Homogeneous Linewidths in the Optical Spectrum of a Single Gallium Arsenide Quantum Dot

The homogeneous linewidths in the photoluminescence excitation spectrum of a single, naturally formed gallium arsenide (GaAs) quantum dot have been measured with high spatial and spectral resolution. The energies and linewidths of the homogeneous spectrum provide a new perspective on the dephasing dynamics of the exciton in a quantum-confined, solid-state system. The origins of the linewidths are discussed in terms of the dynamics of the exciton in zero dimensions, in particular, in terms of lifetime broadening through the emission or absorption of phonons and photons.     

Early Development and Putative Primordial Germ Cells Characterization in Dogs

Previously, three distinct populations of putative primordial germ cells (PGCs), namely gonocytes, intermediate cells and pre‐spermatogonia, have been described in the human foetal testis. According to our knowledge, these PGCs have not been studied in any other species. The aim of our study was to identify similar PGC populations in canine embryos. First, we develop a protocol for canine embryo isolation. Following our protocol, 15 canine embryos at 21–25 days of pregnancy were isolated by ovaryhysterectomy surgery. Our data indicate that dramatic changes occur in canine embryo development and PGCs specification between 21 to 25 days of gestation. At that moment, only two PGC populations with distinct morphology can be identified by histological analyses. Cell population 1 presented round nuclei with prominent nucleolus and a high nuclear to cytoplasm ratio, showing gonocyte morphology. Cell population 2 was often localized at the periphery of the testicular cords and presented typical features of PGC. Both germ cell populations were positively immunostained with anti‐human OCT‐4 antibody. However, at day 25, all cells of population 1 reacted positively with OCT‐4, whereas in population 2, fewer cells were positive for this marker. These two PGCs populations present morphological features similar to gonocytes and intermediate cells from human foetal testis. It is expected that a population of pre‐spermatogonia would be observed at later stages of canine foetus development. We also showed that anti‐human OCT‐4 antibody can be useful to identify canine PGC in vivo.     

A cross-sectional pilot study to estimate the prevalence of and risk factors for leptospirosis in South-Western Victorian dairy herds, 2017

Leptospirosis is a zoonosis, found worldwide, affecting many species of animals. We conducted a cross-sectional study to estimate the prevalence of Leptospira borgpetersenii sv Hardjo and Leptospira interrogans sv Pomona in cattle in dairy herds in South-Western Victoria, Australia. Fifty-three herds were enrolled in the study. Urine samples were collected from 15 late-lactation cows in each herd. A questionnaire was provided to herd managers at the time of each herd visit, asking them to describe the methods they used for controlling leptospirosis, including vaccination. Urine samples were pooled at the herd level and tested for leptospira spp. using real time PCR. Urine samples from individual cows within the positive pooled samples were then tested for Leptospira Hardjo and Leptospira Pomona using qPCR. Four of the 53 herds showed positive leptospirosis results giving an apparent prevalence of 8 (95% CI 2–18) leptospira-positive herds per 100 herds at risk. Based on the 53 completed questionnaires, leptospirosis vaccination programs were not compliant with label directions in 36 of the 52 vaccinated herds: 69 (95% CI 55–81) of 100 herd managers that routinely vaccinated for leptospirosis did not comply with label directions. One herd was completely unvaccinated. Based on our findings, we estimate that approximately 10% of dairy farms in South-Western Victoria are likely to be infected with leptospirosis. While most herds are vaccinating for leptospirosis, most are not doing so according to label directions. We conclude that herd managers need to be better educated regarding leptospirosis vaccination programs.     

Absorption by sheep of dieldrin from contaminated soil

Objective To study the accumulation of dieldrin residues in sheep from ingestion of contaminated soils was studied in two experiments.
Design A controlled feeding study of sheep fed contaminated soils of different type at varying intervals.
Animals and procedure Thirty-four 2-years-old wethers were divided into four groups (one control sheep only) and fed water-soluble dieldrin or soil contaminated with aldrin and dieldrin at varying intervals in the first study. In a second study 34 similar sheep were divided into four treatments with one being a control. Sheep were fed sandy, high clay or high organic matter soils with similar dieldrin and aldrin concentrations.
Results In the first study the concentration of dieldrin in the body fat of sheep dosed with dieldrin-contaminated soil was about half that in the body fat of sheep dosed with an equivalent amount of water-soluble dieldrin. The concentration of dieldrin was almost the same in sheep fed 500 μg of total dieldrin per day as it was in sheep fed 5000 μg every tenth day, over a 50-day period. In the second experiment sheep accumu-lated nearly three times as much pesticide from a soil with a high organic matter content, and about four times as much from a soil with a high clay content, as from a sandy soil with the same dieldrin content, over a 100-day period. The half-life of dieldrin in the fat of all sheep varied between 96 and 116 days after sheep ceased ingesting contaminated soil.
Conclusions Dieldrin concentrations in the fat of sheep that consume dieldrin contaminated soil fall within 10 days of removal from the source of contamination. However, dieidrin accumulates in the wool of sheep that consume dieldrin-contaminated soil.     

Short-term anaesthesia in piglets using a liquid injection, rebreathing, inhaler device

An economical anaesthetic technique of short duration that can be administered to piglets in the field is desirable for humanitarian reasons, for castration, tail docking or other brief procedures. Using the principles of anaesthetic uptake and distribution, an inhaler was developed to vaporize and administer isoflurane to piglets. The inhaler design consisted of a mask, vaporization chamber and a rebreathing bag. A stopcock provided access for injection of liquid isoflurane onto a wick contained in the vaporization chamber. Inspiratory and expiratory flow of air over the wick enhanced anaesthetic vaporization. The amount of liquid isoflurane required for induction and 2–3 minutes of surgical anaesthesia was calculated using the square root of time model proposed by Lowe & Ernst (1981) for liquid injection, closed circuit anaesthesia in people. Calculations were based on an assumed MAC of 1.4% and the achievement of a target alveolar concentration of 1.3 MAC to provide a surgical plane of anaesthesia. The appropriate isoflurane concentrations in the mask, inhaler, rebreathing bag and the piglet's FRC and tissues were calculated. Original calculations were based on metabolic size (BW^0.75) and then converted to weight (kg). Based on the piglet's scale weight, the total microliters of liquid isoflurane required were formulated into a table for field use. Isoflurane was injected into the inhaler stopcock followed by oxygen to fill the rebreathing bag and initiate vaporization. After the mask was placed over the piglet's nose a slide switch was activated to allow gases to move in and out of the inhaler and rebreathing bag. Fifty‐seven male piglets weighing (mean ± SD 3.0 ± 0.7 kg) and aged 7.7 ± 1.0 days were randomly selected to receive anaesthesia prior to castration. Remaining littermates served as controls for assessing morbidity or mortality. The time to induction, recovery and total anaesthetic time were measured. The Pe ′CO₂ was measured at the piglet's nostril immediately after the mask was removed at the end of the surgical procedure. Data were analysed in SAS using the Proc Mixed procedure. Inductions were rapid, 47 ± 9 seconds, generally with minimal or no resistance. The duration of surgery was 1–2 minutes. Anaesthesia was adequate and recovery was rapid, 122 ± 44 seconds. Total time from start to standing was 260 ± 51 seconds. The Pe ′CO₂ was 5.2 ± 1.1 kPa (39.4 ± 8.4 mm Hg). There was no morbidity or mortality associated with either group of piglets. After piglets were standing and mobile, they were returned to the sow and other littermates, where they immediately started nursing and were indistinguishable from littermates except by determination of ear notch number. This technique provides safe, rapid anaesthesia and recovery that is appropriate for use by veterinarians for brief field procedures.     

Interlaboratory comparison of extraction efficiency of pesticides from surface and laboratory water using solid-phase extraction disks

A continuation of an earlier interlaboratory comparison was conducted (1) to assess solid-phase extraction (SPE) using Empore disks to extract atrazine, bromacil, metolachlor, and chlorpyrifos from various water sources accompanied by different sample shipping and quantitative techniques and (2) to compare quantitative results of individual laboratories with results of one common laboratory. Three replicates of a composite surface water (SW) sample were fortified with the analytes along with three replicates of deionized water (DW). A nonfortified DW sample and a nonfortified SW sample were also extracted. All samples were extracted using Empore C(18) disks. After extraction, part of the samples were eluted and analyzed in-house. Duplicate samples were evaporated in a 2-mL vial, shipped dry to a central laboratory (SDC), redissolved, and analyzed. Overall, samples analyzed in-house had higher recoveries than SDC samples. Laboratory x analysis type and laboratory x water source interactions were significant for all four compounds. Seven laboratories participated in this interlaboratory comparison program. No differences in atrazine recoveries were observed from in-house samples analyzed by laboratories A, B, D, and G compared with the recovery of SDC samples. In-house atrazine recoveries from laboratories C and F were higher when compared with recovery from SDC samples. However, laboratory E had lower recoveries from in-house samples compared with SDC samples. For each laboratory, lower recoveries were observed for chlorpyrifos from the SDC samples compared with samples analyzed in-house. Bromacil recovery was <65% at two of the seven laboratories in the study. Bromacil recoveries for the remaining laboratories were >75%. Three laboratories showed no differences in metolachlor recovery; two laboratories had higher recoveries for samples analyzed in-house, and two other laboratories showed higher metolachlor recovery for SDC samples. Laboratory G had a higher recovery in SW for all four compounds compared with DW. Other laboratories that had significant differences in pesticide recovery between the two water sources showed higher recovery in DW than in the SW regardless of the compound. In comparison to earlier work, recovery of these compounds using SPE disks as a temporary storage matrix may be more effective than shipping dried samples in a vial. Problems with analytes such as chlorpyrifos are unavoidable, and it should not be assumed that an extraction procedure using SPE disks will be adequate for all compounds and transferrable across all chromatographic conditions.