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     

Trichromatic color vision in the salamander (Salamandra salamandra)

Spectral sensitivity functions were measured between 334 nm and 683 nm in Salamandra salamandra by utilizing two behavioral reactions: the negative phototactic response, and the prey catching behavior elicited by a moving worm dummy. The action spectrum of the negative phototactic response revealed 3 pronounced maxima: at 360–400 nm, at 520–540 nm, and at 600–640 nm. In the range around 450 nm, there was a reaction gap where sensitivity could not be measured. The action spectrum of the prey catching behavior was entirely different: maximal sensitivity was found at 500 nm and at 570 nm. Between 500 nm and 334 nm sensitivity decreased continuously for about 1 log unit (Fig. 6).Experiments under chromatic adaptation using the prey catching behavior indicate that the relatively high sensitivity in the ultraviolet range is not due to a separate ultraviolet photoreceptor, but is based on the responses of a photoreceptor maximally sensitive at about 500 nm.Color discrimination was tested by moving a colored worm dummy within a differently colored surround of equal subjective brightness. The salamanders were able to discriminate blue from green, and green from red (Fig. 10). The results can be explained by assuming a trichromatic color vision based on 3 photoreceptor types maximally sensitive around 450 nm, 500 nm and 570 nm (Fig. 12).     

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.     

Spectral mechanisms of the compound eye in the fireflyPhotinus pyralis (Coleoptera: Lampyridae)

Summary Electroretinograms (ERG) were recorded from dark- and chromatic-adapted compound eyes in the dusk-active firefly,Photinus pyralis , at different wavelengths ranging from 320 to 700 run and over 4.5 log units change in stimulus intensity. ERG waveforms differed in the short (near-UV and violet) and long (yellow) wavelengths (Fig. 1). Waveform differences were quantitated by analysis of rise and fall times as a function of the amplitude of the response. Rise times were found to be relatively constant for all stimulus wavelengths. However, variations in the fall times were detected and followed characteristically different functions for short and long wavelengths (Fig. 2).No significant differences in the slopes of the Vlog-I curves at different stimulus wavelengths were observed (Fig. 3).Spectral sensitivity curves obtained from the ventral sector in dark- and chromatic-adapted conditions revealed peaks in the short ( max 400 nm: Fig. 4; max 430 nm: Fig. 5 A; and max 380 nm; Fig. 5B) and long ( max 570 nm: Figs. 4, 5) wavelengths, suggesting the presence of two spectral mechanisms. The long wavelength (yellow) mechanism was in close tune with the species bioluminescence emission spectrum (Fig. 4B).This investigation was supported in part by NIH Research Grant # EY-00490 (to R.M.C.); Research Grant # 01794N from the Research Foundation of the City University of New York (to A.B.L.); NIGMS Training Grant #1 TO 2 GM 05010-01 MARC (to J.A.H.); and NSF Grant # HES-75-09824 (to C.O.T.). We thank Tom Jensen for technical assistance, Barry Schuttler for his courtesy in allowing us to collect fireflies at his farm, Jean Lall for editorial assistance, and the two anonymous referees whose comments added considerably to the quality of this paper.     

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.     

Electrophysiological studies on the compound eye of a stalked-eye fly,Cyrtodiopsis dalmanni (Diopsidae,Diptera)

Summary The mass response (ERG) of the compound eye of the Malaysian stalked-eye flyCyrtodiopsis dalmanni was recorded by means of conventional electrophysiological techniques. The ERG consists of a positive on-effect, a sustained negative potential during illumination and a negative off-effect, it resembles that ofCalliphora as described by Autrum (1950). As compared with data derived fromCalliphora under identical conditions the eye ofCyrtodiopsis is more sensitive to weak stimuli and shows considerable adaptation. The spectral response curve reveals peaks at 360 nm, around 450 nm and around 490 nm. Above 550 nm the response curve rises steeply, even with stimuli above 700 nm reactions may be elicited. Most probably this effect is caused by weak absorption of long wavelength radiation in the screening pigments.With simple techniques it is fairly easy to record impulse activity from single units of the optic tract within the eye-stalk. This makesCyrtodiopsis a favorable object for experimental studies on data processing in insect optic centers.The characteristics of the diopsid eye are discussed in context with the environmental conditions in the biotop.I would like to thank the colleagues at the University of Malaya, Kuala Lumpur, Malaysia, for help and hospitality.The investigations were supported by a grant from the Sonderforschungsbereich Vergleichende Sinnes- und Nervenphysiologie at the University of Frankfurt (Main).     

The performance of dogs in detecting α-ionone in the vapor phase

Summary Concentration-response functions for-ionone were established for four German shepherds (Figs. 3 and 4). The dogs were tested in a three choice behavioral apparatus (Fig. 2), and trained, by a restricted operant procedure, to establish an approach-avoidance discrimination between odor and air. Odorant concentrations were presented from an olfactometer calibrated by gas chromatography. Minimum detectable concentrations fell within the range 4.0×10^4.5–4.0×10^6.5 molecules/cm³. Concentration-response curves for three of the dogs show a clear double reversal in slope which is statistically significant and which divides the curve into a slowly descending upper limb, best fitted by a parabolic function, and a rapidly descending lower limb, best fitted by a cubic function (Figs. 5 and 6). There is evidence that this division might reflect a dual receptor mechanism. When performance during testing stabilized for a given concentration and the concentration was then lowered by a certain magnitude, the new performance level depended markedly on that magnitude. No evidence was found to suggest that adaptation to the test odor influenced performance. As defined by a differential threshold fraction (Flow/Flow) one dog's ability to discriminate between differences in flow rate fell in the range 0.12–0.08.We thank the U.S. Air Force, Air Force Office of Scientific Research for their generous support of this work (Grant No. 73-2425 to D.G.Moulton).-ionone was donated by Givaudan Inc. (Dr. J. Dorsky). We also thank Mr. Paul Phillips for able technical assistance and Dr. T. Burlingame for gas chromatographic measurements.     

Photoreceptor-specific efficiencies of β-carotene,zeaxanthin and lutein for photopigment formation deduced from receptor mutant Drosophila melanogaster

Summary Drosophila rearing media had only -carotene, zeaxanthin or lutein as precursors for photopigment chromophores. Zeaxanthin and lutein are potentially optimum sources of the 3-hydroxylated retinoids of visual and accessory photopigments. Mutants made the electroretinogram in white (w) eyes selective for compound eye photoreceptors R1–6, R7 and R8: R1–6 domiantes w's electroretinogram; R7/8 generates w;ora's (ora = outer rhabdomeres absent); R8 generates w sev;- ora's (sev = sevenless). Microspectrophotometry revealed R1-6's visual pigment. In w, all 3 carotenoids yielded monotonic dose-responses for sensitivity (Fig. 4) or visual pigment (Fig. 7). An ultraviolet sensitivity peak from R1-6's sensitizing pigment was present at high but not low doses (Fig. 1). In w;ora, all 3 carotenoids gave similar spectra dominated by R7's high ultraviolet sensitivity (Fig. 2). For w sev;ora, all spectra were the shape expected for R8, peaking around 510 nm (Fig. 3). The sensitivity dose-response was at its ceiling except for low doses in w;ora (Fig. 5) and zero supplementation in w sev;ora (Fig. 6). Hence, without R1-6, most of our dose range mediated maximal visual pigment formation. In Drosophila, -carotene, zeaxanthin and lutein mediate the formation of all major photopigments in R1-6, R7 and R8.Abbreviations ERG electroretinogram - MSP microspectrophotometry - HPLC high pressure liquid chromatography - n.a. numerical aperture - w, sev, ora Drosophila mutants - y, p, r marg types of R7 and R8     

Single Sensillum responses in the male mothAdoxophyes orana (F.v.R.) to female sex pheromone components and their geometrical isomers

Summary A technique is described for the recording of receptor and action potentials from the outer dendritic segments of the olfactory cells in individual antennalSensilla trichodea in insects. The 50 m long olfactory hairs on the antennae of adult male summerfruit toftrix moth,Adoxophyes orana, are shown to possess two cells responsive to the female sex pheromone (a 91 mixture ofcis-9 andcis-11-TDA (= tetradecen-1-ol acetate)). One of these cells (typeB) is sensitive tocis-9-TDA, the other (type A) mainly responds tocis-11-TDA and, to a much smaller extent, tocis-9-TDA. The behavioural inhibitorstrans-9 andtrans-11-TDA evoke small responses in both cells, which may have been caused by contamination of these substances by thecis isomers (Fig. 6).It appears that the pheromone receptor cells are not tuned to the optimal 91 mixture (Fig. 7). Hence, the attractiveness of the pheromone should be determined in the central nervous system by comparison of the responses from theA andB cells.A rough calculation indicates that the males are very well able to discriminate between different mixture ratios. It is suggested that thecis-9-/cis-11-TDA ratio excreted by the females shows a considerable variation.I am much indebted to Prof. Dr. D. Schneider for the use of facilities in his laboratory at the Max-Planck-Institut für Verhaltensphysiologie, Seewiesen (Federal Republic of Germany), and to all colleagues at this laboratory, especially Dr. K.-E. Kaissling, for their help. I am also grateful to Dr. F.W. Maes, Department of Zoology, State University of Groningen (Netherlands), for many discussions and his very valuable suggestions and help. I thank Drs. A.K. Minks and S. Voerman, Laboratory for Research on Insecticides, Wageningen (Netherlands), for the supply of the maleA. orana pupae and the chemicals; Mrs. C. Huss-Hahn, Mrs. G.W. De Vries-Nijboer and Miss M.J. Den Otter for technical assistance; Mr. D. Visser for preparing the figures; and Dr. G. Thomas for correcting the English text and constructive criticism. The investigations were supported by the Alexander von Humboldt-Stiftung and the Netherlands Organization for the Advancement of Pure Research (ZWO).     

AFLP analysis of phylogenetic relationships among myrmecophytic species of Macaranga (Euphorbiaceae) and their allies

The palaeotropic pioneer tree genus Macaranga Thouars (Euphorbiaceae) is characterized by various types of mutualistic interactions with specific ant partners (mainly Crematogaster spp.). About 30 species are obligate ant-plants (myrmecophytes). We used amplified fragment length polymorphism (AFLP) markers to assess phylogenetic relationships among 108 Macaranga specimens from 43 species, including all available taxa from the three sections known to contain myrmecophytes. Eight primer combinations produced 426 bands that were scored as presence/absence characters. Banding patterns were analyzed phenetically, cladistically and by principal coordinates analysis. Monophyly of section Pruinosae is clearly supported. There is also good evidence for a monophyletic section Pachystemon that includes the puncticulata group. The monophyly of section Winklerianae and relationships between the three sections remain ambiguous. Section Pachystemon is subdivided into four well-supported monophyletic subclades that presumably correspond to taxonomic entities.We acknowledge the support by the Deutsche Forschungsgemeinschaft (DFG Fi606/4-1, DFG We1830/2-1, 4-1 and 4-2), which in part was granted in the frame of the DFG-SPP 1127 Radiations: origins of biological diversity. Part of the plant material was kindly supplied by Dr. H. Feldhaar (University of Würzburg), Dr. U. Moog (University of Kassel) and Dr. F. Slik (Leiden University Branch, Nationaal Herbarium Nederland). We thank the University of Malaysia (Dr. Rosli b. Hashim) and Taman Taman Sabah (Datuk Lamri Ali; Dr. J. Nais) for permits and logistic support, and EPU for permission to conduct research in Malaysia.     

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     

Crcadian pacemaker in theBursatella eye: Properties of the rhythm and its effect on locomotor behavior

Summary The eye of the frilled sea hare,Bursatella leachi plei, expresses a circadian rhythm in the frequency of spontaneously occurring optic nerve impulses. The rhythm will free-run for at least 3 cycles in vitro (Fig. 2) and can be entrained by light cycles provided in vivo (Fig. 4 A). While bothBursatella andAplysia eyes contain circadian pacemakers the two rhythms differ in several respects: (1) the peak impulse frequency forBursatella eyes is only 96/h (±36 SD) compared with 247/h (±61 SD) forAplysia. (2) The ocular waveform of theBursatella rhythm exhibits a steep rise and fall from peak frequencies and lacks the delayed falling phase which creates a shoulder on the ocular waveform inAplysia (Fig. 2). (3) The in vitro free-running period of theBursatella ocular rhythm is 21.2 h (±0.6 SD) compared with 24.3 h (±0.9 SD) for theAplysia rhythm (Fig. 2). (4) The steady state phase angle for entrainment differs withBursatella eyes showing a median activity peak at +3 Z.T. compared with a medianAplysia peak at –1 Z.T. (Fig. 4).We also investigated the locomotor rhythm.Bursatella were found to be predominantly diurnal when exposed to LD, 1212 (Fig. 5A) and to exhibit anticipatory locomotor activity when maintained on LD), 915 (Fig. 6). The eyes appear to play a minor role, if any, in timing the locomotor rhythm. EyelessBursatella remained diurnal on LD, 915 and most animals continued to exhibit anticipatory behavior (Fig. 6). These results suggest that theBursatella eye plays a less prominent role than theAplysia eye in controlling locomotor behavior.Abbreviations DD constant darkness - LD 1212 24 h light cycles 12 h light, 12 h dark - EST Eastern Standard Time - Z.T. Zeitgeber Time We would like to thank L. Baird, W. Kilmartin and S. Wallace for help with animal maintenance, data presentation and photography. We also thank T. Breeden for our computer programs. This work was supported by NIH grant NS-15264 to G. Block.     

The cloned cardiac Na channel α-subunit expressed in Xenopus oocytes show gating and blocking properties of native channels

Summary The neonatal rat cardiac Na channel -subunit directed currents in oocytes show characteristic cardiac relative resistance to tetrodotoxin (TTX) block. TTX-sensitive currents obtained by expression in Xenopus oocytes of the -subunits of the rat brain (BrnIIa) and adult skeletal muscle (I) Na channels show abnormally slow decay kinetics. In order to determine if currents directed by the cardiac -subunit (RHI) exhibit kinetics in oocytes like native currents, we compared RHI-directed currents in oocytes to Na currents in freshly isolated neonatal rat myocytes. The decay rate of RHI currents approached that of neonatal myocytes and was faster than BrnIIa and I currents in oocytes. The voltage dependence of availability and activation was the same as that in the rat myocytes except for a 12–19 mV shift in the depolarizing direction. The RHI Na currents were sensitive to Cd²⁺ block, and they showed use dependence of TTX and lidocaine block similar to native currents. The current expressed in oocytes following injection of the cRNA encoding for the -subunit of the cardiac Na channel possesses most of the characteristic kinetic and pharmacological properties of the native cardiac Na current.We are grateful to Dr. Juliet Morgan for providing us with neonatal ventricle cell cultures. We thank Dr. Gail Mandel for providing the pl plasmid and Dr. A. Goldin for rat brain 2a. Aaron Fox kindly provided us with Axobasic 1.0 software and support. We also thank Turi Larsen for oocyte preparation, technical assistance, injections and maintaining the Xenopus colony. Supported by NIH HL 37217, HL 20592, NS 23360-02 and HL 07381, a grant from the International Life Sciences Institute and a grant from the Upjohn Company.     

Lipoprotein crystals in the yolk platelet of a teleost,Pelvicachromis pulcher (Cichlidae)

Summary Yolk-platelet crystals in the oocytes of the teleost Pelvicachromis pulcher (Cichlidae) were shown, using electron diffraction and tilting of thinsectioned specimens, to possess an orthorhombic lattice with unit-cell sides a=8.3 nm, b=16.6 nm and c=18.0 nm. They thus closely resemble the crystals known for a newt (Triturus sp.) and a frog (Xenopus laevis).Supported by the Deutsche Forschungsgemeinschaft, Bonn-Bad Godesberg. The author wishes to thank Dr. R. Riehl, Heidelberg, for taxonomic advice     

Spectral sensitivities of retinular cells measured in intact,living flies by an optical method

Summary The spectral sensitivity of the peripheral retinular cells R1–6 in nine species of intact flies was determined using non-invasive, optical measurements of the increase in reflectance that accompanies the pupillary response. Our technique is to chronically illuminate a localized region of the eye with a long wavelength beam, adjusted to bring pupillary scattering above threshold, then, after stabilization, to stimulate with monochromatic flashes. A criterion increase in scattering is achieved at each wavelength by adjusting flash intensity. Univariance of the pupillary response is demonstrated by Fig. 3.Action spectra measured with this optical method are essentially the same as the published spectral sensitivity functions measured with intracellular electrophysiological methods (Fig. 4 forCalliphora, Fig. 5 forDrosophila, Fig. 7 forEristalis, and Fig. 8 forMusca). This holds for both the long wavelength peak and the high sensitivity in the UV as was consistently found in all investigated fly species.Spectral sensitivity functions for R1–6 of hover flies (family Syrphidae) are quite different in different regions of the same eye. There can also be substantial differences between the two sexes of the same species. The ventral pole of the eye of femaleAllograpta (Fig. 10) contains receptors with a major peak at 450 nm, similar to those ofEristalis. However, the dorsal pole of the same eye contains receptors with a major peak at 495 nm, similar to those ofCalliphom. Both dorsal and ventral regions of the maleToxomerus eye, and the ventral region of the female eye, contain only the 450 nm type of R1-6 (see Fig. 12). However, the dorsal region of the female eye also contains another spectral type of receptor that is maximally sensitive at long wavelength. Eyes of both sexes ofAllograpta (Figs. 10 and 11) contain a mixture of spectral types of receptors R1-6.We thank Dr. Chris Maier of the Connecticut Agricultural Experiment Station, for determination of the Syrphidae. This work was supported by grants EY01140 and EY00785 from the National Eye Institute, U.S.P.H.S., (to GDB), by the Connecticut Lions Eye Research Foundation (to GDB), and by the Netherlands Organization for the Advancement of Pure Research (Z.W.O.), (to DGS).     

Half-lives of oat mRNAs in vivo and in a polysome-based in-vitro system

We have used a cell-free polysome-based in-vitro mRNA-degradation system to investigate the halflives of plant cell mRNAs. In order to establish the fidelity of the in-vitro system, we used cordycepin to determine the in-vivo half-lives of -tubulin and actin mRNAs in the primary leaves of 4-d-old etiolated oat (Avena sativa L.) seedlings. The in-vitro rank order of half-lives for phytochrome A (45 min), -tubulin (105 min), and actin (220 min) mRNAs mimicked the in-vivo rank order. A pulse of red light given to excised etiolated primary leaves caused an in-vivo reduction in the half-life of -tubulin mRNA. The selectivity of the polysome-based system was further demonstrated by the decrease in the half-life of -tubulin mRNA (from 105 min to 60 min) induced by a pulse of red light given to the etiolated oat seedlings prior to isolation of polysomes. Red light did not affect the apparent half-lives of phytochrome A or actin mRNAs.Abbreviations cab gene for chlorophyll-a/b-binding protein - kb(p) kilobase (pair) - phyA gene for type-I phytochrome protein - rbcS gene for ribulose-1,5-bisphosphate-carboxylase small-subunit We thank Dr. Richard B. Meagher for the pSAc3 actin clone. We thank Dr. Cecil Stewart for the use of his density-gradient fractionator, and Dr. Virginia Crane for instruction in using the fractionator. We also appreciate the helpful comments provided by the other members of the laboratory during the course of this research: Dr. Isaac John, Dr. Iffat Rahim, Linda Barnes, Bruce Held, David Higgs, and Theresa Tirimanne. This work was supported by USDA grants CRGO 88-37261-4196 and 91-37304-6397, and the Iowa State University Biotechnology Program.     

Comparative study of structure and function of blood cells from two Drosophila species

Summary Hemocytes of Drosophila melanogaster and Drosophila yakuba larvae have been defined in terms of their ultrastructure and functions in coagulation, wound healing, encapsulation, phenol-oxydase activity, and phagocytosis. The position of these cells among the classical hemocyte types of insects is determined. We distinguish two plasmatocyte types (macrophage plasmatocytes and lamellocytes) which do not seem to belong to the same lineage, and oenocytoids which are the crystal cells of the literature.I should like to thank Dr. N. Plus for her help in this study     

The human rete testis

Summary The human rete testis was examined with regard to 1) the number and distribution of entrances of seminiferous tubules, 2) the light microscopic topography and 3) details of the passages as revealed by scanning and transmission electron microscopy. In a newborn 1474 entrances were counted, approximately 50 % entering from the right and 50 % from the left of the central long axis. Three major subdivisions of the rete were distinguished and described: a septal (or interlobular) part represented by tubuli recti, a tunical (or mediastinal) part which is a true network of channels, and an extratesticular part characterized by dilatations (up to 3 mm wide) which we have called bullae retis. In SEM, cylindrical strands running from wall to wall in the tunical and extratesticular rete spaces are a prominent feature. We have called these chordae retis. They are covered by epithelium and are 5–40 m wide and 15 to more than 100 m long. They contain a peculiar tissue consisting of central myoid cells in a fibroelastic matrix. The smaller chordae are avascular. In the light of these findings the rete is interpreted as a highly complex myoelastic sponge. Its function is discussed.Supported in part by USPHS Grant HD-03752 and by a Senior Scientist Award from the Alexander von Humboldt-Stiftung which made the co-authorship possibleSupported by a grant from the Deutsche ForschungsgemeinschaftFor their kind support in supplying us with material, we are indebted to Dr. Janssen (Institut für Rechtsmedizin, Universität Hamburg), Dr. Mairose (Zentralkrankenhaus der Justizbehörde, Hamburg) and Dr. Hubman (Allgemeines Krankenhaus St. Georg, Hamburg). We thank Dr. Kaiser (Zoologisches Institut, Universität Hamburg) for his friendly, generous and competent help with the scanning electron microscopy. Ms. Joanna Davis gave invaluable help with the laborious reconstruction of the rete entrances     

Spectral responses of sustaining fibers in the optic tracts of crayfish (Procambarus)

Summary Spectral response curves were recorded for 60–70 individual sustaining fibers in the optic nerve of the crayfish Procambarus. These cells belong to at least 8 of the 14 classes of sustaining fibers described by Wiersma and Yamaguchi (1966) on the basis of receptive fields. About 90 percent of the cells receive predominant input from yellow-green receptors and are maximally sensitive at 560 to 570 nm; a much smaller number receive principal input from blue receptors and are maximally sensitive near 460 nm.The wavelength sensitivity of optic fibers receiving their major input from yellow-green receptors depends on the state of dark adaptation of the animal and the intensity of illumination. Early in dark adaptation and at high intensities of stimulation the spectral response curve is distorted by light which has been filtered through the sleeves of red-brown shielding pigment. During dark adaptation a shift in maximum spectral response to shorter wavelengths parallels the retraction of the migratory pigment to the dark position and the development of retinal glow. The effects are reversed by injecting into a dark-adapted animal an extract of eyestalks containing the hormone controlling pigment migration: the pigment sleeves lengthen, retinal glow disappears, and shoulders or peaks of sensitivity appear in the red region of the spectrum.This work was supported by USPHS research grant EY 00222 to Yale University. A. E. R. W. was aided by a Fulbright-Hays travel grant. We are grateful to Prof. C. A. G. Wiersma and Dr. R. M. Glantz for a helpful demonstration of the recording technique.