Body surface rewarming in fully and partially hypothermic king penguins

Penguins face a major thermal transition when returning to land in a hypothermic state after a foraging trip. Uninsulated appendages (flippers and feet) could provide flexible heat exchange during subsequent rewarming. Here, we tested the hypothesis that peripheral vasodilation could be delayed during this recovery stage. To this end, we designed an experiment to examine patterns of surface rewarming in fully hypothermic (the cloaca and peripheral regions (here; flippers, feet and the breast) < 37 °C) and partially hypothermic (cloaca at normothermia ≥ 37 °C, but periphery at hypothermia) king penguins (Aptenodytes patagonicus) when they rewarmed in the laboratory. Both groups rewarmed during the 21 min observation period, but the temperature changes were larger in fully than in partially hypothermic birds. Moreover, we observed a 5 min delay of peripheral temperature in fully compared to partially hypothermic birds, suggesting that this process was impacted by low internal temperature. To investigate whether our laboratory data were applicable to field conditions, we also recorded surface temperatures of free-ranging penguins after they came ashore to the colony. Initial surface temperatures were lower in these birds compared to in those that rewarmed in the laboratory, and changed less over a comparable period of time on land. This could be explained both by environmental conditions and possible handling-induced thermogenesis in the laboratory. Nevertheless, this study demonstrated that appendage vasodilation is flexibly used during rewarming and that recovery may be influenced by both internal temperature and environmental conditions when penguins transition from sea to land. Electronic supplementary material The online version of this article (10.1007/s00360-020-01294-1) contains supplementary material, which is available to authorized users.


Introduction
Seabirds and pinnipeds spend a large part of their lives at sea but periodically come to land for reproduction, moult or rest (Feltz and Fay 1966;Ling 1970;Croxall 1982;Hammond et al. 1988;Watts 1992Watts , 1996. The return to land is a major thermal transition, because air has physical characteristics 1 3 (e.g., thermal conductivity) that substantially reduces the rate of heat loss compared to water (Bullard and Rapp 1970;Nadel 1984;Ponganis 2015) and air temperatures are often higher than sea temperatures.
To reduce the rate of heat loss at sea, the body trunk of marine endotherms is well insulated by dense pelage or a thick layer of subcutaneous fat. Furthermore, marine endotherms generally show local heterothermy in appendages and the body trunk (Culik et al. 1996;Bevan et al. 1997;Handrich et al. 1997;Boyd 2000) which not only extends dive duration by lowering tissue demands for oxygen (Scholander 1940) but also decreases the rate of heat loss by reducing the temperature gradient between the body and the environment. Reduced appendage temperature is achieved by massive peripheral vasoconstriction and countercurrent heat exchange in the appendages (Pabst et al. 1999;Williams and Worthy 2002). The latter is particularly important, because the appendages are relatively fat free, and at most insulated by short feathers or hair. Accordingly, heat loss from the appendages was estimated to 8-28% of total body heat loss in whales and seals (Ryg et al. 1993). However, vasoconstriction may reduce heat loss from the flippers to only 2-6% of total body heat loss in 0 °C water, compared to 19-48% without vasoconstriction at 24 °C (Kvadsheim and Folkow 1997).
In contrast to when they are submerged, marine endotherms typically maintain stable high body temperature on land. For example, dry king penguins (Aptenodytes patgonicus) on land have a core body temperature of 37 °C Lewden et al. 2017a). In seals, vasodilation of the uninsulated appendages can rapidly increase heat loss during periodic haul-outs onto land. This has been proposed to help maintain core body temperature and avoid hyperthermia in the warmer and less conductive air (Watts 1992). For this reason, uninsulated body parts such as appendages have been characterized as 'thermal windows' that allow flexible heat transfer in a range of environments (e.g., Klir and Heath 1992;Williams 1990;Norris et al. 2010;Erdsack et al. 2012;Tattersall et al. 2018). Thermal windows are also found on the body trunk of seals and may facilitate heat dissipation and evaporation of water trapped within the wet pelage (Mauck et al. 2003).
Similar to the appendages of marine mammals, the penguin flipper is a large, relatively uninsulated structure that might serve as a thermal window available for control of heat transfer via vasomotor action and countercurrent heat exchange (Frost et al. 1975;Boyd and Croxall 1996;Thomas 2007;Thomas and Fordyce 2012). This may lead to a large temperature gradient between the distal and proximal flipper in some situations (e.g., during extended periods at sea and during dives) (Prévost and Sapin-Jaloustre 1964;Ponganis et al. 2003), and a uniformly heated flipper that is maintained well above ambient temperature in others (e.g., during rest on land and at the sea surface) (Ponganis et al. 2003;Schmidt 2006). Uninsulated legs and feet of other seabirds have been identified as analogous heat-transfer structures (Irving and Krog 1955;Kilgore and Schmidt-Nielsen 1975;Baudinette et al. 1976) with countercurrent heat exchangers and main blood vessels with sphincteric action (Johansen and Millard 1973;Hargens et al. 1978;Midtgård 1981; see Johansen and Bech 1983 for review) that allows fine-scale control of leg and foot temperature (Kazas et al. 2017).
The aim of this study was to describe patterns of surface rewarming in plausible thermal windows (flippers, feet) in king penguins after their return to land following foraging bouts at sea. We also studied the simultaneous rewarming of surface temperature on the well-insulated body trunk, to gain insights into the relative roles of uninsulated but relatively small, and well insulated, considerably larger, surface areas in the control of heat transfer (McCafferty et al. 2013). Using thermal imaging, we were able to collect rewarming data more closely linked to heat exchange patterns, which is arguably relevant for the study of thermal windows, compared to previous work on rewarming in penguins that used internally implanted sensors (Ponganis et al. 2003;Schmidt 2006). We specifically studied how surface temperature recovery was affected by internal temperature, testing the hypothesis that birds facilitate the recovery of internal temperature by delaying peripheral temperature recovery. This was achieved by performing an experiment where we compared the dynamics of rewarming of king penguins that had just returned from the sea. These individuals showed both low internal and low peripheral temperature (henceforth 'fully hypothermic'; i.e., all tissue temperatures ≥ 2 °C below normothermia), similar to the physiological state of penguins when feeding (Handrich et al. 1997). We then measured the same birds once they had completed recovery (i.e., when internal temperature was ≥ 37 °C and peripheral temperature was stable) and we had induced peripheral hypothermia by cold water immersion (henceforth 'partially hypothermic'). We predicted that we would observe a delay of surface rewarming in fully hypothermic birds compared to partially hypothermic birds, which could indicate that they reduced peripheral circulation until their internal temperature had reached normothermia, or simply reflect differences in heat transfer as the bird rewarms from the inside and out. Because the stress of handling can induce thermoregulatory changes in deep and peripheral tissues in both penguins and other birds (Regel and Pütz 1997;Herborn et al. 2015;Nord and Folkow 2019), we also compared rewarming patterns recorded in the laboratory with those in free-ranging, non-handled, birds in the colony after their return from sea. This study, therefore, provides insights into patterns of rewarming in hypothermic penguins as they transition from prolonged periods at sea to land, and how this process was affected by internal state.

Materials and methods
King penguins were studied during the courtship phase of their breeding cycle in La Baie du Marin on Possession Island, Crozet Archipelago ((46°4′ S, 51°8′ E) from November to March during two consecutive summers (Year 1: 2015(Year 1: -2016Year 2: 2016Year 2: -2017. The experimental design is outlined in Fig. 1.

Effects of internal temperature on surface rewarming-Group 1
Thermal images of individual king penguins (N = 40; Year 1: 24; Year 2: 16) were collected using a thermal imaging camera (ThermaCAM™ P25, FLIR Systems, Orsonville, Florida, USA, accuracy ± 2 °C) to confirm that birds were in a peripherally vasoconstricted state. This was clearly visible as uniformly cold body trunk, head, beak and flippers (Fig. 1).

Fig. 1
Graphic illustration of the experimental protocol used to investigate surface temperature rewarming ashore after a foraging trip in king penguins. Studies were performed on: (1) captive individuals that were measured in the laboratory after their return to the colony from a foraging trip at sea (Group 1); and (2) free-ranging birds that rewarmed in the colony after coming from the sea (Group 2). The birds in Group 1 were measured in two experimental conditions; once in a fully hypothermic state (i.e., directly when they came from the sea; 1A) and again in an experimentally induced partially hypothermic state (1B). The birds in Group 1 in Year 1, and all birds in Group 2, were measured only once. No birds were re-used between years or in the different groups The bird was then captured and transferred to a thermal imaging studio in a nearby laboratory within 2 min (Year 1: 2.07 min ± 0.10 s; Year 2: 2.53 min ± 0.42 s, mean ± s.e.) (Group 1A, Fig. 1). The thermal imaging studio (hereafter referred to as the 'laboratory') provided standardized conditions for thermal imaging by excluding wind, precipitation and solar radiation, and also allowed for a uniform angle and distance (1.1 m) of measurement. We fitted birds with a hood before measurements to reduce stress (Cockrem et al. 2008). We then proceeded to collect thermal images of the ventral surface of the right flipper (T flipper ) and breast (T breast ) just below the axilla. Because the flipper had to be manually opened to expose the ventral side, we only measured rewarming in one flipper to reduce handling stress. We also collected a thermal image of the dorsal area of the right foot (T foot ). This set of two images, i.e., flipper/breast and foot, was collected every 30 s. In Year 1, internal temperature was not measured, but in Year 2, it was measured by inserting a digital thermometer with a flexible tip (Gilbert, Caen, FR) 6-8 cm through the cloaca (T cloacal ). Data in Year 1 were collected for 6.4 min ± 0.5 min (s.e.) after capture (range 6-12 min). To ascertain that birds had sufficient time to reach a stable surface temperature during the experiment, we extended measurement duration to 21.3 min ± 0.5 min in Year 2 (range 16.9-32.4 min). Activity during the measurements were scored on a scale from 1 to 3, where 1 represented a calm individual, and 3, a distressed individual that continuously attempted to escape. Activity level did not affect any measured temperatures (all P > 0.08), and some birds even appeared to be asleep during measurements (AL, pers. obs.). This effect was, therefore, not considered further below. Mean air temperature, T a , in the laboratory was 8.1 ± 1.4 °C (s.d.) during all trials (range 4.7-11.4 °C), which is within the thermoneutral zone of king penguins (i.e., − 5 to + 15 °C; Le Maho and Despin 1976;Froget et al. 2002;Fahlman et al. 2004).
Of the 16 individuals measured when fully hypothermic in Year 2, 14 were subsequently kept in thermoneutrality in an outdoor roofless wooden enclosure (3 × 3 m) without human disturbance for 68.00 ± 3.00 min to allow rewarming to internal normothermia. These birds were then brought back to the laboratory and thermal images of the flipper and the foot were taken, and T cloacal (which was 2.2 ± 0.7 °C greater than when the birds had just returned from sea) was recorded. We then briefly immersed all of the body but the head in cold water (ca. 8 °C) that was available from a freshwater supply at the field site. The water bath had similar temperature to seawater in the adjacent bay (7.7 ± 0.9 °C in the same year; Lewden et al. 2017b). Immersion lasted 4.05 min ± 0.25 s, which was enough to induce peripheral vasoconstriction without changing internal temperature. Accordingly, T cloacal did not differ before (37.3 ± 0.3 °C) and after immersion (37.2 ± 0.2 °C) (paired t test; df = 11 t = − 0.33, P = 0.75), but we observed a significant decrease in T flipper (before: 16.2 ± 1.4 °C; after: 11.0 ± 0.5 °C) (df = 13 t = − 3.22, P = 0.006), T foot (before: 15.8 ± 2.7 °C; after: 10.7 ± 0.5 °C) (df = 8, t = − 0.99, P = 0.035) and T breast (before = 15.5 ± 0.8 °C; after = 12.9 ± 0.5 °C) (df = 13 t = − 2.77, P = 0.0101). Birds were then directly returned to the laboratory to be measured a second time (Group 1B, Fig. 1) during 21.0 min ± 0.1 min (range 17.3-25.3 min). The birds were then released in the colony.

Measurements in the colony-Group 2
Thermal imaging of free-ranging birds (N = 24, Fig. 1), which had not been previously measured in the laboratory, was undertaken during Year 2, by following individuals from the point at which they returned from the sea for as long as possible before they could not be seen by the observer (Fig. 1, Free-ranging-Group 2). Data were collected on days without rain for, on average, 14.53 min ± 2.05 min (range 2.77-38.93 min). Images were collected as frequently as possible when birds were in view and the inside of the flipper was visible. This provided, on average (± s.e.), 22 ± 3 thermal images per bird, collected roughly every 1.6 min. Surface temperature were extracted only from thermal images where the regions of interest where displayed as in the laboratory. T a within the colony was recorded every 3 min with an iButton (MXMDS1921Z-F5; Maxim Integrated, San Jose, CA, USA). We also scored wind speed from low (0) to high (4) and estimated percentage cloud cover. T a ranged from 4.8 to 9.9 °C (mean: 7.4 ± 0.1 °C), cloud cover between 30 and 90% (mean: 69 ± 4%), and mean wind speed score was 1.70.

Thermal image analysis
Mean T flipper and T foot were delineated by fitting polygons around each region of interest with the software Ther-maCAM™ Researcher Pro 2.10 (Flir systems, Wilsonville, Oregon, USA). Emissivity was set to 0.98. Mean T breast was extracted from a region just below the axilla, using a standardized square with length of side equal to the height of the distal flipper. We adjusted all images for variation in T a and measurement distance (which was always 1.1. m in the laboratory). For field measurements, distance was not measured in meters and, therefore, we derived a distance index by counting the number of pixels along a line fitted from the top of the head to base of the foot. A greater number of pixels indicated that an individual was closer to the camera.

Statistical analysis
For laboratory data, general linear mixed models (GLMMs) were used to model the initial temperature and the temperature change (i.e., final temperature-initial temperature; Year 2) for T cloacal , T flipper , T foot , and T breast , using thermal state (fully or partially hypothermic) and ambient temperature (T a ) as explanatory variables, and bird ID as a random factor. For these analyses, only data recorded during Year 2 were used, as birds were not measured in both states in Year 1 (above) and we were specifically interested in comparing temperature change within individuals.
For data collected in the colony, we used GLMMs to model separately T flipper , T foot , and T breast recorded as a function of time on land, distance (as indexed by pixel number; see above), and T a , wind index and cloud cover. Bird ID was used as a random factor to account for repeated measurements.
To compare rewarming patterns in the laboratory and in the colony, we first divided temperature data (for each tissue) into 2.5 min intervals between 0 ≤ t ≤ 5 min, and in 5 min intervals from 5 < t ≤ 25 min. To test if there was a delay, which we defined as the time necessary to measure a significant temperature increase compared to initial values, we then compared time-wise temperature differences for flippers, feet and breast between fully hypothermic birds in the laboratory (Year 1 and 2), partially hypothermic birds in the laboratory (Year 2), and free-ranging birds in the colony (Year 2) using GLMMs including T a , time interval, year nested in thermal state, the interaction between time interval and thermal state (nested in year), and bird ID as random factor. T cloacal , that was measured only in Year 2 in the laboratory, was compared between fully and partially hypothermic birds using a GLMM with T a , time interval and thermal state, and the interaction between time interval and thermal state, as explanatory variables and bird ID as random factor.
Statistical analyses were performed using JMP® v. 13 (SAS Institute Inc., Cary, North Carolina, USA). Results are presented as mean ± s.e. with capital "N" corresponding to the number of individuals and lowercase "n" to the total number of measurements. Non-significant parameters were excluded by backward elimination (Quinn and Keough 2002). A Student's t test was used to compare the significant difference between two groups, whereas a Tukey HSD post hoc was used to compare three, or more, groups.

Effects of internal temperature on surface rewarming-Group 1
In laboratory conditions during Year 2, all tissues reached a high stable temperature at the end of the experiment (mean of 37.3 ± 0.3 °C; 15.9 ± 0.8 °C; 12.5 ± 1.1 °C; and 19.1 ± 0.3 °C, respectively, in the cloacal, flipper, foot and breast areas). However, due to lower initial temperature in fully compared to partially hypothermic birds (Fig. 2), the measured body temperature change was greater in the fully hypothermic birds (Fig. 2).

Measurements in the colony-Group 2
In the colony, we observed a linear increase of T flipper , T foot and T breast with time on land (Table 2; all P < 0.001). Moreover, T foot and T breast , but not T flipper increased with increasing T a (Table 2). We also noted that T flipper , but not T foot and T breast , increased as measurements were closer (Table 2). There was no effect of cloud cover on any surface Fig. 2 Differences in initial temperature (left) and temperature change (i.e., final temperature-initial temperature) (right) in hypothermic (dark boxes) and normothermic (light boxes) birds measured in the second year of the study. The panels show: cloacal temperature (T cloacal ; a), flipper surface temperature (T flipper ; b), foot surface temperature (T foot ; c) and breast surface temperature (T breast ; d). Boxes show medians (white and black lines), and 1st and 3rd quartiles (upper and lower margins of the box). The whiskers extend to the 5th and 95th percentiles. Significance was assessed using a Student's t test post-hoc. The dashed line denotes no change in tissue temperatures. NS non-significant, **P ≤ 0.047 Table 1 Final models of temperature recovery as a function of thermal states in king penguins that rewarmed either in the laboratory (fully and partially hypothermic) or in the colony Data were analysed using general linear mixed effects models with bird ID as a random intercept, with separate models for each tissue. Post hoc tests were performed both between time intervals within thermal state (capital letters to the left of the vertical line) and or the thermal states within time intervals (lowercase letters to the right of the vertical line). Different letters denote significant (P < 0.05) differences temperature (P > 0.1), but we observed a significant negative relationship between T flipper and wind index ( Table 2).

Comparison of rewarming in the laboratory and in the colony
The increase in tissue temperature with time differed between thermal states (i.e., interval × thermal state: P < 0.0001) ( Table 1). There was also a significant positive effect of T a (p < 0.0001), and a strong positive effect of time interval (P < 0.0001) on all tissue temperatures and in all thermal states.

Recovery patterns within individual thermal states
In partially hypothermic birds, T cloacal maintained a stable normothermic value (38.0 ± 0.3 °C) with the 21 min measurement period ( Table 1). The fully hypothermic birds also recovered T cloacal , but this increase was delayed compared to the partially hypothermic birds (Fig. 2a). However, since we recorded the first T cloacal after 5 min (see Methods), we cannot fully compare the recovery pattern at the start of rewarming (Fig. 4a). T flipper in fully hypothermic birds did not increase within the first 5 min on land (Fig. 4b). In partially hypothermic birds, T flipper started to increased immediately, such that it was higher than in the fully hypothermic group after 5 min (Time interval 2.5-5 Table 1; Fig. 4b). T flipper in the colony increased only slightly, but non-significantly so, during the observation period (Fig. 4b).
T foot increased gradually in fully hypothermic birds (Fig. 4c). However, we did not observe any significant change in partially hypothermic birds measured in the laboratory, or in birds measured in the colony (Table 1; Fig. 4c).
T breast started to increase above baseline values only after 5 min on land (Fig. 4d). However, the increase was immediate in the partially hypothermic group, such that T breast was higher than in the fully hypothermic grouped after 2.5 min (Table 1). T breast then remained stable until the end of experiment in both groups (Fig. 4d). There was globally no change in T breast over the observation period in the colony (Table 1; Fig. 4d).

Time-wise differences in recovery patterns between thermal states
Fully hypothermic birds showed a significant lower initial T flipper until 5 min (i.e., a delay of 5 min) compared to the partially hypothermic group and penguins measured in the colony, with no difference between the latter two groups (Table 1; Fig. 4b). Moreover, we noted that at the end of the recovery, the final T flipper was similar in all thermal states (Time interval 20-25 Table 1; Fig. 4b).
T foot in penguins during recovery showed a similar pattern during the first 10 min in all years and thermal states (Table 1; Fig. 4c). The subsequent increase in T foot in fully hypothermic birds (Fig. 4c) resulted in a higher T foot than in the partially hypothermic group and penguins measured in the colony (Time intervals 15-20 and 20-25 Table 1; Fig. 4c).
T breast recorded in the laboratory was constantly higher than in the colony (Fig. 4d). Initial T breast was lower in laboratory during Year 1 than during Year 2 (Time interval 0-2.5 Table 1; Fig. 4d), but this difference disappeared after 2.5 min (Table 1). There was no difference in T breast recovery in fully and partially hypothermic birds (Time interval 20-25 Table 1; Fig. 4d).

Discussion
Our study revealed rapid vasodilation of the king penguin flipper after the return from the sea, though this was only observed when viewed at close proximity when the birds were allowed to recover from their hypothermic state indoors sheltered from the environment in the laboratory (Figs. 2b and 3). Rewarming of T breast followed a similar trajectory, although the thicker insulation covering this part of the body meant we could not image any vasodilation response (Fig. 3). Rewarming of T foot showed a more ambiguous pattern over our observation period, tending to increase only in the fully hypothermic laboratory birds (Figs. 2c and 4c). Our measurement of lower post-recovery T flipper compared to previous studies of king and emperor penguins (Aptenodytes forsteri) (Ponganis et al. 2003;Schmidt 2006) probably reflects the fact that we measured a wholly external temperature that was integrated over the full surface area of the flipper. This temperature is expected to be lower than the recordings from more proximally positioned, internal, sensors (Ponganis et al. 2003;Schmidt 2006). In line with this, maximum T flipper (26.7 ± 0.23 °C; Fig. S1) was well below internal flipper temperatures in previous studies (35-38 °C in Ponganis et al. 2003;around 38 °C in Schmidt 2006).

Effects of internal temperature on surface rewarming
Fully hypothermic birds (i.e., Group 1A), showed relatively large surface temperature changes during measurements (Figs. 2 and 4b-d). During the same time period, cloacal temperature also increased and had attained a stable value well before the end of measurements (Fig. 4a). In contrast, partially hypothermic birds showed a more moderate increase in surface temperature during the same experiment duration, likely because of the higher initial flipper temperature (Figs. 2b and 4b), with only minor changes in foot temperature (Figs. 2c and 4c). Cloacal temperature also increased in the partially hypothermic birds from the first measurement onwards (Fig. 2a), and had reached normothermia before the end of the observation period (Fig. 4a). This confirms that, in king penguins, rewarming of peripheral structures does not prevent recovery of internal temperature. However, according to our prediction, the fact that both flipper and breast temperature started to increase after a delay of 5 min in the fully hypothermic birds (Fig. 4b and d), suggests that low internal temperature modifies the peripheral recovery pattern, most likely because more heat needs to be produced before normothermia is reached. It could also be due to fact that lower internal tissue temperature delays peripheral rewarming when centrally produced heat is transferred through the body before reaching the appendages and body surface. Alternatively, this could indicate that preference is given to reducing heat loss to restore core temperature, but in that case, we probably would not expect a similar onset of rewarming in the two groups of birds.
Some birds maintained vasoconstriction in the flippers and feet during the observation period (Fig. S1). This flexibility of vasomotor states in the appendages, and their superficial vasculature (e.g., Fig. 3), highlight their roles as potential thermal windows. In contrast to studies on seals (Mauck et al. 2003), we did not observe any indication of similar thermal windows over the body trunk. This is expected, because the thick plumage that provides up to 80% of insulation in penguins Le Maho 1977) would leave little room for any meaningful circulatory adjustment of local body trunk temperature. Because we could not image the underlying vasculature, we also do not know if the observed increase in T breast reflected peripheral vasodilation, increased heat production in the underlying pectoral muscles (e.g., Hohtola 2012), or largely a consequence of drying plumage that would improve insulation and decrease evaporative cooling and, hence, reduce heat loss (De Vries and van Eerden 1995). It would be interesting to investigate this potential effect of changes to evaporation during recovery in future studies. Regardless of the mechanism involved, the high absolute T breast combined with the considerably larger surface area of this part of the body compared to that of the appendages, means that the body trunk makes a major contribution to overall heat exchange with the environment, as is also known in the related emperor penguin (McCafferty et al. 2013).

Comparison of rewarming in the laboratory and in the colony
Free-ranging birds in the colony showed very slight rewarming of peripheral regions (Fig. 4), which contrasts with the laboratory results. We do not believe that the different rewarming patterns in the laboratory were entirely a consequence of a thermoregulatory response to capture and handling. For example, if increased T cloacal was caused by stress from repeated handling in the laboratory (e.g., Cabanac and Guillemette 2001), we would not have expected this temperature to stabilize in fully hypothermic birds by the end of the observation period and then to remain relatively stable until the start of the second trial (Fig. 4a). This response was qualitatively similar to that recorded by abdominally implanted temperature sensors in king penguins that were handled in the same way but then left to recover to normothermia in an unrestrained state without human disturbance during 2 h (Lewden et al. in press). There was also no further change in T flipper for about 1 h after the end of handling, neither in birds that rewarmed from hypothermia nor in birds that were captured and handled in a similar way when they were already completely dry and in a presumed normothermic state in the colony (Fig. S2). Had the initial increase in Table 2 Effects of time on land, distance, T a , wind index and cloud cover on T flipper , T foot and T breast surface temperatures in free-ranging king penguins measured in the colony starting immediately upon their return to land after a foraging trip at sea Data were analysed using general linear mixed effects models with bird ID as a random intercept, with separate models for each tissue Year 2: filled squares and solid line), partially hypothermic (light squares and dashed line) and free-ranging birds (filled triangles and solid line). Mean temperatures were calculated by averaging temperatures measured between 00:00 and 2:30 min for the first interval, between 2:31 and 5:00 min for the second interval, between 5:01 and 10:00 min for the third interval, and so on. Results from post hoc comparisons between intevals within thermal states, and between thermal states within intervals, are presented in Table 2 Time on land (min) T flipper indeed been a thermoregulatory response to reduce core temperature after the acute stress response (Briese and Cabanac 1991;Cabanac and Guillemette 2001), we may have expected reversal to a lower baseline starting at the end of handling (Herborn et al. 2015). Finally, there was no effect of activity score on rewarming patterns (see "Materials and methods" section), and we observed that several individuals fell asleep during measurements. This suggests that stress-induced activity metabolism was not obvious. Hence, we do not believe that the recovery pattern measured in the laboratory was driven by the stress of capture, even though it could explain some difference between free-ranging and laboratory birds. Differences between the groups could instead be attributed to differences in the physical environment between the laboratory and the field, manifested e.g. in faster drying of the plumage in the laboratory and consequent higher initial T breast compared to in the colony (Fig. 4d). In line with this, the non-insulated body parts (flippers and feet) showed no difference in initial temperature between the two conditions ( Fig. 4b and c). If variation in the physical environment indeed increased the overall rate of heat transfer in the colony (cf. Gates 1980;Monteith and Unsworth 2013), it is possible that the lack of peripheral rewarming when birds were measured in the free-ranging condition is consistent with vasoconstriction of peripheral and/or poorly insulated structures to avoid excessive heat loss until internal temperature has recovered. To elucidate this possibility, it would be interesting to compare the recovery rates of core and subcutaneous temperatures in free-ranging birds with implanted loggers. Future studies should also aim to extend our experimental protocol by studying rewarming rates in fully hypothermic and partially hypothermic penguins that are allowed to recover in a range of controlled environmental temperatures. Environment (SCENE), University of Glasgow, to undertake thermal image analyses. Funding was also received from the Institut Polaire Français Paul-Emile Victor and by the Centre National de la Recherche Scientifique (CNRS-INEE) (project no. 394). Logistic support in the field was provided by the Terres Australes et Antarctiques Françaises (TAAF). A.L. was the recipient of a scholarship from the French Ministere de l'Education National, de la recherche et de la technologie. A.N. was supported by the Birgit and Hellmuth Hertz Foundation / The Royal Physiographic Society of Lund (grant. no. 2017-39034). The experiment was approved by the French Ethics Committee (APAFIS, permit no. 02015041411414001) and the French Polar Environmental Committee (permit nos. 2014-375 2015-2495).
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