Phenotypic stability of resistance to late blight in potato clones evaluated at eight sites in the United States

Changes in the fungal pathogenPhytophthora infestans in the United States pose a significant threat to potato production. Sources of resistance to these new genotypes of P.infestans need to be identified for potato breeders to have parental materials for crossing, and the phenotypic stability of late blight resistance in these potato clones needs to be determined. Sixteen potato clones which reportedly have some resistance to late blight were evaluated at eight locations: Florida (FL), Maine (ME), Michigan (MI), Minnesota (MN), North Dakota (ND), New York (NY), Pennsylvania (PA) and Wisconsin (WI) in 1996. Percent infected foliage was recorded at approximately weekly intervals following the onset of the disease at each location. Area under the disease progress curve (AUDPC) was calculated. Clones were ranked for mean AUDPC within location and the nonparametric stability statistics, mean absolute rank differences and variance of the ranks, were analyzed for phenotypic stability. Neither of these statistics was significant, indicating a lack of genotype x environment interaction on the rankings of these clones across locations in 1996. The four clones with lowest AUDPC scores were U.S. clones AWN86514-2, B0692-4, B0718-3 and B0767-2. These clones should be useful parental materials for breeders seeking to incorporate genes for late blight resistance into potatoes.     

Self -Compatibility in a Diploid Hybrid Population of <Emphasis Type="Italic">Solanum phureja</Emphasis> – <Emphasis Type="Italic">S. stenotomum</Emphasis>

Recently proposals have been made in both Europe and North America to try to radically change potato breeding strategy from a tetraploid, heterozygous crop to a diploid inbred crop. As part of that effort, clones from the long-day adapted, late blight resistant diploid hybrid Solanum phureja – S. stenotomum population were selfed to begin the process of developing inbred lines. In March of 2016 and 2017, 42 diploid clones from the above-mentioned population were selfed in the greenhouse in Beltsville, MD. In 2016 and 2017, 10 and 13 clones failed to flower, respectively. Among the remaining clones, 716 pollinations were made in 2016, resulting in 57 fruit from 17 clones, and 3742 seeds; 801 pollinations were made in 2017, resulting in 34 fruit from 12 clones, and 1903 seeds. Nine clones were successfully selfed both years. Percent successful selfs was significantly higher in 2016 (7.96%) than in 2017 (4.24%). The most prolific clones in 2016 were BD1241–1 (34% successful selfs, 1090 seed), BD1218–3 (25% successful selfs, 638 seed), BD1215–1 (5% successful selfs, 411 seed), BD1243–1 (23% successful selfs, 232 seed). In contrast, the most prolific clones in 2017 were BD1230–2 (25% successful selfs, 537 seed), BD1203–3 (23% successful selfs, 391 seed), and BD1229–1 (11% successful selfs, 388 seed). These results indicate that there is sufficient self-compatibililty in this population to generate large numbers of inbred individuals, but that genotype x environment interactions are large. Attempts to generate selfed seed should be made over several years to maximize the genetic base of the selfed population.     

Australian surveillance for avian influenza viruses in wild birds between July 2005 and June 2007

Objective   To identify and gain an understanding of the influenza viruses circulating in wild birds in Australia.
Design   A total of 16,303 swabs and 3782 blood samples were collected and analysed for avian influenza (AI) viruses from 16,420 wild birds in Australia between July 2005 and June 2007. Anseriformes and Charadriiformes were primarily targeted.
Procedures   Cloacal, oropharyngeal and faecal (environmental) swabs were tested using polymerase chain reaction (PCR) for the AI type A matrix gene. Positive samples underwent virus culture and subtyping. Serum samples were analysed using a blocking enzyme-linked immunosorbent assay for influenza A virus nucleoprotein.
Results   No highly pathogenic AI viruses were identified. However, 164 PCR tests were positive for the AI type A matrix gene, 46 of which were identified to subtype. A total of five viruses were isolated, three of which had a corresponding positive PCR and subtype identification (H3N8, H4N6, H7N6). Low pathogenic AI H5 and/or H7 was present in wild birds in New South Wales, Tasmania, Victoria and Western Australia. Antibodies to influenza A were also detected in 15.0% of the birds sampled.
Conclusions   Although low pathogenic AI virus subtypes are currently circulating in Australia, their prevalence is low (1.0% positive PCR). Surveillance activities for AI in wild birds should be continued to provide further epidemiological information about circulating viruses and to identify any changes in subtype prevalence.     

Competitive and noncompetitive adsorption of silicate and phosphate by two acid Si-deficient soils and their effects on P and Si extractability

The effects of pH on the adsorption of silicate and phosphate, either singly or in competition, by two acid soils were investigated. Both soils adsorbed two to three times more P than Si and adsorption isotherms at pH 5.0, 5.5, 6.0 and 6.5 showed that increasing pH greatly increased Si adsorption but decreased that of P. Silicate adsorption was very low below pH 5.0, increased rapidly up to pH 9–10 before decreasing again. Adsorption of P was at a maximum at pH 2.0, decreased slowly up to pH 7.0 and then more rapidly above pH 7.0. When Si and P were added at equimolar concentrations, the presence of P decreased Si adsorption between pH 6.0 and 8.0 while the presence of Si decreased P adsorption in the pH region 6.0 and 11. Addition of calcium silicate at rates equivalent to 300, 600 and 1200 kg Si ha^?1 resulted in a progressive increase in soil pH. Separate samples of soil were treated with Ca(OH)₂ to give the same pH values so that the effect of Si could be identified. The highest rate of Si (1200 kg ha^?1 which gave a pH of 6.5) caused a significant decrease in P adsorption (as determined by adsorption isotherms) and an increase in resin-extractable P but the lower rates had little effect. Addition of P to the soil as calcium phosphate at rates equivalent to 30, 60 and 100 kg P ha^?1 all caused a decrease in Si adsorption capacity and an increase in CaCl₂-extractable Si. It was concluded that the strategy of adding Si to lower P requirements in acid soils is not likely to be effective while addition of fertilizer P may well lower Si adsorption and promote Si desorption and its increased mobility.     

Evaluation of chlorfenapyr for control of the bed bug,Cimex lectularius L.

BACKGROUND: The presence of bed bug populations resistant to pyrethroids demands the development of new control tactics, including the use of insecticides with new modes of action. Insecticides that disrupt oxidative phosphorylation in insect mitochondria can be an option. Laboratory assays were used to measure the toxicity of chlorfenapyr to susceptible strains and two strains highly resistant to pyrethroids. The effectiveness of two chlorfenapyr‐based formulations was compared, and behavioral responses of bed bugs to dry residues of aerosol sprays were evaluated. RESULTS: Chlorfenapyr was effective against all bed bug strains, killing them at a similar rate, regardless of their susceptibility status to pyrethroids. Dry residues aged for 4 months were as toxic as fresh dry residues. The aerosol formulation had contact activity and caused faster mortality than a water‐based formulation. Bed bugs did not avoid resting on surfaces treated with aerosol. CONCLUSION: Chlorfenapyr is an option for controlling pyrethroid‐resistant bed bugs. While it does not cause quick knockdown, its long residual activity and no avoidance behavior of bed bugs to dry residues appear to make this insecticide suitable for bed bug control. A faster insecticidal effect is obtained with the aerosol formulation, suggesting greater bioavailablity of the toxicant. Copyright © 2010 Society of Chemical Industry     

Nasopharyngeal trichobezoar foreign body in a cat

CASE SUMMARY: A 5-year-old male neutered indoor cat presented for evaluation and treatment of an acute onset of nasal discharge and open-mouth breathing of 3 days' duration. He had been treated for asthma prior to presentation, but his clinical signs were more consistent with upper airway disease. Thoracic radiographs were suggestive of asthma. However, a soft tissue mass was noted in the nasopharynx on a lateral cervical radiograph. Nasopharyngeal examination revealed the mass to be a trichobezoar (hair ball) lodged in the nasopharynx, removal of which led to resolution of clinical signs. The cat re-presented with a second nasopharyngeal trichobezoar approximately 1 year later, which was also successfully removed. CLINICAL SIGNIFICANCE: Nasopharyngeal disease has myriad potential infectious, inflammatory and neoplastic etiologies. However, simpler causes such as foreign bodies can be considered in cases of acute-onset nasopharyngeal disease. To the authors' knowledge, this is the first reported case of a nasopharyngeal trichobezoar foreign body in a cat.