Martin Wikelski’s research while affiliated with Max Planck Institute of Animal Behavior and other places

What is this page?


This page lists works of an author who doesn't have a ResearchGate profile or hasn't added the works to their profile yet. It is automatically generated from public (personal) data to further our legitimate goal of comprehensive and accurate scientific recordkeeping. If you are this author and want this page removed, please let us know.

Publications (638)


Movement trajectories of all bats and a depiction of the two spatial extents of habitat selection analyses. (A) Attributes of 3D vegetation structure measured at 10 m resolution were limited to the 25 km² site level within the UAV-LiDAR extent of Bouamir Research Site. Bat movement tracks are overlain on a map of canopy height (black = 0 m, white = 55 m). Note that canopy height (height of first LiDAR Return) was included in all models as a quadratic term (canopy height + canopy height²). Vertical complexity: total diversity of 3D point cloud distribution measured from ground to top-of-canopy; Distance to gap: straight-line distance to nearest area with no vegetation > 5 m; Plant Volume Density: leaf area per volume within a specified height bin (10–15 or 15–20 m). Swamp: habitat characterized by seasonal or permanent shallow water and characterized by dominance of Raphia palm species. (B) We used upscaled 3D vegetation structure metrics to quantify habitat selection at the landscape level, which encompassed the full scale of bat movement tracks, including the boundary of the Dja Faunal Reserve. Canopy height: predicted value of 95th percentile relative height (RH 95). Distance to gap: straight-line distance to nearest area with no vegetation > 15 m. Canopy heterogeneity: standard deviation of canopy height at a specified spatial resolution (100–1000 m). Swamp: same as in panel A. (C) The inset photo shows a male hammer-headed bat carrying a 15 g e-obs tag
Log-transformed Relative Selection Strength (log-RSS) for each value of canopy height relative to the mean (indicated by x = 0) at the (A) site level (25 km²) and (B) landscape level (full movement trajectories). Each line represents an individual bat. Negative selection for a canopy height value relative to the mean is indicated where the line takes on values less than y = 0, and positive selection is indicated where the lines take on values greater than y = 0. Note that the plots were generated using a different model structure, and that the limits of both axes differ between the plots
Selection coefficients and 95% confidence intervals (CIs) for each linear environmental predictor of bat movements within Bouamir Research Site (25 km²), including (A) Leaf Area Index, (B) Vertical Complexity Index, (C) Distance to small (50 m² or greater) and (D) large (500 m² or greater) canopy gaps, and (E) Plant Volume Density at a height of 10–15 and (F) 15–20 m. 95% CIs that do not overlap x = 0 indicate a significant effect of the covariate on individual bat habitat selection. Each bat is represented in the y-axes. Note that the order of bats differs for each plot
Difference in step length of bat movements (distance between successive GPS locations) between swamp and non-swamp habitats, including a Wilcoxon signed-rank test comparison (p = 4.8e− 14)
Movement trajectories of each bat plotted over distance to canopy gap (15 m threshold) and the distribution of swamp habitats (gray polygons). Clusters of green, blue, and red points represent areas with the greatest revisitation rates (75th percentile or greater)
Spaceborne and UAV-LiDAR reveal hammer-headed bat preference for intermediate canopy height and diverse structure in a Central African rainforest
  • Article
  • Full-text available

April 2025

·

51 Reads

Movement Ecology

·

·

Valorian Tegebong

·

[...]

·

Background Animals with key ecological roles, such as seed-dispersing fruit bats, rely to varying degrees on habitat structure to indicate the locations of resources and risks. Methods To understand how variation in vegetation structure influences fruit bat habitat selection, we related movement steps of hammer-headed bats (Hypsignathus monstrosus) to attributes of canopy height, vertical and horizontal vegetation structure, and habitat type in a mature rainforest of southern Cameroon. Vegetation structural metrics were measured with UAV-LiDAR at 10 m resolution for a 25 km² study area. Because bats frequently moved outside the study area, we also characterized vegetation height and horizontal complexity over the full extent of bat movement trajectories by upscaling UAV-LiDAR measurements using primarily GEDI LiDAR data. Results At the site level, hammer-headed bats preferred areas of intermediate canopy height (13.9–32.0 m) close to large canopy gaps (≥ 500 m²). Individual bats varied in selection for vertical vegetation complexity, distance to smaller canopy gaps (≥ 50 m²) and plant volume density of intermediate vegetation strata (10–20 m). Over the full extent of movement trajectories, hammer-headed bats consistently preferred intermediate canopy height, and areas closer to canopy gaps. At both spatial extents, bats moved the shortest distances in swamp habitats dominated by Raphia palms. These behaviors indicate the use of forest types that vary structurally, with a preference for open airspace during foraging or moving among resources, and for dense swamp vegetation during roosting and resting periods. In addition, most bats regularly made long flights of up to 17.7 km shortly after sunset and before sunrise and limited their movements to three or fewer destinations throughout the tracking period. Conclusions These results highlight the importance of structurally diverse landscapes for the nightly movements of hammer-headed bats. Our results show how remote sensing methods and animal tracking data can be integrated to understand habitat selection and movement behavior in tropical ecosystems.

Download

Timing of independence is explained by movement ability, but depends on how independence is defined for a long-lived raptor

April 2025

·

83 Reads

Achieving independence from parental care requires animals to learn about their environment while acquiring vital skills. The timing and type of the transition to independence vary across species, with some achieving independence early, while others rely on prolonged parental care presumably to mature and develop vital skills. When independence is delayed until juveniles reach a certain level of skill, we can expect that skill acquisition rate and proficiency will predict the timing of independence. Here, we investigated whether the acquisition of soaring flight skills can predict the latency to engage in extra-territorial excursions and ultimately emigration from the natal territory marking the onset of independence in golden eagles (Aquila chrysaetos). While fine-scale soaring flight did not predict the propensity to go on excursions or the timing of emigration, movement at a daily scale did affect latency to excursions and emigration. Together, this indicates that soaring flight is learned quickly and early in life and that movement at the daily scale likely encompasses more than just flight capacity. Adult-like skill levels appear to be a necessary but not the determining factor for emigration, but may determine the timing of excursions. The difference we discovered between when individuals were capable of independence and when they committed to it may obscure the more general link between skill acquisition and the end of parental care in other systems as well.


Fig. 1. Complete foraging trips recorded by GPS loggers of 114 breeding Swallow-tailed Gulls Creagrus furcatus (one trip per bird) at four colonies across three islands in the Galápagos Islands: one colony at Genovesa, one colony at South Plazas, and two colonies Española (Punta Cevallos and Punta Suarez). Inset: the location of the study site relative to South America is indicated by the red circle.
Fig. 2. Temporal distribution of departures and arrivals for complete foraging trips by 114 Swallow-tailed Gulls Creagrus furcatus (one trip per bird) from four colonies in the Galápagos Islands. Grey vertical shading indicates local nighttime.
The owl gull: exclusively nocturnal foraging by the Swallow-tailed Gull Creagrus furcatus in Galápagos.

April 2025

·

47 Reads

Marine Ornithology

Colony-based observations indicate that Swallow-tailed Gulls Creagrus furcatus go to sea only at night. Here, we use GPS tracking technology to reveal the species' exclusively nocturnal foraging behavior at four colonies in the Galápagos Islands. All nocturnal trips proved to be foraging effort in pelagic waters 19-103 km from nests during breeding. While at sea, individuals spent approximately one-quarter of their time commuting, with half of the time dedicated to area-restricted search behavior. Three years of data from one colony indicate spatial fidelity to a general foraging area. Our research directly confirms that Swallow-tailed Gulls are the only obligate nocturnal foragers among Laridae and contributes to our understanding of nocturnal foraging strategies in tropical seabirds.


Migratory Birds Advance Spring Arrival and Egg-Laying in the Arctic, Mostly by Travelling Faster

April 2025

·

249 Reads

In the current warming climate, many organisms in seasonal environments advance their timing of reproduction to benefit from resource peaks earlier in spring. For migrants, the potential to advance reproduction may be constrained by their migration strategies, notably their ability to advance arrival at the breeding grounds. Recent studies show various changes in migration strategies, including wintering closer to the breeding grounds, earlier departure from the wintering grounds or faster travels by spending less time at stopover sites. However, whether such changes lead to earlier arrival or earlier breeding remains an open question. We studied changes in migration and reproduction timing in 12 populations of nine migratory birds, including seabirds, shorebirds, birds of prey and waterfowl breeding at Arctic sites bordering the Greenland and Barents Sea, a region undergoing rapid climate warming. The timing of migration and reproduction was derived from tracking and field data and analysed to study (1) how timing has changed in response to the changing moment of snowmelt at the breeding grounds and (2) what adjustments in migration strategies this involved. We found that in years with early snowmelt, egg‐laying in multiple populations advanced, but only two waterfowl populations also advanced arrival in the Arctic. In contrast, arrival in the Arctic generally advanced with time, even when snowmelt or egg‐laying dates did not advance. Earlier arrival with time was mostly explained by populations traveling to the Arctic faster, likely spending less time at stopover sites. Inability to forecast conditions in the Arctic may limit birds to adjust migration timing to annually varying snowmelt, but we show that several species, particularly waterfowl, are able to travel faster and advance the timing of migration over the years. The question remains whether this reflects adaptations to Arctic climate change or other factors, for example, environmental changes along the migratory route.



Fig. 1: Conceptual advances provided by movement traits. (A) In trait-based ecological studies, animal movement 137 behaviour is often incorporated via 'proxy traits' -typically morphological and ecological traits, such as body 138 size/mass, wing morphology, or trophic guild, which are typically derived from museum collections and measured 139 only once per individual. This technically allows for quantification of within-species trait variation, although most 140 trait databases typically only contain trait values averaged at the species level, often without reporting the 141 underlying trait measurements, variance measures, or sample sizes. (B) Biologging devices measure behavioural 142 information repeatedly for the same individual in its natural environment and over ecologically meaningful time 143 periods. Building on these repeated individual-level raw data, movement traits can be calculated in a standardised 144 workflow with consistent methodology, achieving (1) more comparable measures including variance estimates 145 and sample sizes, and (2) quantification of both between-species, between-individual and within-individual trait 146 variation. (C) Finally, animals may display considerable plasticity in behavioural reactions to their encountered 147 abiotic and biotic environment. Individual measures of movement traits along environmental gradients facilitate 148 incorporation of behavioural reaction norms, combining consistent between-individual differences in behaviour 149 independent of context (different intercepts) with within-individual behavioural plasticity (individuals adjusting 150 behaviour adaptively to changing conditions; non-zero slopes). Accounting for behavioural reactions norms 151 should enable better predictions of community dynamics and ecosystem processes under global change. Panel C 152 adapted from Hertel et al. (2020). 153
Fig. 2: Trait-based approaches have been used in various ecological disciplines, leading to a plethora of trait 166 concepts, definitions, and categories (Violle et al. 2007). Here, we suggest a 'taxonomy of traits' with movement 167 traits as a subcategory of behavioural traits, as movement always reflects behaviour, but not all behaviour is 168 expressed via movement. However, we note that there can be considerable overlap between trait categories and 169 suggest a pragmatic approach to such classifications. 170
Fig. 3: Examples showcasing the utility of movement traits at the species, individual, and within-individual level, extracted from our first proof-of-concept MoveTraits database. (A) Log-transformed species mean body mass against log-transformed monthly range size for 42 terrestrial mammal species for which monthly range size could be calculated. (B) Between-individual variation in mean daily displacement distance for 27 mammal species for which daily displacements were available. Individual means are indicated with black lines and their overall distribution at the species level with density ridges, with species means indicated by white vertical lines. (C) Illustrative example: Daily displacement distances of two non-migratory mule deer (Odocoileus hemionus) measured along a gradient of human disturbance in the central United States (Utah & Wyoming), quantified by the Human Footprint Index. A significant interaction between individuals and HFI (F(1, 2229679) = 4.863, p = 0.029) suggests that the two individuals adjust movement differently to HFI. Data were collected between March
MoveTraits - A database for integrating animal behaviour into trait-based ecology

March 2025

·

1,019 Reads

Trait-based approaches are key to understanding eco-evolutionary processes but rarely account for animal behaviour despite its central role in ecosystem dynamics. We propose integrating behaviour into trait-based ecology through movement traits - standardised and comparable measures of animal movement derived from biologging data, such as daily displacements or range sizes. Accounting for animal behaviour will advance trait-based research on species interactions, community structure, and ecosystem functioning. Importantly, movement traits allow for quantification of behavioural reaction norms, offering insights into species' acclimation and adaptive capacity to environmental change. We outline a vision for a 'living' global movement trait database that enhances trait data curation by (1) continuously growing alongside shared biologging data, (2) calculating traits directly from individual-level data using standardised, consistent methodology, and (3) providing information on multi-level (species, individual, within-individual) trait variation. We present a proof-of-concept 'MoveTraits' database with 55 mammal and 108 bird species, demonstrating calculation workflows for 5 traits across multiple time scales. Movement traits have significant potential to improve trait-based global change predictions and contribute to global biodiversity assessments as Essential Biodiversity Variables. By making animal movement data more accessible and interpretable, this database could bridge the gap between movement ecology and biodiversity policy, facilitating evidence-based conservation.


Fig. 4 This plot compares the actual behaviours with the classified behaviours throughout the experimental data. The y-axis indicates the different behaviours. The x-axis shows the timesteps. The blue line shows which behaviour was exhibited during the recording, therefore mapping to the actual labels of the time series data. The grey lines connect the behaviour classified by the decision tree with the actual behaviour at that particular timestep. Therefore, the grey lines indicate wrong classifications.
Fig. 5 This image shows the confusion matrix for the decision tree, optimised for the behaviour standing, with a tree depth of 7, belonging to Participant 1. The decision tree has an increased number of misclassifications between sitting, standing and walking. The y-axis shows the actual behaviours and the x-axis what the classifier has predicted.
Data overview per sensor
Decision tree performances by sensor and tree depth
Feature permutations ranked by the chosen quality metrics
Resource efficient data transmission on animals based on machine learning

March 2025

·

31 Reads

Bio-loggers, electronic devices used to track animal behaviour through various sensors, have become essential in wildlife research. Despite continuous improvements in their capabilities, bio-loggers still face significant limitations in storage, processing, and data transmission due to the constraints of size and weight, which are necessary to avoid disturbing the animals. This study aims to explore how selective data transmission, guided by machine learning, can reduce the energy consumption of bio-loggers, thereby extending their operational lifespan without requiring hardware modifications.


Screenshot of the Eoldist application, parameterized for a lesser kestrel (Falco naumanni) in local flight (top left panel) at a wind energy facility with asynchronous machines with 35‐m blades, an initial wind speed of 10 m s⁻¹ and a residual rotation speed of 3 rpm (bottom left panel). The program first displays a frequency distribution of flight (ground)speeds for the species, calculated from source data (top right panel). Underneath this, the program calculates the estimated turbine shutdown time and displays the cumulative cautionary detection distance curve (bottom right panel). On this curve, a dotted line indicates the precise cautionary detection distance in relation to the percentage of detected flights (here 95% of detected flights results in a cautionary detection distance of 315 m).
Turbine shutdown time Tshutdown required for the residual rotation speed to reach ≤ 3 rpm in 90 s as a function of (A) blade length, (B) initial wind speed, and (C) turbine type (Asynch = asynchronous, Synch. = synchronous). The shaded areas represent the 95% confidence intervals of the estimates. Because the model included an interaction, each variable that is not represented was set to its mean, and the machine type was asynchronous. The pattern was similar at a residual rotation speed of 2 rpm.
Effect of blade length, type of machine (synchronous: circles; asynchronous: triangles), and wind speed (5, 10, and 15 m s⁻¹) on cautionary detection distance D of the lesser kestrel (Falco naumanni) in local flight. The effect of wind speed is due to changes in Tshutdown (and not in‐flight speed). Simulations were performed with 95% of detected flights and a residual rotation speed of 3 rpm.
Effect of the percentage of detected flights on cautionary detection distances for two species differing in flight speed variance: Bewick's swan (Cygnus columbianus bewickii) (groundspeed 15.2 ± 0.7 m s⁻¹) and the griffon vulture (Gyps fulvus) (groundspeed 15.3 ± 5.3 m s⁻¹). Simulations were performed with asynchronous turbines with 45‐m blades, an initial wind speed of 10 m s⁻¹, and a residual rotation speed of 3 rpm, resulting in a turbine shutdown time of 35.2 ± 2.1 s.
Cautionary detection distance D as a function of blade length for 10 species of conservation concern in Europe. Variations in mean flight speed affect D with asynchronous turbines with 45‐m blades (circles) and 63‐m blades (triangles). All simulations were performed with an initial wind speed of 10 m s⁻¹, a residual rotation speed of 3 rpm and 95% of flights detected.
Eoldist, a Web Application for Estimating Cautionary Detection Distance of Birds by Automatic Detection Systems to Reduce Collisions With Wind Turbines

January 2025

·

325 Reads

·

2 Citations

The installation of automatic detection systems (ADSs) on operating wind energy facilities is a mitigation measure to reduce bird collisions. The effectiveness of an ADS depends on a combination of parameters, including the detection distance of the bird, its flight speed, and the time to complete the chosen action (e.g., turbine shutdown). We created a web application, Eoldist, to calculate cautionary detection distances required by an ADS, using bird flight speed and turbine shutdown time as input parameters. We compiled a database of the flight speeds of 168 Western Palearctic birds from a review of scientific literature supplemented by an analysis of unpublished GPS‐tracking datasets. To estimate turbine shutdown time, we conducted 137 field trials of experimental shutdown at seven wind farms and found that the duration to reach residual rotor speeds of 3 or 2 rotations per minute (rpm) was respectively 32.2 or 38.8 s on average. Based on this data, Eoldist allows the user to select a species from the database, wind turbine characteristics, and a residual rotor speed (3 or 2 rpm); it then calculates the time to reach the selected threshold and provides a distribution curve for the cautionary detection distance needed to prevent collision. This article includes examples of cautionary detection distances required for several species to demonstrate the sensitivity of key input parameters. Eoldist is freely available and should help the wind energy industry, ADS suppliers, and environmental agencies to define requirements for ADS bird detection that are compatible with the biology of the target species.


Blackbird sampling and population structure. (A) Geographic location of blackbirds sampled: Spain (resident n = 9), France (resident n = 7), Germany (resident n = 12, migratory n = 12), and Russia (migratory n = 9). Circles represent individuals colored according to their population, open circles indicate resident, filled circles migratory phenotypes. The photograph in the upper left corner shows a male blackbird equipped with a radio transmitter (taken by Jesko Partecke). (B) Genome‐wide principal component analysis (PCA) of SNV genotypes. Individuals from the Spanish population are clustered together, with distinct separation on the first principal component, while variation within the French population is captured mostly on the second principal component. Individuals from the German and Russian populations are tightly clustered, especially on the first principal component. (C) PCA of individuals from the German partial migratory populations with 12 resident (filled circles) and 12 migratory individuals (open circles). The lack of clear clusters illustrates that there is no population subdivision corresponding to the migratory phenotype.
Genome‐wide differentiation scans. In (A), we compared geographically separated populations exhibiting the same migratory phenotype (Spain and France) and calculated FST in 2.5 kb windows. We then normalized these estimates by scaffold (FST’) and plotted the running mean over five windows with different shades of blue corresponding to collared flycatcher chromosome models (respective chromosome number indicated on x‐axis in C). Windows above the 99th percentile are shown in red. (B) Comparison between migratory and resident individuals within the partial migratory population (Germany). Net differentiation (ΔFST’ = FST'Spain‐France—FST'GER migratory‐GER resident) is plotted the same way as in (A). While the overall differentiation landscape is similarly heterogeneous compared to the within‐phenotype comparison, there is one region of markedly increased differentiation on the equivalent of collared flycatcher chromosome 9 (indicated by the rectangle). ΔFST’ outlier clusters, that is, five or more consecutive outlier windows are marked by black arrows. Note that only five arrows are visible due to the close proximity of clusters on chromosomes 1, 2, and 9. (C) ΔFST’ for the between‐phenotype comparison between Spain and Russia. A total of 73 outlier windows (in red) are shared between B and C, two of them also occurred in outlier cluster 1 of chromosome 9 in the between‐phenotype comparison in the German population (indicated by the rectangle).
Between‐phenotype German comparison ΔFST’ outlier cluster on the equivalent of flycatcher chromosome 9. (A) Haplotype plot of SNVs. Rows represent individuals, vertical tiles SNV genotypes colored according to genotype. While there are no variants fixed between the two migratory phenotypes, there is a clear separation of haplotypes visible. (B) Windowed (red line indicating the running mean) and per‐SNV FST (black dots) estimates. Yellow bars indicate the two cluster regions with 7 and 12 consecutive outlier windows, respectively. The gene model of the PER2 gene is shown in the lower right corner. (C) Tajima's D estimates in 2.5 kb windows of migratory phenotypes in the German population. The two violin plots indicate the genome‐wide estimates for migratory (pink) and resident (white) phenotypes. Box‐ and jitter plots show estimates for each outlier cluster. Genome‐wide, clusters 1 and 2 on chromosome 9 (orange as in B), and cluster 3 on chromosome 2 estimates are significantly different (Kruskal–Wallis test, p = 1.33⁻¹², 1.75⁻³, 3.77⁻², and 9.02⁻³, respectively).
Putative inversion on chromosome 9. (A) Running mean of FST between the Spanish and Russian population in 2.5 kb windows over chromosome 9. One of the two scaffolds assigned to this chromosome shows elevated differentiation compared to the other scaffold as well as the genome‐wide average. The two scaffolds are separated by a vertical gray line. (B) PCA of individuals from all populations using only SNVs from the scaffold presumably harboring the inversion (Super‐Scaffold_100189). PC1 separates individuals into three clearly distinct clusters, with the middle and right cluster containing only individuals from the Spanish and French populations. (C) Chromosome‐wide linkage disequilibrium (LD) including individuals from all populations. The x‐ and y‐axis represent physical position on chromosome 9, and tiles are colored according to LD between SNVs. Elevated LD is only observed within one scaffold, and does not extend beyond the scaffold boundary (indicated by the gray vertical line; the inverted scaffold is shown left of the gray line).
Combining Individual‐Based Radio‐Tracking With Whole‐Genome Sequencing Data Reveals Candidate for Genetic Basis of Partial Migration in a Songbird

January 2025

·

177 Reads

·

1 Citation

Partial migration is a phenomenon where migratory and resident individuals of the same species co‐exist within a population, and has been linked to both intrinsic (e.g., genetic) as well as environmental factors. Here we investigated the genomic architecture of partial migration in the common blackbird, a songbird that comprises resident populations in the southern distribution range, partial migratory populations in central Europe, and exclusively migratory populations in northern and eastern Europe. We generated whole‐genome sequencing data for 60 individuals, each of which was phenotyped for migratory behavior using radio‐telemetry tracking. These individuals were sampled across the species' distribution range, including resident populations (Spain and France), obligate migrants (Russia), and a partial migratory population with equal numbers of migratory and resident individuals in Germany. We estimated genetic differentiation (FST) of single‐nucleotide variants (SNVs) in 2.5 kb windows between all possible population and migratory phenotype combinations, and focused our characterization on birds from the partial migratory population in Germany. Despite overall low differentiation within the partial migratory German population, we identified several outlier regions with elevated differentiation on four distinct chromosomes. The region with the highest relative and absolute differentiation was located on chromosome 9, overlapping PER2, which has previously been shown to be involved in the control of the circadian rhythm across vertebrates. While this region showed high levels of differentiation, no fixed variant could be identified, supporting the notion that a complex phenotype such as migratory behavior is likely controlled by a large number of genetic loci.


Fig. 1. Female common noctule spring migration. (A) Assigned daily behavior of each tagged bat from evaluations of daily distance and daily VeDBA, a measure of activity. Inactive and foraging (blue and green, respectively) were determined from a threshold of daily total VeDBA, and migration (orange) was estimated from a daily distance threshold. NA (not available) values correspond to locations with missing values for distance or VeDBA, typically representing the day of capture. Each tag ID is associated with a single individual and is ordered chronologically by deployment time. (B) Direction and distance of each migration step for 2022, 2023, and 2024 are colored by the daily VeDBA. The average migration bearing for each year is indicated with an arrow (2022, 63.9°; 2023, 53.3°; 2024, 37.8°). (C) Map of Central Europe showing the individual tracks, connected by solid lines in 2022, dashed lines in 2023, and dotted lines in 2024; each daily point is colored by day of the year. The capture location is shown by a purple triangle in the northeast region of Switzerland.
Bats surf storm fronts during spring migration

January 2025

·

980 Reads

·

4 Citations

Science

Long-distance migration, common in passerine birds, is rare and poorly studied in bats. Piloting a 1.2-gram IoT (Internet of Things) tag with onboard processing, we tracked the daily location, temperature, and activity of female common noctules ( Nyctalus noctula ) during spring migration across central Europe up to 1116 kilometers. Over 3 years, 71 bats migrated tens to hundreds of kilometers per night, predominantly with incoming warm fronts, which provided them with wind support. Bats also showed unexpected flexibility in their ability to migrate across a wide range of conditions if needed. However, females leaving toward the end of the season showed higher total activity per distance traveled, a possible cost for their flexible migration timing.


Citations (56)


... Partial migration refers to the situation in which some individuals within a population migrate post-breeding and some do not, creating a situation in which individuals differ in their response to the same environment. Partial migration is not within the scope of this review, and we therefore suggest Hegemann et al. (2019) and Weissensteiner et al. (2025) who provide recent summaries of physiological and genetic mechanisms associated with partial migration. ...

Reference:

Mechanisms matching timing to resources: comparisons of closely related seasonally sympatric, migratory and non‐migratory populations
Combining Individual‐Based Radio‐Tracking With Whole‐Genome Sequencing Data Reveals Candidate for Genetic Basis of Partial Migration in a Songbird

... So, the arrival of the M. nyctor ancestral lineage in Barbados is quite recent and probably resulted from an extreme overwater dispersal event from South America (Larsen et al. 2012a). Therefore, it is possible to assume that other similar events, perhaps driven by wind streams during tropical storms (Hurme et al. 2025), may have facilitated the invasion of M. nyctor from Barbados into Grenada. Subsequently, introgression of lineages may have occurred through hybridization, which can explain the discordance between the phenotype (like M. attenboroughi) and the genotype (like M. nyctor) of the specimen CM 83427 (JN020562) from Grenada. ...

Bats surf storm fronts during spring migration

Science

... As such, the effects of warming are more easily detectable and are expected to have a large impact on species breeding here. The Arctic is home to many migratory breeding birds, ranging from small passerines to large waterfowl, with migration distances ranging between 1,400 (e.g., rough-legged buzzard Buteo lagopus, Pokrovsky et al. 2024) and 25,000 km (Arctic tern Sterna paradisaea, Egevang et al. 2010). Arctic climate warming is resulting in earlier snowmelt in spring (Box et al. 2019) which is a major determinant of the time suitable for the reproduction of migratory birds. ...

Foxtrot migration and dynamic over-wintering range of an Arctic raptor

eLife

... Areas that are important to animals should be prioritized for protection, and biologging, which enables detailed, long-term tracking of animal movements as well as the measurement of environmental conditions, offers valuable insights for identifying and managing these areas effectively [31]. Long-term data is essential to address these challenges. ...

Tracking individual animals can reveal the mechanisms of species loss
  • Citing Article
  • November 2024

Trends in Ecology & Evolution

... However, our results also showed that the golden eagle was less influenced by increasing temperature compared to the Spanish eagle in the proportion of time flown per hour and flight speed. Although the differences in response between the Spanish and golden eagles were small, they may be related to the fact that soaring flight in golden eagles is also influenced by other factors, for example, gravity waves, and not just by thermal currents (Carrard et al. 2024). ...

Golden eagles regularly use gravity waves to soar in the Alps: new insights from high-resolution weather data

... Movement distances can indicate resource tracking behavior; for example, large birds generally move longer distances through homogeneous habitats to meet resource needs [58]. Black-casqued hornbills (Ceratogymna atrata) exhibit a similar behavior to bats at the Bouamir Research Site, selecting swamps during hotter temperatures and becoming less active [59]; swamps dominated by Raphia palms likely provide a cool location for a day roost and dense vegetation that may conceal birds and bats from predators. Still, we did not detect a population-level signal of bat selection for Plant Volume Density of mid-story vegetation strata (10-20 m), albeit with a small sample size and two-dimensional tracking methods. ...

Three‐dimensional vegetation structure drives patterns of seed dispersal by African hornbills

... Named "Global SnowPack" and being made available on the DLR Geoservice 1 , several combination and interpolation steps are applied to the original snow cover product of the National Snow and Ice Data Center (NSIDC) to ensure continuous information about the presence or absence of snow cover throughout the year. The motivation for this development was the need for continuous, gap-free data for the detection of trends in snow cover duration for hydrological studies (Roessler et al., 2021;Vydra et al., 2024) or analyses in the context of animal migration, long-term changes in animal behaviour 20 (Pokrovsky et al., 2024), or even the impact of snow cover change on genetical, evolutionary aspects (Mills et al., 2018;Zimova et al., 2022). An estimate of the snow cover status below clouds is necessary for such studies, even though they come at the price of slightly reduced accuracy when compared to clear-sky conditions (Gafurov and Bárdossy, 2009). ...

Quick-quick-slow: the foxtrot migration and dynamic non-breeding range of the Arctic raptor
  • Citing Preprint
  • September 2024

... Additionally, other factors, such as brief heavy snowfalls, might have triggered movement, even if these did not result in sustained increases in snow cover (Vansteelant et al., 2011). Alternatively, this phenomenon could have been more complex, with multiple factors possibly acting asynchronously, influencing their over-wintering movements (Yanco et al., 2024). While the ultimate reasons behind the over-wintering movements require further investigation, it is clear that snow cover was a proximate factor driving the birds' continual 1000 km southwest movement during winter (Figure 3). ...

Migratory birds modulate niche tradeoffs in rhythm with seasons and life history

Proceedings of the National Academy of Sciences

... This explanation is supported by a number of studies that have shown that seasonal variation in immune parameters is attributed to increases in parasite prevalence over the breeding season (Merino et al. 2000, Arriero 2009, Emmenegger et al. 2018). The condition-dependent immunoglobulin levels found in our study, along with the fluctuation in energy stores (muscle and fat), seem to support the idea that the variation in immune parameters observed could result from trade-offs mediated by energetic constraints, given the tremendous energetic demands involved in migration (Piersma 2002, Nebel et al. 2012; but see Linek et al. 2024). Therefore, the variation observed may reflect individual flexibility in how animals cope with the environment and may be shaped by the combined effect of immunological responses linked to seasonal variation in infections, and the effect of immunological trade-offs mediated by nutrition and energy stores (Pedersen and Babayan 2011, Hegemann et al. 2012, Arriero et al. 2018, Ohmer et al. 2021. ...

Migratory lifestyle carries no added overall energy cost in a partial migratory songbird

Nature Ecology & Evolution

... [46][47][48][49] In late summer and autumn, before the onset of the mating season, this pattern may reverse, as males in some species prefer normothermia to promote spermatogenesis. 50,51 In contrast, females and juveniles may conserve energy by entering torpor for part of the day during this phase of their annual cycle. [38][39][40]47 Due to the critical importance of roosts for the survival and reproduction of bats, 28 we take a closer look at the different roost types in light of climate change. ...

Heart rate monitoring reveals differential seasonal energetic trade-offs in male noctule bats