Geochronological constraints on the evolution of the Periadriatic Fault System (Alps)

Fault rocks from various segments of the Periadriatic fault system (PAF; Alps) have been directly dated using texturally controlled Rb-Sr microsampling dating applied to mylonites, and both stepwise-heating and laser-ablation ⁴⁰Ar/³⁹Ar dating applied to pseudotachylytes. The new fault ages place better constraints on tectonic models proposed for the PAF, particularly in its central sector. Along the North Giudicarie fault, Oligocene (E)SE-directed thrusting (29-32 Ma) is currently best explained as accommodation across a cogenetic restraining bend within the Oligocene dextral Tonale-Pustertal fault system. In this case, the limited jump in metamorphic grade observed across the North Giudicarie fault restricts the dextral displacement along the kinematically linked Tonale fault to ~30 km. Dextral displacement between the Tonale and Pustertal faults cannot be transferred via the Peio fault because of both Late Cretaceous fault ages (74-67 Ma) and sinistral transtensive fault kinematics. In combination with other pseudotachylyte ages (62-58 Ma), widespread Late Cretaceous-Paleocene extension is established within the Austroalpine unit, coeval with sedimentation of Gosau Group sediments. Early Miocene pseudotachylyte ages (22-16 Ma) from the Tonale, Pustertal, Jaufen and Passeier faults argue for a period of enhanced fault activity contemporaneous with lateral extrusion of the Eastern Alps. This event coincides with exhumation of the Penninic units and contemporaneous sedimentation within fault-bound basins.     

Microbial–silica interactions in Icelandic hot spring sinter: possible analogues for some Precambrian siliceous stromatolites

Silicified deposits, such as sinters, occur in several modern geothermal environments, but the mechanisms of silicification (and crucially the role of microorganisms in their construction) are still largely unresolved. Detailed examination of siliceous sinter, in particular sections of microstromatolites growing at the Krisuvik hot spring, Iceland, reveals that biomineralization contributes a major component to the overall structure, with approximately half the sinter thickness attributed to silicified microorganisms. Almost all microorganisms observed under the scanning electron microscope (SEM) are mineralized, with epicellular silica ranging in thickness from < 5 μm coatings on individual cells, to regions where entire colonies are cemented together in an amorphous silica matrix tens of micrometres thick. Within the overall profile, there appears to be two very distinct types of laminae that alternate repeatedly throughout the microstromatolite: ‘microbial’ layers are predominantly consisting of filamentous, intact, vertically aligned, biomineralized cyanobacteria, identified as Calothrix and Fischerella sp.; and weakly laminated silica layers which appear to be devoid of any microbial component. The microbial layers commonly have a sharply defined base, overlying the weakly laminated silica, and a gradational upper surface merging into the weakly laminated silica. These cyclic laminations are probably explained by variations in microbial activity. Active growth during spring/summer allows the microorganisms to keep pace with silicification, with the cell surfaces facilitating silicification, while during their natural slow growth phase in the dark autumn/winter months silicification exceeds the bacteria’s ability to compensate (i.e. grow upwards). At this stage, the microbial colony is probably not essential to microstromatolite formation, with silicification presumably occurring abiogenically. When conditions once again become favourable for growth, recolonization of the solid silica surface by free‐living bacteria occurs: cell motility is not responsible for the laminations. We have also observed that microbial populations within the microstromatolite, some several mm in depth, appear viable, i.e. they still have their pigmentation, the trichomes are not collapsed, cell walls are unbroken, cytoplasm is still present and they proved culturable. This suggests that the bulk of silicification occurred rapidly, probably while the cells were still alive. Surprisingly, however, measurements of light transmittance through sections of the microstromatolite revealed that photosynthetically active light (PAL) only transmitted through the uppermost 2 mm. Therefore the ‘deeper’ microbial populations must have either: (i) altered their metabolic pathways; (ii) become metabolically inactive; or (iii) the deeper populations may be dominated by different microbial assemblages from that of the surface. From these collective observations, it now seems unequivocal that microstromatolite formation is intimately linked to microbial activity and that the sinter fabric results from a combination of biomineralization, cell growth and recolonization. Furthermore, the similarities in morphology and microbial component to some Precambrian stromatolites, preserved in primary chert, suggests that we may be witnessing contemporaneous biomineralization processes and growth patterns analogous to those of the early Earth.     

Estimation of surface latent heat fluxes from IRS-P4/MSMR satellite data

The brightness temperatures of the Microwave sensor MSMR (Multichannel Scanning Microwave Radiometer) launched in May 1999 onboard Indian Oceansat-1 IRS-P4 are used to develop a direct retrieval method for latent heat flux by multivariate regression technique. The MSMR measures the microwave radiances at 8 channels at frequencies of 6.6, 10.7, 18 and 21 GHz at both vertical and horizontal polarizations. It is found that the surface LHF (Latent Heat Flux) is sensitive to all the channels. The coefficients were derived using the National Centre for Environmental Prediction (NCEP) reanalysis data of three months: July, September, November of 1999. The NCEP daily analyzed latent heat fluxes and brightness temperatures observed by MSMR were used to derive the coefficients. Validity of the derived coefficients was checked within situ observations over the Indian Ocean and with NCEP analyzed LHF for global points. The LHF derived directly from the MSMR brightness temperature (Tb) yielded an accuracy of 35 watt/m². LHF was also computed by applying bulk formula using the geophysical parameters extracted from MSMR. In this case the errors were higher apparently due to the errors involved in derivation of the geophysical parameters.     

A comparison of cytochrome P4501A (CYP1A) mRNA inducibility in four species of Atlantic coast anadromous fishes

Quantification of levels of cytochrome P4501A (CYP1A) gene expression in sentinel species of fishes has been proposed as a management tool to evaluate contamination of aquatic systems. Based on preliminary studies, we hypothesized that differences in CYP1A mRNA inducibility among individuals, populations, or species might lead to spurious conclusions when using this approach in environmental monitoring programs. To address this possibility, we quantitated and compared CYP1A mRNA induction levels in four species of common Atlantic Coast estuarine fish: smooth flounder, hogchoker, striped bass, and Atlantic tomcod, which were treated with model chemicals (beta naphthoflavone (β-NF), or benzo[a]pyrene at 10 ppm) known to induce CYP1A mRNA, or were exposed to contaminated environments. Species-specific CYP1A DNA probes were generated from PCR (polymerase chain reaction) amplification of genomic DNA using conserved oligonucleotide primers, and, along with cloned rainbow trout and Atlantic tomcod CYP1A cDNA probes were used to quantify CYP1A mRNA levels in northern blot analyses. Successful PCR amplification of CYP1A hybridizable DNA fragments was observed for all four species. Results from northern blot analyses showed large differences in CYP1A mRNA induction among species; only Atlantic tomcod exhibited significant induction of CYP1A mRNA for both chemically treated (97-fold) and environmentally exposed fish (34-fold). Significant, although lower, levels of induction were observed in β-NF treated (14-fold) smooth flounder, but not in environmentally exposed smooth flounder. Only low levels (not significant) of CYP1A gene induction were detected in hogchokers and striped bass. We conclude that CYP1A mRNA inducibility differed significantly among fish taxa perhaps due to differences in regulation of gene expression, suggesting that careful selection of sentinel species should be exercised prior to the use of CYP1A mRNA induction in environmental monitoring programs. However, the significance of differences in CYP1A mRNA inducibility in relation to higher level biological endpoints has yet to be determined.     

Endmember graphics

Thek points inp-space corresponding to a specified set ofk (k<p) linearly independent endmember estimates associated with ap-variate (n×p) compositional datasetX, define the vertices of a (k?1) dimensional simplexH. Then estimated mixtures which together account for the systematic variation in the datasetX, are each convex combinations of thek fixed endmember estimates. Accordingly, then-points inp-space which represent these mixtures must be interior points of the simplexH. The purpose of this paper is to describe a simple graphical procedure for examining the positions of the estimated mixtures relative tok=3 or 4 putative endmembers, and for assessing their compliance or otherwise with the convexity constraints. Since the mixture coefficients must be estimated first in order to obtain the mixture estimates, the paper begins with a review of the least-squares partitioning procedure.     

Numerical studies of two-dimensional saturated/ unsaturated drainage models

The partial differential equation which governs the seepage of water in unsaturated and saturated porous media is solved numerically by a generalized Newton iteration technique for two models, one ditch drainage model and one earth dam model. For each model, which is two-dimensional, a few hypothetical soils with different moisture retention curves are considered. In both models only drainage from an initially saturated soil occurs; thus, the problem of hysteresis is avoided. The results of the computations are compared with those of corresponding saturated (pure groundwater) models; solutions obtained earlier by this author and others.

Computational instability phenomena appear when the slope of the retention curves is made steep, i.e., for poorly-graded soils.     

Adjusting to Policy Expectations in Climate Change Modeling

This paper surveys and interprets the attitudes of scientists to the use of flux adjustments in climate projections with coupled Atmosphere Ocean General Circulation Models. The survey is based largely on the responses of 19 climate modellers to several questions and a discussion document circulated in 1995. We interpret the responses in terms of the following factors: the implicit assumptions which scientists hold about how the environmental policy process deals with scientific uncertainty over human-related global warming; the different scientific styles that exist in climate research; and the influence of organisations, institutions, and policy upon research agendas. We find evidence that scientists' perceptions of the policy process do play a role in shaping their scientific practices. In particular, many of our respondents expressed a preference for keeping discussion of the issue of flux adjustments within the climate modeling community, apparently fearing that climate contrarians would exploit the issue in the public domain. While this may be true, we point to the risk that such an approach may backfire. We also identify assumptions and cultural commitments lying at a deeper level which play at least as important a role as perceptions of the policy process in shaping scientific practices. This leads us to identify two groups of scientists, pragmatists and purists, who have different implicit standards for model adequacy, and correspondingly are or are not willing to use flux adjustments.