Equine neural angiostrongylosis

Verminous encephalomyelitis due to Angiostrongylus cantonensis larvae was diagnosed in 2 foals at necropsy. The principal clinical feature was tetraparesis, although history and neurological examination revealed progressive and multifocal neurological disease. At presentation, a tentative diagnosis of parasitic larval migration involving the central nervous system (CNS), presumably due to Strongylus vulgaris, was proposed. Dissection of the spinal cord in one case resulted in recovery of intact larvae of both sexes of A. cantonensis. In both foals, histopathology of the brain and spinal cord revealed nematode sections which were consistent with A. cantonensis larvae.     

A survey of slaughter procedures used in chicken processing plants

Information was collected on the slaughter procedures used in 12 processing plants in Australia. The processing line speed varied from 25 to 125 birds/minute; the voltage in the electrified waterbath varied from 55 to 165 V; the duration of stunning was 2.0 to 7.5 seconds and the time allowed for exsanguination was 45 to 180 seconds. As a result of the variables, some birds were dead on leaving the stunner and prior to exsanguination, while it was probable that others were not dead before entering the scald tank.     

Determination of Venus Winds by Ground-Based Radio Tracking of the VEGA Balloons

A global array of 20 radio observatories was used to measure the three-dimensional position and velocity of the two meteorological balloons that were injected into the equatorial region of the Venus atmosphere near Venus midnight by the VEGA spacecraft on 11 and 15 June 1985. Initial analysis of only radial velocities indicates that each balloon was blown westward about 11,500 kilometers (8,000 kilometers on the night side) by zonal winds with a mean speed of about 70 meters per second. Excursions of the data from a model of constant zonal velocity were generally less than 3 meters per second; however, a much larger variation was evident near the end of the flight of the second balloon. Consistent systematic trends in the residuals for both balloons indicate the possibility of a solar-fixed atmospheric feature. Rapid variations in balloon velocity were often detected within a single transmission (330 seconds); however, they may represent not only atmospheric motions but also self-induced aerodynamic motions of the balloon.     

Rapid Identification of Helicoverpa armigera and Helicoverpa zea (Lepidoptera: Noctuidae) Using Ribosomal RNA Internal Transcribed Spacer 1

Rapid identification of invasive species is crucial for deploying management strategies to prevent establishment. Recent Helicoverpa armigera (Hübner) invasions and subsequent establishment in South America has increased the risk of this species invading North America. Morphological similarities make differentiation of H. armigera from the native Helicoverpa zea (Boddie) difficult. Characteristics of adult male genitalia and nucleotide sequence differences in mitochondrial DNA are two of the currently available methods to differentiate these two species. However, current methods are likely too slow to be employed as rapid detection methods. In this study, conserved differences in the internal transcribed spacer 1 (ITS1) of the ribosomal RNA genes were used to develop species-specific oligonucleotide primers that amplified ITS1 fragments of 147 and 334 bp from H. armigera and H. zea, respectively. An amplicon (83 bp) from a conserved region of 18S ribosomal RNA subunit served as a positive control. Melting temperature differences in ITS1 amplicons yielded species-specific dissociation curves that could be used in high resolution melt analysis to differentiate the two Helicoverpa species. In addition, a rapid and inexpensive procedure for obtaining amplifiable genomic DNA from a small amount of tissue was identified. Under optimal conditions, the process was able to detect DNA from one H. armigera leg in a pool of 25 legs. The high resolution melt analysis combined with rapid DNA extraction could be used as an inexpensive method to genetically differentiate large numbers of H. armigera and H. zea using readily available reagents.     

Development and validation of a quantitative PCR to detect Parvicapsula minibicornis and comparison to histologically ranked infection of juvenile Chinook salmon, Oncorhynchus tshawytscha (Walbaum), from the Klamath River, USA

Parvicapsula minibicornis is a myxosporean parasite that is associated with disease in Pacific salmon during their freshwater life history phase. This study reports the development of a quantitative (real-time) polymerase chain reaction (QPCR) to detect P. minibicornis DNA. The QPCR assay targets the 18S ribosomal subunit gene. A plasmid DNA control was developed to calibrate cycle threshold ( C _T) score to plasmid molecular equivalent (PME) units, a measure of gene copy number. Assay validation revealed that the QPCR was sensitive and able to detect 50 ag of plasmid DNA, which was equivalent to 12.5 PME. The QPCR assay could detect single P. minibicornis actinospores well above assay sensitivity, indicating a single spore contains at least 100 times the 18S DNA copies required for detection. The QPCR assay was repeatable and highly specific; no detectable amplification was observed using DNA from related myxozoan parasites. The method was validated using kidney tissues from 218 juvenile Chinook salmon sampled during the emigration period of March to July 2005 from the Klamath River. The QPCR assay was compared with histological examination. The QPCR assay detected P. minibicornis infection in 88.1% of the fish sampled, while histological examination detected infection in 71.1% of the fish sampled. Good concordance was found between the methods as 80% of the samples were in agreement. The majority of the disconcordant fish were positive by QPCR, with low levels of P. minibicornis DNA, but negative by histology. The majority of the fish rated histologically as having subclinical or clinical infections had high QPCR levels. The results of this study demonstrate that QPCR is a sensitive quantitative tool for evaluating P. minibicornis infection in fish health monitoring studies.     

Contribution of Biological Control to Integrated Pest Management of Tephritid Fruit Flies in the Tropics and Subtropics

The biological control of pest tephritid flies using parasitoids has been successful in relatively few subtropical and tropical regions. The best documented successes were in Hawaii and Florida, USA, Fiji and southern Europe. There were relatively limited successes in Australia, Costa Rica and Mexico. With the accidental establishment of new pest tephritids, such as Bactrocera latifrons (Hendel) in Hawaii or Bactrocera papayae Drew and Hancock in Australia, foreign exploration for new parasitoids is essential. A renewal of interest in classical biological control has recently occurred, although not at the same level as in the 1940s and 1950s. New parasitoid species are currently being obtained for several tephritids, such as Ceratitis capitata (Weidemann), B. latifrons and Anastrepha suspensa (Loew). The advances in mass rearing and quality control technology for parasitoids has enabled researchers to perform large-scale field testing of these parasitoids to determine the potential of augmentative releases. Numerous studies on the augmentative release of parasitoids have been done. Historically, the larval—pupal parasitoid Diachasmimorpha longicaudata (Ashmead) has been the most frequently studied parasitoid, due to the ease of rearing this species. However, recent successes in rearing other species with different biologies, e.g. the egg—pupal parasitoid Biosteres arisanus (Sonan), the gregarious eulophid, Tetrastichus giffardianus (Silvestri) and the pupal parasitoid, Coptera sp., will enable researchers to broaden the repertoire of parasitoid species for the future. Both successes and failures in augmentative releases have occurred. Without knowledge of the behavioural ecology of parasitoids, the reasons for success or failure can only be surmised. Recent research on the dispersal and host habitat finding of tephritid parasitoids will provide insights into improving augmentation and conservation strategies. The integrated pest management (IPM) of tephritid flies in the tropics has been less well-developed than research and programmes for tephritids in temperate zones. Significant emphasis is now being placed on the development of quarantine treatment methods that are environmentally sound; thus IPM will take a larger role. Several existing pest management strategies are reviewed which show the potential for compatibility with the activities of tephritid parasitoids. These include trap cropping, insecticides with selective toxicity to the target pests, mass trapping with parapheromones, the sterile insect technique and field sanitation.     

Soil property predictors of soybean yield using yield contest sites

State yield contests offer a unique opportunity to examine the high end of crop productivity. Yield-contest-entered and average-yielding areas on the same or a similar soil can provide large yield and soil property variations to better examine the relationships among various near-surface soil properties and soybean (Glycine max L. [Merr.]) yield. The objective of this study was to evaluate the relationships among a suite of near-surface soil properties and soybean yield across average- and high-yield areas using state yield-contest sites. Multiple regression analyses were conducted to evaluate best-fit relationships among various soil physical, chemical, and biological properties and yield separately for average- and high-yielding areas and for data combined across yield areas. Soybean yield variation was most explained for the high-yield-area dataset (R² = 73%) and less explained for the average-yield-area (R² = 51%) and the combined (R² = 50%) datasets. Extractable soil Ca and S explained the largest proportion of yield variation (37% and 31% of total sum of squares) in the high-yield setting and both were inversely related to yield. A better understanding of the soil environment may be a key component of more frequent attainment of the 6270 kg ha^?1 (100 bu acre^?1) soybean yield mark. Additional soil properties, beyond those evaluated in this study, may need to be included for a more complete understanding of the soil environment that is associated with high-yield soybean production.