Oliver P. Love’s research while affiliated with University of Windsor and other places

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Publications (163)


Dealing with the heat: Assessing heat stress in an Arctic seabird using 3D-printed thermal models
  • Article

May 2025

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3 Reads

Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology

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David A. Fifield

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Kyle H. Elliott

Climate change could disrupt migratory patterns for an Arctic seabird population

March 2025

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13 Reads

Marine Ecology Progress Series

Climate change is altering the marine environment at a global scale, and these changes could affect the distribution and migration patterns of marine species throughout their annual cycle. Arctic regions are already experiencing some of the most dramatic changes in marine climate, and there is a need for predictive models to understand how these changes could alter the spatio-temporal distributions of Arctic marine species. We used a species distribution model to predict potential future changes in the non-breeding distribution of thick-billed murres Uria lomvia from a colony in Hudson Bay, Canada, from 2021 to 2100 using 3 Coupled Model Intercomparison Project Phase 6 (CMIP6) climate scenarios: low (SSP1-2.6), intermediate (SSP2-4.5), and high (SSP5-8.5) emissions. Under the intermediate- and high-emissions scenarios, suitable habitat within Hudson Bay would become available year-round during the next century. This could lead to a portion of this migratory population becoming year-round residents within the next 80 yr. We predicted a significant northward shift in the winter range, such that little or no habitat would be available below 55°N by 2100. This shift would have significant implications for the murre harvest in Canada because the winter distribution would no longer include coastal Newfoundland where most harvesting occurs, particularly if murres from other colonies show a similar shift in distribution. Although there were projected changes in seasonal distributions under all 3 climate scenarios, dramatic re-distribution of non-breeding habitat could be avoided with policies that limit future emissions.


Dealing with the Heat: Assessing Heat Stress in an Arctic Seabird Using 3d-Printed Thermal Models
  • Preprint
  • File available

January 2025

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39 Reads

Download

Distribution of thick-billed murre foraging tracks around East Digges Island colony. A = Incubation 2014–2015; B = Early chick-rearing 2014 to 2016 (before 9.48 days since median hatching date); C = Late chick-rearing 2016 (after 9.48 days since median hatching date). Dashed and full lines represent 95 and 50% Utilization Distributions, respectively. Black lines and points represent all GPS data available, but only locations associated with water activities were used in the UDs
Correlation between Foraging Range Index, cumulated flight distance, cumulated time spent on water and total energy expenditure for incubating and chick-rearing thick-billed murres at Digges Island in 2014-16. All data are log-transformed. Regression lines from linear models (p < 0.0001) account for years and GPS deployment repeated measures
Correlation of all foraging and foraging effort metrics of interest in thick-billed murres at Digges Island, all years combined. All variables were log-transformed. Descriptions of variables can be found in Table 2. The correlation index shown is Pearson’s correlation coefficient. Significance is based on the result of Pearson’s product-moment correlation coefficient (* p < 0.05; ** p < 0.01; *** p < 0.001)
Principal Component Analysis (PCA) of thick-billed murres foraging trips (blue and yellow dots) and their associated foraging parameters (black arrows, see Table 2). A: Foraging behavior metrics, dim1 had an eigenvalue of 5.23, and dim2 had an eigenvalue of 0.53. dim1 is dominated by parameters representing transit time, dim2 by parameters representing search time. B: Foraging effort proxies, dim1 had an eigenvalue of 2.13, and dim2 had an eigenvalue of 1.21. Dim1 is dominated by the number of foraging trips per day and the proportion of time spent on water, dim2 by distance flown per day, and average energy expenditure over a day. Centroids of the ellipses are represented by a larger colored point
Stage- and sex-dependent changes in foraging behavior in thick-billed murres at Digges Island during the 2014, 2015, and 2016 breeding seasons. Solid lines represent no sex differences. Early chick-rearing refers to prior to 9.48 days since the median hatching date, and Late chick-rearing refers to the past 9.48 days since the median hatching date. The 9.48 threshold was obtained using an automated breakpoint detection algorithm and has been set as the reference point. The lines represent linear mixed-effect model results, accounting for years and GPS deployment repeated measures. Individual models were performed for each breeding stage and combined into a single graph. Full model descriptions are available in supplementary material

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Integrating behavior and physiology supports Storer-Ashmole’s halo in a central place forager

Marine Biology

Central place foraging may lead to local prey depletion as foragers select nearby prey (“Storer-Ashmole’s halo”), causing individuals to forage progressively farther from the central place. We tested this idea by coupling GPS tracking (foraging behavior) and plasma metabolites (nutritional biomarkers) when studying thick-billed murres (Uria lomvia; N = 237), a colonial-nesting seabird where central place foraging constraints are expected to be particularly pronounced due to high transit costs. Foraging range decreased when birds were constrained to visit the central place several times per day (chick-rearing) compared to self-feeding (incubation), illustrating the constraint of central place foraging. Moreover, adult feeding frequency, as determined by plasma triglycerides, were higher during incubation, consistent with the longer fasts (incubation shifts) during that period. Transit time (foraging distance) increased with date during chick-rearing but not incubation, consistent with prey depletion due to central place foraging within the restricted chick-rearing foraging range. During late chick-rearing, when a diet switch to low-quality, smaller prey occurs, birds switched to foraging near the colony, consistent with the foraging range being overextended. Unlike other, smaller colonies where foraging success is higher due to a smaller halo, sexes had similar foraging behaviour in our study, except during early incubation when females foraged more (more flying, more swimming) as they overcame the cost of producing the egg. When we take our results with other lines of evidence (increased foraging distance with colony size, prey switching as birds “feed down the food chain”), we conclude that central place foraging seabirds may cause prey depletion at one of the world’s largest murre colonies.


Influence of sea ice concentration, sex and chick age on foraging flexibility and success in an Arctic seabird

September 2024

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71 Reads

Conservation Physiology

Declining sea ice and increased variability in sea ice dynamics are altering Arctic marine food webs. Changes in sea ice dynamics and prey availability are likely to impact pagophilic (ice-dependent and ice-associated) species, such as thick-billed murres (Uria lomvia), through changes in foraging behaviour and foraging success. At the same time, extrinsic factors, such as chick demand, and intrinsic factors, such as sex, are also likely to influence foraging behaviour and foraging success of adult murres. Here, we use 3 years of data (2017–2019) to examine the impacts of environmental conditions (sea ice concentration and sea surface temperature), sex and chick age (as a proxy for chick demand) on foraging and diving behaviour (measured via biologgers), energy expenditure (estimated from activity budgets) and foraging success (measured via nutritional biomarkers) of thick-billed murres during the incubation and chick-rearing stages at Coats Island, Nunavut. Murres only exhibited foraging flexibility to environmental conditions during incubation, which is also the only stage when ice was present. When more ice was present, foraging effort increased, murres foraged farther and made deeper dives, where murres making deeper dives had higher foraging success (greater relative change in mass). During incubation, murre behaviour was also influenced by sex of the individual, where males made more and shorter trips and more dives. During chick-rearing, murre behaviour was influenced primarily by the sex of the individual and chick age. Males made shallower dives and fewer dive bouts per day, and more dives. Birds made longer, deeper dives as chicks aged, likely representing increased intra-specific competition for prey throughout the season. Our results suggest variation in sea ice concentration does impact foraging success of murres; however, sex-specific foraging strategies may help buffer colony breeding success from variability in sea ice concentration.


Individual mean body temperatures for calm (non-active) snow buntings (Plectrophenax nivalis) implanted intraperitoneally or subcutaneously with temperature sensitive transponder tags. Error bars represent standard deviation. The horizontal dashed lines are the respective mean maximum body temperatures for intraperitoneal and subcutaneous birds when actively flying. All values represent data recorded between sunrise and sunset.
Mean body temperature as a function of air temperature measured in a captive population of calm (non-active) snow buntings (Plectrophenax nivalis). Horizontal lines represent the respective average modal body temperatures for intraperitoneal and subcutaneous birds. Error bars were removed for clarity. All values represent data recorded between sunrise and sunset.
Body temperature patterns in active snow buntings (Plectrophenax nivalis) as a function of a time since entering the aviary and b air temperature. In panel a, negative minutes represent the time span prior to entering the aviary and positive values represent the time span after entering the aviary. The vertical dashed line in panel a represents the start time for each experiment (i.e., Minutes = 0). In panel b, the regression line represents the conditional effect of air temperature on body temperature using the model-averaged regression estimates from the 95% confidence set of the best-ranked models (see Table 4).
The impacts of air temperature on a the percent of actively flying snow buntings (Plectrophenax nivalis) with a body temperature (Tb) greater than or equal to 45 °C and b the percent of buntings exhibiting panting behavior. Note the y-axes are on different scales. The horizontal dashed line in b represents the threshold above which 50% of the study population was dissipating heat through panting behavior. There are fewer data points in b as panting was only recorded during 2020.
Mean hyperthermic scope (i.e., maximum flight body temperature—modal body temperature) as a function of modal body temperature (Tb-mod) among actively flying snow buntings (Plectrophenax nivalis).
An arctic breeding songbird overheats during intense activity even at low air temperatures

July 2024

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59 Reads

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3 Citations

Birds maintain some of the highest body temperatures among endothermic animals. Often deemed a selective advantage for heat tolerance, high body temperatures also limits birds’ thermal safety margin before reaching lethal levels. Recent modelling suggests that sustained effort in Arctic birds might be restricted at mild air temperatures, which may require reductions in activity to avoid overheating, with expected negative impacts on reproductive performance. We measured within-individual changes in body temperature in calm birds and then in response to an experimental increase in activity in an outdoor captive population of Arctic, cold-specialised snow buntings (Plectrophenax nivalis), exposed to naturally varying air temperatures (− 15 to 36 °C). Calm buntings exhibited a modal body temperature range from 39.9 to 42.6 °C. However, we detected a significant increase in body temperature within minutes of shifting calm birds to active flight, with strong evidence for a positive effect of air temperature on body temperature (slope = 0.04 °C/ °C). Importantly, by an ambient temperature of 9 °C, flying buntings were already generating body temperatures ≥ 45 °C, approaching the upper thermal limits of organismal performance (45–47 °C). With known limited evaporative heat dissipation capacities in these birds, our results support the recent prediction that free-living buntings operating at maximal sustainable rates will increasingly need to rely on behavioural thermoregulatory strategies to regulate body temperature, to the detriment of nestling growth and survival.


Phenotypic constraints at the top of the world: an Arctic songbird faces the cumulative cost of maintaining a winter-like phenotype during breeding

April 2024

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81 Reads

Among birds, several body composition traits typically decrease in size or mass during breeding likely as a result of competing demands during this critical life history stage. However, a recent outdoor captive study in an Arctic-breeding cold-specialist songbird (snow buntings – Plectrophenax nivalis) demonstrated that these birds maintain winter cold acclimatization during the spring and summer, despite facing summer temperatures much warmer than on their Arctic breeding grounds. This suggests that buntings may face a cumulative physiological cost during breeding: having to support a winter phenotype while also upregulating additional traits for reproduction. The current study aimed to test this hypothesis. Between 2016 and 2019, we examined how body composition and metabolic performance (thermogenic capacity and physiological maintenance costs) changed from pre-breeding to chick provisioning in free-living birds captured at the northern limit of their breeding range in the Canadian Arctic (Alert, NU, 82°). While body mass and fat reserves deceased significantly between pre-breeding and territory defense independent of thermal conditions, cold endurance and associated traits remained stable and elevated up to the nestling provisioning period, as long as ambient temperature remained below a threshold level of 0–2°C. These results indicate that snow buntings must maintain a high thermogenic capacity after arrival on the breeding grounds if temperatures remain below freezing, regardless of whether birds are actively breeding or not. In this context, our research suggests that these birds, and possibly other arctic breeding songbirds, may experience cumulative physiological costs during years with a late onset of spring, when breeding activities (i.e., egg production and incubation) begin while temperatures are still below 0–2°C.


An interspecific foraging association with polar bears increases foraging opportunities for avian predators in a declining Arctic seabird colony

March 2024

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78 Reads

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2 Citations

Interspecific foraging associations (IFAs) are biological interactions where two or more species forage in association with each other. Climate‐induced reductions in Arctic sea ice have increased polar bear ( Ursus maritimus ) foraging in seabird colonies, which creates foraging opportunities for avian predators. We used drone video of bears foraging within a common eider ( Somateria mollissima ) colony on East Bay Island (Nunavut, Canada) in 2017 to investigate herring gull ( Larus argentatus ) foraging in association with bears. We recorded nest visitation by gulls following n = 193 eider flushing events from nests during incubation. The probability of gulls visiting eider nests increased with higher number of gulls present (β = 0.14 ± 0.03 [SE], p < .001) and for nests previously visited by a bear (β = 1.14 ± 0.49 [SE], p < .02). In our model examining the probability of gulls consuming eggs from nests, we failed to detect statistically significant effects for the number of gulls present (β = 0.09 ± 0.05 [SE], p < .07) or for nests previously visited by a bear (β = −0.92 ± 0.71 [SE], p < .19). Gulls preferred to visit nests behind bears (χ ² = 18, df = 1, p < .0001), indicating gulls are risk averse in the presence of polar bears. Our study provides novel insights on an Arctic IFA, and we present evidence that gulls capitalize on nests made available due to disturbance associated with foraging bears, as eiders disturbed off their nest allow gulls easier access to eggs. We suggest the IFA between gulls and polar bears is parasitic, as gulls are consuming terrestrial resources which would have eventually been consumed by bears. This finding has implications for estimating the energetic contribution of bird eggs to polar bear summer diets in that the total number of available clutches to consume may be reduced due to avian predators.


Photo of trail camera (Browning inc. model: BTC-5HDPX) footage showing a focal incubating female common eider (Somateria mollissima) and polar bear (Ursus maritimus) on East Bay Island, Nunavut, Canada at 9.41 on 1 July 2019.
Comparison of baseline heart rate (beats/10 s) versus heart rate in the presence of a polar bear (Ursus maritimus) in incubating female common eider (Somateria mollissima) on East Bay Island, Nunavut, Canada. Red points correspond to model predicted estimates of heart rate at both baseline and during bear presence, and vertical lines are their associated 95% confidence intervals.
Magnitude of change in log transformed common eider (Somateria mollissima) heart rate (‘ΔHR’, beats/10 s) on East Bay Island, Nunavut, Canada in relation to (a) eider ratio of exposure risk (min m⁻²) to a polar bear, (b) eider incubation stage (days), and (c) air temperature (°C). Solid and dashed lines are based on model predicted values ± 95% confidence intervals, respectively.
A colonial-nesting seabird shows limited heart rate responses to natural variation in threats of polar bears

October 2023

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90 Reads

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1 Citation

Several predator–prey systems are in flux as an indirect result of climate change. In the Arctic, earlier sea-ice loss is driving polar bears (Ursus maritimus) onto land when many colonial nesting seabirds are breeding. The result is a higher threat of nest predation for birds with potential limited ability to respond. We quantified heart rate change in a large common eider (Somateria mollissima) breeding colony in the Canadian Arctic to explore their adaptive capacity to keep pace with the increasing risk of egg predation by polar bears. Eiders displayed on average higher heart rates from baseline when polar bears were within their field of view. Moreover, eiders were insensitive to variation in the distance bears were to their nests, but exhibited mild bradycardia (lowered heart rate) the longer the eider was exposed to the bear given the hen's visibility. Results indicate that a limited ability to assess the risks posed by polar bears may result in long-term fitness consequences for eiders from the increasing frequency in interactions with this predator.


Standardized, model-averaged regression estimates from the 95% confidence set of the best-ranked models explaining variation in body temperature among snow buntings during activity experiments.
Snow Buntings, an arctic cold-specialist passerine, risk overheating under intense activity even at low air temperatures

September 2023

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41 Reads

Birds maintain some of the highest body temperatures (Tb) among endothermic animals. Often deemed a selective advantage for heat tolerance, high Tb also limits the capacity to increase Tb before reaching lethal levels. Recent thermal modelling suggests that sustained effort in Arctic birds might be restricted at mild air temperatures (Ta) during energetically demanding life history stages, which may force reductions in activity to avoid overheating, with expected negative impacts on reproductive performance. Consequently, understanding how Arctic birds will cope with increasing Ta has become an urgent concern. We examined within-individual changes in Tb in response to an experimental increase in activity in outdoor captive Arctic cold-specialised snow buntings (Plectrophenax nivalis), exposed to naturally varying Ta from -15 to 36 °C. Calm buntings exhibited a modal Tb range from 39.9 %—42.6 °C. However, we detected a dramatic increase in Tb within minutes of shifting birds to active flight, with strong evidence for a positive effect of Ta on Tb (slope = 0.04 °C/°C). Importantly, by Ta of 9 °C, flying buntings were already generating Tb ≥ 45°C, approaching the upper thermal limits of organismal performance (i.e., Tb = 45—47 °C). Under scenarios of elevated Tb, buntings must increase rates of evaporative water loss and/or reduce activity to avoid overheating. With known limited evaporative heat dissipation capacities, we argue buntings operating at peak energy levels will increasingly rely on behavioral thermoregulatory strategies (i.e., reducing activity) to regulate Tb, at the potential detriment to nestling growth and survival.


Citations (80)


... The phenotypic flexibility of birds is also governed by ambient temperature in integration with other environmental factors, by metabolic adjustments and other physiological, morphological, and behavioral adaptions, necessary for survival (Kumar et al. 2023). Birds maintain relatively higher body temperatures amongst endothermic animals (O'Connor et al. 2024). In a seasonal study on Common Blackbirds (Turdus merula), it was found that with a decrease in ambient temperature at night, their body temperature also decreased, whereas, this was not the case during daytime (Linek et al. 2021). ...

Reference:

Seasonality in erythrocyte cytomorphometry and physiology of a sub-tropical resident bird, the Scaly-breasted Munia (Lonchura punctulata)
An arctic breeding songbird overheats during intense activity even at low air temperatures

... Several other studies have successfully used heart rate as a metric for perceived risk by eiders. In a recent study, we approached eiders with different predator imagery ( polar bear, Arctic fox and control), and birds displayed a higher magnitude of response to the fox than bear compared with the control, but exhibited a fear bradycardia response leading up to flushing regardless of predator stimulus [32]. This fear bradycardia response was also observed for three nesting eiders encountering actual approaching polar bears in the same study (although this response was never compared with an eider's heart rate in the absence of a polar bear). ...

Heightened heart rate but similar flight responses to evolved versus recent predators in an Arctic seabird

Avian Conservation and Ecology

... Flight relies on triglycerides (fat reserves) as fuel (Hennin et al. 2016;Sorenson 2016;Lamarre et al. 2017). For example, murres have higher plasma-neutral lipids during chick-rearing, consistent with mass loss due to lipid mobilization at that time (Jacobs et al. 2012;Eby et al. 2023). Lipid mobilization allows adults to transfer their reserves to their offspring via higher feeding rates (Gaston and Hipfner 2006a, b). ...

Lower nutritional state and foraging success in an Arctic seabird despite behaviorally flexible responses to environmental change

... For example, sex hormone production was reduced in brown bullhead (Ameiurus nebulosus) exposed to Hg [98]. Increases in Hg cause decreases in prolactin, a reproductive hormone in common eiders (Somateria mollissima) [101]. When whole populations are exposed, this can cause an entire population to decline. ...

Do foraging ecology and contaminants interactively predict parenting hormone levels in common eider?
  • Citing Article
  • March 2023

General and Comparative Endocrinology

... Drone footage is also ideal to spot rare behaviours. When recording bear behaviour using drones, researchers observed conspecific nest attendance by the common eider ducks, Somateria mollissima, in response to polar bear attacks (Simone et al., 2023). Bird nesting behaviours can be observed with little disturbance to the birds and reduced fieldwork effort (Gallego & Sarasola, 2021), allowing the monitoring of birds' breeding success ranging from ravens, Corvus corax (Zawadzki & Zawadzka, 2024), to raptors, Buteo jamaicensis, Buteo regalis, Haliaeetus leucocephalus and Pandion haliaetus (Junda et al., 2015). ...

Conspecific nest attendance behaviour of Common Eider (Somateria mollissima) in response to Polar Bear (Ursus maritimus) foraging activity: error or intent?
  • Citing Article
  • February 2023

The Canadian Field-Naturalist

... As a result, resource availability and abundance likely differ between the Rankin Inlet and Naujaat areas, in turn influencing the potential fish and invertebrate prey species composition. For example, capelin are commonly observed around Rankin Inlet and have only been documented as far north as Coats Island and Southampton Island (∼62 • N-65 • N) along western Hudson Bay (Gaston et al. 2003;Amiraux et al. 2023). Both study sites are also important Inuit subsistence and commercial harvesting locations for Arctic char that are typically fished during the ice-free summer months from mid-June to late-August while Arctic char feed in the marine environment. ...

Tracing carbon flow and trophic structure of a coastal Arctic marine food web using highly branched isoprenoids and carbon, nitrogen and sulfur stable isotopes

Ecological Indicators

... It is now well established that effective animal management and conservation programs should incorporate knowledge of the behavioural ecology of the species under study. More recently, conservation management strategies have integrated animal behaviour with conservation genetics (Holderegger et al. 2019) and conservation physiology (Madliger et al. 2020) to obtain innovative solutions. Increasingly, it is also recognised that there is a need to include sensory ecology (as a subset of behavioural ecology) into conservation management, but this has seldom occurred, particularly in Australia (see reviews by (Dominoni et al. 2020;Elmer et al. 2021;Madliger 2012). ...

Conservation Physiology: Applications for Wildlife Conservation and Management
  • Citing Article
  • November 2020

... Applications that require repetition of the measurements frequently, such as change detection of vegetation or morphology (Ancin-Murguzur et al. 2020;de Almeida et al. 2020;Eltner et al. 2015;Guisado-Pintado et al. 2019) now use UAS widely. Also mapping of rapidly evolving or moving systems, which require capacity to react and to adapt the mapping relative to the target, such as natural disasters (Daud et al. 2022) or wildlife monitoring in hardto-access environments (Geldart et al. 2022;Krishnan et al. 2023) have benefitted from the flexibility of UAS. One of its agreed benefits is that it does not disturb the research target, which has been demonstrated to apply also to wildlife: in a study of Geldart et al. (2022), the heart rates of incubating female birds did not change during a drone-based population survey, when compared to their baseline heart rate. ...

A colonial-nesting seabird shows no heart-rate response to drone-based population surveys

... This footage was originally collected to estimate the energetics of bear foraging on eider eggs, and the authors recorded 31 foraging bouts from 20 individual bears (Jagielski, Dey, Gilchrist, Richardson, Love, & Semeniuk, 2021;. This dataset was previously analyzed to examine the spatial effects of bear foraging on eider flush behaviour ; however, for this current research we (2021), and Barnas, Geldart, et al. (2022) along with the associated drone reporting protocol (Barnas, Chabot, et al., 2020). ...

Predatory cue use in flush responses of a colonial nesting seabird during polar bear foraging

Animal Behaviour

... For species that are adapted to withstand extreme cold temperatures, a warming environment might challenge their survival due to their limited capacity to dissipate heat (Oswald and Arnold, 2012). Thus, despite the limited work on direct effects, heat stress has the potential to affect Arctic wildlife at a much faster rate than indirect effects, leading to expected reductions in breeding success (O'Connor et al. 2022) and mortality events (Gaston et al., 2002;McKechnie & Wolf, 2010). ...

Warming in the land of the midnight sun: breeding birds may suffer greater heat stress at high- versus low-Arctic sites