Analoge und Digitale Hochgeschwindigkeitskinematographie – Eine Übersicht (Analog and Digital High Speed Cinematography – a Review)

2001 ◽  
Vol 68 (11/2001) ◽  
Author(s):  
J. Holzfuss
Keyword(s):  
High Speed ◽  
High Speed Cinematography

New findings on life history traits of Xenos peckii (Strepsiptera: Xenidae)

2014 ◽  
Vol 146 (5) ◽  
pp. 514-527 ◽  
Author(s):  
M. Hrabar ◽  
A. Danci ◽  
S. McCann ◽  
P.W. Schaefer ◽  
G. Gries
Keyword(s):  
Life History ◽  
High Speed ◽  
Life History Traits ◽  
Suture Line ◽  
Paper Wasp ◽  
Anterior Portion ◽  
New Findings ◽  
High Speed Cinematography ◽  
Normal Speed ◽  
Wasp Nests

AbstractWe studied life history traits of Xenos peckii Kirby (Strepsiptera: Xenidae), a little-known parasite of the paper wasp Polistes fuscatus (Fabricus) (Hymenoptera: Vespidae) in North America. We field-collected 24 wasp nests in early July 2012, isolated parasitised wasps, tracked life history events of X. peckii, and recorded such behaviour as emergence of males and mating by normal-speed and high-speed cinematography. To emerge, males first cut the puparium with their mandibles along an ecdysial suture line, and then push aside the pupal cap during emergence. The endoparasitic females engage in active calling (pheromone release) behaviour by slowly inflating their cephalothorax, and then extruding it even farther out of, and tilting it away from, the host wasp abdomen. Seasonal and diel (afternoon) emergence periods of males coincide with seasonal and diel receptivity and calling periods of females. Males approach calling females in a swaying flight with smooth turns. They typically land on the anterior portion of the host wasp's abdomen, and then step backward until they make contact with the cephalothorax of the female. As soon as their mesothoracic legs contact the female's cephalothorax, they curl around it, and the male initiates mating. Thereafter, the female fully retreats and never re-mates.

Angular Momentum Requirements of the Twisting and Nontwisting Forward 1 1/2 Somersault Dive

1987 ◽  
Vol 3 (1) ◽  
pp. 47-62 ◽  
Author(s):  
Ross H. Sanders ◽  
Barry D. Wilson
Keyword(s):  
Angular Momentum ◽  
High Speed ◽  
Center Of Gravity ◽  
Transverse Axis ◽  
Free Position ◽  
High Speed Cinematography ◽  
The Difference ◽  
Hip Flexion ◽  
Commonwealth Games

This study investigated the in-flight rotation of elite 3m springboard divers by determining the angular momentum requirement about the transverse axis through the divers center of gravity (somersault axis) required to perform a forward 1 1/2 somersault with and without twist. Three elite male divers competing in the 1982 Commonwealth Games were filmed using high-speed cinematography while performing the forward 1 1/2 somersault in the pike position and the forward 1 1/2 somersault with one twist in a free position. The film was digitized to provide a kinematic description of each dive. An inclined axis technique appeared to be the predominant means of producing twist after takeoff from the board. The angular momentum about the somersault axis after takeoff was greater for the forward 1 1/2 somersault with twist than the forward 1 1/2 somersault without twist for all three divers. The difference in angular momentum between the two dives of each diver ranged from 6% to 19%. The most observable difference between the dives during the preflight phases was the degree of hip flexion at takeoff. There was more hip flexion at takeoff in 5132D than 103B for all three divers. This difference ranged from 9° to 18° (mean = 14°).

Kinematics of Tongue Projection in Chamaeleo Oustaleti

1991 ◽  
Vol 159 (1) ◽  
pp. 109-133 ◽  
Author(s):  
PETER C. WAINWRIGHT ◽  
DAVID M. KRAKLAU ◽  
ALBERT F. BENNETT
Keyword(s):  
High Speed ◽  
Prey Capture ◽  
Maximum Velocity ◽  
Head Movements ◽  
Florida State University ◽  
State University ◽  
Maximum Acceleration ◽  
Related Family ◽  
High Speed Cinematography ◽  
Tongue Movements

The kinematics of prey capture by the chamaeleonid lizard Chamaeleo oustaleti were studied using high-speed cinematography. Three feeding sequences from each of two individuals were analyzed for strike distances of 20 and 35 cm, at 30°C. Ten distances and angles were measured from sequential frames beginning approximately 0.5 s prior to tongue projection and continuing for about 1.0 s. Sixteen additional variables, documenting maximum excursions and the timing of events, were calculated from the kinematic profiles. Quantified descriptions of head, hyoid and tongue movements are presented. Previously unrecognized rapid protraction of the hyobranchial skeleton simultaneously with the onset of tongue projection was documented and it is proposed that this assists the accelerator muscle in powering tongue projection. Acceleration of the tongue occurred in about 20ms, reaching a maximum acceleration of 486 m s−2 and maximum velocity of 5.8m s−1 in 35 cm strikes. Deceleration of the tongue usually began within 5 ms before prey contract and the direction of tongue movement was reversed within 10 ms of prey contact. Retraction of the tongue, caused by shortening of the retractor muscles, reached a maximum velocity of 2.99 ms−1 and was complete 330 ms after prey contact. Projection distance influences many aspects of prey capture kinematics, particularly projection time, tongue retraction time and the extent of gape and head movements during tongue retraction, all of which are smaller in shorter feedings. Though several features of the chameleon strike have apparently been retained from lizards not capable of ballistic tongue projection, key differences are documented. Unlike members of a related family, the Agamidae, C. oustaleti uses no body lunge during prey capture, exhibits gape reduction during tongue projection and strongly depresses the head and jaws during tongue retraction. Note: Present address: Department of Biological Sciences, Florida State University, Tallahassee, FL 32306, USA.

Kinematic analysis of tongue movements during chemosensory behaviour in the European green lizard, Lacerta viridis (Reptilia: Lacertidae)

1992 ◽  
Vol 70 (10) ◽  
pp. 1886-1896 ◽  
Author(s):  
Véronique Goosse ◽  
Vincent L. Bels
Keyword(s):  
High Speed ◽  
Prey Capture ◽  
Principal Component ◽  
Upward Movement ◽  
High Speed Cinematography ◽  
Tongue Movements ◽  
Lacerta Viridis ◽  
Tongue Flicking ◽  
Stationary Interval ◽  
Tongue Displacement

High-speed cinematography (100 frames/s) was used to allow quantitative analysis of the kinematic profiles of tongue and jaw displacements during chemosensory activities in the scleroglossan lizard Lacerta viridis. The types of tongue flicking were simple downward extensions (SDE), single oscillations (SOC), and submultiple oscillations (SMOC) of the tongue out of the mouth. The SMOC type involves a downward or upward movement of the tongue performed before a typical oscillation and it is therefore suggested that this is an intermediate category of flick between the typical SOC and MOC of lizards. Closing and opening of the mouth in SDE, SOC, and SMOC cycles may or may not be separated by a stationary stage during which the jaws are held open at a constant gape. The duration of this stationary interval increases from SDE to SMOC. Gape cycles do not show any division into slow and fast stages. The gape is produced largely by depression of the lower jaw; the upper jaw is slightly elevated by protrusion of the tongue. Patterns of correlation of kinematic variables depicting jaw and tongue movements differed between SDE, SOC, and SMOC. A principal component analysis shows that the three flick types overlap in a multivariate space constructed from the kinematic variables depicting jaw and tongue displacements. Overlap between SOC and SMOC categories is greater than that between SOC, SMOC, and SDE categories. The kinematic patterns of tongue displacement during SMOC in Lacerta viridis show similarities with those of MOC in other lizards and in snakes. Kinematically, the pattern of jaw and tongue displacements of Lacerta viridis during chemosensory activities shows similarities with those that occur during drinking and prey capture.

scholarly journals THE MECHANISM OF THE NEPHRIDIAL APPARATUS OF PARAMECIUM MUL TIMICRONUCLEATUM

1968 ◽  
Vol 37 (1) ◽  
pp. 139-146 ◽  
Author(s):  
Alan E. Organ ◽  
Eugene C. Bovee ◽  
Theodore L. Jahn ◽  
Duncan Wigg ◽  
James R. Fonseca
Keyword(s):  
Electron Microscopy ◽  
Excretory Pore ◽  
High Speed ◽  
Cell Membranes ◽  
Recent Analysis ◽  
Opposite Wall ◽  
Active Contraction ◽  
High Speed Cinematography ◽  
Excretory Canal

Recent analysis of the mechanism of the nephridial apparatus of Paramecium multimicronucleatum by high-speed cinematography (300 fps at x 250) confirms the observations by electron microscopy (Schneider, 1960) that once the pore is opened, the vesicle is invaginated by adjacent cytoplasm and is emptied by collapsing under pressure from that cytoplasm, aided perhaps by pressure of the fibrils which anchor the ampullae to the excretory canal. There is no indication of active contraction of the vesicle or its membrane. There is no permanent pore to the vesicle. The vesicle is closed by a sealing of the ruptured membrane where it is in contact with the pellicular excretory canal. At onset of expulsion of vesicular fluid the membrane across the basal opening of the excretory canal is ripped along one semicircular portion of the excretory pore and is driven up against the opposite wall as a flap while the water rushes out. A constriction of the vesicular and cell membranes at the base of the excretory canal reseals the opening.

TAIL MUSCLE ACTIVITY PATTERNS IN WALKING AND FLYING PIGEONS (COLUMBA LIVIA)

1993 ◽  
Vol 176 (1) ◽  
pp. 55-76 ◽  
Author(s):  
S. M. Gatesy ◽  
K. P. Dial
Keyword(s):  
Muscle Activity ◽  
High Speed ◽  
Activity Patterns ◽  
Columba Livia ◽  
Trunk Muscles ◽  
Avian Evolution ◽  
Terrestrial Locomotion ◽  
Temporal Flexibility ◽  
High Speed Cinematography ◽  
Tail Muscle

The electrical activity of major caudal muscles of the pigeon (Columba livia) was recorded during five modes of aerial and terrestrial locomotion. Tail muscle electromyograms were correlated with movement using high-speed cinematography and compared to activity in selected muscles of the wings, legs and trunk. During walking, the pectoralis and most tail muscles are normally inactive, but levator muscle activity alternates with the striding legs. In flight, caudal muscles are phasically active with each wingbeat and undergo distinct changes in electromyographic pattern between liftoff, takeoff, slow level flapping and landing modes. The temporal flexibility of tail muscle activity differs significantly from the stereotypic timing of wing muscles in pigeons performing the same flight modes. These neural programs may represent different solutions to the control of flight surfaces in the rapidly oscillating wing and the relatively stationary caudal skeleton. Birds exhibit a novel alliance of tail and forelimb use during aerial locomotion. We suggest that there is evidence of anatomical and functional decoupling of the tail from adjacent hindlimb and trunk muscles during avian evolution to facilitate its specialization for rectricial control in flight.

The Different Connections and Motor Outputs of Lateral and Medial Giant Fibres in the Crayfish

1971 ◽  
Vol 54 (2) ◽  
pp. 391-404
Author(s):  
JAMES L. LARIMER ◽  
ALAN C. EGGLESTON ◽  
LEONA M. MASUKAWA ◽  
DONALD KENNEDY
Keyword(s):  
High Speed ◽  
Motor Neurone ◽  
Giant Axons ◽  
Procion Yellow ◽  
High Speed Cinematography ◽  
Motor Neurones ◽  
Motor Outputs ◽  
Giant Fibres ◽  
Tonic System ◽  
Stimulation Of

1. High-speed cinematography was used to analyse the abdominal movements of crayfish in response to separate stimulation of medial and lateral giant axons. These films showed that the medial giant fibres command complete abdominal flexions with little flaring of the tail appendages. The lateral giants, in contrast, evoked a relatively weak flexion of the middle abdominal segments, accompanied by promotion of the exopodites of the uropods. 2. An examination of the muscles activated by the two types of giant fibres shows that differences in the connexions between the giant fibres and specific motor neurones can account for the behavioural differences observed. 3. The output of the giant fibres was determined in the sixth abdominal ganglion, where their differential effects are most pronounced. The medial giants activate motor neurones whose axons emerge from root 6 of the sixth ganglion. The lateral giants activate motor neurones whose axons emerge via roots 2 and 3, as well as those emerging via root 6. 4. The larger motor neurones associated with the giant axons in the sixth root of the sixth ganglion have been mapped by Procion Yellow injection, and the terminations of the central giant axons in the sixth ganglion have also been determined. The connexions revealed by this technique are consistent with the physiological findings. 5. The evidence suggests that root 6 of the sixth ganglion is homologous with root 3 of the more anterior ganglia. However, the giant motor neurone of the sixth ganglion has not been identified. 6. The medial and lateral giant fibres, and perhaps other specific ‘command’ interneurones, can thus drive specific ensembles of phasic motor neurones to provide a range of stereotyped quick movements. In this respect the organization of the phasic system of interneurones and motor neurones resembles that in the tonic system.

Unilateral ciliary reversal and motor responses during prey capture by the ctenophore Pleurobrachia

1985 ◽  
Vol 114 (1) ◽  
pp. 443-461 ◽  
Author(s):  
S. L. Tamm ◽  
A. G. Moss
Keyword(s):  
High Frequency ◽  
Feeding Behaviour ◽  
High Speed ◽  
Prey Capture ◽  
Reverse Direction ◽  
Motor Responses ◽  
Ciliary Reversal ◽  
High Speed Cinematography

High-speed cinematography of feeding Pleurobrachia revealed a stereo-typed sequence of ciliary motor responses underlying the feeding behaviour of this ctenophore. Prey capture by a tentacle first elicited high frequency beating in all comb rows, propelling the animal forward at a rapid speed for several seconds. This was followed by a brief period of inactivity on some or all comb rows. Then comb rows adjacent to the catching tentacle beat in the reverse direction, causing the ctenophore to spin rapidly toward this side and sweeping the prey-catching tentacle to the opened mouth, which bent towards it. After engulfing the prey, the animal slowly swam forward to re-set the relaxed tentacles as a fishing net. The patterns, timing, onset and coordination of these ciliary responses, particularly the unilateral reversal of comb rows on the catching side, are analysed with respect to possible conducting pathways mediating this behaviour.

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