DNA tracers with information capacity and high detection sensitivity tested in groundwater studies

 In order to investigate the usefulness of unique synthetic DNA tracers in groundwater, a field experiment was conducted in Norway. DNA tracers and a sodium-chloride tracer were injected into an aquifer. The transport of DNA molecules was interpreted by comparing with the plume of chloride ions under forced-gradient steady-state flow conditions. Spatial concentration moments described the migration of conservative tracers. Mobility and migration of DNA in groundwater demonstrate that DNA tracers can be detected by using the polymerase chain reaction (PCR) and DNA sequence analysis. The results indicate that DNA tracers can be valuable tools as tracers in groundwater investigations. Received, June 1997 / Revised, July 1998, December 1998 / Accepted, January 1999     

Impact of UV-B, Heat and Chemicals on Ethylene-Production of Lichens

To assess the impact of UV-B radiation combined with NaHSO₃ in solution under laboratory conditions, we compared the amounts of stress-ethylene produced by two lichen species of the same genus. Ramalina lacera, an epiphytic Mediterranean lichen, was found to be rather sensitive to UV-B combined with NaHSO₃, relative to the epilithic desert lichen R. maciformis. The impact of high temperatures with FeCl₂ in solution, measured by amounts of stress ethylene accentuated the adaptability of R. maciformis to desert conditions, whereas R. lacera appeared to be rather sensitive to extreme temperatures especially in the case of chemical contamination. The adaptability of R. maciformis to UV-B appears to be related to the photoprotective capabilities of lichen substances.     

Role of electrochemical reactions in pressure solution

Using a Surface Forces Apparatus we have measured changes in the electrical potential difference between quartz and mica surfaces that correlate with the changing quartz dissolution rate when surfaces are pressed together at relatively low pressures (2-3 atm) in aqueous electrolyte solutions of 30 mM CaCl₂ at 25 °C. No detectable dissolution or voltage potential difference is measured in symmetrical systems (e.g. mica-mica or quartz-quartz) or between dry surfaces subjected to similar pressures, indicating that the dissolution can not be attributed to a simple pressure effect, slow aging (creep), or plastic deformation of the quartz surface. In quartz-mica systems brought together under pressure or to close proximity in electrolyte solution, the onset of quartz dissolution is marked by a sudden, rapid decrease in the quartz thickness at initial rates in the range from 1 to 4 nm/min, which after several hours settles into a constant rate of approximately 0.01 nm/min (∼5 μm/yr). Concomitantly, the potential drops to a constant value once the dissolution rate has stabilized. The decrease in the decay rate is interpreted as being due to saturation of the confined aqueous film and/or to the buildup of a Stern layer on the quartz surface, and the constant rate as being due to the steady-state chemical dissolution and diffusion of the dissolving silica into the surrounding reservoir. The dissolution is ‘non-uniform’: the surfaces become rough as dissolution proceeds, with the appearance of pits in a manner analogous to corrosion. On occasions, the process of rapid dissolution followed by a gradual transition to steady dissolution repeats itself, suggesting that the pit structure and Stern layer are fragile and subject to collapse and/or expulsion from the gap. Preliminary experiments on the dissolution of multi-faceted milled quartz particles (∼1.0 μm diameter) compressed between two muscovite surfaces suggest an asymmetry in the dissolution rates at different crystallographic planes. The origin of the electrical potential is interpreted as arising from the overlapping of the electric double-layers of two dissimilar surfaces when they are forced into close proximity. This electrical potential difference, for as yet unknown reasons, appears to be the driving force for the dissolution, rather than pressure.     

Developing a Marine Information System by Integrating Existing Ocean Models Using Object-Oriented Technology

Information systems developed for different applications within the environmental domain have common characteristics, which can potentially be abstracted for sharing and reuse of design and software modules. This article presents an approach to designing for reuse by abstracting commonalities in the design of a Marine Information System (MIS), facilitating data management in a prototype operational monitoring, forecasting, and management system for the North Atlantic and the Nordic Seas. A detailed study of the requirements and data analysis was carried out, and Object-Oriented Technology (OOT) is employed to encapsulate abstractions and to promote reuse of code and design. This article identifies the Object-Oriented Frameworks (OOFW) required to build the MIS. It also provides guidelines to environmental scientists for restructuring legacy software and employing modern programming techniques.     

Dissolved organic matter variations in coastal plain wetland watersheds: The integrated role of hydrological connectivity,land use,and seasonality

Dissolved organic matter (DOM) is integral to fluvial biogeochemical functions, and wetlands are broadly recognized as substantial sources of aromatic DOM to fluvial networks. Yet how land use change alters biogeochemical connectivity of upland wetlands to streams remains unclear. We studied depressional geographically isolated wetlands on the Delmarva Peninsula (USA) that are seasonally connected to downstream perennial waters via temporary channels. Composition and quantity of DOM from 4 forested, 4 agricultural, and 4 restored wetlands were assessed. Twenty perennial streams with watersheds containing wetlands were also sampled for DOM during times when surface connections were present versus absent. Perennial watersheds had varying amounts of forested wetland (0.4–82%) and agricultural (1–89%) cover. DOM was analysed with ultraviolet–visible spectroscopy, fluorescence spectroscopy, dissolved organic carbon (DOC) concentration, and bioassays. Forested wetlands exported more DOM that was more aromatic‐rich compared with agricultural and restored wetlands. DOM from the latter two could not be distinguished suggesting limited recovery of restored wetlands; DOM from both was more protein‐like than forested wetland DOM. Perennial streams with the highest wetland watershed cover had the highest DOC levels during all seasons; however, in fall and winter when temporary streams connect forested wetlands to perennial channels, perennial DOC concentrations peaked, and composition was linked to forested wetlands. In summer, when temporary stream connections were dry, perennial DOC concentrations were the lowest and protein‐like DOM levels the highest. Overall, DOC levels in perennial streams were linked to total wetland land cover, but the timing of peak fluxes of DOM was driven by wetland connectivity to perennial streams. Bioassays showed that DOM linked to wetlands was less available for microbial use than protein‐like DOM linked to agricultural land use. Together, this evidence indicates that geographically isolated wetlands have a significant impact on downstream water quality and ecosystem function mediated by temporary stream surface connections.     

Trace element geochemistry of coesite-bearing eclogites from the Roberts Victor kimberlite, Kaapvaal craton

Trace element characteristics of seven coesite-bearing eclogitic xenoliths from the Roberts Victor kimberlite demonstrate that this suite of eclogites originated as gabbroic cumulates in oceanic crust that was subsequently subducted. All but one of the garnets show positive Eu anomalies, accompanied by a flat heavy rare earth pattern, which is atypical of garnet, but characteristic of plagioclase, arguing for a considerable amount of plagioclase in the protoliths. Forward modelling of the accumulation of liquidus minerals from primitive komatiitic, picritic, and basaltic liquids suggests that at least some of the eclogite protoliths were not derived from basaltic parental liquids, whereas derivation from either komatiitic or picritic liquids is possible. The reconstructed eclogite bulk rocks compare favourably with oceanic gabbros from ODP hole 735B (SW Indian Ridge), even to the extent that oxygen isotopic systematics show signs of low-temperature seawater alteration. However, the oxygen isotope trends are the reverse of what is expected for cumulates in the lower section of the oceanic crust. These new findings show that δ¹⁸O values in eclogitic xenoliths, despite being sound indicators for their interaction with hydrothermal fluids at low pressure, do not necessarily bear a simple relationship with the inferred oceanic crustal stratigraphy of the protoliths.