Modeling nutrients profiles at the sediment–water interface. Calibration and validation from two climatically contrasted estuaries: Seine (France) and Somone (Senegal)

The dialysis porewater sampler, type Hesslein, allows sampling of sediment interstitial water according to a continuous gradient between sediment and the water column. Its equilibration time fluctuates according to the nature of sediment, so it has to be measured in each kind of sediment. The aim of this work is to develop a physical diffusion model in order to determine an equilibration time without using extensive field experiments. The model is validated by real nutrient concentration profiles obtained on two estuaries under different climates, moderate climate (estuary of the Seine) and tropical dry climate (estuary of Somone, Senegal). The results highlight that the equilibration of the dialysis porewater sampler is not homogeneous over the full sediment height investigated. Other sediment characteristics as compaction, rate of bioturbation or bacterial density must be taken into account in order to find a well-calculated value of the equilibration time.     

Optical extinction due to aerosols in the upper haze of Venus: Four years of SOIR/VEX observations from 2006 to 2010

The variability of the aerosol loading in the mesosphere of Venus is investigated from a large data set obtained with SOIR, a channel of the SPICAV instrument suite onboard Venus Express. Vertical profiles of the extinction due to light absorption by aerosols are retrieved from a spectral window around 3.0 μm recorded in many solar occultations (～200) from September 2006 to September 2010. For this period, the continuum of light absorption is analyzed in terms of spatial and temporal variations of the upper haze of Venus. It is shown that there is a high short-term (a few Earth days) and a long-term (～80 Earth days) variability of the extinction profiles within the data set. Latitudinal dependency of the aerosol loading is presented for the entire period considered and for shorter periods of time as well.     

Rubber tapper identities: Political-economic dynamics,livelihood shifts,and environmental implications in a changing Amazon

Rubber tappers promoted extractive reserves as a sustainable alternative to forest destruction in the Brazilian Amazon. However, the significance of rubber tapping itself has declined since the creation of extractive reserves, which raises questions about the contemporary cultural content of the rubber tapper identity. This paper therefore evaluates rubber tapper identity, using the case of the Chico Mendes Extractive Reserve (CMER) in Acre, Brazil. We first draw on household survey data from the CMER to construct a statistical model of who self-identifies as a rubber tapper. The model shows that socio-economic background, household assets, institutional context, and knowledge of the CMER’s management plan are relevant to understanding rubber tapper self-identification, but not resource management practices, including rubber tapping itself. We therefore pursue qualitative analysis of key informant interviews to better apprehend contemporary understandings of the “rubber tapper” identity, particularly in light of recent shifts in livelihoods from rubber tapping toward cattle ranching. The qualitative analysis shows that there are now several different foundations for self-identifying as a “rubber tapper,” and that there are disagreements concerning the acceptability of cattle ranching among “rubber tappers.” These findings bear implications for research on the relationship of livelihood-based identities with resource management practices and environmental change, as well as public policies that seek to reconcile regional development with forest conservation.     

Raman spectroscopic properties and Raman identification of CaS‐MgS‐MnS‐FeS‐Cr2FeS4 sulfides in meteorites and reduced sulfur‐rich systems

Raman spectra were acquired on a series of natural and synthetic sulfide minerals, commonly found in enstatite meteorites: oldhamite (CaS), niningerite or keilite ((Mg,Fe)S), alabandite (MnS), troilite (FeS), and daubreelite (Cr₂FeS₄). Natural samples come from three enstatite chondrites, three aubrites, and one anomalous ungrouped enstatite meteorite. Synthetic samples range from pure endmembers (CaS, FeS, MgS) to complex solid solutions (Fe, Mg, Ca)S. The main Raman peaks are localized at 225, 285, 360, and 470 cm^?1 for the Mg‐rich sulfides; at 185, 205, and 285 cm^?1 for the Ca‐rich sulfides; at 250, 370, and 580 cm^?1 for the Mn‐rich sulfides; at 255, 290, and 365 cm^?1 for the Cr‐rich sulfides; and at 290 and 335 cm^?1 for troilite with, occasionally, an extra peak at 240 cm^?1. A peak at 160 cm^?1 is present in all Raman spectra and cannot be used to discriminate between the different sulfide compositions. According to group theory, none of the cubic monosulfides oldhamite, niningerite, or alabandite should present first‐order Raman spectra because of their ideal rocksalt structure. The occurrence of broad Raman peaks is tentatively explained by local breaking of symmetry rules. Measurements compare well with the infrared frequencies calculated from first‐principles calculations. Raman spectra arise from activation of certain vibrational modes due to clustering in the solid solutions or to coupling with electronic transitions in semiconductor sulfides.     

Oxygen Isotope Composition Of Human Teeth And The Record Of Climate Changes In France (Lorraine) During The Last 1700 Years

In order to study climate variations during the last 1700 years in eastern France, fifty-eight oxygen isotope compositions of phosphate were measured in human tooth enamel. The individuals, who lived in Lorraine, are assumed to have drunk local water derived directly from rainfall. According to previous work, drinking water is the main source of oxygen that sets the isotopic composition of phosphatic tissues in humans. The empirical fractionation equation determined from our data combined with those of Longinelli’s one [Geochim. Cosmochim. Acta 48 (1984) 385] was used to calculate the oxygen isotope composition of meteoric waters. The mean air temperature was inferred from these isotope ratios and the Von Grafenstein et al.’s [Geochim. Cosmochim. Acta 60 (1996) 4025] relationship between δ¹⁸O and air temperature. Oxygen isotope composition of present-day individuals yields a mean air temperature of 9.9± 1.7 ^∘C which is consistent with meteorological data. Application of this method to historical individuals results in mean air temperatures estimates 0 to 3 ^∘C higher than present-day air temperature. These warm air temperatures are not realistic during the so-called Little Ice Age for which an air-cooling of about 0.5 to 2 ^∘C has been documented. We propose that these relatively high δ¹⁸O values of human tooth enamel reflect higher mean δ¹⁸O values of meteoric water which can be attributed to an increased proportion of summer rainfall during the “Little Ice Age” time frame in Lorraine.     

The detection of new methanol masers in the 5−1–40 E line

Forty-eight objects were detected in the 5_?1–4₀ E methanol line at 84.5 GHz during a survey of Class I maser sources. Narrow maser features were found in 14 of these. Broad quasi-thermal lines were detected toward other sources. One of the objects with narrow features at 84.5 GHz, the young bipolar outflow L1157, was also observed in the 8₀–7₁ A ⁺ line at 95.2 GHz; a narrow line was detected at this frequency. Analysis showed that the broad lines are usually inverted. The quasi-thermal profiles imply that there are no more than a few line opacities. These results confirm the plausibility of models in which compact Class I masers appear in extended sources as a result of a preferential velocity field.     

Enregistrements sismologiques de l'explosion sur le site de l'usine AZF (Toulouse,France)Seismological records of an explosion at the AZF chemical complex in Toulouse,France

This study presents a detailed analysis of the seismic records of a strong explosion that occurred on 21 September 2001 at a chemical complex located south of Toulouse, France, and provoked important damages. The explosion, which is equivalent to a 3.4 magnitude earthquake, has been recorded at most of the stations of the National Seismological Network, as well as at a station under test at the ‘Observatoire Midi-Pyrénées’, 4.2 km away from the epicentre. The main seismic phases are interpreted using the known crustal structures, and a modelling with synthetic seismograms is performed. To cite this article: A. Souriau et al., C. R. Geoscience 334 (2002) 155–161.     

Quantitative assessment of the reliability of chironomid remains in paleoecology: effects of count density and sample size

Random distributions for a wide range (1–100,000) of chironomid head capsules (HC) were simulated on a 1-m² surface. The number of HC found in circular surfaces equivalent to standard core diameters (90 and 63 mm) was estimated 1000 times, over the range of tested densities. For each number of HC found in the samples, the range of simulated densities was estimated using a threshold probability (p > 0.95). This enabled us to develop equations to infer HC density from sample counts. Because of the threshold probability for comparable sample counts, the equations yield higher estimated densities under a random distribution than for a regular distribution. The probability of sampling at least one HC was >0.95 for densities of 900 HC m^?2 for the 90-mm core and 1400 HC m^?2 for the 63-mm core. For a specific sample count, the range of actual densities was ~10 times higher for the 63-mm core than the 90-mm core. Comparison with field larval densities revealed that most densities were too low to be suitable for annually resolved reconstruction of a quantitative signal, using current corer sizes, although a large number of populations can support sub-decadal analyses. Nonetheless, some lakes exhibit population sizes large enough to reconstruct robust quantitative estimates of past chironomid abundances. This work provides guidance to reconstruct species dynamics and fine-scale time series analyses in paleoecology.     

Major and trace element geochemistry in Zeekoevlei, South Africa: A lacustrine record of present and past processes

This study reports a multi-parameter geochemical investigation in water and sediments of a shallow hyper-eutrophic urban freshwater coastal lake, Zeekoevlei, in South Africa. Zeekoevlei receives a greater fraction of dissolved major and trace elements from natural sources (e.g., chemical weathering and sea salt). Fertilizers, agricultural wastes, raw sewage effluents and road runoff in contrast, constitute the predominant anthropogenic sources, which supply As, Cd, Cu, Pb and Zn in this lake. The overall low dissolved metal load results from negligible industrial pollution, high pH and elevated metal uptake by phytoplankton. However, the surface sediments are highly polluted with Pb, Cd and Zn. Wind-induced sediment resuspension results in increased particulate and dissolved element concentrations in bottom waters. Low C/N ratio (10) indicates primarily an algal source for the sedimentary organic matter. Variation in sedimentary organic C content with depth indicates a change in primary productivity in response to historical events (e.g., seepage from wastewater treatment plant, dredging and urbanization). Primary productivity controls the enrichment of most of the metals in sediments, and elevated productivity with higher accumulation of planktonic debris (and siltation) results in increased element concentration in surface and deeper sediments. Aluminium, Fe and/or Mn oxy-hydroxides, clay minerals and calcareous sediments also play an important role in adsorbing metals in Zeekoevlei sediments.