One Rhodopsin per Photoreceptor: Iro-C Genes Break the Rule

While photoreceptors usually contain a single type of rhodopsin, two rhodopsins are sometimes expressed. This bi-allelic expression appears to be under genetic control, an example of which is discussed in this Primer

Exact spin dynamics of the 1/r^2 supersymmetric t-J model in a magnetic field

The dynamical spin structure factor S^{zz}(Q,omega) in the small momentum region is derived analytically for the one-dimensional supersymmetric t-J model with 1/r^2 interaction. Strong spin-charge separation is found in the spin dynamics. The structure factor S^{zz}(Q,omega) with a given spin polarization does not depend on the electron density in the small momentum region. In the thermodynamic limit, only two spinons and one antispinon (magnon) contribute to S^{zz}(Q,omega). These results are derived via solution of the SU(2,1) Sutherland model in the strong coupling limit.Comment: 20 pages, 8 figures. Accepted for publication in J.Phys.

Derivation of Green's Function of Spin Calogero-Sutherland Model by Uglov's Method

Hole propagator of spin 1/2 Calogero-Sutherland model is derived using Uglov's method, which maps the exact eigenfunctions of the model, called Yangian Gelfand-Zetlin basis, to a limit of Macdonald polynomials (gl_2-Jack polynomials). To apply this mapping method to the calculation of 1-particle Green's function, we confirm that the sum of the field annihilation operator on Yangian Gelfand-Zetlin basis is transformed to the field annihilation operator on gl_2-Jack polynomials by the mapping. The resultant expression for hole propagator for finite-size system is written in terms of renormalized momenta and spin of quasi-holes and the expression in the thermodynamic limit coincides with the earlier result derived by another method. We also discuss the singularity of the spectral function for a specific coupling parameter where the hole propagator of spin Calogero-Sutherland model becomes equivalent to dynamical colour correlation function of SU(3) Haldane-Shastry model.Comment: 36 pages, 8 figure

Coloration principles of the Great purple emperor butterfly (Sasakia charonda)

The dorsal wings of male Sasakia charonda butterflies display a striking blue iridescent coloration, which is accentuated by white, orange-yellow and red spots, as well as by brown margins. The ventral wings also have a variegated, but more subdued, pattern. We investigated the optical basis of the various colors of intact wings as well as isolated wing scales by applying light and electron microscopy, imaging scatterometry and (micro)spectrophotometry. The prominent blue iridescence is due to scales with tightly packed, multilayered ridges that contain melanin pigment. The scales in the brown wing margins also contain melanin. Pigments extracted from the orange-yellow and red spots indicate the presence of 3-OH-kynurenine and ommochrome pigment. The scales in the white spots also have multilayered ridges but lack pigment. The lower lamina of the scales plays a so-far undervalued but often crucial role. Its thin-film properties color the majority of the ventral wing scales, which are unpigmented and have large windows. The lower lamina acting as a thin-film reflector generally contributes to the reflectance of the various scale types

Random array of colour filters in the eyes of butterflies

The compound eye of the Japanese yellow swallowtail butterfly Papilio xuthus is not uniform. In a combined histological, electrophysiological and optical study, we found that the eye of P. xuthus has at least three different types of ommatidia, in a random distribution. In each ommatidium, nine photoreceptors contribute microvilli to the rhabdom. The distal two-thirds of the rhabdom length is taken up by the rhabdomeres of photoreceptors R1­R4. The proximal third consists of rhabdomeres of photoreceptors R5­R8, except for the very basal part, to which photoreceptor R9 contributes. In all ommatidia, the R1 and R2 photoreceptors have a purple pigmentation positioned at the distal tip of the ommatidia. The R3­R8 photoreceptors in any one ommatidium all have either yellow or red pigmentation in the cell body, concentrated near the edge of the rhabdom. The ommatidia with red-pigmented R3­R8 are divided into two classes: one class contains an ultraviolet-fluorescing pigment. The different pigmentations are presumably intimately related to the various spectral types found previously in electrophysiological studies

One rhodopsin per photoreceptor: Iro-C genes break the rule

No abstract availabl

An expanded set of photoreceptors in the Eastern Pale Clouded Yellow butterfly, Colias erate

We studied the spectral and polarisation sensitivities of photoreceptors of the butterfly Colias erate by using intracellular electrophysiological recordings and stimulation with light pulses. We developed a method of response waveform comparison (RWC) for evaluating the effective intensity of the light pulses. We identified one UV, four violet-blue, two green and two red photoreceptor classes. We estimated the peak wavelengths of four rhodopsins to be at about 360, 420, 460 and 560 nm. The four violet-blue classes are presumably based on combinations of two rhodopsins and a violet-absorbing screening pigment. The green classes have reduced sensitivity in the ultraviolet range. The two red classes have primary peaks at about 650 and 665 nm, respectively, and secondary peaks at about 480 nm. The shift of the main peak, so far the largest amongst insects, is presumably achieved by tuning the effective thickness of the red perirhabdomal screening pigment. Polarisation sensitivity of green and red photoreceptors is higher at the secondary than at the main peak. We found a 20-fold variation of sensitivity within the cells of one green class, implying possible photoreceptor subfunctionalisation. We propose an allocation scheme of the receptor classes into the three ventral ommatidial types

A unique visual pigment expressed in green, red and deep-red receptors in the eye of the small white butterfly, Pieris rapae crucivora

The full primary structure of a long-wavelength absorbing visual pigment of the small white butterfly, Pieris rapae crucivora, was determined by molecular cloning. In situ hybridization of the opsin mRNA of the novel visual pigment (PrL) demonstrated that it is expressed in the two distal photoreceptor cells (R3 and R4) as well as in the proximal photoreceptors (R5–8) in all three types of ommatidia of the Pieris eye. The main, long-wavelength band of the spectral sensitivities of the R3 and R4 photoreceptors is well described by the absorption spectrum of a visual pigment with absorption maximum at 563 nm; i.e. PrL is a visual pigment R563. The spectral sensitivities of R5–8 photoreceptors in ommatidial type I and III peak at 620 nm and those in type II ommatidia peak at 640 nm. The large shifts of the spectral sensitivities of the R5–8 photoreceptors with respect to the absorption spectrum of their visual pigment can be explained with the spectral filtering by pale-red (PR) and deep-red (DR) screening pigments that are concentrated in clusters of granules near the rhabdom boundary. The peak absorbance of the two spectral filters appears to be approximately 1 (PR) and 2 (DR)

Tuning of photoreceptor spectral sensitivities by red and yellow pigments in the butterfly Papilio xuthus

The compound eye of the Japanese yellow swallowtail butterfly, Papilio xuthus, consists of different types of ommatidia characterized by the pigmentation around the rhabdom. About 75% of the ommatidia harbor red pigment, whereas the other 25% contain yellow pigment. We find that the pigments function as spectral filters for the proximal photoreceptor cells. Intracellular recordings of the proximal cells yielded spectral sensitivities peaking in the red (λmax = 600 nm) and in the green (λmax = 520 nm), respectively. Staining of the recorded cells and subsequent histology demonstrated that the red receptors contain red pigment and that the green receptors contain yellow pigment. The sensitivity spectrum of the red receptors was considerably narrower compared to the absorption spectrum of a visual pigment peaking at 600 nm. The sensitivity spectrum can be calculated with an optical model for the butterfly rhabdom by incorporating measured absorbance spectra of the red pigments, yielding that the cell contains a visual pigment peaking at about 575 nm. The model also indicated that the spectral sensitivity of the green receptors is produced by the combination of the yellow lateral filter and a visual pigment peaking at 515 nm