An Interface for the Direct Coupling of Small Liquid Samples to AMS.

We describe the moving wire interface attached to the 1-MV AMS system at LLNL's Center for Accelerator Mass Spectrometry for the analysis of nonvolatile liquid samples as either discrete drops or from the direct output of biochemical separatory instrumentation, such as high-performance liquid chromatography. Discrete samples containing at least a few 10s of nanograms of carbon and as little as 50 zmol 14C can be measured with a 3-5% precision in a few minutes. The dynamic range of our system spans approximately 3 orders in magnitude. Sample to sample memory is minimized by the use of fresh targets for each discrete sample or by minimizing the amount of carbon present in a peak generated by an HPLC containing a significant amount of 14C. Liquid Sample AMS provides a new technology to expand our biomedical AMS program by enabling the capability to measure low-level biochemicals in extremely small samples that would otherwise be inaccessible.

A fiber-optic sensor system for monitoring chlorinated hydrocarbon pollutants.

We have developed and field-tested a fiber-optic chemical sensor system for use in environmental monitoring and remediation. The system detects chlorinated hydrocarbon pollutants with colorimetry, and is based on an irreversible chemical reaction between the target compound and a specific reagent. The reaction products are detected by their absorption at 560 nm and can be monitored remotely with optical fibers. Continuous measurements are made possible by renewing the reagent from a reservoir with a miniature pumping system. The sensor has been evaluated against gas chromatography standards and has demonstrated accuracy and sensitivity (5 ppbw) sufficient for the environmental monitoring of trichloroethylene and chloroform. Successful preliminary field tests have been conducted in a variety of contamination monitoring scenarios.

Diagnosis of the Earliest Strain-Specific Interactions between Tobacco Mosaic Virus and Chloroplasts of Tobacco Leaves in Vivo by Means of Chlorophyll Fluorescence Imaging.

Fluorescence imaging was used to diagnose early stages of the strain-specific interactions between tobacco mosaic virus (strain PV230) and chloroplasts following infection of tobacco leaves (Nicotiana tabacum cv Xanthi). The earliest indication of interaction in tissues that ultimately become chlorotic was a reduction in chlorophyll fluorescence, and there was little fluorescence quenching compared with adjacent healthy tissues. Subsequently, fluorescence increased but remained unquenched. In the late stages fluorescence declined again in chlorotic regions as the chloroticmosaic symptoms developed. These in vivo data showing altered fluorescence yields confirm strain-specific interaction of virus coat protein with photosystem II (PSII) components in vitro, leading to photoinhibition and photooxidation of chlorophyll in infected cells and the development of visible chlorotic-mosaic symptoms. Although mechanisms leading to the low, unquenched fluorescence condition are not known, the intermediate high, unquenched fluorescence condition is consistent with impaired PSII electron transport as measured in vitro. Fluorescence lesions appear more rapidly and develop more extensively in high light, consistent with the faster and larger extent of symptom formation in high-light-grown leaves than in low-light-grown leaves.

Topography of photosynthetic activity of leaves obtained from video images of chlorophyll fluorescence.

The distribution of photosynthetic activity over the area of a leaf and its change with time was determined (at low partial pressure of O(2)) by recording images of chlorophyll fluorescence during saturating light flashes. Simultaneously, the gas exchange was being measured. Reductions of local fluorescence intensity quantitatively displayed the extent of nonphotochemical quenching; quench coefficients, q(N), were computed pixel by pixel. Because rates of photosynthetic electron transport are positively correlated with (1 - q(N)), computed images of (1 - q(N)) represented topographies of photosynthetic activity. Following application of abscisic acid to the heterobaric leaves of Xanthium strumarium L., clearly delineated regions varying in nonphotochemical quenching appeared that coincided with areoles formed by minor veins and indicated stomatal closure in groups.

Growth and physiological responses of Pinus ponderosa Dougl ex P. Laws. to long-term elevated CO(2) concentrations.

Seven-year-old ponderosa pine (Pinus ponderosa Dougl. ex P. Laws.) saplings and one- and two-year-old ponderosa pine seedlings of a Sierra Nevada and a Rocky Mountain seed source, respectively, were exposed to CO(2)-enriched atmospheres in an outdoor open-top chamber facility for 2.5 years. Seedling growth (main stem diameter, height, volume) increased with increasing CO(2) concentration, though the two populations exhibited different patterns of response. By the beginning of the last growth season, however, the trees under the highest CO(2) concentrations showed signs of stress that included accelerated needle abscision, chlorosis, and apparent alteration of tolerance to heat. The stress response is at least partly attributable to elevated foliar temperatures resulting from CO(2)-induced stomatal closure, which in turn lowered transpirational cooling of needles.