Iron storage disease in captive Egyptian fruit bats (Rousettus aegyptiacus): relationship of blood iron parameters to hepatic iron concentrations and hepatic histopathology.

This study evaluated the relationship between blood iron parameters and hepatic iron concentrations, and correlation of histologic findings with hepatic iron concentrations in a captive population of Egyptian fruit bats (Rousettus aegyptiacus) and island flying foxes (Pteropus hypomelanus). Blood samples were collected for complete blood counts, plasma biochemical profiles, serum iron concentrations, total iron-binding capacity, whole-blood lead concentrations, and plasma ferritin assays. Liver samples obtained by laparotomy were divided, with one half processed for histologic examination and the other half frozen and submitted for tissue mineral analysis. The histologic sections were scored by two blinded observers for iron deposition, necrosis, and fibrosis. The Egyptian fruit bats had significantly higher liver iron (mean = 3,669 +/- 1,823 ppm) and lead (mean = 8.9 +/- 5.8 ppm) concentrations than the island flying foxes (mean [Fe] = 174 +/- 173 ppm, mean [Pb] = 1.9 +/- 0.5 ppm). Hepatic iron concentrations significantly correlated with tissue lead concentrations, histologic grading for iron and necrosis, serum iron, transferrin saturation, and plasma ferritin (P < 0.001). Blood lead concentrations negatively correlated with tissue lead concentrations (P < 0.001). When the product of transferrin saturation and serum iron was greater than 51, an individual animal had a high probability of having iron overload. When the product of these two variables was greater than 90, there was a high probability that the animal had hemochromatosis. On the basis of this study, it appears that evaluation of serum iron, transferrin saturation, and plasma ferritin are useful and noninvasive methods for diagnosis of hemochromatosis in Egyptian fruit bats.     

Studies on amoebae and cysts associated with the isolation of Spongospora subterranea f.sp. subterranea in vitro

New evidence is presented to support the contention that the amoeba/cyst colonies isolated from surface-sterilized Spongospora subterranea f.sp. subterranea -infected potato tubers and spore balls have a saprophytic phase but are contaminants and not S. subterranea. Amoebae isolated from infected tissues and spore balls formed colonies associated with bacteria on 1% water agar at 18°C and encysted after 5–7 days. These cysts were morphologically distinct from the resting spores of S. subterranea and were formed singly or in a layer, unlike the spore ball (cystosorus) of S. subterranea . Amoebae, cysts and mixtures of amoebae and cysts in primary, secondary and tertiary subcultures failed to infect tomato roots. PCR amplification of DNA from amoebae, cysts and spore balls using the S. subterranea -specific primer pair SsF/R generated a 434-bp product from S. subterranea spore balls only and not from amoebae or cysts. When an amoeba/cyst-specific primer pair AmF/R was designed and used for PCR amplification, a single 411-bp product was generated from DNA of amoebae and cysts, but not from DNA of S. subterranea spore balls. These results are discussed in relation to earlier reports claiming the successful isolation of S. subterranea and other plasmodiophorids in vitro .     

Seasonal patterns of dispersal of ascospores of Cryphonectria parasitica (chestnut blight)

Infected barks of chestnut blight cankers, caused by Cryphonectria parasitica , were collected from a naturally infected orchard and incubated at different temperatures. Cankers started to discharge ascospores about a week after incubation at 15–25°C; most ascospores were collected at 20 and 25°C. When incubated at 5, 10 or 30°C, only a few cankers released a small number of ascospores and only during the later stages of incubation. However, the rate of formation of perithecia was not affected by the incubation temperature. The number of airborne ascospores was monitored using a volumetric spore trap in a chestnut orchard during 1996 and 1997. In both years, the number of ascospores trapped daily varied greatly, but in general it increased sharply from March onwards, reached a peak in May, and then declined steeply. There was a significant correlation between daily counts of ascospores and air temperature. Time-series transfer function (TF) analysis showed a positive association of the daily number of ascospores with increasing temperature, rain events and wet/humid conditions. In general, values predicted by the TF model agreed well with the observed pattern. However, a multiple regression equation based on TF analysis failed to provide a satisfactory prediction of the daily number of ascospores.     

On estimating non-linear response of fungal development under fluctuating temperatures

Published research concerning disease development often shows that the response of fungal development to temperature is non-linear. Unfortunately, this non-linear response has often been ignored when predicting fungal development under varying temperatures using non-linear models and when deriving fungal development models from data collected under fluctuating temperatures. In this paper, the magnitude of non-linear effects on fungal development is shown to depend on the types of non-linear models and on the extent of temperature fluctuations. A method is described, which has been used in other disciplines to fit non-linear models directly to varying temperatures. Hypothetical data were generated to demonstrate the usefulness of this method. With the underlying rate equation being non-linear, models derived from average temperatures underestimate the rates at intermediate temperatures; the greater the temperature fluctuation, the greater this underestimation.     

Phenological patterns in an arable land weed community related to disturbance

The emergence pattern and life cycle of four major species growing in a non–irrigated almond tree grove were analysed in relation to ploughing frequencies and environmental factors. At the community level, the overall emergence pattern was found to be much the same whether or not the soil was disturbed. Nevertheless, soil disturbance in late winter and early spring produced peaks of seedling emergence and brought about an increase in germination. Winter annuals such as Lolium rigidum Gaudin and Diplotaxis erucoides (L.) DC., which emerged in the autumn, started to grow rapidly in winter and spring and were able to pre–empt the environmental resources of the habitat and suppress spring–germinating plants such as Chenopodium album L. and Amaranthus blitoides S. Watson. Late–winter and early–spring disturbances favoured the dominance of summer annuals such as C. album and A. blitoides S. Watson. The different ploughing regimes applied during the first year had effects on plant development and seed production which brought about changes in plant population size during the second year.     

Recessive Genes for Resistance to Puccinia striiformis f. sp. hordei in Barley

ABSTRACT Barley genotypes Abyssinian 14, BBA 2890, Grannelose Zweizeilige, PI 548708, PI 548734, PI 548747, and Stauffers Obersulzer are resistant to all races of Puccinia striiformis f. sp. hordei identified thus far in North America. Astrix, BBA 809, Bigo, Cambrinus, Emir, Heils Franken, Hiproly, I5, Mazurka, Trumpf, and Varunda have specific resistance to certain races, whereas Topper and Steptoe are susceptible to all races. Seedlings of parents and F(1), F(2), and F(3) progeny from crosses of resistant genotypes with Topper and Steptoe were tested for resistance to North American P. striiformis f. sp. hordei races PSH-1, PSH-4, PSH-10, PSH-13, and PSH-20. When tested with PSH-1, one recessive gene was detected in BBA 809, BBA 2890, Bigo, Hiproly, and Grannelose Zweizeilige; two recessive genes were detected in Emir, I5, PI 548708, PI 548734, PI 548747, Varunda, and Astrix; and one dominant gene and one recessive gene were detected in Abyssinian 14 and Stauffers Obersulzer. In tests with PSH-4, one recessive gene was detected in BBA 809, two recessive genes were detected in Trumpf, and two partially recessive genes were detected in Astrix. In tests with PSH-13, one recessive gene was detected in BBA 2890, Grannelose Zweizeilige, I5, and PI 548708 and two recessive genes were detected in Abyssinian 14, Hiproly, PI 548734, and PI 548747. In tests with PSH-20, one recessive gene was detected in Bigo and a recessive gene and a dominant gene were detected in Heils Franken. A gene in Cambrinus for resistance to PSH-10 and a gene in Mazurka for resistance to PSH-20 were dominant on the basis of the response of the first seedling leaf but recessive on the basis of the response of the second leaf. Four different types of epistasis were detected. Information on the number of genes, mode of inheritance, and nonallelic gene interactions should be useful in understanding the host-pathogen interaction and in breeding barley for resistance to stripe rust.     

Soybean Brown Stem Rot, Phytophthora sojae, and Heterodera glycines Affected by Soil Texture and Tillage Relations

ABSTRACT Investigations were conducted to determine whether the effects of tillage practices on the prevalence of brown stem rot of soybean (caused by Phialophora gregata), Heterodera glycines, and Phytophthora sojae were confounded by soil texture in samples collected in the fall of 1995 and 1996. Soil and soybean stem samples, along with tillage information, were collected from 1,462 randomly selected fields in Illinois, Iowa, Minnesota, Missouri, and Ohio in collaboration with the National Agricultural Statistics Service. The incidence of brown stem rot was determined from 20 soybean stem pieces collected from each field in a zigzag pattern. The detection frequency of P. sojae (expressed as percent leaf disks colonized) and population densities of H. glycines were determined from soil cores also collected in a zigzag pattern. The soil samples were grouped into various textural classes, and the effect of soil texture and tillage relations on the activities of each pathogen were determined. Both tillage and soil texture affected the incidence of brown stem rot; however, there was no interaction between tillage and soil texture. Conservation tillage had a greater (P < 0.05) incidence of brown stem rot in clay loam and silty clay loam than did conventional tillage. The detection frequency of P. sojae was not affected by tillage, but a tillage x texture interaction (P = 0.013) indicated that the effect of tillage depended on soil texture. There was a greater (P < 0.05) detection frequency of P. sojae in conservation tillage than in conventional tillage in silt loam and loam soils. However, in sandy loam, the detection frequency of P. sojae was greater (P = 0.0099) in conventional tillage than in conservation tillage. Population densities of H. glycines were significantly affected by both tillage and soil texture, but overall, there was no tillage x texture interaction. There was an inverse relationship between population densities of H. glycines and percent clay (r = -0.81, P = 0.01) in no-till fields, but little or no change in nematode densities was observed with increasing clay content in tilled fields. Population densities of H. glycines were less (P < 0.05) in no-till fields than in tilled fields in silty clay loam and clay soils. There was no difference in H. glycines densities between the tillage categories in soils sandier than silty clay loam or clay. The findings emphasize the need for cautious interpretation of the effects of tillage practices on diseases and pathogens in the absence of information on soil texture.     

Spatial distribution of leaf dry weight per area and leaf nitrogen concentration in relation to local radiation regime within an isolated tree crown

To assess the spatial distribution of photosynthetic capacity within an isolated 20-year-old walnut tree (Juglans regia L.) crown, the distribution of relevant leaf characteristics was measured. Variations in leaf dry weight per area (W(a)), and nitrogen content on a weight (N(w)) and area basis (N(a)) were studied along two horizontal and one vertical gradients of leaf irradiance, at two dates (July 30 and September 3). In addition, the content of total nonstructural carbon on a weight (TNC(w)) and area basis (TNC(a)) was measured on July 30. Concurrently, the spatial distribution of daily integrated leaf irradiance within the crown was simulated by a three-dimensional radiation transfer model over a one week period before sampling at each date. High spatial heterogeneity was observed for W(a) (from 50 to 140 g m(-2)), TNC(a) (from 4 to 17 g m(-2)) and N(a) (from 1.2 to 3.6 g m(-2)) among the foliage. Although TNC(w) and N(w) were not correlated and only weakly correlated to daily leaf irradiance, respectively, W(a), TNC(a) and N(a) were strongly correlated to daily leaf irradiance. The relationship between observed N(a) and simulated daily leaf irradiance was used to assess the spatial distribution of N(a) within the crown at each date. Total leaf nitrogen in the foliage was estimated to be 339 g in late July and 317g in early September. For the whole crown (i.e., 1729 current-year shoots), N(a) increased strongly with basal shoot diameter (an index of "shoot vigor"), highlighting the fact that large shoots were mainly located in sunlit locations and exhibited high photosynthetic capacity.