Journal of Comparative Physiology A

, Volume 199, Issue 2, pp 89–98 | Cite as

The magnetite-based receptors in the beak of birds and their role in avian navigation

  • R. Wiltschko
  • W. Wiltschko
Open Access


Iron-rich structures have been described in the beak of homing pigeons, chickens and several species of migratory birds and interpreted as magnetoreceptors. Here, we will briefly review findings associated with these receptors that throw light on their nature, their function and their role in avian navigation. Electrophysiological recordings from the ophthalmic nerve, behavioral studies and a ZENK-study indicate that the trigeminal system, the nerves innervating the beak, mediate information on magnetic changes, with the electrophysiological study suggesting that these are changes in intensity. Behavioral studies support the involvement of magnetite and the trigeminal system in magnetoreception, but clearly show that the inclination compass normally used by birds represents a separate system. However, if this compass is disrupted by certain light conditions, migrating birds show ‘fixed direction’ responses to the magnetic field, which originate in the receptors in the beak. Together, these findings point out that there are magnetite-based magnetoreceptors located in the upper beak close to the skin. Their natural function appears to be recording magnetic intensity and thus providing one component of the multi-factorial ‘navigational map’ of birds.


Magnetite-based receptors Pulse treatment Trigeminal nerve ‘Fixed direction’ responses Magnetic ‘map’ component 


The literature on the avian magnetic compass, showing its functional properties, the underlying physical radical pair processes and its association with the visual system, has been discussed in several recent reviews (e.g., Ritz et al. 2010; Ritz 2011; W. Wiltschko et al. 2011). The other avian magnetoreception system, based on magnetite and associated with the trigeminal system, has received less attention and has not been summarized in a review so far. In the present paper, we will describe the respective findings, mostly behavioral that support the existence of magnetite-based magnetoreceptors in the beak of birds and also provide some insight in their structure, their function and their role in avian navigation.

Biogenic magnetite and its possible role in magnetoreception

Lowenstam (1962) described magnetite, a form of Fe3O4 in the denticles of the radula of chitons (Mollusca: Polyplacophora), where they seem to be used for hardening the teeth. This was the first time that magnetic material was found in living organisms and proved in principle that magnetic material can be produced by biological means. In the mid-1970s, Blakemore (1975) found intra-cellular magnetite crystals in bacteria, a discovery that was soon followed by many other reports describing the occurrence of magnetite in other bacterial species, protozoa etc., and also in higher animals (see Kirschvink et al. 1985a for a summary up to that date).

Bacteria use their magnetite inclusions for orientation: they become ‘north-seeking’ or ‘south-seeking’; when they are stirred up, they move along the magnetic field lines to reach the ground. This is a mere passive orientation, mediated by the force of the magnetic field acting upon the magnetite crystals. Yet it inspired Yorke (1979) to suggest that magnetite could also be part of magnetoreceptors in higher animals.

The magnetic properties of magnetite depend on the size of the particles: larger particles are multi domain with no net magnetization; smaller crystals are single domains (SD) with a stable magnetic moment, and even smaller ones are superparamagnetic (SPM)—they do not have a stable magnetic moment, but will align their magnetization by an external magnetic field. Kirschvink and Gould (1981) described several ways how magnetite particles could work in a receptor, discussing systems based on single domain magnetite, on superparamagnetic crystals or a combination of both. These first considerations on the function of magnetite in receptors were followed by others proposing modified models and considering various theoretical possibilities how magnetite-based receptors might work and what type of information they might convey (e.g., Kirschvink and Walker 1985; Shcherbakov and Winklhofer 1999; Davila et al. 2003; Fleissner et al. 2007; Solovyov and Greiner 2007; Walker 2008; Winklhofer and Kirschvink 2010).

Magnetite found in birds

Birds were a group of special interest, because their ability to use information from the geomagnetic field for orientation had been demonstrated: migratory birds had been shown to use the magnetic field as a compass (e.g., W. Wiltschko 1968; Keeton 1971), and the behavior of pigeons in a magnetic anomaly suggested a possible use of magnetic components in the navigational ‘map’ (Walcott 1978).

The first report of magnetite in birds was published in 1979, when Walcott et al. (1979), measuring the remanence with a SQUID magnetometer, found permanently magnetic material, presumably single domain magnetite, in the head of pigeons between the brain and the skull, that is, at a location where a sensory function does not seem very likely. Other iron-rich structures were found in the nasal region of birds: based on histological studies with Prussian blue staining, Beason and Nichols (1984) and Beason and Brennan (1986) described such structures in Bobolinks (Dolichonyx oryzivorus: Emberizidae), a passerine migrant, and Williams and Wild (2001) reported similar structures in pigeons. The size of the structures and remanence measurements suggested single domain magnetite. Being associated with the ophthalmic branch of the trigeminal nerve, these structures were discussed as possible magnetoreceptors.

Another type of putative magnetoreceptors involving superparamagnetic magnetite was described in the skin of the upper beak of pigeons. Hanzlik et al. (2000) identified the iron-rich particles crystallographically as magnetite; histological and electron microscopic studies revealed the fine structure, indicating clusters of nanocrystals adjacent to or within dentrites of the ophthalmic nerves (Winklhofer et al. 2001; Fleissner et al. 2003, 2007). An independent histological study and remanence measurements by Tian et al. (2007) supported these findings. Falkenberg et al. (2010) reported similar structures in the beak of domestic chickens (Gallus gallus) and two species of migrating passerines, the Garden Warbler (Sylvia borin) and the European Robin (Erithacus rubecula: Turdidae). These findings have recently been challenged by Treiber et al. (2012) who claim that the iron-containing structures described as potential magnetoreceptors were merely macrophages.

Magnetic material, presumably magnetite, has also been described in other vertebrates. Cells containing single domain magnetite were also found in the nasal regions of fish from the genus Oncorhynchus (Salmonidae), and interpreted to play a role in magnetoreception (e.g., Kirschvink et al. 1985b; Mann et al. 1988; Walker et al. 1997; Diebel et al. 2000; Eder et al. 2012). Remanence measurements indicated magnetite in the newts (Brassart et al. 1999) and in the heads of bats (Tian et al. 2010). Ferrous inclusions, discussed to be magnetite, were also found the cornea of mole-rat (genus Fukomys, Bathyergidae) (Wegner et al. 2006).

The pioneering studies by Beason and Semm

Beason and Semm (1987, 1991); Semm and Beason (1990) recorded electrophysiological responses to magnetic stimulation from the ophthalmic nerve and the trigeminal ganglion of Bobolinks. Their stimuli consisted of changes in direction and intensity of the magnetic field produced by a set of coils. Figure 1a showed the responses to increases of the vertical components of the magnetic field; in Fig. 1b, the number of spikes is plotted as a function of the magnetic intensity, revealing a logarithmic relationship.
Fig. 1

Electrophysiological recordings from the trigeminal ganglion of the bobolink. Left spontaneous activity and responses to various changes in the intensity of the vertical component of the magnetic field. The lines indicate the 50 ms of stimulation (from Semm and Beason 1990). Right recorded activity changes as a logarithmic function of the increased intensity (from Beason and Semm 1991)

From their findings, Beason and Semm drew two conclusions

  1. 1.

    The ophthalmic nerve mediates magnetic information,

  2. 2.

    This information is probably the information on magnetic intensity involved in the navigational ‘map’.


The first conclusion, namely that a branch of the trigeminal nerve mediates magnetic information, has been confirmed in a behavioral study with caged Bobolinks by the authors themselves (Beason and Semm 1996): injecting an anesthetic in the ophthalmic nerve suppressed the effect of a short, strong magnetic pulse (see Fig. 3a below). A conditioning study by Mora et al. (2004) produced corresponding results: after locally anesthetizing or sectioning the ophthalmic nerve, homing pigeons trained to respond to a small, strong magnetic anomaly could no longer perform the task. Similar results were obtained by Freire et al. (2012) with young Pekin Ducks (Anas platyrhynchos domestica) trained to associate a small, strong magnetic anomaly with food: here, too, anesthesia or sectioning the ophthalmic nerve led to a performance at chance level. A recent ZENK-study with European robins (Heyers et al. 2010) likewise confirms the involvement of the trigeminal system in magnetoreception: after magnetic stimulation, a number of ZENK-positive neurons were found in two areas in the trigeminal brain stem, and this number deceased significantly when the ophthalmic nerve was sectioned.

In all studies mentioned above, the magnetic stimuli used do not allow to decide whether the information mediated by the ophthalmic nerve was indeed information on intensity. Behavioral data that will be discussed below support this view, but recent findings show that the situation is rather complex.

Pulse experiments to indicate magnetite

The electrophysiological responses recorded in the ophthalmic nerve after magnetic stimulation suggested these responses originate in the iron-rich structures found by the histological studies and the remanence measurements. Yet more direct evidence for an involvement of magnetite in orientation behavior seemed desirable. A diagnostic tool to identify magnetite is the response to a strong, short magnetic pulse, e.g., 0.5 Tesla with a duration of <5 ms: the pulse must be strong enough to remagnetize single domains, and it must be brief enough to prevent the magnetite crystals to rotate and align in the direction of the pulse. Since the orientation of the magnetite particles was unclear, it was to be expected that such a pulse would remagnetize roughly half of the single domains. A pulse would also disrupt clusters and chains of superparamagnetic magnetite, as experiments with model systems of ferrofluids showed (Davila et al. 2005). In both cases, receptors based on magnetite would be severely disrupted, and their input would be markedly changed. Other types of magnetoreception, like the radical-pair processes in the eye (Ritz et al. 2000, 2004), are not affected by the pulse, however.

The first birds subjected to such a magnetic pulse were Australian Silvereyes (Zosterops lateralis), Australian migrants. In cage studies, the pulse was applied ‘south-anterior’, with the direction of the pulse being towards the beak in birds facing east in the geomagnetic field. This caused a roughly 90° shift to the east during spring as well as during autumn migration (Fig. 2a)—the effect was obviously independent from the migratory direction (W. Wiltschko et al. 1994, 1998). Interestingly, the effect of pulsing was only observed in old, experienced migrants; young birds that had been captured immediately after fledging did not respond to the pulse (Fig. 2b; Munro et al. 1997). Treating the ophthalmic nerve or upper beak of birds with the local anesthetic suppressed this pulse effect (Fig. 3; Beason and Semm 1987; W. Wiltschko et al. 2009).1
Fig. 2

Orientation of migrants after a short, strong magnetic pulse. Upper diagrams responses of Australian Silvereyes showing that adult (ad.) birds respond with a marked deflection to the east, whereas juveniles (juv.) are unaffected. Black open symbols: behavior before pulsing; solid red symbols: behavior on the day of pulsing and the following day (data from Munro et al. 1997). Lower diagrams responses of bobolinks to pulses applied in two different directions. The headings are presented in relation to the orientation before the pulse (C) projected upward (data from Beason et al. 1995). The arrows represent the mean vector in relation to the radius of the circle = 1; the two inner circles are the 5 % (dashed) and 1 % significance border of the Rayleigh test

Fig. 3

The response to the pulse can be abolished by preventing the information from the magnetite-based receptors reaching the brain—in that case, the birds head in their migratory direction with their magnetic compass, indicating that the pulse does not affect the compass. Upper diagrams response of Bobolinks to a pulse ‘south anterior (P) and when the ophthalmic branch of the trigeminal nerve was anesthetized with a local anesthetic (data from Beason and Semm 1996). Lower diagrams orientation of Australian Silvereyes before pulsing (C, black symbols) and after being subjected to the pulse without further treatment (P, red symbols) and with the upper beak locally anesthetized by a local anesthetic, externally applied (P Xy, blue symbols) (data from W. Wiltschko et al. 2009). Symbols as in Fig. 2

Beason et al. (1995) pulsed Bobolinks in two different directions, recorded their activity in cages and found that they deviated in different directions: the bird pulsed ‘south anterior’ headed to the right, those pulsed ‘north anterior’ to the left of their directions before pulsing (Fig. 2c). Deflections to different sides were also observed in homing pigeons that had been displaced after being pulsed ‘south anterior’ and ‘south left’ (Beason et al. 1997). Here, the observed effect was much smaller, probably because the pigeons were released and had, in contrast to the migrants tested in cages, other navigational factors available.

The pulse was found to alter the behavior of migrants only temporarily. The deviations described above are observed only on the day of pulsing and the two following days; after that the birds in the cage studies were disoriented, and about 8–10 days after the pulse, their orientation was back to normal—they again preferred their seasonally appropriate migratory direction (W. Wiltschko et al. 1994, 1998). This transient nature of the effect proved important when wild migrants were subjected to a pulse before they were released and their starting routes were tracked. A first study in America involving Catbirds (Dumetella carolinensis: Mimidae) proved inconclusive because the birds lingered in the area and took off only with considerable delay (Holland et al. 2009). In a second study in spring with European Robins and Reed Warblers (Acrocephalus scirpaceus: Sylviidae), many birds departed in the first days after pulsing, and here, the treated birds showed a significant deviation from the untreated controls, with the amount and direction of this deviation depending on the direction of pulsing (Holland 2010). A subsequent study with robins in autumn showed that juvenile birds were not affected by the pulse and those adult birds that took off within the first 10 days showed a significant deviation from their migratory direction, in contrast to those that departed later (Holland and Helm 2012).

Together, these findings provide some information on the receptors in question: the effect of the strong, short magnetic pulse on the orientation of birds indicates that the receptors are indeed based on magnetic material like magnetite. The observation that the deviations induced by pulsing depended on the direction in which the pulse is applied points out that the pulse does not silence the magnetite-based receptors altogether and that it just alters the information they mediate. At the same time, this observation also suggests that the magnetite particles in the receptors are not evenly or circular-symmetrically arranged, but extend differently to the various sides. From the behavioral point of view, it is interesting that only experienced, but not juvenile birds are affected, as this suggests that the mechanism involved is not innate, but based on experience.

Single domains or superparamagnetic particles?

Pulse experiments were first proposed to find out whether the receptors controlling the respective behaviors contained magnetic material like magnetite. The observed effects of pulsing indeed indicate magnetite-based receptors, but it is not clear what type of particles is involved. Any interpretation of behavioral data in view of this question must necessarily remain speculative. Yet some findings give at least some hints.

Another approach involved pulsing the birds while they are exposed to a strong biasing field that aligns single domain particles (if sufficiently mobile) in one direction—in this case, a pulse parallel to the biasing field should have no effect, whereas an antiparallel pulse should remagnetize a maximum of particles, and thus lead to a marked change in orientation. The results of the two such experiments do not agree: Australian Silvereyes, pulsed parallel in a 100 μT biasing field showed the same axial deviations from their migratory direction as those pulsed antiparallel (W. Wiltschko et al. 2002), whereas Reed Warblers pulsed in a 320 μT biasing field seemed unaffected by a parallel pulse and showed an axial deviation when pulsed antiparallel (Holland 2010). The data of the pulse experiments available so far do not yet allow a decision on the type of particles involved in the magnetite-based receptors.

What kind of information is mediated?

Another question concerns the type of magnetic information these receptors provide—directional information for compass use or a component of the navigational ‘map’. Theoretically, magnetite-based receptors could provide information on both, direction and intensity (e.g., Kirschvink and Gould 1981; Solovyov and Greiner 2007). But these are two different qualities of the magnetic field—we humans measure them with different instruments, a compass and a magnetometer. Hence, it would not be surprising if birds had specialized their magnetic sense in a similar way.

The electrophysiological study by Semm and Beason (1990) pointed towards magnetic intensity, and the observations of Munro et al. (1997) that young Australian Silvereyes remain unaffected by the pulse also speaks in favor of a learned system, which suggests the magnetite-based receptors provide a component of the navigational ‘map’ (see also Deutschlander et al. 2012). At the same time, the data of the respective study (Fig. 2b) clearly show that the young birds, despite the pulse treatment that disrupted their magnetite-based receptors, continued in migratory direction: obviously, their magnetic compass mechanism was not affected. This conclusion is also supported by findings that pulse-treated birds preferred their normal migratory direction when the altered input from the magnetite-based receptors was disrupted, either by anesthetizing the ophthalmic nerve (Fig. 3a; Beason and Semm 1996) or by anesthetizing the skin of the upper beak with the local anesthetic Xylocain, applied externally (Fig. 3b; W. Wiltschko et al. 2009). Testing pulse-treated Silvereyes in a magnetic field with the vertical component reversed showed that these birds located their changed course with their normal inclination compass (W. Wiltschko et al. 2006). Furthermore, in otherwise untreated Robins and Silvereyes, local anesthesia of the upper beak—the same treatment that disrupts the pulse effect—did not affect migratory orientation (R. Wiltschko et al. 2007, 2008).2 Zapka et al. (2009) obtained similar results by cutting the ophthalmic nerve.

All these findings clearly show that the magnetite-based receptors are not involved in the avian magnetic compass. The inclination compass represents a different mechanism based on different physical reactions, namely on radical-pair processes in the eye (Ritz et al. 2000, 2004). The magnetite-based receptors in the beak, in contrast, seem to contribute to the processes that determine the course to be pursued, the avian ‘map’ mechanism. In view of this, it appears most likely that the iron-rich structures mediate information on magnetic intensity.

In rainbow trouts, Oncorhynchus mykiss, two findings that might be parallel cases have been reported. In electrophysiological studies from a branch of the trigeminal nerve, Walker et al. (1997) found responses to changes in intensity, but not to changes in direction alone. In a study by Hellinger and Hoffmann (2012), fish were conditioned to magnetic stimuli; inactivation of the ophthalmic branch of the trigeminal nerve by a local anesthetic abolished the response to changes in intensity, but did not affect the response to changes in direction.

‘Fixed direction’ responses

The cage experiments with migratory birds reported so far were performed under ‘white’ or under very low intensity monochromatic lights from the short-wavelength end of the spectrum—here, the birds prefer their natural migratory direction. In total darkness, under red light or when short-wavelength light is combined with yellow light, birds change their behavior and head in directions that are different from their migratory direction—since these preferences do not show the seasonal change between autumn and spring, they are characterized as ‘fixed direction’ responses (see R. Wiltschko et al. 2010a). In contrast to migratory orientation by the inclination compass which ignores the polarity of the magnetic field (W. Wiltschko and Wiltschko 1972), these ‘fixed direction’ responses are polar responses, that is, they orient by the polarity of the magnetic field. This indicates that they must be based on a mechanism that is fundamentally different from the radical pair processes of the inclination compass.

Several such ‘fixed direction’ responses have been described in European Robins and Australian Silvereyes (e.g., R. Wiltschko et al. 2007, 2008, 2012; Stapput et al. 2008; for review, see R. Wiltschko et al. 2010a). The ones analyzed in detail so far could all be disrupted by local anesthesia of the upper beak (for examples, see Fig. 4)—the magnetic information involved appears to originate in the magnetite-based receptors located there. Obviously, under some extreme light conditions, the normal inclination compass is disrupted, and the receptors in the upper beak can take over and control the directional behavior of birds.
Fig. 4

‘Fixed direction’ responses in Robins, observed under certain light regimes, can be disrupted by local anesthesia of the upper beak. D, orientation in total darkness; GY, orientation under a combination of monochromatic green and yellow light. Black open symbols: untreated controls; blue solid symbols: birds with the upper beak locally anesthetized with an externally applied local anesthetic (data from Stapput et al. 2008; R. Wiltschko et al. 2012). Symbols as in Fig. 2

This means that the magnetite-based receptors do not only provide information on magnetic intensity, but under certain conditions also produce directional information. However, for reasons unknown, this information is not helpful for the birds—they cannot use it for locating their seasonally changing migratory direction. A biological significance of these ‘fixed direction’ responses to the magnetic field is not known; they have been discussed as possible relicts of an ancient, magnetite-based compass mechanism that has been replaced by the radical pair mechanism in birds (e.g., R. Wiltschko et al. 2010a), thus giving the magnetite-based receptors a chance to specialize for a different function. The ‘fixed directions’ depend on the respective light regimes and differ under the various colors and color combinations of light (see Fig. 4). Since the receptors in the upper beak cannot be directly affected by light, this suggests connections between the trigeminal and the visual system at higher levels in the brain.

What is the natural function of the magnetite-based receptors?

So far, the behavioral evidence that indicates the occurrence of magnetite-based receptors in the upper beak involves highly unnatural stimuli: neither spatially limited strong anomalies, nor magnetic pulses or extreme light regimes exist in nature. This leads to the question about the natural role of these receptors. Some of the findings—the electrophysiological recordings by Semm and Beason (1990), the observation that young, inexperienced migrants are not affected by the magnetic pulse (Munro et al. 1997) and that the magnetic compass is not involved (Beason and Semm 1996; W. Wiltschko et al. 2006; R. Wiltschko et al. 2007; Zapka et al. 2009)—suggest that these receptors normally mediate magnetic information as a component of the navigational ‘map’. Pigeons have been shown to respond to temporal fluctuations of the geomagnetic field as reflected by the K-indices or the A p index, with slight shifts in their initial orientation and a lower steadiness of their homing flight (Keeton et al. 1974; Schiffner and Wiltschko 2011), which suggests a sensitivity in the range of at least 20 nT. In Central Europe, the magnetic reference field increases by 2.5 nT/km towards 15° NNE; hence magnetic gradients could be helpful for navigation, provided that the spatial distribution of the geomagnetic field is fairly regular and that the birds are familiar with the local and regional magnetic topography.

In the 1970s, Walcott (1978) released pigeons in a strong, irregular magnetic anomaly in the Northeastern USA and found that the quality of their orientation, represented by the vector length, decreased as the differences in intensity over a distance of 1 km increased. Yet at that time, nothing was known about the receptors that mediate the respective magnetic information. Walcott’s findings have recently been repeated in Germany with pigeons released in the Vogelsberg anomaly (R. Wiltschko et al. 2009); additionally, a marked effect on the vanishing interval (i.e., the time pigeons need to fly out of sight of observers with good binoculars, about 2.5 km) was observed. In a subsequent study, pigeons were released within the anomaly and outside in magnetically quiet terrain with the receptors in the upper beak temporarily deactivated by an externally applied local anesthetic. This affected their behavior considerably. Within the anomaly, the effect was somewhat beneficial: the pigeons with their beak anesthetized had longer vectors and were significantly faster to leave the site than the untreated controls. Anesthesia of the upper beak had obviously removed an impeding input. The controls were rather slow, significantly slower than when released outside the anomaly (Fig. 5; R. Wiltschko et al. 2010b). The hesitance of control pigeons to leave within the anomaly seemed to reflect confusion caused by the irregular magnetic conditions they encountered when flying around. These birds needed some time to realize that the magnetic field was not reliable and finally turn to other, non-magnetic cues. The birds with their beak anesthetized, in contrast, being deprived of the irregular magnetic input, seemed to turn to other cues right away.
Fig. 5

Vanishing intervals of untreated pigeons (Cont., controls) and pigeons with the upper beak anesthetized by an externally applied local anesthetic (Exp., experimentals) within an strong, irregular anomaly and outside in magnetically quiet terrain. The columns indicate mean and standard deviations. Asterisks indicate significant differences: *p < 0.05; ***p < 0.001 (data from R. Wiltschko et al. 2010a, b)

These observations suggest that magnetic information is normally included in navigational decisions. Yet it is only one factor in the multi-factorial navigational ‘map’, which appears to be redundant to a certain degree. Pigeons released in Italy with their trigeminal nerve sectioned did not show navigational deficits (Gagliardo et al. 2008, 2009); the pigeons with the beak anesthetized in the above-mentioned study (R. Wiltschko et al. 2010b) did not show any effect at three of the four control sites, yet at the fourth site, they showed larger deviations from home, shorter vectors and longer vanishing intervals. Apparently, the significance of magnetic cues varies considerably between sites. But they are regularly consulted, as the obvious confusion of the untreated control birds within the anomaly suggests.


Behavioral evidence indicates that there are magnetoreceptors in the beak of birds. These receptors include magnetite, as indicated by the pulse experiments, and they mediate their input to the brain by the ophthalmic nerve and the trigeminal system. They are not involved in the avian magnetic compass; instead, they seem to normally convey information on magnetic intensity. Their natural function appears to be to provide birds with magnetic information as one factor in the multi-factorial navigational ‘map’—not only homing pigeons within their home region, but also migrants when they return to their familiar breeding site or wintering area.

The exact position of these magnetite-based receptors is unclear. The effect of the local anesthetic seemed to speak in favor of the receptors described in the skin of the upper beak (e.g., Hanzlik et al. 2000; Fleissner et al. 2003; Falkenberg et al. 2010), yet the histological study by Treiber et al. (2012) calls the existence of these receptors in question, a finding that received considerable public attention. This may point to the single-domain receptors described in the nasal region (e.g., Beason and Nichols 1984, Beason and Brennan 1986; Williams and Wild 2001), but it appears highly unlikely that the externally applied anesthetic could have reached them. The observation that young chickens with the tip of their beak removed, as routinely done in the poultry industry, were impaired in locating a magnetic anomaly (Freire et al. 2011) also suggests a position of the receptors further in front of the beak.

Future histological studies will have to identify their true location and show details of their structure.


  1. 1.

    The latter findings—normal preference of the migratory direction despite being treated with a pulse—make possible non-specific side-effects of the pulse treatment seem highly unlikely.

  2. 2.

    The observation that birds with the ophthalmic nerve or the upper beak anesthetized oriented in their normal migratory direction and the beneficial effect of local anesthesia of the beak in a magnetic anomaly (see below) speak against adverse effects on other sensory systems or non-specific side effects of these treatments.


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  1. Beason RC, Brennan WJ (1986) Natural and induced magnetization in the Bobolink Dolichonyx oryzivorus (Aves: Icteridae). J Exp Biol 125:49–56Google Scholar
  2. Beason RC, Nichols JE (1984) Magnetic orientation and magnetically sensitive material in a transequatorial migratory bird. Nature 309:151–153CrossRefGoogle Scholar
  3. Beason RC, Semm P (1987) Magnetic responses of the trigeminal nerve system of the Bobolink (Dolichonyx oryzivorus). Neurosci Lett 80:229–234PubMedCrossRefGoogle Scholar
  4. Beason RC, Semm P (1991) Two different magnetic systems in avian orientation. In: Bell BD, Cossee RO, Flux JEC, Heather BD, Hitchmough RA, Robertson CJR, Williams MJ (eds) Acta XX Congr Int Ornithol. New Zealand Ornithol Congr Trust Board, Wellington, pp 1813–1819Google Scholar
  5. Beason RC, Semm P (1996) Does the avian ophthalmic nerve carry magnetic information? J Exp Biol 199:1241–1244PubMedGoogle Scholar
  6. Beason RC, Dussourd N, Deutschlander M (1995) Behavioral evidence for the use of magnetic material in magnetoreception by a migratory bird. J Exp Biol 198:141–146PubMedGoogle Scholar
  7. Beason RC, Wiltschko R, Wiltschko W (1997) Pigeon homing: effect of magnetic pulses on initial orientation. Auk 114:405–415CrossRefGoogle Scholar
  8. Blakemore RP (1975) Magnetotactic bacteria. Science 19:377–379CrossRefGoogle Scholar
  9. Brassart J, Kirschvink JL, Philipps JB, Borland SC (1999) Ferromagnetic material in the eastern red-spotted newt Nothophthalmus visidescens. J Exp Biol 202:3155–3160PubMedGoogle Scholar
  10. Davila AF, Fleissner G, Winklhofer M, Peterson N (2003) A new model for a magnetoreceptor in homing pigeons based on interacting clusters of superparamagnetic magnetite. Phys Chem Earth 28:647–652CrossRefGoogle Scholar
  11. Davila AF, Winklhofer M, Shcherbakov VP, Peterson N (2005) Magnetic pulse affects a putative magnetoreceptor mechanism. Biophys J 89:56–63PubMedCrossRefGoogle Scholar
  12. Deutschlander M, Phillips JB, Munro U (2012) Age-dependent orientation of magnetically-simulated geographic displacement in migratory Australian Silvereyes (Zosterops l. lateralis). Wilson J Ornithol 124:457–477CrossRefGoogle Scholar
  13. Diebel CE, Priksch R, Green CR, Nelson P, Walker MM (2000) Magnetite defines a vertebrate magnetoreceptor. Nature 406:229–301CrossRefGoogle Scholar
  14. Eder SHK, Cadiou H, Muhamad A, McNaughton PA, Kirschvink JL, Winklhofer M (2012) Magnetic characterization of isolated candidate vertebrate magnetoreceptor cells. Proc Natl Acad Sci USA 109:12022–12027PubMedCrossRefGoogle Scholar
  15. Falkenberg G, Fleissner G, Schuchardt K, Kuehbacher M, Thalau P, Mouritsen H, Heyers D, Wellenreuther G, Fleissner G (2010) Avian magnetoreception: elaborate iron mineral containing dendrites in the upper beak seem to be a common feature of birds. PLoS ONE 5:e9231PubMedCrossRefGoogle Scholar
  16. Fleissner G, Holtkamp-Rötzler Hanzlik M, Winklhofer M, Fleissner G, Petersen N, Wiltschko W (2003) Ultrastructural analysis of a putative magnetoreceptor in the beak of homing pigeons. J Comp Neurol 458:350–360PubMedCrossRefGoogle Scholar
  17. Fleissner G, Stahl B, Thalau P, Falkenberg G, Fleissner G (2007) A novel concept of Fe-mineral-based magnetoreception: histological and physicochemical data from the upper beak of homing pigeons. Naturwissenschaften 94:631–642PubMedCrossRefGoogle Scholar
  18. Freire R, Eastwood MA, Joyce M (2011) Minor beak trimming in chickens leads to loss of mechanoreception and magnetoreception. J Anim Sci 89:1201–1206PubMedCrossRefGoogle Scholar
  19. Freire R, Dunston E, Fowler EM, McKenzie GL, Quinn CT, Michelsen J (2012) Conditioned response to a magnetic anomaly in the Pekin Duck (Anas platyrhynchos domestica) involves the trigeminal nerve. J Exp Biol 215:2399–2404PubMedCrossRefGoogle Scholar
  20. Gagliardo A, Ioalè P, Savini M, Wild M (2008) Navigational abilities of homing pigeons deprived of olfactory or trigeminally mediated magnetic information when young. J Exp Biol 211:2046–2051PubMedCrossRefGoogle Scholar
  21. Gagliardo A, Ioalè P, Savini M, Wild M (2009) Navigational abilities of adult and experienced homing pigeons deprived of olfactory or trigeminally mediated magnetic information. J Exp Biol 212:3119–3124PubMedCrossRefGoogle Scholar
  22. Hanzlik M, Heunemann C, Holtzkamp-Rötzler E, Winklhofer M, Petersen N, Fleissner G (2000) Superparamagnetic magnetite in the upper beak of homing pigeons. Biometals 13:325–331PubMedCrossRefGoogle Scholar
  23. Hellinger J, Hoffmann K-P (2012) Magnetic field perception in the rainbow trout Oncyrynchus mykiss: magnetite mediated, light dependent or both? J Comp Physiol 198:593–605CrossRefGoogle Scholar
  24. Heyers D, Zapka M, Hoffmeister M, Wild JM, Mouritsen H (2010) Magnetic field changes activate the trigeminal brainstem complex in a migratory bird. Proc Natl Acad Sci USA 107:9394–9399PubMedCrossRefGoogle Scholar
  25. Holland RA (2010) Differential effects of magnetic pulses on the orientation of naturally migrating birds. J R Soc Interface 7:1617–1625PubMedCrossRefGoogle Scholar
  26. Holland RA, Helm B (2012) The effect of strong magnetic pulses on the behavior on naturally migrating songbirds. Abstract, 6th Eur Conf Behav Biol, EssenGoogle Scholar
  27. Holland RA, Thorup K, Gagliardo A, Bisson IA, Knecht E, Mizrahi D, Wikelski (2009) Testign the role of sensory systems in the migratory heading of a songbird. J Exp Biol 212:4065–4071PubMedCrossRefGoogle Scholar
  28. Keeton WT (1971) Magnets interfere with pigeon homing. Proc Natl Acad Sci USA 68:102–106PubMedCrossRefGoogle Scholar
  29. Keeton WT, Larkin TS, Windsor DM (1974) Normal fluctuations in the earth’s magnetic field influence pigeon orientation. J Comp Physiol 95:95–103CrossRefGoogle Scholar
  30. Kirschvink JL, Gould JL (1981) Biogenetic magnetite as a basis for magnetic field detection in animals. BioSystems 13:181–201PubMedCrossRefGoogle Scholar
  31. Kirschvink JL, Walker MM (1985) Particle-size considerations for magnetite-based magnetoreceptors. In: Kirschvink JL, Jones DS, MacFadden BJ (eds) Magnetite biomineralization and magnetoreception in organisms. Plenum Press, New York, pp 243–256CrossRefGoogle Scholar
  32. Kirschvink JL, Jones DS, MacFadden BJ (eds) (1985a) Magnetite biomineralization and magnetoreception in organisms. Plenum Press, New YorkGoogle Scholar
  33. Kirschvink JL, Walker MM, Chang S-B, Dizon AE, Peterson KA (1985b) Chains of single-domain magnetite particles in Chinook salmon, Oncyrhynchus tshawytscha. J Comp Physiol A 157:375–381CrossRefGoogle Scholar
  34. Lowenstam HA (1962) Magnetite in denticle capping in recent chitons (Polyplacophora). Geol Soc Am Bull 73:435–438CrossRefGoogle Scholar
  35. Mann S, Sparks HCH, Walker MM, Kirschvink JL (1988) Ultrastructure, morphology and organization of biogenic magnetite from Sockeye Salmon, Oncyrhynchus nerka: implications for magnetoreception. J Exp Biol 140:35–49PubMedGoogle Scholar
  36. Mora CV, Davison M, Wild JM, Walker MM (2004) Magnetoreception and its trigeminal mediation on the homing pigeons. Nature 432:508–511PubMedCrossRefGoogle Scholar
  37. Munro U, Munro JA, Phillips JB, Wiltschko R, Wiltschko W (1997) Evidence for a magnetite-based navigational ‘map’ in birds. Naturwissenschaften 84:26–28CrossRefGoogle Scholar
  38. Ritz T (2011) Quantum effects in biology: bird navigation. Procedia Chem 3:262–275CrossRefGoogle Scholar
  39. Ritz T, Adem S, Schulten K (2000) A model for photoreceptor-based magnetorecption in birds. Biophys J 78:707–718PubMedCrossRefGoogle Scholar
  40. Ritz T, Thalau P, Phillips JB, Wiltschko R, Wiltschko W (2004) Resonance effects indicate a radical-pair mechanism for avian magnetic compass. Nature 429:177–180PubMedCrossRefGoogle Scholar
  41. Ritz T, Ahmad M, Mouritsen H, Wiltschko R, Wiltschko W (2010) Photoreceptor-based magneto-receptiom: optimal design of receptor molecules, cells, and neural processing. J R Soc Interface 7 Focus 2:S135–S146CrossRefGoogle Scholar
  42. Schiffner I, Wiltschko R (2011) Temporal fluctuation of the geomagnetic field affect pigeons’ entire homing flight. J Comp Physiol A 197:765–772CrossRefGoogle Scholar
  43. Semm P, Beason RC (1990) Responses to small magnetic variations by the trigeminal system of the bobolink. Brain Res Bull 25:735–740PubMedCrossRefGoogle Scholar
  44. Shcherbakov VP, Winklhofer (1999) The osmotic magnetometer: a new model for magnetite-based magnetoreceptors in animals. Eur Biophys J 28:380–392CrossRefGoogle Scholar
  45. Solovyov IA, Greiner W (2007) Theoretical analysis of an iron-mineral-based magnetoreceptor model in birds. Biophys J 93:1493–1509CrossRefGoogle Scholar
  46. Stapput K, Thalau P, Wiltschko R, Wiltschko W (2008) Orientation of birds in total darkness. Curr Biol 18:602–606PubMedCrossRefGoogle Scholar
  47. Tian L, Xiao B, Lin W, Zhang S, Zhu R, Pan Y (2007) Testing for the presence of magnetite in the upper-beak skin of homing pigeons. Biometals 20:197–203PubMedCrossRefGoogle Scholar
  48. Tian L, Lin W, Zhang S, Pan Y (2010) Bat head contains soft magnetic particles: evidence from magnetism. Bioelectromagnetics 31:499–503PubMedCrossRefGoogle Scholar
  49. Treiber CD, Salzer MC, Riegler J, Edelmann N, Sugar C, Breuss M, Pichler P, Cadiou H, Saunders M, Shaw J, Keays DA (2012) Clusters of iron-rich cells in the upper beak of pigeons are macrophages not magnetosensitive neurons. Nature 484:367–370PubMedGoogle Scholar
  50. Walcott C (1978) Anomalies in the earth’s magnetic field increase the scatter of pigeons’ vanishing bearings. In: Schmidt-Koenig K, Keeton WT (eds) Animal migration, navigation, and homing. Springer, Berlin, Heidelberg, New York, pp 143–151Google Scholar
  51. Walcott C, Gould JL, Kirschvink JL (1979) Pigeons have magnets. Science 205:1027–1029PubMedCrossRefGoogle Scholar
  52. Walker MM (2008) A model for encoding magnetic-field intensity by magnetite based magnetoreceptor cells. J Theor Biol 250:85–91PubMedCrossRefGoogle Scholar
  53. Walker MM, Diebel CE, Haugh CV, Pankhurst PM, Montgomery JC, Green CR (1997) Structure and function of the vertebrate magnetic sense. Nature 390:371–376PubMedCrossRefGoogle Scholar
  54. Wegner R, Begall S, Burda H (2006) Magnetic compass in the cornea: local anesthesia impairs orientation in a mammal. J Exp Biol 209:4747–4750PubMedCrossRefGoogle Scholar
  55. Williams MN, Wild JM (2001) Trigeminally innervated iron-containing structures in the beak of homing pigeons, and other birds. Brain Res 889:243–246PubMedCrossRefGoogle Scholar
  56. Wiltschko W (1968) Über den Einfluß statischer Magnetfelder auf die Zugorientierung der Rotkehlchen (Erithacus rubecula). Z Tierpsychol 25:536–558Google Scholar
  57. Wiltschko W, Wiltschko (1972) The magnetic compass of European Robins. Science 176:62–64PubMedCrossRefGoogle Scholar
  58. Wiltschko W, Munro U, Beason RC, Ford H, Wiltschko R (1994) A magnetic pulse leads to a temporary deflection in the orientation of migratory birds. Experientia 50:697–700CrossRefGoogle Scholar
  59. Wiltschko W, Munro U, Ford H, Wiltschko R (1998) Effect of a magnetic pulse on the orientation of Silvereyes, Zosterops l. lateralis, during spring migration. J Exp Biol 201:3257–3261PubMedGoogle Scholar
  60. Wiltschko W, Munro U, Wiltschko R, Kirschvink J (2002) Magnetite-based magnetoreception in birds: the effect of a biasing field and a pulse on migratory behavior. J Exp Bio 20:3031–3037Google Scholar
  61. Wiltschko W, Munro U, Ford H, Wiltschko R (2006) Bird navigation: what type of information does the magnetite-based receptor provide? Proc R Soc B 273:2815–2850PubMedCrossRefGoogle Scholar
  62. Wiltschko R, Stapput K, Ritz T, Thalau P, Wiltschko W (2007) Magnetoreception in birds: different physical processes for two types of directional responses. HFSP Journal 1:41–47PubMedCrossRefGoogle Scholar
  63. Wiltschko W, Ford H, Munro U, Winklhofer M, Wiltschko R (2007) Magnetite-based magneto-reception: the effect of repeated pulsing on the orientation of migratory birds. J Comp Physiol A 193:515–522CrossRefGoogle Scholar
  64. Wiltschko R, Munro U, Ford H, Stapput K, Wiltschko W (2008) Light-dependent magnetoreception: orientation behaviour of migratory birds under dim red light. J Exp Biol 211:3344–3350PubMedCrossRefGoogle Scholar
  65. Wiltschko R, Schiffner I, Wiltschko W (2009) A strong magnetic anomaly affects pigeon navigation. J Exp Biol 212:2983–2990PubMedCrossRefGoogle Scholar
  66. Wiltschko W, Munro U, Ford H, Wiltschko R (2009) Avian orientation: the pulse effect is mediated by the magnetite receptors in the upper beak. Proc R Soc B 276:2227–2232PubMedCrossRefGoogle Scholar
  67. Wiltschko R, Stapput K, Thalau P, Wiltschko W (2010a) Directional orientation of birds by the magnetic field under different light conditions. J R Soc Interface 7 Focus 2:S163–S177CrossRefGoogle Scholar
  68. Wiltschko R, Schiffner I, Fuhrmann P, Wiltschko W (2010b) The role of the magnetite-based receptors in the beak in pigeon homing. Curr Biol 20:1534–1538PubMedCrossRefGoogle Scholar
  69. Wiltschko W, Wiltschko R, Ritz T (2011) The mechanism of the avian magnetic compass. Procedia Chem 3:276–284CrossRefGoogle Scholar
  70. Wiltschko R, Dehe L, Gehring D, Thalau P, Wiltschko W (2012) Interactions between the visual and the magnetoreception system: Different effects of bichromatic light regimes in the directional behavior of migratory birds. J Physiol Paris.
  71. Winklhofer M, Kirschvink JL (2010) A quantitative assessment of torque-transducer models for magnetoreception. J R Soc Interface 7 Focus 2:S273–S289CrossRefGoogle Scholar
  72. Winklhofer M, Holtkamp-Rötzler E, Hanzlik M, Fleissner G, Petersen N (2001) Clusters of superparamagentic magnetite particles in the upper-beak skin of homing pigeons: evidence of a magnetoreceptor? Eur J Mineral 13:659–669CrossRefGoogle Scholar
  73. Yorke E (1979) A possible magnetic transducer in birds. J Theor Biol 77:101–105PubMedCrossRefGoogle Scholar
  74. Zapka M, Heyers D, Hein CM, Engels S, Schneider N-L, Hans J, Weiler S, Dreyer D, Kishkinev D, Wild JM, Mouritsen H (2009) Visual but not trigeminal mediation of magnetic compass information in a migratory birds. Nature 461:1274–1278PubMedCrossRefGoogle Scholar

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© The Author(s) 2012

Authors and Affiliations

  1. 1.FB BiowissenschaftenJ.W.Goethe-Universität FrankfurtFrankfurt a.MGermany

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