The relationship between the bioavailability of dissolved organic matter (DOM) and its bulk chemical composition was examined on three dates at 10 sites on the Ogeechee River, a blackwater river in Georgia, Samples of riverine DOM were concentrated from filtered river water using reverse osmosis. In addition, particulate organic matter (POM), in the form of leaf litter, algae, and macrophytes, was leached with synthetic rainwater to obtain fresh DOM. Elemental composition, carboxylic acid content, and bacterial growth were measured on all samples. The results of this study indicate that fresh DOM in POM leachates is generally more bioavailable than riverine DOM. The bioavailability of riverine DOM appears to be greater under low discharge conditions and decreases with distance downstream. The bioavailability of all DOM samples is very well predicted (r2 = 0.93, II = 20) by an empirical equation of the form: bioavailability = a,, + a,(H: C) + a,(0 : C) + al(N : C). When compositional data arc plotted on a van Krevelen diagram, it is evident that POM leachates and, to a lesser degree, DOM from headwatcr sites have compositions that differ little from simple mixtures of major components of biomass (lipids, sugars, proteins, and lignins). Father downstream, major diagenetic alteration of organic matter is evident from the compositions of DOM samples, whose H : C and 0 : C ratios are lower and higher, respectively, than for any possible mixture of biomass components. Bioavailability of DOM is closely related to the pcrccntage of aliphatic carbon in a sample, and downstream decreases in bioavailability arc mainly attributable to selective degradation of aliphatic carbon in riverine DOM.Dissolved organic matter (DOM) is an essential component of microbial food webs in natural waters because it is a growth substrate for bacteria that are then consumed by higher trophic levels (Pomeroy 1974). Only a fraction of the DOM present in natural waters supports bacterial growth, and the bioavailability of DOM varies from <1 to >75% for different molecular weight fractions and in different environments (Table I). Because of the significance of DOM in microbial food webs and the great variation in its availability to bacteria, researchers have sought simple physical or chemical indicators of the bioavailability of DOM in natural waters. One approach has been to quantify specific biochemical compounds such as sugars and amino acids, whose concentrations may reflect the bioavailability of DOM. This approach is neither simple nor predictive of bioavailability of the entire DOM pool. Separating riverine DOM by molecular size using ultrafiltration showed that bacteria use DOM fractions in the order small > large > moderate (Meyer et al. 1987); yet high molecular weight oceanic DOM is more available than low (Amon and Benner 1994). Hence one cannot use the size distribution of DOM to predict reliably its bioavailability. A third approach is based on a bioassay of bacterial growth after resins are used to separate Acknowledgments...
Chemiresistive sensors are becoming increasingly important as they offer an inexpensive option to conventional analytical instrumentation, they can be readily integrated into electronic devices, and they have low power requirements. Nanowires (NWs) are a major theme in chemosensor development. High surface area, interwire junctions, and restricted conduction pathways give intrinsically high sensitivity and new mechanisms to transduce the binding or action of analytes. This Review details the status of NW chemosensors with selected examples from the literature. We begin by proposing a principle for understanding electrical transport and transduction mechanisms in NW sensors. Next, we offer the reader a review of device performance parameters. Then, we consider the different NW types followed by a summary of NW assembly and different device platform architectures. Subsequently, we discuss NW functionalization strategies. Finally, we propose future developments in NW sensing to address selectivity, sensor drift, sensitivity, response analysis, and emerging applications.
This communication describes a simple solvent-free method for fabricating chemoresistive gas sensors on the surface of paper. The method involves mechanical abrasion of compressed powders of sensing materials on the fibers of cellulose. We illustrate this approach by depositing conductive layers of several forms of carbon (e.g., single-walled carbon nanotubes [SWCNTs], multi-walled carbon nanotubes, and graphite) on the surface of different papers (Figure 1, Figure S1). The resulting sensors based on SWCNTs are capable of detecting NH3 gas at concentrations as low as 0.5 part-per-million.
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