Influence of carrot psyllid (Trioza apicalis) feeding or exogenous limonene or methyl jasmonate treatment on composition of carrot (Daucus carota) leaf essential oil and headspace volatiles

The effect of carrot psyllid (Trioza apicalis F?rster) feeding and limonene and methyl jasmonate (MeJA) treatments on the essential oil composition and headspace volatiles of carrot (Daucus carota ssp. sativus), cvs. Parano and Splendid, leaves was studied. Carrot psyllid feeding significantly increased the concentrations of sabinene, beta-pinene, and limonene, whereas limonene treatment increased the concentration of (Z)-beta-ocimene in the leaves of both cultivars. The limonene treatment significantly increased the concentration of total phenolics in the leaves of both cultivars, and MeJA treatment increased phenolic concentration in the leaves of Parano. Exogenous limonene spray did not decrease the number of carrot psyllid eggs laid either 2 or 24 h after treatment. The results suggest that carrot psyllid feeding induces changes in the endogenous monoterpene pool in the carrot leaves. Limonene and MeJA treatments affect some induced defenses of the carrot, but the exogenous limonene spray is not an effective oviposition deterrent against carrot psyllid.     

Evaluation of some Methods for Fish Canning Wastewater Treatment

A fish canning facility processes 1900–2000 tons of mackerel and sardine annually at arate of 10–15 tons per day for a total of 200 days yr^-1. This factory generates an average of 20 m³ of industrial wastewaters per day. The objective of our study, which was carried out on a bimonthly basisfrom December 1995 to November 1996, was to determine the overall pollutant load associated with this effluent in relation to the applicable Egyptian Standards and to propose methods for pollutant load reduction before discharging it to the local sewer. The methods were to benefit through the recovery of wasted organic load and transform it into an environmentally safe residue amenable for either immediate reuse or final disposal thereafter. Five chemical coagulation/flocculation treatments were tried using ferric chloride, alum, lime, ferric chloride and lime, and alum and lime. The best method involved the use of FeCl₃ and Ca(OH)₂ (0.4 g Fe L^-1 and 0.2 g Ca L^-1, respectively) which reduced the average influent BOD₅ from 989 to 204 mg L^-1, the COD from 1324 to 320 mg L^-1, TSS from 4485 to 206 mg L^-1, total protein content from 812 to 66 mg L^-1 and oil and grease from 320 to 66 mg L^-1. The separated dried precipitate averaged 50 g L^-1 which was found to contain 40% by weight recovered protein and 20% recovered fat. The solid was ideal for on-site reprocessing as animal feed. As well, the final effluent, if not discharged to the area sewer, was safe for controlled use in some irrigation applications or forestry projects at the desert area surrounding the factory.     

EVALUATION OF THE EXTIRPATED EQUINE EYE USING B-MODE ULTRASONOGRAPHY

B-mode ultrasonography using a 7.5 megahertz (MH^z) transducer was performed on 95 equine cadaver eyes submerged in a water bath. Identification and measurement of the anterior to posterior diameters of the intraocular structures and of the axis bulbi was done. The dorsal ventral axis of the eye was also measured. The eyes were then frozen, sectioned in a saggital plane and the same measurements were made using calipers. Two sets of measurements were then compared statistically.
With the exception of the cornea and the dorsal ventral axis measurements of male horses there was no statistically significant difference in the measurements obtained by the two methods.
The use of B-mode ultrasonography at a frequency of 7.5 MH^z to examine the architecture of the equine eye is suggested as a valuable clinical tool. Biometry of the intraocular structures at this frequency may be reasonably accurate.     

The dispersal of Culicoides brevitarsis in eastern New South Wales and associations with the occurrences of arbovirus infections in cattle

Distributions of the vector Culicoides brevitarsis Kieffer (Diptera: Ceratopogonidae) (determined from light trap data) and 2 arboviruses (determined from seroconversions in sentinel cattle) were studied in eastern New South Wales in 1993–94. C brevitarsis was recorded progressively from endemic areas on the north coast, to Nowra on the south coast, and westward to Scone, in the Hunter Valley. C brevitarsis also survived through winter at Paterson, in the Hunter Valley. Its apparently focal reappearance in this marginal area had no obvious effect on the broad pattern of its progression or the dispersal of Akabane and bluetongue viruses. These viruses were first recorded from foci near Coffs Harbour, on the mid-north coast. Their first occurrences at different locations were associated with those of C brevitarsis, but not with each other. The viruses were found only within the recorded limits of the vector's distribution. Delays between the initial occurrence of C brevitarsis and first evidence of virus transmissions at locations ranged from 2 to 7 months. The delays decreased away from the points of focus and were negatively associated with the time of initial occurrence of the vector. Seroconversions to the viruses were related to the presence of C brevitarsis. However, the densities of C brevitarsis had no apparent effect on the initial numbers of cattle seroconverting to either virus. The results support the conclusion that the progressions of C brevitarsis and Akabane and bluetongue viruses were the result of gradual movements by the vector.     

Biochemical identification of putative GABA/benzodiazepine receptors in house fly thorax muscles

[³H]Flunitrazepam ([³H]Flu) was used to identify benzodiazepine binding sites in house fly thorax muscle membranes using a filter assay. [³H]Flu bound to a finite number of sites in a concentration- and time-dependent manner, reaching equilibrium in 10 min. Scatchard plots of the binding indicated a high-affinity site at 0.2 pmol/mg protein (K_d 24.3 nM) and a low-affinity site at 8.2 pmol/mg protein (K_d994nM). Binding of [³H]Flu to the high-affinity binding site was inhibited by several benzodiazepine analogs, with Flu, diazepam, and Ro 5-4864 being more potent than β-CCE, Ro 5-3027, and Ro 5-2180. Clonazepam was least potent in inhibiting [³H]Flu binding. Thus, the drug specificity of these insect muscle benzodiazepine binding sites was quite different from both the mammalian central and peripheral benzodiazepine receptor sites, though closer to the peripheral ones. GABA (γ-aminobutyric acid) and its agonists enhanced the specific binding of [³H]Flu in a dose-dependent manner, and this effect was inhibited with the GABA antagonist bicuculline. The effect was biphasic since at high GABA concentrations this stimulation was reduced. The data suggest that house fly muscles have benzodiazepine receptors, which are coupled allosterically to GABA receptors, analogous to the GABA/benzodiazepine receptors of vertebrates, but with some differences in their drug specificities.