Can pigeons be fooled about the actual release site position by presenting them information from another site?

Summary The aim of the experiment was to test the hypothesis that pigeons depend on route- and/or site-specific airborne parameters to establish their position relative to the loft. Pigeons were transported to the release site with free access to the environmental air. They were then enclosed in large airtight containers filled with air from the release site and either transported via the loft to a release site in the opposite direction with respect to the loft (experimental birds) or via the loft back to the same site (control birds). Before release the pigeons (still inside the containers) were made anosmic by a local anesthetic applied to the olfactory membranes through the nostrils. Vanishing bearings of experimental birds were on the average in a direction opposite to home while the vanishing bearings of control birds were homeward oriented. For this initial orientation the pigeons seem to rely on airborne cues obtained at a site where they last had access to ambient air or cues obtained from the air inside the sealed containers. Irrespective of the treatment the bearings pooled with respect to north still show a residual orientation to the NE. There was no difference either in the homing speeds or in the homing times of anosmic control and experimental pigeons. We therefore have to assume further mechanisms guiding the pigeons home in addition to a possibly olfactory one.     

Pigeon homing: new airbag experiments to assess the role of olfactory information for pigeon navigation

Summary In three series of experiments we assessed the effects of olfactory and non-olfactory information collected en route or at the release site on the initial orientation of homing pigeons. In the first experiment, pigeons were transported in open crates to two sites located in opposite directions from the home loft. They were left at the site for 1 h, then put into airtight containers filled with air from that site and brought back to the loft. From there, controls were transported back to the original site. Experimentals were transported to the opposite site. Upon arrival at the site, the olfactory mucosae of both groups were anesthetized with Gingicain. Thus in this experiment, control and experimental pigeons were exposed to different olfactory as well as to different non-olfactory information during displacement and at the site. In the second series, controls and experimentals were treated as in the first experiment, except that they were enclosed in the airtight containers at the very beginning of the experiment and were ventilated with synthetic air until arrival at the final release site. This treatment excluded the possibility to perceive olfactory information en route or at the site. In this series, the two groups differed only with respect to non-olfactory information perceived during displacement and/or at the release site. In the third series, we exposed pigeons at the loft to air collected either at the later release site (controls) or to air collected at a site located in opposite direction of the home loft (experimentals). Here the two groups differed only with respect to their exposure to air of different origin. In all three series, the pooled controls showed a directional preference that was statistically indistinguishable from the home direction. All three experimental groups were disoriented. In the first two series, the differences in the initial orientation of control and experimental pigeons were highly significant. In the third experiment, there was only very weak statistical evidence for a difference between controls and experimentals. These results suggest that more than one factor is involved in the pigeons' navigation system. According to the present experiment with synthetic air, pigeons probably gather and process non-olfactory information during the first part of their transport from the home loft to the release site. Thus, some kind of, in this case non-olfactory, route reversal seems to be involved in the homing process. In addition, the experiment involving only manipulations of airborne information indicated some olfactory component. Previous experiments at our loft did not result in disorientation of the pigeons if either only the access to airborne information had been removed or when otherwise unmanipulated pigeons had been transported in detours to the final release site. Therefore, we assume that our pigeons' navigation system relies on several cues. Deletion of one cue can be compensated by other information. Often the initial orientation of our pigeons is disturbed only when at least one cue is removed and another one provides false information.     

Pigeon homing: Olfactory orientation—a paradox

Summary In order to find out whether the different ways that pigeons are raised and maintained at the various lofts affect their orientation behavior, especially the selection of navigational factors, a group of birds was raised according to the procedures of our Italian colleagues in a wind-exposed loft on the roof. The behavior of these R-birds was then compared with that of G-birds living in a garden loft, raised and trained according to the normal Frankfurt procedure. When R-birds were made anosmic by closing the nostril with cotton during transportation and a local anesthetic was used at release, their reaction was similar to that of Italian pigeons: the deviation of their vanishing bearings from the home direction increased significantly, leading to a marked decrease in homeward orientation. In contrast, the orientation of the anosmic G-birds did not differ from that of their controls; their directional selections agreed with those of the controls of the R-group. These data indicate that the conditions of raising and maintaining homing pigeons may be of crucial importance in determining the pigeons' attitude toward olfactory input. Finally, olfactory orientation is discussed; the paradoxical finding that the G-birds, not using olfaction, oriented like the controls of the R-group that did use olfactory input, leads to the question of whether olfactory input really conveys navigational information to the birds.     

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     

Correct and false olfactory orientation of homing pigeons as depending on geographical relationships between release site and home site

Summary Pigeons from two German home sites were released at a site near Mantua in northern Italy. The home sites, Andechs and Würzburg, are 303 and 508 km north of the release site, respectively. Not only the initial bearings but still more the distributions of recoveries after a longer flight distance (median 65 km) were very different in pigeons from these two lofts. While the majority of the Wurzburg birds were found north of the release site, almost all birds from Andechs were found south of it (Fig. 1). Pigeons from both lofts, if made anosmic by sectioning the olfactory nerves, showed no average tendency towards change of latitude. These findings strongly suggest that both correct and false positional information were deduced by the birds from olfactory inputs. A coherent (though very hypothetical) interpretation of these and earlier results is based on regularly varying proportions of chemical tract compounds in the atmospheric boundary layer over the Alps and adjacent regions (Fig. 4).     

Short-term residence in deflector lofts alters initial orientation of homing pigeons

Summary A modification of the deflector-loft technique first outlined by Baldaccini et al. (1975) is presented in which experienced homing pigeons that do not permanently reside in deflector lofts were housed in them for periods of 7–20 days. Upon release these birds consistently exhibited a deflection of mean vanishing bearings in the directions predicted by the olfactory hypothesis of pigeon homing. Two potential explanations for this short-term deflector-loft effect are suggested. One is that the olfactory map sense of homing pigeons is very flexible and capable of accurate readjustment in as short a period as seven days. Alternatively, it may be that nonolfactory cues are being altered by the deflector lofts in such a way as to result in behavior by pigeons that is consistent with the olfactory hypotheses. The short-term technique has the practical benefit of making it possible to conduct far more experiments in a single field season than was possible with the original deflector-loft method.     

Pigeon homing: Different effects of olfactory deprivation in different countries

Summary This study compares the orientation of untreated pigeons and pigeons subjected to olfactory deprivation at two lofts near Pisa, Italy, at a loft at Ithaca, New York, USA, and at a loft at Frankfurt a.M., FRG. The experimental birds were rendered anosmic by nasal plugs until Gingicain, a local anaesthetic, was applied shortly before release. The Italian and American control pigeons appeared to orient towards home equally well, while the control pigeons in Germany frequently preferred directions that deviated significantly from the home direction. The effect of olfactory deprivation was small in the USA and in Germany; it was significantly larger in Italy, indicating that Italian pigeons depend on olfactory information to a much greater extent. These findings suggest that there are important regional differences in the strategies and cues pigeons use to navigate. The varied roles of olfactory information, and the reasons for these differences are discussed.     

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.     

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.     

Bird orientation: Single homing pigeons compared with small flocks

Summary The hypothesis that bird flocks orient more accurately than single individuals was tested on homing pigeons. Birds were released both singly and in flocks of three to six. Vanishing bearings were recorded and it was found that flocks were less scattered around the mean direction than singly released birds. Homing times were found to be shorter for flocks as compared to singles. This suggests that the average homing pigeon can gain in directional accuracy and save energy by joining other pigeons heading for the same goal.     

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     

Homing pigeons do extract directional information from olfactory stimuli

Summary Two groups of pigeons were kept from fledging time in two cages fully exposed to winds. From time to time, the cage containing experimentals was additionally exposed to an artificial air current coming from a specific direction and carrying a scent of benzaldehyde. When both groups were exposed to benzaldehyde scent during transportation and at the release site, the control birds flew homeward, whereas the experimentals oriented in the direction roughly opposite that from which they were used to perceiving the benzaldehyde at the loft. When benzaldehyde was not applied, experimental pigeons were homeward oriented like controls.     

Pigeon homing: a comparison between groups raised under different conditions

Summary The homing ability of a group of pigeons raised under conditions of continuous exposure to windborne information was compared to that of another group subjected to exposure to winds only during the time spent in pre-test training flights. The results of release experiments at sites that were unfamiliar to the pigeons show that both bird groups, which had been made temporarily anosmic, had impaired initial homeward orientation and homing ability. These results, which do not entirely concur with the recent findings of Wiltschko and his coworkers, show that the raising and training procedures we used do not influence the nature of the cues used in pigeon homing. If the exposure of birds to wind-borne information is reduced, this does not bring into play any effective non-olfactory mechanisms of navigation; it simply hinders the development of the olfactory map and impairs the homing ability. Offprint requests to: S. Benvenuti     

Initial orientation of homing pigeons at the magnetic equator with and without sun compass

Summary To test the present hypotheses concerning the functioning of the bird's magnetic compass, pigeons reared near the magnetic and geographic equator (Fortaleza, NE Brasil) were released 300 km NW of their home in the horizontal field at the magnetic equator. Pigeons released in the morning and in the afternoon were roughly homeward oriented whereas pigeons released at noon with the sun near the zenith vanished close to magnetic north. According to the Wiltschko model of the magnetic compass they should not be able to pick up specific directions. A considerable number of young and inexperienced pigeons returned home against a continuously blowing trade wind. This result contradicts the hypothesis of olfactory navigation as currently discussed.     

Further experiments on olfactory navigation and non-olfactory pilotage by homing pigeons

Summary Supplementary to a previous investigation (Wallraff and Neumann 1989), further experiments were conducted with homing pigeons that were either familiar of unfamiliar with the release area, and that had or lacked olfactory access to environmental odours. All four possible pairwise combinations of these factors were tested. The previous results were confirmed, showing that in an unfamiliar area olfactory inputs are necessary for home-related orientation, while in a familiar area both olfactory and non-olfactory information can be utilized and each is more or less redundant as long as the other kind of information is also available. The degree of redundancy of olfactory inputs varies, obviously depending on the pattern of individual local experience. Correspondence to: H.G. Wallraff     

Effects of the Resolution and Kinematics of Olfactory Appendages on the Interception of Chemical Signals in a Turbulent Odor Plume

A variety of animals use olfactory appendages bearing arrays of chemosensory neurons to detect chemical signatures in the water or air around them. This study investigates how particular aspects of the design and behavior of such olfactory appendages on benthic aquatic animals affect the patterns of intercepted chemical signals in a turbulent odor plume. We use virtual olfactory `sensors' and `antennules' (arrays of sensors on olfactory appendages) to interrogate the concentration field from an experimental dataset of a scalar plume developing in a turbulent boundary layer. The aspects of the sensors that we vary are: (1) The spatial and temporal scales over which chemical signals arriving at the receptors of a sensor are averaged (e.g., by subsequent neural processing), and (2) the shape and orientation of a sensor with respect to ambient water flow. Our results indicate that changes in the spatial and temporal resolution of a sensor can dramatically alter its interception of the intermittency and variability of the scalar field in a plume. By comparing stationary antennules with those sweeping through the flow (as during antennule flicking by the spiny lobster, Panulirus argus), we show that flicking alters the frequency content of the scalar signal, and increases the likelihood that the antennule encounters peak events. Flicking also enables a long, slender (i.e., one-dimensional) antennule to intercept two-dimensional scalar patterns.     

Effects of current speed on filtration during suspension feeding in Oligometra serripinna (Echinodermata: Crinoidea)

Suspension feeding by the crinod Oligometra serripinna was studied at Lizard Island, Australia, in 1986. Video recordings were made of 90-m particles interacting with the filter of the crinoid in a laboratory flow chamber. A complete census of particles was possible because both the capture event and the filter area could be defined unequivocally. Also, because O. serripinna is a passive suspension feeder, a census of partcles could be made at different ambient current speeds without interference due to active pumping by the crinoid. Experiments were run at seven current speeds from 0.9 to 13.3 cm s^-1. Particles approaching the filter: (1) were captured, (2) passed through the filter without triggering a capture event, (3) passed through the filter after escaping from an unsuccessful capture event, or (4) were deflected around the filter. With increasing current speed, the proportion of deflections declined and the proportion of particles passing through rose: these results could be partially explained by the progressive widening of the spaces within the filter due to distortion of filter parts by the current. The proportion of captures (normalized to approaches) was comparatively low at 0.9 cm s^-1, rose to a relatively constant maximum from 1.7 to 6.4 cm s^-1, and then declined progressively at 9.5 and 13.3 cm s^-1. These proportions were translated into capture rates for whole crinoids by taking into consideration both the encounters with particles and the reduction of filter area by distortion of body parts at higher speeds. When plotted against current speed, capture rate peaked at 6.4 cm s^-1, which was close to the mean current speed that we measured on the reef in the microhabitat of O. serripinna.     

Sibling recognition in spiny mice (Acomys cahirinus)

Summary Sibling recognition by spiny mice (Acomys cahirinus) was investigated by housing groups consisting of two pairs of littermates together and recording frequency of dyadic pairing. A total of 136 animals (68 pairs of siblings) were tested in three experiments. Sibling pairs were observed more often than pairings between nonsiblings; however, such preferences were no longer evident if the nonsiblings were exposed to one another prior to testing. Animals made anosmic through zinc sulfate treatment did not differ on their frequencies of sibling vs. nonsibling pairing and showed a higher incidence of group huddling (by all four animals) than did intact controls. Weanling A. cahirinus appear to be able to recognize (i.e., are attracted to) their littermate siblings through olfactory cues, which seems to be a modifiable attraction to odors to which the littermates were exposed rather than an irreversible imprinting-like process.The research project reported herein was supported by grant # 00973 from NICHD     

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.     

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