scholarly journals Diminution and enlargement of the mosquito rhabdom in light and darkness.

1975 ◽  
Vol 65 (5) ◽  
pp. 583-598 ◽  
Author(s):  
R H White ◽  
E Lord
Keyword(s):  
Light Intensity ◽  
Aedes Aegypti ◽  
Dark Adaptation ◽  
Light Adaptation ◽  
Constant Volume ◽  
Intensity Level ◽  
Constant Intensity ◽  
Rates Of Change

The rhabdoms of the larval ocelli of the mosquito Aedes aegypti undergo morphological light and dark adaptation over periods of hours. The rhabdom enlarges during dark adaptation and grows smaller during light adaptation. Diminution is exponential, enlargement linear, and rates of change are proportional to log light intensity. Rhabdoms maintained at a constant intensity level off at a constant volume proportional to log intensity. We argue that changes in rhabdom volume after changes in light intensity reflect an influence of light on the turnover of photoreceptro membrane, and that the volumes at which rhabdoms level off represent equilibria between opposed processes of membrane loss and renewal.

scholarly journals Light and dark adaptation in Phycomyces phototropism.

1984 ◽  
Vol 84 (1) ◽  
pp. 101-118 ◽  
Author(s):  
P Galland ◽  
V E Russo
Keyword(s):  
Dark Adaptation ◽  
Time Course ◽  
Growth Response ◽  
Light Adaptation ◽  
Abnormal Behavior ◽  
Adaptation Level ◽  
Intensity Level ◽  
Wild Type ◽  
Adaptation Mechanism ◽  
Intensity Range

Light and dark adaptation of the phototropism of Phycomyces sporangiophores were analyzed in the intensity range of 10(-7)-6 W X m-2. The experiments were designed to test the validity of the Delbrück-Reichardt model of adaptation (Delbrück, M., and W. Reichardt, 1956, Cellular Mechanisms in Differentiation and Growth, 3-44), and the kinetics were measured by the phototropic delay method. We found that their model describes adequately only changes of the adaptation level after small, relatively short intensity changes. For dark adaptation, we found a biphasic decay with two time constants of b1 = 1-2 min and b2 = 6.5-10 min. The model fails for light adaptation, in which the level of adaptation can overshoot the actual intensity level before it relaxes to the new intensity. The light adaptation kinetics depend critically on the height of the applied pulse as well as the intensity range. Both these features are incompatible with the Delbrück-Reichardt model and indicate that light and dark adaptation are regulated by different mechanisms. The comparison of the dark adaptation kinetics with the time course of the dark growth response shows that Phycomyces has two adaptation mechanisms: an input adaptation, which operates for the range adjustment, and an output adaptation, which directly modulates the growth response. The analysis of four different types of behavioral mutants permitted a partial genetic dissection of the adaptation mechanism. The hypertropic strain L82 and mutants with defects in the madA gene have qualitatively the same adaptation behavior as the wild type; however, the adaptation constants are altered in these strains. Mutation of the madB gene leads to loss of the fast component of the dark adaptation kinetics and to overshooting of the light adaptation under conditions where the wild type does not overshoot. Another mutant with a defect in the madC gene shows abnormal behavior after steps up in light intensity. Since the madB and madC mutants have been associated with the receptor pigment, we infer that at least part of the adaptation process is mediated by the receptor pigment.

scholarly journals DARK ADAPTATION IN DINEUTES

1938 ◽  
Vol 21 (3) ◽  
pp. 375-382 ◽  
Author(s):  
Leonard B. Clark
Keyword(s):  
Light Intensity ◽  
Dark Adaptation ◽  
Light Adaptation ◽  
Threshold Intensity

The level of dark adaptation of the whirligig beetle can be measured in terms of the threshold intensity calling forth a response. The course of dark adaptation was determined at levels of light adaptation of 6.5, 91.6, and 6100 foot-candles. All data can be fitted by the same curve. This indicates that dark adaptation follows parts of the same course irrespective of the level of light adaptation. The intensity of the adapting light determines the level at which dark adaptation will begin. The relation between log aI0 (instantaneous threshold) and log of adapting light intensity is linear over the range studied.

scholarly journals VISUAL ADAPTATION AND CHEMISTRY OF THE RODS

1937 ◽  
Vol 21 (1) ◽  
pp. 93-105 ◽  
Author(s):  
George Wald ◽  
Anna-Betty Clark
Keyword(s):  
Dark Adaptation ◽  
Light Adaptation ◽  
Visual Adaptation ◽  
Slow Process ◽  
Constant Intensity ◽  
Visual Threshold ◽  
Chemical Equations ◽  
Chemical Cycle

1. The reality of a chemical cycle proposed to describe the rhodopsin system is tested with dark adaptation measurements. 2. The first few minutes of rod dark adaptation are rapid following short, slower following long irradiation. As dark adaptation proceeds, the slow process grows more prominent, and occupies completely the final stages of adaptation. 3. Light adaptation displays similar duality. As the exposure to light of constant intensity lengthens, the visual threshold rises, and independently the speed of dark adaptation decreases. 4. These results conform with predictions from the chemical equations.

Exposure of Polymeric Glazing Materials Using NREL’s Ultra-Accelerated Weathering System (UAWs)

2010 ◽  
Author(s):  
Carl Bingham ◽  
Gary Jorgensen ◽  
Amy Wylie
Keyword(s):  
Light Intensity ◽  
Thermal Effects ◽  
Outdoor Exposure ◽  
Exposure Chamber ◽  
Accelerated Weathering ◽  
Intensity Level ◽  
Design And Implementation ◽  
Different Temperatures ◽  
Exposure Testing ◽  
Ultraviolet Irradiance

NREL’s Ultra-Accelerated Weathering System (UAWS) selectively reflects and concentrates natural sunlight ultraviolet irradiance below 475 nm onto exposed samples to provide accelerated weathering of materials while keeping samples within realistic temperature limits. This paper will explain the design and implementation of the UAWS which allow it to simulate the effect of years of weathering in weeks of exposure. Exposure chamber design and instrumentation will be discussed for both a prototype UAWS used to test glazing samples as well as a commercial version of UAWS. Candidate polymeric glazing materials have been subjected to accelerated exposure testing at a light intensity level of up to 50 UV suns for an equivalent outdoor exposure in Miami, FL exceeding 15 years. Samples include an impact modified acrylic, fiberglass, and polycarbonate having several thin UV-screening coatings. Concurrent exposure is carried out for identical sample sets at two different temperatures to allow thermal effects to be quantified along with resistance to UV.

scholarly journals PSB27: A thylakoid protein enabling Arabidopsis to adapt to changing light intensity

2015 ◽  
Vol 112 (5) ◽  
pp. 1613-1618 ◽  
Author(s):  
Xin Hou ◽  
Aigen Fu ◽  
Veder J. Garcia ◽  
Bob B. Buchanan ◽  
Sheng Luan
Keyword(s):  
Photosystem Ii ◽  
Light Intensity ◽  
Light Adaptation ◽  
Light Exposure ◽  
Starch Accumulation ◽  
State Transitions ◽  
Potential Candidate ◽  
Subsequent Work ◽  
Variable Intensity ◽  
Changing Light

In earlier studies we have identified FKBP20-2 and CYP38 as soluble proteins of the chloroplast thylakoid lumen that are required for the formation of photosystem II supercomplexes (PSII SCs). Subsequent work has identified another potential candidate functional in SC formation (PSB27). We have followed up on this possibility and isolated mutants defective in the PSB27 gene. In addition to lack of PSII SCs, mutant plants were severely stunted when cultivated with light of variable intensity. The stunted growth was associated with lower PSII efficiency and defective starch accumulation. In response to high light exposure, the mutant plants also displayed enhanced ROS production, leading to decreased biosynthesis of anthocyanin. Unexpectedly, we detected a second defect in the mutant, namely in CP26, an antenna protein known to be required for the formation of PSII SCs that has been linked to state transitions. Lack of PSII SCs was found to be independent of PSB27, but was due to a mutation in the previously described cp26 gene that we found had no effect on light adaptation. The present results suggest that PSII SCs, despite being required for state transitions, are not associated with acclimation to changing light intensity. Our results are consistent with the conclusion that PSB27 plays an essential role in enabling plants to adapt to fluctuating light intensity through a mechanism distinct from photosystem II supercomplexes and state transitions.

The Cockroach DCMD Neurone: I. Lateral Inhibition and the Effects of Light- and Dark-adaptation

1982 ◽  
Vol 99 (1) ◽  
pp. 61-90 ◽  
Author(s):  
DONALD H. EDWARDS
Keyword(s):  
Lateral Inhibition ◽  
Dark Adaptation ◽  
Light Adaptation ◽  
Absolute Intensity ◽  
Recurrent Network ◽  
Light Spot ◽  
Movement Detector ◽  
Threshold Response ◽  
Inhibitory Network ◽  
Local Background

1. The responses of the cockroach descending contralateral movement detector (DCMD) neurone to moving light stimuli were studied under both light- and dark-adapted conditions. 2. With light-adaptation the response of the DCMD to two moving 2° (diam.) spots of white light is less than the response to a single spot when the two spots are separated by less than 10° (Fig. 2). 3. With light-adaptation the response of the DCMD to a single moving light spot is a sigmoidally shaped function of the logarithm of the light intensity (Fig. 3a). With dark-adaptation the response of a DCMD to a single moving light spot is a bell-shaped function of the logarithm of the stimulus intensity (Fig. 3b). The absolute intensity that evokes a threshold response is about one-and-a-half log units less in the dark-adapted eye than in the light-adapted eye. 4. The decrease in the DCMD's response that occurs when two stimuli are closer than 10°, and when a single bright stimulus is made brighter, indicates that lateral inhibition operates among the afferents to the DCMD. 5. It is shown that this inhibition cannot be produced by a recurrent lateral inhibitory network. A model of the afferent path that contains a non-recurrent lateral inhibitory network can account for the response/intensity plots of the DCMD recorded under both light-adapted and dark-adapted conditions. 6. The threshold intensity of the DCMD is increased if a stationary pattern of light is present near the path of the moving spot stimulus. This is shown to be due to a peripheral tonic lateral inhibition that is distinct from the non-recurrent lateral inhibition described earlier. 7. It is suggested that the peripheral lateral inhibition acts to adjust the threshold of afferents to local background light levels, while the proximal non-recurrent network acts to enhance the acuity of the eye to small objects in the visual field, and to filter out whole-field stimuli.

scholarly journals Objective and subjective measures of exercise intensity during thermo-neutral and hot yoga

2018 ◽  
Vol 43 (4) ◽  
pp. 397-402 ◽  
Author(s):  
Corinne N. Boyd ◽  
Stephanie M. Lannan ◽  
Micah N. Zuhl ◽  
Ricardo Mora-Rodriguez ◽  
Rachael K. Nelson
Keyword(s):  
Oxygen Consumption ◽  
Light Intensity ◽  
Exercise Intensity ◽  
Perceived Exertion ◽  
Maximal Oxygen Consumption ◽  
Rating Of Perceived Exertion ◽  
Moderate Intensity ◽  
Subjective Measures ◽  
Moderate Intensity Exercise ◽  
Constant Intensity

While hot yoga has gained enormous popularity in recent years, owing in part to increased environmental challenge associated with exercise in the heat, it is not clear whether hot yoga is more vigorous than thermo-neutral yoga. Therefore, the aim of this study was to determine objective and subjective measures of exercise intensity during constant intensity yoga in a hot and thermo-neutral environment. Using a randomized, crossover design, 14 participants completed 2 identical ∼20-min yoga sessions in a hot (35.3 ± 0.8 °C; humidity: 20.5% ± 1.4%) and thermo-neutral (22.1 ± 0.2 °C; humidity: 27.8% ± 1.6%) environment. Oxygen consumption and heart rate (HR) were recorded as objective measures (percentage of maximal oxygen consumption and percentage of maximal HR (%HRmax)) and rating of perceived exertion (RPE) was recorded as a subjective measure of exercise intensity. There was no difference in exercise intensity based on percentage of maximal oxygen consumption during hot versus thermo-neutral yoga (30.9% ± 2.3% vs. 30.5% ± 1.8%, p = 0.68). However, exercise intensity was significantly higher during hot versus thermo-neutral yoga based on %HRmax (67.0% ± 2.3% vs. 60.8% ± 1.9%, p = 0.01) and RPE (12 ± 1 vs. 11 ± 1, p = 0.04). According to established exercise intensities, hot yoga was classified as light-intensity exercise based on percentage of maximal oxygen consumption but moderate-intensity exercise based on %HRmax and RPE while thermo-neutral yoga was classified as light-intensity exercise based on percentage of maximal oxygen uptake, %HRmax, and RPE. Despite the added hemodynamic stress and perception that yoga is more strenuous in a hot environment, we observed similar oxygen consumption during hot versus thermo-neutral yoga, classifying both exercise modalities as light-intensity exercise.

The Effect of Changed Extracellular Calcium and Sodium Concentration on the Electroretinogram of the Crayfish Retina

1980 ◽  
Vol 35 (3-4) ◽  
pp. 308-318 ◽  
Author(s):  
H. Stieve ◽  
I. Claßen-Linke
Keyword(s):  
Dark Adaptation ◽  
Time Course ◽  
Calcium Concentration ◽  
Light Adaptation ◽  
Sodium Concentration ◽  
Strong Increase ◽  
Calcium Stores ◽  
Half Time ◽  
Astacus Leptodactylus ◽  
External Calcium

Abstract The electroretinogram (ERG) of the isolated retina of the crayfish Astacus leptodactylus evoked by strong 10 ms light flashes at constant 5 min intervals was measured while the retina was continuously superfused with various salines which differed in Ca2+ -and Na+ -concentrations. The osmotic pressure of test- and reference-saline was adjusted to be identical by adding sucrose. Results: 1. Upon raising the calcium-concentration of the superfusate in the range of 20-150 mmol/l (constant Na+ -concentration: 208 mmol/l) the peak amplitude hmax and the half time of decay t2 of the ERG both decrease gradually up to about 50% in respect to the corresponding value in reference saline. 2. The recovery of the ERG due to dark adaptation following the “weakly light adapted state” is greatly diminished in high external [Ca2+]ex. 3. Lowering the external calcium-concentration (10 →1 mmol/l) causes a small increase in hmax and a strong increase of the half time of decay t2 (about 180%). Upon lowering the calcium concentration of the superfusate to about 1 nmol/l by 1 mmol/l of the calcium buffer EDTA, a slowly augmenting diminution of the ERG height hm SLX occurs. How­ever, a strong retardation of the falling phase of the ERG characterized by an increase in t2 occurs quickly. Even after 90 min stay in the low calcium saline the retina is still not inexcitable; hmax is 5 - 10% of the reference value. The diminution of hmax occurs about six-fold faster when the buffer concentration is raised to 10 mmol/l EDTA. 4. Additional lowering of the Na+ -concentration (208 →20.8 mmol/l) in a superfusate with a calcium concentration raised to 150 mmol/l causes a strong reduction of the ERG amplitude hmax to about 10%. 5. In a superfusate containing 1 nmol/l calcium such lowering of the sodium concentration (208 → 20.8 mmol/l) causes a diminution of the ERG height to about 40% and the shape of the ERG to become polyphasic; at least two maxima with different time to peak values are observed. Interpretation: 1. The similarity of effects, namely raising external calcium concentration and light adaptation on the one hand and lowering external calcium and dark adaptation on the other hand may indicate that the external calcium is acting on the adaptation mechanism of the photoreceptor cells, presumably by influencing the intracellular [Ca2+]. 2. The great tolerance of the retina against Ca2+ -deficiency in the superfusate might be effected by calcium stores in the retina which need high Ca2+ -buffer concentrations in the superfusate to become exhausted. 3. In contrast to the Limulus ventral nerve photoreceptor there does not seem to be an antagonis­ tic effect of sodium and calcium in the crayfish retina on the control of the light channels. 4. The crayfish receptor potential seems to be composed of at least two different processes. Lowering calcium-and lowering external sodium-concentration both diminish the height and change the time course of the two components to a different degree. This could be caused by in­ fluencing the state of adaptation and thereby making the two maxima separately visible.

Changes of Acuity during Light and Dark Adaptation in the Dragonfly Compound Eye

1990 ◽  
Vol 45 (1-2) ◽  
pp. 137-142 ◽  
Author(s):  
Eric J. Warrant ◽  
Robert B. Pinter
Keyword(s):  
Dark Adaptation ◽  
Time Course ◽  
Light Adaptation ◽  
Compound Eye ◽  
Sensitivity Function ◽  
The State ◽  
Intracellular Recordings ◽  
Acceptance Angle ◽  
Angular Sensitivity ◽  
Rapid Reduction

Abstract Intracellular recordings of angular sensitivity from the photoreceptors of Aeschnid dragonflies (Hemianax papuensis and Aeschna brevistyla) are used to determine the magnitude and time course of acuity changes following alterations of the state of light or dark adaptation. Acuity is defined on the basis of the acceptance angle, Δρ (the half-width of the angular-sensitivity function). The maximally light-adapted value of Δρ is half the dark-adapted value, indicating greater acuity during light adaptation. Following a change from light to dark adaptation, Δρ increases slowly, requiring at least 3 min to reach its dark-adapted value. In contrast, the reverse change (dark to light) induces a rapid reduction of Δρ , and at maximal adapting luminances, this reduction takes place in less than 10 sec.

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