Stoichiometry of consumer-driven nutrient recycling across nutrient regimes in streams

Stoichiometric constraints within ecological interactions and their ecosystem consequences may depend on characteristics of the abiotic environment such as background nutrient levels. We assessed whether consumer identity, via differing body stoichiometry, could regulate periphyton stoichiometry across nutrient regimes in open systems. In 60 flow-through artificial streams, we factorially crossed dissolved inorganic nitrogen levels (elevated = 294  μ g L⁻¹, ambient = 26  μ g L⁻¹) with dissolved inorganic phosphorus levels (DIP: elevated = 15  μ g L⁻¹, ambient = 3  μ g L⁻¹) and consumer type [crayfish (body N : P = 18), snails (body N : P = 28) or a control]. At ambient DIP, periphyton in the crayfish treatment had a lower %P and a lower C : P than periphyton in the snail treatment suggesting that consumer identity, probably mediated by differing P-excretion, regulated periphyton P content. At high DIP, consumer identity no longer affected periphyton elemental composition. Therefore, the stoichiometry of consumer-driven nutrient recycling and consumer identity may be less important to ecosystem functioning in environments with elevated nutrient levels.     

Internalization and recycling of transferrin and its receptor. Effect of trifluoperazine on recycling in human erythroleukemic cells

When human erythroleukemic (K562) cells were incubated with 25 microM trifluoperazine (TFP), a drug that inhibits both calmodulin-dependent and calcium-activated phospholipid-dependent kinases, the number of transferrin receptors detected on the cell surface was reduced to approximately half with no change in the affinity of the remaining surface receptors. Removal of the TFP from the incubation medium reversed the loss of surface receptors and they returned to the cell surface in an apparently synchronous manner. As a result, the number of receptors detected on the cell surface exceeded the original level but later returned to normal. Measurements of the total number of receptors available to transferrin in TFP-treated cells suggested that the lost receptors were not participating in the internalization and recycling pathway but instead were probably trapped at an intracellular location. However, those receptors that remained on the cell surface continued to internalize transferrin and to recycle apotransferrin to the cell surface albeit more slowly than in cells that had not been treated with TFP. Using transferrin that had been labeled with iron-59, it was found that although iron uptake was reduced in line with the diminished number of surface receptors, iron still accumulated within TFP-treated cells, suggesting that in the presence of the drug, transferrin-transferrin receptor complexes continued to migrate through an intracellular compartment that contained a low pH.     

Enzymatic digestion of spent yeast cells for nutrient recycling in inulase production

Summary An enzyme complex capable of lysing yeast cells was produced byArthrobacter sp. in a medium containing live cells ofKluyveromyces fragilis as the sole source of nutrients. The enzyme complex caused a 90% reduction in the optical density of viable yeast cells in 6 h at 25°C. This yeast cell hydrolysate can be used as a source of nitrogen, vitamins and minerals for subsequent growth of yeast cells (8.3 mg/ml) and further production of inulase (167 U/ml) representing 88 and 87% yield respectively, compared to cells grown on a standard yeast extract (1%) and sucrose (2%) medium.     

Persistence and coexistence in zooplankton-phytoplankton-nutrient models with instantaneous nutrient recycling

We consider plankton-nutrient interaction models consisting of phytoplankton, herbivorous zooplankton and dissolved limiting nutrient with general nutrient uptake functions and instantaneous nutrient recycling. For the model with constant nutrient input and different constant washout rates, conditions for boundedness of the solutions, existence and stability of non-negative equilibria, as well as persistence are given. We also consider the zooplankton-phytoplankton-nutrient interaction models with a fluctuating nutrient input and with a periodic washout rate, respectively. It is shown that coexistence of the zooplankton and phytoplankton may arise due to positive bifurcating periodic solutions.Research has been supported in part by a University of Alberta Ph.D. Scholarship and is in part based on the author's Ph.D. thesis under the supervision of Professor H. 1. Freedman, to whom the author owes a debt of appreciation and gratitude for his kind advice, helpful comments and continuous encouragement     

Transferrin receptor 2: evidence for ligand-induced stabilization and redirection to a recycling pathway

Transferrin receptor 2 (TfR2) is a homologue of transferrin receptor 1 (TfR1), the protein that delivers iron to cells through receptor-mediated endocytosis of diferric transferrin (Fe(2)Tf). TfR2 also binds Fe(2)Tf, but it seems to function primarily in the regulation of systemic iron homeostasis. In contrast to TfR1, the trafficking of TfR2 within the cell has not been extensively characterized. Previously, we showed that Fe(2)Tf increases TfR2 stability, suggesting that trafficking of TfR2 may be regulated by interaction with its ligand. In the present study, therefore, we sought to identify the mode of TfR2 degradation, to characterize TfR2 trafficking, and to determine how Fe(2)Tf stabilizes TfR2. Stabilization of TfR2 by bafilomycin implies that TfR2 traffics to the lysosome for degradation. Confocal microscopy reveals that treatment of cells with Fe(2)Tf increases the fraction of TfR2 localizing to recycling endosomes and decreases the fraction of TfR2 localizing to late endosomes. Mutational analysis of TfR2 shows that the mutation G679A, which blocks TfR2 binding to Fe(2)Tf, increases the rate of receptor turnover and prevents stabilization by Fe(2)Tf, indicating a direct role of Fe(2)Tf in TfR2 stabilization. The mutation Y23A in the cytoplasmic domain of TfR2 inhibits its internalization and degradation, implicating YQRV as an endocytic motif.     

Effects of nutrient recycling by zooplankton and fish on phytoplankton communities

In laboratory experiments we tested the hypothesis that nutrients supplied by fish and zooplankton affect the structure and dynamics of phytoplankton communities. As expected from their body size differences, fish released nutrients at lower mass-specific rates than Daphnia. On average, these consumers released nutrients at similar N:P ratios, although the ratios released by Daphnia were more variable than those released by fish. Nutrient supply by both fish and Daphnia reduced species richness and diversity of phytoplankton communities and increased algal biomass and dominance. However, nutrient recycling by fish supported a more diverse phytoplankton community than nutrient recycling by Daphnia. We conclude that nutrient recycling by zooplankton and fish have different effects on phytoplankton community structure due to differences in the quality of nutrients released. Received: 21 December 1998 / Accepted: 31 May 1999     

Ion chromatographic determination of taurine in medicine, nutrient capsule and human urine with electrochemical detection

A very simple and sensitive method for the determination of taurine by ion chromatography with electrochemical integrated pulsed amperometry is firstly described. Taurine was determined using 160 mmol/l NaOH as eluent and a Dionex CarboPac™ PA1 separation column (250×4 mm I.D.) without the interference with ten kinds of common amino acids. The peak area response of taurine was linear in the range 0.1–20 μg/ml, the detection limit was 0.034 μg/ml. The method has been applied successfully in the determination of taurine in medicinal granule, nutrient capsule and human urine. The content determined in medicinal granule is consistent with that marked by the manufacturer.     

Measurement of 6-hydroxymelatonin in human urine and its diurnal variations

A gas chromatographic-mass spectrometric assay has been developed and applied to the measurement of the major melatonin metabolite in human urine. In seven normal adult male subjects, the mean daily urinary conjugated 6-hydroxymelatonin was 15.5 μg (6.5 ? 22.8 μg rang). Urine samples at 6 hour intervals clearly demonstrated a ten-fold diurnal variation, from 0.8 μg/6 hr during the day to 8.6 μg/6 hr at night.     

Morphometry and sedimentation as regulating factors for nutrient recycling and trophic state in coastal waters

The aim of this work is to quantify the importance of morphometry and sedimentation/resuspension on nutrient recycling and trophic characteristics in coastal waters. Extensive field work has been carried out in 23 coastal areas in the Swedish and Finnish part of the Baltic Proper. Sediment traps were deployed for two one-week periods in all areas. On average, 56% of the total sedimentation in sediment traps 3 m below the water surface (SedS) and 62% of the total sedimentation on sediment traps 1 m above the bottom (SedB) was resuspended material. Coastal morphometric parameters, surface water retention time and bottom dynamic conditions were determined for all areas. There is a marked relationship between SedS and inorganic-N concentration in the surface water. The relationship was improved significantly by using sedimentation of the resuspended fraction at 3 m water depth (SedR) instead of SedS.This led to the hypothesis that increased concentration of inorganic nitrogen in the surface water results from increased mineralisation of resuspended organic particles. A model describing SedS is presented where inorganic nitrogen concentration, the water surface area and the surface water retention time can explain 82% of the variation in SedS. In another model inorganic nitrogen and water surface area can explain as much as 93% of the variation in SedR.These results emphasise the importance of resuspension for nutrient recycling and trophic state in coastal waters. The importance of coastal morphometry and surface water retention time on total sedimentation and nutrient recycling makes it possible to classify coastal areas in terms of potential nutrient recycling capacity/trophic state from these simple sensitivity parameters.     

Models of competition in the chemostat with instantaneous and delayed nutrient recycling

Two models for competition of two populations in a chemostat environment with nutrient recycling are considered. In the first model, the recycling is instantaneous, whereas in the second, the recycling is delayed. For each model an equilibrium analysis is carried out, and persistence criteria are obtained. This paper extends the work done by Beretta et al. (1990) for a single species.Research partially supported by the Natural Sciences and Engineering Research Council of Canada, Grant NSERC A4823Research carried out at the University of Alberta while on a Canada-China Scholarly Exchange Program     

Neural network modeling for nutrient dynamics in a recycling piggery slurry treatment system

A recycling reactor system operated under sequential anoxic and oxic conditions was evaluated, in which the nutrients of piggery slurry were anaerobically and aerobically treated and then a portion of the effluent was recycled to the pigsty. The most dominant aerobic heterotrophs from the reactor were Alcaligenes faecalis (TSA-3), Brevundimonas diminuta (TSA-1) and Abiotrophia defectiva (TSA-2) in decreasing order, whereas lactic acid bacteria, LAB (MRS-1, etc.) were most dominantly observed in the anoxic tank. Here we have tried to model the nutrient removal process for each tank in the system based on population densities of heterotrophic and LAB. Principal component analysis (PCA) was first applied to delineate a relationship between input (microbial densities and treatment parameters such as population densities of heterotrophic and LAB, suspended solids (SS), COD, NH₄ ⁺–N, ortho-phosphorus, and total phosphorus) and output. Multi-layer neural networks using an error back-propagation learning algorithm were then employed to model the nutrient removal process for each tank. PCA filtration of microbial densities as input data was able to enhance generalization performance of the neural network, and this has led to a better prediction of the measured data. Neural networks independently trained for each treatment tank and the combined analysis of the subsequent tank data allowed a successful prediction of the treatment system for at least 2 days.     

Gas chromatograph-mass spectrometric method for the determination of carvedilol and its metabolites in human urine

A sensitive and efficient method was developed for the determination of carvedilol and its metabolites in human urine by gas chromatography-mass spectrometry (GC-MS). Urine samples were hydrolyzed with beta-glucuronidase/arylsulfatase (from Helix pomatia) and the target compounds were extracted with liquid-liquid extraction. The extracts were completely derivatized with MSTFA and MBTFA and analyzed by GC-MS using an Ultra-2 column. The linearity of the assay ranges were 0.75-75 ngmL(-1) for carvedilol and o-desmethyl carvedilol (o-DMC), and 3.0-75 ngmL(-1) for 4-hydroxyphenyl carvedilol (4-HPC) and 5-hydroxyphenyl carvedilol (5-HPC). The absolute recovery of carvedilol and its metabolites added to a blank urine sample was 80.1-97.8%. The limits of detection (LOD) and quantitation (LOQ) of carvedilol and o-DMC were 0.30 and 0.75 ngmL(-1), and its of 4-HPC and 5-HPC were 0.75 and 3.0 ngmL(-1), respectively. The reproducibilities were 1.86-11.5% for the intra-day assay, and 0.70-1.71% for the inter-day assay precision and the degree of inaccuracy was -3.0 to 3.9% at the concentration of 75 ngmL(-1). The proposed GC-MS method was effective for the determination of carvedilol and its three metabolites in human urine.     

The metamicrobiome: key determinant of the homeostasis of nutrient recycling

The metamicrobiome is an integrated concept to study carbon and nutrient recycling in ecosystems. Decomposition of plant-derived matter by free-living microbes and fire – two key recycling pathways – are highly sensitive to global change. Mutualistic associations of microbes with plants and animals strongly reduce this sensitivity. By solving a fundamental allometric trade-off between metabolic and homeostatic capacity, these mutualisms enable continued recycling of plant matter where and when conditions are unfavourable for the free-living microbiome. A diverse metamicrobiome – where multiple plant- and animal-associated microbiomes complement the free-living microbiome – thus enhances homeostasis of ecosystem recycling rates in variable environments. Research into metamicrobiome structure and functioning in ecosystems is therefore important for progress towards understanding environmental change.     

Retinol-binding protein from human urine and its interaction with retinol and prealbumin

In freshly collected urine from a patient with glomerulotubular proteinuria there were two bands which contained retinol-binding proteins. The cathodal band showed fluorescence in the ultraviolet. After extraction with organic solvents only the anodal non-fluorescent band remained. After addition of an excess retinol only one band remained which by mobility corresponded to the cathodal band.The anodal of the two bands was therefore probably the apo form and the cathodal the holo form of the same retinol-binding protein. Their proportions, determined by densitometric scanning were approximately 4/1 (anodal/cathodal band). More than 85% of the retinol-binding protein in the urine bound to prealbumin-Sephrose. The apo retinol-binding protein from urine had the same electrophoretic mobility on agarose gel el-ctrophoresis and the same pattern on isoelectric focusing as an retinol-binding protein prepared from serum. The carboxy-terminal amino acid sequence of the retinol-binding protein from freshly collected urine that bound to prealbumin-Sepharose, was -Arg-Leu. The amino-terminal sequence was Glu-Arg-Asp-Cys-Arg-Val-Ser-X-Phe-Arg-Val-Lys-Glu-Asn-Phe-Asp-Lys-Ala-Arg-Phe-X-Gly-Thr-Trp-Tyr-. This sequence and the amino acid composition are compatible with the view that the retinol-binding protein in urine is the same as in plasma.