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D Osorio

Publications and source records attributed to D Osorio.

34 records · Page 2Linked to original sources
PubMed1997

Stomatopod photoreceptor spectral tuning as an adaptation for colour constancy in water.

Where colour is used in communication absolute judgement of signalling spectra is important, and failures of colour constancy may limit performance. Stomatopod crustaceans have unusual eyes in which the midband contains ten or more classes of photoreceptor. For constancy based on receptor adaptation to a fixed background, elementary theory predicts and we confirm by modelling, that stomatopods' narrow-band receptors outperform more broadly tuned receptors. Similar considerations could account for the small spectral separation of receptors in each midband row. Thus, stomatopods seem to trade-off sensitivity and signal-to-noise ratio for increased colour constancy.

Adaptation, Ocular↗
PubMed1997

Eosinophilic gastroenteritis: diagnostic laparoscopy.

We report a case of eosinophilic gastroenteritis. The initial diagnosis was made by laparoscopic inspection of the lesion during exploration of the abdomen. We immediately carried out an extracorporeal resection using a laparoscopic surgical technique. Pathological examination confirmed our diagnosis. Eosinophilic gastroenteritis is an infrequent condition, and this definitive description of a lesion as seen in the magnified field of the laparoscope demonstrates the effectiveness of laparoscopy as a diagnostic tool to diagnose the cause of ill-defined abdominal discomfort with inconclusive laboratory findings that formerly would have needed a more surgically aggressive laparotomy to resolve.

Abdominal Pain↗
PubMed1996

Colour vision as an adaptation to frugivory in primates.

Most mammals possess two classes of cone, sensitive to short and to long wavelengths of light, but Old World primates (Catarrhini) have distinct medium and long wavelength sensitive classes. The sensitivities of these cones photopigments are alike in all catarrhines with peaks at about 440 nm ('blue'), 533 nm ('green') and 565 nm ('red'). One possible reason for the evolution and conservatism of catarrhine trichromacy is that colour vision is a specialization for finding food. A model of retinal coding of natural spectra, based on discrimination thresholds, is used to examine the usefulness of dichromatic and trichromatic vision for finding fruit, and for identifying fruit and leaves by colour. For identification tasks the dichromat's eye is almost as good as a trichromat's, but the trichromat has an advantage for detecting fruit against a background of leaves.

Adaptation, Physiological↗
PubMed1996

Characterisation of columnar neurons and visual signal processing in the medulla of the locust optic lobe by system identification techniques.

We describe visual responses of seventeen physiological classes of columnar neuron from the retina, lamina and medulla of the locust (Locusta migratoria) optic lobe. Many of these neurons were anatomically identified by neurobiotin injection. Characterisation of neuronal responses was made by moving and flash stimuli, and by two system identification techniques: 1. The first-order spatiotemporal kernel was estimated from response to a spatiotemporal white-noise stimulus; 2. A set of kernels to second order was derived by the maximal-length shift register (M-sequence) technique, describing the system response to a two-channel centre-surround stimulus. Most cells have small receptive fields, usually with a centre diameter of about 1.5 degrees, which is similar to that of a single receptor in the compound eye. Linear response components show varying spatial and temporal tuning, although lateral inhibition is generally fairly weak. Second-order nonlinearities often have a simple form consistent with a static nonlinear transformation of the input from the large monopolar cells of the lamina followed by further linear filtering.

Animals↗
PubMed1994

A good eye for arthropod evolution.

Insect and crustacean lineages diverged over 500 Myr ago, and there are continuing uncertainties about whether they evolved from a common arthropod ancestor or, alternatively, they evolved independently from annelid worms. Despite the diversity of their limbs and lifestyles, the nervous systems of insects and crustaceans share many common features both in development and in function. Cellular and molecular embryology techniques reveal good evidence for homologies in the developing segmental ganglia. In the visual system, this seemingly common programme of insect and crustacean CNS development culminates in common adult neural function. Comparisons of the cellular anatomy and physiology of animals as diverse as flies and crayfishes indicate that the neural circuits in the lamina of their optic lobe have been inherited largely unchanged from a common ancestor with good compound eyes.

Animals↗
PubMed1993

The tuning of human photopigments may minimize red-green chromatic signals in natural conditions.

Humans and other Old World primates (Catarrhini) share very similar L (long-wavelength, 'red') and M (medium-wavelength, 'green') cone photopigment spectral sensitivities, with peaks at around 563 nm and 535 nm, respectively. Changes of single amino acid residues at critical sites in photopigment opsins can alter this peak tuning. Moreover, the photopigment alleles and spectral sensitivities of human populations are polymorphic, so there is potential for adaptive change or genetic drift. The manifest lack of variability suggests that the tuning of the L and M photopigments has adaptive significance, but the reason for this conservatism is unclear. To assess how natural spectral reflectances may have influenced pigment tuning, we have measured the chromatic (i.e. difference) signals available in natural scenes, and estimated how these signals would vary if spectral sensitivities of the pigments moved to longer or to shorter wavelengths. The size of the chromatic signal is, predictably, dependent principally on the spectral separation of the photopigments, but in addition we find that for a fixed separation there is a marked dependence on the specific peak tuning of the photopigments. Indeed, the naturally occurring L and M cone peaks may be set at a pair of points on the spectrum that on average minimizes the 'L-M' (i.e. red-green) chromatic signal. This somewhat paradoxical observation supports the view that red-green vision has evolved for a specific task, such as finding fruit, whilst minimizing interference by the chromatic signal in luminance vision to which both L and M cones contribute.

Adaptation, Physiological↗
PubMed1992

Human cone-pigment spectral sensitivities and the reflectances of natural surfaces.

The evolution of visual pigment spectral sensitivities is probably influenced by the reflectance spectra of surfaces in the animal's environment. These reflectances, we conjecture, fall into three main classes: i. Most inorganic and many organic surfaces, including tree bark, dead leaves and animal melanin pigmentation, whose reflectance increases gradually as a function of wavelength. ii. Living leaves, which contain chlorophyll, have a sharp reflectance peak at about 555 nm. iii. Flowers, fruit and other signaling colours that have co-evolved with animal vision typically do not reflect strongly at the same wavelength as leaves, and present a colour contrast against a leafy background. These three spectral functions we call 'grey-red', 'leaf-green' and 'leaf-contrast' respectively. This simple categorisation allows us to interpret the spectral tuning of human cone pigments in a way that might not seem possible given the wide variety of colours present in nature. In particular L-(red) cones will capture the highest possible proportion of photons reflected by leaves, and M-(green) cones will capture about 10% fewer photons both from leaves and from 'grey-red' surfaces. These observations have some clear implications for our understanding of the evolution of trichomacy and the trade-off between chromatic and luminance vision in Old-World Primates.

Humans↗
PubMed1991

Camouflage by edge enhancement in animal coloration patterns and its implications for visual mechanisms.

Animal camouflage patterns may exploit, and thus give an insight into, visual processing mechanisms. In one common type of camouflage the borders of the coloured patterns are enhanced by high contrast lines. This type of camouflage is seen on many frogs and we use it as the basis for speculating about vision in a small, frog-eating snake. It is argued that a simple categorization of intensity profiles, such as that invoked by a mechanism that detects phase-congruence, occurs at an early stage of snake vision. We show that edge-detectors using a phase-congruence strategy will be unable to distinguish between 'natural' step-edges and the enhanced border profiles commonly seen on cryptic animals, and that the camouflage will be effective over a wide range of spatial scales.

Adaptation, Physiological↗
PubMed1991

Mechanisms of early visual processing in the medulla of the locust optic lobe: how self-inhibition, spatial-pooling, and signal rectification contribute to the properties of transient cells.

In the arthropod medulla, which is the second ganglion on the afferent visual pathway, a column of about 40 cells represents each point in space (i.e. compound eye facet). Some stages of visual processing underlying the responses of one class of cells in the locust medulla have been identified. These transient cells give very similar responses to intensity increments and decrements, and also to pulses and steps; there is no spontaneous activity and a stimulus causes one or two spikes to fire at fixed latencies. Movement, however, produces a prolonged spike discharge by successive excitation of subunits within the receptive field. One of the main features of the transient cells' responses is a self-inhibition which attenuates responses to successive stimuli at one point. This inhibition is restricted to the outputs of single receptor (rhabdom), it decays after about 100 ms, and is polarity sensitive so that stimuli of one polarity (e.g. dimming) do not inhibit responses to stimuli of the opposite polarity (e.g. brightening). The inhibition effectively alters the contrast threshold of the cells, because after adaptation with stimuli of one contrast, a modest (less than 20%) increase in contrast is sufficient to elicit an unadapted response. Transient cells are not directionally selective and there are no local spatio-temporal interactions of the kind necessary for directional selectivity. But, by analogy with the directional veto in directionally selective cells in the rabbit retina (Barlow & Levick, 1965), self-inhibition is suggested as a mechanism of non-directional motion detection. After the inhibition, there is some spatial pooling of signals which is followed by rectification. The transient cells' spiking outputs could abstract a refined subset of visual information which may encode the presence, but not the direction, amplitude, or polarity of moving object borders.

Afferent Pathways↗
PubMed1990

Shift of edge-taxis to scototaxis depends on mean luminance and is predicted by a matched filter theory on the responses of fly lamina LMC cells.

The strength of the flanking inhibitory regions of the receptive fields of fly lamina cells (LMC) decreases as the mean luminance is lowered. Simultaneously, the biphasic temporal flash (impulse) response of the lamina cells becomes monophasic on lowering luminance. For a moving-edge stimulus at high mean luminance, this implies that the spatial integration by the lamina cell yields a temporal waveform which is congruent to the waveform of the temporal impulse response of the lamina cell. In other words, the temporal waveform generated by the moving edge is matched to the temporal waveform most preferred by the lamina cell. The edge is the stimulus causing the largest amplitude response at high (above 1 cd/m2) levels of luminance. On lowering luminance, the now monophasic nature of the spatial and temporal impulse responses of the lamina gives a preference not for the edges but for the center of a uniform region. We describe this theory and its behavioral corroboration in walking flies (Lucilia cuprina).

Animals↗
PubMed1990

What causes edge fixation in walking flies?

The orientation of freely walking flies (female Lucilia cuprina) to lines and stripes in a circular arena is described. The following observations were made. 1. The flies walked straight towards a dark line using the frontal eye region, but a pale line on a dark background was only weakly attractive. 2. In bright conditions flies walked in a curved line towards a black-white edge, the path being convex towards the dark side of the border. The curves indicated that the flies were heading for a point about 5-10 degrees to the dark side of the edge. 3. In dim conditions the edge of a dark region was not especially attractive and flies headed towards any point in the dark area. These observations can be accounted for by assuming that the fly walks towards the darkest region in its visual field (scototaxis). In bright conditions the edges of a dark region become more attractive than its centre. This change could be explained if lateral inhibition creates a 'Mach-band' effect, making the edges appear darker than the centre. Thus, fixation behaviour in walking Lucilia females seems to be a simple taxis.

Animals↗
PubMed1987

Bi-partitioning and boundary detection in natural scenes.

We propose a strategy for early vision which tailors visual channels to the object-oriented characteristics of natural scenes. This strategy involves essentially two types of channel, one for encoding the locally dominant edges which form the boundaries of 'objects', and another for 'filling in' the regions within them. The selection of contrasts which characterize object boundaries rather than textural detail can be enhanced by making an estimate local of contrast, and setting a threshold accordingly. This procedure and other aspects of the model were first suggested by observations of insect visual cells.

Animals↗
PubMed1986

Directionally selective cells in the locust medulla.

Intracellular recordings of a distinctive class of directionally selective cell from the medulla of the locust, Locusta migratoria, optic lobe are described. Dye marking shows that these cells arborize in the distal part of the medulla, and project through the lobula complex. The cells are excited by upward movement and have receptive fields of about 20 degrees in diameter. They are sensitive to a wide range of angular velocities from 0.02 degrees/s to over 200 degrees/s. The cells are sensitive to stationary flicker and have different latencies to dimming and brightening. Evidence is presented which suggests that directional computation depends, at least in part, on an inhibitory interaction between flicker sensitive channels.

Action Potentials↗