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1.
1.  Bees were trained to enter the central hole in a disc containing 89 holes and collect sugar-water from a box placed behind it (Fig. 1). Visual marks were offered on the inner surface of a cylinder placed in front of the disc (Fig. 2), thus projecting onto peripheral (nonfrontal) regions of the bees' eye. The trained bees were tested by recording their choices among the holes.
2.  Bees use the memorized position of peripheral marks to localize the frontally positioned goal (Figs. 6–9). The effectiveness of a mark depends on its retinal position, the most effective marks being lateral ones (Figs. 8, 9).
3.  Altering the dimensions of the mark does not influence the distribution of the bees' choice (Figs. 11–13). Thus, image motion rather than image size is used for distance estimation in the present task.
4.  Cinematographic recordings (Fig. 14) revealed that the searching bees' whereabouts are correlated with the choice distribution (Fig. 6a). The hypothesis that the bees stabilize the mark in the trained retinal position by correcting for retinal image slip is proposed.
5.  Experiments using coloured patterns revealed that the bees' performance is mediated by the green-sensitive channel (Figs. 17–22), as predicted by the above hypothesis.
Dedicated to Prof. Dr. Rüdiger Wehner on the occasion of his 50th birthday, in great appreciation for both his scientific work and his personality.  相似文献   

2.
1.  The behaviour of isolated individual forager honeybees during the night has been investigated with a variety of experimental methods. Prolonged rest in these diurnal insects is accompanied by: reduced muscle tone (Figs. 1, 6, 10–12), decreased motility (Figs. 2, 3, Table 1), lowered body temperature (Figs. 7, 8) and raised reaction threshold (Fig. 9). These phenomena strongly resemble four characteristic features of sleep in humans, mammals and birds. It is thus very likely that the profound rest which forager bees experience at night is sleep. This assumption is further supported by the results of previous investigations of visual interneurones in the bee.
2.  The antennae of sleeping bees manifest characteristic postural constellations (Fig. 6). High reaction thresholds are associated with particular antennal positions.
3.  The total sleep time (duration of antennal immobility plus duration of small antennal movements) in 24 h for two bees was 7.6 h and 4.9 h (Table 1).
4.  Bees which rest in a hive at night also display phenomena which have been encountered during the laboratory investigations.
5.  Sleep in mammals is an active, controlled process; the same seems to be true of sleep in honeybees (Figs. 3, 4). Unlike mammals, bees experience their deepest sleep towards the end of the sleep phase (Figs. 3, 9, 10, 12).
Dedicated to Prof. Dr. D. Burkhardt on the occasion of his 60th birthday  相似文献   

3.
1.  The excitatory and inhibitory influences on the gill ofAplysia Juliana, which are mediated by the branchial nerve, were studied by means of electrophysiological techniques. Excitatory and inhibitory pathways in the nerve were stimulated simultaneously or selectively.
2.  The branchial nerve was found to contain both excitatory and inhibitory pathways which did not contain synapses in the branchial ganglion. The excitatory pathways caused longitudinal shortening of the gill along the efferent branchial vessel and the inhibitory pathways were modulatory, depressing the longitudinal shortening.
3.  Branchial nerve stimulation elicited two types of excitatory junctional potential (EJP), which were not mediated by the branchial ganglion, in a muscle cell of the efferent branchial vessel. One type was attributed to the central motor neuron and the other type to a motor neuron which is probably situated in the neural plexus of the gill periphery.
4.  Four inhibitory pathways from the central nervous system to the gill were found.
5.  Inhibitory junctional potentials (IJPs) recorded from muscle cells of the efferent branchial vessel in response to branchial nerve stimulation did not have monosynaptic characteristics. It is thought that inhibitory motor neurons which were activated by the branchial nerve might exist at the neural plexus of the gill.
6.  A single EJP which has been induced by a stimulus pulse applied to the excitatory pathway of the branchial nerve may be depressed in an all-or-none manner by a stimulus pulse applied to the inhibitory pathway, if this is done within a distinct short period prior to or after the stimulus inducing the EJP. This indicates that the central motor neuron receives presynaptic inhibition at its periphery.
7.  The motor neurons of the neural plexus seem to receive inhibitory innervation. Suppression of endogenous EJPs in the efferent vessel persisted for a long period even after cessation of stimulation.
8.  A certain branchioganglionic neuron (BGN) was found to receive inhibitory postsynaptic potential (IPSP) inputs from the branchial nerve.
9.  The multimodality of both the excitatory and the inhibitory pathways in the branchial nerve may explain the compound neural modulations of gill movements.
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4.
Artificial magnetic fields (MF) influence physiological processes in bees.
1.  An inhomogeneous, static magnetic field (IMF) reduces the flying activity of bees and increases their life span by more than 60%.
2.  The content of the ageing pigment lipofuscin in brain and, to a lesser extent, in thorax muscles increases with the physiological age. The content of lipofuscin of the thorax muscle is only 1/5 that of the brain.
3.  Despite their increased chronological age (60–74%) brain lipofuscin of bees under conditions of an inhomogeneous, static magnetic field is slightly reduced compared with bees in natural earth's magnetic field (EMF) conditions. No effects could be registered in the muscle lipofuscin of the thorax.
4.  There was no correlation between the content of lipofuscin and the chronological age.
5.  Flying activity is also reduced by horizontal magnetic fields (0.40–1.45 Oe).
6.  Dance tempo is reduced in compensated EMF and amplified static magnetic fields (0.84 Oe). Dance tempo is drastically reduced if compensation of the EMF is followed by application of a 5 Hz magnetic field with 1.04 Oepp, directed E-W.
Dedicated to Prof. Dr. Drs. h.c. M. Lindauer on the occasion of his 70th birthday  相似文献   

5.
The caudal photoreceptors (CPRs) of crayfish (Procambarus clarkii) can trigger walking and abdominal movements by their response to light.
1.  In a restrained, inverted crayfish, illumination of A6 evoked a CPR discharge followed by leg movements and bursting from the abdominal tonic flexor (TF) motoneurons. Intracellular electrical stimulation of a single CPR at high frequency (80 Hz) evoked similar responses.
2.  Responses only occurred when a single CPR axon was driven at 60 Hz or more and outlasted the stimulus.
3.  CPR stimulation also excites the pattern-initiating network (Moore and Larimer 1987) in the abdomen.
4.  The axon of the CPR projects from ganglion A6 to the brain. Terminal branches occur in the subesophageal ganglion and the brain. A small descending interneuron is dye-coupled to CPR in the subesophageal ganglion.
5.  In animals with cut circumesophageal connectives, the CPRs can evoke walking and the abdominal motor pattern.
6.  The relationship of the abdominal motor pattern to walking is altered by restraint and/or inversion. In freely moving crayfish, the cyclic abdominal motor pattern is only observed with backward walking. In restrained, inverted crayfish, the motor pattern occurs with both forward or backward walking.
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6.
1.  Honey bees (Apis mellifera, worker) were trained to discriminate between two random gratings oriented perpendicularly to each other. This task was quickly learned with vertical, horizontal, and oblique gratings. After being trained on perpendicularly-oriented random gratings, bees could discriminate between other perpendicularly-oriented patterns (black bars, white bars, thin lines, edges, spatial sinusoids, broken bars) as well.
2.  Several tests indicate that the stimuli were not discriminated on the basis of a literal image (eidetic template), but, rather, on the basis of orientation as a single parameter. An attempt to train bees to discriminate between two different random gratings oriented in the same direction was not successful, also indicating that the bees were not able to form a template of random gratings.
3.  Preliminary experiments with oriented Kanizsa rectangles (analogue of Kanizsa triangle) suggest that edge detection in the bee may involve mechanisms similar to those that lead to the percept of illusory contours in humans.
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7.
1.  Seasonal changes in the half-times (0.5) for calcium influx and outflux in bone, skin and scales, and soft-tissue compartments ofF. kansae were measured.
2.  The size of diffusible calcium pools in the three compartments was estimated from the ratio of the loading and unloading half-times. Both the bone and skin and scales compartments contain diffusible calcium pools which increase in size during the summer months.
3.  The calcium in the soft-tissue compartment is all diffusible, and the kinetics indicate that this compartment receives calcium from the other two compartments.
4.  Hypophysectomy reduced the rate of calcium turnover in summer animals to the levels measured in intact winter animals. Such treatment also affected the distribution of radiocalcium within the animal.
5.  It is concluded that acellular bone is a metabolically active tissue.
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8.
Stinging behavior has been extensively studied in honey bees at the level of the individual, that is, in terms of stimuli that release stinging in adult bees, and in terms of integration of individual behavior into colony defense. Yet very little is known about the physiological basis for this behavior. Using an isolated abdominal preparation factors that influence peripheral control of the sting extension response are analyzed. Results show that:
1.  Electromyogram activity released by severing the ventral nerve cord changed during the first few days of adult life but not later. Abdomens from older bees (nurses, guards, foragers) showed significantly higher EMG activity than newly emerged or 24 h-old bees.
2.  The reflex matured over 5–7 days after emergence as an adult.
3.  Younger bees (24h) had a lower threshold for initiating sting extension than older bees. However, the threshold for initiating the full sting response, i.e., extension and venom pumping, did not differ due to age.
4.  Caste status was not correlated to any of the parameters of sting extension, indicating that any effect of caste on stinging behavior must arise in more anterior ganglia and/or in the brain.
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9.
1.  Certain species of tiger moths emit clicks when stimulated by bat-like sounds. These clicks are generated by modified thoracic episterna (tymbals) (Fig. 1) and constitute a rhythmic behaviour activated by simple sensory input.
2.  Tymbal periods are indirectly related to stimulus intensity and periods (Fig. 3). Moths initiate sounds with the tymbal opposite to the stimulated ear and once a sequence commences it continues in an undisrupted fashion.
3.  The tymbal is innervated by a pleural branch (IIIN2a) of the metathoracic leg nerve, a similar anatomy to that in the unmodified episterna of silent moths (Fig. 5). Backfills of the IIIN2a in Cycnia tenera reveal sensory fibres and a cluster of 5–9 motor neurons with densely overlying dendritic fields (Fig. 6).
4.  Extracellular recordings of the IIIN2a reveal a large impulse preceding each tymbal sound (Fig. 7). I suggest that this impulse results from the synchronous firing of 2–3 motor neurons and is the motor output of the tymbal central pattern generator (CPG). The spikes alternate (Figs. 9, 10) and are bilaterally co-related (Fig. 11) but with an phase asymmetry of 2–3 ms (Fig. 12).
5.  Normal motor output continues in the absence of tymbal sounds (Fig. 13) and when all nerve-tymbal connections are severed (Fig. 14, Table 1) therefore this CPG operates independent of sensory feedback. A model is proposed for the tymbal circuitry based upon the present data and the auditory organization of related noctuid moths (Fig. 15). I propose that the tymbal response in modern arctiids evolved from either flight or walking CPGs and that preadaptive circuitry ancestral to tymbal movements still exists in modern silent Lepidoptera.
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10.
In the rift valley (North-East of France/South-West of Germany), the Rhine runs freely for 300 km from South to North. The absence of natural obstacles allows the development of a very regular profile of the river. We have therefore an opportunity to study very gradual modifications of the alluvial forest communities of the fluvial corridor from upstream to downstream, according to the gradual evolution of the ecological factors, related to slope decrease and hydrological modifications.We describe, from Basel to Mainz:
1)  modification of dynamic processes in the forest communities such as successional sequences or sylvigenetic mosaïcs of the terminal stages.
2)  modification of species richness.
3)  reduction of species diversity.
4)  simplification of the forest stratification.
5)  modification of efficiency of the biogeochemical cycling.
6)  ecological vicariances.
7)  modification in species behaviour.
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11.
1.  Non-visual sensory systems are likely to be important in antarctic fish since these fish inhabit an area where low light levels occur for long periods. This study was undertaken to examine the suitability of the lateral line system for prey detection.
2.  Recordings were made from afferent fibres of the anterior lateral line in the antarctic fishPagothenia borchgrevinki.
3.  A vibrating probe was used to stimulate the lateral line at a range of frequencies between 10 and 100 Hz.
4.  Most units responded best at a stimulus frequency of 40 Hz. Below the best frequency the response typically declined steeply and at higher frequencies it was usually better sustained.
5.  Crustacea identified as major components of the diet ofPagothenia borchgrevinki were individually attached to a force transducer to determine the vibrations produced by swimming movements.
6.  The Fourier amplitude spectra of swimming crustaceans exhibited prominent low frequency peaks at 3–6 Hz and higher frequency peaks in the 30–40 Hz range.
7.  It is concluded that the overlap in the frequency response characteristics of the anterior lateral line and the frequencies produced by crustacean prey clearly establishes the suitability of the lateral line for prey detection.
8.  In several instances recordings were made from fish primary afferent neurons responding to a swimming amphipod. These recordings confirm that crustacean swimming is indeed a potent natural stimulus of the lateral line system.
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12.
In a task designed to simulate olfactory-guided foraging, the ability of squirrel monkeys to discriminate an artificial 12-component odorant from 3-, 6-, 9- or 11- component submixtures was investigated. A combination of factors was found to contribute to the animals' performance:
1.  Discriminability generally decreased as the number of components in the submixture increased.
2  Submixtures did not contribute equally to mixture perception, and one component in particular (cineole) disproportionately influenced stimulus discriminability.
3.  Interactive effects between submixtures resulted in marked deviations from the general pattern of discriminability.
4.  Changes in the relative concentration of submixtures could also influence discriminability.
5.  Finally, individual differences in responsiveness to particular stimuli were apparent.
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13.
1.  Two campaniform sensilla (CS) on the proximal tibia of a hindleg monitor strains set up when a locust prepares to kick, or when a resistance is met during locomotion. The connections made by these afferents with interneurones and leg motor neurones have been investigated and correlated with their role in locomotion.
2.  When flexor and extensor tibiae muscles cocontract before a kick afferents from both campaniform sensilla spike at frequencies up to 650 Hz. They do not spike when the tibia is extended actively or passively unless it encounters a resistance. The fast extensor tibiae motor neurone (FETi) then produces a sequence of spikes in a thrusting response with feedback from the CS afferents maintaining the excitation. Destroying the two campaniform sensilla abolishes the re-excitation of FETi.
3.  Mechanical stimulation of a single sensillum excites extensor and flexor tibiae motor neurones. The single afferent from either CS evokes EPSPs in the fast extensor motor neurone and in certain fast flexor tibiae motor neurones which follow each sensory spike with a central latency of 1.6 ms that suggests direct connections. The input from one receptor is powerful enough to evoke spikes in FETi. The slow extensor motor neurone does not receive a direct input, although it is excited and slow flexor tibiae motor neurones are unaffected.
4.  Some nonspiking interneurones receive direct connections from both afferents in parallel with the motor neurones. One of these interneurones excites the slow and fast extensor tibiae motor neurones probably by disinhibition. Hyperpolarization of this interneurone abolishes the excitatory effect of the CS on the slow extensor motor neurone and reduces the excitation of the fast. The disinhibitory pathway may involve a second nonspiking interneurone with direct inhibitory connections to both extensor motor neurones. Other nonspiking interneurones distribute the effects of the CS afferents to motor neurones of other joints.
5.  The branches of the afferents from the campaniform sensilla and those of the motor neurones and interneurones in which they evoke EPSPs project to the same regions of neuropil in the metathoracic ganglion.
6.  The pathways described will ensure that more force is generated by the extensor muscle when the tibia is extended against a resistance. The excitatory feedback to the extensor and flexor motor neurones will also contribute to their co-contraction when generating the force necessary for a kick.
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14.
Looking at the on-going discussions, integrated product policy seems to become important for the LCA community and should therefore be reflected in the International Journal of LCA. Reasons include that IPP:
–  clearly follows life cycle thinking,
–  encourages the usage of the life cycle tool box, e.g. for product-innovation,
–  could become a political umbrella for a new co-operation along the life cycle - beyond the old roles of life cycle stakeholders acting on their own,
–  faces similar issues as the LCA community looking e.g. at environmental value / objective setting.
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15.
1.  The self-adapting effects of chemical backgrounds on the response of primary chemoreceptor cells to superimposed stimuli were studied using lobster (Homarus americanus) NH4 receptor cells.
2.  These receptors responded for several seconds to the onset of the backgrounds, and then returned to their initial level of spontaneous activity (usually zero). The strongest response always occurred only during the steepest concentration change; the response then decayed back to zero or to the earlier spontaneous firing level, while the background concentration was still rising, and remained silent during the entire time that the background was maintained constant (20–30 min) (Fig. 2).
3.  Exposure to constant self-adapting backgrounds eliminated the responses of NH4 receptor cells to stimuli of concentration lower than the background, and reduced the responses to all higher stimulus concentrations tested by a nearly equal amount. This resulted in a parallel shift of the stimulus-response function to the right along the abscissa (Figs. 3 and 4).
4.  Since the response threshold was completely re-set by adaptation to backgrounds, NH4 receptors seem to function mostly as detectors of relative rather than absolute stimulus intensity across their entire dynamic range: the response to a given stimulus-to-background ratio remained the same over 3 log step increases of background concentration (Fig. 6).
5.  As in other sensory modalities, a parallel shift of response functions appears to be an important property of chemoreceptor cells, allowing for this sensory system to function over a wider stimulus intensity range than the instantaneous dynamic range of individual receptor cells.
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16.
We have identified a nerve carrying auditory afferents and characterized their physiological responses in the tiger beetle,Cicindela marutha.
1.  The tympana are located at the lateral margins of the first abdominal tergum. The nerve carrying the tympanal afferents is a branch of the dorsal root from the first abdominal ganglion.
2.  Both male and female auditory afferent responses are sharply tuned to 30 kHz with sensitivities of 50–55 dB SPL.
3.  The auditory afferents show little adaptation and accurately code the temporal characteristics of the stimulus with the limit of a resolution of 6–10 ms.
4.  The difference in threshold between contralateral and ipsilateral afferents for lateral stimuli is greatest at 30 kHz and is at least 10–15 dB.
5.  Ablation studies indicate that the floppy membrane in the anterolateral corner of the tympanum is crucial for transduction while the medial portion of the tympanum is less important.
6.  The tiger beetle and acridid (locust and grasshopper) ears have evolved independently from homologous peripheral structures. The neural precursor of the tympanal organs in both animals is likely the pleural chordotonal organ of the first abdominal segment.
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17.
1.  The head-bobbing rhythm previously reported in pigeons Columba livia during approximately level landing flights also occurs in upwards landing flights. This finding strengthens the evidence that head-bobbing in flight is linked specifically to approach to a landing target, and that the behaviour has a visual function.
2.  In both level and upwards flights, head-bobbing arises from an oscillating flexion and extension of the neck. Rhythms in translation and rotation of the body do not make a detectable contribution to head-bobbing.
3.  Head-bobbing occurs at the same frequency as the wingbeat cycle and in a fixed phase relationship to it.
4.  The orientation of the head relative to the horizontal is correlated with the trajectory of upwards approach to a perch. In contrast to downwards landing flights, this relationship cannot have the function of keeping the perch in focus during landing. It is proposed instead that it enables the head to be bobbed along the axis which maximizes amplification of optic flow.
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18.
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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19.
1.  In the tortoise the capability of the spinal cord of generating rhythmic motor activity and of modulating reflex transmission depending on the motor cycle was investigated.
2.  In the intact animal co-ordinated locomotion was only observed if the feet had ground contact. Without ground contact only rhythmic struggling movements occurred. After spinalization some peripheral input was needed to initiate and sustain struggling movements in the air; the pattern of the movements was changed but not the frequency. After paralyzation the capability of generating a rhythmic activity was distinctly depressed in the spinal tortoise. The frequency of a rhythmic activity which could be induced in such a preparation by peripheral stimulation was very low, even after premedication with nialamide and DOPA.
3.  In the spinal paralyzed preparation during rhythmic motor activity a modulation of the membrane potential of motoneurones occurred with phases of depolarization and hyperpolarization. The latter at least partly were due to synaptic inhibition.
4.  In the spinal paralyzed preparation the transmission in excitatory reflex pathways from peripheral flexor reflex afferents (FRA) to motoneurones was phasically modulated during rhythmic motor activity in the way that the transmission was facilitated during the active phase of a motoneurone pool and inhibited during the reciprocal phase. In the inhibitory FRA pathways partly a particular kind of modulation of the transmission during the different phases was observed.
5.  The results indicate that the rhythmic motor activity in the spinal paralyzed tortoise which largely matched the activity found in cats, resembles in some aspects locomotor activity and therefore by analogy with findings in cats and turtles may be denoted as fictive locomotion.
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20.
(1)  The inactivation of various forms of nucleoside transport with reagents blocking thiol groups was studied in whole cells ofE. coli B. No positive correlation between the efficiency of active transport and the extent or rate of inactivation could be demonstrated.
(2)  The most efficient constitutive nucleoside-transporting system was found to comprise a specific thiol component characterized by low rate of inactivation with N-ethylmaleimide; the less efficient inducible transport and the facilitated diffusion of guanosine require the integrity of another thiol component which is rapidly inactivated with N-ethylmaleimide.
(3)  The constitutive nucleoside-transporting system is completely inactivated with T4 phage, while other modes of nucleoside transport are much less affected.
(4)  Inactivation of constitutive transporting system in cells exposed to N-ethylmaleimide for a limited period of time continues long after the inhibitor has been removed, indicating storage of the inhibitor in some cellular compartment. Addition of dithiothreitol stops the inactivation immediately.
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