Emission of coherent THz radiation from superconductors

Compact solid-state sources of terahertz (THz) radiation are being sought for sensing, imaging, and spectroscopy applications across the physical and biological sciences. We demonstrate that coherent continuous-wave THz radiation of sizable power can be extracted from intrinsic Josephson junctions in the layered high-temperature superconductor Bi2Sr2CaCu2O8. In analogy to a laser cavity, the excitation of an electromagnetic cavity resonance inside the sample generates a macroscopic coherent state in which a large number of junctions are synchronized to oscillate in phase. The emission power is found to increase as the square of the number of junctions reaching values of 0.5 microwatt at frequencies up to 0.85 THz, and persists up to approximately 50 kelvin. These results should stimulate the development of superconducting compact sources of THz radiation.     

Der Fe(III)-Reduktionstest - ein einfaches Verfahren zur Abschätzung der Wirkung von Umweltchemikalien auf die mikrobielle Aktivität in Böden

The Fe(III)-reduction test - a simple procedure to determine the effects of environmental chemicals on the microbial activity in soils A new simple microorganism test is described. The test is based on the fact that the degree of microbial reduction in waterlogged soils is influenced by the addition of different amounts of toxic chemicals. The microbial activity under reducing conditions can be measured by the degree of the microbial reduction of easily reducable Fe(III)-oxides (ferrihydrites) to soluble Fe²⁺-ions. The influence of different test parameters, the reproducibility and limitations of the proposed test are described. Toxicity indices of the investigated chemicals are derived graphically from the resulting dose effect curves. Values are determined for those concentrations which cause no (Non Effect Level, NEL) and a 50%-inhibition (ED₅₀) of the microbial activity in soil samples. By representing some results for 2,4-D, 2,4,5-T, LAS, Cd and Hg the scope of the test is described. First results show that the effective toxicity of chemicals is strongly influenced by the adsorption capacity of the soils. Furthermore the relation of toxic substances to nutrients in the soil solution causing competition or antagonistic and synergistic effects during uptake and also within the organisms can substantially influence the toxicity of chemicals.     

Dosis- Wirkungs-Beziehungen zur Erfassung von Chemikalienwirkungen auf die mikrobielle Aktivität von Böden: I. Kurvenverläufe und Auswertungsmöglichkeiten

Dose response curves: their use in soil microbiological research and possibilities of evaluation The relation between different concentrations of a toxicant in soils and the resulting effects on biological parameters can be described with dose response curves. Dose response curves make it possible to determine the concentrations of a chemical that create definite effects (?Effective Doses”?, e.g. ED₁₀ and ED₅₀ for 10- and 50% inhibitory effects) or to evaluate the rate of increase of inhibition with increasing concentrations. Some of the mostly used ways to extract these parameters from dose response curves are presented and examined with regard to their suitability in soil microbiological research. Besides graphical procedures for the evaluation of dose response curves a mathematical model for fitting quantitative dose response curves is introduced. With this model the confidence intervals of effective doses can be computed. By showing eight frequently appearing shapes of dose response curves the advantages and limitations of different ways to calculate effective doses are discussed.     

The impact of boreal forest fire on climate warming

We report measurements and analysis of a boreal forest fire, integrating the effects of greenhouse gases, aerosols, black carbon deposition on snow and sea ice, and postfire changes in surface albedo. The net effect of all agents was to increase radiative forcing during the first year (34 +/- 31 Watts per square meter of burned area), but to decrease radiative forcing when averaged over an 80-year fire cycle (-2.3 +/- 2.2 Watts per square meter) because multidecadal increases in surface albedo had a larger impact than fire-emitted greenhouse gases. This result implies that future increases in boreal fire may not accelerate climate warming.     

Adsorption and solubility of ten metals in soil samples of different composition

We conducted batch experiments for ten metals [Mg, Cr(III), Fe(III), Co, Ni, Cu, Zn, Sr, Cd, Pb] and four soil samples of different composition to determine the relation of the soluble fraction (’intensity’︁) to an adsorbed or precipitated metal pool (’quantity’︁) and, thus, to investigate the buffer function of soils. The soil samples were spiked with 6 to 12 exponentially increasing metal doses added as metal nitrates. The native metal pool involved in sorption processes was characterized by an extraction with 0.025 M (NH₄)₂EDTA (pH 4.6). The quantity-intensity (Q/I) relations of eight metals [except Cr(III) and Fe(III)] were governed by sorption and complexation processes and can be fitted by Freundlich isotherms. Q/I relations for Cr(III) and two soils indicate a sorption maximum, which can be approximated with the Langmuir isotherm. In a calcareous soil high Cr doses induced the precipitation of a Cr oxide. The solution concentrations of Fe are primarily a function of the pH-dependent solubility of ferrihydrite. For all metals pH was the predominant factor controlling the partitioning between the solid and the liquid phase. Drastic losses in the buffer function of soils primarily occurred in the slightly acidic range. Furthermore, adsorption was also metal specific. On the basis of median Freundlich K values, adsorption increased in the order [median K_F values and K_F range (mg kg^—1) in brackets]: Mg (2.9: 0.9—19) < Sr (4.7: 0.6—21) << Co (17.7: 1.1—143) < Zn (26.7: 1.8—301) = Ni (27.6: 2.4—120) < Cd (71: 2.5—405) << Cr(III) (329: 45—746) < Cu (352: 30—1200) < Pb (1730: 76—4110).     

Repeated monitoring of organic carbon stocks after eight years reveals carbon losses from intensively managed agricultural soils in Western Germany

Past land‐use changes, intensive cropping with large proportions of root crops, and preferred use of mineral fertilizer have been made responsible for proceeding losses of soil organic C (SOC) in the plough layer. We hypothesized that in intensive agriculturally managed regions changes in SOC stocks would be detectable within a decade. To test this hypothesis, we tracked the temporal development of the concentrations and stocks of SOC in 268 arable sites, sampled by horizon down to 60 cm in the Cologne‐Bonn region, W Germany, in 2005 and in 2013. We then related these changes to soil management data and humus balances obtained from farmers' surveys. As we expected that changes in SOC concentrations might at least in part be minor, we fractionated soils from 38 representative sites according to particle size in order to obtain C pools of different stability. We found that SOC concentrations had increased significantly in the topsoil (from 9.4 g kg^?1 in 2005 to 9.8 g kg^?1 in 2013), but had decreased significantly in the subsoil (from 4.1 g kg^?1 in 2005 to 3.5 g kg^?­1 in 2013). Intriguingly, these changes were due to changes in mineral‐bound SOC rather than to changes in sand‐sized organic matter pools. As bulk density decreased, the overall SOC stocks in the upper 60 cm exhibited a SOC loss of nearly 0.6 t C (ha · y)^?1 after correction by the equivalent soil mass method. This loss was most pronounced for sandy soils [?0.73 t SOC (ha · y)^?1], and less pronounced for loamy soils [?0.64 t SOC (ha · y)^?1]; silty soils revealed the smallest reduction in SOC [?0.3 t SOC (ha · y)^?1]. Losses of SOC occurred even with the overall humus balances having increased positively from about 20 kg C (ha · y)^?1 (2003–2005) to about 133 kg C (ha · y)^?1 (2005–2013) due to an improved organic fertilization and intercropping. We conclude that current management may fail to raise overall SOC stocks. In our study area SOC stocks even continued to decline, despite humus conservation practice, likely because past land use conversions (before 2005) still affect SOC dynamics.     

Soil heterogeneity at the field scale: a challenge for precision crop protection

Crop protection seldom takes into account soil heterogeneity at the field scale. Yet, variable site characteristics affect the incidence of pests as well as the efficacy and fate of pesticides in soil. This article reviews crucial starting points for incorporating soil information into precision crop protection (PCP). At present, the lack of adequate field maps is a major drawback. Conventional soil analyses are too expensive to capture soil heterogeneity at the field scale with the required spatial resolution. Therefore, we discuss alternative procedures exemplified by our own results concerning (i) minimally and non-invasive sensor techniques for the estimation of soil properties, (ii) the evidence of soil heterogeneity with respect to PCP, and (iii) current possibilities for incorporation of high resolution soil information into crop protection decisions. Soil organic carbon (SOC) and soil texture are extremely interesting for PCP. Their determination with minimally invasive techniques requires the sampling of soils, because the sensors must be used in the laboratory. However, this technique delivers precise information at low cost. We accurately determined SOC in the near-infrared. In the mid-infrared, texture and lime content were also exactly quantified. Non-invasive sensors require less effort. The airborne HyMap sensor was suitable for the detection of variability in SOC at high resolution, thus promising further progress regarding SOC data acquisition from bare soil. The apparent electrical conductivity as measured by an EM38 sensor was shown to be a suitable proxy for soil texture and layering. A survey of arable fields near Bonn (Germany) revealed widespread within-field heterogeneity of texture-related ECa, SOC and other characteristics. Maps of herbicide sorption and application rate were derived from sensor data, showing that optimal herbicide dosage is strongly governed by soil variability. A phytoassay with isoproturon confirmed the reliability of spatially varied herbicide application rates. Mapping areas with an enhanced leaching risk within fields allows them to be kept free of pesticides with related regulatory restrictions. We conclude that the use of information on soil heterogeneity within the concept of PCP is beneficial, both economically and ecologically.     

Inhibitory effects of the total and water-soluble concentrations of nine different metals on the dehydrogenase activity of a loess soil

 This study focuses on a comparison of the microbial toxicity of nine metals, including As as a metalloid and two species of Cr. A loess soil [Ap horizon, clay 15.2%, organic C 1.12%, pH(CaCl₂) 7.02] was spiked with 8–12 geometrically increasing doses of the metals. The dehydrogenase assay (2-p-iodophenyl-3-p-nitrophenyl-5-phenyltetrazoliumchloride method) was combined with sorption and solubility experiments. The resulting dose-response curves and sorption isotherms were used to derive total doses that caused definite percentage inhibitions [i.e. effective doses (ED) causing a 10–90% reduction in dehydrogenase activity (dha)] as well as the corresponding toxic solution concentrations causing the same reductions in dha (i.e. effective concentrations; EC₁₀–EC₉₀). Based on total doses, the toxicity decreased in the following order with ED₅₀ values (mg kg^–1) given in brackets: Hg (2.0)>Cu (35)>Cr(VI) (71)>Cr(III) (75)>Cd (90)>Ni (100)>Zn (115)>As (168)>Co (582)>Pb (652). With regard to solution concentrations, toxicity decreased in the order (EC₅₀ in mg l^–1): Hg (0.003)>Pb (0.04)>Cu (0.05)>Cd (0.14)>Zn (0.19)>Cr(III) (0.62)>Ni (0.69)>Co (30.6)>As (55.5)>Cr(VI) (78.1). The retention of the metals by the soil differed strongly. Pb, Cu, and Hg exhibited the highest and Ni, As, and Cr(VI) the lowest sorption constants (Freundlich K values: 2455, 724, 348, 93, 13, and 0.06 mg kg^–1, respectively). The sorptivity of the metals and their microbial toxicity in the aqueous phase were characteristically related: metals with a strong toxic action in the soil solution were adsorbed by the soil to a high degree and vice versa. Therefore, especially for metals with a high inherent toxicity, sorption is an effective way of immobilizing them and temporarily detoxifying soil. Received: 2 July 1998     

Einfluß von Bodenreaktion,Redoxbedingungen und organischer Substanz auf die Phosphatgehalte der Bodenlösung

Influence of soil reaction, redox conditions and organic matter on the phosphate content of soil solutions Samples of seven agriculturally used soils of different composition (A_p-horizons), one marine underwater soil and two garbage composts were adjusted in suspensions (soil-water-ratio 1:3) to different pH values between 3 and 8 by additions of NaOH or HCl. By a different degree of aeration the redox potential was kept constant at selected values between +600 and ?300 mV. After an incubation period of 22–24 days under controlled E_h-pH-conditions the content of total phosphate and orthophosphate was measured in the equilibrium solutions. At oxidizing conditions all soil and compost samples show the lowest phosphate content in solution at pH S6. At higher and lower pH values the phosphate content increases. The results indicate that the phosphate concentration is determined by adsorption/desorption processes – mainly connected with iron oxides – and not by dissolution or precipitation of definite phosphorus compounds. Under reducing conditions the phosphate content increases in the equilibrium solutions of all samples. Especially in samples with high content of sulphides a considerable increase of the phosphate concentration could be measured at Eh values below +300 mV at pH 5, +200 mV at pH 6, and ± 0 mV at pH7 and 8. Below these values phosphate containing iron(II1) oxides were reduced and – with further decreasing redox potentials – transformed to iron sulphides. In samples without sulphide formation the phosphate mobilization is much lower. With increasing amount of soluble organic matter the phosphate content of the solutions also increases because of phosphate desorption by organic anions or complexation of aluminium and iron from phosphate adsorbing compounds. But also the content of soluble organically bound phosphate increases and may amount to 70 % of the total phosphate content in solution.     

Control of prostaglandin-induced parturition in sows by injection of the beta-adrenergic blocking agent carazolol or carazolol and oxytocin

Although parturition commonly is induced in swine with prostaglandin F2 alpha or one of its analogs, variation in response to the treatment is large. The purpose of this investigation was to more precisely terminate parturition. Two experiments were conducted. Sows all received prostaglandin analog followed, 20 h later, by different doses of the beta-adrenergic blocking agent carazolol and(or) oxytocin. Treatment with 3 mg of carazolol alone caused parturition to commence within 2.6 +/- .23 (SEM) h after injection. Parturition was complete in 2.0 +/- .13 h and proceeded smoothly without the necessity of manual assistance. Adding 2.5 I.U. of oxytocin to the 3 mg of carazolol speeded the onset of labor (1.7 +/- .17 h). However, in some cases parturition was interrupted and the time passing between the birth of the first and the last piglet was prolonged to 2.5 +/- .28 h. We conclude that by applying carazolol 20 h after a prostaglandin analog, parturition in swine may be terminated very effectively.