An architectural model of spring wheat: Evaluation of the effects of population density and shading on model parameterization and performance

ADELwheat is an architectural model that describes development of wheat in 3D. This paper analyzes the robustness of the parameterization of ADELwheat for spring wheat cultivars in relation to plant population density and shading. The model was evaluated using data from two spring wheat experiments with three plant population densities and two light regimes. Model validation was done at two levels of aggregation: (a) by comparing parameterization functions used as well as parameter values to the data (leaf and tiller appearance, leaf number, blade dimensions, sheath length, internode length) and (b) by comparing ground cover (GC) and leaf area index (LAI) of simulated virtual wheat plots with GC and LAI calculated from data. A sensitivity analysis was performed by modulating parameters defining leaf blade dimensions and leaf or tiller appearance rate.In contrast to population density, shading generally increased phyllochron and delayed tiller appearance. Both at the level of the organ and at the level of the canopy the model performed satisfactorily. Parameterization functions in the model that had been established previously applied to independent data for different conditions; GC and LAI were simulated adequately at three population densities. Sensitivity analysis revealed that calibration of phyllochron and blade area needs to be accurate to prevent disproportional deviations in output.The robustness of the model parameterization and the simulation performance confirmed that the model is a complete architectural model for aboveground development of spring wheat. It can be used in studies that require simulation of spring wheat structure, such as studies on plant–insect interaction, remote sensing, and light interception.     

Von der Erkenntnis zur Entscheidung

This contribution highlights the role and importance of ecotoxicology in regulatory decisions of chemicals legislation focussing on the responsibilities of the German Federal Environmental Agency (UBA). Therefore, organisational structures and processes relevant for making decisions concerning the risks of chemicals to men and the environment are described. As any regulatory decision starts with scientific findings, a brief overview of UBA’s activities with regard to own research and to initiate research in the area of ecotoxicology is provided. In addition, the vast importance of standardisation and international harmonisation of guidelines for testing and assessment of chemicals is illustrated, including the time- and ressource consuming character of these harmonisation processes. Subsequently, the involvement of regulatory decision making in intense and controversial scientific and political debates is emphasised. The transparency of these discussions and the independence of science is critically addressed in this context. In a final chapter the job requirements and options for qualification in Germany are described, ending up with a brief summary of the positive experiences with UBA’s contribution to the new advanced training course in ecotoxiciology realised by GDCh/SETAC GLB. A summary of the discussions on these different topics emphasises the specific challenge in regulatory ecotoxicology: To generate knowledge relevant for decision making, while acting in an area of conflict between scientific demands and economical as well as political interests.     

Monitoring of waste deposit derived groundwater contamination with organic tracers

Specific anthropogenic substances derived from seepage and leakage water from a waste deposit landfill were analysed in groundwater and drainage effluents using gas chromatography-mass spectrometry (GC/MS). Here, we demonstrate the application of an organic marker approach to study lateral and vertical distribution of contamination as well as the long-term emission behaviour. Source-specific and environmentally-stable pesticides, plasticisers and pharmaceuticals, such as N,N-diethyl toluamide, N-butyl benzene sulfonamide, clofibric acid, mecoprop and bisphenol A, were quantitatively analysed. A distinct lateral expansion was detected. Although temporal variations were high, no significant trend was observed.     

A Bayesian network approach to modelling land-use decisions under environmental policy incentives in the Brazilian Amazon

ABSTRACT

Deforestation driven by agricultural expansion is a major threat to the biodiversity of the Amazon Basin. Modelling how deforestation responds to environmental policy implementation has thus become a policy relevant scientific undertaking. However, empirical parameterization of land-use/cover change (LUCC) models is challenging due to the high complexity and uncertainty of land-use decisions. Bayesian Network (BN) modelling provides an effective framework to integrate various data sources including expert knowledge. In this study, we integrate remote sensing products with data from farm-household surveys and a decision game to model LUCC at the BR-163, in Brazil. Our ‘business as usual’ scenario indicates cumulative forest cover loss in the study region of 8,000 km² between 2014 and 2030, whereas ‘intensified law-enforcement’ would reduce cumulative deforestation to 1,600 km² over the same time interval. Our findings underline the importance of conservation law enforcement in modulating the impact of agricultural market incentives on land cover change.     

Toxicity of octameric elemental sulphur in aquatic sediments

The proportions of elemental sulphur species in sediment from a contaminated area and a reference sediment sample were compared with the acute toxicity measured in short-term toxicity tests. Octameric elemental sulphur was separated into three operationally defined fractions. Here we show that octameric elemental sulphur contributes to the acute toxicity measured by bioluminescence inhibition. Our findings show that only a small part of extractable elemental sulphur was effective during exposure to the test organisms. A firmly bound fraction of sulphur was found in a contaminated sediment. This information has to be taken into account while interpreting the acute sediment toxicity.     

Neocembrene A, a major component of the trail-following pheromone in the genus Prorhinotermes (Insecta, Isoptera, Rhinotermitidae)

Summary. The diterpene neocembrene A or (1E,5E,9E,12R)-1,5,9-trimethyl-12-(1-methylethenyl)-1,5,9-cyclotetradecatriene, known as the trail-following pheromone of the advanced Termitidae Nasutitermitinae Nasutitermes exitiosus and Trinervitermes bettonianus, has been identified after SPME-GC/MS as the major component of the trail-following pheromone of the Rhinotermitidae Prorhinotermitinae, Prorhinotermes canalifrons and P. simplex. In all the other Rhinotermitidae studied until now, the major component of their trail pheromones is dodecatrienol ((3Z,6Z,8E)-dodeca-3,6,8-trien-1-ol). This biochemical data further add to the anatomical and molecular characteristics that give a special status to the taxon Prorhinotermes among Rhinotermitidae. In Prorhinotermes canalifrons and P. simplex, neocembrene A was the only secretory compound specific to the sternal gland surface that could be detected after SPME. It elicited orientation as well as recruitment behavioral effects. However, the comparison of the respective biological activities triggered by neocembrene A and by sternal gland secretion suggests that minor components of the latter are acting in synergy with neocembrene A.     

Identification and quantitation of dinaphthylsulfones in particulate matter of the Elbe river,Germany. Part VI of organic compounds as contaminants of the Elbe river and its tributaries

Gas chromatographic-mass spectrometric (GC/MS) analysis of particulate matter of the Elbe river and its tributaries Havel, Spree and Mulde revealed a group of three dinaphthylsulfone isomers as sedimentary and suspended particulate matter (SPM) contaminants. The mass spectra of dinaphthylsulfones are characterized by the molecular ion (m/z 318), and the naphthyl fragment ion m/z 127. Losses of HSO(2) and C(10)H(7)O from the molecular ion lead to different mass spectra for each isomer. The gas phase infrared spectra exhibit isomer specific bands in the spectral region between 900 and 700 wave numbers. A synthetic mixture of dinaphthylsulfones was used for isomer identification and the assignment of the gas chromatographic retention behaviour of the dinaphthylsulfone isomers. Quantitative GC/MS analysis of dinaphthylsulfones in 44 sediment and SPM samples provided comprehensive information on the overall distribution and distinct sources of dinaphthylsulfones in the Elbe river drainage system. The results indicate emissions of these compounds over prolonged times and their environmental stability in anaerobic sediments.     

Temporal variation of trace metal geochemistry in floodplain lake sediment subject to dynamic hydrological conditions

Climate change and land use may significantly influence metal cycling in dynamic river systems. We studied temporal variation of sediment characteristics in a floodplain lake, including concentrations of dissolved organic carbon, acid volatile sulfide and trace metals. The sampling period included a severe winter inundation and a dramatic water level drop during summer. Temporal changes were interpreted using multivariate analysis and chemical equilibrium calculations. Metal concentrations in sediment increased with depth, indicating a gradual improvement of sediment quality. In contrast, dissolved metal concentrations were highest in top layers due to mobilization from oxyhydroxides and precipitation with sulfides in deeper layers. Inundation had a mobilizing effect as it stimulated resuspension and oxygenation of sediment top layers. Water table lowering combined with organic matter decomposition led to immobilization due to sulfide formation. The chemistry of the sediments was consistent with model calculations, especially for macro-elements. The results illustrate the importance of seasonality for metal risk assessment.     

Formation of polychlorobiphenyls in silicone rubber

In silicone rubber crosslinked with bis(2,4-dichlorobenzoyl) peroxide (DCBP) as initiator about 0.1% of DCBP is converted into polychlorobiphenyls (PCBs). The PCB content in silicone rubber determined by high resolution gas chromatography (HRGC) after its destruction by HF is around 10 mg/kg. 29 PCB congeners were detected. Instead of the expected PCB-47, lower chlorinated congeners are predominant. Some possible pathways of their origin are presented.