Impacts of growth in resource use and human population on the Nechako River: A major tributary of the Fraser River, British Columbia, Canada

Hydroelectric development, forest exploitation, agricultural land use and related human population numbers have increased rapidly during the last 40 years, in the basin of the Nechako River, a major tributary system of the Fraser River. The Kemano project of the Aluminum Company of Canada Ltd. begun in 1950, was the largest industrial scheme in the area. A key feature of the first stage of it was a dam which diverted about 40% of flow of the south branch of the Nechako River, through a tunnel in the mountains, to the Pacific Ocean. In 1987 an agreement for the Kemano Completion Project (KCP), which would have diverted 87% of the flow, was signed. This final phase of the project would have put important fisheries resources of the upper Fraser River at high risk. Mitigation for fisheries protection were inadequate or untested in the system at the time. Potential cumulative impacts of water abstraction, elevated pollution levels, increased water temperature and natural sediment were not addressed. In January 1995 KCP was cancelled but there remain at present no adequate measures to protect the fish and the river ecosystem. These measures are to be negotiated in the future. Future management of the whole Kemano development must provide biologically realistic flow and temperature regimes in the Nechako River, and must deal with cumulative impacts of population and industrial growth. To achieve sustainability of fisheries in the Nechako River and upper Fraser watershed the present approach to the Kemano development must be changed fundamentally. The future of the Kemano development must be set in the context of the whole future of the upper Fraser system. Continued growth and development, as has occurred in the upper Fraser and total basin, can not go on without inimical changes to ecosystem conditions and loss of fisheries resources.     

Photochemistry and Vertical Transport in Io's Atmosphere and Ionosphere

We present an updated model for the photochemistry of Io's atmosphere and ionosphere and use this model to investigate the sensitivity of the chemical structure to vertical transport rates. SO₂is assumed to be the dominant atmospheric gas, with minor molecular sodium species such as Na₂S or Na₂O released by sputtering or venting from the surface. Photochemical products include SO, O₂, S, O, Na, NaO, NaS, and Na₂. We consider both “thick” and “thin” SO₂atmospheres that encompass the range allowed by recent HST and millimeter-wave observations, and evaluate the possibility that O₂and/or SO may be significant minor dayside constituents and therefore likely dominant nightside gases. The fast reaction between S and O₂limits the column abundance of O₂to ∼10⁴less than that calculated by Kumar (J. Geophys. Res.87, 1677–1684, 1982; 89(A9), 7399–7406, 1984) for a pure sulfur/oxygen atmosphere. If a significant source of NaO₂or Na₂O were supplied by the surface and mixed rapidly upward, then oxygen liberated in the chemical reactions which also liberate free Na would provide an additional source of O₂. Fast eddy mixing will enhance the transport of molecular sodium species to the exobase, in addition to increasing the vertical transport rate of ions. Ions produced in the atmosphere will be accelerated by the reduced corotation electric field penetrating the atmosphere. These ions experience collisions with the neutral gas, leading to enhanced vertical ion diffusion. The dominant ion, Na⁺, is lost primarily by charge exchange with Na₂O and/or Na₂S in the lower atmosphere and by diffusion through the ionopause in the upper atmosphere. The atmospheric column abundance of SO, O₂, and the upper atmosphere escape rates of Na, S, O, and molecular sodium species are all strong functions of the eddy mixing rate. Most atmospheric escape, including that of molecular sodium species, probably occurs from the low density “background” SO₂atmosphere, while a localized high density “volcanic” SO₂atmosphere can yield an ionosphere consistent with that detected by the Pioneer 10 spacecraft.     

Coronal magnetic fields from microwave polarization observations

The solar active region (AR) 7530 was observed at 6 cm on July 3 and 4, 1993 with the Westerbork Synthesis Radio Telescope, using a multi-channel receiver with very narrow bandwidth. We compare the radio data with Yohkoh SXT observations and with the magnetic field extrapolated from the Marshall vector magnetograms in the force-free and current-free approximations. The comparison with soft X-rays shows that, although a general agreement exists between the shape of the radio intensity map and the X-ray loops, the brightness temperature, T _b, obtained using the parameters derived from the SXT is much lower than that observed. The comparison with the extrapolated photospheric fields shows instead that they account very well for the observed T _b above the main sunspots, if gyroresonance emission is assumed. In the observation of July 4 an inversion and strong suppression of the circular polarization was clearly present above different portions of the AR, which indicates that particular relationships exist between the electron density and the magnetic field in the region where the corresponding lines of sight cross the field quasi-perpendicularly. The extrapolated magnetic field at a much higher level ( 10¹⁰ cm), satisfies the constraints required by the wave propagation theory all over the AR. However, a rather low electron density is derived.     

Reservoir timescales for anthropogenic CO2 in the atmosphere

Non-steady state timescales are complicated and their application to specific geophysical systems requires a common theoretical foundation. We first extend reservoir theory by quantifying the difference between turnover time and transit time (or residence time) for time-dependent systems under any mixing conditions. We explicitly demonstrate the errors which result from assuming these timescales are equal, which is only true at steady state. We also derive a new response function which allows the calculation of age distributions and timescales for well-mixed reservoirs away from steady state, and differentiate between timescales based on gross and net fluxes. These theoretical results are particularly important to tracer-calibrated "box models" currently used to study the carbon cycle, which usually approximate reservoirs as well-mixed. We then apply the results to the important case of anthropogenic CO2 in the atmosphere, since timescales describing its behavior are commonly used but ambiguously defined. All relevant timescales, including lifetime, transit time, and adjustment time, are precisely defined and calculated from data and models. Apparent discrepancies between the current, empirically determined turnover time of 30-60 years and longer model-derived estimates of expected lifetime and adjustment time are explained within this theoretical framework. We also discuss the results in light of policy issues related to global warming, in particular since any comparisons of the "lifetimes" of different greenhouse gases (CO2, CH4, N2O, CFC's etc.) must use a consistent definition to be meaningful.     

Cu 2p absorption spectroscopy as a probe for the site occupancy of (ZnxCu1−x)WO4 solid solution

The solid solution sanmartinite (ZnWO₄)—cuproscheelite (CuWO₄) has been studied using Cu 2p X-ray absorption spectroscopy. While a single L₃ absorption peak is observed for CuWO₄, two distinct L₃ absorption peaks with a separation of ～0.8 eV are observed for the intermediate samples in the solid solution. The two peaks represent distinct Cu sites: one with all CuO₆ next nearest neighbours in the (Cu,Zn)O₆ chains, another having at least one ZnO₆ next nearest neighbour. Both sites show a linear increase in covalency as a function of increasing Cu-content. The relative intensities of the two absorption peaks is dependent upon the Cu-content and has been used to model the site occupancies. The results reveal that the local structural effects can be associated with a composition-dependent structural phase transition from P2/c (ZnWO₄) to P $\bar 1$ (CuWO₄). Deviations from a single-site model are explained in terms of the local environments, and evidence for site preferences and local clustering are explored.     

Isotope and trace element evidence for three component mixing in the genesis of the North Luzon arc lavas (Philippines)

Post-3Ma volcanics from the N Luzon arc exhibit systematic variations in ⁸⁷Sr/⁸⁶Sr (0.70327–0.70610), ¹⁴³Nd/¹⁴⁴Nd (0.51302–0.51229) and ²⁰⁸Pb^*/²⁰⁶Pb^* (0.981–1.035) along the arc over a distance of about 500 km. Sediments from the South China Sea west of the Manila Trench also exhibit striking latitudinal variations in radiogenic isotope ratios, and much of the isotopic range in the volcanics is attributed to variations in the sediment added to the mantle wedge during subduction. However, Pb-Pb isotope plots reveal that prior to subduction, the mantle end-member had high 8/4, and to a lesser extent high 7/4, similar to that in MORB from the Indian Ocean and the Philippine Sea Plate. Th isotope data on selected Holocene lavas indicate a source with unusually high Th/U ratios (4.5–5.5). Combined trace element and isotope data require that three end-members were implicated in the genesis of the N Luzon lavas: (1) a mantle wedge end-member with a Dupal-type Pb isotope signature, (2) a high LIL/HFS subduction component interpreted to be a slab-derived hydrous fluid, and (3) an isotopically enriched end-member which reflects bulk addition (<5%) of subducted S China Sea terrigenous sediment. The ⁸⁷Sr/⁸⁶Sr ratios in the volcanics show a restricted range compared with that in the sediments, and this contrasts with ¹⁴³Nd/¹⁴⁴Nd and ²⁰⁸Pb^*/²⁰⁶Pb^*, both of which have similar ranges in the volcanics and sediments. Such differences imply that whereas the isotope ratios of Nd, Pb and Th are dominated by the component from subducted sediment, those of Sr reflect a larger relative contribution from the slab-derived fluid.     

The inverse planetary problem: a numerical treatment

The so-called inverse planetary problem can be stated as follows: given the distances from the centre, masses, and radii of (say) three planets of a planetary system, find the optimum polytropic index, mass, and radius of their star, and also other quantities of interest, which depend either explicitly or implicitly on the foregoing ones (e.g., central and mean density, central and mean pressure, central and mean temperature, etc.). It is hereafter tacitly assumed that the system is opaque with respect to observations concerning periods of planetary otbits; hence, we cannot have any relevant estimates due to the well-known period laws. In the present paper, the inverse planetary problem is treated numerically on the basis of the so-called global polytropic model, developed recently by the first author.     

Quasi-periodical structures in the galaxy populations: mass and luminosity functions for the cluster galaxies

A search and estimation of the statistical significance of the quasi-periodical structures (QPS) has been carried out: for the luminosity function of the galaxies in a few rich clusters; for the integrated mass function of galaxies in the superclusters identified via = 21 cm observations. Some statistically significant QPS have been revealed. The periods for these structures are in agreement between each other, at this basis the hypothesis has been proposed that an effect of the QPS at the level of galaxies has some universal character. Frequency doubling has been discovered for these QPS.     

Interstellar water in meteorites?

D/H ratios of two meteorites (Renazzo CR and Semarkona LL3), which are known to exhibit the largest departures from the terrestrial hydrogen isotopic ratios, have been determined with the CRPG Nancy ion microprobe. Correlations between the D/H ratios and the chemical compositions (H2O, K, Si, C/H) of plausible hydrogen carriers were observed. From these correlations, it is possible to show that, contrary to previous interpretations, phyllosilicates are the carriers of the deuterium-rich hydrogen in Semarkona and Renazzo: 870 x 10(-6) > or = D/H > or = 670 x 10(-6) (+4600 > or = deltaD > or = 3300%) and > or = 320 x 10(-6) (deltaD > or = 1050%), respectively. Hydrogen is also present in the chondrules of these two deuterium-rich meteorites. The large differences in D/H ratios between matrix (up to 700 x 10(-6), deltaD up to +3500%) and chondrules (from 120 x 10(-6) (deltaD = -230%) to 230 x 10(-6) (deltaD = +475%)) show that hydrogen in chondrules cannot originate from the matrix by simple contamination or diffusion processes. The high D/H ratios measured in water-bearing minerals could not have been produced thermally within a dense solar nebula. Chemical reactions (i.e., involving ions or radicals), taking place in interstellar space or in the outer regions of the nebula at 110-140K are presently the only conceivable mechanisms capable of yielding such isotopic enrichments. Water in these meteorites should no longer be considered as a simple product of nebular condensation under equilibrium thermodynamic conditions at T > or = 160K.