Seasonal changes of gastrointestinal nematode populations in yearling beef cattle in Louisiana with emphasis on prevalence of inhibition in Ostertagia ostertagi

Investigation of seasonal changes in the composition of nematode populations, principally Ostertagia oslertagi, was conducted over 3 years at three locations in Louisiana. This is the most commonly occurring parasite of cattle in the state. Naturally infected yearling cattle were killed monthly over extended periods and tracer calves were grazed for monthly intervals from late autumn to summer at two locations in 1978–1979. Major objectives were to determine seasonal incidence of common gastrointestinal nematodes and for O. ostertagi, in particular, the time period during which larval inhibition was prevalent, circumstances under which larvae were conditioned to inhibition, and the duration of inhibition. Small numbers of inhibited O. ostertagi were recovered between November and February. Large numbers were found initially in March and increased numbers in April and May. Both normally developing and inhibition prone larvae were acquired during late winter-early spring, with the proportion of the latter being more prevalent in April and May. Evidence from tracer calves indicated that few O. ostertagi larvae were acquired after early June. Large burdens of inhibited larvae persisted in yearling cattle through summer; numbers of developing larvae and adults were minimal. Maturation of inhibited larvae occurs from August to October and in one instance was associated with cases of clinical parasitism. Factors responsible for inhibition were not defined, but increasing temperatures of late winter-early spring, host resistance, and density-dependence of populations were considered. Other abomasal genera were most prevalent in spring while intestinal genera were most common during autumn through spring.     

Resolving UV Bioactinometric Results with Intensity and Time Distributions

A UV reactor with an annular design, a total liquid volume of 460[emsp4 ]ml, and outfitted with a single lamp with 1690[emsp4 ]mW of germicidal power was tested. Coliphage MS2 was used as a bioactinometer to measure the UV dose at a flow rate of 56.7[emsp4 ]ml/sec in water with a very low absorbance. The Beers Law coefficient was A₁₀0.003. The measured dose (MS2 bioactinometry) was 35.2±1.1[emsp4 ]mW-sec/cm².A retention time distribution was generated with a dye tracer study. The reactor was modeled as if flow was confined to ten equal volume paths existing as concentric rings around the lamp. The UV intensity along each path (ith intensity) was calculated to generate a simulated distribution of UV intensity in the reactor. The retention time distribution was subdivided to estimate the retention time associated with each decile jth time) of the total flow.Seven methods of associating the ith intensity with the jth retention time were used to produce simulated dose distributions for the reactor. The average UV dose for each distribution was calculated as the average of the products of I and t (AP protocol) and by the apparent survival (AS protocol), in which the predicted survival along each path was averaged to back-calculate dose from the reference batch inactivation curve. The average dose predicted assuming that time and intensity were independent was 51.5[emsp4 ]mW-sec/cm² based on the arithmetic average (AP protocol). Using the apparent survival method, the predicted dose for the independent distribution (I independent of t) was 36.4[emsp4 ]mW-sec/cm². Three methods of developing dependent structure between time and intensity were tested. In the best possible case for stratified flow (I negatively correlated with t) the calculated (AS) intensity was 46.3[emsp4 ]mW-sec/cm^2. In the worst case for stratified flow (I positively correlated with t) the AS intensity was 32.0[emsp4 ]mW-sec/cm². In a rational case where flows were assumed to be distributed parabolically (low flow at the wall and at the lamp) produced an AS intensity of 37.7[emsp4 ]mW-sec/cm². When either time or intensity was averaged, while the other variable was allowed to keep its distribution, the (AS) dose (time averaged 43.3[emsp4 ]mW-sec/cm², intensity averaged 41.0[emsp4 ]mW-sec/cm²), yielded a poor prediction compared to the measured value.The errors associated with averaging time, intensity, or both, far outweigh the errors associated with choosing a rational distribution or an independent distribution of time and intensity in the prediction. This observation is generally true whenever an organism is exposed to UV light in a flow through reactor such that the range of doses is within the portion of the inactivation curve exhibiting strong exponential decay.     

Studies on Sporopollenin Biosynthesis in Tulipa Anthers

Investigations were carried out to clarify sporopollenin biosynthesis. Tracer experiments were focussed on the incorporation of specifically labeled ¹⁴C-phenylalanine into sporopollenin. In addition, the incorporation of further ¹⁴C-labeled substances, such as glucose, acetate, malonic acid, mevalonate and tyrosine, was investigated. The sporopollenin fraction was isolated and purified by a gentle method including extractions by different solvents, incubations with hydrolyzing enzymes and fractionated saponifications. During the purification procedure the whereabouts of the initially applied radioactivity was followed. After each step the remaining as well as the released radioactivity was determined. Saponification of samples labeled after application of phenylalanine yielded p-coumaric acid and p-coumaric acid methyl ester as labeled products. In comparison with the other substances applied, the highest incorporation rates were obtained with phenylalanine, regardless of the position of labeling. After degradation of the sporopollenin sample labeled with ring-¹⁴C-phenylalanine, p-hydroxybenzoic acid was detected as the main labeled product. These results unequivocally show that an integral incorporation of the aromatic ring system occurred. Tracer experiments were carried out at different stages of development. Their results show that, although the incorporation rates of ¹⁴C-phenylalanine into sporopollenin differ, the substantial incorporation of this substance is not bound to defined stages of development.