Magnetic Orientation in Solenopsis sp. Ants

It is known that magnetic fields affect ants behavior. It has been shown that Solenopsis ants are sensitive to magnetic fields but there is no experimental evidence for magnetic orientation. In this paper experiments were done to verify the magnetic orientation of Solenopsis sp. ants. The spontaneous orientation of ants in a circular arena was studied in two different magnetic conditions: in the natural geomagnetic field and under an altered magnetic field, with the horizontal geomagnetic axis shifted in 90?o. Our results show that ants consistently change their orientation direction when the magnetic field was altered. Axial circular statistics analysis showed that, in the absence of other cues, ants orient spontaneously to the horizontal geomagnetic field axis. The present paper shows for the first time magnetic orientation in Solenopsis sp. ants.     

A comprehensive hypothesis on the migration of European glass eels (Anguilla anguilla)

The European eel (Anguilla anguilla) is a catadromous fish that spawns in the Sargasso Sea. As larvae, eels cross the Atlantic Ocean and reach the continental slope of Europe, where they metamorphose into post‐larval glass eels. These reach the continent, where some enter fresh water, some remain in marine waters, and others move between fresh and marine waters. After 5–25 years, as adult silver eels, they migrate back from fresh water to the Sargasso Sea to spawn and die. The glass eel stage is a critical step during which the eels cross the continental shelf and recruit to estuaries, where they facultatively transition to fresh water. Extensive research has been conducted to understand the behavioural mechanisms and environmental cues that aid and guide glass eels' migration. Glass eels follow odours and salinity gradients, they avoid light, and they change orientation and depth according to the tides. Recent work revealed that European glass eels also use Earth's magnetic field and lunar cues to orient. However, while we understand many aspects of their orientation behaviour, a unifying theory describing how glass eels migrate from the continental slope to fresh water is lacking. The goal of this review is to develop a comprehensive hypothesis on the migration of European glass eels, integrating previous knowledge on their orientation behaviour with recent findings on magnetic and celestial orientation. This review follows the journey of a hypothetical glass eel, describing the nature and the role of orientation cues involved at each step. I propose that, although glass eels have the sensory capacity to use multiple cues at any given time, their migration is based on a hierarchical succession of orientation mechanisms dictated by the physical properties of the environments that they occupy: (i) lunar and magnetic cues in pelagic water; (ii) chemical and magnetic cues in coastal areas; and (iii) odours, salinity, water current and magnetic cues in estuaries.     

Celestial orientation in the marbled newt (Triturus marmoratus)

Orientation toward breeding ponds plays an important role in the seasonal movements of amphibians. In this study, adult marbled newts were tested in a circular arena to determine sensory cues used to locate breeding ponds. Animals were collected from a temporary pond situated in northern Spain, taken to the experimental site 340 m distant, and tested for orientation under a variety of conditions (i.e., orientation under a clear night sky, orientation under an overcast night sky, and orientation under a clear night sky in the presence of an altered geomagnetic field). These investigations have demonstrated that the marbled newt is able to orient using celestial cues. Animals chose a compass course in the direction of their breeding pond only when celestial cues were available. Conversely, the ambient geomagnetic field does not seem to be relevant to orientation of marbled newts since they were unable to orient themselves using the ambient geomagnetic field in the absence of celestial cues. Electronic Publication     

Experimental evidence for geomagnetic orientation in juvenile salmon, Oncorhynchus tschawytscha Walbaum

Juvenile chinook salmon, Oncorhynchus tschawytscha , kept under artificial light in a rectangular holding tank aligned east/west for 18 months, showed a preferred temporal and directional orientation of 270° with respect to water flow and the source of food.
Individual fish transferred from the holding/training tank to an unfamiliar circular test arena in another room devoid of local directional cues showed a mean of means preferred unimodal orientation of 264°.
Controlled re-introduction of individual stimuli revealed a hierarchy of orientation cues; one of these was a response to magnetism. A 90° clockwise shift in the horizontal component of the earth's magnetic field was followed by a significant change in the mean of means axial orientation, for the fish under test, from 258°/78° to 354°/174°. After restoration of the normal magnetic field the mean of means axial orientation reverted to 274°/94°.     

Anguilla japonica is already magnetosensitive at the glass eel phase

Magnetosensitivity of the Japanese eel Anguilla japonica at the glass eel phase (newly metamorphosed juveniles) was examined by conditioning and electrocardiography. The glass eels were conditioned to an imposed magnetic field of 192 473 nT parallel to the fish body placed along the earth's west‐east axis. After 10 to 40 conditioning runs, all the glass eels exhibited a significant conditioned response ( i.e . slowing of the heart beat) to a 192 473 nT magnetic field and even to a 12 663 nT magnetic field that combined with the geomagnetic field (32 524 nT) at the laboratory and produced a resultant magnetic field of 21° easterly. These results indicate that glass eels have high magnetosensitivity and probably acquire geomagnetic information early in life. It is hypothesized that silver‐phase adult eels find their way back to the oceanic spawning ground by reversing the geomagnetic direction that had been detected and 'memorized' during the glass eel phase when migrating from the open ocean towards the continental shelf and coastal waters.     

Behavioural responses of European silver eels(Anguilla anguilla) to the geomagnetic field

Magnetic orientation of European silver eels(Anguilla anguilla) was tested in an octagonal tank. Orientation was determined from photo-registrations of eel positions in tests performed alternately in the natural magnetic field and a field with the horizontal component rotated 180°. Tests were performed in LD 11 : 13. At a daytime light intensity of 100 lux the fish were diurnally active, while at 0.10 lux crepuscular or nocturnal activity dominated. The eels probably differed in preferred orientation, largely depending on the clockwise or anti-clockwise swimming of some of the animals. Therefore there was no preferred direction common to all eels. The orientation of single eels differed, however, significantly between the two magnetic fields, suggesting that the eels responded to the geomagnetic field.     

A geomagnetic declination compass for horizontal orientation in fruit flies

The Earth's geomagnetic field (GMF) is known to act as a sensory cue for magnetoreceptive animals such as birds, sea turtles, and butterflies in long‐distance migration, as well as in flies, cockroaches, and cattle in short‐distance movement or body alignment. Despite a wealth of information, the way that GMF components are used and the functional modality of the magnetic sense are not clear. A GMF component, declination, has never been proven to be a sensory cue in a defined biological context. Here, we show that declination acts as a compass for horizontal food foraging in fruit flies. In an open‐field test, adopting the food conditioning paradigm, food‐trained flies significantly orientated toward the food direction under ambient GMF and under eastward‐turned magnetic field in the absence of other sensory cues. Moreover, a declination change within the natural range, by alteration only of either the east–west or north–south component of the GMF, produced significant orientation of the trained flies, indicating that they can detect and use the difference in these horizontal GMF components. This study proves that declination difference can be used for horizontal foraging, and suggests that flies have been evolutionarily adapted to incorporate a declination compass into their multi‐modal sensorimotor system.     

Compass Orientation During Dispersal of Freshwater Hatchling Snapping Turtles (Chelydra serpentina) and Blanding's Turtles (Emydoidea blandingii)

Freshwater turtle hatchlings primarily use visual cues for orientation while dispersing from nests; however, hatchlings rapidly develop a relationship between a sun or geomagnetic compass and a dispersal target that allows them to maintain an established direction of movement when target habitats are not visible. We examined dispersal patterns of hatchling snapping turtles (Chelydra serpentina) and Blanding's turtles (Emydoidea blandingii) dispersing in large arenas in a mowed field and in dense corn. The dispersal of three categories of hatchlings were examined: (1) naïve individuals (no previous dispersal experience), (2) arena‐experienced (limited dispersal experience in arenas in natural habitat), and (3) natural‐experienced hatchling Blanding's turtles (captured after extensive experience dispersing W in natural habitats toward wetlands). Experienced hatchlings were assigned to treatments consisting of having a magnet or a non‐magnetic aluminum sham or nothing glued to their anterior carapace before release in the corn arena. Dispersal patterns of naïve hatchlings of both species were strongly directional in the field arena with visible target horizons and primarily random in the corn arena where typical target horizons were blocked. When released in corn, dispersal patterns were similar for arena‐experienced hatchlings with magnets or shams attached and differed from their prior dispersal headings in the field arena as naïve hatchlings. Natural‐experienced hatchling Blanding's turtles with and without magnets were able to accurately maintain their prior headings to the WNW while dispersing in the field or corn arenas (i.e., the presence of a magnet did not disrupt their ability to maintain their prior heading). Based on the assumption that no other type of compass exists in hatchlings, we conclude that they were not using a geomagnetic compass, but by default were using sun compass orientation to maintain dispersal headings in dense corn where no typical target habitats were visible.     

Influence of magnetic field on the spatial orientation in zebrafish (<Emphasis Type="Italic">Danio rerio</Emphasis>) (Cyprinidae) and Roach (<Emphasis Type="Italic">Rutilus rutilus</Emphasis>) (Cyprinidae)

Preferred direction of motion under influence of geomagnetic field and its modifications was registered in zebrafish (Danio rerio) raised in laboratory culture and in roach (Rutilus rutilus) from the Rybinsk Reservoir. In the geomagnetic field, specimens of zebrafish prefer two opposite directions oriented towards the north and south, while they prefer towards east and west at 90° turning of the horizontal component of geomagnetic field. The specimens of roach in the geomagnetic field prefer only the direction oriented towards east–northeast. This direction coincides with the direction along the canal where roach was sampled to the main river channel part of the Rybinsk Reservoir. At 90° rotation of the horizontal component of geomagnetic field, the direction turns to the south–southeast. The reasons for selection of certain directions in the geomagnetic field are discussed.     

Avian orientation: effects of cue-conflict experiments with young migratory songbirds in the high Arctic

The migratory orientation of juvenile white-crowned sparrows, Zonotrichia leucophrys gambelli, was investigated by orientation cage experiments in manipulated magnetic fields performed during the evening twilight period in northwestern Canada in autumn. We did the experiments under natural clear skies in three magnetic treatments: (1) in the local geomagnetic field; (2) in a deflected magnetic field (mN shifted −90°); and (3) after exposure to a deflected magnetic field (mN −90°) for 1 h before the cage experiment performed in the local geomagnetic field at dusk. Subjects showed a mean orientation towards geographical east in the local geomagnetic field, north of the expected migratory direction towards southeast. The sparrows responded consistently to the shifted magnetic field, demonstrating the use of a magnetic compass during their first autumn migration. Birds exposed to a cue conflict for 1 h on the same day before the experiment, and tested in the local geomagnetic field at sunset, showed the same northerly orientation as birds exposed to a shifted magnetic field during the experiment. This result indicates that information transfer occurred between magnetic and celestial cues. Thus, the birds' orientation shifted relative to available sunset and geomagnetic cues during the experimental hour. The mean orientation of birds exposed to deflected magnetic fields prior to and during testing was recorded up to two more times in the local geomagnetic field under natural clear and overcast skies before release, resulting in scattered mean orientations.Copyright 2002 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved .     

Shifted magnetic fields lead to deflected and axial orientation of migrating robins,Erithacus rubecula,at sunset

The migratory orientation of the robin was tested in shifted magnetic fields during the twilight period after sunset, under clear skies and under simulated total overcast. The horizontal direction of the geomagnetic field was shifted 90° to the right or left in relation to the local magnetic field, without changing either the intensity of the field or its angle of inclination. Experiments were conducted during both spring and autumn, with robins captured as passage migrants at the Falsterbo and Ottenby bird observatories in southern Sweden as test subjects. Generally, the orientation of robins was affected by magnetic shifts compared to controls tested in the natural geomagnetic field. Autumn birds from the two capture sites differed in their responses, probably because of different migratory dispositions and body conditions. The robins most often changed their orientation to maintain their typical axis of migration relative to the shifted magnetic fields. However, preferred directions in relation to the shifted magnetic fields were frequently reverse from normal, or axial rather than unimodal. These results disagree with suggested mechanisms for orientation by visual sunset cues and with the proposed basis of magnetic orientation. They do, however, demonstrate that the geomagnetic field is involved in the sunset orientation of robins, probably in combination with additional visual or non-visual cues that contribute to establish magnetic polarity.     

Memory of Location and Site Recognition in the Ant Formica uralensis (Hymenoptera: Formicidae)

Spatial recognition cues used in site fidelity in the ant Formica uralensis Ruzsky were studied using outdoor and laboratory arenas. Ant workers visiting symmetrically spaced feeders were colour-marked corresponding to the initial feeder visited during sampling. The effect of manipulating environmental cues on the mean 'spatial specialization' of the population was measured. Site recognition appears to be based on visual landmark/canopy cues. However, ants maintained some fidelity when shielded from these cues, suggesting the involvement of additional cues. When ridding our experimental device of olfactory deposits and shielding visual cues, site fidelity was lost. Idiothetic and/or geomagnetic cues are thought to provide spatial references to visual or olfactory landmarks. Altering nest position relative to the arena and changing the geomagnetic field within the arena in our study, however, did nothing to the site fidelity of visually deprived and non-deprived foragers.
We conclude that site fidelity is developed in a visually structured environment but supplemented by an olfactory backup system that is probably based on discrete home range markings rather than radial odour trails. We demonstrate furthermore that the visual component involved in site location can be stored in the memory of individual F. uralensis foragers during a 6-month hibernation period.     

Orientation in pied flycatchers: the relative importance of magnetic and visual information at dusk

We investigated the orientation of juvenile pied flycatchers, Ficedula hypoleuca, during autumn migration in south Sweden using orientation cage experiments, to study the relative importance of visual and magnetic information at sunset. We performed cage tests under 12 experimental conditions that manipulated the geomagnetic and visual sunset cues available for orientation: natural clear skies in the local or a vertical magnetic field; simulated total overcast in the local or a vertical magnetic field; natural pattern of skylight polarization and directional information from stars screened off, with the sun's position as normal or shifted 120 degrees anticlockwise with mirrors; reduced polarization in the local or a vertical magnetic field; directions of polarization (e-vector) NE/SW and NW/SE, respectively, in the local or a vertical magnetic field. The pied flycatchers were significantly oriented towards slightly south of west when they could use a combination of skylight and geomagnetic cues. The mean orientation was significantly shifted along with the deflection of the sunset position by mirrors. Reduced polarization had no significant effect on orientation either in the local, or in a vertical, magnetic field. The birds tended to orient parallel with the axis of polarization, but only when the artificial e-vector was aligned NW/SE. The mean orientation under simulated total overcast in a vertical, and in the local, magnetic field was not significantly different from random. It is difficult to rank either cue as dominant over the other and we conclude that both visual and magnetic cues seem to be important for the birds' orientation when caught and tested during active migration. Copyright 1999 The Association for the Study of Animal Behaviour.     

Avian orientation at steep angles of inclination: experiments with migratory white-crowned sparrows at the magnetic North Pole

The Earth's magnetic field and celestial cues provide animals with compass information during migration. Inherited magnetic compass courses are selected based on the angle of inclination, making it difficult to orient in the near vertical fields found at high geomagnetic latitudes. Orientation cage experiments were performed at different sites in high Arctic Canada with adult and young white-crowned sparrows (Zonotrichia leucophrys gambelii) in order to investigate birds' ability to use the Earth's magnetic field and celestial cues for orientation in naturally very steep magnetic fields at and close to the magnetic North Pole. Experiments were performed during the natural period of migration at night in the local geomagnetic field under natural clear skies and under simulated total overcast conditions. The experimental birds failed to select a meaningful magnetic compass course under overcast conditions at the magnetic North Pole, but could do so in geomagnetic fields deviating less than 3 degrees from the vertical. Migratory orientation was successful at all sites when celestial cues were available.     

Navigation by green turtles: which strategy do displaced adults use to find Ascension Island?

Sea turtles are known to perform long-distance, oceanic migrations between disparate feeding areas and breeding sites, some of them located on isolated oceanic islands. These migrations demonstrate impressive navigational abilities, but the sensory mechanisms used are still largely unknown. Green turtles breeding at Ascension Island perform long oceanic migrations (>2200 km) between foraging areas along the Brazilian coast and the isolated island. By performing displacement experiments of female green turtles tracked by satellite telemetry in the waters around Ascension Island we investigated which strategies most probably are used by the turtles in locating the island. In the present paper we analysed the search trajectories in relation to alternative navigation strategies including the use of global geomagnetic cues, ocean currents, celestial cues and wind. The results suggest that the turtles did not use chemical information transported with ocean currents. Neither did the results indicate that the turtles use true bi-coordinate geomagnetic navigation nor did they use indirect navigation with respect to any of the available magnetic gradients (total field intensity, horizontal field intensity, vertical field intensity, inclination and declination) or celestial cues. The female green turtles successfully locating Ascension Island seemed to use a combination of searching followed by beaconing, since they searched for sensory contact with the island until they reached positions NW and N of the Island and from there presumably used cues transported by wind to locate the island during the final stages of the search.     

Wintergoldh?hnchen (Regulus regulus) besitzen einen Inklinationskompa?

During autumn migration, orientation tests were performed with Goldcrests in the morning immediately after the birds had been caught. In the local geomagnetic field (vertical component pointing downward), they showed a significant tendency towards 144° SE; in a magnetic field with the vertical component pointing upward, their mean was at 321° NW. This response to an inversion of the vertical component reveals that the Goldcrests used the magnetic field for orientation and that their magnetic compass is an inclination compass as it has been described for several other species of migrants.     

Magnetic Compass Orientation in Larval Iberian Green Frogs, Pelophylax Perezi

Experiments were carried out to investigate whether Iberian green frog tadpoles Pelophylax perezi (formerly Rana perezi) are able of using the geomagnetic field for y‐axis orientation (i.e. orientation toward and away from shore). Tadpoles were trained outdoor for 5 d, in two different training configurations: (i) a training tank aligned along the magnetic north–south axis, with shore facing south, and (ii) a training tank aligned along the magnetic east–west axis, with shore located east, and similar to the shore–deep water axis (‘y‐axis’) found in their home stream, which flows from south to north. After training, tadpoles were individually tested for magnetic orientation in a water‐filled circular outdoor arena surrounded by a pair of orthogonally aligned cube‐surface‐coils used to alter the alignment of the earth's magnetic field. Tadpoles held in the east–west training tank oriented towards shore, indicating that they were able to distinguish between the shoreward and waterward direction along the y‐axis. Tadpoles trained in the tank that was aligned along the north–south axis showed bimodal magnetic compass orientation along the shore–deep water magnetic axis. These findings provide evidence for the use of magnetic compass cues for y‐axis orientation by P. perezi tadpoles.     

Orientation of Dunnocks (Prunella modularis) at Sunset

To find out the relative importance of the geomagnetic and solar cues for the orientation at the time of sunset, dunnocks were tested outdoors during the spring migration periods of 1982 and 1983. Experimental magnetic fields were produced by Helmholtz coils. In the various magnetic conditions, the following results were obtained:

• 1 In the local geomagnetic field, the dunnocks oriented in a seasonally appropriate northerly direction.
• 2 In a magnetic field the north of which was shifted 120° clock-wise to ESE, the birds showed a corresponding shift in their orientation.
• 3 In a vertical magnetic field without meaningful directional information, birds previously tested in either the local geomagnetic field or the shifted magnetic field now displayed axially bimodal orientation, with the axes of the two groups differing.

These findings indicate that for migratory dunnocks, the magnetic field plays a dominant role in determining their orientation at the time of sunset, and that magnetic information may affect the dunnocks' response to other directional, presumably solar cues as well.     

The role of skylight polarization in the orientation of a day-migrating bird species

To assess the role of skylight polarization in the orientation system of a day-migrating bird, Yellow-faced Honeyeaters (Lichenostomus chrysops, Meliphagidae) were tested in funnel cages for their directional preferences. In control tests in the natural local geomagnetic field under the clear natural sky, they preferred their normal migratory course. Manipulations of the e-vector by depolarizing the skylight or rotating the axis of polarization failed to affect the orientation as long as the natural geomagnetic field was present. When deprived of magnetic information, the birds continued in their normal migratory direction as long as they had access to information from the natural sky, or when either the sun or polarized light was available. However, when sun was hidden by clouds, depolarizers caused disorientation. — These findings indicate that polarized skylight can be used for orientation when no other known cues are available. However in the hierarchy of cues of this species, the polarization pattern clearly ranks lower than information from the geomagnetic field.     

Experimental evidence for juvenile Chinook salmon, Oncorhynchus tschawytscha Walbaum, orientation at night and in sunlight after a 7° change in latitude

A group of eighteen young chinook salmon, Oncorhynchus tschawytscha Walbaum, trained to orientate in the direction 270°, showed a unimodal orientation of 264° and a mean bimodal axis of orientation of 258°/078° (magnetic) within confidence limits of 218°←→285°: 038°←→105° when tested under controlled conditions in Auckland. Two years later 12 of these fish were transferred to a new test arena in Christchurch, south (7° latitude) of the original location, for individual re-testing at night in a light-proof room and also in sunlight; in the absence of ‘local’ Auckland cues/clues. These fish had been kept in artificial light but six fish were exposed to sunlight in Auckland 2 weeks before moving to Christchurch. At night each fish showed consistent non-random orientation and nine out of 10 fish showed a mean bimodal orientation that fell within the confidence limit established in Auckland; the mean of means axis of orientation for 10 fish was 270°/090°. In sunlight each individual fish showed a consistent, non-random mean bimodal orientation that fell outside the confidence limits established in Auckland and, at night, in Christchurch. The mean of means axis of orientation was 001°/181° (magnetic); the map direction from Christchurch to Auckland is 15°. The principal findings in this study were: (a) ‘Local’ Auckland cues were not essential for location of the learnt direction. (b) A non-visual ‘universal’ cue was used as a reference for location of direction at night. (c) Daylight orientation was influenced by anisotropic radiance, even though the sun image was obscured by the test arena cover. (d) The concentration of data at midday and sunset in artificial light and perhaps at midnight, may indicate the presence of a non-visual zeitgeber. (e) A correlation between time and direction, in light and in darkness, which by implication involves a co-ordination process. (f) The fish under test apparently imprinted on some aspect of the sun (in Auckland) within a 2-day period at the age of 2 years. (g) Displacement, by 7° in latitude, may have been detected by both visual and non-visual means. It is proposed that directional information from the geomagnetic field and the anisotropic radiance of sunlight provides a complementary cross reference which would be sufficient for positional orientation, in relation to some fixed landmark, within coastal waters; but would not suffice for spatial orientation in mid-ocean.