Response of Paddy (Oryza sativa) as Influenced by Zinc Application and Available Zinc Status of Soils

The influence of zinc application on yield, Zn concentration and its uptake by paddy crop (Oryza sativa) was studied in a pot experiment in alluvial soils from Gwalior district. All the soils having less than 3.0 ppm 0.1 N HCl-extractable soil Zn showed significant yield response to application of Zn. The latter also resulted in significant increase in Zn concentration and its uptake by the crop. The plant tissue Zn was found to be significantly correlated at 1 % level with the soil Zn (r=0.82) and Bray's per cent grain yield (r=0.82). Critical level Zn in rice plant taken from top 15 cm of the plant was worked out by statistical procedure of Cate and Nelson and found to be 13.5 ppm below which response to applied Zn is expected.     

Elevated CO2 Improves Growth and Phosphorus Utilization Efficiency in Cereal Species Under Sub-Optimal Phosphorus Supply

Cultivars of Triticum aestivum, T. durum, and Secale cereale were grown at low (2 μM) and sufficient (500 μM) phosphorus (P) under ambient carbon dioxide (380 μmol mol^?1; aCO₂) and elevated CO₂ (700 μmol mol^?1, eCO₂) to study responses of cereal species in terms of growth and P utilization efficiency (PUE) under P x CO₂ interaction. Dry matter accumulation increased under eCO₂ with sufficient P. Nevertheless, dry matter accumulated at eCO₂ with low-P was similar to that obtained at aCO₂ with sufficient P. Leaf area was 43% higher under eCO₂ with sufficient P. Significant increase in lateral root density, length and surface area were noted at low-P under eCO₂. Phosphorus use efficience (PUE) increased by 59% in response to eCO_2­ in low-P plants. Thus, eCO₂ can partly compensate effect of low-P supply because of improved utilization efficiency. Among cereals, durum wheat was more suitable in terms of PUE under high CO₂ and limiting P supply.     

Toxoplasmosis and other causes of abortions in sheep from north central United States

Between 1983 and 1989, we examined 1,201 aborted fetuses and dead lambs from the north central United States. Toxoplasmosis was diagnosed in 17.5%, campylobacteriosis in 9.9%, chlamydiosis in 4.7%, and miscellaneous infections in 15.1%. Inflammatory lesions suggestive of infectious causes were seen in 13%. Noninfectious causes were identified in 6.1%, and a diagnosis was not reached in 33.3%. An agglutination test was used to detect Toxoplasma gondii-specific antibodies in ovine fluids. Toxoplasma gondii antibodies were detected in 223 of 1,064 (20.9%) fluids from fetuses and dead lambs. Of 201 seropostive (greater than or equal to 16) fetuses and lambs, T gondii antibody titers (reciprocal) were 16 (21 fetuses and lambs), 32 (10 fetuses and lambs), 64 (2 fetuses and lambs), 128 (7 fetuses and lambs), 256 (9 fetuses and lambs), 512 (5 fetuses and lambs), 1,024 (15 fetuses and lambs), 2,048 (13 fetuses and lambs), 4,096 (13 fetuses and lambs), 8,196 (13 fetuses and lambs), 16,392 (19 fetuses and lambs), and greater than or equal to 32,784 (74 fetuses and lambs).     

Neospora-like protozoan infection as a major cause of abortion in California dairy cattle

Ninety-five aborted bovine fetuses received from California dairies over a 4.5-year period had histologic lesions of focal encephalitis. Protozoa that reacted with Neospora caninum antiserum were detected in the brain of 88 of these fetuses and in the heart of 1 fetus. Sarcocystis spp schizonts were seen in the vascular endothelium of 1 fetus. It was concluded that a Neospora-like cyst-forming coccidian may be a major cause of abortion in California dairy cattle.     

Lesions in fetal pigs with transplacentally-induced toxoplasmosis

Two sows (Nos. 1, 2) were each fed 1,000 Toxoplasma gondii oocysts. Sow No. 1 was fed oocysts at 60 day of gestation and was euthanatized 49 days later. Sow No. 2 was fed oocysts at day 45 of gestation and euthanatized 62 days later. Sow No. 1 had eight dead fetuses of which one was mummified and unsuitable for histologic study. Sow No. 2 had 11 fetuses, of which four fetuses were mummified and unsuitable for histologic examination, two fetuses were dead and five were live. Lesions and Toxoplasma parasites were identified in seven fetuses from sow No. 1 and three fetuses from sow No. 2. No lesions were found in four fetuses from sow No. 2. Toxoplasma gondii was present in trophoblasts and produced areas of necrosis of the chorioallantois with focal placental separation. The predominant lesions were necrotizing placentitis, non-suppurative encephalomyelitis, and myocardial degeneration, necrosis and mineralization. Numerous tachyzoites were seen in trophoblast cells lining areolae in placenta.     

Sarcocystis infections in mule deer (Odocoileus hemionus) in Montana and the descriptions of three new species

Four structural types of sarcocysts of Sarcocystis were found in skeletal muscles of mule deer in Montana. Type I sarcocysts were thin walled (1 to 3 micron) and belonged to S hemionilatrantis. Types II to IV sarcocysts were thick walled (2 to 10 microns) and new names were proposed for them. Type II sarcocysts with long villar projections were named S hemioni. Type III sarcocysts with club-shaped villi of uneven thickness were named S youngi. Type IV sarcocysts with walls of uneven thickness and containing hair-like protrusions were named S americana.     

Sarcocystosis in goats: clinical signs and pathologic and hematologic findings

Clinical sarcocystosis was studied in 37 goats after inoculation with graded doses of sporocysts of Sarcocystis capracanis. Eight uninoculated goats served as controls. Clinical response varied with the dose. Goats inoculated with 10-40 million sporocysts died between 11 and 13 days after inoculation (DAI), from interstitial pneumonia, vasculitis, and necrosis of mesenteric lymph nodes. All goats inoculated with 100,000 or 1 million sporocysts died between 19 and 23 DAI; clinical signs were anorexia, fever (40-41 C), anemia, and weight loss. Four of 4 goats inoculated with 50,000 sporocysts and 1 of 4 inoculated with 10,000 sporocysts died 24, 28, 39, 68, and 61 DAI, respectively. Goats inoculated with 1,000 sporocysts and uninoculated goats remained clinically normal. After day 18 and before day 68, packed cell volume and hemoglobin content decreased to as low as 11% and 3.6 g/dl, respectively. Alanine aminotransferase and lactic dehydrogenase activities were inconsistently increased. Blood urea nitrogen and bilirubin values were increased, reaching as high as 63 mg/dl and 10 mg/dl, respectively. Histologically, thymic atrophy, vasculitis, hepatitis, cholangitis, myocarditis, generalized myositis, and encephalomyelitis were the main microscopic findings. The cause of the anemia in goats that died after day 19 was not determined.     

Distribution of cysts and tachyczoites in calves and pregnant cows inoculated with toxoplasma gondii oocysts

Sixteen calves and 6 cows were each inoculated with 100 000 infective oocytes of the GT-1 strain of Toxoplasma gondii. Cattle were necropsied between 3 and 287 days post-inoculation (DPI) and their tissues were inoculated into mice or fed to Toxoplasma-free cats for the detection of Toxoplasma in bovine tissues. Ten to 10 000-fold more T. gondii were recovered from small intestine and mesenteric lymph nodes of calves at 3 and 6 DPI than from lungs and liver, and the number of T. gondii in bovine tissues was reduced 1000-fold between 6 and 8 DPI. By using the pepsin digestion technique, or feeding tissues to Toxoplasma-free cats, it was demonstrated that T. gondii encysted in bovine tissues as early as 11 DPI and persisted as late as 287 DPI. More Toxoplasma gondii cysts occurred in livers than in any other bovine tissue. Of the 6 cows inoculated at 95–155 days after breeding, 5 delivered normal calves and T. gondii was isolated from only one of these calves. One cow was barren. Toxoplasma gondii was not isolated either by mouse inoculation or by feeding cats tissues from 2 cows killed 132 and 190 DPI. Toxoplasma gondii was not isolated in mice inoculated with tissues of cows killed 98 and 109 DPI, but cats fed on bovine tissues shed T. gondii oocysts. The organism, however, was isolated in mice inoculated with the mesenteric lymph nodes of 1 of the 2 cows killed 162 and 168 DPI, and from the small intestine of the other. Cats fed tissues of these cows later shed T. gondii oocysts.