Streamflow variability and its relationship with climate indices in western rivers of Argentina

The objective of this study was to examine the streamflow variability of Argentinean Andean basins (22°–52°S). Trends and step changes of seven hydrological variables were analysed. In addition, relationships between the hydrological variables and Pacific Decadal Oscillation (PDO), Niño 3.4, and Southern Annular Mode (SAM) indices were analysed. Most streamflow variables showed upward trends in the northwest and central-western basins, while downward trends were identified in the Patagonia (southwestern) region. Streamflow of the central-western and Patagonian basins was positively correlated with the Niño 3.4 index. Moreover, an inverse relationship with the SAM was found in watersheds south of 37°S. Positive step changes associated with the PDO phases in the north and central-western basins in the mid-1970s were detected, while negative step changes resulted in Patagonia between 1970 and 2000. This research provides new evidence of the influence of major climate modes on streamflow variability in the western rivers of Argentina.     

Off-shelf fluxes of labile materials by an upwelling filament in the NW Iberian Upwelling System

Daily changes in the concentrations of carbon and nitrogen species were monitored during the course of a Lagrangian drifter experiment in a recurrent upwelling filament south of Cape Finisterre (NW Iberian Upwelling System). A drifting buoy released at the southern edge of the upwelling centre generated by the Cape moved 60km southwestwards from 3 to 7 August 1998. Organic matter in the 50m deep study water mass (average 77±2 μM C) consisted of: 57μM C of dissolved organic matter (DOM) with a C/N molar ratio of 19±2; 6μM C of DOM with a C/N ratio of 9±2, and 14μM C of 50% DOM and 50% suspended organic matter (POM_susp) with a C/N ratio of 6.0±0.4.Net conversion of consumed inorganic salts into accumulated TOM=POM_susp+DOM was 40% for nitrogen and 30% for carbon. Since the parcel of water crossed the shelf-edge, these conversion efficiencies are equivalent to net horizontal export-ratio of 0.4 and 0.3 respectively. A second drifter was deployed in the offshore-end of the filament, and was displaced 20km west between 14 and 17 August 1998. Nitrate was exhausted in the surface water and no significant changes were observed in the variables measured during the course of the second experiment. Low C/N ratios (6.5±0.4) and rapid POM_susp/DOM inter-conversion in the 20 μM C excess observed in the study volume points to the persistence of the labile materials formed on the shelf during transport to the ocean. Our data demonstrate

a) the key role of upwelling filaments in off-shelf export of organic materials and

b) the major contribution of DOM to this horizontal export, a previously unaccounted amount.

The high nitrogen content of the materials exported make them attractive organic substrates for use by microbial populations in the adjacent oligotrophic ocean.     

Negligent killing of scientific concepts: the stationarity case

Abstract

In scientific vocabulary, the term “process” is used to denote change in time. Even a stationary process describes a system changing in time, rather than a static one that keeps a constant state all the time. However, this is often missed, which has led to misuse of the term “nonstationarity” as a synonym of “change”. A simple rule to avoid such misuse is to answer the question: can the change be predicted in deterministic terms? Only if the answer is positive is it legitimate to invoke nonstationarity. In addition, we should have in mind that models are made to simulate the future rather than to describe the past; the past is characterized by observations (data). Usually future changes are not deterministically predictable and thus the models should, on the one hand, be stationary and, on the other hand, describe in stochastic terms the full variability, originating from all agents of change. Even if the past evolution of the process of interest contains changes explainable in deterministic terms (e.g. urbanization), it is better to describe the future conditions in stationary terms, after “stationarizing” the past observations, i.e. adapting them to represent the future conditions.     

A site amplification factor map of the Iberian Peninsula and the Balearic Islands

Considering the lack of site effect cartography in the Iberian Peninsula region to be related to the strong motion data, we present a site amplification factor map covering the Iberian Peninsula and the Balearic Islands. Steps leading to produce the map have included the classification of geological units from the 1:1,000,000 scale Geological Map of Spain into six site classes characterized on a seismic response basis, and the calculation, for every site class, of both short-period and mid-period amplification factors. In order to test the validity and applicability of the map, we have calculated the synthetic seismic intensity in the particular localities where several past earthquakes were felt, supposing a point source approximation. The synthetic intensities have been obtained with and without site amplification factors, resulting in two types of synthetic isoseismals maps that have been compared with the corresponding observed isoseismals. As the amplification factors obtained are only applicable to the linear domain, the synthetic intensities greater than VII are only illustrative. A main conclusion has been drawn about the fact that synthetic isoseismals with site amplification factor approach to the related observed isoseismals in a higher degree than synthetic isoseismals without site amplification factor. In addition, the resemblances between the synthetic isoseismals produced with site amplification factors and the corresponding observed isoseismals have been found to be more evident at shorter epicentral distances, provided that intensities are lower than VIII, and therefore, we remain in the linear domain.     

Mechanistic and Kinetic Study of the Gas-Phase Reaction of Atomic Chlorine with Cyclohexanone using an Absolute and a Relative Technique; Influence of Temperature

The reaction of Cl with cyclohexanone (1) was investigated, for the first time, as a function of temperature (273–333 K) and at a low total pressure (1 Torr) with helium as a carrier gas using a discharge flow-mass spectrometry technique (DF-MS). The resulting Arrhenius expression is proposed, k ₁= (7.7 ± 4.1) × 10^–10 exp[–(540 ± 169)/T]. We also report a mechanistic study with the quantitative determination of the products of the reaction of Cl with cyclohexanone. The absolute rate constant derived from this study at 1 Torr of total pressure and room temperature is (1.3 ± 0.2) × 10^–10 cm³ molecule^–1 s^–1. A yield of 0.94 ± 0.10 was found for the H-abstraction channel giving HCl. In relative studies, using a newly constructed relative rate system, the decay of cyclohexanone was followed by gas chromatography coupled with flame-ionisation detection. These relative measurements were performed at atmospheric pressure with synthetic air and room temperature. Rate constant measured using the relative method for reaction (1) is: (1.7 ± 0.3) × 10^–10 cm³ molecule^–1 s^–1. Finally, results and atmospheric implications are discussed and compared with the reactivity with OH radicals.     

3EG J2020+4017, the γ-Cygni source—before GLAST

The Cygnus region of the Milky Way is prolific in star formation and presents extended diffuse γ-ray emission with a few γ-ray point sources. Among them is 3EG J2020+4017, the brightest of the unidentified EGRET sources, positionally coincident with the supernova remnant G78.2+2.1. Even though the EGRET and multi-wavelength data have not provided a conclusive identification for this γ-ray loud, but otherwise faint object, the evidence favors a pulsar like source. The EGRET photon data lack the signal-to-noise ratio required for a period search, but will serve as a valuable timing baseline extension in the case that GLAST confirms the pulsar nature of the γ-Cygni source. Work sponsored by CONACyT grant SEP-2003-C02-42611.     

Do we have enough pieces of the jigsaw to integrate CO2 fluxes in the coastal ocean?

Annually integrated air-water CO₂ flux data in 44 coastal environments were compiled from literature. Data were gathered in 8 major ecosystems (inner estuaries, outer estuaries, whole estuarine systems, mangroves, salt marshes, coral reefs, upwelling systems, and open continental shelves), and up-scaled in the first attempt to integrate air-water CO₂ fluxes over the coastal ocean (26×10⁶ km²), taking into account its geographical and ecological diversity. Air-water CO₂ fluxes were then up-scaled in global ocean (362×10⁶ km²) using the present estimates for the coastal ocean and those from Takahashi et al. (2002) for the open ocean (336×10⁶ km²). If estuaries and salt marshes are not taken into consideration in the up-scaling, the coastal ocean behaves as a sink for atmospheric CO₂(−1.17 mol C m⁻² yr⁻¹) and the uptake of atmospheric CO₂ by the global ocean increases by 24% (−1.93 versus −1.56 Pg C yr⁻¹). The inclusion of the coastal ocean increases the estimates of CO₂ uptake by the global ocean by 57% for high latitude areas (−0.44 versus −0.28 Pg C yr⁻¹) and by 15% for temperate latitude areas (−2.36 versus −2.06 Pg C yr⁻¹) At subtropical and tropical latitudes, the contribution from the coastal ocean increases the CO₂ emission to the atmosphere from the global oceam by 13% (0.87 versus 0.77 Pg C yr⁻¹). If estuaries and salt marshes are taken into consideration in the upscaling, the coastal ocean behaves as a source for atmospheric CO₂ (0.38 mol C m⁻² yr⁻¹) and the uptake of atmospheric CO₂ from the global ocean decreases by 12% (−1.44 versus −1.56 Pg C yr⁻¹) At high and subtropical and tropical latitudes, the coastal ocean behaves as a source for atmospheric CO₂ but at temperate latitudes, it still behaves as a moderate CO₂ sink. A rigorous up-scaling of air-water CO₂ fluxes in the coastal ocean is hampered by the poorly constrained estimate of the surface area of inner estuaries. The present estimates clearly indicate the significance of this biogeochemically, highly active region of the biosphere in the global CO₂ cycle.     

Water column characterisation on the Azores platform and at the sea mounts south of the archipelago

This study provides data concerning the hydrography and water chemistry of the Atlantic region between 29-38° N and 27-31° W, and establishes background values for dissolved Cu, Cd, Pb and As. Three water masses were identified: the Eastern North Atlantic Central Water (ENACW), the Mediterranean Water (MW) and the North Atlantic Deep Water (NADW). The ENACW exhibits a clear meridional gradient of temperature and salinity, with comparatively high values at the southern sites and lower values on the Azores platform. The ENACW, which includes the euphotic zone, also had comparatively high concentrations of oxygen and lower concentrations of nutrients and metals. The Cu, Cd and Pb results suggest that new background concentrations for OSPAR Region V (the Wider Atlantic) should be established as follows: 0.15-13nM for Cu, 0.05-1.4nM for Cd and 0.03-5nM for Pb. The background concentrations of As for OSPAR Region V should be 7-28nM.     

The effect of the Fernando de Noronha plume on the mantle lithosphere in north-eastern Brazil

New xenolith occurrences in the Cenozoic alkali basalts of north-eastern Brazil have been studied in order to constrain the possible imprint on the continental mantle lithosphere of its passage over the Fernando de Noronha plume and the regional mantle processes. Texturally, the lherzolite and harzburgite xenoliths define three groups: group 1, porphyroclastic; group 2, protogranular; group 3, transitional between groups 1 and 2. Equilibrium temperatures are highest for group 1 and lowest for group 2. Clinopyroxenes from group 1 peridotites have Primitive Mantle (PM)-normalised REE patterns varying from L-MREE-enriched convex-upward, typical of phases in equilibrium with alkaline melts, to LREE-enriched, spoon-shaped, to LREE-enriched, steadily fractionated in a wehrlite. Group 2 clinopyroxenes show patterns slightly depleted in LREE to nearly flat. The M-HREE are at 3–5 ×PM concentration level, as typical in fertile lithospheric lherzolites. Most of group 3 clinopyroxenes show LREE-depleted patterns similar to the group 2 ones, but in two samples the clinopyroxenes are characterised by LREE-enriched, spoon-shaped profiles. Sr and Nd isotopes of the group 1 clinopyroxenes form an array between DM and EMI-like components, both of them are also present in the host basalts. Melts estimated to be in equilibrium with the group 1 clinopyroxenes having L-MREE-enriched, convex-upward patterns are similar to the Cenozoic alkaline magmas. The groups 2 and 3 clinopyroxenes define two distinct compositional fields at higher ¹⁴³Nd/¹⁴⁴Nd values, correlated with their LREE composition. The isotopes of the groups 2 and 3 LREE-depleted clinopyroxenes form an array from DM towards the isotopic composition of Mesozoic tholeiitic basalts from north-eastern Brazil. Melts in equilibrium with these clinopyroxenes are similar to these basalts, thus suggesting that such xenoliths record geochemical imprint from older melt-related processes.

The LREE-enriched spoon-shaped group 3 clinopyroxenes are characterised by the highest ¹⁴³Nd/¹⁴⁴Nd values at any given ⁸⁷Sr/⁸⁶Sr composition. These results are interpreted in terms of a lithospheric mantle section which underwent thermo-chemical and mechanical erosion by infiltration of asthenospheric alkali basalts having EMI-like isotope characteristics during Cenozoic time. At that time, the lithospheric mantle consisted of fertile lherzolites and harzburgites recording the geochemical imprint of Mesozoic mantle processes. The onset of the interaction between lithospheric peridotites and alkaline melts was characterised by the porous flow percolation of small melt volumes that induced chromatographic enrichments in highly incompatible elements and the isotope signature of the spoon-shaped, group 3 clinopyroxenes. Group 1 peridotites represent the base of the lithospheric column eroded by the ascending alkaline melts, whereas the group 2 documents the shallower lithospheric section, with group 3 being the transition. The similarity of processes and isotope components in the protogranular xenoliths from Fernando de Noronha area and north-eastern Brazil supports the hypothesis that the lithosphere beneath Fernando de Noronha is a detached portion of the continental one. Furthermore, the similarity in terms of textural and geochemical features documented by the mantle samples coming from the two different regions seems to confirm the interference of the two regions with the same plume.