The antenna of the final instar larva of Tenebrio molitor has three segments. The reduced third (terminal) segment bears a large trichoid sensillum, four uniporous peg sensilla, one blunt tipped peg sensillum, and one papillate sensillum. The second segment bears a very large multiporous placoid sensillum, three uniporous peg sensilla, one blunt-tipped peg sensillum, and one papillate sensillum. The numbers and arrangement of these sensilla are usually stereotyped, but variations occur.The trichoid sensillum is a long, thin, unsocketed, aporous hair. It is innervated by two (sometimes one) bipolar neurones and has five sheath cells. The three sheath cells which distally delimit the large sensillar sinus have extremely elaborate microvillate inner borders. The uniporous peg sensillum is a short, stout, socketed peg with a single terminal pore. It is innervated by two to six (usually six) bipolar neurones. The dendrite from one of these always ends as a tubular body in the base, while the dendrites from the others extend to the tip of the peg. This sensillum has a small sensillar sinus and only four sheath cells. The inner sheath cell of both types of sensilla forms a cylindrical, nonlapped sleeve around the dendrite bundles.

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Rifamycins are a class of antibiotic compounds of which rifampicin is the most commonly prescribed. Conventional electron-impact mass spectrometry of rifampicin has not been found to provide useful data. Thermospray and electrospray mass spectrometry are studied as potential tools for the analysis of rifampicin, rifamycin SV, and rifamycin B. Using thermospray and electrospray ionization, all three compounds provide significant ion intensity for either the [MH]+ or [MNa]+ ions. In addition, combined high-performance liquid chromatography-thermospray mass spectrometry provides useful analytical data for a mixture of the three rifamycins.

Efforts to restore function to the neurologically disabled lower urinary tract by direct electrical stimulation of the bladder wall have met with only very limited success. This has been due to pain and cocontraction of bladder outlet mechanisms caused by presumed spread of the large currents required to effectively directly stimulate the detrusor muscle. Stimulation at the four anatomical sites of the sacral neural outflow on the other hand has been more successful. Conus medullaris stimulation has resulted in "good results" in just over half of the 28 patients so treated. Acceptance of this technique has been limited by the poor selectivity of the intramedullary electrodes in stimulating only the target motor neurons and the resultant clinical problems with the consequent stimulus current spread. Sacral anterior root stimulation has been used in at least 88 patients with generally good results. Cocontraction of the detrusor and external urethral sphincter are circumvented by the use of an intermittent pattern of stimulation. The primary disadvantage of this technique is the obligatory placement of the electrodes within the cerebrospinal fluid compartment. Clinical experience with stimulation of the extradural sacral mixed nerves is limited. Experimental studies indicate that success with this technique requires dorsal rhizotomy and pudendal neurotomy. Preliminary clinical experience suggests that these surgical manipulations may not be necessary for a successful outcome. The literature on clinical application of pelvic nerve stimulation is too limited for detailed comment on this technique. A definitive technique for restoration of bladder function by electrical stimulation remains to be developed.

Each antenna of a final instar Tenebrio molitor larva has two blunt-tipped pegs and two papillate sensilla. The former are short pegs with fluted cuticle and a terminal moulting pore and are set in deep sockets. Two large microtubule-filled dendrites fill a dense dendritic sheath within the peg; below the base of the peg they are joined by a lamellate dendrite and a dendrite resembling a scolopidial cilium. There are four accessory cells, the innermost resembling a scolopale cell. This sensillum may be thermo- and hygro-receptive.Superficially the papillate sensillum is radially symmetrical with a central zone of small cuticular papillae surrounded by one or two rings of smooth cuticle. Three or four dendrites (of five) end under a turret of longer papillae at the center of the papillate cuticle. Fine pores from the dendritic canal extend to the surface between the papillae. One or two dendrites, one of which may be lamellate, end well below the end organ. There are five accessory cells. The sensillar and ciliary sinuses are large and the bounding membranes of the sheath cells highly elaborated. The function of this sensillum is uncertain.