RESUMEN
Grasslands throughout the world are responding in diverse ways to changing climate and environmental conditions. In this study we analyze indicators of phosphorus limitation including phosphorus concentrations, phosphorus to nitrogen, and carbon ratios, oxygen isotope ratios of phosphate in vegetation, and phosphatase enzyme activity in soil to shed light on potential effects of climate change on phosphorus availability to grassland vegetation. The study was conducted at the Jasper Ridge Global Change Experiment (JRGCE), California where manipulations mimicking increases in temperature, water, nitrogen and carbon-dioxide have been maintained for over 15 years. We compare our results to an earlier study conducted 3 years after the start of the experiment, in order to assess any change in the response of phosphorus over time. Our results suggest that a decade later the measured indicators show similar or only slightly stronger responses. Specifically, addition of nitrogen, the principle parameter controlling biomass growth, increased phosphorus demand but thresholds that suggest P limitation were not reached. A study documenting changes in net primary productivity (NPP) over time at the JRGCE also could not identify a progressive effect of the manipulations on NPP. Combined these results indicate that the vegetation in these grassland systems is not very sensitive to the range of climate parameters tested.
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Cambio Climático , Fósforo , California , Ecosistema , Pradera , SueloRESUMEN
Stable isotopes present in water (δ2H, δ18O) have been used extensively to evaluate hydrological processes on the basis of parameters such as evaporation, precipitation, mixing, and residence time. In estuarine aquatic habitats, residence time (τ) is a major driver of biogeochemical processes, affecting trophic subsidies and conditions in fish-spawning habitats. But τ is highly variable in estuaries, owing to constant changes in river inflows, tides, wind, and water height, all of which combine to affect τ in unpredictable ways. It recently became feasible to measure δ2H and δ18O continuously, at a high sampling frequency (1 Hz), using diffusion sample introduction into a cavity ring-down spectrometer. To better understand the relationship of τ to biogeochemical processes in a dynamic estuarine system, we continuously measured δ2H and δ18O, nitrate and water quality parameters, on board a small, high-speed boat (5 to >10 m s-1) fitted with a hull-mounted underwater intake. We then calculated τ as is classically done using the isotopic signals of evaporation. The result was high-resolution (â¼10 m) maps of residence time, nitrate, and other parameters that showed strong spatial gradients corresponding to geomorphic attributes of the different channels in the area. The mean measured value of τ was 30.5 d, with a range of 0-50 d. We used the measured spatial gradients in both τ and nitrate to calculate whole-ecosystem uptake rates, and the values ranged from 0.006 to 0.039 d-1. The capability to measure residence time over single tidal cycles in estuaries will be useful for evaluating and further understanding drivers of phytoplankton abundance, resolving differences attributable to mixing and water sources, explicitly calculating biogeochemical rates, and exploring the complex linkages among time-dependent biogeochemical processes in hydrodynamically complex environments such as estuaries.
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Monitoreo del Ambiente , Agua , Isótopos , Nitratos , RíosRESUMEN
Stable isotopes are extensively used as tracers for the study of plant-water sources. Isotope-ratio infrared spectroscopy (IRIS) offers a cheaper alternative to isotope-ratio mass spectroscopy (IRMS), but its use in studying plant and soil water is limited by the spectral interference caused by organic contaminants. Here, we examine two approaches to cope with contaminated samples in IRIS: on-line oxidation of organic compounds (MCM) and post-processing correction. We assessed these methods compared to IRMS across 136 samples of xylem and soil water, and a set of ethanol- and methanol-water mixtures. A post-processing correction significantly improved IRIS accuracy in both natural samples and alcohol dilutions, being effective with concentrations up to 8% of ethanol and 0.4% of methanol. MCM outperformed the post-processing correction in removing methanol interference, but did not effectively remove interference for high concentrations of ethanol. By using both approaches, IRIS can overcome with reasonable accuracy the analytical uncertainties associated with most organic contaminants found in soil and xylem water. We recommend the post-processing correction as the first choice for analysis of samples of unknown contamination. Nevertheless, MCM can be more effective for evaluating samples containing contaminants responsible for strong spectral interferences at low concentrations, such as methanol.
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Plantas/química , Espectrofotometría Infrarroja/métodos , Agua/química , Deuterio , Etanol/química , Funciones de Verosimilitud , Metanol/química , Compuestos Orgánicos/aislamiento & purificación , Isótopos de Oxígeno , Contaminantes Químicos del Agua/aislamiento & purificaciónRESUMEN
The functions of the bromodomain and extra terminal (BET) family of proteins have been implicated in a wide range of diseases, particularly in the oncology and immuno-inflammatory areas, and several inhibitors are under investigation in the clinic. To mitigate the risk of attrition of these compounds due to structurally related toxicity findings, additional molecules from distinct chemical series were required. Here we describe the structure- and property-based optimization of the in vivo tool molecule I-BET151 toward I-BET282E, a molecule with properties suitable for progression into clinical studies.