scholarly journals The Behaviour of Minnows in Relation to Light Intensity

1956 ◽  
Vol 33 (2) ◽  
pp. 271-281
Author(s):  
F. R. HARDEN JONES

1. Minnows kept in a tank are active during the day and quiet at night. Their behaviour is reversed if they are given hollow bricks in which they take cover and so avoid bright light. When cover is available they are very active at sunrise and sunset. 2. Minnows have no inherent daily rhythm of locomotory activity. 3. Blind minnows respond to daily variations in light intensity, and are more active at night than during the day. 4. Minnows will not cross a light-dark boundary when the intensity on the light side is greater than 0.17-0.08 m.c 5. A minnow shoal disperses between intensities of 0.024 and 0.0034 m.c. 6. Minnows catch Dapknia better in bright light than in the dark. The change from visual to ‘dark’ feeding takes place between 0.0007 and 0.00007 m.c. 7. Minnows appear to avoid bright light by a comparison of intensities if the light-dark boundary is sharp, but they may also respond to light photokinetically. 8. It should be noted that these results, obtained in the laboratory, may not be true for minnows under natural conditions.

2018 ◽  
Vol 50 (2) ◽  
pp. 222-231 ◽  
Author(s):  
María Cristina Scaglione ◽  
Raúl Delmar Cerutti ◽  
Francesca Arfuso ◽  
Maria Rizzo ◽  
Michela Pugliese ◽  
...  

1961 ◽  
Vol 45 (1) ◽  
pp. 69-76 ◽  
Author(s):  
J. Woodland Hastings ◽  
Lazarus Astrachan ◽  
Beatrice M. Sweeney

The luminescent marine dinoflagellate, Gonyaulax polyedra, exhibits a diurnal rhythm in the rate of photosynthesis and photosynthetic capacity measured by incorporation of C14O2, at different times of day. With cultures grown on alternating light and dark periods of 12 hours each, the maximum rate is at the 8th hour of the light period. Cultures transferred from day-night conditions to continuous dim light continue to show the rhythm of photosynthetic capacity (activity measured in bright light) but not of photosynthesis (activity measured in existing dim light). Cultures transferred to continuous bright light, however, do not show any rhythm. Several other properties of the photosynthetic rhythm are similar to those of previously reported rhythms of luminescence and cell division. This similarity suggests that a single mechanism regulates the various rhythms.


2017 ◽  
Vol 32 (2) ◽  
pp. 130-142 ◽  
Author(s):  
Ruth I. Versteeg ◽  
Dirk J. Stenvers ◽  
Dana Visintainer ◽  
Andre Linnenbank ◽  
Michael W. Tanck ◽  
...  

Ambient light intensity is signaled directly to hypothalamic areas that regulate energy metabolism. Observational studies have shown associations between ambient light intensity and plasma glucose and lipid levels, but human data on the acute metabolic effects of light are scarce. Since light is the main signal indicating the onset of the diurnal phase of physical activity and food intake in humans, we hypothesized that bright light would affect glucose and lipid metabolism. Therefore, we determined the acute effects of bright light on plasma glucose and lipid concentrations in 2 randomized crossover trials: (1) in 8 healthy lean men and (2) in 8 obese men with type 2 diabetes. From 0730 h, subjects were exposed to either bright light (4000 lux) or dim light (10 lux) for 5 h. After 1 h of light exposure, subjects consumed a 600-kcal mixed meal. Primary endpoints were fasting and postprandial plasma glucose levels. In healthy men, bright light did not affect fasting or postprandial plasma glucose levels. However, bright light increased fasting and postprandial plasma triglycerides. In men with type 2 diabetes, bright light increased fasting and postprandial glucose levels. In men with type 2 diabetes, bright light did not affect fasting triglyceride levels but increased postprandial triglyceride levels. We show that ambient light intensity acutely affects human plasma glucose and triglyceride levels. Our findings warrant further research into the consequences of the metabolic effects of light for the diagnosis and prevention of hyperglycemia and dyslipidemia.


1983 ◽  
Vol 102 (1) ◽  
pp. 253-271 ◽  
Author(s):  
F. Claire Rind

1. In the moth, Manduca sexta, a pair of neurones, one on each side of the brain, were characterized morphologically and physiologically as descending interneurones, selective for horizontal motion over a large area of the moth's visual field. 2. Their cell bodies and dendritic processes are located in the protocerebrum of the brain. Their axons, 12–15 [μm diameter, project down the ipsilateral connective, branching profusely on the ipsilateral side of the suboesophageal, prothoracic and pterothoracic ganglia. 3. Each neurone responds to movement over either retina. Their preferred directions are from front to back across the ipsilateral eye and back to front over the contralateral one. Movement in the opposite direction supresses their usual ‘resting’ discharge. The neurones are particularly sensitive to movements within the frontal, ventral visual field. 4. Each neurone responds repeatedly, for up to 5 h, to a stimulus oscillating back and forth across the retinae. The response is not diminished during concurrent wing flapping. 5. An increase in the velocity of stimulus movement produces a proportional increase in firing frequency. For stripes of 2.5 cm wavelength and subtending 32° at the eye, the maximum response occurs at a velocity of 3cm/s which gives a contrast frequency of 1.2 Hz. 6. The latency of the neurone's response, measured from its axon as it enters the pterothoracic ganglion, depends on at least two factors: light intensity and the speed of stimulus movement. 7. The neurone gives a directional response to stripes of period 6–4° in bright light. The response falls to 16° in dim light. 8. At night, in dim light, the latency of response is much reduced and the threshold light intensity, necessary for a directional response, decreases by two orders of magnitude.


2008 ◽  
Vol 88 (8) ◽  
pp. 1607-1609 ◽  
Author(s):  
Shin Kubota

At the end of the breeding season in autumn, under natural conditions, mature medusae of Eugymnanthea japonica are released from its host Mytilus galloprovincialis at night-time. In laboratory experiments, mature medusae of the congeneric species E. inquilina are also released at night-time in autumn. At that time of the year, sunset is earlier and the water temperature is lower than in summer, when, under natural conditions, medusa release of E. japonica takes place at sunset instead. The release thus takes place at the same hours of the day in summer as well as in autumn. The circadial timing of medusa release of E. japonica is likely constant throughout the whole period in the breeding season and not correlated with the decrease of light intensity at sunset.


2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Stefania Romeo ◽  
Daniela Di Camillo ◽  
Alessandra Splendiani ◽  
Marta Capannolo ◽  
Cristina Rocchi ◽  
...  

Recent data indicates that prolonged bright light exposure of rats induces production of neuromelanin and reduction of tyrosine hydroxylase positive neurons in thesubstantia nigra. This effect was the result of direct light reaching thesubstantia nigraand not due to alteration of circadian rhythms. Here, we measured the spectrum of light reaching thesubstantia nigrain rats and analysed the pathway that light may take to reach this deep brain structure in humans. Wavelength range and light intensity, emitted from a fluorescent tube, were measured, using a stereotaxically implanted optical fibre in the rat mesencephalon. The hypothetical path of environmental light from the eye to thesubstantia nigrain humans was investigated by computed tomography and magnetic resonance imaging. Light with wavelengths greater than 600 nm reached the ratsubstantia nigra, with a peak at 709 nm. Eyes appear to be the gateway for light to the mesencephalon since covering the eyes with aluminum foil reduced light intensity by half. Using computed tomography and magnetic resonance imaging of a human head, we identified the eye and the superior orbital fissure as possible gateways for environmental light to reach the mesencephalon.


1956 ◽  
Vol 13 (3) ◽  
pp. 309-325 ◽  
Author(s):  
William S. Hoar

Pink salmon fry which have never schooled are negatively phototactic, prefer a cover of stones and do not emerge into bright light. Those which have schooled show a strong cover reaction when exposed to a rapid increase in light intensity but do not seek cover unless the change is abrupt. In general they remain in bright light after they have schooled. This change in behaviour occurs rapidly (15 minutes or less) when the fry school for the first time. Chum salmon fry establish a definite direction of swimming in the quiet water of a circular channel or basin. The established direction is stable and not permanently disturbed by light or darkness, by water currents, by strong avoiding reactions, by changing the location or by excluding direct skylight. The direction may be initially established in relation to water currents.


1932 ◽  
Vol 9 (2) ◽  
pp. 180-211
Author(s):  
GEORGE L. CLARKE

1. A quantitative study of the responses of Daphnia magna to light was made with the use of an experimental trough illuminated horizontally through one end by a uniform beam of light. The intensity of light was changed by shifting the position of a neutral glass "wedge" interposed in the beam of light. 2. The difference in the position of Daphnia when positively phototropic and when negatively phototropic is a difference in the postural angle at which the antennae are held, and not a difference in the direction of orientation of the whole organism--the animal's back being toward the light under all circumstances. 3. The primary sign of phototropism is not altered according to the absolute intensity of the light, but is affected by (1) the age of the individual, (2) the temperature of the water, and (3) the condition of the culture medium. Sometimes a "spontaneous" change in the primary sign of phototropism occurs. 4. The occasional movements observed to occur in the direction opposite to that of the primary sign of phototropism appear to be essentially periodic in respect to their times of inception and their duration. These periodic movements of Daphnia are not due to recurring periods of increased or of decreased activity, but probably represent periodic changes in the underlying photic mechanism. 5. "Variability" of the responses of Daphnia to successive identical tests gives evidence of being fundamentally periodic. A system of experimentation was devised to eliminate the error due to this variability, in so far as this was possible. 6. It was found that the rate and the magnitude of the change of illumination must rise above a certain threshold to be effective in causing a reversal of phototropic sign. A minimum length of exposure to bright light before the test is made is also necessary. 7. The relations of (1) length of the latent period, (2) speed of response, (3) magnitude of response, and (4) duration of response to (a) amount of reduction of light intensity, (b) duration of previous exposure to light, (c) duration of previous sojourn in dark, and (d) temperature of the water, were investigated, and the results have been summarised in Table XIII. 8. My observations are consistent with Ewald's conclusions that orientation of Daphnia is based on a mechanism which is entirely distinct from that responsible for the other three aspects of phototropism, namely (1) persistent phototropic swimming under any constant illumination, (2) periodic changes of phototropic sign under constant low illumination, and (3) reversal of phototropism produced by changes of light intensity. 9. It is shown that these other aspects of phototropism of Daphnia could be accounted for by one mechanism of excitation, if it were photoreversible and properly controlled. A theory is proposed that this mechanism is a reversible photochemical system such as that used by Hecht. The theoretical requirements of the mechanism would be fulfilled on the assumption (1) that equilibrium in the system would result in the maintenance of the persistent primary sign of phototropism, and (2) that the upsetting of this equilibrium would result in the production of the secondary signs. Upsetting of the equilibrium by some internal rhythmic process and by changes of illumination would account for periodic phototropic movements and for induced reversals of phototropic sign, respectively. 10. The results of the experiments on the photic responses have been reviewed in the terms of the proposed theory, and it is found that the evidence strongly supports the hypothesis that a reversible photochemical system is the basis for these aspects of the phototropism of Daphnia.


1998 ◽  
Vol 112 (2) ◽  
pp. 113-124 ◽  
Author(s):  
Johannes Oberwinkler ◽  
Doekele G. Stavenga

Light adaptation in insect photoreceptors is caused by an increase in the cytosolic Ca2+ concentration. To better understand this process, we measured the cytosolic Ca2+ concentration in vivo as a function of adapting light intensity in the white-eyed blowfly mutant chalky. We developed a technique to measure the cytosolic Ca2+ concentration under conditions as natural as possible. The calcium indicator dyes Oregon Green 1, 2, or 5N (Molecular Probes, Inc., Eugene, OR) were iontophoretically injected via an intracellular electrode into a photoreceptor cell in the intact eye; the same electrode was also used to measure the membrane potential. The blue-induced green fluorescence of these dyes could be monitored by making use of the optics of the facet lens and the rhabdomere waveguide. The use of the different Ca2+-sensitive dyes that possess different affinities for Ca2+ allowed the quantitative determination of the cytosolic Ca2+ concentration in the steady state. Determining the cytosolic Ca2+ concentration as a function of the adapting light intensity shows that the Ca2+ concentration is regulated in a graded fashion over the whole dynamic range where a photoreceptor cell can respond to light. When a photoreceptor is adapted to bright light, the cytosolic Ca2+ concentration reaches stable values higher than 10 μM. The data are consistent with the hypothesis that the logarithm of the increase in cytosolic Ca2+ concentration is linear with the logarithm of the light intensity. From the estimated values of the cytosolic Ca2+ concentration, we conclude that the Ca2+-buffering capacity is limited. The percentage of the Ca2+ influx that is buffered gradually decreases with increasing Ca2+ concentrations; at cytosolic Ca2+ concentration levels above 10 μM, buffering becomes minimal.


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