Visual fields in the Stone-curlew Burhinus oedicnemus

The Stone-curlew Burhinus oedicnemus is a short-billed terrestrial wading bird (Burhinidae; Charadriiformes) which forages primarily for surface living invertebrates in open, sparsely vegetated habitats during twilight and nighttime. Visual field topography in restrained alert birds was investigated using an ophthalmoscopic reflex technique. The visual fields have the following features: (1) Eye movements of significant amplitude appear to be absent. (2) The retinal binocular field is relatively small, with the bill placed near its centre. It extends vertically through 80° in the median sagittal plane with a maximum width of 18° occurring 5° above the bill. (3) With the head in a typical posture (eye-bill-tip angle approximately 15° below the horizontal), the binocular field stretches from 60° below to 20° above the horizontal. (4) The blind area behind the head is relatively narrow (15° at the horizontal), giving the bird near panoramic vision in the horizontal plane, but the widest blind area (32°) occurs directly above the head. (5) Monocular retinal fields in the horizontal plane are 182° wide and are asymmetric about the optic axis. (6) There is a blind sector of 7–12° at the margin of the optical fields, indicating that binocular field widths are not maximized. Interspecific comparisons of these visual field features suggest that the foraging of Stone-curlews is guided primarily by visual cues.     

Visual fields in woodcocks Scolopax rusticola (Scolopacidae; Charadriiformes)

Woodcocks, Scolopax rusticola, are long-billed terrestrial wading birds (Scolopacidae; Charadriiformes) which forage primarily by probing in soft substrates for invertebrates. Visual field topography in restrained alert birds was investigated using an ophthalmoscopic reflex technique.

1. Eye movements of significant amplitude are absent.
2. The retinal binocular field is long and narrow. It extends through 190° in the median sagittal plane. When the head adopts a normal posture (bill at an angle of 40° below the horizontal) the binocular field stretches from 25° above the bill to 5° above the horizontal behind the head. Thus, woodcocks have comprehensive visual coverage of the hemisphere above them but the bill falls outside the visual field. Maximum binocular field width equals 12° and occurs perpendicular to the line of the bill. To the rear of the head binocular field width is less than 5° except in an area 40° above the horizontal where it increases to 7°.
3. Monocular retinal fields in the horizontal plane are 182° wide. There is no blind sector at the margin of the optical fields.
4. The general structure of woodcock skulls facilitates panoramic vision in a horizontal plane.
5. Interspecific comparisons are consistent with the hypothesis that visual field topography among birds is closely associated with the role of vision in foraging. Comprehensive visual coverage of the celestial hemisphere probably occurs only in species, such as woodcocks, which rely primarily upon senses other than vision to guide foraging.

     

The lumbosacral transition: morphologic variations and their functional significance

The articular facet of a superior articular process of the sacrum is directed backward, inward, and upward with marked variations. 4 angles characterize the orientation of this facet: a) The relative angle of tilt: i.e. the angle between the articular facet and the upper end-plate of the sacrum, measured in a sagittal plane. b) The absolute angle of tilt: i.e. the angle between the articular facet and the horizontal plane, measured in a sagittal plane. c) The tilted part-angle of opening: i.e. the angle between the articular facet and the sagittal plane, measured in a plane parallel to the upper end-plate of the sacrum. d) The horizontal part-angle of opening: i.e. the angle between the articular facet and the sagittal plane, measured in a horizontal plane. These 4 angles are determined by characteristic straights within the articular facet and certain reference planes (upper end-plate of the sacrum, horizontal plane, sagittal plane). Only 2 intersecting straights suffice for an adequate determination of a geometrical plane; therefore, if we know the relative angle of tilt and the tilted part-angle of opening, we are able to construct or to calculate the absolute angle of tilt as well as the horizontal part-angle of opening by using the range of inclination of the sacrum. The shape as well as the orientation of the articular facets at the superior articular processes of the sacrum do not depend on the inclination of the pelvis nor on the inclination of the sacrum nor on the range of the lumbosacral angle. Only the absolute angle of tilt shows a reference to the inclination of the sacrum because the relative angle of tilt shows a certain constancy. The orientation of the articular facets is slightly influenced by static moments, but considerably determined by dynamical requirements. At spines with irregular numbers of praesacral vertebrae, the orientation of the lumbosacral articular facets do not differ from the orientation of these facets at spines with the regular number of 24 praesacral vertebrae. This, however, does not prove right at spines, that have a lumbosacral "transitional vertebra". Such lumbosacral transitional vertebrae detract much from the stability of the lumbosacral region of the spine.     

The visual field and visually guided behavior in the zebra finch (Taeniopygia guttata)

Summary Measurements were made of the physical properties of the visual system of the zebra finch, a bird with laterally placed eyes. The use of the visual system in pecking and courtship behavior was examined. It was demonstrated that the optical axis and the fovea of the eye point in a direction about 62° from the sagittal axis of the head. The visual field of each eye covers about 170° in the horizontal plane. In the frontal region there is an overlap of about 30°–40° where the birds can see binocularly; caudally there is a gap in the visual field of 60°. The point of best binocular viewing is in the sagittal plane at 16.5° below the beak.Concerning movement detection, the upper threshold is 540°/s for the binocular (frontal) part of the visual field and about 1100°/s for the monocular (lateral) part. Most fixations before pecking occur monocularly. A preference for one eye during pecking was not detected. During the courtship song, a male bird directs its head towards the female. The results are discussed in comparison with findings in pigeons and chickens.     

The visual perception of relative distances in the wood-cricket, Nemobius sylvestris

ABSTRACT. In post-embryonic development, the visual system of the cricket Nemobius sylvestris (Bosc) shows a regular increase in the length and number of the ommatidia and a decrease of inter-ommatidial angle so that the adult's is a third of the value in the first larval instar. Further, a 20° widening of the binocular visual field, in the horizontal plane at least, and a three-fold increase of the inter-ocular distance improve the potential for binocular vision. Behavioural experiments showed that the insect orientates with differing precision depending on the distances to targets of constant angular size. Further, in a choice situation between two such vertical targets, the cricket orientates most strongly towards the closer of the two, even at target distances of 52 and 130 cm from its point of decision. In fixed tethered animals, discrimination between a close and a distant target is still possible, but disappears when the head is waxed to the thorax, so that any relative movement between the animal and the object is prevented. As these capabilities exceed the possibilities of binocular triangulation, the possible role of other mechanisms is discussed, particularly that involving movement parallax using both eyes.     

Three‐dimensional flight tracking shows how a visual target alters tsetse fly responses to human breath in a wind tunnel

Tsetse flies Glossina spp. (Diptera; Glossinidae) are blood‐feeding vectors of disease that are attracted to vertebrate hosts by odours and visual cues. Studies on how tsetse flies approach visual devices are of fundamental interest because they can help in the development of more efficient control tools. The responses of a forest tsetse fly species Glossina brevipalpis (Newstead) to human breath are tested in a wind tunnel in the presence or absence of a blue sphere as a visual target. The flight responses are video recorded with two motion‐sensitive cameras and characterized in three dimensions. Although flies make meandering upwind flights predominantly in the horizontal plane in the plume of breath alone, upwind flights are highly directed at the visual target presented in the plume of breath. Flies responding to the visual target fly from take‐off within stricter flight limits at lower ground speeds and with a significantly lower variance in flight trajectories in the horizontal plane. Once at the target, flies fly in loops principally in the horizontal plane within 40 cm of the blue sphere before descending in spirals beneath it. Successful field traps designed for G. brevipalpis take into account the strong horizontal component in local search behaviour by this species at objects. The results suggest that trapping devices should also take into account the propensity of G. brevipalpis to descend to the lower parts of visual targets.     

Evasive behaviour in the cave-cricket, Troglophilus cavicola

ABSTRACT. Cave crickets of the genus Troglophilus occur in caves of the Alps and Dinarides generally in wintertime. Most hibernation sites in caves were inclined at more than 60° to the horizontal. The crickets show a striking escape behaviour which is strongly influenced by the inclination of the surface on which they are standing: stimulated adequately, they readily jump from horizontal surfaces, but only rarely from the side walls or roofs of caves. An arena with a tiltable floor was used to quantify this and other behavioural effects in relation to the degree of inclination of the floor, and gave the following results, (a) From 0° to 60° the rate of evasive jumping was inversely related to the steepness of the floor; above 60° jumping was almost completely inhibited. (b) Below 75° more than half the crickets showed a positive thigmotaxis to the arena walls, above 75° this thigmotaxis was much weaker, (c) The effect of blinding was to reduce these levels of thigmotaxis at inclinations lower than 60° and to increase the thigmotactic response at steeper inclinations, (d) Standing orientation was generally upwards at inclinations steeper than 60°; below 45°, the steeper the floor, the greater this upward orientation tendency, (e) If the cricket was standing orientated downwards, evasive jumping was less inhibited on slopes between 15° and 60°.     

New model for the avian magnetic compass

It is proposed that the avian magnetic compass depends on the angle between the horizontal component B(h) of the geomagnetic field (GMF) and E(r), the radial electric field distribution generated by gamma-oscillations within the optic tectum (TeO). We hypothesize that the orientation of the brain relative to B(h) is perceived as a set of electric field ion cyclotron resonance (ICR) frequencies that are distributed in spatially recognizeable regions within the TeO. For typical GMF intensities, the expected ICR frequencies fall within the 20-50 Hz range of gamma-oscillation frequencies observed during visual stimulation. The model builds on the fact that the superficial lamina of the TeO receive signals from the retina that spatially map the visual field. The ICR frequencies are recruited from the local wide-band gamma-oscillations and are superposed on the tectum for interpretation along with other sensory data. As a first approximation, our analysis is restricted to the medial horizontal plane of the TeO. For the bird to fly in a preferred, previously mapped direction relative to B(h), it hunts for that orientation that positions the frequency maxima at appropriate locations on the TeO. This condition can be maintained even as B(h) varies with geomagnetic latitude during the course of long-distance flights. The magnetovisual coordinate system (straight phi, omega) overlaying the two halves of the tectal surface in a nonsymmetric way may imply an additional orienting function for the TeO over and above that of a simple compass (e.g., homing navigation as distinct from migrational navigation).     

Nonlinear analysis of the dynamics of the human balance control system during fixation and smooth pursuit of visual target

The similarity between the dynamics of the human balance control system in the frontal and sagittal planes during the fixation of visual stimulus and smooth pursuit of its sinusoidal movements in the horizontal plane with a frequency of 0.1 or 0.01 Hz (so-named fast and slow pursuit) has been investigated by the nonlinear method of analysis. The experiments were carried out according to the notion that it is possible to describe the process of orthograde standing by a two-segment model--upper and lower segments which are connected by a hip joint (other joints were fixed). It was shown that during fixation the similarity between the dynamics of orthostatic control system in the frontal plane is higher than in the sagittal plane. A slow pursuit does not influence the similarity, but a fast one decreases the similarity in the frontal plane. The indices of similarity between the dynamics of the system in the sagittal plane for all the conditions are close and do not differ significantly. The changes in similarity during fast pursuit are supposed to be connected with the different inertia of eyes and body movements. The differences between dynamic similarity in the frontal and sagittal planes are probably connected with the peculiarities of both balance control during joint fixation and AP-ML control (Winter et al., 1993) under conditions investigated.     

MPI CyberMotion Simulator: implementation of a novel motion simulator to investigate multisensory path integration in three dimensions

Path integration is a process in which self-motion is integrated over time to obtain an estimate of one's current position relative to a starting point (1). Humans can do path integration based exclusively on visual (2-3), auditory (4), or inertial cues (5). However, with multiple cues present, inertial cues - particularly kinaesthetic - seem to dominate (6-7). In the absence of vision, humans tend to overestimate short distances (<5 m) and turning angles (<30°), but underestimate longer ones (5). Movement through physical space therefore does not seem to be accurately represented by the brain. Extensive work has been done on evaluating path integration in the horizontal plane, but little is known about vertical movement (see (3) for virtual movement from vision alone). One reason for this is that traditional motion simulators have a small range of motion restricted mainly to the horizontal plane. Here we take advantage of a motion simulator (8-9) with a large range of motion to assess whether path integration is similar between horizontal and vertical planes. The relative contributions of inertial and visual cues for path navigation were also assessed. 16 observers sat upright in a seat mounted to the flange of a modified KUKA anthropomorphic robot arm. Sensory information was manipulated by providing visual (optic flow, limited lifetime star field), vestibular-kinaesthetic (passive self motion with eyes closed), or visual and vestibular-kinaesthetic motion cues. Movement trajectories in the horizontal, sagittal and frontal planes consisted of two segment lengths (1st: 0.4 m, 2nd: 1 m; ±0.24 m/s(2) peak acceleration). The angle of the two segments was either 45° or 90°. Observers pointed back to their origin by moving an arrow that was superimposed on an avatar presented on the screen. Observers were more likely to underestimate angle size for movement in the horizontal plane compared to the vertical planes. In the frontal plane observers were more likely to overestimate angle size while there was no such bias in the sagittal plane. Finally, observers responded slower when answering based on vestibular-kinaesthetic information alone. Human path integration based on vestibular-kinaesthetic information alone thus takes longer than when visual information is present. That pointing is consistent with underestimating and overestimating the angle one has moved through in the horizontal and vertical planes respectively, suggests that the neural representation of self-motion through space is non-symmetrical which may relate to the fact that humans experience movement mostly within the horizontal plane.     

Variations in the off-axis refractive state in the eye of the Vietnamese leaf turtle (<Emphasis Type="Italic">Geoemyda spengleri</Emphasis>)

Lower-field myopia has been described for various vertebrates as an adaptation that permits the animal to keep the ground in focus during foraging, and, at the same time, to look out for distant objects, such as predators, in the upper visual field. Off-axis measurements with infrared photoretinoscopy in the eye of Geoemyda spengleri revealed a constant refractive state in the horizontal plane of the visual field but variable refraction in the vertical plane. In the three turtles investigated, the refractions increased continuously from the ventral to the dorsal visual field over a range of 35, 40 and 56 D, respectively. While this finding confirms the presence of an adaptive change of the refractive state equivalent to lower field myopia, subsequent measurements with a rotated retinoscope showed that at least part of the variation in the ventral field was attributed to astigmatism. The reason for this astigmatism is unknown. Anatomical investigation of the retina revealed that the constant refractive values in the horizontal plane corresponded to a stripe of increased ganglion cell density. A maximum density of 4,200 ganglion cells mm^–2 was counted in the centre of this visual streak.     

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°.     

Visual discrimination by the honeybee (Apis mellifera): the position of the common centre as the cue

Abstract. Bees can be trained to discriminate between a target with a 20° spot above a 10° spot of the same colour, and another target with the spots exchanged in position. Tests show that they do not remember the separate positions of spots of the same colour (including black) on the same target. The bees discriminate the difference in positions, in the vertical direction, of the common centres of the spots taken together, with or without green contrast.
Similar results are obtained in discriminations of a fixed T shape, each composed of two broad black bars subtending 8 by 24°, vs the same shape inverted. The trained bees fail to discriminate between the T shapes when the centroids are at the same level in the vertical direction. Moving the shapes in the horizontal direction in tests has less effect. Quite different results are obtained when the two bars of the T shape differ in colour. The bees discriminate the positions of the two colours separately, but they still fail to discriminate the shape of the T. The results can be explained by filters that detect the intensities within their fields, irrespective of shape, and weigh them according to their vertical angles from the horizontal midline. The normal function of these filters could be to detect the levels of objects relative to the horizon when the bee is in flight.     

Anteroposterior dynamic balance reactions induced by circular translation of the visual field

The anteroposterior sway of subjects under conditions of spontaneous dynamic balance on a wobbly platform was measured during visual stimulation by a visual target executing a circular trajectory in the frontal plane. The target was either a component of the whole moving visual scene or moving on a stationary background. With the former stimulation, obtained through the use of rotating prismatic glasses, every point of the visual field appeared to describe a circular trajectory around its real position so that the whole visual field apeared to be circularly translated, undistorted, inducing a binocular pursuit movement. Under these conditions, stereotyped anteroposterior dynamic balance reactions synchronous with the position of the stimulus were elicited. The latter stimulation consisted of pursuing a luminous target describing a trajectory similar to that of the fixation point seen through the rotating prisms on the same, this time stable, visual background. Although pursuit eye movements were comparable, as demonstrated by electro-oculographic recordings, no stereotyped equilibration reaction was induced. It is concluded that the translatory motion of the background image on the retina in the latter experiments contributed to the body's stability as well as to the perception of a stable environment.     

Effects of Auditory Stimuli in the Horizontal Plane on Audiovisual Integration: An Event-Related Potential Study

This article aims to investigate whether auditory stimuli in the horizontal plane, particularly originating from behind the participant, affect audiovisual integration by using behavioral and event-related potential (ERP) measurements. In this study, visual stimuli were presented directly in front of the participants, auditory stimuli were presented at one location in an equidistant horizontal plane at the front (0°, the fixation point), right (90°), back (180°), or left (270°) of the participants, and audiovisual stimuli that include both visual stimuli and auditory stimuli originating from one of the four locations were simultaneously presented. These stimuli were presented randomly with equal probability; during this time, participants were asked to attend to the visual stimulus and respond promptly only to visual target stimuli (a unimodal visual target stimulus and the visual target of the audiovisual stimulus). A significant facilitation of reaction times and hit rates was obtained following audiovisual stimulation, irrespective of whether the auditory stimuli were presented in the front or back of the participant. However, no significant interactions were found between visual stimuli and auditory stimuli from the right or left. Two main ERP components related to audiovisual integration were found: first, auditory stimuli from the front location produced an ERP reaction over the right temporal area and right occipital area at approximately 160–200 milliseconds; second, auditory stimuli from the back produced a reaction over the parietal and occipital areas at approximately 360–400 milliseconds. Our results confirmed that audiovisual integration was also elicited, even though auditory stimuli were presented behind the participant, but no integration occurred when auditory stimuli were presented in the right or left spaces, suggesting that the human brain might be particularly sensitive to information received from behind than both sides.     

Visual fields in hornbills: precision-grasping and sunshades

Retinal visual fields were determined in Southern Ground Hornbills Bucorvus leadbeateri and Southern Yellow-billed Hornbills Tockus leucomelas (Coraciiformes, Bucerotidae) using an ophthalmoscopic reflex technique. In both species the binocular field is relatively long and narrow with a maximum width of 30° occurring 40° above the bill. The bill tip projects into the lower half of the binocular field. This frontal visual field topography exhibits a number of key features that are also found in other terrestrial birds. This supports the hypothesis that avian visual fields are of three principal types that are correlated with the degree to which vision is employed when taking food items, rather than with phylogeny. However, unlike other species studied to date, in both hornbill species the bill intrudes into the binocular field. This intrusion of the bill restricts the width of the binocular field but allows the birds to view their own bill tips. It is suggested that this is associated with the precision-grasping feeding technique of hornbills. This involves forceps-like grasping and manipulation of items in the tips of the large decurved bill. The two hornbill species differ in the extent of the blind area perpendicularly above the head. Interspecific comparison shows that eye size and the width of the blind area above the head are significantly correlated. The limit of the upper visual field in hornbills is viewed through the long lash-like feathers of the upper lids and these appear to be used as a sunshade mechanism. In Ground Hornbills eye movements are non-conjugate and have sufficient amplitude (30–40°) to abolish the frontal binocular field and to produce markedly asymmetric visual field configurations.     

Horizontal-vertical filters in early vision predict anomalous line-orientation identification frequencies.

A characteristic of early visual processing is a reduction in the effective number of filter mechanisms acting in parallel over the visual field. In the detection of a line target differing in orientation from a background of lines, performance with brief displays appears to be determined by just two classes of orientation-sensitive filter, with preferred orientations close to the vertical and horizontal. An orientation signal represented as a linear combination of responses from such filters is shown to provide a quantitative prediction of the probability density function for identifying the perceived orientation of a target line. This prediction was confirmed in an orientation-matching experiment, which showed that the precision of orientation estimates was worst near the vertical and horizontal and best at about 30 degrees each side of the vertical, a result that contrasts with the classical oblique effect in vision, when scrutiny of the image is allowed. A comparison of predicted and observed frequency distributions showed that the hypothesized orientation signal was formed as an opponent combination and horizontal and vertical filter responses.     

Scanning eye movements of the stomatopod crustacean,Neogonodactylus oerstedii,in polarized light fields

ABSTRACT

Stomatopod crustaceans have highly mobile, independently moving compound eyes that are sensitive to both linearly and circularly polarized light. They rotate their eyes to predictable angles when viewing a linearly polarized target, and they scan their eyes frequently to sample the visual field. Angles of scans are roughly perpendicular to the plane of the midband (a set of specialized parallel rows of equatorial ommatidia). We investigated scanning eye movements in one Caribbean stomatopod species (Neogonodactylus oerstedii) in uniform visual fields that were vertically polarized, horizontally polarized, or depolarized. We found that mean eye rotation and scan angles differed significantly among these different treatments. Average scan angles differed by 12°, being more horizontal in a vertically polarized field than in a horizontally polarized one, and also more horizontal in a vertically polarized field than in a depolarized field. Thus, these stomatopods adjusted visual scanning to the polarization of the visual environment.     

Motion sensitive interneurons in the optomotor system of the fly

The functional properties of the three horizontal cells (north horizontal cell, HSN; equatorial horizontal cell, HSE; south horizontal cell, HSS) in the lobula plate of the blowflyCalliphora erythrocephala were investigated electrophysiologically. 1. The receptive fields of the HSN, HSE, and HSS cover the dorsal, equatorial and ventral part of the ipsilateral visual field, respectively. In all three cells, the sensitivity to visual stimulation is highest in the frontal visual field and decreases laterally. The receptive fields and spatial sensitivity distributions of the horizontal cells are directly determined by the position and extension of their dendritic fields in the lobula plate and the dendritic density distributions within these fields. 2. The horizontal cells respond mainly to progressive (front to back) motion and are inhibited by motion in the reverse direction, the preferred and null direction being antiparallel. The amplitudes of motion induced excitatory and inhibitory responses decline like a cosine function with increasing deviation of the direction of motion from the preferred direction. Stimulation with motion in directions perpendicular to the preferred direction is ineffective. 3. The preferred directions of the horizontal cells show characteristic gradual orientation changes in different parts of the receptive fields: they are horizontally oriented only in the equatorial region and increasingly tilted vertically towards the dorsofrontal and ventrofrontal margins of the visual field. These orientation changes can be correlated with equivalent changes in the local orientation of the lattice of ommatidial axes in the pertinent compound eye. 4. The response amplitudes of the horizontal cells under stimulation with a moving periodic grating depend strongly on the contrast frequency of the stimulus. Maximal responses were found at contrast frequencies of 2–5 Hz. 5. The spatial integration properties of the horizontal cells (studied in the HSE) are highly nonlinear. Under stimulation with extended moving patterns, their response amplitudes are nearly independent of the size of the stimuli. It is demonstrated that this response behaviour does not result from postsynaptic saturation in the dendrites of the cells. The results indicate that the horizontal system is essentially involved in the neural control of optomotor torque responses performed by the fly in order to minimize unvoluntary deviations from a straight flight course.     

Secondary dormancy in Avena fatua: Effect of temperature and after-ripening

To evaluate the effect of after-ripening on secondary dormancy induction in pure genetic lines of Avena fatua L., seed samples were periodically removed from standard conditions of storage and the caryopses then subjected to anoxia. Anoxia did not induce secondary dormancy in SH430, a line characterized by no primary dormancy at harvest maturity; secondary dormancy was induced in caryopses of other lines that had been after-ripened to over-come primary dormancy ranging in duration from a few days (CS40, CS166) to several months (AN51, AN127). Germination response to low GA₃ concentrations indicated that secondary dormancy in CS40 and CS166 was less intense than in AN51 and AN127. The longer the period of dry after-ripening prior to anoxia treatment, the lower the intensity of secondary dormancy induced. After a period of dry after-ripening, which was characteristic for each line, anoxia became an ineffective dormancy-inducing treatment. Caryopses selected for their response to dormancy induction by anoxia were subjected to temperatures from 5 to 35°C to investigate the effect of low (5 to 18°C) and high (20 to 35°C) temperatures on both thermo- and secondary dormancy induction. SH430 was not responsive to any treatment, while CS40, CS166 and AN51 were induced into a thermo-dormancy at temperatures above 20°C and CS166 and AN51 were induced into secondary dormancy by anoxia at temperatures from 5 to 35°C. The effect of anoxia on secondary dormancy induction in a range of pure genetic lines is discussed with reference to primary dormancy, after-ripening and temperature.