The structures of milled wood lignin (MWL), cellulolytic enzyme lignin (CEL), and residual lignin (REL) from a loblolly pine were analyzed using a modified derivatization followed by reductive cleavage (DFRC) method developed to allow the quantitative determination of three different structural monomeric products originating in lignin: phenolic beta-O-4, alpha-O-4, and etherified beta-O-4 structures. Results show that MWL and CEL are structurally identical, with an increased phenolic beta-O-4 content compared to that of the original Wiley milled wood. These results indicate that the portion of lignin linked to carbohydrates and that not linked to carbohydrates are structurally the same. Modified DFRC analysis of the effect of ball milling on the structure of lignin in wood, MWL, CEL, and REL indicate that vibratory ball milling does not change the lignin structure provided certain precautions are taken. Specifically, dry vibratory ball milling under a nitrogen atmosphere causes substantial structural changes including condensation, whereas vibratory ball milling in toluene had little effect on the lignin structure. This indicates that the structural differences observed in MWL and CEL arise because of the extraction procedure, which preferentially extracts phenolic lignin structures. MWL and CEL are representative of the total lignin in wood; however, due primarily to the solvent extraction process, higher phenolic hydroxyl contents are observed. Nitrobenzene oxidation showed structural results similar to those from the modified DFRC method.
[1] Mesozooplankton are significant consumers of phytoplankton, and have a significant impact on the oceanic biogeochemical cycles of carbon and other elements. Their contribution to vertical particle flux is much larger than that of microzooplankton, yet most global biogeochemical models have lumped these two plankton functional types together. In this paper we bring together several newly available data syntheses on observed mesozooplankton concentration and the biogeochemical fluxes they mediate, and perform data synthesis on flux rates for which no synthesis was available. We update the equations of a global biogeochemical model with an explicit representation of mesozooplankton (PISCES). We use the rate measurements to constrain the parameters of mesozooplankton, and evaluate the model results with our independent synthesis of mesozooplankton concentration measurements. We also perform a sensitivity study to analyze the impact of uncertainty in the flux rates. The standard model run was parameterized on the basis of the data synthesis of flux rates. The results of mesozooplankton concentration in the standard run are slightly lower than the independent databases of observed mesozooplankton concentrations, but not significantly. This shows that structuring and parameterizing biogeochemical models on the basis of observations without tuning is a strategy that works. The sensitivity study showed that by using a maximum grazing rate of mesozooplankton that is only 30% higher than the poorly constrained fit to the observations, the model mesozooplankton concentration gets closer to the observations, but mesozooplankton grazing becomes higher than what is currently accounted for. This is an indication that food selection by mesozooplankton is not sufficiently quantified at present. Despite the amount of effort that is represented by the data syntheses of all relevant processes, the good results that were obtained for mesozooplankton indicate that this effort needs to be applied to all components of marine biogeochemistry. The development of ecosystem models that better represent key plankton groups and that are more closely based on observations should lead to better understanding and quantification of the feedbacks between marine ecosystems and climate.
A model for chemotaxis in a bacteria-substrate mixture introduced by Keller and Segel, which is described by nonlinear partial differential equations, is studied analytically. The existence of traveling waves is shown for the system in which the substrate diffusion is taken into account and the chemotactic coefficient is greater than the motility one, and the instability of traveling waves is discussed.
Respiration (= oxygen consumption) rates and electron transport system (ETS) enzyme activities in conjunction with body carbon and nitrogen composition (for respiration) or protein (for ETS) were determined for over 50 copepod species from the mesopelagic (M; 500 to 1000 m), upperbathypelagic (UB; 1000 to 2000 m) and lower-bathypelagic (LB; 2000 to 3000 m) zones of the western subarctic Pacific. Calculated specific respiration rates (SR, a fraction of body carbon respired) at in situ temperatures (3, 2 and 1.5°C for the M, UB and LB zones, respectively) were greater for the M zone copepods (mean: 1.1% body C d ). Respiration rates adjusted to those at 1°C by using a Q 10 value (2.0), and to those of specimens with 1 mg body nitrogen by using a body mass exponent ( 0.8) , showed the same depth-related decline from the M zone to the LB zone. Stepwise regression analysis revealed that stage/sex, feeding type and/or reaction speeds (as judged by the presence/absence of myelin sheath enveloping axons) of copepods were possible additional variables affecting their respiration rates and ETS activities. The reduction in respiration rates and ETS activities from the M zone to the UB or LB zone is more pronounced when respiration rate data on Arctic/Antarctic epipelagic copepods is added; the same is true for ETS activities when respiration rate data is added from copepods dominant in the subarctic Pacific. The present results are compared with those of micronektonic crustaceans and fishes reported for specimens collected from 500 to 2000 m in other regions and discussed in the light of the 'visual interactions' hypothesis. KEY WORDS: Mesopelagic · Bathypelagic · Copepods · Respiration · ETS activity · Western North PacificResale or republication not permitted without written consent of the publisher
We have developed an environmentally benign large-scale (50 kg wood meal per batch) lignin production plant, operating based on acid-catalyzed polyethylene glycol (PEG) solvolysis of softwood biomass. The motivation for the proposed process was to promote technological innovation in biomass utilization systems in Japanese rural areas based on widely abundant Japanese cedar (sugi) biomass. In this study, the process was evaluated by investigating the effects of the source sugi wood meal size and the solvent PEG molecular mass on the yield, chemical structure, molecular mass, and thermal properties of the resultant PEG-modified lignin derivatives, glycol lignins (GLs). Reducing the source wood meal size and PEG solvent molecular mass not only promoted lignin PEGylation but also the subsequent acid-induced chemical rearrangements of the GLs as demonstrated by chemical analyses, 2D NMR, and size exclusion chromatography (SEC). Reducing the source wood meal size and/or increasing the solvent PEG molecular mass enhanced the thermal properties of GLs as determined by thermomechanical analysis (TMA) and thermogravimetric analysis (TGA). We considered that the proposed process can efficiently produce lignin derivatives with substantial control over the chemical structure and thermal properties to meet commercial and industrial needs for lignin-based advanced material production.
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