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This dataset provides comprehensive measurements of nutrient concentrations and fluxes in foliage, fine roots, wood, litterfall, and throughfall in hardwood and conifer stands across temperate forest stands at three long-term ecological research sites in the northeastern United States: Cone Pond, NH, Hubbard Brook, NH, and Sleepers River, VT. These sites vary in bedrock composition, parent material, and soil chemistry, but share similar climatic characteristics. Tissue nutrient concentrations were determined in leaves, fine roots, wood, and branches using site- and tissue-specific methods, with additional quality control through certified standards and duplicate sampling. Nutrient fluxes via litterfall and throughfall were measured over multiple years. Nutrient fluxes in roots were estimated from minirhizotron-based turnover rates and fine root biomass. Annual nutrient accumulation and uptake were calculated by integrating biomass production and nutrient concentrations. This dataset supports cross-site comparisons of forest biogeochemistry and provides a basis for evaluating nutrient limitations, cycling processes, and ecosystem responses to environmental gradients in northeastern temperate forests. 

In the northeastern United States, both hardwood and conifer forests have developed on sites with contrasting soils, allowing an examination of the effect of site and forest type on ecosystem nutrient cycling. We measured biomass production and nutrient fluxes in northern hardwood and conifer stands at three sites differing in soil fertility. We found that leaf, root, and wood concentrations of calcium (Ca), magnesium (Mg), and potassium reflected differences in soil base cation availability, while concentrations of nitrogen (N) and phosphorus (P) were more consistent across sites. Nutrient uptake was calculated as the sum of litterfall, net throughfall (throughfall minus precipitation), root turnover, and accumulation in perennial tissues (wood). We propose a novel metric of nutrient cycling, the nutrient retention fraction (NRF), defined as the proportion of annual nutrient uptake retained in biomass accretion. Because the NRF is unitless, it can be compared across nutrients; Ca and Mg had the highest NRF and P the lowest ( p = 0.05). Across sites and elements, NRFs were lower for conifers (5.0 ± 0.6%) than for hardwoods (7.2 ± 0.5%), associated with their lower productivity. Nutrient-use efficiency (biomass production divided by nutrient uptake) tended to be high where foliar concentrations indicated low availability of that nutrient. Nutrient retention of N and P was higher where availability of the other element was high, which could be a mechanism contributing to N and P co-limitation. 

We demonstrate the ability of a non-heme iron containingl-lysine dioxygenase to perform sequential oxidation on its native substrate and computationally explore structural elements that promote this reactivity. 

Previously unobserved (carbamoyl)disulfanyl chlorides were prepared by (i) addition of limiting aromatic secondary amine to (chlorocarbonyl)disulfanyl chloride; (ii) Harris reactions of sulfur dichloride with appropriate O-alkyl N-methyl-N-arylthiocarbamates; and (iii) regiospecific chlorolysis of bis(N-methyl-N-arylcarbamoyl)disulfanes. The newly synthesized unstable species were observed in situ by 1H NMR and were trapped with alkenes, thiocarbamates, and thiols using methods precedented by the chemistry of analogous (carbamoyl)sulfenyl chlorides. Furthermore, each of the trapped products was synthesized by an alternate route, reinforcing conclusions about their structures. While (N-methyl-N-phenylcarbamoyl)disulfanyl chloride was unstable and decomposed quickly or cyclized intramolecularly, introduction of the N,2,6-trimethylphenyl moiety led to significantly improved stability. As part of this study, an interesting, unexpectedly stable 1,2,4-dithiazinone was discovered and its structure was established by X-ray crystallography. The new heterocycle, with its twisted out-of-plane disulfide bond in a six-membered ring, readily donated a sulfur atom to triphenylphosphine; this reaction resulted in the formation of triphenylphosphine sulfide, along with the corresponding highly stable heterocycle in which the single sulfur that remains is part of a planar five-membered ring, fused to a co-planar aryl moiety. 

We construct a sequence of multisite gates which transform an easily constructed product state into an approx- imation to the superfluid ground state of the Bose-Hubbard model. The mapping is exact in the one-dimensional hard-core limit and for noninteracting particles in both one and two dimensions. The gate sequence has other applications, such as being used as part of a many-body interferometer which probes the existence of doublons. 

Baeyer-Villiger oxidation of alpha-alkoxy ketones 1 provides lactone acetals 2, which react with the lithium salts of di-methyl(alkyl) phosphonates in the presence of LaCl3•2LiCl to provide cyclic enones 3 in good to excellent yields after treatment with dilute aqueous potassium carbonate. Thus, five-, six-, and seven-membered lactones are con-verted to five-, six-, and seven membered cyclic enones. The utility of this two-step ring expansion method is demonstrated in the synthesis of (±)-1-epi-xerantholide from 5-methyl-2-cyclohexen-1-one. 

van der Waals materials support numerous exotic polaritonic phenomena originating from their layered structures and associated vibrational and electronic properties. However, many van der Waals materials' unique properties are most prominent at cryogenic temperatures. This presents a particular challenge for polaritonics research, as reliable optical constant data are required for understanding light-matter coupling. This paper presents a cryogenic Fourier transform infrared microscope design constructed entirely from off-the-shelf components and associated fitting procedures for determining optical constants in the infrared. Data correction techniques were developed to directly quantify systematic errors in the fitting procedure. We use this microscope to present the first temperature-dependent characterization of the optical properties of hexagonal boron nitride enriched with isotopically pure boron. Our full analysis of the infrared dielectric function shows small but significant tuning of the optical constants, which is highly consistent with Raman data from the literature. We then use this dielectric data to perform and analyze the polariton propagation properties, which agree exceptionally well with published cryogenic scattering-type near-field microscopy results. In addition to the insights gained into hyperbolic polaritons in hBN, our paper represents a transferable framework for characterizing exfoliated infrared polaritonic materials and other infrared devices. This could accelerate discoveries in different material systems, especially those that are spatially inhomogeneous or cannot be prepared as large single crystals. 

We examine the microfluidic postprocessing soft colloidal dispersions and reveal a variety of microflow regimes between nanoscale emulsions and solvents.