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1.
1.  At ambient temperatures (T a) between 39 and 43°C, specimens of the waterproof treefrogChiromantis xerampelina, resting quietly in wind tunnels, adjust rates of evaporative water loss (EWL), maintaining body temperature (T b) 2–4°C belowT a.
2.  Brain heating and cooling, respectively, increased and decreased steady-state rates of thermoregulatory evaporative water loss (EWL), driving negative feedback changes inT b.
3.  Continuous infusions of epinephrine resulted in specific, dose-dependent, saturable increases in EWL; isoproterenol was more potent than epinephrine, which was more potent than phenylephrine. Tyramine injection also stimulated EWL.
4.  Non-specific increases in EWL stimulated by injections of cholinergic agonists were weakly antagonized by atropine, but thermally induced EWL, as well as adrenergically and cholinergically stimulated increases in EWL, were abolished by beta-adrenergic antagonists.
5.  Sweating decreased andT b increased during ganglionic blockade.
6.  The observations suggest thatC. xerampelina controls thermoregulatory EWL by modulating the sympathetic nervous outflow stimulating beta-adrenergic receptors on cutaneous mucous glands.
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2.
1.  Under laboratory conditions complete development of H. sparsutum is shown within a temperature range of-0.7°C to +8°C. Constant temperatures above 10°C are lethal to the population. Larval growth (L1 to L5) is strictly temperature-dependent between-0.7 and +3.5°C, but slightly temperature compensated between +3.5 and +8°C.
2.  Rate of egg production is highest at an average daily temperature of-0.7°C.
3.  The sixth larval stage (L6) can be subdivided into a wandering and feeding period of about 40 days (at 7.3°C) and a following prepupal resting stage (PPR) with a high variability in duration, even at one and the same temperature, which ends with pupation.
4.  Entrance into this resting stage seems to be independent of environmental changes and can occur at every time of the year. Termination of the PPR depends upon light stimuli received during the entire larval period.
5.  Readiness for pupation exists when the photoperiod in the PPR exceeds that during hatching of first larva. A decreasing photoperiod during PPR triggers pupation in prepupae of various age.
6.  The diapause stage seems to be a primary factor synchronizing the life cycle with seasonal changes in the environment.
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3.
The effects of temperature, over the range 10–40 °C, on properties of locust (Schistocerca gregaria) ocellar L-neurones and of their interconnections have been investigated. At cooler temperatures, a small change in temperature has a larger effect than an equivalent change at warmer temperatures. An increase in temperature leads to the following:
1.  A decrease in input resistance, which typically halves in value as temperature increases from 15 °C to 35 °C. When synaptic transmission between photoreceptor cells and L-neurones is blocked with cobalt, temperature still affects L-neurone resistance. The membrane time constant also decreases, but the resting potential is unaffected.
2.  An increase in the sizes of rebound spikes, which are produced when hyperpolarizing pulses end. Above 35 °C, the maximum size of rebound spike is smaller than that at cooler temperatures.
3.  A decrease in the latency to response to light, and an increase in the speeds of the transient responses to changes in light.
4.  A decrease in the latency of transmission at both excitatory and inhibitory synapses between L-neurones.
5.  At excitatory synapses between L-neurones, an increase in the postsynaptic current. This is compensated by a decrease in postsynaptic membrane resistance, so that there is little effect on the size of the postsynaptic potential.
6.  At inhibitory synapses between L-neurones, a decrease in the time for the postsynaptic potential to reach its peak. The time for recovery of transmission at inhibitory synapses is unaffected by temperature.
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4.
1.  Brain (hypothalamic) and cloacal temperatures were measured in heat-stressed Lesser Nighthawks (Chordeiles acutipennis), Mallards (Anas platyrhynchos), Pigeons (Columba livia), and White-Necked Ravens (Corvus cryptoleucus) and in one Roadrunner (Geococcyx californianus). Range of mean body masses was 0.047 to 1.156 kg.
2.  In all these species brain temperatures were always below cloacal temperatures (Fig. 1). The body-to-brain temperature difference was maintained nearly constant within a species over a wide range of cloacal and air temperatures, and varied in magnitude from 0.80°C in the Roadrunner to 1.29°C in Mallards.
3.  The presence of arete mirabile ophthalmicum was demonstrated in all five species. This rete may be associated with the observed pattern of brain temperature control.
4.  The body-to-brain temperature difference may be important in avoiding brain damage during core hyperthermia.
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5.
1.  At 28°C conversion efficiency of total nitrogen (TN) was inversely related to size.
2.  In the pre-adult stage protein nitrogen (PN) conversion efficiency was high whereas in the Post-adult stage non-protein nitrogen (NPN) conversion efficiency was high.
3.  Lower temperature (20°C) was not congenial for PN conversion.
4.  Higher temperature favoured PN conversion for smaller fish but NPN for larger fish.
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6.
1.  The ommatidia of the butterfly Papilio have a fused and tiered rhabdom. The distal tier of the rhabdom is made up of four distal photoreceptors (R1–4), whereas the proximal tier is made up of four proximal (R5–8) and one basal photoreceptor cell (R9).
2.  We first confirmed by light microscopy that the ommatidia of Papilio are not twisted, i.e. have the same spatial organization all about the longitudinal axis. The polarization method, previously applied to the distal tier, hence is applicable to identify the photoreceptor location from the peak angle of the polarization sensitivity.
3.  We determined the polarization and spectral sensitivity of in total 109 proximal and basal photoreceptors in the lateral looking eye region. All of the photoreceptors were either green or red type, most of which fall into three classes as judged by the peak angles of the polarization sensitivity: around 40°, 150°, and 180° (= 0°) with respect to the dorso-ventral axis. The first two classes are formed by the proximal photoreceptors with straight microvilli oriented at the average angle of 39° (R6, 8) and 144° (R5, 7) respectively, and the third is formed by the basal photoreceptors R9 with straight microvilli oriented at 180° (= 0°). The mean polarization sensitivity (PS = maximal sensitivity/minimal sensitivity) was about 2.
4.  75% of the proximal and 48% of the basal photoreceptors were of the red type.
5.  A single ommatidium of Papilio appears to contain two to four types of spectral receptors.
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7.
1.  Optical and electrophysiological measurements on the eyes of living moths,Ephestia kuehniella, show that aggregation of secondary pigment cell granules occurs only in the temperature range 5 to 37°C. At temperatures outside this range the granules are always dispersed, even when the moths are in the dark. The state of aggregation is maximal at about 20°C, as measured by reflectance. The temperature-dependent decrease in reflectance induced by test illuminations (identical in wavelength, intensity and flash duration), as an indication of the translocation of the granules towards the dispersed state, is strongest at about 25°C.
2.  Electroretinograms (ERGs) were recorded in the range from –5 to 42°C. The temperature dependence of ERGs gives an asymmetrical curve with a maximum between 10 and 15°C. The difference in the position of this maximum compared to those of reflectance values is discussed, together with results from a white-eyed mutant.
3.  Oxygen consumption of moth heads is independent of light or dark adaptation in both wildtype and mutant moths. TheQ 10 values of oxygen consumption are between 2 and 3. Inhibition of the aggregation of screening pigment granules by colchicine does not change O2 consumption. When mixtures of oxygen and nitrogen (O2/N2) are applied to mealmoths, aggregation of granules does not occur with less than 3% O2. At O2 levels between 10% and 100%, granule migration is constant. At O2 levels between 3 and 10%, change in reflectance after a given light stimulus increases with decreasing O2 concentration.
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8.
1.  Physiological adaptation to hypothermia were studied in newly hatched great snipe chicks (Gallinago media) by measuring oxygen uptake (VO2), heart rate (HR), respiratory frequency (RF), and body temperature (Tb) at different ambient temperatures (Ta).
2.  Tb of 1-day-old chicks at Ta of 35°C stabilized at about 40°C. At Ta between 20 and 30°C the chicks maintained a Tb about 8°C above Ta. Hatchlings maintained a higher gradient when active than when resting. Below 20°C they were unable to maintain a stable Tb.
3.  In resting hatchlings VO2 was similar at Ta between 35 and 20°C (Tb 40–30°C), VO2 range 1.7–2.5 ml·g-1·h-1. Below 20°C, VO2 declined with time.
4.  The HR of 1-day-old chicks fell linearly with Tb during cooling. The Q10 of the HR was 1.7 at Tb 38°C and increased to 3.0 at 29°C. The RF showed a slight tendency to decrease with decreasing Tb.
5.  It is concluded that the ability to maintain normal dexterity at low Tb is an important aspect of snipe survival strategy. Maintaining a temperature gradient rather than a constant high Tb presumably saves energy. It is suggested that the mechanisms whereby VO2 is maintained at a low Tb may involve isoenzymes and adaptations of the nervous system. However, such adaptations would not seem to affect the pacemaker mechanism as evidenced by the high Q10 of the HR.
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9.
1.  The overall rate of feeding at 28°C bears an inverse relationship to size; the time course of feeding appears to be size-independent and shows a decline with increase in time.
2.  Absorption efficiency is independent of size.
3.  The rates of absorption and conversion and conversion efficiency are inversely related to size.
4.  The rate of feeding is reflected on the rates of absorption and conversion.
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10.
1.  Intracellular recordings of suboesophageal neurons were performed in the cricketGryllus bimaculatus during applied changes of head temperature in the range 8 to 32.5 °C. The temperature was controlled by perfusing the head with Ringer solution of appropriate temperature. Subsequent staining with Lucifer Yellow revealed descending, ascending or T-shaped cells with ventrally located somata (Fig. 1).
2.  In 6 out of 7 neurons recorded (Fig. 1, neurons A, B, C, D, E, G) the firing rate was correlated with abdominal ventilatory pumping (Fig. 2a, b). These neurons also received input from cereal sensory hairs (Fig. 2c). Furthermore, one of them (Fig. 1, neuron A) showed responses to auditory (Fig. 2d) and another (Fig. 1, neuron E) to visual input (Fig. 2e).
3.  Activity of every tested neuron was correlated with the temperature of the perfusing Ringer solution: the amplitude and duration of spikes and excitatory postsynaptic potentials increased with cooling (Fig. 3). Two types of temperature-dependent changes in firing rate were identified. In type I the spiking rate was higher at higher temperature (Figs. 4a, b; 5). In type II spiking rate was related to the direction of temperature change (Fig. 4c, d).
4.  The possible involvement of one of the recorded cells (Fig. 1, neuron F) in thermoreception processes is discussed. Activity of this neuron was not related to the rhythm of abdominal ventilatory pumping, nor did the cell receive cereal, visual or auditory input. Its activity was related mainly to the direction of temperature changes i.e. with an increase in firing rate during cooling, independent of the temperature at which the cooling started and with a transient decrease in firing rate during warming from starting point of 10 °C.
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11.
1.  Filiform hairs of various lengths on the cerci of adult crickets vibrate in a sound field. These movements were measured with a photodetector for sound frequencies from 10 Hz to 200 Hz in the species Acheta domestica, Gryllus bimaculatus and Phaeophilacris spectrum.
2.  With low air-particle velocities, the hair shafts were deflected sinusoidally from their resting position, without bending or secondary oscillations (Figs. 2 A, 3 A). At higher velocities (from ca. 80 mm/s peak velocity, depending on the properties of the individual hairs), the shaft struck the cuticular rim of the socket in which the base of the hair is seated (Fig. 2B). This contact was made at an average angular displacement from the resting position of 5.16°±1.0°.
3.  The best frequencies of the hairs were found to be between 40 Hz and 100 Hz (Fig. 5A). The slope of the amplitude curve for constant peak air-particle velocity at frequencies below the best frequencies was between 0 and 6 dB/octave. Long hairs had smaller slope values than short hairs (Fig. 5C).
4.  At its best frequency the ratio of maximal tip displacement of a hair to the displacement of the air particles in the sound field was between 0.2 and 2. Only a small number of hairs (2 out of 36) showed tip displacements exceeding twice the air-particle displacement. The values of maximal angular displacement were not correlated to hair length (Fig. 5 B).
5.  The angular displacement of the hairs was phase shifted with respect to the air-particle velocity by 0° to +45° (phase lead) at sound frequencies around 10 Hz and by -45° to -120° (phase lag) at 200 Hz (Figs. 3C, 4B). At a particular frequency long hairs tended to have larger phase lags than shorter hairs (Fig. 5D).
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12.
1.  Chronic ingestion of caffeine by male NIH strain mice alters the density of a variety of central receptors.
2.  The density of cortical A1 adenosine receptors is increased by 20%, while the density of striatal A2A adenosine receptors is unaltered.
3.  The densities of cortical 1 and cerebellar 2 adrenergic receptors are reduced byca. 25%, while the densities of cortical 1 and 2 adrenergic receptors are not significantly altered. Densities of striatal D1 and D2 dopaminergic receptors are unaltered. The densities of cortical 5 HT1 and 5 HT2 serotonergic receptors are increased by 26–30%. Densities of cortical muscarinic and nicotinic receptors are increased by 40–50%. The density of cortical benzodiazepine-binding sites associated with GABAA receptors is increased by 65%, and the affinity appears slightly decreased. The density of cortical MK-801 sites associated with NMDA-glutaminergic receptors appear unaltered.
4.  The density of cortical nitrendipine-binding sites associated with calcium channels is increased by 18%.
5.  The results indicate that chronic ingestion of caffeine equivalent to about 100 mg/kg/day in mice causes a wide range of biochemical alterations in the central nervous system.
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13.
1.  The larva of the tiger beetle (Cicindela chinensis) possesses six stemmata on either side of the head. Optical and physiological properties of two pairs of large stemmata and a pair of anterior medium sized stemmata, and responses of second-order visual interneurons (medulla neurons) have been examined.
2.  Objects at infinite distance were estimated to focus 50 m deep in the retina in the large stemmata. Receptive fields of four large stemmata, the acceptance angle of each being 90°, largely overlapped one another.
3.  The stemmata possessed a single type of retinular cell with a maximal spectral sensitivity at 525 nm, and a flicker fusion frequency of 25–50 Hz.
4.  Medulla neurons expanded fan-shaped dendrites in the medulla neuropil, and their axons extended into the protocerebrum. They responded to illumination with a variety of discharge patterns. They also responded with spike discharges to moving objects and to apparent movements provided by sequential illumination or extinction of LEDs. They did not show directional selectivity. They possessed well-defined receptive fields ranging from 30° to 105°.
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14.
1.  The actions of GABA on three classes of visual interneurons in crayfish, Procambarus clarkii, medulla externa are examined. The effect of GABA on the visual response is compared to GABA's action on agonist-elicited responses purported to mediate the visual response.
2.  GABA produces a shunting type of inhibition in medullary amacrine cells which is associated with a small depolarization (Figs. 2, 3), a large increase in input conductance (Gn) and a reversal potential close to rest (Fig. 4). GABA is a potent antagonist to the depolarizing action of acetylcholine (ACh) (Fig. 5).
3.  GABA depolarizes dimming fibers (Fig. 2), and the response is mediated by an increase in Gn (Fig. 6). GABA antagonizes the light-elicited IPSP and the hyperpolarizing action of ACh (Fig. 7).
4.  Sustaining fibers (SF) do not appear to have GABA receptors but GABA inhibits the excitatory visual input pathway to the SFs (Fig. 8). Conversely, the GABA antagonist, bicuculline, potentiates the SF light response (Fig. 9).
5.  GABA has at least three different modes of antagonist action in the medulla: i) Increased conductance and depolarization in dimming fibers and medullary amacrine neurons; ii) Decreased chloride conductance in tangential cells; and iii) An inhibitory action on the visual pathway which drives SFs.
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15.
1.  We used laser vibrometry and free field sound stimulation to study the frequency responses of the eardrum and the lateral body wall of awake male Eleutherodactylus coqui.
2.  The eardrum snowed one of two distinct frequency responses depending on whether the glottis was open (GO response) or closed (GC response) during the measurement.
3.  The lateral body wall vibrated with a maximum amplitude close to that of the eardrum and in the same frequency range.
4.  Covering the frog's body wall with vaseline reduced the vibration amplitude of the GC response by up to 15 dB.
5.  When a closed sound delivery system was used to stimulate a local area of the body wall the eardrum also showed one of two types of responses.
6.  These results suggest that sound is transmitted via the lung cavity to the internal surface of the eardrum. This lung input has a significant influence on the vibrations of the eardrum even when the glottis is closed.
7.  The vibration amplitude of the eardrum changed with the angle of sound incidence. The directionality was most pronounced in a narrow frequency range between the two main frequencies of the conspecific advertisement call.
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16.
1.  The activity of tympanal high- and low-frequency receptors in the migratory locustLocusta migratoria was recorded with glass capillary microelectrodes, and Lucifer Yellow was then injected through the microelectrode to reveal the cells' metathoracic projections.
2.  A photodetector device was used to monitor the abdominal respiratory movements, which caused clearly visible deflections of the tympanal membrane.
3.  The auditory receptors respond not only to sound stimuli but also to the respiratory movements; these phasic (Figs. 1–3) or tonic (Fig. 4) responses are especially pronounced during the inspiration and expiration movements, and less so during the constriction phases.
4.  The magnitude of the response to sound depends on the phase of the stimulus with respect to the respiratory movements. At certain phases sound elicits no response at all (Fig. 5).
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17.
1.  We have obtained a cDNA clone encoding a human retinal D2 dopamine receptor.
2.  The longest open reading frame (1242 bp) of this clone encodes a protein of 414 amino acids having a predicted molecular weight of 47,000 and a transmembrane topology similar to that of other G protein-coupled receptors.
3.  Transient transfection of COS-7 cells with an expression vector containing the clone resulted in expression of a protein possessing a pharmacological profile similar to that of the D2 dopamine receptor found in striatum and retina.
4.  Northern blot analysis indicated that, in rat brain and retina, the mRNA for this receptor was 2.9 kb in size.
5.  In situ hybridization was performed to examine the distribution of the mRNA for this receptor in human retina. Specific hybridization was detected in both the inner and the outer nuclear layers.
6.  These findings are consistent with prior physiological and autoradiographic studies describing the localization of D2 dopamine receptors in vertebrate retinas. Our observations suggest that photoreceptors as well as cells in the inner nuclear layer of human retinas may express the mRNA for this D2 dopamine receptor.
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18.
Müller  D. G.  Frenzer  K. 《Hydrobiologia》1993,(1):37-44
Culture studies with healthy and virus-infected isolates of Ectocarpus siliculosus, Feldmannia simplex and F. irregularis gave the following results:
–  Virus particles are produced in deformed reproductive organs (sporangia or gametangia) of the hosts and are released into the surrounding seawater.
–  Their infective potential is lost after several days of storage under laboratory conditions.
–  New infections occur when gametes or spores of the host get in contact with virus particles. The virus genome enters all cells of the developing new plant via mitosis.
–  Virus expression is variable, and in many cases the viability of the host is not impaired. Infected host plants may be partly fertile and pass the infection to their daughter plants.
–  Meiosis of the host can eliminate the virus genome and generate healthy progeny.
–  The genome of the Ectocarpus virus consists of dsDNA. Meiotic segregation patterns suggest an intimate association between virus genome and host chromosomes.
–  An extra-generic host range has been demonstrated for the Ectocarpus virus.
–  Field observations suggest that virus infections in ectocarpalean algae occur on all coasts of the world, and many or all Ectocarpus and Feldmannia populations are subject to contact with virus genomes.
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19.
1.  By penetrating axons in the ventral nerve cord of the dragonfly, Aeshna umbrosa, we measured the intracellular responses of target-selective visual interneurons to movement of black square targets ranging from 1° to 32° visual angle at several levels of mean background luminance.
2.  Neuronal responses, measured both in number of spikes and in the magnitude of integrated postsynaptic potentials, showed a preference for larger target size at lower mean luminance (Table 1, Figs. 1–3). The latency of postsynaptic potential (psp) and spike responses from onset of target movement increased with a decrease in mean luminance (Fig. 1).
3.  A measure of mean target size preference (Eqn. 1) for one identified interneuron (MDT4) in both laboratory and outdoor lighting shows a continuous decrease of preferred size with increases of mean luminance over more than 4 orders of magnitude.
4.  The time to reach the new steady state of cell response after the decrease of mean luminance was ordinarily less than 30 s, but sometimes longer (Fig. 4).
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20.
1.  The daily (circadian) rhythm of activity and rest of common redpolls (Acanthis f. flammea L.) from 65°N lat. was measured for about one year in individuals outdoors at two latitudes (48° and 65°N). During winter at both latitudes, activity-time () of common redpolls approximated the duration of daylight (including civil twilights); onset of activity, however, occurred at lower light intensities than end of activity. During mid-summer, a rest-time (p) of ca. 5 h was maintained at both latitudes. During the times of spring and fall migration (extending into summer or winter, respectively), common redpolls showed nightly unrest or shifted their onset of daily activity into the pre-dawn hours.
2.  Redpolls of two subspecies (A. f. flammea and A. f. cabaret Müller) resident at different latitudes (ca. 65° and 49°N) were maintained and measured under the same light conditions at 48°N lat. The two populations showed significant differences in their responses to the same annual changes in day length which included: (i) differences in the timing of the circadian activity rhythm with respect to the daily solar cycle; (ii) differences in the amount and range of seasonal changes in nightly unrest; (iii) differences in the mean level and range of seasonal changes of body weight; and (iv) differences in the timing of postnuptial molt.
3.  In all experimental groups of redpolls, the highest precision (i.e. lowest mean day-to-day variation) in onset and end of activity was observed when both phases occurred during the twilights. The different effects of annually changing light conditions on onset and end of activity with respect to solar time indicated that timing of these two phases of the activity rhythm is independently controlled. It is further indicated that an annually changing sensitivity to light controls the termination of activity in common redpolls, although ambient temperature can modify this response.
4.  Besides the direct influence of latitude on timing and the amount of changes of various circadian and annual functions throughout the year, the important role of long-term (genetic?) adaptation to the light and temperature conditions prevailing in the respective habitats of redpoll populations is emphasized by the results of this study.
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