Crystal Structure of Cucumene Synthase, a Terpenoid Cyclase That Generates a Linear Triquinane Sesquiterpene
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99 GENERAL AND MISCELLANEOUS↗
Engineering topics
Chow, J.
Publications and source records attributed to Chow, J..
Mercury in Active-Layer Tundra Soils of Alaska: Concentrations, Pools, Origins, and Spatial Distribution
Tundra soils serve as major sources of mercury (Hg) input to the Arctic Ocean via river runoff and coastal erosion; yet little information is available on tundra soil Hg concentrations, pool sizes, origins, and dynamics. We present a detailed investigation of Hg in the active layer (upper ~100 cm subject to seasonal thaw) of tundra soils across 11 sites in Alaska. Soil Hg concentrations in organic horizons (151 ± 7 μg/kg) were in the upper range of temperate soil organic horizons, and concentrations in mineral horizons (98 ± 6 μg/kg) were much higher than in temperate soils. Soil Hg concentrations declined from inland to coastal sites, in contrast to a hypothesized northward increase expected because of proximity to coastal atmospheric mercury depletion events. Principle component analyses and elemental ratios results show that exogenic sources dominated over geogenic sources—in A-horizons (66 ± 4%) and mineral B-horizons (51 ± 1%). 14 C age-dating suggested recent origins of Hg in surface soils but showed that mineral soils (more than 7,300 years old) must have accumulated atmospheric inputs across millennia leading to high soil concentrations and pools. We estimated a total Northern Hemisphere active-layer tundra soil Hg pool of 184 Gg (range of 136 to 274 Gg), suggesting a globally important Hg storage pool. Tundra soils are subject to seasonal thaw and freeze dynamics, thereby providing large inputs to rivers, lakes, and the Arctic Ocean. Understanding processes that mobilize Hg from tundra soils will be critical to understanding future Arctic wildlife and human Hg exposures.
54 ENVIRONMENTAL SCIENCES↗
Comparison of automated pre-column and post-column analysis of amino acid oligomers
It has been shown that various amino acids will polymerize under plausible prebiotic conditions on mineral surfaces, such as clays and soluble salts, to form varying amounts of oligomers (n = 2-6). The investigations of these surface reactions required a quantitative method for the separation and detection of these amino acid oligomers at the picomole level in the presence of nanomole levels of the parent amino acid. In initial high-performance liquid chromatography (HPLC) studies using a classical postcolumn o-phthalaldehyde (OPA) derivatization ion-exchange HPLC procedure with fluorescence detection, problems encountered included lengthy analysis time, inadequate separation and large relative differences in sensitivity for the separated species, expressed as a variable fluorescent yield, which contributed to poor quantitation. We have compared a simple, automated, pre-column OPA derivatization and reversed-phase HPLC method with the classical post-column OPA derivatization and ion-exchange HPLC procedure. A comparison of UV and fluorescent detection of the amino acid oligomers is also presented. The conclusion reached is that the pre-column OPA derivatization, reversed-phase HPLC and UV detection produces enhanced separation, improved sensitivity and faster analysis than post-column OPA derivatization, ion-exchange HPLC and fluorescence detection.
NASA Discipline Exobiology↗
Cognitive memory
Perceptive cognition system structurally analyzed with semantic techniques for parsing and compiling
Arnold, P.↗