Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “ORIENTATION”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,117 records · Page 62Linked to original sources

Dynamics of orientation tuning in macaque V1: the role of global and tuned suppression.

The temporal development of neural selectivity to physical attributes of a visual stimulus, such as its orientation and spatial frequency, can provide important clues about mechanisms of cortical tuning. We measured the dynamics of orientation tuning in macaque primary visual cortex (V1) and found several dynamical features in the data: changes in global enhancement and suppression, narrowing of orientation bandwidth, small but significant shifts in preferred orientation, and "Mexican-hat" tuning curves. The dynamics data were analyzed with a model that sums two fixed, tuned components (enhancement and suppression) and one global (untuned) component. The analysis suggests that there is early global enhancement followed by global and tuned suppression. Tuned suppression accounts for the dynamical reduction of orientation bandwidth and for the generation of Mexican-hat tuning profiles. Our findings imply that global and tuned suppression are important factors that determine the selectivity and dynamics of V1 responses to orientation.

Animals↗

Quantitative studies of single-cell properties in monkey striate cortex. II. Orientation specificity and ocular dominance.

1. Quantitative analyses of orientation specificity and ocular dominance were carried out in striate cortex of the rhesus monkey. 2. Sharpness of orientation selectivity was greater for simple (S type) than for complex (CX type) cells. CX-type cells became more broadly tuned in the deeper cortical layers: S-type cells were equally well tuned throughout the cortex. 3. Sharpness of orientation selectivity for S-type cells was similar at all retinal eccentricities studied (0 degrees - 20 degrees from the fovea):in CX-type cells orientation selectivity decreased slightly with increasing eccentricity. 4. The orientation tuning of binocular cells was similar when mapped separately through each eye. 5. Orientation selectivity and direction selectivity are independent of each other, suggesting that separate neural mechanisms give rise to them. 6. More CX-type cells can be binocularly activated than S-type cells (88% versus 49%). The ocular dominance of S-type cells is similar in all cortical layers: for CX-type cells there is an increase in the number of cells in ocular-dominance category 4 in layers 5 and 6.

Animals↗

Effects of bilateral and unilateral ablation of auditory cortex in cats on the unconditioned head orienting response to acoustic stimuli.

1. Reflexive head orienting responses (ORs) elicited by bursts of wide-band noise were investigated in cats after bilateral or unilateral ablation of the auditory cortex, and the cats' performance was compared with that of control cats. The OR was used as an indication of ability to orient toward the azimuthal direction of a source of sound. 2. To adequately test this ability, a unique combination of stimulus duration and position of the sound source was selected on each trial. Stimulus durations (0.1, 0.3, and 1.5 s) were selected so that the offset of a burst of noise occurred before, during, or after an OR. The stimuli were produced from speakers positioned approximately at the interaural horizontal plane within each quadrant of a cat's auditory field. The ORs were recorded on moving film and analyzed quantitatively. 3. In the control cats, the trajectory of the OR was characterized by a saccadic profile (rapid steplike movement, monophasic velocity, and biphasic acceleration). The accuracy of the OR varied directly with stimulus duration, suggesting that the response was modified by auditory feedback produced by a head movement during the stimulus. Corrective responses executed during long-duration (1.5 s) stimuli reduced residual mean error to < 7 degrees in each of the control animals. The mean error in orientation was smaller for sources located in the frontal sound field than for sources located behind the coronal plane the head (> 90 degrees). When brief (0.1 s) stimuli were presented behind the head, the cats confused back with front directions on most of the trials. 4. Compared with performance in the control cats, bilateral destruction of the auditory geniculocortical system severely impaired a cat's ability to orient consistently and accurately toward a source of sound. Latencies to the onset of ORs were increased, the magnitudes of ORs were reduced, average error in orienting to a sound source was larger under every stimulus duration-source position combination, relatively few corrective responses were executed, and residual mean error was significantly elevated (bilateral = 28.1 degrees; control = 3.1 degrees). Several animals with bilateral lesions also made vertical errors in orienting to azimuthal sources of sound. 5. However, in the bilateral lesion group, ORs were initiated in the correct right or left direction; and, rather than eliminating accurate responses altogether, the lesions reduced the probability of their occurrence. Furthermore, the saccadic profile of the response was preserved, providing evidence that the motor control system for the OR was not perturbed by the bilateral lesions.(ABSTRACT TRUNCATED AT 400 WORDS)

Acoustic Stimulation↗

Fastigial nucleus activity during different frequencies and orientations of vertical vestibular stimulation in the monkey.

Neurons in the rostral part of the fastigial nucleus (FN) respond to vestibular stimulation but are not related to eye movements. To understand the precise role of these vestibular-only neurons in the central processing of vestibular signals, unit activity in the FN of alert monkeys (Macaca mulatta) was recorded. To induce vestibular stimulation, the monkey was rotated sinusoidally around an earth-fixed horizontal axis at stimulus frequencies between 0.06 (+/-15 degrees) and 1.4 Hz (+/-7.5 degrees). During stimulation head orientation was changed continuously, allowing for roll, pitch, and intermediate planes of orientation. At a frequency of 0.6 Hz, 59% of the neurons had an optimal response orientation (ORO) and a null response (i.e., no modulation) 90 degrees apart. The phase of neuronal response was constant except for a steep shift of 180 degrees around the null response. This group I response is compatible with a semicircular canal input, canal convergence, or a single otolith input. Several other features indicated more complex responses, including spatiotemporal convergence (STC). 1) For 35% of the responses at 0.6 Hz, phase changes were gradual with different orientations. Fifteen percent of these had a null response (group II), and 20% showed only a minimal response but no null response (group III). The remaining responses (6%), classified as group IV, were characterized by a constant sensitivity at different orientations in most instances. 2) For the vast majority of neurons, the stimulus frequency determined the response group, i.e., an individual neuron could show a group I response at one frequency and a group II (III or IV) response at another frequency. 3) ORO changed with frequency by >45 degrees for 44% of the neurons. 4) Although phase changes at different frequencies were close to head velocity (+/-45 degrees ) or head position (+/-45 degrees ) for most neurons, they exceeded 90 degrees for 29% of the neurons between 0.1 and 1.0 Hz. In most cases, this was a phase advance. The change in sensitivity with change in frequency showed a similar pattern for all neurons; the average sensitivity increased from 1.24 imp. s-1. deg-1 at 0.1 Hz to 2.97 imp. s-1. deg-1 at 1.0 Hz. These data demonstrate that only an analysis based on measurements at different frequencies and orientations reveals a number of complex features. They moreover suggest that for the vast majority of neurons several sources of canal and otolith information interact at this central stage of vestibular information processing.

Acoustic Stimulation↗

Neuronal mechanisms for the control of body orientation in Clione I. Spatial zones of activity of different neuron groups.

The marine mollusk Clione limacina, when swimming, can stabilize different body orientations in the gravitational field. Here we describe one of the modes of operation of the postural network in Clione-maintenance of the vertical, head-up orientation. Experiments were performed on the CNS-statocyst preparation. Spike discharges in the axons of different types of neurons were recorded extracellularly when the preparation was rotated in space through 360 degrees in different planes. We characterized the spatial zones of activity of the tail and wing motor neurons as well as of the CPB3 interneurons mediating the effects of statocyst receptor cells on the tail motor neurons. It was found that the activity of the tail motor neurons increased with deviation of the preparation from the normal, rostral-side-up orientation. Their zones of activity were very wide ( approximately 180 degrees ). According to the zone position, three distinct groups of tail motor neuron (T1-T3) could be distinguished. The T1 group had a center of the zone near the ventral-side-up orientation, whereas the zones of T2 and T3 had their centers near the left-side-up and the right-side-up positions, respectively. By comparing the zone of activity with the direction of tail bending elicited by each of the groups, one can conclude that gravitational reflexes mediated by the T1, T2, and T3 groups will evoke turning of the animal toward the head-up orientation. Two identified wing motor neurons, 1A and 2A, causing the wing beating, were involved in gravitational reactions. They were activated with the downward inclination of the ipsilateral side. Opposite reactions were observed in the motor neurons responsible for the wing retraction. A presumed motor effect of these reactions is an increase of oscillations in the wing that is directed downward and turning of Clione toward the head-up orientation. Among the CPB3 interneurons, at least four groups could be distinguished. In three of them (IN1, IN2, and IN3), the zones of activity were similar to those of the three groups (T1, T2, and T3) of the tail motor neurons. The group IN4 had the center of its zone in the dorsal-side-up position; a corresponding group was not found among the tail motor neurons. In lesion experiments, it was found that gravitational input mediated by a single CPB3 interneuron produced activation of its target tail motor neurons in their normal zones, but the strength of response was reduced considerably. This finding suggests that several interneurons with similar spatial zones converge on individual tail motor neurons. In conclusion, because of a novel method, activity of the neuronal network responsible for the postural control in Clione was characterized in the terms of gravitational responses in different neuron groups comprising the network.

Animals↗

Spatial orientation of caloric nystagmus in semicircular canal-plugged monkeys.

We studied caloric nystagmus before and after plugging all six semicircular canals to determine whether velocity storage contributed to the spatial orientation of caloric nystagmus. Monkeys were stimulated unilaterally with cold ( approximately 20 degrees C) water while upright, supine, prone, right-side down, and left-side down. The decline in the slow phase velocity vector was determined over the last 37% of the nystagmus, at a time when the response was largely due to activation of velocity storage. Before plugging, yaw components varied with the convective flow of endolymph in the lateral canals in all head orientations. Plugging blocked endolymph flow, eliminating convection currents. Despite this, caloric nystagmus was readily elicited, but the horizontal component was always toward the stimulated (ipsilateral) side, regardless of head position relative to gravity. When upright, the slow phase velocity vector was close to the yaw and spatial vertical axes. Roll components became stronger in supine and prone positions, and vertical components were enhanced in side down positions. In each case, this brought the velocity vectors toward alignment with the spatial vertical. Consistent with principles governing the orientation of velocity storage, when the yaw component of the velocity vector was positive, the cross-coupled pitch or roll components brought the vector upward in space. Conversely, when yaw eye velocity vector was downward in the head coordinate frame, i.e., negative, pitch and roll were downward in space. The data could not be modeled simply by a reduction in activity in the ipsilateral vestibular nerve, which would direct the velocity vector along the roll direction. Since there is no cross coupling from roll to yaw, velocity storage alone could not rotate the vector to fit the data. We postulated, therefore, that cooling had caused contraction of the endolymph in the plugged canals. This contraction would deflect the cupula toward the plug, simulating ampullofugal flow of endolymph. Inhibition and excitation induced by such cupula deflection fit the data well in the upright position but not in lateral or prone/supine conditions. Data fits in these positions required the addition of a spatially orientated, velocity storage component. We conclude, therefore, that three factors produce cold caloric nystagmus after canal plugging: inhibition of activity in ampullary nerves, contraction of endolymph in the stimulated canals, and orientation of eye velocity to gravity through velocity storage. Although the response to convection currents dominates the normal response to caloric stimulation, velocity storage probably also contributes to the orientation of eye velocity.

Animals↗

The orientation of the cervical vertebral column in unrestrained awake animals. II. Movement strategies.

Previously we demonstrated a stereotyped resting posture of the head-neck arrangement in a number of vertebrates: the cervical vertebral column is oriented vertically to form one portion of the partial S-shaped configuration of the entire spine. The present investigation quantified the various strategies of head-neck movements employed by different mammalian species (human, monkeys, cats, rabbits and guinea pigs) using cineradiography. At rest, bipeds and quadrupeds hold their heads at the extreme point of flexion of the passive atlanto-occipital range of motion. In this posture, the horizontal semicircular canals are tilted upward from earth horizontal by 5 to 10 degrees and roughly parallel the plane determined by the two obliquus capitis posterior muscles. Furthermore, at this head position, the utricular maculae become oriented earth-horizontally. In quadrupedal animals, head-neck movements in the sagittal plane result from movement at the atlanto-occipital articulation (head/C1) and at the multi-articular cervico-thoracic junction (C6-Th3). Only very small flexion/extension movements occur within the body of the cervical vertebral column (C2-C5). Lowering the head from the resting position is only possible by flexion at the C6-Th3 vertebrae. Raising of gaze from the resting position is only possible by extension of the head at the atlanto-occipital articulation. By contrast, sagittal plane head movements in bipeds are largely confined to the cervico-thoracic junction. This is related to a significantly reduced range of motion of the atlanto-occipital articulation. In monkeys and humans, it range of motion is about 13 and 8-11 degrees, respectively, compared to 105 degrees in rabbits. Our cineradiographic data demonstrated different strategies for head movements in the sagittal plane between quadrupeds and bipeds. At one end of the spectrum, in the case of rabbits, there was no systematic relationship between head and neck orientation. Rabbits stabilized head posture by using the head-neck structure in a parallelogram fashion, which resulted in head posture being largely independent of cervical vertebral column orientation. In monkeys and humans, however, orientation of the head depended almost entirely on the orientation of the cervical vertebral column. In such case, head movements in the sagittal plane almost exclusively relied on the positioning of the cervico-thoracic junction. These different strategies again correlate with the different ranges of motion of the atlanto-occipital articulation. We suggest that vertebrates use mechanical constraints and preferred planes of action for head-neck movement control to simplify sensory-motor transformations subserving motor control and plasticity and to minimize neuronal operations.

Animals↗

Two corticotectal areas facilitate multisensory orientation behavior.

It had previously been shown that influences from two cortical areas, the anterior ectosylvian sulcus (AES) and the rostral lateral suprasylvian sulcus (rLS), play critical roles in rendering superior colliculus (SC) neurons capable of synthesizing their cross-modal inputs. The present studies examined the consequences of selectively eliminating these cortical influences on SC-mediated orientation responses to cross-modal stimuli. Cats were trained to orient to a low-intensity modality-specific cue (visual) in the presence or absence of a neutral cue from another modality (auditory). The visual target could appear at various locations within 45 degrees of the midline, and the stimulus effectiveness was varied to yield an average of correct orientation responses of approximately 45%. Response enhancement and depression were observed when the auditory cue was coupled with the target stimulus: A substantially enhanced probability in correct responses was evident when the cross-modal stimuli were spatially coincident, and a substantially decreased response probability was obtained when the stimuli were spatially disparate. Cryogenic blockade of either AES or rLS disrupted these behavioral effects, thereby eliminating the enhanced performance in response to spatially coincident cross-modal cues and degrading the depressed performance in response to spatially disparate cross-modal cues. These disruptive effects on targets contralateral to the deactivated cortex were restricted to multisensory interactive processes. Orientation to modality-specific targets was unchanged. Furthermore, the pattern of orientation errors was unaffected by cortical deactivation. These data bear striking similarities to the effects of AES and rLS deactivation on multisensory integration at the level of individual SC neurons. Presumably, eliminating the critical influences from AES or rLS cortex disrupts SC multisensory synthesis that, in turn, disables SC-mediated multisensory orientation behaviors.

Acoustic Stimulation↗

Orienting attention to locations in internal representations.

Three experiments investigated whether it is possible to orient selective spatial attention to internal representations held in working memory in a similar fashion to orienting to perceptual stimuli. In the first experiment, subjects were either cued to orient to a spatial location before a stimulus array was presented (pre-cue), cued to orient to a spatial location in working memory after the array was presented (retro-cue), or given no cueing information (neutral cue). The stimulus array consisted of four differently colored crosses, one in each quadrant. At the end of a trial, a colored cross (probe) was presented centrally, and subjects responded according to whether it had occurred in the array. There were equivalent patterns of behavioral costs and benefits of cueing for both pre-cues and retro-cues. A follow-up experiment used a peripheral probe stimulus requiring a decision about whether its color matched that of the item presented at the same location in the array. Replication of the behavioral costs and benefits of pre-cues and retro-cues in this experiment ruled out changes in response criteria as the only explanation for the effects. The third experiment used event-related potentials (ERPs) to compare the neural processes involved in orienting attention to a spatial location in an external versus an internal spatial representation. In this task, subjects responded according to whether a central probe stimulus occurred at the cued location in the array. There were both similarities and differences between ERPs to spatial cues toward a perception versus an internal spatial representation. Lateralized early posterior and later frontal negativities were observed for both pre- and retro-cues. Retro-cues also showed additional neural processes to be involved in orienting to an internal representation, including early effects over frontal electrodes.

Adult↗

An "Oblique Effect" in infants' haptic perception of spatial orientations.

The present research addresses the question of the "oblique effect" (better discrimination of the vertical orientation than of an oblique orientation) in manual haptic perception of orientations (without visual control) by 5-month-old infants. A familiarization/reaction to novelty procedure was used. The results revealed the occurrence of a haptic oblique effect. These findings are similar to those obtained in infant visual perception. We suggest that 5-month-old infants predominately use vertical orientation as a reference norm to perceive haptically spatial orientations. We discuss the implications of these results for both orientation processing and anatomofunctional level contributing specifically to the haptic oblique effect.

Discrimination, Psychological↗

Cueing of object orientation facilitates attentional selection of relevant objects.

Three experiments investigated the effects of advance information about orientation on the processing of relevant and irrelevant objects, as indicated by Stroop effects from color words located in either object. Four results were obtained. First, participants showed the expected modulation of the Stroop effect: words in the relevant object produced much larger Stroop effects than words in the irrelevant object or words in the background. Second, blocking of object orientation had no effects. Third, informative orientation cues facilitated processing of the relevant object, but cueing did not affect processing of the irrelevant object. Fourth, effects of informative orientation cues were restricted to the first part of each experiment. Results suggest that observers can use advance information about object orientation for improving attentional selection of a visual object. In addition, the results revealed some constraints for the effective use of orientation cues, and discard possible explanations for the observed modulation of Stroop effects.

Adult↗

Spatial, colour and contrast response characteristics of mechanisms which mediate discrimination of pattern orientation and magnification.

We have measured response times for the detection of a single target presented against a set of reference elements which are characterised by combinations of four different stimulus parameters; colour, contrast polarity, magnification and orientation. The aim of the experiments was to determine the response characteristics of visual mechanisms which mediate target detection through the discrimination of orientation and magnification. In the first experiments, we determined sensitivity to differences in colour and contrast polarity, and show that the mechanisms responsible for the discrimination of orientation and of magnification are both selective in their responses to colour and to contrast polarity. There are, nonetheless, residual interactions between patterns of different contrast polarities and between those of different colour, and in the latter case, weak interactions persist under equiluminance conditions. In a second set of experiments, we examined the interactions between orientation and magnification. We conclude that the responses of visual mechanisms which mediate target detection through discrimination of orientation are markedly dependent on stimulus magnification whereas those which mediate detection through discrimination of magnification are, in contrast, relatively insensitive to stimulus orientation.

Adult↗

Lateral modulation of contrast discrimination: flanker orientation effects.

We used a dual-masking paradigm to study how contrast discrimination is influenced by the presence of adjacent stimuli differing in orientation. The task of the observer was to detect a vertical Gabor target superimposed on a vertical Gabor pedestal in the presence of flankers. The Gabor flankers had orientations ranging from 0 degrees (parallel to the target) to 90 degrees (orthogonal). The flankers had two different facilitatory effects: (a) Threshold facilitation. The flankers facilitated target detection at low pedestal contrasts. This facilitation was narrowly tuned to flanker orientation. (b) Pedestal enhancement. The flankers at high contrast enhanced the masking effectiveness of the pedestal. This pedestal enhancement changed little with flanker orientation. We fitted the data with a sensitivity modulation model in which the flanker effects were implemented as multiplicative factors modulating the sensitivity of the target mechanism to both excitatory and inhibitory inputs. The model parameters showed that, (a) pedestal enhancement occurs when flanker facilitation to the pedestal is greater than to the target; (b) while the sensitivity modulation was tuned sharply with flanker orientation, the ratio between the excitatory and the inhibitory factors remained constant. The explanation of the flanker orientation effect requires the both the values of each factor and the ratio between them.

Contrast Sensitivity↗

Leg orientation as a clinical sign for pusher syndrome.

BACKGROUND: Effective control of (upright) body posture requires a proper representation of body orientation. Stroke patients with pusher syndrome were shown to suffer from severely disturbed perception of own body orientation. They experience their body as oriented 'upright' when actually tilted by nearly 20 degrees to the ipsilesional side. Thus, it can be expected that postural control mechanisms are impaired accordingly in these patients. Our aim was to investigate pusher patients' spontaneous postural responses of the non-paretic leg and of the head during passive body tilt. METHODS: A sideways tilting motion was applied to the trunk of the subject in the roll plane. Stroke patients with pusher syndrome were compared to stroke patients not showing pushing behaviour, patients with acute unilateral vestibular loss, and non brain damaged subjects. RESULTS: Compared to all groups without pushing behaviour, the non-paretic leg of the pusher patients showed a constant ipsiversive tilt across the whole tilt range for an amount which was observed in the non-pusher subjects when they were tilted for about 15 degrees into the ipsiversive direction. CONCLUSION: The observation that patients with acute unilateral vestibular loss showed no alterations of leg posture indicates that disturbed vestibular afferences alone are not responsible for the disordered leg responses seen in pusher patients. Our results may suggest that in pusher patients a representation of body orientation is disturbed that drives both conscious perception of body orientation and spontaneous postural adjustment of the non-paretic leg in the roll plane. The investigation of the pusher patients' leg-to-trunk orientation thus could serve as an additional bedside tool to detect pusher syndrome in acute stroke patients.

Adult↗

Use of multiple orientation cues by juvenile loggerhead sea turtles Caretta caretta.

Although the orientation cues used by hatchling sea turtles have been studied extensively, little is known about the mechanisms of orientation and navigation that guide older turtles. To investigate the orientation cues used by juvenile loggerheads Caretta caretta L., captured turtles were tethered in a water-filled arena located outdoors. Turtles tested under these conditions established and maintained headings in specific directions in the absence of wave cues, familiar landmarks and chemical gradients. Distorting the magnetic field around the anterior part of a turtle's body did not disrupt orientation if vision remained unimpaired. Similarly, eliminating visual cues by attaching frosted goggles did not disrupt orientation if the magnetic environment was undisturbed. However, when turtles experienced a simultaneous disruption of magnetic and visual cues, their orientation was altered. These results imply that sea turtles, like migratory birds and homing pigeons, are able to maintain headings using multiple sources of directional information.

Animals↗

The role of orientation flights on homing performance in honeybees.

Honeybees have long served as a model organism for investigating insect navigation. Bees, like many other nesting animals, primarily use learned visual features of the environment to guide their movement between the nest and foraging sites. Although much is known about the spatial information encoded in memory by experienced bees, the development of large-scale spatial memory in naive bees is not clearly understood. Past studies suggest that learning occurs during orientation flights taken before the start of foraging. We investigated what honeybees learn during their initial experience in a new landscape by examining the homing of bees displaced after a single orientation flight lasting only 5-10 min. Homing ability was assessed using vanishing bearings and homing speed. At release sites with a view of the landmarks immediately surrounding the hive, 'first-flight' bees, tested after their very first orientation flight, had faster homing rates than 'reorienting foragers', which had previous experience in a different site prior to their orientation flight in the test landscape. First-flight bees also had faster homing rates from these sites than did 'resident' bees with full experience of the terrain. At distant sites, resident bees returned to the hive more rapidly than reorienting or first-flight bees; however, in some cases, the reorienting bees were as successful as the resident bees. Vanishing bearings indicated that all three types of bees were oriented homewards when in the vicinity of landmarks near the hive. When bees were released out of sight of these landmarks, hence forcing them to rely on a route memory, the 'first-flight' bees were confused, the 'reorienting' bees chose the homeward direction except at the most distant site and the 'resident' bees were consistently oriented homewards.

Animals↗

The role of extraocular photoreceptors in newt magnetic compass orientation: parallels between light-dependent magnetoreception and polarized light detection in vertebrates.

Theoretical models implicating specialized photoreceptors in the detection of the geomagnetic field have been the impetus for studying the effects of light on magnetic compass orientation. Magnetic orientation in flies, amphibians and birds has been found to be influenced by light, and in all these groups a shift of approximately 90 degrees in the direction of magnetic compass orientation has been observed under certain wavelengths and/or intensities of light. In the eastern red-spotted newt Notophthalmus viridescens, wavelength-dependent effects of light on magnetic compass orientation appear to result from an antagonistic interaction between short-wavelength (< or = 450 nm) and long-wavelength (> or = 500 nm) photoreception mechanisms. We have demonstrated that at least the short-wavelength input to the newt's magnetic compass is mediated by extraocular photoreceptors located in or near the pineal organ, and here we present new findings that indicate that the putative long-wavelength mechanism is also associated with pineal photoreceptors. Interestingly, the amphibian pineal organ mediates orientation to both the e-vector of plane-polarized light and the magnetic field. Although the wavelength-dependence of the polarized light orientation in amphibians has not been studied, polarization sensitivity in fishes appears to be mediated by two antagonistic photoreception mechanisms that have similar spectral characteristics to those of the newts' magnetic compass response. These parallels, along with similarities in the types of receptors that are expected to be involved in light-dependent magnetoreception and polarized light detection, suggest that similar photoreception mechanisms may mediate the light-dependent magnetic and polarized light compasses.

Animals↗

Harmonic oscillatory orientation relative to the wind in nocturnal roosting flights of the swift Apus apus.

Swifts regularly spend the night flying at high altitude. From previous studies based on tracking radar observations, we know that they stay airborne during the night and prefer to orient themselves into the wind direction with an increased angular concentration with increasing wind speed. In this study, we investigated the orientation relative to the wind of individual swifts by frequency (discrete Fourier transform) and autocorrelation analysis based on time series (10s intervals) of the angle between the swifts' heading and the wind direction for radar trackings of long duration (9-60 min). The swifts often showed a significant harmonic oscillation of their heading direction relative to the wind, with a frequency mostly in the range 1-17 mHz, corresponding to cycle periods of 1-16 min. The swifts also sometimes performed circling flights at low wind speeds. Wind speed ranged from 1.3 to 14.8 m s(-1), and we expected to find different patterns of orientation at different wind speeds, assuming that the swifts adapt their orientation to avoid substantial displacement during their nocturnal flights. However, oscillatory orientation was found at all wind speeds with variable frequencies/periods that did not show any consistent relationship with wind speed. It remains to be shown whether cyclic heading changes are a regular feature of bird orientation.

Adaptation, Physiological↗