When does bearing magnets affect the size of deflection in clock-shifted homing pigeons?

Pigeons whose internal clock is shifted by 6 h show deflections from the direction of untreated controls, yet these deflections are often smaller than predicted. Magnets temporarily disabling the magnetic compass increased these the deflections significantly (R. Wiltschko and Wiltschko 2001), indicating a compromise between sun compass and magnetic compass. – Recently, Ioalé et al. (2006) claim that they could not replicate our findings. The reason lies in a difference in the behavior of the clock-shifted pigeons without magnets: in the study of Ioalè et al. (2006), their deflections was already almost as large as that of our pigeons carrying magnets. This difference is probably caused by the limited experience of the pigeons of Ioalè et al. (2006): Their birds, in contrast to ours, had not used their sun’ compass during extended homing flights at various times of the year and, not having been faced with the necessity to compensate the saisonal changes of the sun’s arc, gave the sun compass more weight than our birds did.A comment to the paper by Ioalè, Odetti and Gagliardo (2006) Behav Ecol Sociobiol 60: 516–521.     

The development of sun compass orientation in young homing pigeons

Summary A series of clock-shift experiments with young homing pigeons of various ages was performed to determine at what age they normally learn sun compass orientation. The response of untrained pigeons to shifting of their internal clock seems to depend on their age. When the clock-shifted birds were tested at an age of 11 weeks and younger, their departure bearings did not differ significantly from those of controls (Fig. 1, diagrams on the right); in tests with birds 12 weeks and older the characteristic deviation indicating the use of the sun compass was observed (Figs. 2 and 3). Birds that had participated in a short training program, however, used the sun compass at 8 weeks, the earliest age tested (Fig. 1, diagrams on the left). These findings show that the time of development of the sun compass strongly depends on flying experience. Within the first months of a bird's life, it seems to take place after the bird has been confronted with the need to orient, either spontaneously during extended exercise flights around its loft or imposed by training releases.The departure bearings of the very young, inexperienced birds that did not rely on the sun compass, however, were already oriented homeward. This indicates that the ability to navigate develops independently of the sun compass, before the sun compass is learned.Dedicated to Prof. Dr. F.W. Merkel for his 70th birthday     

Re-orientation in clock-shifted homing pigeons subjected to a magnetic disturbance: a study with GPS data loggers

Some authors have proposed that homing pigeons are able to correct the error in orientation following a phase-shift treatment by using the magnetic compass reference. They reported that clock-shifted pigeons bearing magnets display a greater deflection compared to magnetically unmanipulated clock-shifted birds. However, this hypothesis tested by recording pigeons’ vanishing bearings has led to contradictory results. The present study reports pigeons’ tracks recorded with a GPS and shows that clock-shifted pigeons bearing magnets displayed a greater deviation through the whole route compared to the magnetically unmanipulated shifted pigeons. Moreover, the analysis of the tracks shows that the birds belonging to both experimental groups stop in coincidence with their subjective night. When re-starting their journey, the birds corrected the clock-shift induced error in orientation, but the magnetically manipulated pigeons were less efficient in doing so. Our results are consistent with the hypothesis that homing pigeons released from unfamiliar location re-orient after clock shift by using the magnetic compass.     

Do bearing magnets affect the extent of deflection in clock-shifted homing pigeons?

When released after clock-shift, homing pigeons fail to orient towards the home direction but display a consistent deflection of their initial orientation due to the difference between the real sun azimuth and the computed azimuth according to the subjective time of each single bird. It has been reported that the size of the observed deflection is frequently smaller than expected and a discussion on the possible factors affecting the size of deflection has emerged. Some authors have proposed that the major factor in reducing the deflection after clock-shift is the simultaneous use of both the magnetic and the sun compasses, giving true and erroneous information, respectively, about the home direction. Therefore, a magnetic disturbance, by impeding the use of the geomagnetic information in determining the home direction, is presumed to increase the size of the deflection up to the levels of the expectation. To test this hypothesis, we released three groups of clock-shifted birds from unfamiliar locations (unmanipulated pigeons, pigeons bearing magnets on their head, and pigeons bearing magnets on their back) together with a group of unshifted control birds. As no difference in the orientation of the three groups emerged, we were not able to confirm the hypothesis of the role of the magnetic compass in reducing the expected deflection after clock-shift.Communicated by W. Wiltschko     

Pigeon homing: sun compass use in the southern hemisphere

Although the sun compass of birds is based on learning the sun's arc during development, it was unclear whether birds can use the sun when its apparent movement is reversed, in particular, whether northern birds that have been introduced into the southern hemisphere can use the southern sun. To answer this question, clock-shift experiments were performed with local homing pigeons in Auckland, New Zealand (37°S). In three fast-shift tests and two slow-shift tests, the experimental birds showed deflections from the untreated controls that were the mirror images of those observed in the northern hemisphere. These results clearly show that homing pigeons in New Zealand use a sun compass that is adapted to the situation in the southern hemisphere. The learning processes establishing the compensation mechanisms thus appear to be free of constraints concerning the direction of the sun's movement. Differences from recent findings with migratory birds, where the direction of celestial rotation proved of crucial importance for establishing the migratory direction, are discussed: the differences may arise from the different orientation tasks, in particular, from the involvement of innate information in establishing the migratory direction. Received: 13 November 1997 / Accepted after revision: 28 February 1998     

Navigational strategies of homing pigeons at familiar sites: do landmarks reduce the deflections induced by clock-shifting?

To analyze the navigational strategy of homing pigeons at familiar sites in view of a possible role of local landmarks, two groups of pigeons—one familiar to the release site, the other unfamiliar—were released with their internal clock shifted 6 h fast, with untreated birds of both groups serving as controls. The two groups showed median deflections of 67% and 57%, respectively, of the expected size, with no consistent difference in the size of the deflection between familiar and unfamiliar birds. This clearly shows that familiarity with the release site and with the local landscape features does not affect the size of the deflections induced by clock-shifting. Obviously, pigeons familiar with the release site do not change their navigational strategy, but still continue to determine their home course solely as a compass course. General problems with orientation by landmarks are discussed; however, landmarks may help birds to recognize a site and recall the respective course.

---

The effect of a “permanent” clock-shift on the orientation of experienced homing pigeons

Summary A group of experienced homing pigeons vas subjected to a 6 h slow shift of their internal clock and kept under these conditions for more than 2 months. During the overlap time between the natural and artificial photoperiods they were released for training flights to familiarize them with an area while living in a permanent shift.Tested outside the permanent shift training range, the experimentals always deviated about 30° clockwise from the mean of their controls, markedly less than in a regular 6 h slow shift. Inside the permanent shift training range, however, they oriented like the controls (Fig. 2). When their internal clock was returned to normal, the birds showed a larger counterclockwise deflection on their first flight, which was roughly comparable to the effect of a regular 6 h fast shift (Fig. 3). On later flights after normalization, this large shift was no longer found; instead we observed a roughly 30° counterclockwise deflection when they were released inside the permanent shift training range in the morning. This deflection did not seem to occur in the afternoon or outside the permanent shift training range (Figs. 4, 5), and it disappeared when the birds were repeatedly released from the same site (Fig. 6).The occurrence or non-occurrence of the deflection was independent of the duration of the shift or the time passed after normalization; it seemed to depend solely on whether the birds had become familiar with a given site in the situation of the permanent shift. This argues against an effect based on the sun compass. We tend to assume that the still unknown navigational map is involved. In this case, however, as the deflection is independent of the home direction and the type of release site bias, the factors in question would act very differently from the gradients on which the traditional concepts of the navigational map are based. The processes establishing and updating the map and their possible differences are discussed.Died on August 17, 1980     

A comparison of sound propagation and song frequency in temperate marsh and grassland habitats

Summary Attenuation of pure tones was measured in marsh and grassland habitat. At surface level, in grassland, the ground effect strongly attenuated frequencies below 2.0 kHz (Fig. 2). The ground effect was reduced by increasing source-receiver elevation. In marsh habitat the ground effect did not occur, and low frequencies were optimal for sound propagation (Fig. 3). As predicted from sound propagation tests, analysis of recorded songs of seven grassland and six marsh species indicated that minimum and emphasized frequency were significantly lower in songs of marsh birds. Maximum frequency did not differ between habitats (Table 4). Buzzing songs of yellow-headed blackbirds were broadcast and re-recorded at 1 and 50 m from the speaker in marsh and grassland habitats. Low frequency components attenuated more rapidly than higher frequency components in grassland, and the reverse occurred in marsh. Results suggested that the ground effect restricts the use of low frequencies by grassland birds. This evidence is consistent with the sound window hypothesis of Morton.     

Magnetic compass orientation in the yellow-faced honeyeater,Lichenostomus chrysops,a day migrating bird from Australia

Summary In Australia, the southern populations of the yellow-faced honeyeater, Lichenostomus chrysops (Meliphagidae), perform annual migrations, with routes following the eastern coastline. In order to assess the role of magnetic cues in the migratory orientation of this diurnal migrant, its directional behaviour was recorded in recording cages under natural and experimentally manipulated magnetic-field conditions. During autumn the birds tested indoors in the local geomagnetic field showed a directional change from north initially to northwest later in the season (Fig. 1 a, b), which corresponds well with the general pattern of movement of this species in the field. Deflecting magnetic north to ESE resulted in a clockwise shift of the mean direction by 77° and 71°, respectively (Fig. 1 c, d), while no significant directional tendencies were observed in a magnetic field with a compensated horizontal component (Fig. 1 e, f; see Table 1). In outdoor tests in spring, the birds preferred southerly directions when tested in the local geo-magnetic field. In a magnetic field with a reversed vertical component (i.e. with an inclination pointing down instead of upwards) the birds reversed their directional tendencies and oriented northward (Fig. 2, Table 2). These results clearly show: (1) that yellow-faced honeyeaters can use the magnetic field for direction finding, and (2) that their magnetic compass functions as an inclination compass, as has been shown for several holarctic migrants.Correspondence to: W. Wiltschko     

The magnetic compass mechanism of birds and its possible association with the shifting course directions of migrants

Summary Many birds of the northern hemisphere shift their migratory course to more southerly directions when moving from northern to southern latitudes. Birds from Central Europe, for example, change their course from SW to S or from SE to S respectively (Fig. 1). This also seems to apply to some other animals.The hypothesis presented here explains the observed shifts in migratory direction on the basis of changes in the parameters of the earth's magnetic field and hence would make a genetic fixation of shifts in the migratory direction unnecessary.To determine the direction of migration birds do not refer to the polarity of the magnetic field but to its dip (=). According to the hypothesis presented here, the birds, however, do not refer to the direction of dip as previously believed but to the individual apparent angle of dip (=), this angle changes depending on the heading of the bird (see Fig. 3 and Eq. 1). Maintaining a species specific or population specific the bird will move in its predetermined migratory direction. Changes in the dip of the earth's magnetic field correspond to changes in latitude. According to the hypothesis with fixed, the migratory direction will change when the dip changes. Given the hypothesis and the parameters of the earth's field theoretical migratory paths of birds between summer and winter quarters may be calculated (Figs. 8–11). The calculated tracks and the actually observed migratory routes agree well. This is also confirmed by radar and other observations of migratory directions in areas of different dip angles (Fig. 13). Displacing migrating birds to areas of smaller dip angles (= lower magnetic latitudes) results in predeterminable shifts in the birds migratory direction (Figs. 5, 6). The hypothesis also accounts for the so far unexplained orientation behaviour of transequatorial migrants under the magnetic equator.A very simple model of this hypothetical compass mechanism may be based on the assumption of the sensor axis is supposed to correspond to the apparent angle of dip when moving in the migratory direction. In this position the difference between the apparent angle of dip and the angle of the sensor is zero. Any change in the direction of movement, however, will result in a difference leading to a response of an assumed receptor. When maintaining the zero difference the bird invariably sticks to its migratory course. The proposed mechanism is a null instrument unaffected by changes in field intensity and not depending on the measurement of absolute values.     

Orientation of juvenile barn swallows (<Emphasis Type="Italic">Hirundo rustica</Emphasis>) tested in Emlen funnels during autumn migration

Although hirundines have been used extensively in homing experiments, to date no investigation of their migratory orientation has been carried out, despite the well-known migratory habits of many species of this family. This paper reports on a study of the orientation of the barn swallow (Hirundo rustica), a typical diurnal trans-Saharan migrant. Modified Emlen funnels were used to verify the suitability of this species for cage experiments and investigate the role of visual and magnetic cues during the birds first migratory journey. Juvenile swallows were mist-netted at a roost site in central Italy and then tested in a site 19 km apart. Orientation experiments were performed under four experimental conditions: natural clear sky and simulated overcast, in both local and shifted magnetic fields (magnetic North=geographical West). Under clear sky, the swallows tended to orient phototactically toward the best-lit part of the funnel and failed to respond to the magnetic field shift. Under overcast conditions, they oriented northward and modified their directional choices as expected in response to the shifted magnetic North. On the whole, our data indicate that swallows can use magnetic information for compass orientation. Possible explanations for the northward orientation of birds tested under overcast conditions are discussed.Communicated by W. Wiltschko     

Sunset and the orientation of a nocturnal bird migrant: A mirror experiment

Summary If savannah sparrows, (Passerculus sandwichensis), a North American night migrant, select a migratory heading based upon the setting sun, a shift in the position of that cue should produce a predictable shift in the migrant's nocturnal orientation. I tested this hypothesis by shifting the sunst position with mirrors and by recording the bird's orientation in Emlen funnels. The control group displayed directionality appropriate for spring migration (=342°). The mean heading of experimentals (=272°), which were exposed to a cue-shifted situation, was in the expected westerly direction relative to the control mean (P<0.05, V-test). The setting sun appears to be a sufficient source of directional information for this avian migrant.     

Interaction between solar orientation and landscape visibility in Talitrus saltator (Crustacea: Amphipoda)

A series of experiments on the littoral amphipod Talitrus saltator (Montagu) was carried out between April and September, 1978–1981, both under natural conditions and inland with artificial landscapes of different heights on the horizon, in order to assess the visual importance of the landscape in zonal orientation in populations from the Mediterranean coast, and to determine interactions between solar orientation and orientation based on the landscape. Inland, orientation in controls (permitting only vision of the sky and the sun) was compared to that of the experimental individuals, who could see a simulated landscape positioned landwards to them and seawards. In nature, sandhoppers released in a level arena with the landscape screened from view were compared with others released in an unscreened arena and on the sand in absolutely natural conditions. Situations where solar orientation contradicted local cues were produced both by releasing the sandhoppers on a shore diversely orientated to their own, and by shifting their internal clock by nine hours. Results show that T. saltator uses the landscape as a cue in its orientation towards the sea, in conjunction with solar orientation: the latter being the principal factor involved even when the sandhoppers are separated from the local optical factor in the sky (in trials at a distance from the sea). In fact, with the artificial landscape set seawards, none of the populations we studied showed any orientation based on the landscape comparable in accuracy to orientation based exclusively on the sun. From the experiments carried out in natural conditions, it is possible to deduce that conflicting conditions gave rise to two types of results: deviation from the mean direction and an increase in dispersion, up to total dispersion when the local factors were in total contrast to solar orientation (clock-shifted sandhoppers released on the sand).     

Detour experiments with homing pigeons: information obtained during the outward journey is included in the navigational process

Summary To test the hypothesis that information on the route of the outward journey is involved in the orientation of displaced homing pigeons, we compared the behavior of control pigeons that had been displaced by the most direct route with that of experimental pigeons that had been transported along detours to the same release sites. At distances of 40 km we found no consistent effect. At distances between 75 and 130 km, however, deviations to the left of the direct route induced deflections to the left, while deviations to the right induced deflections to the right, i.e. the deflections of the vanishing bearings tended to compensate for the initial detour of the outward journey. The deflections were smaller than the deviations of the routes; they were not related to the routes themselves or the location of the release sites. A significant correlation emerged with the vector length of the controls, as longer vectors were associated with smaller deflections. This suggests that information on the route of the outward journey is used together with local map information in the navigational process, the significance of the route-specific information apparently depending on quality and reliability of the available local information. The nature of factors controlling the detour effect is still open.Correspondence to: R. Wiltschko     

Contribution of olfactory navigation and non-olfactory pilotage to pigeon homing

Summary By means of training flights (mostly flock releases), two groups of young homing pigeons were made familar with a larger area asymmetrically extending from the loft toward SW and NE, respectively. Thereafter, birds of both groups were released within each of the training areas with which one sort of birds was familiar (F⁺), the other unfamiliar (F^-). Even the F⁺ pigeons had never been released at the test site itself (nearest previous release 10 km apart). Half of each group was allowed to smell environmental odors (O⁺); the other half breathed charcoal-filtered air during transportation and at the release site until a few minutes before release when they were deprived of olfaction by intranasal application of Xylocain (O^-). The two test sites were 53 km distant from home. There was little difference in initial orientation as well as in homing performance between pigeons that were allowed to smell natural air and were familiar with the area (F⁺O⁺) and those that were privileged in only one respect (F⁺O^- and F^-O⁺). Yet if none of the preconditions was met (F^-O^-), performances were drastically reduced. The findings show that pigeons make use of two independent homing methods, olfactory navigation (presumably based on a navigational map) and non-olfactory pilotage (presumably based on a topographical map). The latter method is restricted to a more or less familiar area determined by individual experience. Its boundaries are poorly defined and can be estimated by the experimenter only in rough approximation. Within this area, the homing system takes advantage of more or less redundant inputs. Outside of it, olfactory information seems indispensable.     

Calibration of the sun compass by sunset polarized light patterns in a migratory bird

Summary Migrating birds derive compass information from the sun, stars, geomagnetic field and polarized light, but relatively little is known about how these multiple sources of directional information are integrated into a functional orientation system. We found that migratory warblers exposed to a rotated polarized light pattern at sunset oriented at a constant angle to the axis of polarization. When polarized light cues were eliminated, this shifted orientation was maintained relative to the setting sun. Polarized light patterns, thus, appear to provide a calibration reference for the sun compass in nocturnal migrants, and may also play a role in calibrating other compass systems. Correspondence to: J.B. Phillips     

Sunset orientation of robins,Erithacus rubecula,with different fields of sky vision

Summary Migratory orientation of robins (Erithacus rubecula) at sunset was recorded using orientation cages, under clear autumn skies. The aim of the experiments was to examine the importance of different visible sky sections for the orientation of robins. I obtained the following results: (1) Robins tested with the visible sky section limited to 90° around zenith (45° above the horizon) showed a mean orientation that coincided with the average sunset azimuth, with little scatter around the mean angle (Fig. 2). (2) When the birds were allowed a more extensive field of sky vision (maximum 160°), they chose headings on an approximate north-south axis, significantly different from tests with a restricted view of the sky (Fig. 3). (3) Experiments were also performed in which the response of robins to a mirror deflection (about 120° counterclockwise) of visual cues in the lower parts of the sunset sky was examined. The outcome indicated that visual information in the lower part of the sky may be critical for the orientation of robins (Fig. 5). These results, together with recent findings that robins captured and tested at two nearby sites show distinctly different orientation behavior in relation to experimental manipulations of the magnetic field, suggest that priorities among orientation cues may differ depending on the migratory situation encountered.     

Migratory orientation of red-eyed vireos,Vireo olivaceus,in relation to energetic condition and ecological context

How and when migrants integrate directional information from different sources may depend not only on the bird’s internal state, including fat stores, but also on the ecological context during passage. We designed experiments to (1) examine the influence of stored fat on the decision to migrate and on the choice of migratory direction and (2) investigate how the integration of orientation cue information is tied to energetic status in relation to migration across an ecological barrier. Migratory orientation of red-eyed vireos (Vireo olivaceus) at twilight was recorded using two different techniques, orientation cage experiments and free-flight release tests, during both fall and spring migration. During fall migration, the amount of stored fat proved decisive for directional selections of the vireos. Fat birds chose directions in accordance with migration across the Gulf of Mexico. Lean birds oriented either parallel to the coast line (cage tests) or moved inland (free-flight releases). Whereas only fat birds showed significant responses to experimental deflections of the geomagnetic field, lean birds displayed a tendency to shift their activity in the expected direction, making it difficult to evaluate the prediction that use of the magnetic compass is context dependent. Fat loads also had a significant effect on the decision to migrate, i.e., fat individuals were more likely to embark on migration than were lean birds (true for both cage and release experiments). During spring migration, a majority of experimental subjects were classified as lean, following their arrival after crossing the Gulf of Mexico, and oriented in seasonally appropriate directions. The vireos also showed significant responses to experimental deflections of the geomagnetic field regardless of their energetic status. Free-flight release experiments during spring migration revealed a significant difference in mean directions between clear sky and overcast tests. The difference may indicate a compensatory response to wind drift or possibly a need for celestial cues to calibrate the magnetic compass. Finally, this is the first demonstration of magnetic compass orientation in a North American vireo. Received: 15 December 1995/Accepted after revision: 24 March 1996     

Parental care of nestlings by male red-winged blackbirds

Summary Nestling feeding by males is less common among birds with polygynous mating systems than in monogamous species, because of the pronounced trade-off between parental behavior and the attraction of additional mates. In this study, however, we found that male red-winged blackbirds (Agelaius phoeniceus) commonly assisted females in feeding nestlings in several Ontario marshes. Male parental care was additional to that provided by females, and it significantly enhanced the fledging success of nests (Table 2). Male redwings did not help to feed all nests on their territories: primary and secondary nests were much more likely to receive male parental care than tertiary and later nests. Contrary to expectation, male parental care was not restricted to the nests of primary females: a greater proportion of secondary than primary nests were assisted (Tables 4a and b). The presence of new females settling on the territory at the same time that a resident female had nestlings, resulted in males deferring parental care until a later brood. This suggests that males trade off the recruitment of females against parental care to an existing brood. Although the number of nestlings fledging from a male's territory was strongly influenced by the number of females in the harem, males could additionally increase their reproductive success by feeding nestlings in one or more nests on their territories (Fig. 2). The reproductive success of females was significantly enhanced by male assistance in feeding nestlings (Table 3). However, those females not receiving male assistance on territories of feeding males did not suffer a significantly reduced reproductive success in comparison to females on territories of non-feeding males (Table 2). Males varied considerably in the quality of brood care given. We therefore suggest that the quality of male parental care may be a factor considered by females in choosing a breeding situation.     

The “dawn chorus” and incubation in the coot (Fulica atra L.)

Summary It has been proposed that both acoustic and non-acoustic factors could explain the dawn peak of territorial advertisement in birds. The coot is a territorial waterbird which does not use vocal advertisement either to attract mates or defend territory boundaries. In spite of the absence of acoustic factors affecting the time budgeting of advertisement, this species shows a dawn peak of display and aggressive behaviours. This trend occurs both in the presence and absence of non-territorial prospecting birds, but the trends are quantitatively different in these two cases (Fig. 1). Males participate in display and fighting more often than females, probably because of their greater size and effectiveness in defence. This asymmetry in defence abilities governs the time budgeting of incubation, the male tending to take time off the nest when territorial defence is most necessary (Fig. 2).