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Notes: Near-field scanning optical microscopy (NSOM) and electron probe microanalysis (EPMA) were used to study the topographic and microscopic optical properties of indium–gallium–phosphide (In1−xGaxP) samples grown by liquid phase epitaxy on gallium–arsenide substrates. NSOM imaging found strong and highly localized variations in the photoluminescence (PL) intensity for samples that were highly lattice mismatched with the substrate. The topography and optical features were roughly spatially correlated for these samples. Shifts in the PL peak energy position (by as much as 27 meV) were found during scans across highly mismatched samples, whereas no shifts were seen for In1−xGaxP films with a nearly lattice matched composition. Compositional fluctuations were determined to be the cause of these PL peak energy shifts. EPMA provided corroborating evidence that compositional fluctuations are spatially correlated with the topography. These composition fluctuations arise from the known solid–solid miscibility gap in the In1−xGaxP system at temperatures used for the growth of these samples. © 2002 American Institute of Physics.

Notes: The surface chemistry and electronic properties of n-GaN surfaces were studied via x-ray photoemission spectroscopy before and after wet chemical treatments. Shifts of the surface Fermi level were measured with the change in position of the Ga 3d core level peak. HCl treatment of n-GaN led to a 0.9 eV shift of the surface Fermi level toward the conduction band minimum, while KOH treatment led to a 0.3 eV shift of the surface Fermi level toward the valance band maximum. These shifts lead to a reduction in the surface barrier for HCl-treated n-GaN and for KOH-treated p-GaN, potentially improving contact resistance. The changes in surface chemistry indicate that a N (or Ga) deficiency with HCl(KOH) treatment alters the surface state density through the formation of donor (acceptor)-like states. © 2002 American Institute of Physics.

Notes: A near-field scanning optical microscope (NSOM) was developed to perform photoreflectance (PR) spectroscopy experiments at high spatial resolution (∼1 μm). Representative PR spectra are shown, along with an image illustrating the capability of observing contrast in images due to the strength of a PR feature. It was found that sufficiently high intensity light from the NSOM tip can produce photovoltages large enough to limit the spatial resolution of the electric field determination by PR. The photovoltage effect is measured as a function of light intensity, and the results are discussed in terms of a simple photovoltage expression. © 2000 American Institute of Physics.

Notes: Over 18 months after infectious pancreatic necrosis virus (IPNV) was first detected in fish (80 g–4 kg) on a halibut farm, the stocks were found to be still carrying the virus. This suggests that long-term persistence of IPNV occurs in farmed Atlantic halibut. A non-destructive test was applied to blood adherent leucocytes by placing 100 μL of whole blood collected in a heparinized tube into 96-well plates. After overnight incubation, the non-adherent cells were washed off, the remaining adherent cells lysed in a lysis buffer and inoculated onto CHSE-214 cells. The resulting cytopathic effect was confirmed as IPNV positive by enzyme-linked immunosorbent assay. In a sample of 10 fish tested by this method, all were positive for IPNV while only two were positive by the standard method for virus culture from sonicated kidney homogenates and only one fish, which was positive by the standard method, was positive by reverse transcription polymerase chain reaction on kidney tissue. The test on blood leucocytes is shown to be simple to perform on samples taken under field conditions.

Notes: In populations of Atlantic salmon in sea water, infectious pancreatic necrosis virus (IPNV) could be detected by standard virological culture methods in sonicated kidney homogenates and in mucus samples (gill, skin and rectum) from 14 and nine of 25 fish, respectively, but all fish were positive by virus culture from lysates of kidney macrophages and adherent blood leucocytes. In fish which tested negative for IPNV by the standard method of detection, the virus could be detected using adherent blood leucocytes isolated on a Percoll gradient from as little as 10 μL of blood. The blood sample could be stored for at least 3 days in a heparinized tube on ice before preparing the plastic adherent leucocytes. Furthermore, the latter could be prepared without prior fractionation on Percoll simply by incubating whole blood (33 μL) in cell culture medium (66 μL) in 96-well plates overnight and washing away the non-adherent cells before lysing the adherent cells and inoculation of the lysate onto CHSE-214 cells. This highly sensitive method for detecting IPNV-carriers is therefore very suitable for non-destructive sampling of fish in the field.

Notes: Atlantic salmon smolts, previously unexposed to infectious pancreatic necrosis virus (IPNV), were placed into tanks of sea water at 10 °C. After 4 weeks, 40 fish were injected intraperitoneally (i.p.) with homogenized and filter-sterilized kidney material obtained from salmon with clinical IPN in a marine farm in Shetland. The injected fish were cohabited with 40 untreated fish. Mortalities began in the injected fish on day 7 and reached a peak of 48% on day 14. In the cohabitation group, mortalities began on day 14 and reached a peak of 70% on day 27. The IPNV in the Shetland kidney homogenate was cultured in Chinook salmon embryo (CHSE) cells and passed twice. This cultured virus was injected i.p. into fish at various doses ranging from 10 to 107 TCID50 fish−1 4 weeks after seawater transfer. Challenge tanks contained 30 injected fish and 30 cohabitees. Mortality rates and levels were dose-dependent. The highest dose used resulted in a similar mortality pattern as obtained with a similar dose of the Shetland kidney homogenate, indicating that virulence was retained after two passes in tissue culture. Even with the lowest dose, mortality reached 12% in the injected group and 23% in the cohabitees. The IPNV titres were high (106−109 i.u. g−1 kidney) in fish which died during the experiment and low (〈105 i.u. g−1 kidney) or undetectable in surviving fish. The cultured virus (pass 3) was used in a challenge model where the population density of fish in the tanks was high (50 injected and 50 cohabitees) or low (15 injected and 15 cohabitees). In the high stocking density tank, mortalities peaked at about 35% in the injected group and at 52% in the cohabitees. In the low stocking density tank, mortalities peaked at about 40% in the injected fish but no mortality occurred in the cohabitees. However, IPNV was detected (up to 104 i.u. g−1 kidney) in 82% of cohabitees sampled on day 30. These data suggest that lethal lateral transmission of the virus is dependent on the infectious pressure from the injected group. A further trial was conducted to investigate the effect of time post-seawater transfer on the susceptibility of post-smolts to IPN. Groups of fish were challenged every 2 weeks from week 0–10. Few mortalities occurred at week 0 and virus titres were high in these fish. Most survivors became carriers, some with titres 〉106 i.u. IPNV g−1 kidney. From 2 to 10 weeks after seawater transfer, mortalities in both injected and cohabitees were substantial with viral titres 〉107 i.u. g−1 kidney. Survivors had lower titres and in many virus was undetectable. Throughout the experiments, moribund fish were sampled for histology and all showed typical IPN histopathology.

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