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1.
Yasuo Nakaoka 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1989,165(5):637-641
1. | Paramecium bursaria was stimulated by a light spot of 10–15 m diameter, and the photosensitive site was searched by recording responses in swimming behavior and in membrane potential. |
2. | Local stimulation to the anterior half of the cell caused an avoiding response. |
3. | Stimulation to the cells deciliated by ethanol treatment elicited a depolarization of the membrane potential. |
4. | Local stimulation to the anteroventral portion elicited a depolarization, but stimulation to the dorsal side induced no change in the membrane potential. |
5. | The action spectrum of depolarization elicited by local stimulation to the anteroventral surface showed two main peaks at 420 nm and 560 nm, corresponding to those of light stimulation of the whole cell. |
6. | It is concluded that a photosensitive site exists on the anteroventral surface ofParamecium, in particular within the oral groove of the cell. This local photosensitivity is discussed with respect to the mating reaction. |
2.
J. B. Phillips O. Sayeed 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1993,172(3):303-308
1. | Wildtype Oregon-R Drosophila melanogaster were trained in the ambient magnetic field to a horizontal gradient of 365 nm light emanating from one of the 4 cardinal compass directions and were subsequently tested in a visually-symmetrical, radial 8-arm maze in which the magnetic field alignment could be varied. When tested under 365 nm light, flies exhibited consistent magnetic compass orientation in the direction from which light had emanated in training. |
2. | When the data were analyzed by sex, males exhibited a strong and consistent magnetic compass response while females were randomly oriented with respect to the magnetic field. |
3. | When tested under 500 nm light of the same quantal flux, females were again randomly oriented with respect to the magnetic field, while males exhibited a 90° clockwise shift in magnetic compass orientation relative to the trained direction. |
4. | This wavelength-dependent shift in the direction of magnetic compass orientation suggests that Drosophila may utilize a light-dependent magnetic compass similar to that demonstrated previously in an amphibian. However, the data do not exclude the alternative hypothesis that a change in the wavelength of light has a non-specific effect on the flies' behavior, i.e., causing the flies to exhibit a different form of magnetic orientation behavior. |
3.
Gerbera Nalbach 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1989,164(3):321-331
1. | Several larval diets (Table 1) were developed for rearing the tobacco hornworm mothManduca sexta in an effort to control the synthesis of adult visual pigments (generically, rhodopsins) through the availability of their chromophore, retinaldehyde or, more likely, 3-hydroxyretinaldehyde. |
2. | Rhodopsin was measured in difference spectra from detergent extracts of adult retinas. Opsin was identified and measured on SDS gels after electrophoretic separation of retinal proteins reduced with cyanoborohydride to convert rhodopsin to fluorescent N-retinyl opsin. The density of P-face particles in photoreceptor membranes was measured in freeze-fracture preparations. Visual sensitivity of compound eyes was measured from the electroretinogram (ERG). |
3. | One diet containing corn meal and soy flour, rich sources of potential carotenoid precursors of the chromophore, producedfortified animals with the highest level of rhodopsin: 60 pM/retina. The addition of spinach leaves to the fortified diet did not increase the amount of rhodopsin. A second diet containing wheat germ producedintermediate moths with about 25% of the visual pigment of the fortified group. A third diet containing potato starch and lacking all sources of carotenoids except for a small amount of yeast produceddeprived animals whose visual pigment could not be measured but must have been less than 0.6 pM/retina (Fig. 1B). |
4. | A band at 35–38 kDa on SDS gels prepared from cyanoborohydride-reduced extracts of fortified retinas was identified as n-retinyl opsin from its intense fluorescence. The fluorescence of the band was less intense in preparations from intermediate retinas. No fluorescence was detected in preparations of deprived retinas. However, this relatively insensitive assay would not allow detection of rhodopsin levels less than 6 pM/retina. When the gels were stained for protein, the density of the 35 kDa band from intermediate and deprived retinas was about 45% and 6%, respectively, of that from fortified retinas. Thus the relative density of the band from preparations of deprived retinas is about 6 times greater than the estimated maximum amount of rhodopsin present in extracts. Either there is excess opsin in the deprived retinas, or another minor protein runs at the same position on the gel as opsin (Fig. 2). |
5. | P-face particle densities of rhabdomeric membrane ranged from 104/m2 in the fortified animals to 4×103/m2 in intermediate animals to 5×102/m2 in deprived moths (Figs. 3, 4 and Table 2). |
6. | The sensitivity of the intermediate and deprived animals averaged 55% and 0.06%, respectively, of that of the fortified animals (Fig. 1 A). Measurement of the ERG proved to be the simplest and most sensitive method for measuring visual impairment. If sensitivity remains linear with rhodopsin content at low concentrations, deprived retinas contain about 0.04 pM of rhodopsin. |
7. | Visual sensitivity increased by 10 to 40-fold following the addition of-carotene or xanthophyll to the deprived diet. Addition of either retinol or retinal did not significantly increase sensitivity (Fig. 1A). |
4.
J. Pernberg H. Machemer 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1989,164(4):551-562
1. | Properties of the membrane currents ofDidinium nasutum have been investigated under voltage clamp in different solutions and after deciliation. |
2. | Theearly transient Ca2+ inward current activates in a voltage-dependent manner. Inactivation is both Ca2+ -dependent and voltage-dependent. |
3. | Alate Ca2+ current rises with time to peak > 50 ms and decays in the order of seconds. |
4. | Activation and inactivation of the late Ca2+ current is voltage-dependent. |
5. | The delayed outward current is activated by voltage. The kinetics of this K+ current, but not its amplitude, are enhanced in the presence of intracellular EGTA. |
6. | The two voltage-dependent Ca2+ channels are located in the cilia, whereas all K+ channels are restricted to the somatic membrane. |
5.
K. Arikawa H. Uchiyama 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1996,178(1):55-61
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. |
6.
Rolf Bergmann 《Antonie van Leeuwenhoek》1989,55(2):143-152
Thiolutin was found to inhibit the utilization of glucose and other growth substrates in Escherichia coli. The inhibition was detected by a sharp drop of the respiration rate after addition of the antibiotic. The actual function affected was allocated to the cytoplasmic membrane of the bacterial cells by the following evidence:
It was concluded that the transport of certain substrates across the membrane was inhibited. 相似文献
| - spheroplasts were affected like intact cells, |
| - individual reactions of either the electron transport chain or the glycolytic pathway were not inhibited, |
| - glucose consumption in the culture stopped and the cells accumulated guanosine tetraphosphate as under starvation conditions, |
| - activation of the cell's apo-glucose dehydrogenase restored respiration via bypassing the glucose phosphotransferase system. |
7.
Victy Mercy Gerald 《Hydrobiologia》1976,49(1):77-85
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. |
8.
Jens Meyer Norbert Elsner 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1995,176(4):563-573
1. | Up to 9 kHz, the tympanal membrane of the grasshopper Chorthippus biguttulus responds with equal sensitivity at the attachment sites of the low and the high-frequency receptors; at the latter site it is also particularly sensitive between 10 and 20 kHz. |
2. | The frequency spectra of the songs of both sexes exhibit maxima at 7–8 kHz, to which the membrane is well matched. In the high-frequency region, where the male songs have a peak at 30 kHz, there is no corresponding maximum in the membrane oscillation. |
3. | Because the tympanal membrane is immediately adjacent to air sacs in the tracheal system, it is deflected inward and outward by as much as 80 m during the respiratory cycle. |
4. | Measurements by laser vibrometry show that acoustically induced membrane oscillations are attenuated severely due to the respiratory displacement of the membrane for frequencies up to 10–12 kHz. By contrast, at higher frequencies the membrane sensitivity is doubled or tripled. |
5. | As a result of these membrane effects, the discharge in the tympanal nerve was profoundly reduced in the low-frequency range, whereas above 11 kHz there was a marked increase. This modulation of auditory sensitivity affects the animals' ability to detect conspecific songs. |
9.
P. J. Simmons 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1993,173(5):635-648
Intracellular recordings have been made of responses to step, ramp and sinusoidal changes of light by second-order L-neurones and a third-order neurone, DNI, of locust (Locusta migratoria) ocelli.
相似文献
1. | The membrane potential at the peak response by an L-neurone to a change in light is proportional to the light increment or decrement, independent of background, over a range of at least 4 log units. As background increases, response latency and time-course decrease, and responses become more phasic (Fig. 1). |
2. | Adaptation to a changed mean light level involves a change in sensitivity and a slow change in resting membrane potential, which never adapts completely to dark resting potential in the presence of light (Fig. 3). |
3. | L-neurones can follow changes in light which last several seconds, but responses to fast changes are enhanced in amplitude (Figs. 4, 5). An increase in background light causes an increase in the frequency of sinusoidally modulated light at which the largest response occurs (Fig. 4). |
4. | The responses of DNI to increased light saturate at lower intensities than those of L-neurones. During adaptation to different background light intensities, there is no change in the input-output relation of the synapse between an L-neurone and DNI (Figs. 6, 7). |
5. | For a rapid decrease in light, DNI produces a rebound spike, followed by a period of silence (Figs. 5, 8). |
10.
Peter J. Simmons 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1990,166(4):575-583
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:
相似文献
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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13.
Volkmar Bruns 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1976,106(1):87-97
1. | The cochlea of the horseshoe bat,Rhinolophus ferrumequinum, was frequency mapped by exposing for 30 min to one or two continuous pure tones of intensities between 70 and 110 dB SPL. The evaluation was made by differentiating between normal and swollen nuclei of the outer hair cells (OHC) of the organ of Corti and by measuring the diameter of the nuclei of the OHC. |
2. | In control animals the radial diameter of the OHC nuclei varies systematically from a mean of 2.85 m at the base to 3.2 um at the apex (Fig. 1). |
3. | All frequencies used for exposure were normalized to the resting frequency (FR), which is the frequency of the pure tone component of the orientation sound in a non-flying bat. The individual FR lay between 82.6 and 83.3 kHz. |
4. | For analysing the small frequencies between 83.0 to 86.0 kHz in which relevant echoes occur, 3.15 mm length of the basilar membrane is used, about the same length as for the octaves from FR/4 to FR/2 (2.85 mm) and from FR/2 to FR (3.2 mm) (Fig. Ca, b). |
5. | The discontinuity of the mechanical data at 4.5 mm of the length of the basilar membrane (part I of this paper) coincides with FR and the less pronounced discontinuity at 7.8 mm coincides with FR/2. |
6. | Location and mechanism of the auditory filter are discussed. |
14.
Morten Buhl Jørgensen Barbara Schmitz Jakob Christensen-Dalsgaard 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1991,168(2):223-232
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. |
15.
Yasuo Nakaoka Hans Machemer 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1990,166(3):401-406
1. | Coupling mechanisms between ciliary beating and the membrane potential in Paramecium were investigated under voltage clamp applying intracellular pressure injection of cAMP, cGMP and Ca-EGTA buffer. Ciliary responses following step changes in membrane potential were recorded by high-speed video on magnetic tape. |
2. | Injections of cAMP and cGMP up to millimolar concentrations caused no detectable changes in the frequency voltage relationship. A minor effect was that the ciliary reorientation towards the anterior cell end (reversal) tended to be inhibited with depolarization up to 10 mV. |
3. | Injection of Ca2+ into the cell clamped at the resting potential caused a transient anteriad ciliary reorientation and a simultaneous increase in the beating frequency. |
4. | Injection of EGTA (to buffer Ca2+ below 10–8 M) was ineffective in relation to frequency for several minutes. After this time, hyperpolarization- and depolarization activated frequency responses of EGTA-injected cells were increasingly inhibited. The ciliary reorientation following depolarization was not affected by EGTA. |
5. | A posterior contraction of the cell diameter was noticed upon membrane hyperpolarization. The contraction coincided in time with the increase in beating frequency. |
6. | The results support the view that the voltage-dependent augmentation of the ciliary beating rate is not directly mediated by an intracellular increase in either cAMP or cGMP. |
7. | The role of Ca2+ as intracellular messenger in the ciliary and somatic compartments is discussed. |
16.
W. Junger 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1991,169(5):633-639
Waterstriders on ponds and creeks compensate for displacement caused by wind or water current with periodical jumps against the direction of drift. This behavior is mediated by visual stimuli.
相似文献
1. | Waterstriders are able to detect the direction and extent of their displacement on an artificial canal when visual cues are reduced to a single point-like light source above the upstream end of the canal. They adjust the frequency and direction of the compensatory jumps to keep their mean position on the canal constant. The mean amplitude of the jumps is constant and independent of the stream velocity. |
2. | During drift compensation the light spot is kept in the frontal visual field at a fixed angle of elevation. This set angle differs among individuals and can be changed with time. |
3. | The station-keeping ability can hardly be explained by a velocity servo system since there is no accumulating position error. The average compensatory movements are governed by a discontinuously working position servo. |
4. | When the light spot is switched off, a few jumps are still performed. Jumps, therefore, are not triggered individually by visual cues. Waterstriders must possess an endogenous jump-generator. |
17.
John C. Montgomery John A. Macdonald Gary D. Housley 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1988,163(6):827-833
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. |
18.
3DFS is a 3D flexible searching system for lead discovery. Version 1.0 of 3DFS was published recently (Wang, T.; Zhou, J. J. Chem. Inf. Comput. Sci., 1998, 38, 71–77). Here version 1.2 represents a substantial improvement over version 1.0. There are six major changes in version 1.2 compared to version 1.0.
Besides the above, this paper supplies:
Supplementary material to this paper is available in electronic form at http://dx.doi.org/10.1007/s0089490050231 相似文献
1. | A new rule of aromatic ring recognition. |
2. | The inclusion of multiple-type atoms and chains in queries. |
3. | The inclusion of more spatial constraints, especially the directions of lone pairs. |
4. | The improvement of the query file format. |
5. | The addition of genetic search for flexible search. |
6. | An output option for generating MOLfiles of hits. |
1. | More query examples. |
2. | A comparison between genetic search and Powell optimization. |
3. | More detailed comparison between 3DFS and Chem-X. |
4. | A preliminary application of 3DFS to K+ channel opener studies. |
19.
Culture studies with healthy and virus-infected isolates of Ectocarpus siliculosus, Feldmannia simplex and F. irregularis gave the following results:
相似文献
| 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. |
20.
B. Hedwig 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1988,162(2):237-246
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). |