Biological effects and metabolism of fenoxycarb after treatment of the fourth and the fifth instars of the tobacco budworm,Heliothis virescens F.

Treatment of 4th and 5th instar larvae of Heliothis virescens with different amounts of fenoxycarb induced an increase in weight of the 5th larval instar, prolongation of the 5th larval instar period, or the formation of dauer larvae. No effects were observed during the 4th instar and the moult to the 5th larval instar. To check whether these effects were due to persistence of fenoxycarb in treated larvae, metabolism of this chemical was analysed. Larvae were fed with radio-labelled fenoxycarb at the first day of the 4th or at the first day of the 5th larval instar. Behaviour of the radio-labelled compounds was followed during each instar. At the time of gut purge, the whole of the radio-labelled material was excreted. The effects observed during the 5th instar of 4th-instar-treated larvae do not appear to be due to the persistence of fenoxycarb. The main metabolites of fenoxycarb were identified using coupled gas chromatography and mass spectrometry.     

Uptake and utilisation of phosphonate ions by Phytophthora citrophthora and Nectria haematococca in relation to their selective toxicity

Phosphonate ions, which are degradation products of aluminium tris-O-ethyl phosphonate (fosetyl-aluminium) in plant tissues, had more effect in vitro against Phytophthora citrophthora than against Nectria haematococca. Both fungi were able to take up phosphonate ions. This uptake was realised against a concentration gradient and was affected by metabolic inhibitors. When examined over a 0.5 to 6.0 mm concentration range, phosphonate was carried by a single transport process obeying Michaelis-Menten kinetics, with a low affinity (high K′_m). Further analysis by means of Hofstee plots indicated a somewhat faster phosphonate uptake by N. haematococca than by P. citrophthora, so it appears clearly that uptake was not involved in the selective toxicity of this compound. The continuous uptake of phosphonate by N. haematococca is correlated with an important utilisation of this ion by the fungal cells. This fact could be explained by a detoxification process corresponding to the oxidation of phosphonate to phosphate which could account for the low sensitivity of this fungus. Phosphonate uptake by P. citrophthora reached a maximum level after 20 min and then decreased to a constant level over the following period. During the incubation period phosphonate was incorporated directly without oxidation into phosphate. This incorporation could lead to a disturbance of the cell metabolism.     

Distribution of glyphosate and of its target enzyme inside wheat plants

Enolpyruvylshikimate phosphate (EPSP) synthase activity has been measured in different organs of 1–14-day-old wheat seedlings growing in culture chambers. Enzyme activity was first detected after two days, and reached its maximum value at day 4. It remained almost unchanged for 14 days thereafter. During germination, one of the most important sources of enzyme was the seed scutellum. Later, the developed leaves contained 43% of the whole stock of enzyme. Although the enzyme distribution was not identical under light or in the dark, there was no evident light induction of EPSP synthase. High enzyme activity was found in the coleoptile, continuing for the whole life-time of this organ, and which might be associated with its lignification. Five to 40% of the total enzyme was found in the roots, reaching a maximum at 14 days. At this stage, glyphosate applied to the first grown leaf was phloem-transported to the sink organs, with no clear relationship being shown between EPSP synthase activity and herbicide quantity in each organ. At day 4, glyphosate treatment, by soaking the seedlings in the herbicide solution, was followed by an active phloem transport from the scutellum to the growing parts. The average internal concentration of radiolabelled compounds (glyphosate plus its possible derivatives) which induced wheat seedling growth decrease, was shown to reach 50 to 100 μM under our conditions.     

The Role of the Bark Beetle, Hylastes ater (Coleoptera: Scolytidae), as a Sapstain Fungi Vector to Pinus radiata Seedlings: A Crisis for the New Zealand Forestry Industry?

The role of the bark beetle Hylastes ater in the re-establishment of Pinus radiata forest in New Zealand is discussed. H. ater was found to be a dominant factor in seedlings mortality in the first year following planting. However, seedling mortality is usually relatively low. In contrast, it was found the large numbers of seedlings were sub-lethally damaged by H. ater feeding attempts, particularly in high risk sites. High risk sites were identified as sites that were harvested during March and April (autumn) when the peak flight activity of H. ater occurred, and subsequently planted with P. radiata seedlings the following winter. H. ater was found to vector sapstain fungi to seedlings during feeding attempts, and a strong relationship between the severity of damage and presence of sapstain fungi was identified. The role of H. ater as a vector of these fungi and the potential implications to the New Zealand forest industry are discussed.     

Evaluation of PCR,IEF and ELISA techniques for the detection and identification of potato cyst nematodes from field soil samples in England and Wales

Effective management of potato cyst nematodes (PCNs) requires simple, rapid and accurate identification and quantification of field populations. Soil samples from a survey of 484 fields in potato rotations in England and Wales were used to compare the identification and quantification of PCNs using IEF, PCR, ELISA and bait plant tests. The cyst counts and bait plant test revealed that 64.3% of field samples contained PCNs. Bait plant tests increased the detection rate of PCNs in field samples by 4–6.4%. This means that some infestations are cryptic and would not normally be detected by standard counts. IEF, PCR and ELISA methods distinguished between Globodera rostochiensis and G pallida and were able to register mixed populations; however they were not in full agreement. All methods suggested that G pallida is the dominant species in the field samples tested. The PCR results indicated that 66% of field samples contained pure G pallida, 8% contained pure G rostochiensis and 26% contained mixtures of the two species. Estimates of the relative process times taken per sample in the PCR, IEF and ELISA techniques are given. © 2001 Society of Chemical Industry     

Evaluation of Protein Quality in Microbound Starter Diets Made with Decapsulated Cysts of Artemia and Fishmeal for Fish Larvae

Abstract.— The protein quality of carboxymethylcellulose microbound diets (MBDs) made with decapsulated cysts of Artemia andlor fishmeal as protein sources was used as an indicator of their suitability as starter feed for fish larvae. Studies on the proximate, fatty acid and amino acid composition. in vitro protein digestibility. diet solubility, and protein structure were combined with an in vivo feeding experiment with African catfish Clarias gariepinus larvae to evaluate the protein quality of the MBDs and a commercial diet. The growth of catfish larvae was higher when fed Artemia -based MBDs than with fishmeal-based MBDs, despite the higher protein and amino acid content of the latter. The in vitro protein digestibility was high for all the MBDs in comparison to a commercial diet. Differences were found in the protein molecular weight among the diets. Most of the proteins in the fishmeal-based diets had low molecular weight in the range between 7.4 and 49.2 kDa. The Artemia-based MBDs had larger protein fractions between 29.4 and 82 kDa. Decapsulated cysts improved the utilization of the MBDs when used in combination with fishmeal. Besides the effect of chemical attractants, the explanation for the positive effect of Artemia has yet to be elucidated. However, attention should be given to interactions between nutrients (e.g., protein-lipid) in live food, which might have an effect on the functional properties of food proteins.     

Flowering-pattern and yield components at inflorescence nodes of snap bean as affected by irrigation and plant density

This paper reports the results of a 2 × 2 factorial experiment on bush snap beans ‘Oregon 1604’. The treatments were 2 contrasted irrigation regimes and 2 contrasted plant densities, and were applied in 1978 and repeated in 1979. Data were collected on the number of flowers and pods, and pod size, at each node of the terminal inflorescence (6-T) of the main stem, and at each node of the oldest inflorescence (2-A) at Node 2. High and low plant densities were 45 and 18 plants m^?2 in 1978 and 54 and 33 plants m^?2 in 1979. High temperatures, frequently above 32°C, prevailed during bloom and pod development in 1978, but for the most part occurred only during the week prior to bloom in 1979. Inflorescences 6-T and 2-A usually formed 4 and 3 RN's, respectively, in 1978 and 3 and 2 RN's in 1979. The flowers at the proximal nodes of each inflorescence all opened within a few days of one another (duration of flowering at proximal nodes between 3 and 5 days); the flowering-periods of adjacent nodes overlapped, and the flowering period increased acropetally within the inflorescence (duration of flowering at distal nodes between 7 and 13 days). In general, number of flowers, pods formed, pods harvested and percent set decreased acropetally within each inflorescence. The rate of acropetal decline was lessened by high irrigation or low plant density. In both years, high irrigation increased the percent set of all RN's of the 2-A inflorescences, but few other consistent effects between years were observed. The 2 most proximal RN's together produced 93% or more of the yield of each inflorescence. High irrigation significantly increased the total number of pods harvested from these RN's of inflorescences 6-T and 2-A, and low density had a similar effect on 2-A.     

Safety of a modified-live combination vaccine against respiratory and reproductive diseases in pregnant cows

A combination vaccine (Bovi-Shield FP4 + L5, Pfizer Animal Health) containing modified-live virus (MLV) components against bovine herpesvirus-1 (BHV-1), bovine viral diarrhea virus BVDV), parainfluenza virus-3 (PI3), bovine respiratory syncytial virus (BRSV), and inactivated cultures of Leptospira canicola, grippotyphosa, hardjo, icterohaemorrhagiae, and pomona was evaluated for safety in pregnant beef and dairy animals. Heifers vaccinated prebreeding with the minimum immunizing dose (lowest antigen level initiating immunizing effects) of the vaccine's MLV BHV-1 or BVDV components and during pregnancy (approximately 200 days of gestation) with vaccine containing 10x doses of the same BHV-1 and BVDV components delivered live, healthy calves that were determined to be serologically negative (titer less than 1:2) for neutralizing antibodies to BHV-1 and BVDV prior to nursing. Additionally, in three field safety studies, previously vaccinated cows and heifers that received a field dose (vaccine containing antigen levels required for commercial sale of the MLV combination vaccine during either the first, second, or third trimester of pregnancy had abortion rates similar to those of pregnant cows and heifers vaccinated during the same stage of pregnancy with sterile water diluent.     

Influence of glucosamine on matrix metalloproteinase expression and activity in lipopolysaccharide-stimulated equine chondrocytes

OBJECTIVE: To characterize potential mechanisms of action of glucosamine inhibition of matrix metalloproteinase (MMP) expression and activity in lipopolysaccharide (LPS)-stimulated equine chondrocytes. SAMPLE POPULATION: Chondrocytes cultured from samples of metacarpophalangeal articular cartilage collected from cadaveric limbs of horses. PROCEDURE: The effect of glucosamine on MMP activity in conditioned medium from LPS-stimulated cartilage explants was determined by a colorimetric assay with azocoll substrate. Treatments consisted of negative and positive controls, glucose (50 mM), and glucosamine (50, 25, 6.25, 3, and 1.5 mM). The influence of glucosamine on MMP synthesis was determined in chondrocytes in pellet culture incubated with LPS (20 microg/mL). Concentration of MMP-13 was quantified in spent medium via ELISA; nonspecific MMP activity was determined via azocoll digestion in organomercurial-activated medium. Effects of glucosamine on MMP mRNA concentration in similarly treated chondrocytes were determined by northern blot hybridization with MMP-1, -3, and -13 probes. Statistical analyses were performed with 2-way ANOVA. RESULTS: Glucosamine had no effect on activated MMP activity but inhibited MMP protein expression, as determined by azocoll digestion (glucosamine, 3 to 50 mM) and MMP-13 ELISA (glucosamine, 1.5 to 50 mM). Resting mRNA concentrations for MMP-1, -3, and -13 mRNA were significantly lower in cultures exposed to glucosamine at concentrations of 50 and 25 mM than those of positive controls. CONCLUSIONS AND CLINICAL RELEVANCE: Glucosamine appears capable of pretranslational, and possibly also translational, regulation of MMP expression; data suggest a potential mechanism of action for chondroprotective effects of this aminomonosaccharide.