The influence of the herbicide 2-methyl-4-chlorophenoxyacetic acid (MCPA) on the mineralization of litter-derived alkanes and the abundance of the alkane monooxygenase gene (alkB) in the detritusphere of Pisum sativum (L.)

In the present study, the temporal and spatial variation of the abundance of the alkane monooxygenase gene alkB and 16S rRNA genes in different soil compartments was analysed in the presence or absence of 2-methyl-4-chlorophenoxyacetic acid (MCPA) after the addition of pea litter to soil in a microcosm study. Samples were analysed shortly after litter addition (T0) and 1?week (T1), 3?weeks (T3) and 6?weeks (T6) after the addition of litter. In addition also, the quantity and quality of litter-derived alkanes was analysed and measured. The results revealed a fast and complete degradation of MCPA in all compartments throughout the experiment. Nevertheless, significant changes in the distribution patterns of short- and middle-chained alkanes suggest an interaction of MCPA and alkane degradation. alkB gene copy numbers were highly influenced by the time point of analysis and by the investigated soil compartment. Overall, an increase in alkB gene copy numbers from T0 to T3 was visible in the upper soil compartments whereas a decrease compared to T0 was measured in the deeper soil compartments. MCPA addition resulted in an increase of alkB abundance at T6. Gene copy numbers of 16S rRNA were not influenced by sampling time and soil compartment. In contrast to the control treatments, a slight increase in 16S rRNA gene copy numbers was visible at T1 and T3 compared to T0 in all soil compartments.     

Does the “high sugar” trait of perennial ryegrass cultivars express under temperate climate conditions?

The objective was to evaluate water‐soluble carbohydrate (WSC) and crude protein (CP) concentration of perennial ryegrass (PRG) cultivars with different genetic potential for producing WSC under two contrasting agronomic managements in temperate climate (southern Chile). A 4 × 2 factorial design was randomly allocated to 24 plots (31 m² each, three blocks): four PRG cultivars (diploid standard cultivar, “2nSt”; tetraploid standard cultivar, “4nSt”; diploid high sugar cultivar developed in New Zealand, “2nHSNZ”; and tetraploid high sugar cultivar developed in Europe, “4nHSEU”) and two agronomic managements (“favourable,” defoliations at three leaves per tiller and nitrogen (N) fertilization rate of 83.3 kg N ha^?1 year^?1; “unfavourable,” defoliations at two leaves per tiller and N fertilization rate of 250 kg N ha^?1 year^?1). Herbage samples were collected in early spring, spring, summer and autumn. Concentration of WSC did not differ among cultivars in spring and summer, averaging 194 and 251 g/kg DM, respectively. The cultivar 4nHSEU had the greatest WSC concentration in early spring and autumn (187 and 266 g/kg DM, respectively) and the greatest CP concentration across samplings (average 230 g/kg DM). Favourable management improved WSC concentrations in early spring and summer and decreased CP in spring, summer and autumn. Annual DM yield did not vary with cultivar or management, averaging 8.43 t/ha. Within a 12‐month study at one site in a temperate environment in southern Chile, PRG cultivars have not shown a consistent expression of the “high sugar” trait, where a genetic × environment interaction might be operating.     

Exhaustive Screening of Long-Term Pollutants in Riverbank Sediments of the Wurm River,Germany

Fluvial sediments can act as archives for long-term pollution. However, in environmental studies, often only preselected contaminants and, therefore, only a limited part of the pollution are considered. Herein, geochemical investigations of riverbank samples of the Wurm River (catchment <?400 km²) depict the anthropogenic impact of the city Aachen (250,000 inhabitants) to its main outlet resulting in an exhaustive list of present pollutants including their concentrations. The study is based on 14 riverbank sediment samples at eight sampling sites on a 7.6-km-long segment of the Wurm River. The sediment samples were analyzed for grain size composition (laser diffraction particle size analyzer), total organic carbon (TOC), trace element inventory (X-ray fluorescence), and organic compounds (chromatography-mass spectrometry). Here, we report quantitative data for 71 persistent organic substances as well as six trace elements (Cu, Zn, As, Ba, Hg, and Pb) entering the Wurm River due to domestic and industrial emissions. In general, a slight decline of, e.g., PTEs, DDX, and PCB concentrations with decreasing sampling depth points to a steady improvement of conditions. Whereas no clear trends can be seen for organic pollutants along the investigated reach with increasing distance to the main source of pollution (Aachen city). As obtained concentrations for organic pollutants indicate a rather low level of pollution, trace element values exceed geogenic background values by far. Furthermore, we used selected compounds as time markers for a rough estimation of sedimentation rates. Obtained values point to a highly complex morphodynamic regime with changing sedimentation rates (0.6 to 3.0 cm a^?1) within barely 100 m of river course.     

The accumulation of phytolith-occluded carbon in soils of different grasslands

Purpose

A better understanding of the role of grassland systems in producing and storing phytolith-occluded carbon (PhytOC) will provide crucial information in addressing global climate change caused by a rapid increase in the atmospheric CO₂ concentration.

Materials and methods

Soil samples of typical steppe, meadow steppe, and meadow in Inner Mongolia, China, were taken at 0–10-, 10–20-, 20–40-, and 40–60-cm depths in July and August of 2015. The soil phytoliths were isolated by heavy liquid (ZnBr₂), and the soil PhytOC was determined by the traditional potassium dichromate method.

Results and discussion

The results of our study showed that the storage of soil phytoliths was significantly higher in the meadow (33.44 ± 0.91 t ha^?1) cf. meadow steppe (26.8 ± 0.98 t ha^?1) and typical steppe (21.19 ± 4.91 t ha^?1), which were not different. The soil PhytOC storage was significantly different among grassland types, being: meadow (0.39 ± 0.01 t ha^?1) > meadow steppe (0.29 ± 0.02 t ha^?1) > typical steppe (0.23 ± 0.02 t ha^?1). PhytOC storage in typical steppe soil within the 0–60-cm soil layer is the lowest and that in meadow soils is the highest. The grassland type and the soil condition play significant roles in accumulation of phytoliths and PhytOC in different grassland soils. We suggest that the aboveground net primary productivity (ANPP) is important in soil phytolith accumulation and PhytOC content.

Conclusions

Phytolith and PhytOC storages in grassland soil are influenced by factors such as grass type, local climate and soil conditions, and management practices. Management practices to increase grass biomass production can significantly enhance phytolith C sequestration.

     

Wheat straw biochar application increases ammonia volatilization from an urban compacted soil giving a short-term reduction in fertilizer nitrogen use efficiency

Journal of Soils and Sediments - The potential for using biochar to reclaim degraded urban land into productive land needs to be verified to address the incipient loss of agricultural land. A pot...     

Mobilities of Organic Compounds in Reconstituted Cuticular Wax of Barley Leaves: Effects of Monodisperse Alcohol Ethoxylates on Diffusion of Pentachlorophenol and Tetracosanoic Acid

Effects of monodisperse alcohol ethoxylates on mobilities of ¹⁴C-labelled pentachlorophenol (PCP) and tetracosanoic acid (C₂₄AC) in reconstituted cuticular wax of barley leaves were measured. Depending on the respective alcohol ethoxylate investigated, the diffusion coefficient (D) of PCP in barley wax was increased by factors ranging from 3·3 to 19·6, whereas D of C₂₄AC, was increased by factors varying between 22 and 315. In order to analyse the relationship between the concentration of surfactants in the wax and their effects on D, the amounts of alcohol ethoxylates dissolved in the wax at equilibrium with external concentrations well above the critical micelle concentration (CMC) were determined. Wax/water partition coefficients (K_ww) of the alcohol ethoxylates were about one order of magnitude lower than cuticle/water partition coefficients (K_cw), which is a consequence of the semi-crystalline structure of the wax compared with amorphous cutin. Correlations between effects on D and maximum amounts of alcohol ethoxylates dissolved in the wax were obtained indicating an unspecific wax/surfactant interaction. This was solely dependent on the amount of surfactant sorbed to the wax, leading to increased mobilities of pesticides in the wax. Applying ESR-spectroscopy, which gave an insight into the molecular structure of the wax, supported this interpretation of an unspecific plasticising effect of the alcohol ethoxylates on the molecular structure of the wax. The results obtained in this study are in good accordance with the results obtained in a recent study investigating the effects of the same group of alcohol ethoxylates on mobilities of pesticides in isolated, but intact, cuticular membranes of Citrus. This demonstrates that the investigation of isolated and subsequently reconstituted cuticular wax is a useful model system analysing the mechanisms of the surfactant interaction with the transport-limiting barrier of plant cuticles.     

Influence of litter chemistry and stoichiometry on glucan depolymerization during decomposition of beech (Fagus sylvatica L.) litter

Glucans like cellulose and starch are a major source of carbon for decomposer food webs, especially during early- and intermediate-stages of decomposition. Litter quality has previously been suggested to notably influence decomposition processes as it determines the decomposability of organic material and the nutrient availability to the decomposer community. To study the impact of chemical and elemental composition of resources on glucan decomposition, a laboratory experiment was carried out using beech (Fagus sylvatica, L.) litter from four different locations in Austria, differing in composition (concentration of starch, cellulose and acid unhydrolyzable residue or AUR fraction) and elemental stoichiometry (C:N:P ratio). Leaf litter was incubated in mesocosms for six months in the laboratory under controlled conditions. To investigate the process of glucan decomposition and its controls, we developed an isotope pool dilution (IPD) assay using (13)C-glucose to label the pool of free glucose in the litter, and subsequently measured the dilution of label over time. This enabled us to calculate gross rates of glucose production through glucan depolymerization, and glucose consumption by the microbial community. In addition, potential activities of extracellular cellulases and ligninases (peroxidases and phenoloxidases) were measured to identify effects of resource chemistry and stoichiometry on microbial enzyme production. Gross rates of glucan depolymerization and glucose consumption were highly correlated, indicating that both processes are co-regulated and intrinsically linked by the microbial demand for C and energy and thereby to resource allocation to enzymes that depolymerize glucans. At early stages of decomposition, glucan depolymerization rates were correlated with starch content, indicating that starch was the primary source for glucose. With progressing litter decomposition, the correlation with starch diminished and glucan depolymerization rates were highly correlated to cellulase activities, suggesting that cellulose was the primary substrate for glucan depolymerization at this stage of decomposition. Litter stoichiometry did not affect glucan depolymerization or glucose consumption rates early in decomposition. At later stages, however, we found significant negative relationships between glucan depolymerization and litter C:N and AUR:N ratio and a positive relationship between glucan depolymerization and litter N concentration. Litter C:N and C:P ratios were negatively related to cellulase, peroxidase and phenoloxidase activities three and six months after incubation, further corroborating the importance of resource stoichiometry for glucan depolymerization after the initial pulse of starch degradation.