Pattern‐process relationships in surface hydrology: hydrological connectivity expressed in landscape metrics

The degree of hydrological connectivity is mainly determined by the spatial organisation of heterogeneity. A meaningful and aggregate abstraction of spatial patterns is one of the promising means to gain fundamental insights into this complex interaction and can, moreover, be used as a tool to acquire a profound understanding of the major controls of catchment hydrology. In order to disclose such controls, pattern‐process relationships and the explanatory power of landscape metrics were tested by simulating the runoff of differently patterned virtual basins, generated by neutral landscape models and fractal networks and solved by a surface hydrological model composed of kinematic wave routing and Green‐Ampt infiltration. A total of 23 landscape metrics quantified the spatial patterns and were subsequently related to the functional connectivity, assessed as the proportion of internal runoff generation constituting the hydrological response at the outlet. Landscape metrics allowed the identification of dominant features of heterogeneity that explained the observed connectivity, and to disclose changes in control with class abundance. Therefore, landscape metrics are a useful tool for basin comparison and classification in terms of the dominant processes and the corresponding model structure requirements. Copyright © 2011 John Wiley & Sons, Ltd.     

Dependence of clinopyroxene composition on cooling rate in basaltic magmas: Implications for thermobarometry

The compositional variation of clinopyroxene and the partitioning of major elements between clinopyroxene and melt are estimated as a function of the cooling rate. Clinopyroxenes were crystallized under variable cooling regimes (15, 9.4, 3, 2.1, and 0.5 °C/min from 1250 down to 1000 °C) and at isothermal conditions of 1000 °C from a basaltic composition at a pressure of 500 MPa under anhydrous and hydrous (H₂O = 1.3 wt.%) conditions. The clinopyroxene chemistry shows that, as the cooling rate increases, crystals are progressively depleted in Ca, Mg, Fe²⁺ and Si and enriched in Na, Fe³⁺, Al (mainly Al^IV), and Ti. Di and Hd versus CaTs and CaFeTs form a continuous binary solid solution characterized by higher amounts of tschermakitic components with increasing cooling rate. Two parameters (DH = Di + Hd and TE = CaTs + CaFeTs + En) are calculated to describe the effect of cooling rate on the clinopyroxene composition. The variation of DH/TE with increasing cooling rate evidences the kinetic process induced by rapid cooling in basic rocks under hydrous and anhydrous conditions.Dynamic crystallization conditions affect the partitioning of major elements between clinopyroxene and melt; with increasing cooling rate, the value of crystal–melt partition coefficient departs from that obtained at the isothermal condition. However, in spite of these variations, the values of ^cpx–meltKd_Fe–Mg remain almost constant. Therefore, the Fe²–Mg exchange between clinopyroxene and melt is not suitable to prove the (dis)equilibrium conditions in basaltic cooling magmas, giving rise to possible mismatches in the application of thermobarometers. The results of our study are consistent with that observed at the margin of dikes or in the exterior portions of lavas, where the cooling rate is maximized and disequilibrium compositions of clinopyroxene have been found.     

Is there a possibility to correct fossil n-alkane data for postsedimentary alteration effects?

The long chain n-alkane composition of plant material can significantly differ between plant groups e.g. trees and grasses. Due to their relative recalcitrance, they have been employed in paleoecological research as molecular proxies for different types of vegetation. Most of those paleoenvironmental studies rely on the assumption that characteristic molecular fingerprints of plant material are preserved in the fossil organic material without significant alteration. However, there exists evidence that n-alkane distributions may change in the course of plant litter degradation. Here, the authors propose and discuss a conceptual approach to the correction of n-alkane patterns in paleosols and terrestrial sediments for postsedimentary alteration effects. This might have potential to improve paleoenvironmental reconstructions derived from these molecular fossils. In soil depth profiles typically a correlation between the OEP (odd over even predominance) and paleoecological valuable long-chain n-alkane ratios (LARs) can be found. Similar relationships have been also obtained from n-alkane records in paleosols. With the OEP serving as a proxy of microbial reworking, the correction procedure applies OEP vs. LAR regression functions to correct fossil LARs for degradation effects. The regression functions have been derived from modern soils. The application of the procedure and its significance for paleoecological interpretations is demonstrated on a case study of a loess-paleosol sequence (∼400–700 ka) in Romania. It is shown that changes in the C27/C31 n-alkane ratio at this site are closely related to degradation effects rather than to changes in the paleovegetation (e.g. tree vs. grass abundance). However, it was found that the C29/C31 ratio is a more suitable paleoenvironmental proxy at the Mircea Voda site. The results indicate that there is a future potential to correct fossil n-alkane ratios via the OEP/LAR relationship, however at the moment a general straight forward application of this approach might be critical due to lack of extended and diverse n-alkane records from modern soils. The need of more systematic n-alkane studies on soil profiles is highlighted to improve knowledge concerning dynamics and actual mechanisms of postsedimentary LAR and OEP changes.     

Precise two chronometer dating of Pleistocene travertine: The Th/U and Raex/Ra(0) approach

In order to determine the geochemical evolution of a freshwater limestone cave system located in central Switzerland (Hell Grottoes at Baar/Zug,) young postglacial tufaceous limestone and travertine precipitates were investigated using the ²³⁰Th/²³⁴U ingrowth system. Additional analyses of further radionuclides within the ²³⁸U decay chain, i.e. ²²⁶Ra and ²¹⁰Pb, showed that the Th/U chronometer started with insignificant inherited ²³⁰Th over the entire formation period of the travertine setting (i.e. ²³⁰Th(0)=0). A contribution from detrital impurities with ²³⁰Th/²³⁴U in secular equilibrium could be precisely subtracted by applying isochron dating of cogenetic phases and recently formed travertine. The resulting precise ²³⁰Th/²³⁴U formation ages were found to be consistent with the geological stratigraphy and were furthermore used to demonstrate the applicability of the next geologically important chronometer in the ²³⁸U-decay series, based on decay of excess ²²⁶Ra normalized to the initial, i.e.²²⁶Ra_ex/²²⁶Ra(0). This system is suitable for dating phases younger than 7000 yr when the correction of a detritus component increasingly limits the precision of the ²³⁰Th/²³⁴U chronometer. Analytical solutions of the coupled ²³⁴U/²³⁰Th/²²⁶Ra radionuclide system predicted that the ²²⁶Ra_ex/²²⁶Ra(0) chronometer is independent of the actual ²³⁰Th activity build up from decay of ²³⁴U, if the systems starts with zero inherited ²³⁰Th(0). The data set confirmed this hypothesis and showed furthermore that the initially incorporated ²²⁶Ra excess must have remained almost uniform in all limestone over a period of at least 7000 yr, i.e. 4–5 half-lives of ²²⁶Ra. This is concluded because (i) the ²²⁶Ra_ex/²²⁶Ra(0) ages agreed well with those derived from ²³⁰Th/²³⁴U, (ii) all data plot within uncertainty on the ²²⁶Ra_ex/²²⁶Ra(0) decay curve and (iii) the atomic Ba/Ca ratio was found to be constant in the travertine material independent of the sample ages. Provided that such boundary conditions hold, ²²⁶Ra_ex/²²⁶Ra(0) should be applicable to materials which are suitable for ²³⁰Th/²³⁴U dating in sedimentology and oceanography, i.e. travertine, corals, phosphorites, etc., and should strongly support ²³⁰Th/²³⁴U for samples that have been formed a few thousand years ago.     

Calpionellid biostratigraphy of the Upper Tithonian–Upper Valanginian interval in Western Sicily (Italy)

A revision of the calpionellid bio-chronostratigraphy in Western Sicily (Italy) was carried out, in order to update the taxonomy of this group, through the identification of some genera (Borziella, Longicollaria, Chitinoidella, Dobeniella, Sturiella, Borzaiella and Praecalpionellites) and species (Remaniella catalanoi Pop, Remaniella duranddelgai Pop, Remaniella colomi Pop, Remaniella borzai Pop, Remaniella filipescui Pop) recorded for the first time in the area. The studied sections, belonging to the Trapanese and Saccense Domains (Western Sicily), include at the base the upper portion of the Rosso Ammonitico Unit (Upper Tithonian), followed by the Lattimusa Formation (Lower Cretaceous). The quantitative and biostratigraphic analysis of the calpionellid assemblages allowed us to identify 13 assemblages and to define some important bioevents for the Upper Tithonian–Valangianian interval. The recorded calpionellid bioevents allowed us to recognize Zone/Subzone schema, which have been correlated with the bio-chronostratigraphy previously proposed for the Western Tethys. Editorial handling: M. Chiari (Guest) & J.-P. Billon-Bruyat     

Source and turnover of organic matter in agricultural soils derived from n-alkane/n-carboxylic acid compositions and C-isotope signatures

Agricultural soils are regarded as one potential sink for atmospheric CO₂ via photosynthetic fixation in plant biomass and subsequent transformation into soil organic matter upon soil diagenesis. The difference in C-isotope signatures of C₃- vs. C₄-plants allows for a natural isotopic labelling of soil organic matter after changes from C₃- to C₄-cropping. In this study, we demonstrate that isotopic shifts are paralleled by molecular signatures of C₃- vs. C₄-crop alkyl lipids. Turnover times vary significantly, based on cropping techniques. For grain-maize cropped soils at steady state average turnover times of 40 years for bulk SOC, 35 years for n-alkanes and 21 years for n-carboxylic acids were determined. Turnover times for silage-maize cropped soil at steady state were on average 250 years for bulk SOC, 60 years for n-alkanes and 49 years for n-carboxylic acids. Turnover times reported here for silage-maize cropped soils may be taken as maximum values only, because they derive from a single trial, which was affected by addition of anthropogenic refractory carbon. Discrimination of input from various plant parts (roots, stems and leaves) based on bulk C-isotopes is not feasible but can easily be achieved using compositions of carboxylic acids, especially the ratio of n-C₂₄ vs. n-C₂₂₊₂₆ and their respective C-isotope values. This enables delineation of the influence of different cropping techniques, e.g., silage- or grain-maize, on carbon storage in soils. Admixture of external sources of organic matter to the soil organic carbon pool of an urban site in Halle, Germany was identified based on alkyl lipid distributions. Nearby lignite mining was identified as a source for non-crop-derived alkyl lipids, primarily based on the elevated n-C₂₆-carboxylic acid content and heavier carbon isotopic signatures.     

Fault geometries from the space distribution of the 1990–1997 Sannio–Benevento earthquakes: inferences on the active deformation in Southern Apennines

In this study, we analyze the recent (1990–1997) seismicity that affected the northern sector (Sannio–Benevento area) of the Southern Apennines chain. We applied the Best Estimate Method (BEM), which collapses hypocentral clouds, to the events of low energy (M_{d max}=4.1) seismic sequences in order to constrain the location and geometry of the seismogenetic structures. The results indicate that earthquakes aligned along three main structures: two sub-parallel structures striking NW–SE (1990–1992, Benevento sequence) and one structure striking NE–SW (1997, Sannio sequence). The southernmost NW–SE structure, which dips towards NE, overlies the fault that is likely to be responsible for a larger historical earthquake (I_{o max}=XI MCS, 1688 earthquake). The northernmost NW–SE striking structure dips towards SW. The NE–SW striking structure is sub-vertical and it is located at the northern tip of the fault segment supposed to be responsible for the 1688 earthquake. The spatio-temporal evolution of the 1990–1997 seismicity indicates a progressive migration from SE (Benevento) to NW (Sannio) associated to a deepening of hypocenters (i.e., from about 5 to 12 km). Hypocenters cluster at the interface between the major structural discontinuities (e.g., pre-existing thrust surfaces) or within higher rigidity layers (e.g., the Apulia carbonates). Available focal mechanisms from earthquakes occurred on the recognized NW–SE and NE–SW faults are consistent with dip-slip normal solutions. This evidences the occurrence of coexisting NW–SE and NE–SW extensions in Southern Apennines.     

Adaptations and lifestyle in polar marine environments: a biological challenge for the study of fish evolution

The climatic features of Antarctic waters are more extreme and constant than in the Arctic. The Antarctic has been isolated and cold longer than the Arctic. The polar ichthyofaunas differ in age, endemism, taxonomy, zoogeographic distinctiveness and physiological tolerance to environmental parameters. The Arctic is the connection between the Antarctic and the temperate-tropical systems. Paradigmatic comparisons of the pathways of adaptive evolution of fish from both poles address the oxygen-transport system and the antifreezes of northern and southern species, (i) Haemoglobin evolution has included adaptations at the biochemical, physiological and molecular levels. Within the study of the molecular bases offish cold adaptation, and taking advantage of the information on haemoglobin amino acid sequence, we analysed the evolutionary history of the α and β globins of Antarctic, Arctic and temperate haemoglobins as a basis for reconstructing phylogenetic relationships. In the trees, the constant physico-chemical conditions of the Antarctic waters are matched by clear grouping of globin sequences, whereas the variability typical of the Arctic ecosystem corresponds to high sequence variation, reflected by scattered intermediate positions between the Antarctic and non-Antarctic clades. (ii) Antifreeze (glyco)proteins and peptides allow polar fish to survive at sub-zero temperatures. In Antarctic Notothenioidei the antifreeze gene evolved from a trypsinogen-like serine protease gene. In the Arctic polar cod the genome contains genes which encode nearly identical proteins, but have evolved from a different genomic locus–a case of convergent evolution.     

The Influence of Strong-Motion Duration on the Seismic Response of Masonry Structures

The influence of strong-motion duration on the response of saturated soils is clearly recognised and accounted for in the assessment of liquefaction potential. The degree to which duration of shaking influences damage to structures, however, remains a topic of debate, with resolution of the issue complicated by the variety of definitions of duration and the variety of structural behaviours, as well as the difficulty of decoupling the specific effect of duration from other features of the ground motion. A suite of seven structural models with strength and stiffness degrading characteristics, designed to reflect the seismic behaviour of masonry structures commonly encountered in many parts of Europe, are analysed using a suite of almost 500 strong-motion accelerograms. Correlations are explored between the damage, measured in terms of the strength degradation, and a range of strong-motion parameters, demonstrating that Arias intensity and spectral acceleration at the fundamental initial period of the structure are both reasonably good damage indicators for such structures. A significantly improved correlation is obtained by using the elastic spectral accelerations averaged over a period range from the initial period of the structure to a value approximately three times greater, reflecting the stiffness degradation as the shaking progresses. The scatter in the correlation is shown to be partially explained by differences in duration. This revised version was published online in July 2006 with corrections to the Cover Date.