HVSR of ambient noise in Ston (Croatia): comparison with theoretical spectra and with the damage distribution after the 1996 Ston-Slano earthquake

Horizontal-to-vertical spectral ratios (HVSR) of ambient vibrations measured in the ancient town of Ston (Croatia) on 99 locations, are shown to be well matched to the theoretical ones computed for body-waves as well as for the surface waves. This match is poorer for sites on the slopes of nearby hills. The ratios of measured peak horizontal ground acceleration during the damaging earthquake in 1996 (M _L = 6.0) and the ones obtained using empirical attenuation laws is approximately equal to the mapped value of the dynamic amplification factor determined on the basis of observed HVSR in the vicinity of the accelerometric station. The HVSR of the accelerogram is very similar to the HVSR of the ambient noise. The damage to the building stock in the old town centre caused by the earthquake series of 1996 is closely related to the estimated soil amplification and its fundamental frequency. More measurements in buildings are needed to arrive at confident conclusions about possible soil-structure resonance.     

Multi-disciplinary earthquake researches in Western Turkey: Hints to select sites to study geochemical transients associated to seismicity

Warm and hot spring water as well as soil gas radon release patterns have been monitored in the Aegean Extensional Province of Western Turkey, alongside regional seismic events, providing a multi-disciplinary approach. In the study period of 20 months, seven moderate earthquakes with M _L between 4.0 and 4.7 occurred in this seismically very active region; two earthquakes with magnitude 5.0 also occurred near the study area. Seismic monitoring showed no foreshock activity. By contrast, hydro-geochemical anomalies were found prior to these seismic events, each lasting for weeks. The anomalies occurred foremost in conjunction with dip-slip events and seem to support the dilatancy and water diffusion hypothesis. Increased soil gas radon release was recorded before earthquakes associated with strike-slip faults, but no soil radon anomalies were seen before earthquakes associated with dip-slip faults. Geochemical anomalies were also noticeably absent at some springs throughout the postulated deformation zones of impending earthquakes. The reason for this discrepancy might be due to stress/strain anisotropies.     

Determination of focal depth by two waveformbased methods: A case study for the 2008Panzhihua earthquake

With the 2008 M_S6.1 Panzhihua earthquake as a case study, we demonstrate that the focal depth of the main shock can be well constrained with two approaches: (1) using the depth phase sPL and (2) using full waveform inversion of local and teleseismic data. We also show that focal depths can be well constrained using the depth phase sPL with single broadband seismic station. Our study indicates that the main shock is located at a depth of 11 km, much shallower than those from other studies, confirming that the earthquake occurs in upper crust. Aftershocks are located in the depth range of 11-16 km, which is consistent with a ruptured near vertical fault whose width is about 10 km, as expected for an M_S6.1 earthquake.     

Geochemical Atlas of Slovakia and examples of its applications to environmental problems

Results of comprehensive geochemical mapping and thematic studies of the Slovak territory (rocks, soils, stream sediments, groundwaters, biomass, and radioactivity) in the first half of the 1990s led to several new research programmes in Slovakia, within the frame of which new methodologies for geochemical data evaluation and map visualization were elaborated. This study describes the application and elaboration of data from the Geochemical Atlas of the Slovak Republic at national and regional levels. Based on the index of environmental risk (I_ER = ΣPEC/PNEC), the level of contamination for the geological component of the environment in Slovakia was evaluated. Approximately 10.5% of Slovakia’s territory was characterized as being environmentally disturbed to highly disturbed. In the areas where environmental loadings have accumulated, 14 regions where environmental risks existed due to high element concentrations were defined. The model calculations of health risk estimates based on the databases of the Geochemical Atlas for groundwater and soils indicate that the possible risk occurrence of carcinogenic diseases from groundwater arsenic contents is high in more than 10% of Slovakia, whereas the chronic risk is negligible. To determinate the background and threshold levels a combined statistical–geochemical approach was developed and applied as an example for groundwater at the national level as well as for single groundwater bodies. The results of statistical method application for the whole groundwater body (GBW) were compared with the background values for anthropogenically non-influenced areas in GBW. Final background value took into account time variations and spatial distribution of the element in GBW. Furthermore, based on the database from the Geochemical Atlas for groundwater, groundwater bodies potentially at qualitative risk were delineated for the whole of Slovakia. From a total of 101 groundwater bodies 17 were characterized as being at risk and 22 as being at possible risk.     

On the occurrence,trace element geochemistry,and crystallization history of zircon from in situ ocean lithosphere

We characterize the textural and geochemical features of ocean crustal zircon recovered from plagiogranite, evolved gabbro, and metamorphosed ultramafic host-rocks collected along present-day slow and ultraslow spreading mid-ocean ridges (MORs). The geochemistry of 267 zircon grains was measured by sensitive high-resolution ion microprobe-reverse geometry at the USGS-Stanford Ion Microprobe facility. Three types of zircon are recognized based on texture and geochemistry. Most ocean crustal zircons resemble young magmatic zircon from other crustal settings, occurring as pristine, colorless euhedral (Type 1) or subhedral to anhedral (Type 2) grains. In these grains, Hf and most trace elements vary systematically with Ti, typically becoming enriched with falling Ti-in-zircon temperature. Ti-in-zircon temperatures range from 1,040 to 660°C (corrected for a _TiO2 ≈ 0.7, a _SiO2 ≈ 1.0, pressure ≈ 2 kbar); intra-sample variation is typically ~60–150°C. Decreasing Ti correlates with enrichment in Hf to ~2 wt%, while additional Hf-enrichment occurs at relatively constant temperature. Trends between Ti and U, Y, REE, and Eu/Eu* exhibit a similar inflection, which may denote the onset of eutectic crystallization; the inflection is well-defined by zircons from plagiogranite and implies solidus temperatures of ~680–740°C. A third type of zircon is defined as being porous and colored with chaotic CL zoning, and occurs in ~25% of rock samples studied. These features, along with high measured La, Cl, S, Ca, and Fe, and low (Sm/La)_N ratios are suggestive of interaction with aqueous fluids. Non-porous, luminescent CL overgrowth rims on porous grains record uniform temperatures averaging 615 ± 26°C (2SD, n = 7), implying zircon formation below the wet-granite solidus and under water-saturated conditions. Zircon geochemistry reflects, in part, source region; elevated HREE coupled with low U concentrations allow effective discrimination of ~80% of zircon formed at modern MORs from zircon in continental crust. The geochemistry and textural observations reported here serve as an important database for comparison with detrital, xenocrystic, and metamorphosed mafic rock-hosted zircon populations to evaluate provenance.     

Phyllocladane in brown coal from Handlová, Slovakia: Isolation and structural characterization

Aliphatic diterpenes were isolated from brown coal from Handlová, Slovakia, using microwave assisted extraction of mechanically activated coal powder. The parameters of the extraction procedure were optimized to get the target compounds in high yield. The total extract was separated using adsorption chromatography. GC–MS revealed tetracyclic and tricyclic diterpanes in the aliphatic fraction; they were identified as 16α(H)-phyllocladane (83%), isopimarane (11%), 18-norisopimarane (4%), abietane (2%) and fichtelite (<0.1%). It was found that more than 2 g of the most abundant diterpane, 16α(H)-phyllocladane could be extracted from 1 kg of Handlová coal. Because of the scarcity of relevant analytical data, 16α(H)-phyllocladane was thoroughly characterized by spectroscopic and chromatographic methods. A complete set of ¹H and ¹³C NMR data is given including their comparison with published values and ab initio calculations. EI mass and IR spectra of 16α(H)-phyllocladane are shown and discussed. Kováts retention indices measured on two common GC stationary phases are also given.     

Preliminary health risk assessment for polybrominated diphenyl ethers and polybrominated dibenzo-p-dioxins/furans in seafood from Guangzhou and Zhoushan, China

Dietary intake is one of the important routes of human exposure to brominated flame retardants (BFRs) such as polybrominated diphenyl ethers (PBDEs). The use of PBDEs may also result in exposure to polybrominated dibenzo-p-dioxins and dibenzofurans (PBDDs/DFs), as these compounds are impurities in technical mixtures of BFRs and can also be formed unintentionally by the same processes that generate chlorinated dioxins. This study determined the concentrations of polybrominated compounds in common seafood in Guangzhou and Zhoushan, and assessed the health risks of these chemicals via consumption of contaminated seafood. Seafood samples (fish, bivalves, shrimp, crab, and cephalopods) purchased from local markets in 2003 and 2004 were analyzed for PBDEs and PBDDs/DFs. The highest concentration of total PBDEs (46.3 ng g(-1) lipid wt.) was detected in fish from Guangzhou, in which BDEs 47 and 209 were the two predominant congeners. The total daily intakes of PBDEs, PBDDs, and PBDFs were, 946, 6.39, and 6.54 pg kg(-1) body weight (bw) in Guangzhou, and 489, 4.99, and 7.65 pg kg(-1) bw in Zhoushan, respectively. The hazard ratios for PBDDs and PBDFs were both greater than unity, indicating that these compounds may pose some health risks to the local population.