The spectral sensitivity of a littoral annelid:Nereis mediator

Summary The spectral sensitivities of the four eyes ofNereis mediator (Polychaeta, Annelida) were measured from 400 nm to 600 nm by determining the reciprocal of the number of quanta required to elicit a constant electroretinogram of 350 V.N. mediator is maximally sensitive at 480 nm, although it is very sensitive over a broad range from 400 nm to 540 nm (Fig. 4). Selective adaptation experiments (Fig. 5) and changes in the time characteristics of the electroretinogram under conditions of dark and green adaptation (Fig. 2) indicate the presence of a multi-receptor system.We thank Dr. Olga Hartman and Dr. Kristian Fauchald for their help with the natural history and identification of specimens. We also thank Josephine Yingst for her help in collection of specimens. This research was supported by a USC Biomedical Grant 5730 and by AFOSR Contract F 44620-70-C-0113.     

Vision in the fireflyPhoturis lucicrescens (Coleoptera: Lampyridae): Spectral sensitivity and selective adaptation in the compound eye

Summary The waveform of the electroretinograms (ERGs) recorded from the compound eyes in the dark-active fireflyPhoturis lucicrescens was different in the short (near-UV and violet) and long (green-yellow) wavelengths (Fig. 1). The spectral sensitivity curves in the dark and chromatic adaptation conditions suggested the presence of receptor types in the short (near-UV, Fig. 4, and violet, Fig. 5) and long wavelength (green; max 550 nm, Figs. 3–5) regions of the spectrum. The green peak is in correspondence with the species' bioluminescence emission peak at 554 nm (Fig. 3c).Abbreviations DA dark-adapted - ERG electroretinogram - VP visual pigment Contribution No. 1112 of the McCollum-Pratt Institute and Department of Biology, The Johns Hopkins University     

Spectral and polarized light sensitivity of photoreceptors in the compound eye of the cricket (Gryllus bimaculatus)

Summary Retinula cells in the compound eye of the cricket (Gryllus bimaculatus) were recorded intracellularly and stained with Lucifer yellow. Two different methods were used to determine the spectral sensitivity of these cells: a) the spectral scanning method, and b) the conventional flash method. Three spectral types, with S()-curves close to the rhodopsin-absorption functions, were found with _max at 332 nm (UV), 445 nm (blue) and 515 nm (green), respectively.Blue receptors were only recorded in the anatomically specialized dorsal rim area (DRA), and UV and green receptors in the dorsal region of the pigmented part of the eye, whereby green receptors were only found in the ventral eye. On the basis of these results, model calculations are presented for di- and trichromatic colour vision in the cricket.The fluorescence markings revealed green receptors whose axons project with short visual fibres to the lamina, and a UV receptor with a long visual fibre which projects through the lamina to the medulla. The blue receptors send their axons either to the lamina and medulla (long visual fibres) or only to the lamina (short visual fibres).The temporal dynamics of the three receptor types were examined. The blue receptors lack a phasic component of the receptor potential, and the time from stimulus on-set to peak potential is strongly increased compared to the UV and green receptors. Light adaptation reduces the latency to less than half of the dark adapted state.Spectral adaptation experiments revealed an unidirectional coupling between UV and green receptors, and it was found that polarization sensitivity (PS) in blue cells was much higher (PS= 6.5±1.5) than that of UV (PS=1.76±0.05) and green (2.26±0.57) receptors. The functional aspects of the three receptor types are discussed with respect to the presented physiological and morphological data.Abbreviations DA dorsal area - DRA dorsal rim area - PS polarization sensitivity     

Sensitivity and adaptation in R7, an ultraviolet photoreceptor,in theDrosophila retina

Summary Receptor deficient mutants and chromatic adaptation were used to isolate the contribution of R7 to the electroretinogram (ERG) ofDrosophila. R7 was found to be a single-peaked ultraviolet (UV) receptor (Fig. 1). Photoconversion of the UV absorbing rhodopsin (R) to its stable 470–495 nm metarhodopsin (M) was shown to elicit a long-lived negative (depolarizing) afterpotential (Fig. 3) while inactivating R7. Photoreconversion ofM toR reactivates R7 (Fig. 2) and repolarizes the ERG (Fig. 3). The intensities of light needed to elicit afterpotentials by photointerconverting R7 photopigment were found to be about 2 log units greater than for R1-6 photopigment (Fig. 4). Vitamin A deprivation decreases R7 (as well as R8) sensitivity by about 2 log units (through decreased photopigment levels) without changing spectral sensitivity shape (Fig. 5). Vitamin A deprivation further eliminates the light-induced inactivation of R7 allowing experiments designed to characterize the in vivo spectral absorption of R7M. R7M was found to have UV and 495 nm maxima (Fig. 6). No polarization sensitivity was detected in the R7 ERG component. The adaptational properties of R7 are similar to the properties previously established for R1-6 but different from the properties of R8.Supported by NSF grants BMS-74-12817 and BNS 76-11921. I thank M. Chapin, R. Greenberg, K. Hu, A. Ivanyshyn, D. Lakin, G. Pransky, D. Sawyer, J. Walker and W. Zitzmann for technical assistance.     

Spectral sensitivities of photoreceptors and lamina monopolar cells in the dragonfly,Hemicordulia tau

Summary Five spectral types of photoreceptors with peak sensitivities at 330 nm, 410 nm, 460 nm, 525 nm and 630 nm were recorded from the ventral eye of the dragonfly, Hemicordulia tau. Often the 525 nm photoreceptors presented broader, and the 630 nm photoreceptors narrower, spectral sensitivities than would be excepted of a photopigment with the same peak sensitivity. Four types of lamina monopolar cells (cell types 1–4) were recognised from their dark-adapted spectral sensitivities and their anatomy. The anatomical identification allows tentative assignation to the monopolar cell classification from Sympetrum rubicundulum obtained using Golgi staining (Meinertzhagen and Armett-Kibel 1982). When dark-adapted, the monopolar cells had peak spectral sensitivities that were similar to single photoreceptors or appeared to pool receptor outputs, but in some cases spectral sensitivity changed markedly upon adaptation to white and to chromatic light, in one case (cell type 2) apparently switching off a UV-sensitive input.     

Is histamine a neurotransmitter in insect photoreceptors?

Summary Intracellular recordings were made from the large monopolar cells (LMC's) in the first visual neuropil (lamina) of the flyMusca, whilst applying pharmacological agents from a three-barrelled ionophoretic pipette (Fig. 1). Most of the known neurotransmitter candidates (except the neuropeptides) were tested. The LMC's were most sensitive to histamine, saturating with ionophoretic pulses of less than 2 nC. The responses to histamine were fast hyperpolarizations with maximum amplitudes similar to that of the light-induced response (Fig. 3). Like the light response, the histamine response was associated with a conductance increase (Fig. 5). The histamine responses were not blocked by a synaptic blockade induced by ionophoretic application of cobalt ions (Fig. 6). Several histamine antagonists, and also atropine, were effective at blocking or reducing both the response to histamine and the response to light (Fig. 7). Other transmitter candidates having marked effects on the LMC's were: a) the acidic amino-acids, L-aspartate and L-glutamate, which evoked slower hyperpolarizations that could be blocked by cobalt (Fig. 11); b) GABA, which induced a depolarization associated with an inhibition of the light response (Fig. 9); and c) acetylcholine which also caused a depolarization (Fig. 10). Substances with no obvious effect on the LMC's included serotonin (5-HT),-alanine, dopamine, octopamine, glycine, taurine and noradrenalin. Together with the evidence of Elias and Evans (1983), which shows the presence, synthesis and inactivation of histamine in the retina and optic lobes of the locust, the data suggest that histamine is a neurotransmitter in insect photoreceptors.Abbreviations HA histamine - GABA -amino butyric acid - ACh acetylcholine - 5-HT 5-hydroxy-tryptamine (or serotonin) - R1-6 class of fly photoreceptors - LMC large monopolar cell - L1, L2 andL3 classes thereof     

The effect of UV irradiation on the capacity of an Hfr recA strain of Escherichia coli to act as donor

Summary The ability of a recA Hfr strain of Escherichia coli to form colonies is extremely sensitive to inhibition by ultraviolet light (Fig. 2). Furthermore, in this strain the synthesis of DNA is stopped completely by a dose of 385 ergs/mm² of UV (Fig. 3). Nevertheless, the ability of this recA Hfr strain to act as a donor in sexual recombination was no more sensitive to UV than that of a wild type donor (Fig. 1). Furthermore, when irradiated and mated with a recA female, in which DNA synthesis was also inhibited by UV (Fig. 3), there was a net synthesis of DNA as measured by the incorporation of C¹⁴ thymidine (Fig. 4). By using nalidixic acid resistant recA donors and recipients in all combinations, irradiating with UV and treating with nalidixic acid during mating, it is shown that DNA was synthesized by the donor (Fig. 5). It is concluded that synthesis of DNA directed by the sex factor during mating in a recA donor is not as sensitive to inhibition by UV as normal DNA synthesis in a recA donor.     

Photoreceptor spectral sensitivity in island and mainland populations of the bumblebee, <Emphasis Type="Italic">Bombus terrestris</Emphasis>

Most species of flower-visiting Hymenoptera are trichromatic, with photoreceptor spectral sensitivity peaks in the UV, blue and green regions of the spectrum. Red flowers, therefore, should be relatively difficult to detect for such insects. Nevertheless, in population biological studies in the bumblebee, Bombus terrestris, the Sardinian island population (B. t. sassaricus) displayed significantly higher responses to red artificial flowers (in tests of innate colour choice and detectability) than several mainland populations of the same species (Chittka et al. in Cognitive ecology of pollination, pp 106–126, 2001; Popul Ecol 46:243–251, 2004). Since there is relatively little physiological data on population differences in sensory systems, we used intracellular recording to compare photoreceptor spectral sensitivity in B. t. sassaricus and the southern European and Mediterranean population, B. t. dalmatinus. The results show both populations to be UV–blue–green trichromats, but with a small but significant increase in long-wave sensitivity in island bees. Spectral peaks were estimated at 348, 435 and 533 nm (B. t. dalmatinus) and 347, 436 and 538 nm (B. t. sassaricus) for UV, blue and green receptors, respectively. There were no significant differences in UV and blue receptor sensitivities. We found no photoreceptors maximally sensitive to red spectral light in the Sardinian population and model calculations indicate that the behavioural population differences in colour responses cannot be directly explained by receptor population differences. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Electrophysiology of the visual system in the cricket Gryllus firmus (Orthoptera: Gryllidae): Spectral sensitivity of the compound eyes

The electroretinographic spectral sensitivity of the cricket compound eyes shows the presence of two receptor types, a dominant one at 520 nm and another in the near-u.v. (λ_max 355 ± 5 nm) under dark- and intense chromatic adaptation conditions (Fig. 3). The waveform of the electrical responses elicited by short-wavelength stimuli differ from those elicited by long wavelength stimuli (Fig. 1).     

Le contrôle automatique du flux lumineux dans l'oeil composé des Diptères

In the compound eye of the fly Musca, tiny pigment granules move within the cytoplasm of receptor cells Nos. 1–6 and cluster along the wall of the rhabdomeres under light adaptation, thus attenuating the light flux to which the visual pigment is exposed (Kirschfeld and Franceschini, 1969). Two recently developed optical methods (the neutralization of the cornea and the deep pseudopupil) combined with antidromic and orthodromic illumination of the eye (Fig. 1) make it possible to analyse the properties of the mechanism at the level of the single cell, in live and intact insects (Drosophila and Musca). The mechanism is shown to be an efficient attenuator in the spectral range (blue-green) where cells Nos. 1–6 have been reported to be maximally sensitive (Figs. 4c and d, 5b and 11b). In spite of the fact that the granules do not penetrate into the rhabdomere, the attenuation spectrum they bring about closely matches the absorption spectrum of the substance of which they are composed (ommochrome pigment, dotted curve in Fig. 11b). The dramatic increase in reflectance of the receptors after light adaptation (Figs. 3, 4b, 5a and 11a) can be explained as a mere by-product of the high absorption index of the ommochrome pigment, especially if one takes into account the phenomenon of anomalous dispersion (Chapter 8). The vivid green or yellow colour of the rhabdomeres would thus have a physical origin comparable to a metallic glint. Contrasting with the lens eye in which the pupillary mechanism is a common attenuator for both receptor types (rods and cones), the compound eye of higher Diptera is equiped with two types of pupils adapted respectively to both visual subsystems. A scotopic pupil is present in each of the six cells (Nos. 1–6) whose signals are gathered in a common cartridge of the first optic ganglion. This pupil comes into play at a moderate luminance (0,3 cd/m² in Drosophila; 3 to 10 cd/m² in Musca. Figs 13, 14, 15, 16). A photopic pupil is present in the central cell No. 7 whose signal reaches one column of the second optic ganglion. Attenuating the light flux for both central cells 7 and 8, the photopic pupil has its threshold about two decades higher than the scotopic pupil, just at the point where the latter reaches saturation (Fig. 3b, e-State II of Figs. 6b and 15). The photopic pupil itself saturates at a luminance one to two decades higher still (Fig. 3c, f=State III of Figs. 6c and 15). The two-decades-shift in threshold of these pupil-mechanisms supports the view that receptors 1–6 are a scotopic subsystem, receptors 7 and 8 a photopic subsystem of the dipteran eye. The luminance-threshold of the scotopic pupil (as determined with the apparatus described in Fig. 2) appears to be located at least 3.5 decades (Drosophila) or even 5 decades (Musca) higher than the absolute threshold of movement perception (Fig. 16). After a long period (1 hr) of darkness a light step of high intensity can close the scotopic pupil within about 10 sec (time constant 2 sec as in Fig. 9) and the photopic pupil within no less than 30–60 sec. Some mutants of Drosophila possess only a scotopic pupil (w , Figs. 4 and 5) whereas ommochrome deficient mutants lack both types of pupil (v, cn, see Fig. 7c, d). Comparable reflectance changes, accomplished within about 60 sec of light adaptation, are described for two insects having fused rhabdomes: the bee and the locust (Fig. 17).     

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°, 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.Abbreviations LMC large monopolar cell - LVF long visual fibre - RF receptive field - SMC small monopolar cell - SVF short visual fibre     

Retinal receptor types inAglais urticae andPieris brassicae (Lepidoptera), revealed by analysis of the electroretinogram obtained with Fourier interferometric stimulation (FIS)

Summary Electroretinograms obtained in the butterfliesAglais urticae andPieris brassicae by the procedure of Fourier interferometric stimulation (FIS) were used to construct spectral sensitivity curves. These curves, representing the combined responses of several receptor types, were approximated by summation of spectral sensitivity curves for individual pigments, and the presence of these pigments was corroborated by chromatic adaptation experiments. The results show that the retina in the compound eye ofAglais urticae contains 3 photopigments, with maximal absorption at ca. 360 nm, 460 nm and 530 nm, respectively (Fig. 5). The retina in the compound eye ofPieris brassicae has two subdivisions. In the dorsal region of the eye 3 photopigments were found, with maxima at ca. 360 nm, 450 nm and 560 nm (Fig. 8). In the medioventral region pigments with essentially the same maxima are present together with an additional, fourth long-wavelength component with effective maximal absorption at ca. 620 nm (Fig. 11). Its absorption curve is considerably narrower than would be expected for a rhodopsin with the same absorption maximum, and presumably results from the spectral combination of a photopigment and a photostable screening pigment.Abbreviations FIS Fourier interferometric stimulation - WLP White-light position - ERG Electroretinogram     

Electroretinogram Characteristics and the Spectral Mechanisms of the Median Ocellus and the Lateral Eye in Limulus polyphemus

Electrical responses (ERG) to light flashes of various wavelengths and energies were obtained from the dorsal median ocellus and lateral compound eye of Limulus under dark and chromatic light adaptation. Spectral mechanisms were studied by analyzing (a) response waveforms, e.g. response area, rise, and fall times as functions of amplitude, (b) slopes of amplitude-energy functions, and (c) spectral sensitivity functions obtained by the criterion amplitude method. The data for a single spectral mechanism in the lateral eye are (a) response waveforms independent of wavelength, (b) same slope for response-energy functions at all wavelengths, (c) a spectral sensitivity function with a single maximum near 520 mµ, and (d) spectral sensitivity invariance in chromatic adaptation experiments. The data for two spectral mechanisms in the median ocellus are (a) two waveform characteristics depending on wavelength, (b) slopes of response-energy functions steeper for short than for long wavelengths, (c) two spectral sensitivity peaks (360 and 530–535 mµ) when dark-adapted, and (d) selective depression of either spectral sensitivity peak by appropriate chromatic adaptation. The ocellus is 200–320 times more sensitive to UV than to visible light. Both UV and green spectral sensitivity curves agree with Dartnall's nomogram. The hypothesis is favored that the ocellus contains two visual pigments each in a different type of receptor, rather than (a) various absorption bands of a single visual pigment, (b) single visual pigment and a chromatic mask, or (c) fluorescence. With long duration light stimuli a steady-state level followed the transient peak in the ERG from both types of eyes.     

Sensitivity and photopigments of R1-6, a two-peaked photoreceptor,inDrosophila, Calliphora andMusca

Summary Low vitamin A rearing decreases sensitivity and eliminates the ultraviolet but not the blue sensitivity maximum in R1-6 inDrosophila, Calliphora andMusca (Figs. 2–4). Spectral adaptation functions for control and vitamin A deprived flies yielded derived stable metarhodopsin absorption spectra from spectral sensitivity. Metarhodopsin has a long wavelength maximum and also has an ultraviolet maximum especially in the normal vitamin A condition (Figs. 2–4). M-potentials (fast early-receptor-like potentials) were obtained (Fig. 1) from all three genera in normal vitamin A rearing and were used for spectral adaptation studies (Figs. 2–3); the latter data are approximate inverses of sensitivity based spectral adaptation data. Thus, sensitivity must reflect proportion of rhodopsin, with metarhodopsin being inert in receptor potential generation.Vitamin A effects on spectral functions were further investigated inDrosophila. Ultraviolet (370 nm) and visible (470 nm) sensitivities varied approximately linearly with dietary vitamin A dose (Fig. 5); 370 nm sensitivity decreased more than 470 nm sensitivity at lower doses. Increasing adaptation intensities of 370 and 470 nm caused parallel decreases in spectral sensitivity assayed at 370 and 470 nm in normal vitamin A flies (Fig. 6); the adapting intensities were sufficient to convert photopigment. These and previous results suggest that the two R1-6 spectral peaks are ultimately mediated by one rhodopsin. R1-6 rhabdomeres were structurally similar in high and low vitamin A flies but emitted a long wavelength fluorescence to ultraviolet excitation in high vitamin A flies only (Fig. 7). These results suggest some form of energy transfer; i.e., a carotenoid may capture ultraviolet quanta and transfer energy to rhodopsin via inductive resonance. Spectral adaptation data are consistent with a calculated high rhabdomeric optical density of ECL=0.26 (i.e., 45% of incident light is absorbed) derived from presently available data onDrosophila. Calculations show electro-retinographic sensitivity to be extremely high, perhaps measurable at less than one absorbed quantum per rhabdomere.Supported by NSF grants BMS-74-12817 and BNS-76-11921. We thank M. Chapin, K. Hu, D. Lakin, G. Pransky, D. Sawyer and W. Zitzmann for technical assistance. We are indebted to numerous colleagues especially W. Harris, for comments and suggestions.Chalky Calliphora were obtained from the laboratories of Dr. G. McCann at Caltech and Dr. L. Bishop at the University of Southern California.W-II Musca were from Dr. D. Wagoner at the U.S.D.A. in Fargo, North Dakota.     

Specific receptor input into spectral preference inDrosophila

Summary Drosophila have 3 types of retinal receptors, R1–6, R7 and R8. Using visual mutant strains lacking function in one or two receptor types, spectral preference in walking fast (30 s) phototaxis was measured. High correlations for intensity-response functions were obtained (Fig. 2 and 5). With a 467 nm choice standard, which could saturate R1–6, white-eyed strains with only R8 or with R1–6 plus R8 functional exhibited similar spectral sensitivities with a broad peak at visible wavelengths (Fig. 3) not unlike the electrophysiological characterization of R8 (Fig. 1). Strains with R7 plus R8 or with all receptors intact exhibited similar functions with a high ultraviolet (UV) peak (Fig. 4), like the electrophysiological characterization of R7 plus R8. The presence of R1–6 did not alter the profiles mediated by R8 alone or by R7 plus R8.With a 572 nm standard, which should maintain R1–6 function, white- and red-eyed wild-type strains with all receptors intact exhibited similar UV dominated spectral sensitivities, probably from R7 plus R8, with weak visible secondary peaks possibly from R1–6 or R8 (Fig. 6). However, even with a very dim 572 nm standard or with no standard at all, unequivocal evidence for R1–6 input was not found and intensity-response function correlations were low. This finding and other recent studies suggest that specific phototactic or optomotor tasks and conditions (e.g., adaptation level) determine the extent to which each receptor input is utilized.Spectral preference with a bright 365 nm standard was difficult to measure because of the strong UV preference in phototaxis. In pilot studies, an ocelliless strain showed strong fast phototaxis.Supported by NSF grants BMS-74-12817 and BNS-76-11921. We thank D. Lakin, A. Ivanyshyn, R. Greenberg, M. Chapin, D. Fritzberg, and W. Hamilton for technical assistance. We also thank R. Schümperli for suggestions, for his permission to redraw his data and for confirming the conversions we made.     

Behavioral experiments on the visual processing of color stimuli inPieris brassicae L. (Lepidoptera)

Summary In spontaneous-choice experiments on the butterflyPieris brassicae L. (Pieridae), spectral-effectiveness and spectral-sensitivity functions were obtained for various behaviors.Pilot experiments with colored PVC films, for which the relative number of reflected quanta with regard to the given illumination had been calculated, showed that the feeding response is distinctly intensity-dependent (Fig. 4). The animals are also capable of color discrimination independent of this intensity discrimination;P. brassicae prefers blue to other colors (e.g., orange, red and purple) with higher relative quantum numbers (Fig. 3) and distinguishes golden yellow and red from gray shades as well as from black and white (Fig. 5a, b).The results of subsequent spontaneous-choice experiments, using as stimuli monochromatic lights with known quantum flux, indicate that the various visually controlled functional categories of behavior can be assigned to the following spectral regions (Figs. 6, 8): 1. The open-space reaction corresponds to the UV and violet region, ca. 320–420 nm; 2. The feeding reaction corresponds to the blue region, ca. 420–500 nm, and the orange-red region, ca. 590–610 nm; 3. Egg-laying and drumming correspond to the green-yellow region, ca. 520–580 or 590 nm, respectively. The intensity dependence of the individual responses is again apparent in these experiments with monochromatic light stimuli (Figs. 7, 11, 12a).Even at very high intensities and when the content of the relevant wavelength is high, white light is practically ineffective for the feeding reaction (Fig. 9), drumming and egg-laying (cf. Results), regardless of its UV content. The open-space reaction, however, can be elicited by white light according to its UV content (Fig. 12 b).P. brassicae cannot be trained to give a feeding response to monochromatic light stimuli (Fig. 10).Experiments with mixtures of wavelengths have shown that the combination of the two maxima in the spectral sensitivity curve for the feeding reaction (=600 plus 447 nm) is just as effective as =447 nm alone (Fig. 13, left). Moreover, the mixture producing the hypothetical Pieris purple (=600 plus 370 nm) is no more or less effective in eliciting the feeding and open-space reactions than the more effective component for each of these reactions when presented alone (Fig. 13, right). With the mixture of =600 plus 558 nm, both the feeding reaction and drumming are distinctly reduced (Fig. 13, middle). This mixed color, unlike the other two mixtures tested, has a color quality different from that of the component colors.That the behavior ofP. brassicae is exclusively wavelength-specific can thus be ruled out. There are indications that wavelength-specific behavior and color vision are both present.Abbreviation RNQ relative number of quanta This publication is dedicated to Professor Dr. Dr.h.c. H. Autrum on the occasion of his 80th birthday     

The Spectral Sensitivities of Single Cells in the Median Ocellus of Limulus

The spectral sensitivities of single Limulus median ocellus photoreceptors have been determined from records of receptor potentials obtained using intracellular microelectrodes. One class of receptors, called UV cells (ultraviolet cells), depolarizes to near-UV light and is maximally sensitive at 360 nm; a Dartnall template fits the spectral sensitivity curve. A second class of receptors, called visible cells, depolarizes to visible light; the spectral sensitivity curve is fit by a Dartnall template with λ_max at 530 nm. Dark-adapted UV cells are about 2 log units more sensitive than dark-adapted visible cells. UV cells respond with a small hyperpolarization to visible light and the spectral sensitivity curve for this hyperpolarization peaks at 525–550 nm. Visible cells respond with a small hyperpolarization to UV light, and the spectral sensitivity curve for this response peaks at 350–375 nm. Rarely, a double-peaked (360 and 530 nm) spectral sensitivity curve is obtained; two photopigments are involved, as revealed by chromatic adaptation experiments. Thus there may be a small third class of receptor cells containing two photopigments.     

The influence of color stimuli on visually controlled behavior inAglais urticae L. andPararge aegeria L. (Lepidoptera)

Summary In spontaneous-choice experiments on the butterfliesAglais urticae L. (Nymphalidae) andPararge aegeria L. (Satyridae) the spectral effectiveness and spectral sensitivity of various behaviors were investigated and compared.Pilot experiments with colored PVC films showed indications of an intensity dependence of the feeding reaction inP. aegeria. Moreover, they revealed a color discrimination independent of this intensity discrimination:P. aegeria distinguishes red from grey shades as well as from black and white (Fig. 3).According to subsequent spontaneous-choice experiments using monochromatic light stimuli, the various visually controlled functional categories of behavior can be assigned to the following spectral regions: 1. The open-space reaction corresponds to the UV and violet region, ca. 320–420 nm, inP. aegeria (Figs. 4, 7). 2. The feeding reaction corresponds to the blue region, ca. 420–500 nm, inA. urticae (Fig. 1) andP. aegeria (Fig. 4), and the yellow region, ca. 550–590 nm, inA. urticae (Fig. 1) and the orange-red region, ca. 570–670 nm, inP. aegeria (Fig. 4).In these experiments with monochromatic light stimuli the intensity dependence of the reactions is also obvious (Figs. 2, 5, 6).The open-space reaction is elicited inP. aegeria by white light dependent on its UV content (Fig. 8). This is also valid for the feeding reaction inP. aegeria (Fig. 5b). To elicit this reaction it was necessary to offer light stimuli simultaneously with the odour stimulus of honey water. As the latter was of the same quality in combination with all light stimuli the results can be attributed definitely to the different effectiveness of the various light stimuli.Pure wavelength-specific behavior can be ruled out inA. urticae andP. aegeria. Wavelength-specific behavior and color vision are probably present simultaneously.Abbreviation RNQ relative number of quanta Supported by the Deutsche Forschungsgemeinschaft Ko 445/5-3