Simplifying Dynamic River Water Quality Modelling: A Case Study of Inorganic Nitrogen Dynamics in the Crocodile River (South Africa)

The ultimate goal of this study is to develop a simple dynamic river water quality model that can be applicable in a data limited situation and is compatible with typical activated sludge models, so that the model can be used in integrated modelling of wastewater and river water quality in the future. A simplified river water quality model was formulated based on a conceptual hydraulic sub-model and simplification of an existing river water quality model. The simplified water quality was derived from the River Water Quality Model No. 1, which is one of the most comprehensive basic river water quality models available in literature. The applicability of the simplified model in data limited situations was investigated using a case study of inorganic nitrogen (nitrate and ammonia) in the Crocodile River (South Africa). The model was calibrated and validated on the basis of independent data collected for four years (1987–1990). The results show that the model can adequately describe the seasonal dynamics of inorganic nitrogen in the Crocodile River. The sensitivity of the model output to the model inputs was also analysed, and the results indicate that the model is most sensitive to the microbial biomass (nitrifier) followed by hydraulic parameters. The relation of river flow versus concentration of inorganic nitrogen in the downstream section of the river was also examined in order to identify the main source and critical time for nitrate pollution.     

Long-term effect on the equine eye of an intravitreal device used for sustained release of cyclosporine A

OBJECTIVE: To determine the long-term toxicity of an intravitreal device releasing continuous cyclosporinee A (CsA) in normal eyes of horses by evaluating clinical signs, electroretinography, and histopathology. Animals Studied Ten adult horses with normal ophthalmic examinations were used in this study Procedure(s) Four horses had one eye implanted with a CsA device, and six horses had the right eye implanted with a CsA-containing device (10 eyes with CsA in total) and the left eye (six eyes in total) with the device without drug (control). The implants were placed in the vitreous of the eyes through a sclerotomy 1 cm posterior to the limbus in the dorso-temporal quadrant of the eye. Scotopic electroretinograms were performed prior to implantation and at 1 week, and at 1, 3, 6, 9, and 12 months postimplantation. Two of the unilaterally implanted horses were euthanized at 1 weeks postimplantation, and two at 6 weeks postimplantation. Two of the bilaterally implanted horses were euthanized at 6 months, two at 9 months, and two at 12 months postimplantation. At euthanasia, the eyes were removed, aqueous and vitreous humor aspirated, and tissues fixed in 10% buffered formalin and processed for histopathology. CsA concentrations were measured by high pressure liquid chromatography in the aqueous and vitreous humors, and in peripheral blood. RESULTS: The devices were tolerated well in 14 of 16 eyes. There was minimal postoperative inflammation in most eyes, with a normal appearance within 7 days. In two eyes implanted with the CsA device, severe inflammation resulted in phthisis bulbi by 28 days. One of these eyes exhibited suspected bacterial endophthalmitis, and one had a sterile endophthalmitis and cataract presumably from trauma to the lens during implantation. In the other 14 eyes, no change was observed in the scotopic electroretinograms (ERG) from preoperative results, and no significant differences between the right (CsA) and left (control device) eyes were observed. CsA levels in the aqueous and vitreous humor, and peripheral blood were below the detection limit of the HPLC. Histologic findings revealed only a mild lymphoplasmacytic cellular infiltrate in the ciliary body and pars plana near the implantation site. CONCLUSIONS: The CsA devices were well tolerated with no long-term complications from the implants themselves. However, complications may occur from inadvertent implantation trauma or contamination during surgery. The long-term safety of the device may make it useful for delivery of CsA in the control of equine recurrent uveitis.     

Currents, landscape structure, and recruitment success along a passive–active dispersal gradient

There exists a gradient in dispersal behavior from passive to active, which reflects organisms’ dependence upon currents vs. self-propelled movement. We asked: Do currents modify organism–landscape interactions to influence recruitment success along this dispersal gradient? Using a spatially-explicit cellular model, we simulated the recruitment success of three generalized dispersal strategies (walkers, swimmers, and drifters) through hierarchically structured benthic landscapes. We evaluated the relative recruitment success (recruited population size, overall area occupied, time to recruit) of the three dispersal strategies in similar landscapes, as well as the consequences of varying the total proportion of habitat suitable for recruitment, and the scale and pattern of habitat patchiness on recruitment success. In the presence of currents, swimmers and drifters generally recruited over larger areas and in less time than walkers. Differences among the dispersal strategies’ recruitment success were most pronounced when an intermediate number of good habitat cells (16–48% of landscape) were broadly dispersed across the landscape. Although recruitment success always increased with increasing proportion of good habitat, drifters were more sensitive, and swimmers less sensitive, to these landscape changes than walkers. We also found that organisms dispersing within currents typically responded non-linearly (logarithmically or exponentially) to increasing proportion of total good habitat, whereas walkers more often responded linearly.     

A STUDY OF THE POSSIBLE ROLE OF CHELATION IN THE OCCURRENCE OF HYPOMAGNESAEMIA IN SHEEP

Wethers fitted with permanent rumen cannulae were used in a study of the effect of various doses of ammonium salts and E. D.T. A. (ethylene-diamine-tetra-acetic acid, disodium salt) on the pH of rumen digesta and the levels of serum calcium and magnesium. Doses of up to 200 g ammonium acetate had little effect on the pH of rumen contents or on serum Mg levels, but appeared to produce a fall in serum Ca. Ammonium carbonate, however, when given alone or with E. D.T. A., caused a marked increase in the pH of rumen fluid and a temporary fall in the serum Ca level. When given singly, neither ammonium carbonate nor E. D.T. A. significantly affected the levels of serum Mg which were, however, reduced when these compounds were given together, possibly because the increased pH of rumen contents produced by the ammonium carbonate was conducive to chelation of Mg by the E. D.T. A. High levels of ammonia may occur in rumen liquor after the ingestion of young nitrogen-rich herbage, and it is suggested that chelation of dietary Mg by such compounds as amino acids and peptides, which abound in young herbage, may be a factor concerned in the low 'availability' of this form of Mg.     

Investigation of the effect of pamidronate disodium on the in vitro viability of osteosarcoma cells from dogs

OBJECTIVE: To determine the effect of pamidronate disodium on the in vitro viability of osteosarcoma cells and non-neoplastic cells from dogs. SAMPLE POPULATION: 3 osteosarcoma and 1 fibroblast cell lines derived from dogs. PROCEDURE: Cell counts and cell viability assays were performed in cultures of osteosarcoma cells (POS, HMPOS, and COS31 cell lines) and fibroblasts after 24, 48, and 72 hours of incubation with pamidronate at concentrations of 0.001 to 1000 microM or with no drug (control treatment). Percentage viability was determined in cell samples for each concentration of pamidronate and each incubation time. A DNA fragmentation analysis was performed to assess bisphosphonate-induced apoptosis. RESULTS: Osteosarcoma cell viability decreased significantly in a concentration- and time-dependent manner at pamidronate concentrations ranging from 100 to 1000 microM, most consistently after 48 and 72 hours' exposure. In treated osteosarcoma cells, the lowest percentage cell viability was 34% (detected after 72 hours' exposure to 1000 microM pamidronate). Conversely, 72 hours' exposure to 1000 microM pamidronate did not significantly reduce fibroblast viability (the lowest percentage viability was 76%). After 72 hours of exposure, pamidronate did not cause DNA fragmentation in POS or HMPOS cells. CONCLUSIONS AND CLINICAL RELEVANCE: Results indicate that pamidronate may have the potential to inhibit osteosarcoma growth in dogs, possibly through a nonapoptotic mechanism. The clinical relevance of these in vitro findings remains to be determined, but administration of pamidronate may potentially be indicated as an adjuvant treatment in chemotherapeutic protocols used in dogs.     

Equine herpesvirus-1 infected peripheral blood mononuclear cell subpopulations during viremia

Infection with equine herpesvirus-1 (EHV-1) causes respiratory disease, late term abortions and equine herpesvirus myeloencephalitis (EHM) and remains an important problem in horses worldwide. Despite increasing outbreaks of EHM in recent years, our understanding of EHM pathogenesis is still limited except for the knowledge that a cell-associated viremia in peripheral blood mononuclear cells (PBMCs) is a critical link between primary respiratory EHV-1 infection and secondary complications such as late-term abortion or EHM. To address this question our objective was to identify which PBMC subpopulation(s) are infected during viremia and may therefore play a role in transmitting the virus to the vascular endothelium of the spinal cord or pregnant uterus. PBMCs from 3 groups of animals were collected between days 4 and 9 following experimental infection with EHV-1 strain Findlay/OH03 or strain Ab4. PBMCs were labeled with primary antibodies selective for CD4+ or CD8+ T lymphocytes, B-lymphocytes, or monocytes and positively selected using magnetic bead separation. Cell numbers and EHV-1 genome numbers in each subpopulation were then determined using quantitative PCR for β-actin and the EHV-1 glycoprotein B, respectively. Viral genomic DNA was found in all PBMC subpopulations; the CD8+ lymphocytes were most frequently positive for viral DNA, followed by B-lymphocytes. These differences were statistically significant in horses infected with the EHV-1 strain Findlay/OH03, and ponies with Ab4. These results differ from what has been reported in in vitro studies, and indicate that different PBMC subpopulations may play different roles in EHV-1 viremia.