Time course of the Houseflies' landing response

The landing response of stationary flying houseflies Musca domestica has been recorded on video tape. The leg movements were quantitatively evaluated. It could be demonstrated that:

1. only the first two pairs of legs are involved in the reaction (Fig. 1). Prothoracic tarsi are lifted beyond the head, mesothoracic tarsi are lowered and moved sidewards (Fig. 2a and b).
2. the movement of the tarsal tips is mainly due to an opening of one single joint per leg, i.e. the femurtibia joint of the prothoracic leg (Fig. 2c), and the coxa-femur joint of the mesothoracic leg.
3. the landing reaction is a fixed action pattern which does not seem to require further sensory input once it is released (Fig. 4d).
4. the landing responses to a light-off stimulus and to expanding patterns with different angular velocities are indistinguishable (compare Fig. 3a-c with Fig. 2a-c). The only parameter that is obviously dependent on the stimulus conditions, is the latency of the reaction (Fig. 4a-c).

     

Multisensory control of escape in the cockroach Periplaneta americana

1. All giant interneurons (GIs) were ablated from the nerve cord of cockroaches by electrocautery, and escape behavior was analyzed with high-speed videography. Animals with ablations retained the ability to produce wind-triggered escape, although response latency was increased (Table 1, Fig. 4). Subsequent lesions suggested that these non-GI responses depended in part on receptors associated with the antennae.
2. Antennal and cereal systems were compared by analyzing escape responses after amputating either cerci or antennae. With standard wind stimuli (high peak velocity) animals responded after either lesion. With lower intensity winds, animals lost their ability to respond after cereal removal (Fig. 6).
3. Removal of antennae did not cause significant changes in behavioral latency, but in the absence of cerci, animals responded at longer latencies than normal (Fig. 7).
4. The cercal-to-GI system can mediate short latency responses to high or low intensity winds, while the antennal system is responsive to high intensity winds only and operates at relatively longer latencies. These conclusions drawn from lesioned animals were confirmed in intact animals with restricted wind targeting the cerci or antennae only (Fig. 9).
5. The antennae do not represent a primary wind-sensory system, but may have a direct mechanosensory role in escape.

     

Selective phonotaxis to advertisement calls in the gray treefrog Hyla versicolor: behavioral experiments and neurophysiological correlates

1. The significance of particular acoustic properties of advertisement calls for selective phonotaxis by the gray treefrog, Hyla versicolor (= HV), was studied behaviorally and neurophysiologically. Most stimuli were played back at 85 dB SPL, a level typically measured at 1–2 m from a calling male.
2. Females preferred stimuli with conspecific pulse shapes at 20° and 24°C, but not at 16°C. Tests with normal and time-reversed pulses indicated the preferences were not influenced by the minor differences in the long-term spectra of pulses of different shape.
3. Pulse shape and rate had synergistic or antagonistic effects on female preferences depending on whether the values of one or both of these properties in alternative stimuli were typical of those in HV or heterospecific (H. chrysoscelis = HC) calls.
4. More auditory neurons in the torus semicircularis were temporally selective to synthetic calls (90%) than to sinusoidally AM tones and noise (< 70%).
5. Band-pass neurons were tuned to AM rates of 15–60 Hz. Neurons were more likely to be tuned to HV AM rates ( < 40 Hz) when stimuli had pulses with HV rather than HC shapes.
6. Sharp temporal tuning was uncommon and found only in neurons with band-pass or low-pass characteristics.
7. Many neurons differed significantly in response to HV and HC stimulus sets. Maximum spike rate was more often elicited by an HV stimulus (74%) than by an HC stimulus (24%).
8. Differences in spike rates elicited by HV and HC stimuli were attributable to combinations of differences in the rise times and shapes of the pulses.

     

Discrimination of phase spectra in complex sounds by the bullfrog (Rana catesbeiana)

1. Male bullfrogs at two different natural calling sites were presented with playbacks of synthetic advertisement calls differing in phase spectra. Sounds were presented in a ABA design to analyze the ability of the animals to perceive changes in repeated series of stimuli.
2. The number of individual croaks in an answering call significantly increased over repeated presentations of two of the three stimulus phase types in condition A1. There were significantly fewer croaks to the third stimulus. These data suggest that two stimuli were perceived in a similar manner.
3. Latency of calling to stimuli presented in conditions A and B changed in response to shifts in phase spectrum at a low density calling site. These differences were significant when comparing latency to playbacks where shifts in the phase spectrum changed the temporal fine-structure and waveform periodicity of the stimulus.
4. The increase in number of croaks and decrease in response latency across condition A1 and the increase in latency in condition B suggest that discrimination may take the form of stimulus-specific sensitization. In this context, sensitization might reflect an increase in arousal due to repeated presentation of a salient stimulus.
5. The operation of a hypothetical ‘mating call detector,’ based on linear summation of temporal responses from the eighth nerve, provides output similar to the behavioral results.

     

The effect of temperature on the consumption,absorption and conversion of food in Ophiocephalus punctatus bloch

1. The overall feeding rate is maximum at 28°C and decreases at 20°C and 33°C for all sizes.
2. The smaller fish are cold-sensitive. At 28°C and at 33°C the time course rate shows the same decline, whereas at 20°C the response was anomalous.
3. Absorption efficiency is independent of size and temperature.
4. Rate of absorption and hence rate of conversion is primarily conditioned by rate of feeding.
5. At 20°C the conversion efficiency is directly related to size whereas at 28°C and 33°C it is inversely related to size.

     

The effect of starvation on energy turnover and protein metabolism in Ophiocephalus punctatus bloch

1. At 20°C, fish starved for various durations took less food than unstarved fish. At 28°C, 20-day starved fish alone consumed more food.
2. The maximum feeding was during the second ten days at 28°C but in the first ten days at 20°C.
3. Absorption efficiency was unaffected by temperature and starvation.
4. Absorption rate reflected feeding rate.
5. At 28°C the conversion efficiency was high for the ten-day starved fish but at 20°C the 30-day starved fish showe high conversion efficiency.
6. Conversion rate is governed not only by feeding rate but also by conversion efficiency.
7. At 28°C the 20-day starved fish alone compensated for loss of energy, total and protein nitrogen. At 20°C the loss was compensated for by all fish.

     

A study on the rate of water transport of the clam katelysia opima in relation to environmental conditions

1. The neutral red technique was employed to study the rate of filtration in Katelysia opima.
2. The weight specific water filtration was found to be greater for younger clams compared to the older ones.
3. The rate of water filtration increased with decreasing salinity.
4. Water filtration was found to increase as temperature increased, reaching a maximum at 35°C. but then sharply decreasing at 39°C.
5. Light had no significant effect on the rate of filtration.
6. Suspended matter was found to affect the rate of water filtration.
7. The rate of filtration was low at high pH and high in low pH.
8. The rate of water filtration was found to be faster during high tide than during low tide.
9. The presence of the parasitic crab, Pennotheris sp., in the mantle cavity of clams had a marked effect on the particle filtration.
10. Accidental cut of the siphon tips had no effect on the rate of filtration.

     

Phase reversal in the lateral line of the ruff (Acerina cernua) as cue for directional sensitivity

• 1.1. The afferent response recorded from single fibres innervating canal neuromasts on the head of the ruff shows phase shifts of 180°, depending on stimulus location.
• 2.2. Based on these recordings it is shown, that in the flow field of a nearby moving object, the cupulae of adjacent neuromasts can be deflected in opposite directions.
• 3.3. This information may, in addition to other cues, enable localization of the stimulus source.

     

Wind-evoked evasive responses in flying cockroaches

1. A standing cockroach (Periplaneta americana) responds to the air displacement made by an approaching predator, by turning away and running. The wind receptors on the cerci, two posterior sensory appendages, excite a group of ventral giant interneurons that mediate this response. While flying, these interneurons remain silent, owing to strong inhibition; however, the dorsal giant interneurons respond strongly to wind. Using behavioral and electromyographic analysis, we sought to determine whether flying cockroaches also turn away from air displacement like that produced by an approaching flying predator; and if so, whether the cerci and dorsal giant interneurons mediate this response.
2. When presented with a wind puff from the side, a flying cockroach carries out a variety of maneuvers that would cause a rapid turn away and perhaps a dive. These are not evoked if the cerci are ablated (Figs. 4, 5, 6).
3. This evasive response appears to be mediated by a circuit separate from that mediating escape when the cockroach is standing (Fig. 7).
4. The dorsal giant interneurons respond during flight in a directional manner that is suited to mediate this behavior (Fig. 8).
5. Recordings of the wind produced by a moving model predator (Fig. 9), together with measurements of the behavioral latency of tethered cockroaches, suggest that the evasive response would begin just milliseconds before a predator actually arrives. However, as explained in the Discussion section, under natural conditions, the evasive response may well begin earlier, and could indeed be useful in escaping from predators.
6. If cockroaches had a wind-mediated yaw-correcting behavior, as locusts have, this could conflict with the wind-evoked escape. In fact, cockroaches show the opposite, yaw-enhancing response, mediated by the cerci, that does not present a conflict with escape (Figs. 10–14).

     

Polarization sensitivity in crayfish lamina monopolar neurons

1. Polarization sensitivity (PS) was examined in photoreceptors and lamina monopolar cells (LMCs) in two species of crayfish, Procambarus clarkii and Pacifasticus leniusculus. The measurements were made with intracellular recordings and broad field illumination.
2. PS is about 40% greater in Pacifasticus than in Procambarus (Table 1). In both species the LMC stationary PS profiles (estimated with flashes) are similar to those of receptors (Figs. 1 and 2). Both receptor and LMC sensitivity profiles are well described by cos² θ functions (Fig. 3). PS was observed in all receptors and 78% of LMCs.
3. When stimulated with a rotating polarizer, receptors and LMCs exhibit membrane potential modulation with phase predicted by the stationary PS profile (Fig. 5). In photoreceptors, the polarization-elicited percent modulation falls off steeply as intensity increases. The LMC modulation is stronger than that in receptors and relatively insensitive to the mean intensity (Figs. 6 to 8). For low intensities the LMC modulation is 100%. The LMC dynamic behavior is consistent with either an opponency mechanism or strong but polarization-insensitive lateral inhibition.
4. Receptors and LMCs exhibit steady-state differential sensitivity to stationary e-vector orientation (Fig. 9).
5. About 10% of the LMC neurons exhibit PS maxima separated by 90°. These results imply a nonlinear summation of signals from orthogonal receptor channels (Fig. 10).

     

Frequency as a releaser in the courtship song of two crickets,Gryllus bimaculatus (de Geer) and Teleogryllus oceanicus: a neuroethological analysis

1. The courtship behavior of male field crickets, Gryllus bimaculatus (De Geer) and Teleogryllus oceanicus, is a complex, multimodal behavioral act that involves acoustic signals (a courtship song; Fig. 1A,B). The dominant frequency is 4.5 kHz for T. oceanicus song (Fig. 1A) and 13.5 kHz for G. bimaculatus (Fig. IB).
2. When courting males are deprived of their courtship song by wing amputation, their courtship success declines markedly but is restored when courting is accompanied by tape-recordings of their courtship songs or a synthetic courtship song with only the dominant frequency of the natural song; other naturally occurring frequency components are ineffective for restoring mating success (Figs. 4, 5).
3. It has been suggested that an identified auditory interneuron, AN2, plays a critical role in courtship success. Chronic recordings of AN2 in an intact, tethered female show that AN2's response to the natural courtship song and synthesized songs at 4.5 and 13.5 kHz is similar in T. oceanicus. By contrast, in G. bimaculatus, AN2's response to the natural courtship song and synthesized song at 13.5 kHz, but not at 4.5 kHz, is similar (Figs. 2,3).
4. In behavioral experiments, playback of a 30 kHz synthetic courtship song in G. bimaculatus does not restore courtship success, yet this same stimulus elicits as strong a response from AN2 as does the normal courtship song (Fig. 6). Thus, contrary to earlier work by others, we conclude AN2 is not, by itself, a critical neural link in the courtship behavior of these two species of crickets.

     

Survival,osmoregulatory ability,and respiration of idotea chelipes (Crustacea,Isopoda) from lake veere in different salinities and temperatures

1. An ecological and physiological study ofI. chelipes from Lake Veere, The Netherlands, was made.
2. Both osmoregulatory capacity and survival decrease with increasing temperature as well as with decreasing salinity.
3. Respiration experiments suggest that the need of energy by osmoregulatory activity may be supplied at the cost of other physiological processes, at any rate at temperatures of 10°C and higher.
4. It may be expected that, if temperatures higher than 15°C and salinities lower than 8‰ coincide, the population ofI. chelipes will be affected negatively.

     

Stiffness changes in chick hair bundles following in vitro overstimulation

1. The in vitro effect of intense stimulation on the micromechanical stiffness of hair cell sensory hair bundles was studied at three locations on the chick basilar papilla. Threshold levels of hair bundle motion, produced by a water jet stimulus, were examined before and after exposure to a 300 Hz water jet stimulus set at 25 dB above the pre-exposure threshold level.
2. Threshold levels of motion were systematically examined in 8 unexposed control cells. The level of water jet stimulus needed to achieve the detection threshold of motion remained constant in these cells when periodically tested over a 36.5-min interval.
3. Post-exposure changes in the motion detection threshold of hair bundles were examined in 82 hair bundles, and a number of effects were identified: 2.4% of the hair bundles showed no threshold change; 31.7% of the hair bundles had threshold shifts which indicated an increase in stiffness; 18.3% exhibited a threshold shift that indicated a decrease in hair bundle stiffness, but with no recovery; and 47.6% had thresholds that indicated a decrease in hair bundle stiffness with recovery to pre-exposure levels within 16–18 min.
4. The results suggest that chick hair bundles exhibit complex and varied responses to overstimulation which are very different from that seen in the mammal.

     

Comparison between the movement detection systems underlying the optomotor and the landing response in the housefly

Flies evaluate movement within their visual field in order to control the course of flight and to elicit landing manoeuvres. Although the motor output of the two types of responses is quite different, both systems can be compared with respect to the underlying movement detection systems. For a quantitative comparison, both responses were measured during tethered flight under identical conditions. The stimulus was a sinusoidal periodic pattern of vertical stripes presented bilaterally in the fronto-lateral eye region of the fly. To release the landing response, the pattern was moved on either side from front to back. The latency of the response depends on the stimulus conditions and was measured by means of an infrared light-beam that was interrupted whenever the fly lifted its forelegs to assume a preprogrammed landing posture (Borst and Bahde 1986). As an optomotor stimulus the pattern moved on one side from front to back and on the other side in the opposite direction. The induced turning tendency was measured by a torque meter (Götz 1964). The response values which will be compared are the inverse latencies of the landing response and the amplitude of the yaw torque.

1. Optomotor course-control is more sensitive to pattern movement at small spatial wavelengths (10° and 20°) than the landing response (Fig. 1a and b). This suggests that elementary movement detectors (EMDs, Buchner 1976) with large detection base (the distance between interacting visual elements) contribute more strongly to the landing than to the optomotor system.
2. The optimum contrast frequencies of the different responses obtained at a comparatively high pattern contrast of about 0.6 was found to be between 1 and 10 Hz for the optomotor response, and around 20 Hz for the landing response (Fig. 2a and b). This discrepancy can be explained by the fact that the optomotor response was tested under stationary conditions (several seconds of stimulation) while for the landing response transient response characteristics of the movement detectors have to be taken into account (landing occurs under these conditions within less than 100 ms after onset of the movement stimulus). To test the landing system under more stationary conditions, the pattern contrast had to be reduced to low values. This led to latencies of several seconds. Then the optimum of the landing response is around 4 Hz. This is in the optimum range of the optomotor course-control response. The result suggests the same filter time constants for the movement detectors of both systems.
3. The dependence of both responses on the position and the size of the pattern was examined. The landing response has its optimum sensitivity more ventrally than the optomotor response (Fig. 3a and b). Both response amplitudes increase with the size of the pattern in a similar progression (Fig. 3c and d).

In first approximation, the present results are compatible with the assumption of a common set of movement detectors for both the optomotor course-control and the landing system. Movement detectors with different sampling bases and at different positions in the visual field seem to contribute with different gain to both responses. Accordingly, the control systems underlying both behaviors are likely to be independent already at the level of spatial integration of the detector output.     

Development and efficiency of a new generation of bioreactors

The development and investigation of high-efficiency bioreactors is one of the primary problems bioprocess engineers have to solve. With increasing efficiency of the bioreactor the downstream processes will be much simplified, energy and costs will be substantially reduced. According to fundamental research on the properties of stirred tank bioreactors the following rules for the design of bioreactors should be observed:

1. Prevent rotational motion of the biosuspension.
2. Generate motion of the biosuspension in the radial and axial direction.
3. Prevent fluid flow in big spaces.

These design rules are in general observed in the development of high-efficiency bioreactors. A selected group of such bioreactors is described.     

Development and efficiency of a new generation of bioreactors

The development and investigation of high-efficiency bioreactors is one of the primary problems bioprocess engineers have to solve. With increasing efficiency of the bioreactor the downstream processes will be much simplified, energy and costs will be substantially reduced. According to fundamental research on the properties of stirred tank bioreactors the following rules for the design of bioreactors should be observed:

1. Prevent rotational motion of the biosuspension.
2. Generate motion of the biosuspension in the radial and axial direction.
3. Prevent fluid flow in big spaces.

These design rules are in general observed in the development of high-efficiency bioreactors. A selected group of such bioreactors is described.     

Manipulations of polarized skylight calibrate magnetic orientation in a migratory bird

1. Young migratory birds enter the world with two representations of the migratory direction, one coded with respect to the magnetic field, the other with respect to celestial rotation. The preferred magnetic direction of migratory orientation is malleable early in life: it may be calibrated by celestial rotation, observed either in daytime or at night.
2. Previous experiments showed that early experience with skylight polarization was necessary for calilbration to occur in daytime. In this study, we performed a direct manipulation of patterns of polarized skylight at dawn and dusk.
3. Hand-raised Savannah sparrows (Passerculus sandwichensis) were allowed to observe the clear sky for 1 h prior to local sunrise and for one h following local sunset. They never saw the Sun nor stars. The birds observed the sky through bands of polarizing material (HNP'B) aligned with the e-vector axis in one of three orientations with respect of the azimuth of sunrise and sunset: group 1) 90°; group 2) 45° CW; group 3) 45° CCW.
4. Tested indoors in covered cages in both shifted and unshifted magnetic fields, the autumn migratory orientation of the three groups differed significantly. Group 1 oriented magnetic N-S, group 2 oriented magnetic NW-SE, and group 3 oriented magnetic NNE-SSW. These observed orientation directions are very close to those predicted by the manipulations of polarized skylight.
5. These results indicated that a fairly simplified, static polarized light pattern viewed a limited number of times only in dawn and dusk snapshots is sufficient to produce calibration of the preferred magnetic migratory orientation direction.

     

Basic processes of locomotor coordination in the rock lobster

Rock lobsters are able to perform long and stereotyped stepping sequences above a motor driven treadmill. Forward walking samples are estimated by mean of statistical methods to draw out the basic rules involved in the locomotor behaviour (Fig. 1).

- The spatial and temporal parameters defined in a single propulsive leg are either invariable in respect to the imposed speed, as the mean step length (L), the return stroke duration (Tr) and the pause times (T's, T'r), or speed dependent as the power stroke duration (Ts) and the whole period (Figs. 2 and 3).

- The interleg phase coupling is strong and stable in the ipsilateral rear pairs (4–5), these legs acting most of the time in absolute coordination (1:1) or in harmonic ratio (2:1). In the contralateral pairs (R4-L4, R5-L5) the legs roughly operate in antiphase, but the relationship appears much weaker and variable, with frequent episodes of relative coordination (Fig. 4).

- The time intervals between the ground contact of any leg and the swing initiation in the nearest ones appear somewhat constant and could be closely related to the mechanism of stepping synchronization. The “5 on - 4 off” delay, very stable and always positive, suggests that the rear legs could exert a predominant influence upon the rhythmical movements of the next anterior ipsilateral appendages (Fig. 5).

- To test the contralateral relationships, the treadmill belts can be decoupled in order to impose different walking speeds on each side. Such a conflicting stimulus reveals that:

1. The relative hierarchy always observed between the ipsilateral legs can be artificially created between the two sides (Fig. 6).
2. The driving influence of a given leg is closely linked to the intensity of EMG's discharges in its power stroke muscles.
3. The contralateral appendages are able to walk in absolute coordination despite a large speed difference between the two sides (up to 4 cm/s). Under such a constraint, the walking legs alter its invariable parameters (L and Tr) to reach a common step period and steadily maintain the alternating pattern (Figs. 6 and 7).

     

Improvements of the membrane filter method for DNA:rRNA hybridization

We describe and recommend the following improvements of DNA:rRNA membrane filter hybridization methods. One of our aims was to avoid DNA release from filter discs during hybridization.

1. Our hybridization conditions are 2 SSC in aq. dest., with 20% formamide, 50 C, overnight for 16 hr.
2. Duplexing is over in 8–10 hr.
3. Formamide has to be very pure (O.D.≤0.2/cm light path at 270 nm).
4. RNAase treatment: 250 μg/5 ml 2 SSC/filter at 37 C for 1 hr.
5. Our conditions for stepwise thermal denaturation are: 5°C steps from 50C to 90C in 1.5 SSC in 20% formamide.
6. Single-stranded DNA, fixed on membrane filters, and stored in vacuo at 4C, can be used reliably for hybridization for up to 20 months.
7. Concentrated DNA in 0.1 SSC, quick-frozen at ?50 C and stored at ?90 C for up to 2 years can be used for hybridization without much change.
8. A CsCl gradient purification step yields much purer DNA, but increases the release of DNA from filters by about 20%. Filters with 20% more DNA is a compensation.
9. rRNA can be stored for 20 months in SSC or 2 SSC at ?12C without changing the hybridization results.