Measurement of Magnetic Cavitation Driven by Heat Flow in a Plasma.

We describe the direct measurement of the expulsion of a magnetic field from a plasma driven by heat flow. Using a laser to heat a column of gas within an applied magnetic field, we isolate Nernst advection and show how it changes the field over a nanosecond timescale. Reconstruction of the magnetic field map from proton radiographs demonstrates that the field is advected by heat flow in advance of the plasma expansion with a velocity v_{N}=(6±2)×10^{5} m/s. Kinetic and extended magnetohydrodynamic simulations agree well in this regime due to the buildup of a magnetic transport barrier.

The tympanal hearing organ of the parasitoid fly Ormia ochracea (Diptera, Tachinidae, Ormiini).

Tympanate hearing has evolved in at least 6 different orders of insects, but had not been reported until recently in the Diptera. This study presents a newly discovered tympanal hearing organ, in the parasitoid tachinid fly, Ormia ochracea. The hearing organ is described in terms of external and internal morphology, cellular organization of the sensory organ and preliminary neuroanatomy of the primary auditory afferents. The ear is located on the frontal face of the prothorax, directly behind the head capsule. Conspicuously visible are a pair of thin cuticular membranes specialized for audition, the prosternal tympanal membranes. Directly attached to these membranes, within the enlarged prosternal chamber, are a pair of auditory sensory organs, the bulbae acusticae. These sensory organs are unique among all auditory organs known so far because both are contained within an unpartitioned acoustic chamber. The prosternal chamber is connected to the outside by a pair of tracheae. The cellular anatomy of the fly's scolopophorous organ was investigated by light and electron microscopy. The bulba acustica is a typical chordotonal organ and it contains approximately 70 receptor cells. It is similar to other insect sensory organs associated with tympanal ears. The similarity of the cellular organization and tympanal morphology of the ormiine ear to the ears of other tympanate insects suggests that there are potent constraints in the design features of tympanal hearing organs, which must function to detect high frequency auditory signals over long distances. Each sensory organ is innervated by a branch of the frontal nerve of the fused thoracic ganglia. The primary auditory afferents project to each of the pro-, meso-, and metathoracic neuropils. The fly's hearing organ is sexually dimorphic, whereby the tympanal membranes are larger in females and the spiracles larger in males. The dimorphism presumably reflects differences in the acoustic behavior in the two sexes.

The tympanal hearing organ of a fly: phylogenetic analysis of its morphological origins.

A key adaptation for any parasitoid insect is the sensory modality that it uses to locate its host insect. All members of the speciose family Tachinidae (Diptera) are parasitoids, but only flies of the tribe Ormiini use acoustic cues to find their hosts. Ormiine flies are parasitoids of various genera of crickets and katydids. Gravid females of one ormiine species, Ormia ochracea, hear the reproductive calling song of male field crickets and home in on those calls to locate their hosts. While many flies possess various kinds of "ears" to detect airborne sounds, only ormiine flies have been reported to possess true tympanal hearing organs. Such organs are well-known to occur in their cricket and katydid hosts. The ormiine ear is an evolutionary innovation within Diptera. Our objective was to trace the phylogenetic origins of the tympanal hearing organ among higher flies. Since the ormiine hearing organ is a complex organ within the prothorax, we examined possible precursor structures in the prothoraces of selected Diptera. We have uncovered a suite of characters that define the ormiine ear. These characters in the prothorax include a pair of prosternal tympanal membranes, a pair of chordotonal sensory organs, and modifications of the tracheal system. We have been able to identify and trace the presumptive homologs of these ormiine characters through selected species of related Diptera, using the method of outgroup comparison.

A tympanal hearing organ in scarab beetles.

We describe the paired hearing organ of the scarab beetle Euetheola humilis. The auditory structures of the beetle are typical of other insect ears in that they have a thinned tympanic membrane backed by a tracheal airsac with associated chordotonal sensory structures. The tympanic membranes of the beetle are part of its cervical membrane and are located behind the head, where the cervix attaches dorsally and laterally to the pronotum. Each membrane is approximately 3 microns thick. The chordotonal sensory organ, which lies within the tracheal airsac, contains 3-8 scolopidia that attach by accessory cells directly to the tympanic membrane. Neurophysiological recordings from the neck connective of the beetle revealed that the auditory system is sensitive to frequencies between 20 and 80 kHz and has a minimum threshold of approximately 58 dB at 45 kHz. The neurophysiological audiogram is identical to the behavioral audiogram for a head roll, one behavioral component of the beetle's startle response elicited by ultrasound. Blocking experiments show that the membranous structures on the cervix are indeed the hearing organs. Neurophysiologically determined thresholds increased by more than 35 dB when drops of water covered the tympanic membranes and were essentially restored to the control level when the water was later removed. At least three other genera of Dynastinae scarabs have similar tympanum-like structures located in their cervical membranes. Behavioral and neurophysiological data show that the frequency tuning of species in two of these genera, Cyclocephala and Dyscinetus, is nearly identical to that of E. humilis. Our discovery represents only the second group of beetles known to respond to airborne sounds. However, the hearing organs of these scarab beetles differ in structure and placement from those of the tiger beetles, and thus they represent an independent evolution of auditory organs in the Coleoptera.

Tympanal hearing in tachinid flies (Diptera, Tachinidae, Ormiini): the comparative morphology of an innovation.

Tympanal hearing organs have been reported only recently for Diptera. All the cases documented so far relate to parasitoid tachinid flies of the ormiine tribe. In the ormiine flies, the presence of tympanal hearing is functionally linked to their reproductive behavior. Indeed, female ormiine flies detect and localize their host, typically singing orthopterans, by hearing their calling songs. The three ormiine fly species investigated here at the comparative level share the key morphological features associated with tympanal hearing. The extent of these structural modifications becomes evident in the light of comparison with the closely related atympanate tachinid Myiopharus doryphorae. We document a series of eight characters that constitute specialized modifications of the ventral prothorax: (1) an inflation of the probasisternum, providing a rigid frame to span the large tympanal membranes; (2) an increased surface area of the prosternal membranes that constitute very thin, corrugated tympanal membranes; (3) a forked, broad presternum with tympanal pits to which the sensory organs directly attach; (4) several modifications of the tracheal system comprising the enlargement of the prosternal air sac, a supplementary tracheal tube to the prosternal air sac accompanied by a subpartioning of the spiracular atrium, and larger mesothoracic spiracles; (5) the presence of two scolopophorous chordotonal organs in the unpartitioned prosternal air sac; (6) stiff cuticular apodemes linking the chordotonal organs to the presternum; (7) reduction in size of the cervical sclerites; and (8) several structural modifications of the prosternal apophyses, creating new attachment sites for neck muscles. This comparative approach brings out differences and similarities of the homologous cuticular structures found on the ventral prothorax of both tympanate and atympanate tachinids. It is proposed that, given the degree of similarity between the ormiine hearing organs, the ormiine tribe is monophyletic, whereby all members of this tribe evolved from a common ancestor, an acoustic parasitoid of a singing orthopteran insect.

A dose titration study on the effect of virginiamycin on specific blood parameters and milk quality in the sow.

The present study investigates the changes in blood cholesterol and total lipids concentrations, as well as changes in milk fat, protein, lactose and total solids content of sows after the long-term administration of virginiamycin (VM) in the feed. Seventy-two (72) healthy Dalland gilts, in 18 groups of four (2 + 2) siblings were used in total. The gilts of each group of siblings were randomly allocated to one of the following four dietary treatments: VM0 = negative control, virginiamycin 0 mg/kg, VM20 = virginiamycin 20 mg/kg feed, VM40 = virginiamycin 40 mg/kg feed and VM60 = virginiamycin 60 mg/kg of feed. Treatments started at the age of 6 months covering three complete breeding cycles (up to the third weaning). The first eight groups of siblings (eight gilts per treatment/32 gilts in total) were used for blood sampling (blood group), while the remaining 10 groups of siblings (10 gilts per treatment/40 gilts in total) were used for milk sampling (milk group). Feeds given at insemination, pregnancy and lactation did not contain any other antibacterial or performance enhancer. The results indicate that all three levels of VM supplementation of gilt/sow feed influenced certain blood parameters by increasing (P < 0.05) both cholesterol and total lipids concentrations on the 30th and 60th day of each pregnancy, at each farrowing and at each weaning. The effect of dietary VM on these blood parameters remained constant throughout three consecutive parities. Moreover, the results indicate a beneficial effect of dietary VM on the milk quality of the sows during the third lactation by increasing (P < 0.05) (i) the mean fat content, (ii) the mean protein content, (iii) the mean lactose content and (iv) the mean total solids content. The highest (P < 0.05) levels in both blood and milk parameters were noticed at the inclusion level of 40 mg/kg of feed.