Parasitoid-induced mortality of house fly pupae by Pteromalid wasps in the laboratory

House fly, Musca domestica L., pupae were exposed to six species of pteromalid parasitoids, Muscidifurax zaraptor Kogan and Legner, M. raptor Girault and Sanders, M. raptorellus Kogan and Legner, Pachycrepoideus vindemiae (Rondani), Spalangia nigroaenea Curtis, and Urolepis rufipes Ashmead. Exposures were made for 48 h at six parasitoid-to-host ratios to measure the effect of parasitoid density on parasitoid-induced mortality (PIM) of hosts (excluding mortality as measured by parasitoid emergence). PIM was evident at all parasitoid-to-host ratios for all six species. Fly eclosion declined with a corresponding increase in the parasitoid-to-host ratio; the reverse was generally true for PIM. Parasitoid emergence increased initially with a corresponding increase in the parasitoid-to-host ratio to a point (depending on the parasitoid species), but then declined. The three Muscidifurax spp. and P. vindemiae exhibited similar behavior and generally avoided previously stung hosts until ovipositional restraints broke down at the higher parasitoid-to-host ratios. S. nigroaenea and U. rufipes exhibited little ovipositional restraint, resulting in a high proportion of PIM of hosts. Understanding factors that influence PIM will provide better evaluations of field releases of parasitoids to control flies and will aid in the development of the most economic procedures for large scale rearing of pteromalid parasitoids.     

Maximum airflow through the nose in humans

Inspiratory and expiratory flow via the nose and via the mouth during maximum-effort vital capacity (VC) maneuvers have been compared in 10 healthy subjects. Under baseline conditions maximum flow via the nose was lower than that via the mouth in the upper 50-60% of the VC on expiration and throughout the VC on inspiration. The mean ratio of maximum inspiratory to maximum expiratory flow at mid-VC was 1.38 during mouth breathing and 0.62 during nasal breathing. Inspiratory flow limitation with no increase in flow through the nose as driving pressure was increased above a critical value (usually between 12 and 30 cmH2O) was found in all six subjects studied. Stenting the alae nasi in seven subjects increased peak flow via the nose from a mean of 3.49 to 4.32 l/s on inspiration and from 4.83 to 5.61 l/s on expiration. Topical application of an alpha-adrenergic agonist in seven subjects increased mean peak nasal flow on inspiration from 3.25 to 3.89 l/s and on expiration from 5.03 to 7.09 l/s. Further increases in peak flow occurred with subsequent alan stenting. With the combination of stenting and topical mucosal vasoconstriction, nasal peak flow on expiration reached 81% and, on inspiration, 79% of corresponding peak flows via the mouth. The results demonstrate that narrowing of the alar vestibule and the state of the mucosal vasculature both influence maximum flow through the nose; under optimal conditions, nasal flow capacity is close to that via the mouth.     

Factors in acid treated bagasse inhibiting ethanol production from d-xylose by Pachysolen tannophilus

The fermentation of d-xylose, the major sugar-cane bagasse hemicellulose component, to ethanol by Pachysolen tannophilus is inhibited by various factors produced or released during the acid hydrolysis of the bagasse or during the fermentation process. These include ethanol, iron, chromium, copper, nickel, acetic acid and furfural. Ethanol production by P. tannophilus is inhibited by ethanol fconcentrations >24 g l^?1. Furfural and acetic acid concentrations as low as 0.3 and 7 g l^?1, respectively, and iron, chromium, nickel and copper at concentrations of 0.07, 0.01, 0.01 and 0.004 g l^?1, respectively. Similar concentrations may be found in acid-hydrolysed bagasse. The removal of these factors by treatment with ion-exchange resin resulted in the fermentation of the sugars to ethanol. The d-glucose was used rapidly and completely whereas d-xylose utilization was slow and incomplete. An ethanol concentration of 4.1 g l^?1 was produced and an ethanol yield of 0.32 was obtained. Xylitol in significant amounts was produced.     

Genetic and molecular characterization of the Pseudomonas plasmid pVS1

A restriction map of the 30-kb nonconjugative Pseudomonas plasmid pVS1 was constructed. Derivatives of pVS1 obtained in vitro by successive deletions were used to localize on the physical map the determinant for resistance to mercuric ions (carried by transposon Tn501), the gene(s) encoding sulfonamide resistance, a 1.6-kb region affecting plasmid stability and establishment in P. fluorescens ATCC 13525, and a segment required for mobilization of pVS1 by plasmid RP1. The sulfonamide resistance determinant of pVS1 appeared to be closely related to that of transposon Tn21. A mini-pVS1 replicon, pME259, consisting of an essential 1.55-kb segment (designated rep and thought to carry the origin of replication) and a mercury resistance determinant was able to replicate P. aeruginosa PAO but selective pressure was needed for plasmid maintenance. The copy number of pVS1 derivatives was estimated to be 6-8 per chromosome equivalent. Plasmids possessing the essential rep segment plus the adjacent stability region could be established in strains of P. aeruginosa, P. putida, P. fluorescens, P. acidovorans, P. cepacia, P. mendocina, P. stutzeri, P. syringae, Agrobacterium tumefaciens, and Rhizobium leguminosarum.     

Self cleavage of a precursor RNA from bacteriophage T4

We found that a precursor of an RNA molecule from T4-infected Escherichia coli cells (p2Spl; precursor of species 1) has the capacity to cleave itself in a specific position. This cleavage is similar to a cleavage carried out by the aid of a protein, RNase F, that has been previously identified. This cleavage could lead to the maturation of an RNA (species 1) found in T4-infected E. coli cells. The reaction is time and temperature-dependent and is relatively slow as compared to the protein-dependent reaction. It requires at least a monovalent cation and is aided by non-ionic detergents. In the absence of detergent the cleavage can occur but at a reduced rate. The substrate does not contain hidden nicks and a variety of experiments suggest that it does not contain a protein. Moreover, we found no indication that the cleavage is due to contaminating nucleases in the substrate or in the reagents. The intact secondary and tertiary structures of the molecule are necessary for the cleavage to occur. The finding of a self cleaving RNA molecule has interesting evolutionary implications.     

Oscillatory mechanics of the respiratory system in ozone-exposed rats

The respiratory system impedance of tracheostomized cardiorespiratory disease-free Sprague-Dawley rats was measured from 20 to 90 Hz at constant flow amplitudes in 10 rats exposed to 0.64 ppm (UV) ozone for 7 days, and eight rats exposed to the same level of ozone for 20 days. This data was compared with respiratory system impedence spectra of 24 normal rats obtained in the same manner. When compared with control, the real part (effective resistance) was significantly different at several frequencies in the 7-day group (P less than 0.05), and group means were higher at all frequencies. The 20-day group showed no significant differences in effective resistance. The imaginary part (effective reactance) was significantly lower at higher frequencies (f greater than 36) in both exposure groups (P less than 0.05). When the impedance curves for each individual were fit to a lumped six-parameter model, and the parameters were compared, only the peripheral resistance parameter of the 7-day group was significantly different from control (P less than 0.05). We conclude that ozone exposure at this level causes changes in respiratory system impedance, that these changes consist primarily of decreased reactances at higher frequencies, and that at 7 days these changes can be modeled by an increase in peripheral resistance.     

Voluntary hyperventilation changes recruitment order of parasternal intercostal motor units

The order of recruitment of single-motor units in parasternal intercostal muscles during inspiration was studied in normal human subjects during quiet breathing and voluntary hyperventilation. Electromyograms were recorded from the second and third intercostal spaces by means of bipolar fine wire electrodes. Flow at the mouth, volume, end-expired CO2, and rib cage and abdominal anterior-posterior diameters were monitored. Single-motor units were identified using criteria of amplitude and shape, and the time of first appearance of each unit in each inspiration was noted. Hyperventilation was performed with visual feedback of the display of rib cage and abdomen excursions, keeping the ratio of rib cage to abdominal expansion. Subjects were normocapnic in quiet breathing and developed hypocapnia during hyperventilation. Recruitment order was stable in quiet breathing, but in some cases was altered during voluntary hyperventilation. Some low threshold units that fired early in the breath in quiet breathing fired earlier at the beginning of a period of voluntary hyperventilation but progressively later in the breath as hyperventilation went on, whereas later firing units moved progressively toward the early part of inspiration. This suggests that different groups of motoneurons in the pool supplying parasternal intercostal muscles receive different patterns of synaptic input.     

Microinjection of transforming ras protein induces c-fos expression.

Microinjection of p21ras induced c-fos protein accumulation in three types of 3T3 cells. The induction was rapid and efficient and persisted for many hours. In addition, anti-ras antibody dramatically reduced c-fos accumulation after serum stimulation of injected cells. However, cells which expressed p21ras continuously did not maintain a high level of c-fos expression.     

The distribution of GABA-like immunoreactivity in relation to ganglion structure in the abdominal nerve cord of the locust (Schistocerca gregaria)

Summary An antiserum raised against GABA was used to stain the abdominal nervous system of the locust. To interpret the results, however, it was first necessary to describe the structure of the free abdominal and terminal ganglia. This was done on the basis of ethyl-gallate staining. The free abdominal ganglia are similar in structure to the abdominal neuromeres of the metathoracic ganglia. The terminal ganglion is composed of four neuromeres (representing ganglia 8–11), but only three can be distinguished in the adult on morphological grounds. The eighth neuromere resembles the free ganglia, but the ninth lacks DCI (dorsal commissure I) and the T tracts. In the tenth, only DCII and III are recognisable of the commissures, but two more posterior ones of uncertain homology are also present. Immunocytochemistry reveals three populations of somata in each abdominal ganglion. Of these only one, the medial posterior group, is found in the thoracic ganglia. DCIV and the supra-median commissure are composed of stained neurites, DCII and V contain both unstained neurites and DCI, III and VI are unstained. With the exception of the median ventral tract, all the longitudinal tracts contain some stained axons.     

Selective catalysis of A.T base pair proton exchange in DNA complexes: imino proton NMR analysis.

Polyaromatic molecules with amino chain substituents, upon binding with DNA, selectively catalyze exchange of the A.T base pair protons with bulk water protons. The amine-catalyzed exchange is mediated by compounds which are A.T and G.C base sequence specific, intercalators, and outside binders. A mechanism for the selective exchange, involving transient opening and closing of individual A.T base pairs in the duplex, is discussed.