelled to non‐breeding quarters south of the equator, mainly along the coasts of Namibia and South Africa. One juvenile common tern was tracked during the first twenty months of its life. This bird spent its first northern winter in South Africa, after which it migrated north of the equator to spend the northern summer as a one‐year‐old non‐breeder in tropical waters off Ghana, after which it returned to South Africa for its second northern winter. This record demonstrates that one‐year‐old terns may undertake extensive intra‐African migration to distant over‐summering areas. Comparing geolocator results from Swedish and Dutch black tern populations indicate that they have similar migration habits, with a possible tendency of relatively more individuals migrating south of the equator in the more northerly Swedish population (leap‐frog migration). Comparing geolocator and ringing results among common tern populations indicates a fascinating and complex pattern of scale‐dependent geographic segregation and intermixing along the coasts of Africa.


Locations of study sites. (a) The dotted line marks the approximate breeding range of the taiga bean goose in Finland. Hollow circles show the trapping sites and filled circles are the release sites. The solid square denotes the location of the aviary geese were kept in until release. (b) Schematic depiction of the experiment and hypothesized outcomes. The black line, connecting hollow (breeding area) and filled (moult site) triangles, shows an approximate normal moult migration route. A hollow inverted triangle shows an example of a displacement site. In outcome 1 (red dotted line), displaced one‐year‐old birds compensate for displacement and fly directly to the correct moulting grounds (‘goal‐area navigation'). In outcome 2 (orange dotted line), displaced birds migrate the same length and in the same direction as wild control birds and end up in a correspondingly shifted moulting area marked with a filled inverted triangle (‘clock and compass navigation'). Outcome 3 (blue arrows), displaced birds fail to migrate and randomly disperse around the release site.
Tracks of control groups. (a) Moult migration route of the four wild control birds from trapping (hollow triangles) sites to moulting sites in Novaya Zemlya (filled triangles). (b) Track of the only procedural control bird that executed moult migration. Three procedural control birds (Y29, Y37, Y33) moulted at or near the release site and thus are not plotted on the map. The black line shows the moult migration route of Y38 from the release site (hollow triangle) to the moult site (filled triangle) in Novaya Zemlya.
Tracks of translocated one‐year‐old taiga bean geese from their release sites to their moulting sites. (a) Tracks of birds that moulted in Finland. (b) Tracks of birds that moulted in Russia. Hollow triangles mark release sites and solid triangles the moulting sites.
Efficiency of travel coefficient from the release site to the moulting site. The y‐axis shows the ratio of the total travel distance (km) over the great circle distance (km) from the release site to the moulting site for three different treatment groups. Translocated birds reached moulting grounds through much less efficient routes than the other two groups (F2 = 8.82, p = 0.004). Letters denote statistically different groups according to the post hoc HSD Tukey test (Alpha = 0.5).
Translocation experiment of taiga bean geese Anser fabalis provides evidence for oblique social learning of moult migration

November 2024

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112 Reads

While there is ample evidence supporting genetic control of migratory behaviour in short‐lived passerines, long‐lived social species have been assumed to rely solely on cultural inheritance of migratory routes. Evidence from experimental studies supporting this idea is scarce. We tested whether the moult migration in taiga bean geese Anser fabalis has an inherited component or whether the birds need oblique social learning (where knowledge on migration is transferred from any experienced individual to any naïve individual conspecific) to carry out this journey. In many waterfowl species, non‐breeders and failed breeders migrate to remote places for wing moult while successful breeders stay at the breeding grounds and moult with their chicks. We translocated one‐year‐old taiga bean geese before their first moult migration to sites outside of the breeding range to examine whether they display innate moult migration behaviour without experienced conspecifics or not. The birds were equipped with GPS‐transmitters and released in randomly assigned groups of two. Wild control one‐year‐old birds were released immediately after capture with other non‐breeding geese, while a procedural control group consisting of older birds was held in captivity until being released at the same time with the translocated one‐year‐old birds but in the place where they were captured. Most translocated birds found conspecifics and either joined locally moulting breeders or followed experienced birds to moulting sites in Russia. Two of the translocated birds did not find other bean geese and settled to moult together in southwest Finland. The wild control birds moult‐migrated as expected, while only one of the procedural control birds moult‐migrated to Russia and the remaining three stayed with locally moulting breeders in Finland. Our results support the idea that moult migration in geese is culturally inherited, highlighting the importance of the non‐relative, experienced adult individuals in maintaining population‐specific behaviours.


Tracks of common terns fitted with GPS tags (a), solar geolocators ‘GLS' (b), and MOTUS nanotags (c). Sample sizes are labeled on plots (a)–(c) as (n = ) and in plot (d) as (Ntag type = ), i.e. NGLS = or Nnanotags = .GPS and MOTUS nanotag fixes were summarized on a grid (0.75 × 0.75°). GLS location estimates (a million particles per day per individual) were summarized on the same grid, providing a measure of relative time spent accounting for the spatial inaccuracy of the method. Panel (d) provides a summary of migration schedules by region (Lake Erie, southern Atlantic Coast, and Florida; top to bottom) for birds fitted with GLS and MOTUS nanotags. Beneath each phenology density plot by region, triangles (arrival) and circles (departure) grouped by dashed grey rectangles, show individuals with at least two tracks from different years. Breeding colony locations where tracking devices were deployed are indicated by white diamonds with black outline and include: 1) Lake Winnipeg, 2) Lake Superior, 3) northern Lake Huron and 4) Oneida Lake. Map made with Natural Earth.
Box plots of arrival (first detection) and departure (last detection) of adult and juvenile common terns by region (Lake Erie (n = 9 Adult; n = 11 Juvenile), southern Atlantic Coast (n = 7 Adult; n = 5 Juvenile), and Florida (n = 3 Adult; n = 3 Juvenile)). Midline values represent median date (Julian day). The upper and lower limits of the boxes represent the 75th and 25th quartiles, respectively, with whiskers representing minimum and maximum values (< 1.5 × inter‐quartile range). Only raw data points are shown for both adult and juvenile birds in Florida where only three individuals of each age class were detected.
Graph network showing spatial (a), spatiotemporal (b), and region‐specific spatiotemporal associations (c) of adult common terns breeding at two colonies on Lake Superior (thick black and grey circles) during the non‐breeding season. Nodes represent individuals (with numeric ids) differentiated by sex and breeding colony location (color) within western Lake Superior (Minnesota and Wisconsin, USA). The links provide spatial and spatiotemporal associations among individuals. The network structure (e.g. relative location of nodes/individuals) is fixed to the location of individuals from the spatial association network (a). The regional maps in (c) provide the filtered links between two fixes of different individuals that occurred within a period of 2 days. The total number of links is given for each network. The regional maps describe regions in North America (1) Lake Erie, (2) southern Atlantic Coast, and (3) western coast of Florida, in Mexico (4) northwestern coast of the Yucatan Peninsula and in South America (5) northwestern coastal Peru. Map made with Natural Earth.
Stopover regions, phenology, and spatiotemporal group dynamics of adult and juvenile common terns Sterna hirundo from inland lakes in North America

November 2024

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105 Reads

Understanding the behavior of migratory birds can help determine levels of connectivity and inform conservation actions for species of conservation concern. The common tern Sterna hirundo is a long‐distance migratory seabird that is considered a species of conservation concern in the North American Great Lakes region and that has experienced significant declines in breeding numbers across large lakes in Manitoba. To better understand the movement ecology of common terns, we used data from multiple tracking technologies (solar geolocation, GPS tracking, and Motus radio tracking) obtained from individuals (n = 83) across five breeding colonies on four inland lakes in North America. We identified key stopover regions used during southward migration and explored how demographics and social interactions influence connectivity. We identified three key stopover regions (Lake Erie, the southern Atlantic Coast, and Florida) and documented, for the first time, differences in post‐natal and post‐breeding migration for inland nesting terns. Juveniles arrived, on average, three weeks later than unrelated adults to their first major staging area. Although adult female arrival to and departure from Lake Erie was similar to adult males, female schedules became significantly earlier than males as southward migration progressed. Using a graph network to describe the spatiotemporal associations among adults from the same inland lake, individuals appeared to be highly connected, meeting up in different regions throughout the non‐breeding season, suggesting that social interactions may play an important role in maintaining spatial connectivity. Despite differences in migration schedules by sex and arrival to the first major staging area by age class, birds appeared to rely on the same key stopover regions during southward migration. The stopover regions identified in this study can help identify potential bottlenecks and guide future research aimed at assessing the impacts of climate change and human disturbance on common terns breeding in North America.



Schematic overview of the geographic distributions of the four major tick genera (Amblyomma (yellow), Ixodes (orange), Haemaphysalis (green), Hyalomma (blue)) found on birds within the African–Western Palearctic region (Keve et al. 2022). Colors correspond to tick genera with the mapped distribution of the respective genera based on published distribution maps of all species belonging to a given genus found in the compiled dataset (Walker et al. 2003, Estrada‐Peña et al. 2004, 2017). Migratory bird corridors (black arrows) show the proposed major flyways between European breeding grounds and non‐breeding grounds in Africa or Europe of bird species identified in the compiled dataset (Briedis et al. 2020). Black stars show the sampling locations for all 35 studies which were included in the compiled dataset.
Overview of collected data from 35 studies in relation to ticks moving with migratory birds along African–Western Palearctic flyways. The left plot shows a bar plot reporting the number of independent studies for which a bird species was observed whereas the right plot shows a boxplot of mean tick load (MTL, no. of ticks per unit bird of a given species) per bird species over all studies. Bird species are organized by taxonomic family and only bird species which were found in at least two independent studies are shown. Outlying MTL values above 10 (n = 2) are not shown for ease of reading, but were included in all statistical analysis. See the Supporting information for a full version of this figure showing all bird species found, including those in singular studies and MTLs above 10.
Point estimates for bird/tick species interactions for all tick species belonging to the following tick genera found on infested migratory birds: (A) Ixodes, (B) Hyalomma, (C) Haemaphysalis, (D) Amblyomma, (E) Dermacentor and (F) Rhipicephalus. The dataset was filtered for bird species which were present in at least two independent studies (n = 1102 observations). The model was run with a gamma error distribution with a log link function using the brms command from the ‘brms' package (Bürkner 2017) as implemented in R ver. 4.1.2 (www.r‐project.org). Full outputs including convergence statistics (Material and methods) can be found in the Supporting information. The dotted line refers to the log‐transformed average of all mean tick loads included in the dataset. Interactions were considered significant if the estimates and 95% confidence intervals did not overlap this mean value (i.e. always higher or lower than the average tick load over the full dataset) and are shown in bold.
Point estimates for tick species/migratory season interactions for all tick species in the reported dataset. The dataset was filtered for bird species which were present in at least two independent studies and where a clear migratory season was reported by the original study (n = 865 observations). The model was run with a gamma error distribution with a log link function using the brms command from the ‘brms' package (Bürkner 2017) as implemented in R ver. 4.1.2 (www.r‐project.org). Full outputs including convergence statistics (Material and methods) can be found in the Supporting information. The dotted line refers to the log‐transformed average of all mean tick loads included in the dataset. Interactions were considered significant if the estimates and 95% confidence intervals did not overlap this mean value (i.e. always higher or lower than the average tick load over the full dataset) and are shown in bold. Migratory season is shown either in yellow (spring) or blue (autumn).
Beware of hitchhiking ticks? Clarifying the variable roles of bird species in tick movement along migratory routes

November 2024

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105 Reads

Ticks are blood‐feeding parasites which act as major vectors for various pathogenic microorganisms affecting both animal and human health. Hard ticks are known to move passively (i.e. ‘hitchhike') on migratory birds as they transit between breeding and non‐breeding grounds. This potentially leads to exchange and establishment of non‐endemic tick species in novel environments. However, it is not yet clear if all migratory bird taxa play an equal role in movement of specific tick species, especially outside of medically important tick taxa. To clarify these interactions, we performed a systematic literature review regarding primary data of ticks moving on migratory birds within the African–Western Palearctic flyways. In total, 35 studies were found which showed 123 bird species from 37 families and 12 orders connected to potential movement of 30 tick species representing six genera (Amblyomma, Dermacentor, Haemaphysalis, Hyalomma, Ixodes, Rhipicephalus). Most tick species did not show high abundance for any bird species, or, if they did, only on very few. Only Ixodes ricinus and Hyalomma marginatum were estimated to be carried at above average burdens by multiple bird species. This could indicate an increased likelihood of these species to be moved during migration. Specific tick species or whole genera were only found in certain migratory seasons as expected based on their geographic distributions. Even so, species found in both migratory seasons did not differ in their estimated abundances on birds between seasons. This result could suggest that tick abundance on migrating birds is not always a direct result of geographic distribution and may suggest an understudied importance of stopover sites towards potential tick introduction or turnover. Taken together, the results presented here provide guiding information for future analyses integrating individual level variation into the current understanding of tick movement with migratory birds.


Using metabolic data to investigate the role of brood size in the development of endothermy

November 2024

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45 Reads

Altricial songbirds transform themselves from naked poikilotherms to fully feathered endothermic homeotherms over a matter of days from hatching to fledging. The ontogeny of endothermy is a developmental milestone for birds that not only face warmer average temperatures, but also increasingly frequent cold snaps and extreme weather. The timing of development of endothermy has been studied in altricial birds for over half a century. However, the determinants and constraints of the onset of endothermy are not yet fully understood. We experimentally investigated whether brood size influences the ontogeny of endothermic heat production in 4–8 day‐old nestling blue tits Cyanistes caeruleus in southern Sweden. The thermogenic response to a cooling challenge (15°C) increased with age overall. We found that 8‐day‐old nestlings from reduced broods had a slightly increased capacity for endothermic heat production compared to enlarged broods. This difference cannot be explained by body mass because this trait did not differ between brood size categories. Although a metabolic response was present in most nestlings by day 6, it was brief, not lasting more than a few minutes, and not sufficient to maintain a stable body temperature in any age group. Our study shows that incipient endothermy is present at an early age in nestling blue tits and may advance faster in reduced broods, but that individual nestlings lack sufficient insulation and thermogenic performance to maintain homeothermy independently during the first week of life.


Distributions with thin lines correspond to individual niches for sparrows captured in the spring (blue) and summer (orange) of juveniles (A)–(B) and adults (C)–(D) generated from δ¹⁵N values of blood plasma, red blood cells, and claw tips. Distributions with thick lines represent the corresponding total niche width (TNW), which were scaled equally for the four groups enabling direct comparison.
Trophic levels of juvenile and adult sparrows during spring (blue) and summer (orange), calculated using δ¹⁵N isotopic values from diet and bird tissues. The error bars represent the 95% confidence intervals.
The interplay of resource availability and parent foraging strategies on juvenile sparrow individual specialization

October 2024

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62 Reads

Temporal variation in resource availability, amplified by global change, may have strong impacts on species breeding at temperate and high latitudes that cue their reproduction to exploit seasonal resource pulses. This study examines how resource availability and parental care influence niche partitioning between and within age classes in the rufous‐collared sparrow, which provides extensive parental care. We hypothesized juveniles would exhibit narrower niches focused on high‐quality resources compared to adults, regardless of resource availability. We used stable isotope analysis to quantify individual and population niches in juveniles and adults across the breeding season in two cohorts experiencing contrasting resource landscapes. Contrary to our initial hypothesis, juveniles exhibited greater among‐individual diet variation and smaller total niche widths (i.e. higher levels of individual specialization, IS) during periods of high food availability in comparison to periods of food scarcity. Interestingly, total niche width and IS of adults remained stable across seasons despite a shift in trophic level, highlighting their potential role in providing a consistent diet for their young. These findings reveal a dynamic interplay between resource availability, parental care, and IS, with important implications for understanding population resilience under variable resource scenarios. The study also suggests that adult sparrows modify their provisioning strategies based on resources, potentially buffering offspring from environmental fluctuations. Understanding age‐specific responses to resource variation is crucial for predicting species responses to ecological conditions, particularly in regions like central Chile where seasonal resource limitation is expected to become more variable in response to climate change.


A diagram showing the relationship between phonological syntax, lexical syntax, sequential syntax, and dialectic syntax. Syntax exists as an orderly arrangement of parts. If the structure of the syntax is not associated with a semantic meaning, it is considered sequential syntax. Dialectic syntax is a type of sequential syntax that is population specific. If syntax does convey a semantic meaning, it is considered phonological syntax at the first level and if the resulting meaningful units are combined again, it is considered lexical syntax.
An example of sequential and dialectic syntax in the songs of Bachman's sparrows. (A) The organization of notes into syllables is an example of sequential syntax. (B) The organization of an introductory note and syllables to create a song type is an example of second‐level sequential syntax. (C) The organization of specific song types into a preferred transition pattern that is highly shared within a population is an example of dialectic syntax.
Syntax in animal communication: its study in songbirds and other taxa

October 2024

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46 Reads

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1 Citation

Many building blocks of human language can be found within the vocal communication systems of other species, most notably songbirds. One of the most prominent of these building blocks is syntax. While studies of syntax are abundant, a lack of consensus on the definition of syntax in non‐human animal communication studies has led to much debate. Consistent and deliberate use of terminology is needed to facilitate understanding across disciplines. In addition, new terminology may better describe syntactic structure found in vocal signals that are devoid of semantic associations, such as birdsong. Here, we propose two terms to describe the types of syntax commonly found in birdsong: sequential syntax and dialectical syntax. Sequential syntax can be defined as the rules that govern the patterns of sound without regard to semantic meaning. Dialectic syntax can be defined as sequential syntax that is distinct among different populations or groups with behavioral significance for those groups. Taken together, these two terms can describe the type of syntax seen in ornamental signals, such as birdsong.


GPS tracks of 10 adult Wahlberg's eagles between 2018 and 2022 during their migration, based on 1 point/hour. Red = pre‐breeding migration; yellow = post‐breeding migration. Land cover background data from GeoPortal (https://www.africageoportal.com/maps/africa::africa‐land‐cover/about). Horizontal lines indicate the 4.4°N and 2.8°N lines where non‐breeding areas start for the long‐distance and short‐distance migrants, respectively.
Latitude plotted against date at 1 point/hour/individual, for 10 adult Wahlberg's eagles between 2018 and 2022. The transition between migration north and non‐breeding (blue vertical line) was defined as a 13 latitude of 2.8°N for short‐distance migrants and 4.4°N for long‐distance migrants.
Timing of migratory phases during the annual cycle for 10 adult Wahlberg's eagles (7 short‐distance migrants, SDMs; 3 long‐distance migrants, LDMs) tracked in 2018–2022. The earliest start date and latest end date of any individual within each population was used to delineate the four phases.
The effect of population for 10 adult Wahlberg's eagles (7 short‐distance migrants, SDMs; 3 long‐distance migrants, LDMs) tracked in 2018–2022 on (A) the proportion of time spent on breeding versus non‐breeding areas, (B) the proportion of time spent on post‐ and pre‐breeding migrations, and (C) the number of travel days on post‐ and pre‐breeding migrations. Error bars represent the standard errors. Significant differences are indicated with letters.
The effect of population for 10 adult Wahlberg's eagles (7 short‐distance migrants, SDMs; 3 long‐distance migrants, LDMs) tracked in 2018–2022 on (A) the total migratory distance on post‐ and pre‐breeding migrations, (B) the square root transformed daily distance (in kilometers) on post‐ and pre‐breeding migrations, and (C) on overall migration speed on post‐ and pre‐breeding migrations. Error bars represent the standard errors. Significant differences are indicated with letters.
Different migration patterns of Wahlberg's eagles Hieraaetus wahlbergi across Africa

October 2024

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86 Reads

Intra‐Africa movements of most African migratory birds remain an enigma. We describe the migrations of Wahlberg's eagle Hieraaetus wahlbergi using GPS‐GSM transmitters on adult eagles in their South African (n = 3) and Kenyan (n = 7) breeding areas between 2018 and 2022. The dataset included 57 migratory tracks, 29 post‐breeding and 28 pre‐breeding. We found long‐distance migrants (LDMs; from South Africa) and short‐distance migrants (SDMs; from Kenya) using common non‐breeding areas centered in the Sudans and Central African Republic. The timing of annual phases was similar, but LDMs departed on their pre‐breeding migration on average later than SDMs (13 August versus 31 July) and arrived later on their breeding grounds (13 September versus 10 August). Conversely, the average departure date on the post‐breeding migration was 4 April for SDM and 23 March for LDMs. LDMs spent significantly less time of the year than SDMs on breeding grounds (44 versus 57%), and slightly but not significantly more time (40 versus 38%) on non‐breeding areas. The post‐breeding migration distance was on average 3413.9 ± 170.9 km for LDMs and 491.9 ± 158.5 km for SDMs. At non‐breeding areas, LDMs reached more northerly latitudes than SDMs, increasing the pre‐breeding migration distance to 4495.9 ± 372.5 km for LDMs versus 1701.9 ± 167.3 for SDMs. Daily flight distances back to the breeding areas averaged 153.4 ± 130.3 km for LDMs and 167.4 ± 122.3 km for SDMs and to non‐breeding areas were shorter for SDMs (124.8 ± 113.0 km) than LDMs (178.0 ± 134.4 km). Migration speed was similar across populations and for pre‐ and post‐breeding migrations. LDMs used more stopover days than SDMs. We conclude that Wahlberg's eagles from different parts of Africa have adapted their migration to differences in timing of the breeding season, distance of travel, and resources in the landscapes encountered during migration.


Daily and seasonal use of vocalizations by nesting black‐tailed godwits

October 2024

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45 Reads

Ground‐nesting shorebirds must balance the need for acoustic communication at the nest with the constant threat posed by predators. Although it may seem likely that their calls are adapted to minimize detection by predators, little is known about how these birds communicate at the nest or whether they employ cryptic strategies to avoid predation. Using passive acoustic devices and software to analyse extensive acoustic data, we quantified and categorised the calls of black‐tailed godwits Limosa limosa limosa recorded throughout the whole incubation at eight nests at a dairy farm in the Netherlands in March–June 2021. While incubating, godwits frequently use five main call types, with distinct diurnal patterns and high variation in the number of calls between breeding pairs. Birds used two quiet calls, one for communication at the nest and a second without an easily suggested meaning. Three loud calls were presumably used for predator alert, territory establishment, and long‐range communication. Interestingly, although nests were close to each other and exposed to the same aerial predators, the involvement of incubating birds in predator alert calling consistently differed. Furthermore, we described the relationship between the number of predator alert calls and the probability of a godwit flying off the nest. Our findings show that incubating godwits predominantly use loud vocalizations during the day, with only a few calls at night, which were more frequent on nights with a full moon. These descriptive findings for a single godwit community should now be expanded to other contexts, experimental situations, and shorebird species.


Map of the potential distribution area of Tetrao urogallus and the surveyed leks. Five of the surveyed leks were located in Ariège (France) and one in Andorra.
Number of capercaillies obtained by surveying with each method. For the N^o obtained with M0 the associated CI (95%) is represented by bars. In the surveys 2017‐2, 2018‐1, 2018‐2 and 2019‐1 the walk‐based approach was not performed (np). MPE: minimum population estimate.
Comparison between the number of male capercaillies detected during lek counts with the N^o obtained from the M0 model.
Improving population size estimation at western capercaillie leks: lek counts versus genetic methods

October 2024

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90 Reads

The western capercaillie Tetrao urogallus, hereafter capercaillie, is the largest galliform bird present in the boreal and montane forests of the Western Palearctic. Precise and accurate methods for estimating the number of individuals and/or their densities are crucial for the proper management of its free‐ranging populations. However, obtaining reliable estimates of the abundance of populations of wild species and, particularly, of birds is not a simple task. In the case of lek‐mating birds such as capercaillie, surveys are traditionally based on lek counts, that is, counts of calling males present in their mating areas: the leks. This study was carried out on the Pyrenees at six capercaillie leks where two different lek counting approaches were performed: hide‐based and walk‐based. The results were compared with those obtained from an estimate of minimum population size (MPE) derived from genotyping all faeces samples found in the lek area, and with a population size estimate derived from a genetic mark‐recapture model (N^o) of each capercaillie lek. The results of N^o were used to estimate the detection rate (D) of both lek count approaches. Our results show that traditional lek counts do not detect all male capercaillies since the detection rate was 0.34 (95% CI: 0.26–0.43) for hide‐ and 0.56 (95% CI: 0.43–0.68) for walk‐based lek counts. Our results suggest that the walk‐based lek counts were more efficient than the hide‐based ones, providing more accurate results compared to the N^o estimate. The combination of non‐invasive sampling with genetic mark‐recapture model was found to be the most reliable method for obtaining the N^o of leks given that traditional lek counts underestimate the number of capercaillie and, furthermore, can cause disturbance to the species at these sites.


Example plots of the temporal sequence of two movement metrics (home range size as 95% minimum convex polygon, and median daily travel distance, both calculated over 5‐day windows with a 2‐day overlap between adjacent windows) for three adult female red kite individuals that initiated a breeding attempt (left), did not breed (centre), and exhibited behaviour that resulted in uncertain (assignment probability > 25% and < 75%) classification (right).
Example plots of the temporal sequence of three movement metrics (median daily time spent at the nest, median of the daily maximum distance from the nest, and maximum length of time consecutively away from nest, all calculated over 5‐day windows with a 2‐day overlap between adjacent windows) for three adult female red kite individuals that failed in their nesting attempt (left), bred successfully (centre), and exhibited behaviour that resulted in an uncertain classification with an assignment probability > 25% and < 75% (right).
Extracting reproductive parameters from GPS tracking data for a nesting raptor in Europe

October 2024

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182 Reads

Understanding population dynamics requires estimation of demographic parameters like mortality and productivity. Because obtaining the necessary data for such parameters can be labour‐intensive in the field, alternative approaches that estimate demographic parameters from existing data can be useful. High‐resolution biologging data are frequently available for large‐bodied bird species and can be used to estimate survival and productivity. We extend existing approaches and present a freely available tool (‘NestTool') that uses GPS tracking data at hourly resolution to estimate important productivity parameters such as home range establishment, breeding initiation, and breeding success. NestTool first extracts 42 movement metrics such as time spent within a user‐specified radius, number of revisits, home range size, and distances between most frequently used day and night locations from the raw tracking data for each individual breeding season. These variables are then used in three independent random forest models to predict whether individuals exhibited home range behaviour, initiated a nesting attempt, and successfully raised fledglings. We demonstrate the use of NestTool by training models with data from 258 individual red kites Milvus milvus from Switzerland tracked for up to 7 years, and then applied those models to tracking data from different red kite populations in Germany where detailed observations of nests and their outcomes existed for validation. The models achieved > 90% accurate classification of home range and nesting behaviour in validation data, but slightly lower (80–90%) accuracy in classifying the outcome of nesting attempts, because some individuals frequently returned to nests despite having failed. NestTool provides a graphical user interface that allows users to manually annotate individual seasons for which model predictions exceed a user‐defined threshold of uncertainty. NestTool will facilitate the estimation of demographic parameters from tracking data to inform population assessments, and we encourage ornithologists to test NestTool for different species.


Associations of malondialdehyde (MDA) and uric acid (UA) with migration distance in birds. Phylogenetic distribution of MDA, UA and migration distance is shown across bird species (a). Estimates of regression coefficients from the full models presented in Table 1 for MDA (b) and UA (c) are: β (SE) = 0.05 (0.01) and β (SE) = 0.06 (0.02). Values of oxidative parameters are best linear unbiased estimates (Material and methods). Fitted lines were obtained from the respective full models.
Oxidative state is associated with migration distance, but not traits linked to flight energetics

October 2024

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27 Reads

Flight can be highly energy demanding, but its efficiency depends largely on flight style, wing shape and wing loading, and a range of morphological and lifestyle adaptations that can modify the cost of sustained flight. Such behavioural and morphological adaptations can also influence the physiological costs associated with migration. For instance, during intense flight and catabolism of reserves, lipid damage induced by pro‐oxidants increases, and to keep oxidative physiological homeostasis under control, the antioxidant machinery can be upregulated. Studies on the oxidative physiology of endurance flight have produced contradictory results, making generalization difficult, especially because multispecies studies are missing. Therefore, to explore the oxidative cost of flight and migration, we used samples collected during the breeding season from 113 European bird species and explored the associations of measures of antioxidant capacity (total antioxidant status, uric acid and glutathione concentration) and oxidative damage of lipids (malondialdehyde) with variables reflecting flight energetics (year‐round or specifically during migration) using a phylogenetic framework. We found that none of the traits predicting year‐round flight energy expenditure (flight style, wing morphology and flight muscle morphology) explained any measures of oxidative state. Our results suggest that birds endure their everyday flight exercise without or with low oxidative cost. However, oxidative damage to lipids and one component of the endogenous antioxidant system (uric acid), measured after the end of spring migration on breeding adult birds, increased with migration distance. Our results suggest that migration could have oxidative consequences that might be carried over to subsequent life‐history stages (breeding).


Regression models comparing the standardised percentage of prey type (caterpillars, or ‘other prey') or mean prey size of the items received as a chick and the ones delivered as an adult (n = 47). Only the statistically significant models are shown, in which all of them a negative correlation is found. Regression lines and 95% confidence intervals are shown.
Did you learn what to eat from your parents? A test of the early learning of the foraging niche hypothesis in great tits Parus major

September 2024

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65 Reads

A growing number of studies suggest that individuals can develop long‐term foraging specializations independently of phenotypic or environmental variation, yet little is known about how the foraging niche is acquired. The early learning of the foraging niche hypothesis suggests a key role of vertical cultural transmission in shaping the foraging niche of vertebrates. In birds, direct evidence from natural conditions is limited to a single study that cross‐fostered two related species. To date, no study has tested whether the diet received as an offspring determines the diet delivered as a parent within a single species. We tested the early learning of the foraging niche hypothesis using a Mediterranean population of great tits Parus major, which show great diet variability and moderate consistency in the diet they provide to their offspring across years. To do this, we recorded prey delivered to 9–14 day‐old chicks over twelve years. Then we assessed vertical transmission of dietary specialization using data (percentage of caterpillars, spiders, and other prey types, as well as mean prey size) from individuals recorded as a chick and as an adult. We standardised the data to control for environmental factors and ran a Linear Model for each prey type to measure individuals' consistency within the group (relative consistency), correlating the diet they received as a chick and the one they provided to their own chicks at the adult stage. The correlations between the diet received as a chick and the diet provided as a parent were either not significant or negative. Hence, although individuals showed relatively consistent foraging niches across years regarding their parental provisioning behaviour, these diet preferences were not correlated to the diet they received in the nest. Further research is needed to determine whether the foraging niche is acquired during the post‐fledgling stage.


NMDS plots for all detected analytes. The numeric values and color gradient represent the predicted fuel stores index (FSI; based on the natural logarithm of body mass), with FSI increasing from colder to warmer color shades. Symbols represent individual birds, categorized by site identity (symbol shapes and the connecting hull lines), and observed FSI (symbol size).
Estimated associations between the relative abundance of annotated metabolites (y‐axis) with fuel stores index (FSI; x‐axis; upper panel) and time past sunrise (x‐axis; lower panel). Mean ± SE represents effect sizes; significant effects are colored black (a dashed vertical line indicates zero effect).
Correlation matrices for annotated metabolites, lipophilic (upper pane; A–B), and polar (lower pane; C–D). The left column (A, C) represents Spearman correlations between unmodeled metabolite relative abundances; the right column (B, D) represents modeled residual correlations, i.e. after accounting for fuel stores index (FSI), time past sunrise, and inter‐site random variation, via GLLVM. Color gradient represents correlation coefficient from ‐1 (dark purple) to 1 (yellow); coding of correlation significance: ‘***': p ≤ 0.001, ‘**': 0.001 < p ≤ 0.01, ‘*': 0.01 < p ≤ 0.05.
Fuel stores and time of day account for variation in serum metabolomes of passerine migrants stopping over

September 2024

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125 Reads

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1 Citation

Migratory birds excel in phenotypic flexibility, adapting physiologically as their life histories and environments require. Discerning the metabolic processes underlying migrants' physiology, an emergent property of multiple continuous and dynamic organism–environment interactions, is therefore challenging, particularly under natural conditions. Accordingly, analyses of snapshot‐sampled serum‐circulating metabolites, versatile and readily applicable for migrating birds, have increasingly become the method of choice for such physiologic inference. However, the atemporal nature of single sampling might obscure the links between observed metabolite concentrations and the processes producing them, necessitating an analytical decoupling of focal processes from their broader biochemical background. In the present study, we examined how variation in combined fat and muscle fuel stores, traits pivotal in migratory context, relates to the serum‐circulating metabolomes of spring‐migrating Eurasian blackcaps stopping‐over. Our analyses accounted for potential spatiotemporal influences in the form of time past night's fasting and random local conditions across three sites within the Negev Desert. We shifted the focus from compound‐level analysis of preselected metabolites towards the level of inclusive metabolome, quantifying serum‐circulating lipophilic and polar molecules via UHPLC–MS/MS untargeted metabolomic technique. Our results indicated a general relationship between fuel stores and the metabolome, comprising 16 326 lipophilic and 6923 polar compounds, among which 918 and 44 were annotated, respectively. By applying generalized latent‐variable linear modeling (GLLVM) upon concentrations of annotated metabolites, we identified several candidate biomarkers, some novel in migratory context, notably the fuel‐associated increase in serum ceramides likely derived from circulating very low‐density lipoproteins (VLDLs). Relying on estimated metabolite links with fuel and foraging time and on modeled residual covariations among metabolites, we demonstrate fuel–metabolite associations generally consistent with higher fat‐ and lower protein mobilization in birds having greater stores and with decreased fuel utilization as ingested nutrients accumulate over time, thus introducing a novel approach for the physiological study of migrating birds.


Ways of exposure of birds and eggs and the proposed adverse outcome pathway based on triazoles effects on bird reproduction. The black arrows represent suggested key event relationships; however, not in all cases these relationships have been proven as part of the same assay. References letter means M = Mammals; A = Amphibians; B = Birds; H = Humans; F = Fish; V = Vitro. List of references used: (1) Angelier et al. 2023; (2) Alonso‐Alvarez et al. 2012; (3) Bro et al. 2016; (4) Robinson et al. 2012; (5) EFSA 2009; (6) Mateo et al. 2016; (7) Lopez‐Antia et al. 2014; (8) Lopez‐Antia et al. 2016; (9) Fernández‐Vizcaíno et al. 2022; (10) Fernández‐Vizcaíno et al. 2023; (11) Millot et al. 2015; (12) de Montaigu and Goulson 2022; (13) Esther et al. 2022; (14) Grote et al. 2008; (15) Bellot et al. 2022a, b2022b; (16) Zarn et al. 2003; (17) Poulsen et al. 2015; (18) López‐Antía et al. 2013; (19) López‐Antía et al. 2018; (20) López‐Antía et al. 2021; (21) Fernández‐Vizcaíno et al. 2020; (22) Fernández‐Vizcaíno et al. 2024; (23) Trinh et al. 2017; (24) Lv et al. 2017; (25) Roelofs et al. 2014; (26) Svanholm et al. 2021; (27) Tully et al. 2006; (28) Machado et al. 2021; (29) Serra et al. 2023; (30) Munkboel et al. 2019; (31) Goetz and Dix 2009; (32) Goetz et al. 2007; (33) Ortiz‐Santaliestra et al. 2020; (34) Peffer et al. 2007; (35) Gaffard et al. 2022; (36) Chen et al. 2019; (37) Dimopoulu et al. 2017a; (38) Dimopoulu et al. 2017b; (39) McGraw and Parker 2006.
Integrating adverse effects of triazole fungicides on reproduction and physiology of farmland birds

August 2024

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112 Reads

The extensive use of pesticides has been recognized as one of the major factors negatively impacting birds in agricultural habitats. One of the pesticide groups most used worldwide are triazole fungicides due to their effectiveness in controlling phytopathogenic fungi in cereals, vineyards and orchards. In the last decades, different experimental studies have reported important negative effects on the health and fitness of birds after exposure to triazoles. Birds can be exposed throughout the year through different routes, including oral uptake, dermal contact with treated surfaces and inhalation by overspray. Yet, the ingestion of treated or sprayed material is the principal route. The most alarming effect of triazoles, which can even occur several months after cessation of the exposure, is the decreasing reproductive outputs of birds, including delay in the onset of laying dates, reduced clutch size and hatching rate, and increased mortality of chicks. In order to synthesize the data and knowledge about the toxic effects of triazoles at different levels of biological organization, here we propose an dverse outcome pathway (AOP) on the mechanisms by which triazoles can affect avian reproduction and physiology. The reported effects highlight that the current risk assessment needs some improvements to avoid undesired effects on birds, especially long‐term effects that can influence stability and viability of avian populations from agricultural habitats.


Distribution of T. ruficapillus, sampling information and analyses of mitochondrial DNA. (a) Distribution map (shaded in violet) showing sampling localities, subspecies identity and the type of sequence data obtained for each sample. The distribution map is based on BirdLife International and NatureServe (2014). (b) Median‐joining haplotype network of concatenated mDNA (COI + cyt b; 1,130 bp). Circles represent haplotypes and their size is proportional to haplotype frequency. The length of the branches connecting haplotypes is proportional to the number of nucleotide differences between them, which are indicated by the number of line marks on each branch. Colours represent the subspecies according to the scheme incorporated in the figure. Black circles represent unsampled hypothetical haplotypes. Bird illustrations by Hilary Burn. © Lynx Nature Books. (c) Bayesian phylogenetic tree with divergence times obtained from the analysis of the concatenated mitochondrial dataset (1130 bp). The numbers near the nodes indicate the mean divergence time estimates and the numbers between square brackets correspond to the 95% highest posterior density intervals of those estimates. Divergence times and the numbers between square brackets are in millions of years ago. Posterior probability values are shown below the divergence times. The colours to the right of the tree indicate subspecies information.
Genomic analyses of T. ruficapillus. (a) Principal component analysis (PCA) based on 2306 SNPs (SNPs present in all individuals). (b) Structure plot for K=3 based on 5073 SNPs (one random SNP per RAD locus). (c) Phylogeny inferred with maximum likelihood; the colours to the right of each individual indicate the subspecies. The tree was rooted with Thamnophilus caerulescens. Bootstrap support values are indicated in the nodes.
Demographic reconstruction of T. ruficapillus based on 6165 RADseq loci (13 485 SNPs). Estimates of divergence times (T; in millions of generations), migration rates (mg; in migrants per generation) and current and ancestral effective population sizes (Ne; in millions of individuals) are reported with their 95% confidence intervals.
Analysis of the vocalizations of T. ruficapillus. Song differentiation among subspecies is shown based on a PCA performed with the song variables (mean duration of the note, mean duration of the interval between notes, fundamental frequency, bandwidth of the note and the number of notes in each song; the first four variables were measured for the first note).
Genetic and phenotypic differentiation in Thamnophilus ruficapillus, a Neotropical passerine with disjunct distribution in the Andean and Atlantic forests

August 2024

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113 Reads

The Andean and Atlantic forests are separated by the open vegetation corridor, which acts as a geographic barrier. However, these forests experienced cycles of connection and isolation in the past, which shaped the phylogeographic patterns of their biotas. We analysed the evolutionary history of the rufous‐capped antshrike Thamnophilus ruficapillus, a species with a disjunct distribution in the Atlantic and Andean forests and thus an appropriate model to study the effect of the open vegetation corridor and the Andes on the diversification of the Neotropical avifauna. We performed a phylogenetic/phylogeographic analysis, including the five subspecies, using mitochondrial and nuclear genomic DNA, and studied their differences in vocalizations and plumage coloration. Both the mitochondrial and nuclear DNA evidenced a marked phylogeographic structure with three differentiated lineages that diverged without signs of gene flow in the Pleistocene (1.0–1.7 million years ago): one in the Atlantic Forest and two in the Andean forest. However, the two Andean lineages do not coincide with the two disjunct areas of distribution of the species in the Andes. Vocalizations were significantly different between most subspecies, but their pattern of differentiation was discordant with that of the nuclear and mitochondrial DNA. In fact, we did not find song differentiation between the subspecies of the Atlantic Forest and that of the northwestern Bolivian Andes, even though they differ genetically and belong to different lineages. Consistently, no differences were found in plumage coloration between the subspecies of the Atlantic Forest and that of the southern Andes. Our results suggest a complex evolutionary history in this species, which differentiated both due to dispersion across the open vegetation corridor, likely during a period of connection between the Andean and Atlantic forests, and the effect of the Bolivian Altiplano as a geographic barrier. In both cases, Pleistocene climatic oscillations appear to have influenced the species diversification.


Spectrograms and song parameters of male solos, female solos, and duets in Elliot's laughingthrush Trochalopteron elliotii. (A–C): spectrograms depicting representative male Elliot's laughingthrush solos with 2, 3, 4 notes, respectively. (D), (E): spectrograms depicting representative female Elliot's laughingthrush solos with 6 or 7 notes. (F): male‐initiated overlapping type duet. (G): male‐initiated alternating duet. (H): female‐initiated alternating duet. (I): coordinated alternating type duet.
The boxplots display the comparison of song characteristics between males and females. Each boxplot represents the median (line inside the box), lower quartile (bottom of the box), upper quartile (top of the box), and the range of the data (whiskers). Outliers are displayed as points.
Comparisons of acoustic structures between sexes in a duetting, montane bird

August 2024

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139 Reads

Female song in birds is more widespread than previously thought, and studies across different species are critical for better understanding the entire evolutionary process of bird song. In this study, we recorded the songs of males and females in a duetting, montane bird species, the Elliot's laughingthrush Trochalopteron elliotii, across consecutive breeding seasons. We specifically focused on identifying the number and structure of different song types by males and females, and compared these acoustic structures between the sexes. Our findings revealed that both males and females sang sex‐specific solos. More specifically, females sang a single type of solo that varied significantly in the number of notes, whereas males produced three different solos composed of 2, 3, or 4 notes, respectively. Female solos exhibited significantly more notes and longer song duration compared to males. Male solos typically had a significantly higher maximum frequency for the entire song. No significant differences were observed in the duration of the first note, song rate, and other frequency characteristics between male and female solos. Furthermore, paired males and females coordinated their sex‐specific solos to form duets when challenged by conspecific territory intruders, both within and outside the breeding season. Sex‐specific solos suggested that male and female songs play different roles and may be subject to different selective pressures. Further research is necessary for elucidating the functions of male song, female song, and duets in this montane bird species.


Redstart nest and cavity dimensions measured in the field. (a) Nest cup level. (b) Cup depth (CD), vertical distance (VD) and horizontal distance (HD), nest‐box height (H), width (W) and length (L).
Variation of redstart nest cup composition. Clockwise from top left: mostly feathers (from black grouse male, Lyrurus tetrix), mostly bark (from pine Pinus sp.), a complex mixture of bark (from birch, Betula sp.), pine needles, grass, feathers and a piece of plastic or paper (very rare, therefore it was not quantified), and finally mostly dried grass and roots (note that moss is not part of the nest cup lining but is used in the nest rim) Photos: TG.
Predicted values of the redstart nest cup area in relation to the nest cup location. Relationship of the nest cup area with (a) both centroid coordinates combined, (b) the x coordinate and (c) the y coordinate. The nest‐box entrance hole is placed at zero in both axes.
Predicted values of the probability of cuckoo parasitism in relation to the relevant redstart cavity characteristics and nest design: (a) cavity entrance hole size, (b) nest cup area and (c) nest cup level. The black line and points represent the mean estimate, while the ribbon and coloured lines are the 95% CIs. Note: When testing the probability of cuckoo parasitism in relation to nest design (b) and (c), nests in cavities with entrance holes < 6 cm were excluded (n = 77).
Predicted values of the probability of cuckoo successful laying in relation to redstart nest cup position. The nest cup position is examined in three ways: (a) both nest cup centroid coordinates combined, (b) the x coordinate and (c) the y coordinate. The nest‐box entrance hole is positioned at zero in both axes. In (b) and (c), the black lines represent the mean estimate, while the ribbons are the 95% CIs.
Can nest design hinder brood parasitism success?

August 2024

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121 Reads

Avian nest design varies depending on environmental factors but may also be influenced by between‐species interactions. In the brood parasitism context, hosts may evolve nest architectures that may limit parasite access to the nest cup, reduce parasite laying success or hinder parasite chick success. Therefore, nest characteristics may reduce the likelihood or minimise the costs of being parasitised. The common redstart Phoenicurus phoenicurus is a regular host of the common cuckoo Cuculus canorus, for which cuckoo eggs are often laid outside the nest cup, resulting in low effective parasitism rates. This allowed us to evaluate variation in host nest design and test whether nest design characteristics correlate with brood parasitism likelihood and cuckoo laying success (i.e. cuckoo egg laid in the nest cup versus outside the nest cup). While recording brood parasitism events in two distant redstart populations, we documented nest cup characteristics, such as internal dimensions, materials used and nest cup position, along with the nest‐box dimensions. Cuckoo parasitism likelihood was lower for redstart nests in cavities with smaller entrances, for redstart nests with smaller nest cups and with nest cups that were built level to the rim material. For parasitised nests, cuckoo laying success was lower at redstart nests with nest cups placed further from the cavity entrance. Our results suggest a conditional process, where the cavity entrance size first prevents brood parasites access, then the cup size and the cup level in reference to the rim material affect the cuckoo choice, and finally, the nest cup position hinders cuckoo's laying success. The use of multiple nest design strategies may explain the current low effective parasitism rates in this system. Host nest design may serve as a frontline defence that could shape parasite's preferences, and consequently host nest characteristics.


Adult relative telomere lengths did not differ between rural (black) and urban (gray) habitats, nor did they differ between urban (gray) or rural (black) nestlings from unparasitized nests. Means ± 1 SE are shown with individual data points indicated by open circles.
Relative telomere lengths were significantly longer in nestlings than in adults. Means ± 1 SE are shown with individual data points indicated by open circles.
Urban nestlings that experienced brood parasitism during development had significantly shorter relative telomere lengths than those that did not experience brood parasitism during development. Means ± 1 SE are shown with individual data points indicated by open circles.
Are urbanization and brood parasitism associated with differences in telomere lengths in song sparrows?

August 2024

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58 Reads

Urbanization reflects a major form of environmental change impacting wild birds globally. Whereas urban habitats may provide increased availability of water, some food items, and reduced predation levels compared to rural, they can also present novel stressors including increased light at night, ambient noise, and reduced nutrient availability. Urbanization can also alter levels of brood parasitism, with some host species experiencing elevated levels of brood parasitism in urban areas compared to rural areas. Though the demographic and behavioral consequences of urbanization and brood parasitism have received considerable attention, their consequences for cellular‐level processes are less understood. Telomeres provide an opportunity to understand the cellular consequences of different environments as they are a well‐established metric of biological state that can be associated with residual lifespan, disease risk, and behavior, and are known to be sensitive to environmental conditions. Here we examine the relationships between urbanization, brood parasitism, and blood telomere lengths in adult and nestling song sparrows Melospiza melodia. Song sparrows are a North American songbird found in both urban and rural habitats that experience high rates of brood parasitism by brown‐headed cowbirds Molothrus ater in the urban, but not the rural, sites in our study system. Among adults and nestlings from non‐parasitized nests, we found no differences in relative telomere lengths between urban and rural habitats. However, among urban nestlings, the presence of a brood parasite in the nest was associated with significantly shorter relative telomere lengths compared to when a brood parasite was absent. Our results suggest a novel, indirect, impact of urbanization on nestling songbirds through the physiological impacts of brood parasitism.


Proportion of male chicks in different sized broods (2–4: 11 nests; 5–7: 23 nests; 8–11: 16 nests) plotted against the cumulative rainfall prior to egg laying. Solid line shows line of best fit. To increase clarity, confidence intervals are not shown, but a version of this figure with 95% confidence intervals is available (Supporting information).
Proportion of male and female chicks (322 chicks from 50 nests) as a function of hatching order within broods.
Proportion of male and female chicks (322 chicks from 50 nests) as a function of hatching order and brood size (2–4: 11 nests; 5–7: 23 nests; 8–11: 16 nests).
Offspring sex ratio in a communal breeding bird is male‐biased when pre‐breeding rainfall is low

August 2024

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35 Reads

Offspring sex ratios may deviate from parity when the fitness benefits of producing male or female offspring vary. We tested for sex ratio bias in smooth‐billed anis Crotophaga ani, a communal laying cuckoo with low within‐group relatedness and high offspring dispersal. One male group member performs nocturnal incubation and sires more offspring than other males in the group, suggesting males may have greater reproductive variance than females. We hypothesized that pre‐breeding rainfall influences food availability and offspring sex ratio, predicting that breeding females skew production towards the sex with higher reproductive variance (males) in high food years. Females may also adjust sex ratio across the hatching order to increase survival of the more competitive sex, especially when clutches are larger and within‐brood competition is higher. As adults, male smooth‐billed anis are larger than females, so we assumed male nestlings are more competitive than females and predicted a male‐bias in first hatched chicks in larger broods. Contrary to our first prediction, offspring sex ratio was male biased when pre‐breeding rainfall was lower. In partial support of our second prediction, marginally more first hatched chicks were male in larger broods. To our knowledge, this is the first evidence of offspring sex ratio bias in a communal laying bird species. Future work in this system will attempt to uncover the mechanisms by which co‐breeding females adjust offspring sex ratio and test alternative hypotheses to explain male‐biased offspring sex ratios under different conditions.


The effects of high temperatures and anthropogenic noise on behaviour and cognition. Anthropogenic stressors can affect behaviour both directly and indirectly via effects on cognition. Both high temperatures and anthropogenic noise independently affect various behaviours and cognitive traits; however, whether the simultaneous effect of both anthropogenic stressors will be additive, synergistic, or antagonistic remains unknown, despite the fact that these stressors often co‐occur. Orange bars represent high temperatures; green bars represent anthropogenic noise; yellow bars represent the effect of these two stressors together. Numbers represent the final value of a hypothetical measured response when two co‐occurring stressors have an additive, synergistic, or antagonistic effect relative to the two stressors occurring in isolation.
The importance of investigating the impact of simultaneous anthropogenic stressors: the effects of rising temperatures and anthropogenic noise on avian behaviour and cognition

July 2024

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146 Reads

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1 Citation

Rising temperatures and anthropogenic noise are two of the most pervasive and well researched anthropogenic stressors affecting avian species globally. Despite often triggering similar behavioural responses in birds, and frequently co‐occurring (particularly in urban areas), the impact of these stressors are primarily investigated in isolation. Here, we discuss and compare the most commonly researched effects of anthropogenic noise and rising temperatures on avian behaviour. We then outline recent findings on the impacts of these two stressors on cognition in birds, which underpins many behavioural adjustments. We find that both anthropogenic noise and high temperatures, when investigated in isolation, impact avian behaviours such as foraging, the antipredator response, and interactions with conspecifics. We also find that both these stressors can lead to cognitive impairment, but the occurrence and magnitude of impairment varies depending on the cognitive trait examined. Finally, we discuss the limited studies that have investigated these two anthropogenic stressors simultaneously and outline different scenarios in which additive, synergistic, or antagonistic effects of these stressors may occur. We hope our review will stimulate researchers to investigate the simultaneous effects of these and other anthropogenic stressors on the behaviour and cognition of urban‐living wild birds.


(A) A female superb fairywren incubation call depicting A and B element types. In this example, the call begins with 2 B elements and ends with 3 A elements. (B) Schematics of one experimental playback trial. Embryos were exposed to two playback tracks in random order: one track made of all B elements, and one made of an AB element mix with one minute between tracks. Each of the two playbacks consisted of 30 call stimuli with 5 s of silence between each stimulus. Each stimulus contained a 5‐element sequence (pure B, mix AB) with an inter‐element interval of 0.2 s. Each set was composed of 6 stimuli with 5 s between each set. Each embryo was exposed to two playback tracks in random order: exposure to five sets of all B elements and exposure to five sets of AB elements for a total of 10 sets per embryo.
Heartrate responses of n = 37 embryos to different playback types (treatment: B type stimulus versus AB type stimulus). (A) Baseline heart rate. Raw data are presented as grey circles. There was no significant difference in HR between the two groups. (B) Delta heart rate. The solid red and blue lines indicate the predicted marginal effect mean for treatment AB and treatment B respectively, and coloured band represents 95% confidence intervals. When exposed to B elements, delta HR declined across the five sets. When exposed to AB elements, delta HR remained similar across set 1 to set 5.
Maternal in‐nest call structure reduces habituation risk in songbird embryos

July 2024

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42 Reads

Repetition of the same vocal stimulus during vocal learning may result in habituation. Therefore, selection may favor vocal tutors that produce vocal stimuli with characteristics that reduce the risk of habituation. Superb fairywren Malurus cyaneus mothers produce a two‐element (A and signature B) call to embryos, but embryos only produce one element type (B) after hatching. Why do mothers use the A element to embryos? We broadcast calls with one (B) or two (AB) element types and measured embryo response. Embryos habituated to calls with one element type and remained responsive to calls with both. We conclude that signal characteristics in tutors may guide learning to retain pupil attention during learning.


The wintering range expansion of the Eurasian blackcap. (left) The wintering position of blackcaps that have been caught on the breeding ground and subsequently recovered over the winter. Squares indicate wintering position and are coloured by migratory direction with northwards migrants highlighted in yellow and southwards migrants highlighted in red. (right) A histogram of blackcap ringing effort, coloured by migratory direction (as in left) in autumn. The y‐axis refers to the frequency of birds ringed at the breeding site and recovered > 500 km away (see Methods for further detail). Whilst ringing effort has increased steadily over time, the occurrence of northwards movement is a relatively recent phenomenon.
A null model of blackcap northwards migration. (left) An example of how the distances between the expected wintering site and the observed/null wintering positions vary for a blackcap breeding in south‐west Spain (red). (right) Schematic outlining the quantities used in our statistical analysis: the null migrations generated in our randomisation (light blue, Methods), the observed recovery site (yellow) and the recovery site expected under a model of bi‐axial directional variation (dark blue).
Axial variation in the migratory routes of Eurasian blackcaps. (left) The breeding (red) and wintering (yellow) sites of north‐migrating blackcaps used in this analysis, with each recovery linked by a grey line between the breeding and non‐breeding sites. (right) A histogram showing the mean angular deflection between null recovery sites and the expected recovery site, with the true observed‐to‐expected distance shown as a darker dashed line.
Could bi‐axial orientation explain range expansion in a migratory songbird?

July 2024

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148 Reads

The likelihood of a new migratory route emerging is presumably a function of 1) the associated fitness payoff and 2) the probability that the route arises in the first place. It has been suggested that diametrically opposed ‘reverse' migratory trajectories might be surprisingly common and, if such routes were heritable, it follows that they could underlie the rapid evolution of divergent migratory trajectories. Here, we used Eurasian blackcap (Sylvia atricapilla; ‘blackcap') ringing recoveries and geolocator trajectories to investigate whether a recently evolved northwards autumn migratory route – and accompanying rapid northerly wintering range expansion – could be explained by the reversal of each individual's population‐specific traditional southwards migratory direction. We found that northwards autumn migrants were recovered closer to the sites specified by an axis reversal than would be expected by chance, consistent with the rapid evolution of new migratory routes via bi‐axial variation in orientation. We suggest that the surprisingly high probability of axis reversal might explain why birds expand their wintering ranges rapidly and divergently, and propose that understanding how migratory direction is encoded is crucial when characterising the genetic component underlying migration.


Journal metrics


1.5 (2023)

Journal Impact Factor™


38%

Acceptance rate


3.7 (2023)

CiteScore™


39 days

Submission to first decision


$2,600 / £1,770 / €2,080

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