Biosynthesis,cDNA and amino acid sequences of a precursor of conglutin δ, a sulphur-rich protein from Lupinus angustifolius

The biosynthesis of conglutin has been studied in developing cotyledons of Lupinus angustifolius L. Precursors of conglutin formed the major sink for [³⁵S]-cysteine incorporated by developing lupin cotyledons, and these precursors were rapidly sequestered into the endoplasmic reticulum. The sequence of a cDNA clone coding for one such precursor of conglutin was determined. The structure of the precursor polypeptide for conglutin predicted from the cDNA sequence contained an N-terminal leader peptide of 22 amino acids directly preceding a subunit polypeptide of M _r 4520, together with a linking region of 13 amino acids and a subunit polypeptide of M _r 9558 at the C-terminus. The amino acid sequence predicted from the cDNA sequence showed minor variations from that established by sequencing of the protein purified from mature dried seeds (Lilley and Inglis, 1986). These were consistent with the existence of a multi-gene family coding for conglutin . Comparison of the sequences of conglutin with those of other 2S storage proteins showed that the cysteines involved in internal disulphide bridges between the mature subunits of conglutin , were maintained throughout this family of proteins but that little else was conserved either at the protein or DNA level.     

Early generation intermating for yield improvement in groundnut (Arachis hypogaea L.)

Summary Seeds of 4 crosses of groundnut (Arachis hypogaea L.), Robut 33-1 x Chico, Robut 33-1 x NC Ac 17090, Robut 33-1 x PI 298115 and MK 374 x GAUG 1, were irradiated with 30 kR. In the F₁, some branches of each plant were intermated with other plants at random and others selfed in each cross to produce S₂ and F₂ seeds. They were evaluated for pod yield, shelling percentage and 100-kernel weight. The frequency of plants superior to F[in1] was much higher in S₂ than in F₂, which was, in general, true for the values of yield and its components. The S₂ and F₂ were advanced to third generation by selfing. The families descending from S₂ showed clear superiority over those from F₂. The reason for such superiority was suggested to be the recombination of genes from the upper and lower ends of the genotypic distribution under intermating.     

Temporal and local concentration changes in diffusion layers at cellulose membranes due to concentration differences between the solutions on both sides of the membrane

Summary By means of a laser-interferometrical method diffusion layers at the interface of a noncharged cellulose membrane are studied. These layers are induced by a concentration difference between the NaCl solutions separated by the membrane. The temporal and local shift of the NaCl concentration in the diffusion layers were measured. A steady-state concentration profile could be obtained for times of 121 sect ₀484 sec. The concentration profiles at any time (t ₀900) are not a linear function of the membrane surface, but could be fitted to a quadratic function. The thickness of the diffusion layers is also a function of time and its stationary value in this system is (575±49)×10^–6 m. The role of concentration polarization for the determination of phenomenological thermodynamic coefficients of membranes is discussed and a new method is suggested, which excludes the difficulties of the concentration polarization in the diffusion layers at the membrane.     

Amplification of phleomycin induced death and DNA breakdown by caffeine in Escherichia coli

Summary Caffeine enhanced the degradation of DNA to acid soluble fragments in cultures of Escherichia coli exposed to Phleomycin (2 g/ml). Enhancement was particularly striking with stationary phase cultures, which normally exhibit negligible DNA breakdown when treated with 2 g/ml of Phleomycin. There is little DNA breakdown or death in UVR strains treated with phleomycin (2 g/ml) during exponential growth but when caffeine was present as well as Phleomycin, the kinetics of DNA breakdown and the amounts of DNA degraded were identical in all cultures tested including those of UVR, EXR, B/r type and B strains and equal to the maximum rate observed (with an EXR strain) in the absence of caffeine (ca. 1.7 % per min). High concentrations of Phleomycin (10 g/ml) had the same effect as the caffeine+Phleomycin (2 g/ml) combination and produced a uniform pattern of DNA breakdown in all strains tested. Caffeine did not seem to increase permeability of the bacterial coat. Given to the cells before exposure to Phleomycin it was ineffective in enhancing DNA breakdown. On the other hand, exposure of the bacteria to Phleomycin for a period of 40 min at 37° followed by caffeine was as effective as adding the two drugs together.Caffeine increased the efficiency of Phleomycin as an antibiotic for both growing and stationary phase cultures of e. coli B. It is suggested that caffeine aids the cooperative denaturation of DNA initiated by the attachment of Phleomycin molecules to thymine bases. This would allow single strand-specific endonucleases to attack the DNA and initiate DNA breakdown and cell death.This paper is dedicated to charlotte Auerbach on the occasion of her official retirement.     

The pancreatic islets of the teleost Scorpaena scropha

Summary The principal pancreatic islets of the teleost Scorpaena scropha are found ultrastructurally to contain four different kinds of parenchymal cells, viz. ₁-(= D), ₂-, -and agranular cells. The -cells show considerable variations in the shape of the secretory granules. A peculiar feature is that many of these granules are composed of fibrillar subunits, often in parallel arrangement. All -granules are surrounded by membranes and between the membrane and the granule core there is a moderately wide electron lucent space. The electron density of the cytoplasm in the -cells varies somewhat. The ₂-cells possess typical secretory granules with an electron dense core and a closely applied membrane. The secretory granules in the ₁-cells show also a closely applied membrane but a less dense core. Also in the -cells the electron opacity of the cytoplasm varies. The agranular cells are mainly characterized by low cytoplasmic electron density, narrow cisterns of endoplasmic reticulum and sometimes a laminated Golgi complex. Small immature secretory granules are occasionally seen in the cytoplasm of these cells. The significance of the fibrillar -granules remains obscure.This work was supported by grants from the Nordic Insulin Fund, the Town of Umeå, the Swedish Medical Research Council (Project No. B69-12X-718-04A), and by a postdoctoral fellowship from the United States Public Health Service.     

Electrophysiology of trichobothria in orb-weaving spiders (Agelenidae,Araneae)

Summary Trichobothria of the house spidersTegenaria atrica (C.L. Koch) andTegenaria derhami (Scopoli) were stimulated by linear deflection of the hair from its resting position to one side. The pulse response of the receptor cell was analyzed. At angular deflection velocities of 10^–21 deg/ms the receptor begins to discharge at an angle of 3 degrees. While the mean pulse rate remains constant during deflections of 10^–210^–1deg/ms the pulse train may be interrupted by repeated breaks. Discharge continues when the hair is bent proximally beyond the bothrium edge. When the hair is bent distally and touches the bothrium edge, however, discharge ceases. Responsible for this phenomenon seems to be an asymmetry of hair suspension. — Repeated deflection leads to logarithmically ascending latency curves and logarithmically falling curves of the pulse numbers. The function coefficients depend on velocities and repetition rates of the deflections. The adaptational effect is heightened by preceding stationary deflection in the direction of the dynamical stimulus. The mean pulse rate as a function of hair deflection velocity increases logarithmically. The mean pulse rate as a function of hair movement direction obeys a cosine law, provided that a given velocity and a definite deflection angle are used.Supported by grants of the Deutsche Forschungsgemeinschaft given to Prof. Dr. P. Görner in the field of the Schwerpunktprogramm RezeptorphysiologieThe present paper is part of a doctoral thesis. My thanks are due to Prof. Dr. P. G6rner for the theme, many valuable discussions and his constant readiness to help.     

Reversed bohr and root shifts in hemocyanin of the marine prosobranch,Buccinum undatum: Adaptations to a periodically hypoxic habitat

Summary Oxygen binding properties of the hemocyanin-containing blood ofBuccinum undatum were examined in vitro and in vivo under normoxic ( 150 mmHg) and hypoxic ( 50 mmHg) conditions at 10°C. Blood pH and showed a decrease in vivo under hypoxic conditions. Oxygen uptake at high water , was about 18 ml O₂/kg·h (wet weight) and the critical oxygen tension between 25 and 50 mm Hg. In vitro the O₂ binding to hemocyanin showedn-values independent of pH, while both O₂ affinity and oxygen carrying capacity were strongly pH dependent. Oxygen affinity increased below pH=8.1 and thus showed a pronounced reversed Bohr shift in the physiological pH range (7.5<pH<8.1). The oxygen carrying capacity similarly increased markedly with falling pH in the physiological pH range (reversed Root shift). Astrup titration curves showed a metabolic and respiratory acidosis under hypoxic conditions ( 50 mm Hg). The role of hemocyanin in the transport of oxygen in relation to ambient O₂ availability is discussed.     

Theoretical studies on the necessary number of components in mixtures

Summary Theoretical studies on the optimal numbers of components in mixtures (for example multiclonal varieties or mixtures of lines) have been performed according to phenotypic yield stability (measured by the parameter variance). For each component i, i = 1, 2,..., n, a parameter u_i with 0 u_i 1 has been introduced reflecting the different survival and yielding ability of the components. For the stochastic analysis the mean of each u_i is denoted by u ₁ and its variance by _i ² For the character total yield the phenotypic variance V can be explicitly expressed dependent on 1) the number n of components in the mixture, 2) the mean of the _i ² 3) the variance of the _i ² 4) the ratio and 5) the ratio _i ² /² where denotes the mean of the u _i and _u ² is the variance of the u _j. According to the dependence of the phenotypic stability on these factors some conclusions can be easily derived from this V-formula. Furthermore, two different approaches for a calculation of necessary or optimal numbers of components using the phenotypic variance V are discussed: A. Determination of optimal numbers in the sense that a continued increase of the number of components brings about no further significant effect according to stability. B. A reduction of b % of the number of components but nevertheless an unchanged stability can be realized by an increase of the mean of the u _i by 1% (with and _u ² assumed to be unchanged). Numerical results on n (from A) and 1 (from B) are given. Computing the coefficient of variation v for the character total yield and solving for the number n of components one obtains an explicit expression for n dependent on v and the factors 2.-5. mentioned above. In the special case of equal variances, _i ² = _o ² for each i, the number n depends on v, x = (₀/)² and y = (_u/)². Detailed numerical results for n = n (v, x, y) are given. For x 1 and y 1 one obtains n = 9, 20 and 79 for v = 0.30, 0.20 and 0.10, respectively while for x 1 and arbitrary y-values the results are n = 11, 24 and 95.This publication is an extended version of a lecture given at the 1984-EUCARPIA meeting (Section Biometrics in Plant Breeding) in Stuttgart-Hohenheim (Federal Republic of Germany)     

Ethane production by Methanosarcina barkeri during growth in ethanol supplemented medium

Methanosarcina barkeri strain 227 produced ethane during growth on H₂/CO₂ when ethanol was added to the medium in concentrations of 89–974 mM; ethane production varied from 14 to 38 nmoles per tube (20 ml gas phase, 5.7 ml liquid) with increasing ethanol concentrations. Cells grown to mid-logarithmic phase (A₆₀₀ 0.46, protein = 64 g/ml) on H₂/CO₂, thoroughly flushed with H₂/CO₂, then exposed to ethanol, produced maximal ethane levels (at 585 and 974 mM ethanol) of about 215 nmoles per tube, with an ethane/methane ratio of 1×10^-3. Mid-logarithmic-phase cultures of Methanosarcina barkeri strain Fusaro also produced ethane (up to 20 nmoles per tube) when exposed to ethanol. Cultures of strain 227 growing on methanol in the absence of H₂ produced 6 nmoles per tube of ethane when supplemented with ethanol whereas those lacking ethanol but containing H₂ and/or methanol produced 1.6 nmoles per tube. Cultures of Methanococcus deltae strains LH and RC, Methanospirillum hungatei or Methanobacterium thermoautotrophicum produced 5 nmoles ethane per tube when grown in medium containing ethanol. Ethanol concentrations of 177–886 mM were inhibitory to growth of all methanogens examined. Production of ethane by Methanosarcina was inhibited by >62 mM methanol, and both methanogenic inhibitors tested, CCl₄ and Br–CH₂–CH₂–SO _inf3 ^sup- , inhibited ethane and methane production concurrently. The data suggest that ethanol is converted to ethane by Methanosarcina species using the terminal portion of the methanol-to-methane pathway.     

Optimization of an electroporation procedure for Kluyveromyces lactis transformation

Summary An electroporation method using a Bio-Rad Gene Pulser has been optimized for introducing heterologous DNA into Kluyveromyces lactis yeasts. The plasmid pCR1, derived from a native Kluyveromyces plasmid, was used to transform K. lactis. This plasmid produces a wheat -amylase and contains both the biosynthetic marker URAA and G418 resistance genes. Transformation was optimal at 4500 V/cm, 25 F, and with 0.2 g plasmid DNA. Transformation efficiencies in the range 10⁴–10⁵ transformants/10⁷ cells/g DNA were obtained.     

A method for the investigation of those transformations under which the visual recognition of a given object is invariant

An experiment is described which shows in operation the program set out in Foster (1972a) for the investigation of the invariance transformations of visual recognition. The concern in the present study is with the Lie group of rotations SO(2), and a certain centrally located foveal Landolt ring. By presenting to the visual system this Landolt ring and a rotated image in rapid succession, one attempted to induce a specified rotation-type phi-motion. Two subjects were employed. Both reported the existence of the required type of phi-motion for rotations ₀ of the Landolt ring about the visual axis with -2/72/7. By appealing to the basic Proposition 2 of Foster (1972 a), the conclusion is reached that the visual system appears capable of effecting upon a certain centrally located foveal annulus the local 1-parameter group of rotations about the visual axis ₀, [–2/7,2/7].     

Über die Wirkung von Röntgenstrahlen auf Methionin

Zusammenfassung Durch Untersuchung der Einwirkung von Röntgenstrahlen (50–200 kR) auf Carboxyl-¹⁴C-, 2-¹⁴C- und¹⁴CH₃-markiertes Methionin sowie auf nicht radioaktivmarkiertes Methionin konnte festgestellt werden, daß folgende Umwandlungsprodukte entstehen: Methioninsulfoxyd (MSO),-Hydroxy--methylmercaptobuttersäure (HMMB),-Methylmercaptopropionsäure (MMP) und Homocystein (HO).MSO und die als Zwischenstufe vermutete-Methylmercapto--ketobuttersäure konnten nicht nachgewiesen werden. Außerdem wurde in keinem Versuch eine Abspaltung die S-CH₃-Gruppe (z. B. zu-Aminobuttersäure) und eine Bildung von Methioninsulfon gefunden, die von anderen Autoren nach Einwirkung hoher Dosen beschrieben wurde. Bei einer Dosis 50 kR. konnte als Umwandlungsprodukt nur MSO festgestellt werden.Die Einwirkung von H₂O₂ auf Methionin liefert qualitativ die gleichen Umwandlungsprodukte, jedoch unterscheiden sich die Mengenverhältnisse der gebildeten Produkte deutlich von den Werten, die nach Bestrahlung erhalten werden.Der Deutschen Forschungsgemeinschaft danken wir für eine Sachbeihilfe.     

Über die Bildung der Augenpigmentgranula beiDrosophila v undcn nach Verfütterung von Ommochromvorstufen

Zusammenfassung Bei denDrosophila-Mutantenv undcn, die weder Ommochrom noch leere Pigmentgranula aufweisen, läßt sich durch Verfüttern von Kynurenin, bzw. 3-Hydroxy-kynurenin die Bildung von Pigmentgranula induzieren, die von den Granula des Wildtyps nicht zu unterscheiden sind. Ihr größter Durchmesser beträgt ca. 0,4 , sie sind von einer Membran umgeben und ihre Wachstumsgeschwindigkeit ist identisch.Messung der heranwachsenden Granula in proximalen und distalen Bereichen der Ommatidien erbrachten einen signifikanten Größenunterschied; dieser ist bereits 48 Std nach der Verpuppung erkennbar.

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On the formation of eye pigment granules after feeding ommochrome precursors toDrosophila v andcn

Summary In the mutantsv andcn ofDrosophila, which contain neither ommochrome pigment nor empty pigment granules, feeding of kynurenine or 3-hydroxy-kynurenine causes the formation of pigment granules which cannot be distinguished from wild type granules. Their larger diameter is about 0.4 , they are surrounded by a membrane, and their growth rate is identical.Measurement of growing pigment granules in proximal and more distal regions of the ommatidia has revealed a significant difference in size which can be recognized as early as 48 hours after pupation.

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Wir danken der Deutschen Forschungsgemeinschaft für die finanzielle Unterstützung, Herrn Dr. F. G. Barth, Herrn Prof. H. Altner und seinen Mitarbeitern, sowie Frl. H. Tscharntke für Einweisung und Hilfe in der EM-Technik, und Herrn Dr. F. Schwabl für seinen Rat bei der Auswertung der Messungen.     

Bounds on the learning capacity of some multi-layer networks

We obtain bounds for the capacity of some multi-layer networks of linear threshold units. In the case of a network having n inputs, a single layer of h hidden units and an output layer of s units, where all the weights in the network are variable and shn, the capacity m satisfies 2nmnt logt, where t=1=h/s. We consider in more detail the case where there is a single output that is a fixed boolean function of the hidden units. In this case our upper bound is of order nh logh but the argument which provided the lower bound of 2n no longer applies. However, by explicit computation in low dimensional cases we show that the capacity exceeds 2n but is substantially less than the upper bound. Finally, we describe a learning algorithm for multi-layer networks with a single output unit. This greatly outperforms back propagation at the task of learning random vectors and provides further empirical evidence that the lower bound of 2n can be exceeded.     

Sodium efflux from perfused giant algal cells

Internodal cells of the giant alga Chara corallina were perfused internally to replace the native cytoplasm, tonoplast and vacuole with artificial cytoplasm. Sodium efflux from perfused cells, measured by including ²²Na in the perfusion media, was increased by increasing the internal sodium concentration and by decreasing the external pH, and was inhibited by external application of the renal diuretic amiloride. The sodium efflux was markedly ATP-dependent, with a 50-fold decrease in efflux observed after perfusion with media lacking ATP. Efflux in the presence of ATP was reduced by 33% by inclusion of 10 M N,N-dicyclohexylcarbodiimide in the perfusion medium. The membrane potential of the perfused cells approximated that of intact cells from the same culture. It is suggested that sodium efflux in perfused Chara cells proceeds via a secondary antiporter with protons, regulated by ATP in a catalytic role and with the proton motive force acting as the energy source.Abbreviations DCCD N,N-dicyclohexylcarbodiimide - EGTA ethylene glycol-bis(-aminoethyl ether)-N,N,N,N-tetraacetic acid - Mes 2-(N-morpholino)ethanesulphonic acid - Mops 3(N-morpholino)propanesulphonic acid - Taps tris(hydroxymethyl)methylaminopropanesulphonic acid     

Modulation of formation of tumor metastases by peritoneal macrophages elicited by various agents

Summary We have studied the formation of experimental B16 melanoma metastases in the lungs of mice inoculated IV with tumoricidal or nontumoricidal peritoneal macrophages elicited by various agents. IV inoculation of peritoneal M elicited by Brewer's thioglycollate medium (TG-M) 1 day before the injection of B16 melanoma cells dramatically increased the number of metastatic foci in the lungs. NIH thioglycollate broth and proteose peptone each elicited a relatively low number of M, which were morphologically distinguishable from TG-M and did not influence the yield of B16 melanoma colonies in the lungs. Resident or C. pravum-elicited M also did not augment metastatis formation. TG-M became highly tumoricidal after IP stimulation with poly I: C. However, tumoricidal TG-M inoculated IV 1 day before IV inoculation of B16 melanoma cells did not have an antimetastatic effect. On the contrary, both tumoricidal and nontumoricidal TG-M augmented metastasis formation. Poly I: C treatment had a substantial antimetastatic effect in the normal mice, but not in mice with adoptively transferred TG-M. Histological analysis revealed that IV-inoculated TG-M (tumoricidal or nontumoricidal, either viable or disrupted) induced severe intravascular reaction in the lungs, but not in the liver or kidney. This reaction manifested in the aggregation of the various blood cells, preferentially neutrophils. These reactions were not observed after IV inoculation of PM or NIH TG-M.Intravascular inflammatory reactions induced by TG-M may be responsible for the augmentation of metastasis formation, partly by suppression of NK reactivity and mostly by the acceleration of the processes of tumor cell extravasation. These data may provide some insight into the failure to achieve systemic adoptive immunotherapy using activated peritoneal TG-M. Abbreviations used in this paper are: TG-M, thioglycollate-elicited macrophages; PM, proteose-peptone-elicited macrophages; NIH TG-M, macrophages elicited with NIH thioglycollate broth; CP-M, macrophages; elicited with C. parvum; poly I: C, polyinosinic: polycytidylic acid; TGM, thioglycollate medium; NIHTGB, NIH thioglycollate broth     

Synthesis, Characterization and Antitumor Studies of Mn(II), Ni(II), Cu(II) and Zn(II) Complexes of N-Nicotinoyl-N′-o-Hydroxythiobenzhydrazide

A new ligand N-Nicotinoyl-N-o-hydroxythiobenzhydrazide (H₂Notbh) forms complexes [Mn(Notbh)(H₂O)], [M(Notbh)] [M=Ni(II) Cu(II) and Zn(II)] which were characterized by various physico-chemical techniques. All the metal complexes were observed to inhibit the growth of tumor in vitro, whereas, ligand did not. In vivo administration of these complexes resulted in prolongation of survival of tumor bearing mice. Tumor bearing mice administered with metal complexes showed reversal of tumor growth associated induction of apoptosis in lymphocytes. The paper discusses the possible mechanisms and therapeutic implication of the H₂Notbh and its metal complexes in tumor regression and tumor growth associated immunosuppression.     

Phosphorylation of the triadin cytoplasmic domain by CaM protein kinase in rabbit fast-twitch muscle sarcoplasmic reticulum

Identification of estrogenresponsive genes is important to understand the molecular mechanisms of estrogen action. Suppression subtractive hybridization was employed to screen estrogenresponsive genes in chick liver. A single injection of estrogen into 6weekold chick induced upregulation of several known genes encoded for yolk proteins, such as Vitellogenin I and II and very low density lipoprotein II (apo-VLDL II). One novel sequence displayed a dramatic change (3fold increase) in response to estrogen treatment. This cDNA fragment was extended and the resultant sequence was analyzed. Translated amino acid sequence was 90, 88, 83 and 87% identical to the Larginine:glycine amidinotransferase of pig, rat, frog and human, respectively. The sequence has a conservative catalytic site of Larginine:glycine amidinotransferase. The expression pattern of this gene in organs is consistent with previous reports of Larginine:glycine amidinotransferase in chick. Thus, this clone represented the chicken Larginine:glycine amidinotransferase. It appeared that estrogeninduced alteration of arginine:glycine amidinotransferase was not dependent on protein synthesis, because concurrent administration of cycloheximide did not affect the estrogenmediated expression pattern. This is the first study demonstrating that Larginine:glycine amidinotransferase is a target of the estrogen receptor.     

Effects of UV-B on motility and photoorientation in the cyanobacterium,Phormidium uncinatum

UV-B irradiation has a detrimental effect on the survival of populations of the filamentous cyanobacterium, Phormidium uncinatum, at levels slightly higher than those currently measured at the surface of the earth. The organisms are not damaged or killed by UV-B radiation at 300 nm of 200 Wm^-2 for up to 20 h; but slightly increased levels of UV-B irradiation (2 h of 200 Wm^-2 at 300 nm) drastically impair motility, phototactic orientation and photophobic responses. These photosynthetic organisms require a narrow light intensity range for growth so that any decrease in their ability to actively search for and move into areas of favorable light conditions is bound to affect the survival of a population. The fluorescence yield of both phycobilins and chlorophyll is not altered even after 20 h of UV-B irradiation (200 Wm^-2 at 270 nm) indicating that UV-B at that dose does not affect the photosynthetic apparatus. The organisms are killed either by too bright intensities which bleach the photosynthetic pigments or by the lack of energy when they are unable to avoid moving into dark areas.     

Effects of background structure on the discrimination of configurational moving prey dummies by toadsBufo bufo (L.)

Summary The prey-catching activity of the toadBufo b. bufo was measured in response to various configurational moving two-dimensional black or white stimuli contrasting with various homogeneous or structured backgrounds (Figs. 1 to 5).Area discrimination was tested with squares of different sizes,configurational discrimination with stripes of equal size and different configuration (worm or antiworm), andlength discrimination with worm-like stripes of different length. Signal Extraction. A 2×5 mm² wormlike stripe of a luminanceL _s36 cd×m^–2, for example, was practically not resolved from a homogeneous background of almost the same luminanceL _b = 36. But it could be well detected if the background was structured ( ); at a given luminance ( ) the releasing value of the grey stimulus (L _s= 36) increased to some extent with structure width of the background (Fig. 1 c-e). Configurational Discrimination. The basic stimulus response relationships were maintained, if Configurational stimuli were moved against black, white, grey or structured backgrounds. However, in the range of short stripes (xl= 5 mm) the worm/antiworm discrimination was significantly better withblack stimuli moving against white background than forwhite against black (curvesa andc in Figs. 2A and 3A). The Configurational selectivity in response to white wormlike and antiwormlike stripes increased if stimuli were moved against a grey or a structured background (curvesa andc in Figs. 2 and 3B-E forxl5 mm). Length Discrimination. Relatively short stripes (close to the square configuration) and relatively long ones were discriminated less well than those in a medium size range. The optimal discrimination range was different for black stimuli (range: 3xl ₁6.5 mm) and white stimuli (range: 5xl ₁ 10 mm) (Fig. 4A, B). Discrimination in this range could be enhanced to some extent if the background was structured. These results were consistent for artificially (Fig. 4A) and naturally structured backgrounds (Fig. 5A-C).The results show that stimulus discrimination in toads depends largely on the values of Configurational parameters. The background structure may have distinct effects on stimulus perception, i.e., either masking or facilitation.